Bacilli are gram-positive bacteria that secrete a number of industrially useful enzymes, which can be produced cheaply in high volume by fermentation. Examples of secreted Bacillus enzymes are the subtilisin serine proteases, zinc containing neutral proteases, alpha-amylases, and cellulases. Bacillus proteases are widely used in the textile, laundry and household industries (Galante, Current Organic Chemistry, 7:1399-1422, 2003; and Showell, Handbook of Detergents, Part D: Formulation, Hubbard (ed.), NY: Taylor and Francis Group, 2006). The classification of proteases found in microorganisms is based on their catalytic mechanism which results in four groups: the serine proteases; metallo-proteases; cysteine proteases; and aspartic proteases. The serine proteases have alkaline pH optima, the metalloproteases are optimally active around neutrality, and the cysteine and aspartic enzymes have acidic pH optima (Biotechnology Handbooks, Bacillus. vol. 2, edited by Harwood, 1989 Plenum Press, New York). Although serine proteases have long been known in the art of industrial enzymes, there remains a need for engineered proteases that are suitable for particular conditions and uses.
The present disclosure provides, inter alia, thermolysin enzymes, nucleic acids encoding the same, and compositions and methods related to the production and use thereof.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position of the thermolysin enzyme variant, wherein at least 75% of the modifications tested at the productive position meet at least one of the following criteria: a) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.9, and in addition have a PI for any one of these tests that is greater than or equal to 1.0; b) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.8, and in addition have a PI for any one of these tests that is greater than or equal to 1.2; c) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.5, and in addition have a PI for any one of these tests that is greater than or equal to 1.5; and wherein the productive position is selected from the group consisting of 2, 26, 47, 49, 53, 65, 87, 91, 96, 108, 118, 128, 154, 179, 196, 197, 198, 199, 209, 211, 217, 219, 225, 232, 256, 257, 259, 261, 265, 267, 272, 276, 277, 286, 289, 290, 293, 295, 298, 299, 300, 301, 303, 305, 308, 311, and 316, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the modification is selected from the group consisting of 2 (T,F,L,P,S,V,W,Y,Q,A,C,I,K,M), 26 (T,K,L,R,V,Y,W,F,G,H,I,M,C,D), 47 (R,A,C,H,K,N,D,E,G,L,M,Q,T), 49 (T,A,D,F,H,I,S,W,L,N,Q,V,E,M,Y), 53 (S,F,H,I,M,Q,T,W,K,R,A,N,V,C,L), 65 (S,I,M,Q,V,L,T,W,A,D,E,P,Y), 87 (V,D,E,G,I,S,P,R,T,C,K,L,M,N,Q,W,Y), 91 (L,D,E,F,K,M,P,Q,S,A,N,R,W,Y), 96 (N,C,D,I,V,F,T,G,H,Q,R,S,W,K,L,Y), 108 (Q,C,E,F,H,A,D,I,K,N,L,M), 118 (S,C,G,E,A,D,M,Q,R,T,V), 128 (Q,C,D,E,R,S,V,I,K,A,L,Y), 154 (G,L,Q,S,T,D,I,W,C,N,A,H,K,M,Y), 179 (Y,A,D,H,M,N,Q,S,T,W,F), 196 (G,D,E,T,K,R,V,H,L,Y,A,W), 197 (I,D,K,L,T,V,W,Y,A,H,N,E,Q,R,F,C), 198 (S,C,E,F,G,H,I,P,Q,T,V,M,N,R,W,A,K), 199 (G,C,E,F,H,Q,S,T,W,L,A,Y), 209 (A,D,E,L,S,T,V,G,I,K,P,R,Y,C,M), 211 (Y,A,C,D,F,G,H,I,L,N,Q,S,T,E,R), 217 (Y,Q,S,T,V,W,G,A,F,M,N,C,L), 219 (K,D,F,G,H,I,M,N,Q,T,A,E,R,S), 225 (Q,D,G,H,I,P,V,W,A,M,R,C,E,K,L,S), 232 (I,C,E,F,K,M,N,Q,W,G,L,R,S,T,V,Y), 256 (V,L,T,K,A,D,F,G,H,R,S,N), 257 (G,C,D,E,L,N,P,Q,S,T,Y,K,R), 259 (G,A,C,E,F,H,L,M,W,K,R,N,S,T), 261 (D,A,N,P,V,W,G,H,I,S), 265 (K,A,C,D,M,P,Q,S,G,I,L,R,N), 267 (F,E,G,N,S,V,W,A,C,H,I,K,L,M,T,Y), 272 (T,E,L,V,W,P,Y,C,F,N,Q,A,K), 276 (T,C,F,I,P,Q,W,H,A,L,V,Y), 277 (P,Q,S,T,E,F,G,H,N,R,V,W,A,D,Y), 286 (A,D,E,F,G,H,I,S,P,C,Q,R,T,K,L,M,N,Y), 289 (V,C,E,F,G,I,N,S,W,R,T,L,M,Y,A), 290 (Q,C,D,F,G,L,W,Y,R,T,V,A,H,N), 293 (T,C,E,F,G,H,Q,S,N,V,W,A,I,K,L,M,Y), 295 (L,C,I,N,T,V,F,G,A,K,M,W), 298 (S,C,T,W,Y,E,N,P,A,G,K,M,R), 299 (T,C,F,L,M,R,W,P,D,Q,N,A,K), 300 (S,C,K,M,R,Y,I,L,H,P,V,W,A,G,T,D,N), 301 (Q,E,H,P,R,L,C,F,G,W,M,S,T,V,K), 303 (V,C,H,G,K,L,R,W,A,P,Y), 305 (S,G,I,L,N,W,Y,Q,H,T,V,A,K,M), 308 (Q,C,D,F,G,I,M,R,V,W,Y,A,L), 311 (D,C,E,F,G,I,Q,S,T,A,K,L,M,V,W,Y), and 316 (K,D,E,F,G,H,L,N,P,Q,R,S,V,W,Y,A,M), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position of the thermolysin enzyme variant, wherein at least 40% but less than 75% of the modifications tested at the productive position meet at least one of the criteria listed in a, b, and c (supra), and wherein the productive position is selected from the group consisting of 1, 4, 17, 25, 40, 45, 56, 58, 61, 74, 86, 97, 101, 109, 149, 150, 158, 159, 172, 181, 214, 216, 218, 221, 222, 224, 250, 253, 254, 258, 263, 264, 266, 268, 271, 273, 275, 278, 279, 280, 282, 283, 287, 288, 291, 297, 302, 304, 307, and 312, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the modification is selected from the group consisting of 1 (I,K,M,V,A,H,W,Y,C,L), 4 (T,E,A,N,R,V,K,L,M,Y), 17 (Q,I,W,Y,C,R,V,T,L), 25 (S,D,F,A,C,K,M,R), 40 (F,E,G,M,Q,S,Y,W,A,K,L), 45 (K,E,L,S,F,H,Q,Y,A,G,M), 56 (A,K,Q,V,W,H,I,Y,E,M), 58 (A,N,Y,C,V,E,L), 61 (Q,M,R,W,F,V,C,I,L), 74 (H,E,L,V,C,F,M,N,Q,W), 86 (N,L,S,Y,A,C,E,F,G,K,D), 97 (N,K,C,R,S,Y,E,M), 101 (R,T,C,L,S,H), 109 (G,A,L,S,E,M,R,W), 149 (T,M,V,A,L,D,S,N), 150 (D,A,F,K,N,Q,T,V,S), 158 (Q,A,K,M,N,L,R,Y,S), 159 (N,R,W,A,C,G,M,T,S,Y), 172 (F,G,L,M,Q,S,V,W,Y,D,H), 181 (N,L,A,G,K,M,T,S), 214 (P,C,G,K,S,N,A,R), 216 (H,C,E,S,T,R,A), 218 (S,K,L,Y,F,G,T,V), 221 (Y,K,N,Q,R,S,T,V,A,F,G,M), 222 (T,C,D,L,Y,I,V,A,M,K), 224 (T,K,M,F,L,P,Q,V,Y,E,H), 250 (H,A,C,K,M,N,P,Q,R,V,Y), 253 (V,N,T,I,R,Y,M,Q), 254 (S,A,M,R,Y,K,L,N,V,W), 258 (I,E,L,M,N,R,S,A,C,K,Q,V), 263 (L,C,I,Q,T,H,K,N,V,A,M), 264 (G,C,R,A,N,P,Q,S,T), 266 (I,A,F,L,S,C,M,T,V), 268 (Y,M,Q,V,A,S,K), 271 (L,A,D,F,I,N,Y,H), 273 (Q,A,H,Y,C,S,W,E,G,N), 275 (L,I,M,V,C,Q,S,T), 278 (T,G,K,R,Y,C,H,M,N,Q,S), 279 (S,A,D,I,L,M,N,Q,T,G), 280 (N,A,C,D,E,G,Q,H,T), 282 (S,K,N,R,A,H,L,M,T), 283 (Q,K,L,P,R,W,Y,S), 287 (A,I,L,N,V,Y,K,R,T,D,C), 288 (A,C,I,S,T,V,Y,N,L,M), 291 (S,E,I,L,M,N,V,A,T), 297 (G,A,M,R,Y,C,F,K,T,D,N), 302 (E,K,L,G,T,V,D,Q,A), 304 (A,C,D,L,N,R,S,T,W,E,K,Y), 307 (K,A,C,G,I,M,N,Q,R,W,Y,H), and 312 (A,G,M,V,L,N,R,T,C), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position of the thermolysin enzyme variant, wherein at least 15% but less than 40% of the modifications tested at the productive position meet at least one of the criteria listed in a, b, and c (supra), and wherein the productive position is selected from the group consisting of 5, 9, 11, 19, 27, 31, 33, 37, 46, 64, 73, 76, 79, 80, 85, 89, 95, 98, 99, 107, 127, 129, 131, 137, 141, 145, 148, 151, 152, 155, 156, 160, 161, 164, 168, 171, 176, 180, 182, 187, 188, 205, 206, 207, 210, 212, 213, 220, 227, 234, 235, 236, 237, 242, 244, 246, 248, 249, 252, 255, 270, 274, 284, 294, 296, 306, 309, 310, 313, 314, and 315, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the modification is selected from the group consisting of 5 (S,D,N,P,H,L), 9 (V,L,T,I), 11 (R,I,Y,K), 19 (N,L,Y,K,S), 27 (Y,W,A,M,V,C,L), 31 (Q,A,K,V,I,C,Y), 33 (N,S,T,K,A,C,L,M), 37 (N,D,Q,R,L,K), 46 (Y,L,H,N,C), 64 (A,H,Q,T,D,E), 73 (A,I,F,L,M,W), 76 (Y,H,L,M,Q,T), 79 (V,L,Q,T,A,N,S), 80 (T,I,D,A,L,N), 85 (K,E,A,L,N,R,S), 89 (N,L,M,H), 95 (G,A,D,H,M,N,S), 98 (A,C,E,H,R,Y,K,V), 99 (A,E,K,P,R,S), 107 (S,D,K,Y,A,G), 127 (G,C,D,E), 129 (T,I,R,E,Y,L,M), 131 (I,Y,W,L), 137 (I,P,A,E,T,V,L), 141 (A,S,C,G), 145 (T,A,C,E,G,M,N,Q), 148 (V,L,N,Y,M,A,Q), 151 (Y,K,G,H,S,W), 152 (T,S,L,M,G), 155 (L,C,I,M), 156 (I,M,T,L,Q), 160 (E,L,Y,Q), 161 (S,A,N,P,T), 164 (I,L,N,S,T,V,C,A), 168 (I,A,M,T,L), 171 (I,C,E,F,L,S,G), 176 (V,L,N,C), 180 (A,E,G,K,T,S), 182 (K,L,A,W), 187 (E,L,D), 188 (I,L,V), 205 (M,L,A,V,Q), 206 (S,A,C,K,L,M,R), 207 (D,A,H,N), 210 (K,I,L,V), 212 (G,Y,A,D,Q), 213 (D,N,S,L,A,G,W), 220 (R,K,V,A), 227 (N,D,L,Y,A), 234 (S,D,N,A,C), 235 (G,M,C,Q,S,A), 236 (I,M,A,C), 237 (I,N,F,M), 242 (Y,C,F,N,V), 244 (I,T,V,F,A,M,L), 246 (Q,E,N,T,L,C,D), 248 (G,A,E,S), 249 (T,K,M,N,L,Y,P), 252 (G,K,Y,A,S,T,W), 255 (V,L,P,A,Y,M,N), 270 (A,C,F,I,L,S,G), 274 (Y,F,H,A,C,Q,T,M), 284 (L,V,W,A,M,Y), 294 (D,A,V,Q,N), 296 (Y,N,L,R,H,W,M), 306 (V,A,S,F,I,L,T), 309 (A,G,S,T,V,C), 310 (F,A,C,W,M), 313 (V,T,A,G,L,I,C), 314 (G,A,E,H,M,S,W,Q), and 315 (V,A,C,I,M,L,T), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position of the thermolysin enzyme variant, wherein at least one modification but less than 15% of the modifications tested at the productive position meet at least one of the criteria listed in a, b, and c (supra), and wherein the productive position is selected from the group consisting of 3, 6, 7, 20, 23, 24, 44, 48, 50, 57, 63, 72, 75, 81, 92, 93, 94, 100, 102, 103, 104, 110, 117, 120, 134, 135, 136, 140, 144, 153, 173, 174, 175, 178, 183, 185, 189, 193, 201, 223, 230, 238, 239, 241, 247, 251, 260, 262, 269, and 285, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the modification is selected from the group consisting of 3 (G,Y), 6 (T,C,V), 7 (V,L,I), 20 (I,L,V), 23 (T,F,W), 24 (Y,W), 44 (A,C), 48 (T,E,D), 50 (L,P), 57 (D,K), 63 (F,Y,C), 72 (D,F,W), 75 (Y,A), 81 (Y,F), 92 (S,L), 93 (Y,T,C), 94 (D,T), 100 (I,L,V), 102 (S,G,N), 103 (S,T), 104 (V,A), 110 (Y,L), 117 (G,H), 120 (M,L), 134 (S,A,P), 135 (G,A), 136 (G,A,S), 140 (V,D), 144 (L,T), 153 (A,T), 173 (G,A,C), 174 (T,C,A), 175 (L,H,S), 178 (F,H,Y), 183 (N,S), 185 (D,E), 189 (G,A), 193 (Y,F), 201 (S,C,A), 223 (G,D,K), 230 (V,A), 238 (N,L,M), 239 (K,A), 241 (A,L,S), 247 (G,A,S), 251 (Y,M), 260 (R,A,N), 262 (K,A), 269 (R,V,K), and 285 (R,K,Y), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is an activity combinable mutation, wherein at least one modification of the modifications tested at the activity combinable meet the following criteria: a position wherein the minimum performance indices (PI) relative to Thermolysin parent for expression and detergent stability or thermostability are greater than or equal to 0.5, and PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba greater than or equal to 1.5; and wherein the activity combinable position is selected from the group consisting of 17, 19, 24, 25, 31, 33, 40, 48, 73, 79, 80, 81, 85, 86, 89, 94, 109, 117, 140, 141, 150, 151, 152, 153, 156, 158, 159, 160, 161, 168, 171, 174, 175, 176, 178, 180, 181, 182, 183, 189, 205, 206, 207, 210, 212, 213, 214, 218, 223, 224, 227, 235, 236, 237, 238, 239, 241, 244, 246, 248, 249, 250, 251, 252, 253, 254, 255, 258, 259, 260, 261, 262, 266, 268, 269, 270, 271, 272, 273, 274, 276, 278, 279, 280, 282, 283, 294, 295, 296, 297, 300, 302, 306, 310, and 312, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the modification is selected from the group consisting of 17 (E,F,P), 19 (A,D,H,I,R,T,V), 24 (F,H), 25 (H), 31 (L), 33 (Q), 40 (C), 48 (A,R), 73 (Y), 79 (C), 80 (C,R), 81 (H), 85 (C,M,Y), 86 (V), 89 (K,R,T,V), 94 (E), 109 (D), 117 (A,K,R,T), 140 (S), 141 (T), 150 (E,M,W), 151 (A,C,E,I), 152 (D), 153 (V), 156 (H,R), 158 (F,G,I,V), 159 (F,I,K), 160 (S), 161 (Y), 168 (N), 171 (D), 174 (S,V), 175 (C,E,F,G,I), 176 (E,Q), 178 (C,M), 180 (L,W), 181 (Y), 182 (F,R), 183 (H,I,L,M,Q,R,T), 189 (C), 205 (C,F), 206 (F,H,I,T,V,Y), 207 (T), 210 (A,E,F,G,H,T), 212 (F,H,K,M,N,R,S,T), 213 (I,K,R,V,Y), 214 (Q), 218 (R), 223 (Y), 224 (I,R), 227 (C,E,G,K,Q,R,S,T,V), 235 (D,L,T), 236 (P), 237 (A,Q), 238 (A,C,D,E,R,S), 239 (C,G,H,L,Q,R,S,V,Y), 241 (E,F,G,I,T,V), 244 (Q), 246 (K,R), 248 (C,H), 249 (G,V), 250 (F,S), 251 (H), 252 (F,I,L), 253 (A,D,E,P), 254 (C,F,G,H,I,P), 255 (F,Q), 258 (F), 259 (I), 260 (C,D,I), 261 (K,R,T), 262 (C,F,H,L,P,R), 266 (W), 268 (F,R), 269 (P,T,W,Y), 270 (M,N,P,V), 271 (V), 272 (R), 273 (R), 274 (D,E), 276 (G,S), 278 (V), 279 (E), 280 (P,R,V), 282 (P), 283 (A,C,E,G,H,T,V), 294 (T), 295 (R), 296 (E,I), 297 (I,V), 300 (Q), 302 (W), 306 (Y), 310 (I,N), and 312 (Q), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the thermolysin enzyme variant has an improved PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba or detergent stability or thermostability compared to the parent thermolysin enzyme, and wherein the modification is at a position having a temperature factor greater than 1.5 times the observed variance above the mean main chain temperature factor for all residues in the amino acid sequence of thermolysin set forth in SEQ ID NO: 3; and wherein the residue position is selected from the group consisting of 1, 2, 127, 128, 180, 181, 195, 196, 197, 198, 199, 211, 223, 224, 298, 299, 300, and 316, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the thermolysin enzyme variant has an improved detergent stability or thermostability compared to the parent thermolysin enzyme, and wherein the modification is at a position having a temperature factor greater than 1.5 times the observed variance above the mean main chain temperature factor for all residues in the amino acid sequence of thermolysin set forth in SEQ ID NO: 3; wherein the modification is selected from the group consisting of 1 (I,V), 2 (T,C,I,M,P,Q,V), 127 (G,C), 128 (Q,C,E,F,I,L,V,Y), 180 (A,E,N), 181 (N,A,G,Q,S), 196 (G,L,Y), 197 (I,F), 198 (S,A,C,D,E,H,I,M,P,Q,T,V,Y), 211 (Y,A,C,E,F,H,I,Q,S,T,V,W), 224 (T,D,H,Y), 298 (S,A,C,E,F,G,K,M,N,P,Q,R,T,W,Y), 299 (T,A,C,D,F,G,H,I,K,L,M,N,P,Q,R,S,W), and 316 (K,A,D,E,H,M,N,P,Q,S,T,V,Y), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position of the thermolysin enzyme variant, wherein at least 75% of the modifications tested at the productive position meet at least one of the following criteria: a) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.9, and in addition have a PI for any one of these tests that is greater than or equal to 1.0; b) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.8, and in addition have a PI for any one of these tests that is greater than or equal to 1.2; c) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.5, and in addition have a PI for any one of these tests that is greater than or equal to 1.5; and wherein the productive position is selected from the group consisting of 2, 87, 96, 198, 277, 293, 295, 298 and 301, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
1. In further embodiments, the productive position is selected from the group consisting of 2 (T,F,L,P,S,V,W,Y,Q,A,C,I,K,M), 87 (V,D,E,G,I,S,P,R,T,C,K,L,M,N,Q,W,Y), 96 (N,C,D,I,V,F,T,G,H,Q,R,S,W,K,L,Y), 198 (S,C,E,F,G,H,I,P,Q,T,V,M,N,R,W,A,K), 277 (P,Q,S,T,E,F,G,H,N,R,V,W,A,D,Y), 293 (T,C,E,F,G,H,Q,S,N,V,W,A,I,K,L,M,Y), 295 (L,C,I,N,T,V,F,G,A,K,M,W), 298 (S,C,T,W,Y,E,N,P,A,G,K,M,R), 301 (Q,E,H,P,R,L,C,F,G,W,M,S,T,V,K), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is a productive position wherein the modifications tested at the productive position meet the following criteria: a position wherein the minimum performance indices (PI) relative to Thermolysin parent for at least three of the parameters of expression, detergent stability, thermostability, PAS-38 microswatch cleaning activity, or activity on Abz-AGLA-Nba are greater than or equal to 1, and; wherein the productive position is selected from the group consisting of 278, 283, 180, 244, 48 and 63, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
IN further embodiments, the productive position is selected from the group consisting of T278R, Q283E, A180E, I244T, T48E and F63C, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the invention is a thermolysin enzyme variant or an active fragment thereof comprising an amino acid modification to a parent thermolysin enzyme, wherein the modification is at a productive position, wherein at least one modification of the modifications tested at the productive position meet the following criteria: a position wherein the minimum performance indices (PI) relative to Thermolysin parent for at least all of the parameters of expression, detergent stability, thermostability, PAS-38 microswatch cleaning activity, or activity on Abz-AGLA-Nba are greater than or equal to 0.5 and no more than one of the parameters is less than 0.8, and wherein the productive position is selected from the group consisting of 019, 025, 026, 063, 091, 096, 097, 101, 109, 118, 131, 140, 158, 159, 175, 180, 219, 225, 232, 244, 246, 261, 277, 293, 300, 301, 301, 303, 305, and 311, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In further embodiments, the productive position is selected from the group consisting of N019D, S025A, T026R, S065A, L091M, N096Q, N096R, N096Y, N097K, R101M, G109A, S118A, I131L, V140D, Q158A, N159E, N159K, L175V, A180R, G196T, G196Y, K219S, Q225E, I232R, I244L, Q246D, D261N, P277G, T293Y, S300G, Q301F, Q301M, V303R, S305A, D311A, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In some embodiments, the thermolysin enzyme variant is an M4 peptidase. In some embodiments, the thermolysin enzyme variant is a member of the MA clan. In some embodiments, the thermolysin enzyme variant is a member of the PepSY˜Peptidase_M4˜Peptidase_M4_C family. In some embodiments, the variant has at least 50% identity to a thermolysin of thermolysin set forth in SEQ ID NO: 3. In some embodiments, the thermolysin enzyme variant is from a genus selected from the group consisting of Bacillus, Geobacillus, Alicyclobacillus, Lactobacillus, Exiguobacterium, Brevibacillus, Paenibacillus, Herpetosiphon, Oceanobacillus, Shewanella, Clostridium, Staphylococcus, Flavobacterium, Stigmatella, Myxococcus, Vibrio, Methanosarcina, Chryseobacterium, Streptomyces, Kribbella, Janibacter, Nocardioides, Xanthamonas, Micromonospora, Burkholderia, Dehalococcoides, Croceibacter, Kordia, Microscilla, Thermoactinomyces, Chloroflexus, Listeria, Plesiocystis, Haliscomenobacter, Cytophaga, Hahella, Arthrobacter, Brachybacterium, Clavibacter, Microbacterium, Intrasporangium, Frankia, Meiothermus, Pseudomonas, Ricinus, Catenulispora, Anabaena, Nostoc, Halomonas, Chromohalobacter, Bordetella, Variovorax, Dickeya, Pectobacterium, Citrobacter, Enterobacter, Salmonella, Erwinia, Pantoea, Rahnella, Serratia, Geodermatophilus, Gemmata, Xenorhabdus, Photorhabdus, Aspergillus, Neosartorya, Pyrenophora, Saccharopolyspora, Nectria, Gibberella, Metarhizium, Waddlia, Cyanothece, Cellulphaga, Providencia, Bradyrhizobium, Agrobacterium, Mucilaginibacter, Serratia, Sorangium, Streptosporangium, Renibacterium, Aeromonas, Reinekea, Chromobacterium, Moritella, Haliangium, Kangiella, Marinomonas, Vibrionales, Listonella, Salinivibrio, Photobacterium, Alteromonadales, Legionella, Teredinibacter, Reinekea, Hydrogenivirga, and Pseudoalteromonas. In some embodiments, the thermolysin enzyme variant is from a genus selected from the group consisting of Bacillus, Geobacillus, Alicyclobacillus, Lactobacillus, Exiguobacterium, Brevibacillus, Paenibacillus, Herpetosiphon, Oceanobacillus, Shewanella, Clostridium, Staphylococcus, Flavobacterium, Stigmatella, Myxococcus, Vibrio, Methanosarcina, Chryseobacterium, and Pseudoalteromonas. In some embodiments, the thermolysin enzyme is from the genus Bacillus.
In some embodiments, the invention is a cleaning composition comprising at least one variant as listed above. In some embodiments, the cleaning composition is a granular, powder, solid, bar, liquid, tablet, gel, or paste composition. In some embodiments, the cleaning composition is a detergent composition. In some embodiments, the cleaning composition is a laundry detergent composition, a dish detergent composition, or a hard surface cleaning composition. In some embodiments, the dish detergent is a hand dishwashing detergent composition or an automatic dishwashing detergent composition. In some embodiments, the cleaning composition is a laundry detergent composition. In some embodiments, the cleaning composition further comprises at least one bleaching agent. In some embodiments, the cleaning composition is phosphate-free. In some embodiments, the cleaning composition contains phosphate. In some embodiments, the cleaning composition further comprises at least one additional enzyme. In some embodiments, the at least one additional enzyme is selected from the group consisting of acyl transferases, alphaamylases,beta-amylases, alpha-galactosidases, arabinosidases, aryl esterases, betagalactosidases, carrageenases, catalases, cellobiohydrolases, cellulases, chondroitinases, cutinases, endo-beta-1,4-glucanases, endo-beta-mannanases, esterases, exo-mannanases, galactanases, glucoamylases, hemicellulases, hyaluronidases, keratinases, laccases, lactases, ligninases, lipases, lipoxygenases, mannanases, oxidases, pectate lyases, pectin acetyl esterases, pectinases, pentosanases, peroxidases, phenoloxidases, phosphatases, phospholipases, phytases, polygalacturonases, proteases, pullulanases, reductases, rhamnogalacturonases, beta-glucanases, tannases, transglutaminases, xylan acetyl-esterases, xylanases, xyloglucanases, and xylosidases, additional metallopotease enzymes and combinations thereof.
In some embodiments, the invention is a method of cleaning using a cleaning composition as listed above. A method of cleaning, comprising contacting a surface or an item with a cleaning composition comprising at least one thermolysin enzyme variant of any one of claims 1-33. In some embodiments, the method comprises contacting a surface or an item with a cleaning composition set forth above. In some embodiments, the method comprises rinsing said surface or item after contacting said surface or item, respectively, with said cleaning composition. In some embodiments, the item is dishware. In some embodiments, the item is fabric. In some embodiments, the method comprises the step of rinsing said surface or item after contacting said surface or item with said cleaning composition. In some embodiments, the method comprises the step of drying said surface or item after said rinsing of said surface or item. In some embodiments, the method comprises providing a cleaning composition set forth above and a surface or item in need of cleaning; and contacting said cleaning composition with said surface or item in need of cleaning under conditions suitable for the cleansing of said surface of said surface or item, to produce a cleansed surface or item. In some embodiments, the method comprises the step of rinsing said cleansed surface or item to produce a rinsed surface or item. In some embodiments, the method further comprises the step of drying said rinsed surface or item.
The present invention provides improved metalloprotease enzymes, especially enzymes useful for detergent compositions. Specifically, the present invention provides metalloprotease enzyme variants having one or more modifications, such as a substitution, as compared to a parent metalloprotease enzyme. This can be achieved by making improvements to the enzyme by improving wash performance, stability of the enzyme in detergent compositions, and/or thermostability of the enzyme that improve effectiveness of the enzyme in a wash cycle. The present invention provides variant metalloprotease enzymes, including, but not limited to, variant thermolysis metalloprotease enzymes, that are particularly well suited to and useful in a variety of cleaning applications. The invention includes compositions comprising at least one of the variant metalloprotease enzymes (e.g., variant thermolysins) set forth herein. Some such compositions comprise detergent compositions. The invention provides various species, including Bacillus and Geobacillus species variant metalloprotease enzymes and compositions comprising one or more such variant thermolysins. The metalloprotease enzyme variants of the present invention can be combined with other enzymes useful in detergent compositions. The invention also provides methods of cleaning using metalloprotease enzyme variants of the present invention.
The invention includes enzyme variants of metalloprotease enzymes having one or more modifications from a parent metalloprotease enzyme. The enzyme variants can be useful in a detergent composition by having a minimum performing index for wash performance, stability of the enzyme in detergent compositions and thermostability of the enzyme, while having at least one of these characteristics improved from a parent metalloprotease enzyme.
Additionally, the invention provides modifications, such as a substitution, at one or more amino acid positions in a metalloprotease enzyme which can be useful in a detergent composition where favorable modifications result in a minimum performing index for wash performance, stability of the enzyme in detergent compositions and thermostability of the enzyme, while having at least one of these characteristics improved from a parent metalloprotease enzyme. These modifications are considered suitable modifications of the invention. These amino acid positions can be considered useful positions for combinatorial modifications to a parent metalloprotease enzyme. Metalloprotease enzyme amino acid positions found to be useful positions can be further characterized by having multiple modifications that are suitable for use in a detergent composition. For each position, greater numbers of possible suitable modifications denotes a higher productivity of a particular position.
In addition, the present invention provides compositions comprising these metalloprotease variants. In some embodiments, the present invention provides cleaning compositions comprising at least one of these metalloprotease variants.
It is to be appreciated those certain feature of the invention, which are, for clarity, described above and below in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various feature of the invention that are, for brevity, described in the context of a single embodiment, may also be provided separately or in any sub-combination.
Unless otherwise indicated, the practice of the present invention involves conventional techniques commonly used in molecular biology, protein engineering, microbiology, and recombinant DNA, which are within the skill of the art. Such techniques are known to those of skill in the art and are described in numerous texts and reference works well known to those of skill in the art. All patents, patent applications, articles and publications mentioned herein, both supra and infra, are hereby expressly incorporated herein by reference.
Unless defined otherwise herein, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. Many technical dictionaries are known to those of skill in the art. Although any methods and materials similar or equivalent to those described herein find use in the practice of the present invention, some suitable methods and materials are described herein. Accordingly, the terms defined immediately below are more fully described by reference to the Specification as a whole. Also, as used herein, the singular “a”, “an” and “the” includes the plural reference unless the context clearly indicates otherwise. Numeric ranges are inclusive of the numbers defining the range. Unless otherwise indicated, nucleic acids are written left to right in 5′ to 3′ orientation; amino acid sequences are written left to right in amino to carboxy orientation, respectively. It is to be understood that this invention is not limited to the particular methodology, protocols, and reagents described, as these may vary, depending upon the context they are used by those of skill in the art.
The practice of the present invention employs, unless otherwise indicated, conventional techniques of protein purification, molecular biology, microbiology, recombinant DNA techniques and protein sequencing, all of which are within the skill of those in the art.
Furthermore, the headings provided herein are not limitations of the various aspects or embodiments of the invention which can be had by reference to the specification as a whole. Accordingly, the terms defined immediately below are more fully defined by reference to the specification as a whole. Nonetheless, in order to facilitate understanding of the invention, a number of terms are defined below.
It is intended that every maximum numerical limitation given throughout this specification include every lower numerical limitation, as if such lower numerical limitations were expressly written herein. Every minimum numerical limitation given throughout this specification will include every higher numerical limitation, as if such higher numerical limitations were expressly written herein. Every numerical range given throughout this specification will include every narrower numerical range that falls within such broader numerical range, as if such narrower numerical ranges were all expressly written herein.
As used herein, the terms “protease” and “proteinase” refer to an enzyme protein that has the ability to break down other proteins. A protease has the ability to conduct “proteolysis,” which begins protein catabolism by hydrolysis of peptide bonds that link amino acids together in a peptide or polypeptide chain forming the protein. This activity of a protease as a protein-digesting enzyme is referred to as “proteolytic activity.” Many well known procedures exist for measuring proteolytic activity (See e.g., Kalisz, “Microbial Proteinases,” In: Fiechter (ed.), Advances in Biochemical Engineering/Biotechnology, (1988)). For example, proteolytic activity may be ascertained by comparative assays which analyze the respective protease's ability to hydrolyze a commercial substrate. Exemplary substrates useful in the analysis of protease or proteolytic activity, include, but are not limited to, di-methyl casein (Sigma C-9801), bovine collagen (Sigma C-9879), bovine elastin (Sigma E-1625), and bovine keratin (ICN Biomedical 902111). Colorimetric assays utilizing these substrates are well known in the art (See e.g., WO 99/34011 and U.S. Pat. No. 6,376,450, both of which are incorporated herein by reference). The pNA assay (See e.g., Del Mar et al., Anal. Biochem. 99:316-320 [1979]) also finds use in determining the active enzyme concentration for fractions collected during gradient elution. This assay measures the rate at which p-nitroaniline is released as the enzyme hydrolyzes the soluble synthetic substrate, succinyl-alanine-alanine-proline-phenylalanine-p-nitroanilide (suc-AAPF-pNA). The rate of production of yellow color from the hydrolysis reaction is measured at 410 nm on a spectrophotometer and is proportional to the active enzyme concentration. In addition, absorbance measurements at 280 nanometers (nm) can be used to determine the total protein concentration. The active enzyme/total protein ratio gives the enzyme purity.
As used herein, the term “thermolysin” refers any member of the M4 protease family as described in MEROPS—The Peptidase Data base (See, Rawlings et al., MEROPS: the peptidase database, Nucl Acids Res, 34 Database issue, D270-272 [2006]), of which thermolysin (TLN; EC 3.4.24.27) is the prototype. The amino acid sequence of thermolysin, (EC 3.4.24.27) the neutral metallo endo-peptidase secreted from Bacillus thermoproteolyticus was first reported by Titani et al (Titani et al, (1972), Amino-acid sequence of thermolysin. Nature New Biol. 238:35-37). Subsequently, the gene for this enzyme was cloned by O'Donohue et al (O'Donohue, M. J (1994) Cloning and expression in Bacillus subtilis of the npr gene from Bacillus thermoproteolyticus Rokko coding for the thermostable metalloprotease thermolysin. Biochem. J. 300:599-603) and the sequence set forth as UniProtKB/Swiss-Prot Accession No. P00800 (SEQ ID NO:4). The only differences between the protein sequences reported by Titani et al and O'Donohue et al are the confirmation of Asn at position 37 (instead of Asp) and Gln at position 119 (instead of Glu). As such the terms “thermolysin,” “stearolysin”, “bacillolysin,” “proteinase-T”, “PrT”, “Thermolysin-like protease”, and “TLPs”, are used interchangeably herein to refer to the neutral metalloprotease enzyme of Bacillus thermoproteolyticus.
As used herein, the term “variant polypeptide” refers to a polypeptide comprising an amino acid sequence that differs in at least one amino acid residue from the amino acid sequence of a parent or reference polypeptide (including but not limited to wild-type polypeptides).
As used herein, “the genus Bacillus” includes all species within the genus “Bacillus,” as known to those of skill in the art, including but not limited to B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. clausii, B. halodurans, B. megaterium, B. coagulans, B. circulans, B. lautus, and B. thuringiensis. It is recognized that the genus Bacillus continues to undergo taxonomical reorganization. Thus, it is intended that the genus include species that have been reclassified, including but not limited to such organisms as B. stearothermophilus, which is now named “Geobacillus stearothermophilus.” The production of resistant endospores in the presence of oxygen is considered the defining feature of the genus Bacillus, although this characteristic also applies to the recently named Alicyclobacillus, Amphibacillus, Aneurinibacillus, Anoxybacillus, Brevibacillus, Filobacillus, Gracilibacillus, Halobacillus, Paenibacillus, Salibacillus, Thermobacillus, Ureibacillus, and Virgibacillus.
The terms “polynucleotide” and “nucleic acid,” which are used interchangeably herein, refer to a polymer of any length of nucleotide monomers covalently bonded in a chain. DNA (deoxyribonucleic acid), a polynucleotide comprising deoxyribonucleotides, and RNA (ribonucleic acid), a polymer of ribonucleotides, are examples of polynucleotides or nucleic acids having distinct biological function. Polynucleotides or nucleic acids include, but are not limited to, a single-, double- or triple-stranded DNA, genomic DNA, cDNA, RNA, DNA-RNA hybrid, or a polymer comprising purine and pyrimidine bases, or other natural, chemically, biochemically modified, non-natural or derivatized nucleotide bases. The following are non-limiting examples of polynucleotides: genes, gene fragments, chromosomal fragments, expressed sequence tag(s) (EST(s)), exons, introns, messenger RNA (mRNA), transfer RNA (tRNA), ribosomal RNA (rRNA), ribozymes, complementary DNA (cDNA), recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers.
As used herein, the term “mutation” refers to changes made to a reference amino acid or nucleic acid sequence. It is intended that the term encompass substitutions, insertions and deletions.
As used herein, the term “vector” refers to a nucleic acid construct used to introduce or transfer nucleic acid(s) into a target cell or tissue. A vector is typically used to introduce foreign DNA into a cell or tissue. Vectors include plasmids, cloning vectors, bacteriophages, viruses (e.g., viral vector), cosmids, expression vectors, shuttle vectors, and the like. A vector typically includes an origin of replication, a multicloning site, and a selectable marker. The process of inserting a vector into a target cell is typically referred to as transformation. The present invention includes, in some embodiments, a vector that comprises a DNA sequence encoding a metalloprotease polypeptide (e.g., precursor or mature metalloprotease polypeptide) that is operably linked to a suitable prosequence (e.g., secretory, signal peptide sequence, etc.) capable of effecting the expression of the DNA sequence in a suitable host, and the folding and translocation of the recombinant polypeptide chain.
As used herein, the term “expression cassette,” “expression plasmid” or “expression vector” refers to a nucleic acid construct or vector generated recombinantly or synthetically for the expression of a nucleic acid of interest in a target cell. An expression vector or expression cassette typically comprises a promoter nucleotide sequence that drives expression of the foreign nucleic acid. The expression vector or cassette also typically includes any other specified nucleic acid elements that permit transcription of a particular nucleic acid in a target cell. A recombinant expression cassette can be incorporated into a plasmid, chromosome, mitochondrial DNA, plastid DNA, virus, or nucleic acid fragment. Many prokaryotic and eukaryotic expression vectors are commercially available.
In some embodiments, the ends of the sequence are closed such that the DNA construct forms a closed circle. The nucleic acid sequence of interest, which is incorporated into the DNA construct, using techniques well known in the art, may be a wild-type, mutant, or modified nucleic acid. In some embodiments, the DNA construct comprises one or more nucleic acid sequences homologous to the host cell chromosome. In other embodiments, the DNA construct comprises one or more non-homologous nucleotide sequences. Once the DNA construct is assembled in vitro, it may be used, for example, to: 1) insert heterologous sequences into a desired target sequence of a host cell; and/or 2) mutagenize a region of the host cell chromosome (i.e., replace an endogenous sequence with a heterologous sequence); 3) delete target genes; and/or 4) introduce a replicating plasmid into the host. “DNA construct” is used interchangeably herein with “expression cassette.”
As used herein, a “plasmid” refers to an extrachromosomal DNA molecule which is capable of replicating independently from the chromosomal DNA. A plasmid is double stranded (ds) and may be circular and is typically used as a cloning vector.
As used herein in the context of introducing a nucleic acid sequence into a cell, the term “introduced” refers to any method suitable for transferring the nucleic acid sequence into the cell. Such methods for introduction include but are not limited to protoplast fusion, transfection, transformation, electroporation, conjugation, and transduction (See e.g., Ferrari et al., “Genetics,” in Hardwood et al. (eds.), Bacillus, Plenum Publishing Corp., pp. 57-72 [1989]).
Transformation refers to the genetic alteration of a cell which results from the uptake, optional genomic incorporation, and expression of genetic material (e.g., DNA).
As used herein, a nucleic acid is “operably linked” with another nucleic acid sequence when it is placed into a functional relationship with another nucleic acid sequence. For example, a promoter or enhancer is operably linked to a nucleotide coding sequence if the promoter affects the transcription of the coding sequence. A ribosome binding site may be operably linked to a coding sequence if it is positioned so as to facilitate translation of the coding sequence. Typically, “operably linked” DNA sequences are contiguous. However, enhancers do not have to be contiguous Linking is accomplished by ligation at convenient restriction sites. If such sites do not exist, synthetic oligonucleotide adaptors or linkers may be used in accordance with conventional practice.
As used herein the term “gene” refers to a polynucleotide (e.g., a DNA segment), that encodes a polypeptide and includes regions preceding and following the coding regions as well as intervening sequences (introns) between individual coding segments (exons).
As used herein, “recombinant” when used with reference to a cell typically indicates that the cell has been modified by the introduction of a foreign nucleic acid sequence or that the cell is derived from a cell so modified. For example, a recombinant cell may comprise a gene not found in identical form within the native (non-recombinant) form of the cell, or a recombinant cell may comprise a native gene (found in the native form of the cell) but which has been modified and re-introduced into the cell. A recombinant cell may comprise a nucleic acid endogenous to the cell that has been modified without removing the nucleic acid from the cell; such modifications include those obtained by gene replacement, site-specific mutation, and related techniques known to those of ordinary skill in the art. Recombinant DNA technology includes techniques for the production of recombinant DNA in vitro and transfer of the recombinant DNA into cells where it may be expressed or propagated, thereby producing a recombinant polypeptide. “Recombination,” “recombining,” and “recombined” of polynucleotides or nucleic acids refer generally to the assembly or combining of two or more nucleic acid or polynucleotide strands or fragments to generate a new polynucleotide or nucleic acid. The recombinant polynucleotide or nucleic acid is sometimes referred to as a chimera. A nucleic acid or polypeptide is “recombinant” when it is artificial or engineered.
As used herein, the term nucleic acid or gene “amplification” refers to a process by which specific DNA sequences are disproportionately replicated such that the amplified nucleic acid or gene becomes present in a higher copy number than was initially present in the genome. In some embodiments, selection of cells by growth in the presence of a drug (e.g., an inhibitor of an inhabitable enzyme) results in the amplification of either the endogenous gene encoding the gene product required for growth in the presence of the drug or by amplification of exogenous (i.e., input) sequences encoding this nucleic acid or gene product or both.
“Amplification” is a special case of nucleic acid replication involving template specificity. It is to be contrasted with non-specific template replication (i.e., replication that is template-dependent but not dependent on a specific template). Template specificity is here distinguished from fidelity of replication (i.e., synthesis of the proper polynucleotide sequence) and nucleotide (ribo- or deoxyribo-) specificity. Template specificity is frequently described in terms of “target” specificity. Target sequences are “targets” in the sense that they are sought to be sorted out from other nucleic acid. Amplification techniques have been designed primarily for this sorting out.
As used herein, the term “primer” refers to an oligonucleotide (a polymer of nucleotide residues), whether occurring naturally as in a purified restriction digest or produced synthetically, which is capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of a primer extension product which is complementary to a nucleic acid strand is induced (i.e., in the presence of nucleotides and an inducing agent such as DNA polymerase and at a suitable temperature and pH). A primer is preferably single stranded for maximum efficiency in amplification, but may alternatively be double stranded. If double stranded, the primer is first treated to separate its strands before being used to prepare extension products. In some embodiments, the primer is an oligodeoxyribonucleotide. The primer must be sufficiently long to prime the synthesis of extension products in the presence of the inducing agent. The exact length of a primer depends on a variety of factors, including temperature, source of primer, and the use of the method.
As used herein, the term “probe” refers to an oligonucleotide, whether occurring naturally as in a purified restriction digest or produced synthetically, recombinantly or by PCR amplification, which is typically capable of hybridizing to another oligonucleotide of interest. A probe may be single-stranded or double-stranded. Probes are useful in the detection, identification and isolation of particular gene sequences. It is contemplated that any probe used in the present invention will be labeled with any “reporter molecule,” so that it is detectable in any detection system, including, but not limited to enzyme (e.g., ELISA, as well as enzyme-based histochemical assays), fluorescent, radioactive, and luminescent systems. It is not intended that the present invention be limited to any particular detection system or label.
As used herein, the term “target,” when used in reference to the polymerase chain reaction, refers to the region of nucleic acid bounded by the primers used for polymerase chain reaction. Thus, the “target” is sought to be sorted out from other nucleic acid sequences. A nucleotide “segment” is a region of a nucleic acid within the target nucleic acid sequence.
As used herein, the term “polymerase chain reaction” (PCR) refers to the methods of U.S. Pat. Nos. 4,683,195 4,683,202, and 4,965,188, hereby incorporated by reference, which include methods for increasing the concentration of a segment of a target sequence in a mixture of genomic DNA without cloning or purification. This process for amplifying the target sequence is well known in the art.
As used herein, the term “amplification reagents” refers to those reagents (e.g., deoxyribonucleotide triphosphates, buffer, etc.) needed for amplification except for primers, nucleic acid template, and the amplification enzyme. Typically, amplification reagents along with other reaction components are placed and contained in a reaction vessel (test tube, microwell, etc.).
As used herein, the term “restriction endonuclease” or “restriction enzyme” refers to an enzyme (e.g., bacterial enzyme) that is capable of cutting double-stranded or single-stranded DNA at or near a specific sequence of nucleotides known as a restriction site. The nucleotide sequence comprising the restriction site is recognized and cleaved by a given restriction endonuclease or restriction enzyme and is frequently the site for insertion of DNA fragments. A restriction site can be engineered into an expression vector or DNA construct.
“Homologous recombination” refers to the exchange of DNA fragments between two DNA molecules or paired chromosomes at the site of identical or nearly identical nucleotide sequences. In some embodiments, chromosomal integration is homologous recombination.
A nucleic acid or polynucleotide is said to “encode” a polypeptide if, in its native state or when manipulated by methods known to those of skill in the art, it can be transcribed and/or translated to produce the polypeptide or a fragment thereof. The anti-sense strand of such a nucleic acid is also said to encode the sequence.
“Host strain” or “host cell” refers to a suitable host for an expression vector comprising a DNA sequence of interest.
A “protein” or “polypeptide” comprises a polymeric sequence of amino acid residues. The terms “protein” and “polypeptide” are used interchangeably herein. The single and 3-letter code for amino acids as defined in conformity with the IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN) is used through out this disclosure. The single letter X refers to any of the twenty amino acids. It is also understood that a polypeptide may be coded for by more than one nucleotide sequence due to the degeneracy of the genetic code. Mutations can be named by the one letter code for the parent amino acid, followed by a position number and then the one letter code for the variant amino acid. For example, mutating glycine (G) at position 87 to serine (S) is represented as “G087S” or “G87S”. Mutations can also be named by using the three letter code for an amino acid followed by its position in the polypeptide chain as counted from the N-terminus; for example, Ala10 for alanine at position 10. Multiple mutations are indicated by inserting a “-” between the mutations. Mutations at positions 87 and 90 are represented as either “G087S-A090Y” or “G87S-A90Y” or “G87S+A90Y” or “G087S+A090Y”. For deletions, the one letter code “Z” is used. For an insertion relative to the parent sequence, the one letter code “Z” is on the left side of the position number. For a deletion, the one letter code “Z” is on the right side of the position number. For insertions, the position number is the position number before the inserted amino acid(s), plus 0.01 for each amino acid. For example, an insertion of three amino acids alanine (A), serine (S) and tyrosine (Y) between position 87 and 88 is shown as “Z087.01A-Z087.02S-Z087.03Y.” Thus, combining all the mutations above plus a deletion at position 100 is: “G087S-Z087.01A-Z087.02S-Z087.03Y-A090Y-A100Z.” When describing modifications, a position followed by amino acids listed in parentheses indicates a list of substitutions at that position by any of the listed amino acids. For example, 6 (L,I) means position 6 can be substituted with a leucine or isoleucine.
A “prosequence” or “propeptide sequence” refers to an amino acid sequence between the signal peptide sequence and mature protease sequence that is necessary for the proper folding and secretion of the protease; they are sometimes referred to as intramolecular chaperones. Cleavage of the prosequence or propeptide sequence results in a mature active protease. Bacterial metalloproteases are often expressed as pro-enzymes.
The term “signal sequence” or “signal peptide” refers to a sequence of amino acid residues that may participate in the secretion or direct transport of the mature or precursor form of a protein. The signal sequence is typically located N-terminal to the precursor or mature protein sequence. The signal sequence may be endogenous or exogenous. A signal sequence is normally absent from the mature protein. A signal sequence is typically cleaved from the protein by a signal peptidase after the protein is transported.
The term “mature” form of a protein, polypeptide, or peptide refers to the functional form of the protein, polypeptide, or peptide without the signal peptide sequence and propeptide sequence.
The term “precursor” form of a protein or peptide refers to a mature form of the protein having a prosequence operably linked to the amino or carbonyl terminus of the protein. The precursor may also have a “signal” sequence operably linked to the amino terminus of the prosequence. The precursor may also have additional polypeptides that are involved in post-translational activity (e.g., polypeptides cleaved therefrom to leave the mature form of a protein or peptide).
The term “wild-type” in reference to an amino acid sequence or nucleic acid sequence indicates that the amino acid sequence or nucleic acid sequence is native or naturally occurring sequence. As used herein, the term “naturally-occurring” refers to anything (e.g., proteins, amino acids, or nucleic acid sequences) that are found in nature.
As used herein, the term “non-naturally occurring” refers to anything that is not found in nature (e.g., recombinant nucleic acids and protein sequences produced in the laboratory), as modification of the wild-type sequence.
As used herein with regard to amino acid residue positions, “corresponding to” or “corresponds to” or “corresponds” refers to an amino acid residue at the enumerated position in a protein or peptide, or an amino acid residue that is analogous, homologous, or equivalent to an enumerated residue in a protein or peptide. As used herein, “corresponding region” generally refers to an analogous position in a related proteins or a reference protein.
The terms “derived from” and “obtained from” refer to not only a protein produced or producible by a strain of the organism in question, but also a protein encoded by a DNA sequence isolated from such strain and produced in a host organism containing such DNA sequence. Additionally, the term refers to a protein which is encoded by a DNA sequence of synthetic and/or cDNA origin and which has the identifying characteristics of the protein in question. To exemplify, “proteases derived from Bacillus” refers to those enzymes having proteolytic activity which are naturally produced by Bacillus, as well as to serine proteases like those produced by Bacillus sources but which through the use of genetic engineering techniques are produced by non-Bacillus organisms transformed with a nucleic acid encoding the serine proteases.
The term “identical” in the context of two nucleic acids or polypeptide sequences refers to the residues in the two sequences that are the same when aligned for maximum correspondence, as measured using one of the following sequence comparison or analysis algorithms.
As used herein, “homologous genes” refers to a pair of genes from different, but usually related species, which correspond to each other and which are identical or very similar to each other. The term encompasses genes that are separated by speciation (i.e., the development of new species) (e.g., orthologous genes), as well as genes that have been separated by genetic duplication (e.g., paralogous genes).
As used herein, “% identity or percent identity” refers to sequence similarity. Percent identity may be determined using standard techniques known in the art (See e.g., Smith and Waterman, Adv. Appl. Math. 2:482 [1981]; Needleman and Wunsch, J. Mol. Biol. 48:443 [1970]; Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444 [1988]; software programs such as GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package (Genetics Computer Group, Madison, Wis.); and Devereux et al., Nucl. Acid Res. 12:387-395 [1984]). One example of a useful algorithm is PILEUP. PILEUP creates a multiple sequence alignment from a group of related sequences using progressive, pair-wise alignments. It can also plot a tree showing the clustering relationships used to create the alignment. PILEUP uses a simplification of the progressive alignment method of Feng and Doolittle (See, Feng and Doolittle, J. Mol. Evol. 35:351-360 [1987]). The method is similar to that described by Higgins and Sharp (See, Higgins and Sharp, CABIOS 5:151-153 [1989]). Useful PILEUP parameters include a default gap weight of 3.00, a default gap length weight of 0.10, and weighted end gaps. Other useful algorithm is the BLAST algorithms described by Altschul et al., (See, Altschul et al., J. Mol. Biol. 215:403-410 [1990]; and Karlin and Altschul, Proc. Natl. Acad. Sci. USA 90:5873-5787 [1993]). The BLAST program uses several search parameters, most of which are set to the default values.
The NCBI BLAST algorithm finds the most relevant sequences in terms of biological similarity but is not recommended for query sequences of less than 20 residues (Altschul, S F et al. (1997) Nucleic Acids Res. 25:3389-3402 and Schaffer, A A et al. (2001) Nucleic Acids Res. 29:2994-3005). Example default BLAST parameters for a nucleic acid sequence searches are:
Neighboring words threshold: 11
E-value cutoff: 10
Scoring Matrix: NUC.3.1 (match=1, mismatch=−3)
and the following parameters for amino acid sequence searches:
Word size: 3
E-value cutoff: 10
Gap extension: 1
A percent (%) amino acid sequence identity value is determined by the number of matching identical residues divided by the total number of residues of the “reference” sequence including any gaps created by the program for optimal/maximum alignment. If a sequence is 90% identical to SEQ ID NO: A, SEQ ID NO: A is the “reference” sequence. BLAST algorithms refer the “reference” sequence as “query” sequence.
The CLUSTAL W algorithm is another example of a sequence alignment algorithm. See Thompson et al. (1994) Nucleic Acids Res. 22:4673-4680. Default parameters for the CLUSTAL W algorithm are:
Gap opening penalty: 10.0
Gap extension penalty: 0.05
Protein weight matrix: BLOSUM series
DNA weight matrix: IUB
Delay divergent sequences %: 40
Gap separation distance: 8
DNA transitions weight: 0.50
List hydrophilic residues: GPSNDQEKR
Use negative matrix: OFF
Toggle Residue specific penalties: ON
Toggle hydrophilic penalties: ON
Toggle end gap separation penalty OFF.
In CLUSTAL algorithms, deletions occurring at either terminus are included. For example, a variant with five amino acid deletion at either terminus (or within the polypeptide) of a polypeptide of 500 amino acids would have a percent sequence identity of 99% (495/500 identical residues×100) relative to the “reference” polypeptide. Such a variant would be encompassed by a variant having “at least 99% sequence identity” to the polypeptide.
A polypeptide of interest may be said to be “substantially identical” to a reference polypeptide if the polypeptide of interest comprises an amino acid sequence having at least about 60%, least about 65%, least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or at least about 99.5% sequence identity to the amino acid sequence of the reference polypeptide. The percent identity between two such polypeptides can be determined manually by inspection of the two optimally aligned polypeptide sequences or by using software programs or algorithms (e.g., BLAST, ALIGN, CLUSTAL) using standard parameters. One indication that two polypeptides are substantially identical is that the first polypeptide is immunologically cross-reactive with the second polypeptide. Typically, polypeptides that differ by conservative amino acid substitutions are immunologically cross-reactive. Thus, a polypeptide is substantially identical to a second polypeptide, for example, where the two peptides differ only by a conservative amino acid substitution or one or more conservative amino acid substitutions.
A nucleic acid of interest may be said to be “substantially identical” to a reference nucleic acid if the nucleic acid of interest comprises a nucleotide sequence having least about 60%, least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, or at least about 99.5% sequence identity to the nucleotide sequence of the reference nucleic acid. The percent identity between two such nucleic acids can be determined manually by inspection of the two optimally aligned nucleic acid sequences or by using software programs or algorithms (e.g., BLAST, ALIGN, CLUSTAL) using standard parameters. One indication that two nucleic acid sequences are substantially identical is that the two nucleic acid molecules hybridize to each other under stringent conditions (e.g., within a range of medium to high stringency).
A nucleic acid or polynucleotide is “isolated” when it is at least partially or completely separated from other components, including but not limited to for example, other proteins, nucleic acids, cells, etc. Similarly, a polypeptide, protein or peptide is “isolated” when it is at least partially or completely separated from other components, including but not limited to for example, other proteins, nucleic acids, cells, etc. On a molar basis, an isolated species is more abundant than are other species in a composition. For example, an isolated species may comprise at least about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or about 100% (on a molar basis) of all macromolecular species present. Preferably, the species of interest is purified to essential homogeneity (i.e., contaminant species cannot be detected in the composition by conventional detection methods). Purity and homogeneity can be determined using a number of techniques well known in the art, such as agarose or polyacrylamide gel electrophoresis of a nucleic acid or a protein sample, respectively, followed by visualization upon staining. If desired, a high-resolution technique, such as high performance liquid chromatography (HPLC) or a similar means can be utilized for purification of the material.
“Hybridization” refers to the process by which one strand of nucleic acid forms a duplex with, i.e., base pairs with, a complementary strand. A nucleic acid sequence is considered to be “selectively hybridizable” to a reference nucleic acid sequence if the two sequences specifically hybridize to one another under moderate to high stringency hybridization and wash conditions. Hybridization conditions are based on the melting temperature (Tm) of the nucleic acid binding complex or probe. For example, “maximum stringency” typically occurs at about Tm-5° C. (5° below the Tm of the probe); “high stringency” at about 5-10° C. below the Tm; “intermediate stringency” at about 10-20° C. below the Tm of the probe; and “low stringency” at about 20-25° C. below the Tm. Functionally, maximum stringency conditions can be used to identify sequences having strict identity or near-strict identity with the hybridization probe; while intermediate or low stringency hybridization can be used to identify or detect polynucleotide sequence homologs.
Moderate and high stringency hybridization conditions are well known in the art. Stringent hybridization conditions are exemplified by hybridization under the following conditions: 65° C. and 0.1×SSC (where 1×SSC=0.15 M NaCl, 0.015 M Na3 citrate, pH 7.0). Hybridized, duplex nucleic acids are characterized by a melting temperature (Tm), where one half of the hybridized nucleic acids are unpaired with the complementary strand. Mismatched nucleic acids within the duplex lower the Tm. Very stringent hybridization conditions involve 68° C. and 0.1×SSC. A nucleic acid encoding a variant metalloprotease can have a Tm reduced by 1° C.-3° C. or more compared to a duplex formed between the nucleic acid of SEQ ID NO: 4 and its identical complement.
Another example of high stringency conditions includes hybridization at about 42° C. in 50% formamide, 5×SSC, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured carrier DNA followed by washing two times in 2×SSC and 0.5% SDS at room temperature and two additional times in 0.1×SSC and 0.5% SDS at 42° C. An example of moderate stringent conditions include an overnight incubation at 37° C. in a solution comprising 20% formamide, 5×SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulfate and 20 mg/ml denatured sheared salmon sperm DNA, followed by washing the filters in 1×SSC at about 37-50° C. Those of skill in the art know how to adjust the temperature, ionic strength, etc. to accommodate factors such as probe length and the like.
The term “purified” as applied to nucleic acids or polypeptides generally denotes a nucleic acid or polypeptide that is essentially free from other components as determined by analytical techniques well known in the art (e.g., a purified polypeptide or polynucleotide forms a discrete band in an electrophoretic gel, chromatographic eluate, and/or a media subjected to density gradient centrifugation). For example, a nucleic acid or polypeptide that gives rise to essentially one band in an electrophoretic gel is “purified.” A purified nucleic acid or polypeptide is at least about 50% pure, usually at least about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, about 99.5%, about 99.6%, about 99.7%, about 99.8% or more pure (e.g., percent by weight on a molar basis). In a related sense, the invention provides methods of enriching compositions for one or more molecules of the invention, such as one or more polypeptides or polynucleotides of the invention. A composition is enriched for a molecule when there is a substantial increase in the concentration of the molecule after application of a purification or enrichment technique. A substantially pure polypeptide or polynucleotide of the invention (e.g., substantially pure metalloprotease polypeptide or polynucleotide encoding a metalloprotease polypeptide of the invention, respectively) will typically comprise at least about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98, about 99%, about 99.5% or more by weight (on a molar basis) of all macromolecular species in a particular composition.
The term “enriched” refers to a compound, polypeptide, cell, nucleic acid, amino acid, or other specified material or component that is present in a composition at a relative or absolute concentration that is higher than a starting composition.
In a related sense, the invention provides methods of enriching compositions for one or more molecules of the invention, such as one or more polypeptides of the invention (e.g., one or more metalloprotease polypeptides of the invention) or one or more nucleic acids of the invention (e.g., one or more nucleic acids encoding one or more metalloprotease polypeptides of the invention). A composition is enriched for a molecule when there is a substantial increase in the concentration of the molecule after application of a purification or enrichment technique. A substantially pure polypeptide or polynucleotide will typically comprise at least about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98, about 99%, about 99.5% or more by weight (on a molar basis) of all macromolecular species in a particular composition.
As used herein, the term “combinatorial mutagenesis” or “combinatorial” refers to methods in which libraries of nucleic acid variants of a reference nucleic acid sequence are generated. In these libraries, the variants contain one or several mutations chosen from a predefined set of mutations. The methods also provide means to introduce random mutations which were not members of the predefined set of mutations. Some such methods include those set forth in U.S. Pat. No. 6,582,914, hereby incorporated by reference. Some such combinatorial mutagenesis methods include and/or encompass methods embodied in commercially available kits (e.g., QUIKCHANGE® Multi Site-Directed Mutagenesis Kit (Stratagene), PCR fusion/extension PCR).
As used herein, “having improved properties” used in connection with a variant protease refers to a variant protease with improved or enhanced wash or cleaning performance, and/or improved or enhanced stability optionally with retained wash or cleaning performance, relative to the corresponding reference protease (e.g., wild-type or naturally-occurring protease). The improved properties of a variant protease may comprise improved wash or cleaning performance and/or improved stability. In some embodiments, the invention provides variant proteases of the invention that exhibit one of more of the following properties: improved hand wash performance, improved hand or manual dishwashing performance, improved automatic dishwashing performance, improved laundry performance, and/or improved stability relative to a reference protease (e.g., wild-type protease, such as a wild-type thermolysin).
As used herein, the term “functional assay” refers to an assay that provides an indication of a protein's activity. In some embodiments, the term refers to assay systems in which a protein is analyzed for its ability to function in its usual capacity. For example, in the case of enzymes, a functional assay involves determining the effectiveness of the enzyme in catalyzing a reaction.
As used herein, the term “target property” refers to the property of the starting gene that is to be altered. It is not intended that the present invention be limited to any particular target property. However, in some embodiments, the target property is the stability of a gene product (e.g., resistance to denaturation, proteolysis or other degradative factors), while in other embodiments, the level of production in a production host is altered.
The term “property” or grammatical equivalents thereof in the context of a nucleic acid, as used herein, refer to any characteristic or attribute of a nucleic acid that can be selected or detected. These properties include, but are not limited to, a property affecting binding to a polypeptide, a property conferred on a cell comprising a particular nucleic acid, a property affecting gene transcription (e.g., promoter strength, promoter recognition, promoter regulation, enhancer function), a property affecting RNA processing (e.g., RNA splicing, RNA stability, RNA conformation, and post-transcriptional modification), a property affecting translation (e.g., level, regulation, binding of mRNA to ribosomal proteins, post-translational modification). For example, a binding site for a transcription factor, polymerase, regulatory factor, etc., of a nucleic acid may be altered to produce desired characteristics or to identify undesirable characteristics.
The term “property” or grammatical equivalents thereof in the context of a polypeptide (including proteins), as used herein, refer to any characteristic or attribute of a polypeptide that can be selected or detected. These properties include, but are not limited to oxidative stability, substrate specificity, catalytic activity, enzymatic activity, thermal stability, alkaline stability, pH activity profile, resistance to proteolytic degradation, KM, kcat, kcat/kM ratio, protein folding, inducing an immune response, ability to bind to a ligand, ability to bind to a receptor, ability to be secreted, ability to be displayed on the surface of a cell, ability to oligomerize, ability to signal, ability to stimulate cell proliferation, ability to inhibit cell proliferation, ability to induce apoptosis, ability to be modified by phosphorylation or glycosylation, and/or ability to treat disease, etc.
As used herein, the term “screening” has its usual meaning in the art. In one exemplary screening process, a mutant nucleic acid or variant polypeptide encoded therefrom is provided and a property of the mutant nucleic acid or variant polypeptide, respectively, is assessed or determined. The determined property of the mutant nucleic acid or variant polypeptide may be compared to a property of the corresponding precursor (parent) nucleic acid or to the property of the corresponding parent polypeptide, respectively.
It will be apparent to the skilled artisan that the screening procedure for obtaining a nucleic acid or protein with an altered property depends upon the property of the starting material the modification of which the generation of the mutant nucleic acid is intended to facilitate. The skilled artisan will therefore appreciate that the invention is not limited to any specific property to be screened for and that the following description of properties lists illustrative examples only. Methods for screening for any particular property are generally described in the art. For example, one can measure binding, pH, specificity, etc., before and after mutation, wherein a change indicates an alteration. Preferably, the screens are performed in a high-throughput manner, including multiple samples being screened simultaneously, including, but not limited to assays utilizing chips, phage display, and multiple substrates and/or indicators.
As used herein, in some embodiments, a screening process encompasses one or more selection steps in which variants of interest are enriched from a population of variants. Examples of these embodiments include the selection of variants that confer a growth advantage to the host organism, as well as phage display or any other method of display, where variants can be captured from a population of variants based on their binding or catalytic properties. In some embodiments, a library of variants is exposed to stress (e.g., heat, denaturation, etc.) and subsequently variants that are still intact are identified in a screen or enriched by selection. It is intended that the term encompass any suitable means for selection. Indeed, it is not intended that the present invention be limited to any particular method of screening.
The terms “modified nucleic acid sequence” and “modified gene” are used interchangeably herein to refer to a nucleic acid sequence that includes a deletion, insertion or interruption of naturally occurring (i.e., wild-type) nucleic acid sequence. In some embodiments, the expression product of the modified nucleic acid sequence is a truncated protein (e.g., if the modification is a deletion or interruption of the sequence). In some embodiments, the truncated protein retains biological activity. In alternative embodiments, the expression product of the modified nucleic acid sequence is an elongated protein (e.g., modifications comprising an insertion into the nucleic acid sequence). In some embodiments, a nucleotide insertion in the nucleic acid sequence leads to a truncated protein (e.g., when the insertion results in the formation of a stop codon). Thus, an insertion may result in either a truncated protein or an elongated protein as an expression product.
A “mutant” nucleic acid sequence typically refers to a nucleic acid sequence that has an alteration in at least one codon occurring in a host cell's wild-type sequence such that the expression product of the mutant nucleic acid sequence is a protein with an altered amino acid sequence relative to the wild-type protein. The expression product may have an altered functional capacity (e.g., enhanced enzymatic activity).
As used herein, the phrase “alteration in substrate specificity” refers to changes in the substrate specificity of an enzyme. In some embodiments, a change in substrate specificity is defined as a change in kcat and/or Km for a particular substrate, resulting from mutations of the enzyme or alteration of reaction conditions. The substrate specificity of an enzyme is determined by comparing the catalytic efficiencies it exhibits with different substrates. These determinations find particular use in assessing the efficiency of mutant enzymes, as it is generally desired to produce variant enzymes that exhibit greater ratios of kcat/Km for substrates of interest. However, it is not intended that the present invention be limited to any particular substrate composition or substrate specificity.
As used herein, “surface property” is used in reference to electrostatic charge, as well as properties such as the hydrophobicity and hydrophilicity exhibited by the surface of a protein.
As used herein, the term “net charge” is defined as the sum of all charges present in a molecule. “Net charge changes” are made to a parent protein molecule to provide a variant that has a net charge that differs from that of the parent molecule (i.e., the variant has a net charge that is not the same as that of the parent molecule). For example, substitution of a neutral amino acid with a negatively charged amino acid or a positively charged amino acid with a neutral amino acid results in net charge of −1 with respect to the parent molecule. Substitution of a positively charged amino acid with a negatively charged amino acid results in a net charge of −2 with respect to the parent. Substitution of a neutral amino acid with a positively charged amino acid or a negatively charged amino acid with a neutral amino acid results in net charge of +1 with respect to the parent. Substitution of a negatively charged amino acid with a positively charged amino acid results in a net charge of +2 with respect to the parent. The net charge of a parent protein can also be altered by deletion and/or insertion of charged amino acids
The terms “thermally stable” and “thermostable” and “thermostability” refer to proteases that retain a specified amount of enzymatic activity after exposure to identified temperatures over a given period of time under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process of the invention, while being exposed to altered temperatures. “Altered temperatures” encompass increased or decreased temperatures. In some embodiments, the proteases retain at least about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 92%, about 95%, about 96%, about 97%, about 98%, or about 99% proteolytic activity after exposure to altered temperatures over a given time period, for example, at least about 60 minutes, about 120 minutes, about 180 minutes, about 240 minutes, about 300 minutes, etc.
The term “enhanced stability” in the context of an oxidation, chelator, thermal and/or pH stable protease refers to a higher retained proteolytic activity over time as compared to other proteases (e.g., thermolysin proteases) and/or wild-type enzymes.
The term “diminished stability” in the context of an oxidation, chelator, thermal and/or pH stable protease refers to a lower retained proteolytic activity over time as compared to other proteases (e.g., thermolysin proteases) and/or wild-type enzymes.
The term “cleaning activity” refers to a cleaning performance achieved by a variant protease or reference protease under conditions prevailing during the proteolytic, hydrolyzing, cleaning, or other process of the invention. In some embodiments, cleaning performance of a variant protease or reference protease may be determined by using various assays for cleaning one or more various enzyme sensitive stains on an item or surface (e.g., a stain resulting from food, grass, blood, ink, milk, oil, and/or egg protein). Cleaning performance of a variant or reference protease can be determined by subjecting the stain on the item or surface to standard wash condition(s) and assessing the degree to which the stain is removed by using various chromatographic, spectrophotometric, or other quantitative methodologies. Exemplary cleaning assays and methods are known in the art and include, but are not limited to those described in WO 99/34011 and U.S. Pat. No. 6,605,458, both of which are herein incorporated by reference, as well as those cleaning assays and methods included in the Examples provided below.
The term “cleaning effective amount” of a variant protease or reference protease refers to the amount of protease that achieves a desired level of enzymatic activity in a specific cleaning composition. Such effective amounts are readily ascertained by one of ordinary skill in the art and are based on many factors, such as the particular protease used, the cleaning application, the specific composition of the cleaning composition, and whether a liquid or dry (e.g., granular, tablet, bar) composition is required, etc.
The term “cleaning adjunct material” refers to any liquid, solid, or gaseous material included in cleaning composition other than a variant protease of the invention. In some embodiments, the cleaning compositions of the present invention include one of more cleaning adjunct materials. Each cleaning adjunct material is typically selected depending on the particular type and form of cleaning composition (e.g., liquid, granule, powder, bar, paste, spray, tablet, gel, foam, or other composition). Preferably, each cleaning adjunct material is compatible with the protease enzyme used in the composition.
The term “enhanced performance” in the context of cleaning activity refers to an increased or greater cleaning activity by an enzyme on certain enzyme sensitive stains such as egg, milk, grass, ink, oil, and/or blood, as determined by usual evaluation after a standard wash cycle and/or multiple wash cycles.
The term “diminished performance” in the context of cleaning activity refers to a decreased or lesser cleaning activity by an enzyme on certain enzyme sensitive stains such as egg, milk, grass or blood, as determined by usual evaluation after a standard wash cycle.
Cleaning performance can be determined by comparing the variant proteases of the present invention with reference proteases in various cleaning assays concerning enzyme sensitive stains such as grass, blood, ink, oil, and/or milk as determined by usual spectrophotometric or analytical methodologies after standard wash cycle conditions.
As used herein, the term “consumer product” means fabric and home care product. As used herein, the term “fabric and home care product” or “fabric and household care product” includes products generally intended to be used or consumed in the form in which they are sold and that are for treating fabrics, hard surfaces and any other surfaces, and cleaning systems all for the care and cleaning of inanimate surfaces, as well as fabric conditioner products and other products designed specifically for the care and maintenance of fabrics, and air care products, including: air care including air fresheners and scent delivery systems, car care, pet care, livestock care, personal care, jewelry care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, pre-treatment cleaning compositions, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, glass cleaners and/or treatments, tile cleaners and/or treatments, ceramic cleaners and/or treatments, and other cleaning for consumer or institutional use. In some embodiments, the fabric and home care products are suitable for use on wounds and/or skin. “Fabric and home care product” includes consumer and institutional products.
As used herein, the term “non-fabric and home care products” refers to compositions that are added to other compositions to produce an end product that may be a fabric and home care product.
As used herein, the term “institutional cleaning composition” refers to products suitable for use in institutions including but not limited to schools, hospitals, factories, stores, corporations, buildings, restaurants, office complexes and buildings, processing and/or manufacturing plants, veterinary hospitals, factory farms, factory ranches, etc.
As used herein, the term “cleaning and/or treatment composition” is a subset of fabric and home care products that includes, unless otherwise indicated, compositions suitable for cleaning and/or treating items. Such products include, but are not limited to, products for treating fabrics, hard surfaces and any other surfaces in the area of fabric and home care, including: air care including air fresheners and scent delivery systems, car care, dishwashing, fabric conditioning (including softening and/or freshening), laundry detergency, laundry and rinse additive and/or care, hard surface cleaning and/or treatment including floor and toilet bowl cleaners, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use: car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets.
Indeed, as used herein, “cleaning composition” or “cleaning formulation” of the invention refers to any composition of the invention useful for removing or eliminating a compound (e.g., undesired compound) from an object, item or surface to be cleaned, including, but not limited to for example, a fabric, fabric item, dishware item, tableware item, glassware item, contact lens, other solid substrate, hair (shampoo) (including human or animal hair), skin (soap or and cream), teeth (mouthwashes, toothpastes), surface of an item or object (e.g., hard surfaces, such as the hard surface of a table, table top, wall, furniture item, floor, ceiling, non-dishware item, non-tableware item, etc.), filters, membranes (e.g., filtration membranes, including but not limited to ultrafiltration membranes), etc. The term encompasses any material and/or added compound selected for the particular type of cleaning composition desired and the form of the product (e.g., liquid, gel, granule, spray, or other composition), as long as the composition is compatible with the protease and other enzyme(s) used in the composition. The specific selection of cleaning composition materials are readily made by considering the surface, object, item, or fabric to be cleaned, and the desired form of the composition for the cleaning conditions during use.
Cleaning compositions and cleaning formulations include any composition that is suited for cleaning, bleaching, disinfecting, and/or sterilizing any object, item, and/or surface. Such compositions and formulations include, but are not limited to for example, liquid and/or solid compositions, including cleaning or detergent compositions (e.g., liquid, tablet, gel, bar, granule, and/or solid laundry cleaning or detergent compositions and fine fabric detergent compositions; hard surface cleaning compositions and formulations, such as for glass, wood, ceramic and metal counter tops and windows; carpet cleaners; oven cleaners; fabric fresheners; fabric softeners; and textile, laundry booster cleaning or detergent compositions, laundry additive cleaning compositions, and laundry pre-spotter cleaning compositions; dishwashing compositions, including hand or manual dishwash compositions (e.g., “hand” or “manual” dishwashing detergents) and automatic dishwashing compositions (e.g., “automatic dishwashing detergents”).
Cleaning composition or cleaning formulations, as used herein, include, unless otherwise indicated, granular or powder-form all-purpose or heavy-duty washing agents, especially cleaning detergents; liquid, granular, gel, solid, tablet, or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid (HDL) detergent or heavy-duty powder detergent (HDD) types; liquid fine-fabric detergents; hand or manual dishwashing agents, including those of the high-foaming type; hand or manual dishwashing, automatic dishwashing, or dishware or tableware washing agents, including the various tablet, powder, solid, granular, liquid, gel, and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, including antibacterial hand-wash types, cleaning bars, mouthwashes, denture cleaners, car shampoos, carpet shampoos, bathroom cleaners; hair shampoos and/or hair-rinses for humans and other animals; shower gels and foam baths and metal cleaners; as well as cleaning auxiliaries, such as bleach additives and “stain-stick” or pre-treat types. In some embodiments, granular compositions are in “compact” form; in some embodiments, liquid compositions are in a “concentrated” form.
As used herein, “fabric cleaning compositions” include hand and machine laundry detergent compositions including laundry additive compositions and compositions suitable for use in the soaking and/or pretreatment of stained fabrics (e.g., clothes, linens, and other textile materials).
As used herein, “non-fabric cleaning compositions” include non-textile (i.e., non-fabric) surface cleaning compositions, including, but not limited to for example, hand or manual or automatic dishwashing detergent compositions, oral cleaning compositions, denture cleaning compositions, and personal cleansing compositions.
As used herein, the term “fabric and/or hard surface cleaning and/or treatment composition” is a subset of cleaning and treatment compositions that includes, unless otherwise indicated, granular or powder-form all-purpose or “heavy-duty” washing agents, especially cleaning detergents; liquid, gel or paste-form all-purpose washing agents, especially the so-called heavy-duty liquid types; liquid fine-fabric detergents; hand dishwashing agents or light duty dishwashing agents, especially those of the high-foaming type; machine dishwashing agents, including the various tablet, granular, liquid and rinse-aid types for household and institutional use; liquid cleaning and disinfecting agents, car or carpet shampoos, bathroom cleaners including toilet bowl cleaners; fabric conditioning products including softening and/or freshening that may be in liquid, solid and/or dryer sheet form; as well as cleaning auxiliaries such as bleach additives and “stain-stick” or pre-treat types, substrate-laden products such as dryer added sheets. All of such products which are applicable may be in standard, concentrated or even highly concentrated form even to the extent that such products may in certain aspect be non-aqueous.
As used herein, the term “detergent composition” or “detergent formulation” is used in reference to a composition intended for use in a wash medium for the cleaning of soiled or dirty objects, including particular fabric and/or non-fabric objects or items. Such compositions of the present invention are not limited to any particular detergent composition or formulation. Indeed, in some embodiments, the detergents of the invention comprise at least one variant protease of the invention and, in addition, one or more surfactants, transferase(s), hydrolytic enzymes, oxido reductases, builders (e.g., a builder salt), bleaching agents, bleach activators, bluing agents, fluorescent dyes, caking inhibitors, masking agents, enzyme activators, antioxidants, and/or solubilizers. In some instances, a builder salt is a mixture of a silicate salt and a phosphate salt, preferably with more silicate (e.g., sodium metasilicate) than phosphate (e.g., sodium tripolyphosphate). Some compositions of the invention, such as, but not limited to, cleaning compositions or detergent compositions, do not contain any phosphate (e.g., phosphate salt or phosphate builder).
As used herein, the term “bleaching” refers to the treatment of a material (e.g., fabric, laundry, pulp, etc.) or surface for a sufficient length of time and/or under appropriate pH and/or temperature conditions to effect a brightening (i.e., whitening) and/or cleaning of the material. Examples of chemicals suitable for bleaching include, but are not limited to, for example, ClO2, H2O2, peracids, NO2, etc.
As used herein, “wash performance” of a protease (e.g., a variant protease of the invention) refers to the contribution of a variant protease to washing that provides additional cleaning performance to the detergent as compared to the detergent without the addition of the variant protease to the composition. Wash performance is compared under relevant washing conditions. In some test systems, other relevant factors, such as detergent composition, sud concentration, water hardness, washing mechanics, time, pH, and/or temperature, can be controlled in such a way that condition(s) typical for household application in a certain market segment (e.g., hand or manual dishwashing, automatic dishwashing, dishware cleaning, tableware cleaning, fabric cleaning, etc.) are imitated.
The term “relevant washing conditions” is used herein to indicate the conditions, particularly washing temperature, time, washing mechanics, sud concentration, type of detergent and water hardness, actually used in households in a hand dishwashing, automatic dishwashing, or laundry detergent market segment.
The term “improved wash performance” is used to indicate that a better end result is obtained in stain removal under relevant washing conditions, or that less variant protease, on weight basis, is needed to obtain the same end result relative to the corresponding wild-type or starting parent protease.
As used herein, the term “disinfecting” refers to the removal of contaminants from the surfaces, as well as the inhibition or killing of microbes on the surfaces of items. It is not intended that the present invention be limited to any particular surface, item, or contaminant(s) or microbes to be removed.
The “compact” form of the cleaning compositions herein is best reflected by density and, in terms of composition, by the amount of inorganic filler salt. Inorganic filler salts are conventional ingredients of detergent compositions in powder form. In conventional detergent compositions, the filler salts are present in substantial amounts, typically about 17 to about 35% by weight of the total composition. In contrast, in compact compositions, the filler salt is present in amounts not exceeding about 15% of the total composition. In some embodiments, the filler salt is present in amounts that do not exceed about 10%, or more preferably, about 5%, by weight of the composition. In some embodiments, the inorganic filler salts are selected from the alkali and alkaline-earth-metal salts of sulfates and chlorides. In some embodiments, the filler salt is sodium sulfate.
The position of an amino acid residue in a given amino acid sequence is typically numbered herein using the numbering of the position of the corresponding amino acid residue of the G. caldoproteolyticus thermolysin amino acid sequence shown in SEQ ID NO: 3. The G. caldoproteolyticus thermolysin amino acid sequence shown in SEQ ID NO: 3, thus serves as a reference sequence. A given amino acid sequence, such as a variant protease amino acid sequence described herein, can be aligned with the G. caldoproteolyticus sequence (SEQ ID NO: 3) using an alignment algorithm as described herein, and an amino acid residue in the given amino acid sequence that aligns (preferably optimally aligns) with an amino acid residue in the G. caldoproteolyticus sequence can be conveniently numbered by reference to the corresponding amino acid residue in the thermolysin G. caldoproteolyticus sequence.
Generally, the nomenclature used herein and many of the laboratory procedures in cell culture, molecular genetics, molecular biology, nucleic acid chemistry, and protein chemistry described below are well known and commonly employed by those of ordinary skill in the art. Methods for production and manipulation of recombinant nucleic acid methods, nucleic acid synthesis, cell culture methods, and transgene incorporation (e.g., transfection, electroporation) are known to those skilled in the art and are described in numerous standard texts. Oligonucleotide synthesis and purification steps are typically performed according to specifications. Techniques and procedures are generally performed according to conventional methods well known in the art and various general references that are provided throughout this document. Procedures therein are believed to be well known to those of ordinary skill in the art and are provided for the convenience of the reader.
As used herein, a thermolysin enzyme includes an enzyme, polypeptide, or protein, or an active fragment thereof, exhibiting a proteolytic activity. This includes members of the peptidase family M4 of which thermolysin (TLN; EC 3.4.24.27) is the prototype.
The invention provides amino acid positions in a thermolysin enzyme which can be useful in a detergent composition where favorable modifications result in a minimum performing index for wash performance, stability of the enzyme in detergent compositions and thermostability of the enzyme, while having at least one of these characteristics improved from a parent thermolysin enzyme. These modifications are considered suitable modifications of the invention.
The stability of thermolysin enzymes of the present invention can be compared to the stability of a standard, for example, the G. caldoproteolyticus thermolysin of SEQ ID NO: 3.
The terms “thermal stability” and “thermostability” refer to thermolysins of the present disclosure that retain a specified amount of enzymatic activity after exposure to an identified temperature, often over a given period of time under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process disclosed herein, for example while exposed to altered temperatures. Altered temperatures include increased or decreased temperatures. In some embodiments, the variant thermolysin variant retains at least about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 92%, about 95%, about 96%, about 97%, about 98%, or about 99% thermolysin activity after exposure to altered temperatures over a given time period, for example, at least about 60 minutes, about 120 minutes, about 180 minutes, about 240 minutes, about 300 minutes, etc.
As used herein, improved properties of a variant thermolysin enzyme includes a variant thermolysin enzyme with improved or enhanced wash or cleaning performance, and/or improved or enhanced stability optionally with retained wash or cleaning performance, relative to the corresponding parent thermolysin enzyme (e.g., wild-type or naturally-occurring thermolysin enzyme). The improved properties of a variant thermolysin enzyme may comprise improved wash or cleaning performance and/or improved stability. In some embodiments, the invention provides variant thermolysin enzymes of the invention that exhibit one of more of the following properties: improved hand wash performance, improved hand or manual dishwashing performance, improved automatic dishwashing performance, improved laundry performance, and/or improved stability relative to a reference parent thermolysin enzyme (e.g., wild-type thermolysin enzyme, such as a wild-type thermolysin having the sequence of SEQ ID NO: 3).
Productive positions are described as those positions within a molecule that are most useful for making combinatorial variants exhibiting an improved characteristic, where the position itself allows for at least one combinable mutation. Combinable mutations can be described as those substitutions in a molecule that can be used to make combinatorial variants. Combinable mutations are ones that improve at least one desired property of the molecule, while not significantly decreasing either: expression, activity, or stability.
Combinable mutations are ones that improve at least one desired property of the molecule, while not significantly decreasing either: expression, activity, or stability. For example, Combinable mutations in thermolysin can be determined using performance index (PI) values resulting from the assays described in Example 1: Abz-AGLA-Nba protease assay (activity), PAS-38 microswatch assay (activity), detergent stability and thermostability assays, and protein determination (expression).
In addition to Combinable mutations, a second group of mutations for thermolysin is Activity Combinable mutations. Activity Combinable mutations are ones that improve at least one activity property of the molecule, with a performance index greater than or equal to 1.5, while not decreasing either expression or stability PI values below 0.5. These Activity Combinable mutations can be used to modify the molecule in order to achieve a desired property without significantly decreasing other known and desired properties of the molecule (e.g. expression or stability).
Thermolysin enzyme amino acid positions found to be useful positions can have different modifications that are suitable for use in a detergent composition. Modifications can include an insertion, deletion or substitution at the particular position. In one embodiment, a modification is a substitution. For each position, greater numbers of possible suitable modifications results in a higher productivity score for the position. For example, amino acid positions can have at least 75%, 40% or 15% of the modifications tested at a productive position as suitable modifications, wherein the modification meets at least one of the following suitability criteria:
a) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.9, and in addition have a PI for any one of these tests that is greater than or equal to 1.0;
b) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.8, and in addition have a PI for any one of these tests that is greater than or equal to 1.2; or
c) a position wherein the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.5, and in addition have a PI for any one of these tests that is greater than or equal to 1.5.
Thermolysin enzymes positions of the present invention that have at least 75% of the modifications tested as suitable modifications include positions 2, 26, 47, 49, 53, 65, 87, 91, 96, 108, 118, 128, 154, 179, 196, 197, 198, 199, 209, 211, 217, 219, 225, 232, 256, 257, 259, 261, 265, 267, 272, 276, 277, 286, 289, 290, 293, 295, 298, 299, 300, 301, 303, 305, 308, 311, and 316, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3. Suitable modifications include 2 (T,F,L,P,S,V,W,Y,Q,A,C,I,K,M), 26 (T,K,L,R,V,Y,W,F,G,H,I,M,C,D), 47 (R,A,C,H,K,N,D,E,G,L,M,Q,T), 49 (T,A,D,F,H,I,S,W,L,N,Q,V,E,M,Y), 53 (S,F,H,I,M,Q,T,W,K,R,A,N,V,C,L), 65 (S,I,M,Q,V,L,T,W,A,D,E,P,Y), 87 (V,D,E,G,I,S,P,R,T,C,K,L,M,N,Q,W,Y), 91 (L,D,E,F,K,M,P,Q,S,A,N,R,W,Y), 96 (N,C,D,I,V,F,T,G,H,Q,R,S,W,K,L,Y), 108 (Q,C,E,F,H,A,D,I,K,N,L,M), 118 (S,C,G,E,A,D,M,Q,R,T,V), 128 (Q,C,D,E,R,S,V,I,K,A,L,Y), 154 (G,L,Q,S,T,D,I,W,C,N,A,H,K,M,Y), 179 (Y,A,D,H,M,N,Q,S,T,W,F), 196 (G,D,E,T,K,R,V,H,L,Y,A,W), 197 (I,D,K,L,T,V,W,Y,A,H,N,E,Q,R,F,C), 198 (S,C,E,F,G,H,I,P,Q,T,V,M,N,R,W,A,K), 199 (G,C,E,F,H,Q,S,T,W,L,A,Y), 209 (A,D,E,L,S,T,V,G,I,K,P,R,Y,C,M), 211 (Y,A,C,D,F,G,H,I,L,N,Q,S,T,E,R), 217 (Y,Q,S,T,V,W,G,A,F,M,N,C,L), 219 (K,D,F,G,H,I,M,N,Q,T,A,E,R,S), 225 (Q,D,G,H,I,P,V,W,A,M,R,C,E,K,L,S), 232 (I,C,E,F,K,M,N,Q,W,G,L,R,S,T,V,Y), 256 (V,L,T,K,A,D,F,G,H,R,S,N), 257 (G,C,D,E,L,N,P,Q,S,T,Y,K,R), 259 (G,A,C,E,F,H,L,M,W,K,R,N,S,T), 261 (D,A,N,P,V,W,G,H,I,S), 265 (K,A,C,D,M,P,Q,S,G,I,L,R,N), 267 (F,E,G,N,S,V,W,A,C,H,I,K,L,M,T,Y), 272 (T,E,L,V,W,P,Y,C,F,N,Q,A,K), 276 (T,C,F,I,P,Q,W,H,A,L,V,Y), 277 (P,Q,S,T,E,F,G,H,N,R,V,W,A,D,Y), 286 (A,D,E,F,G,H,I,S,P,C,Q,R,T,K,L,M,N,Y), 289 (V,C,E,F,G,I,N,S,W,R,T,L,M,Y,A), 290 (Q,C,D,F,G,L,W,Y,R,T,V,A,H,N), 293 (T,C,E,F,G,H,Q,S,N,V,W,A,I,K,L,M,Y), 295 (L,C,I,N,T,V,F,G,A,K,M,W), 298 (S,C,T,W,Y,E,N,P,A,G,K,M,R), 299 (T,C,F,L,M,R,W,P,D,Q,N,A,K), 300 (S,C,K,M,R,Y,I,L,H,P,V,W,A,G,T,D,N), 301 (Q,E,H,P,R,L,C,F,G,W,M,S,T,V,K), 303 (V,C,H,G,K,L,R,W,A,P,Y), 305 (S,G,I,L,N,W,Y,Q,H,T,V,A,K,M), 308 (Q,C,D,F,G,I,M,R,V,W,Y,A,L), 311 (D,C,E,F,G,I,Q,S,T,A,K,L,M,V,W,Y), and 316 (K,D,E,F,G,H,L,N,P,Q,R,S,V,W,Y,A,M), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
Thermolysin enzymes positions of the present invention that have at least 40% but less than 75% of the modifications tested as suitable modifications include positions 1, 4, 17, 25, 40, 45, 56, 58, 61, 74, 86, 97, 101, 109, 149, 150, 158, 159, 172, 181, 214, 216, 218, 221, 222, 224, 250, 253, 254, 258, 263, 264, 266, 268, 271, 273, 275, 278, 279, 280, 282, 283, 287, 288, 291, 297, 302, 304, 307, and 312, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3. Suitable modifications include 1 (I,K,M,V,A,H,W,Y,C,L), 4 (T,E,A,N,R,V,K,L,M,Y), 17 (Q,I,W,Y,C,R,V,T,L), 25 (S,D,F,A,C,K,M,R), 40 (F,E,G,M,Q,S,Y,W,A,K,L), 45 (K,E,L,S,F,H,Q,Y,A,G,M), 56 (A,K,Q,V,W,H,I,Y,E,M), 58 (A,N,Y,C,V,E,L), 61 (Q,M,R,W,F,V,C,I,L), 74 (H,E,L,V,C,F,M,N,Q,W), 86 (N,L,S,Y,A,C,E,F,G,K,D), 97 (N,K,C,R,S,Y,E,M), 101 (R,T,C,L,S,H), 109 (G,A,L,S,E,M,R,W), 149 (T,M,V,A,L,D,S,N), 150 (D,A,F,K,N,Q,T,V,S), 158 (Q,A,K,M,N,L,R,Y,S), 159 (N,R,W,A,C,G,M,T,S,Y), 172 (F,G,L,M,Q,S,V,W,Y,D,H), 181 (N,L,A,G,K,M,T,S), 214 (P,C,G,K,S,N,A,R), 216 (H,C,E,S,T,R,A), 218 (S,K,L,Y,F,G,T,V), 221 (Y,K,N,Q,R,S,T,V,A,F,G,M), 222 (T,C,D,L,Y,I,V,A,M,K), 224 (T,K,M,F,L,P,Q,V,Y,E,H), 250 (H,A,C,K,M,N,P,Q,R,V,Y), 253 (V,N,T,I,R,Y,M,Q), 254 (S,A,M,R,Y,K,L,N,V,W), 258 (I,E,L,M,N,R,S,A,C,K,Q,V), 263 (L,C,I,Q,T,H,K,N,V,A,M), 264 (G,C,R,A,N,P,Q,S,T), 266 (I,A,F,L,S,C,M,T,V), 268 (Y,M,Q,V,A,S,K), 271 (L,A,D,F,I,N,Y,H), 273 (Q,A,H,Y,C,S,W,E,G,N), 275 (L,I,M,V,C,Q,S,T), 278 (T,G,K,R,Y,C,H,M,N,Q,S), 279 (S,A,D,I,L,M,N,Q,T,G), 280 (N,A,C,D,E,G,Q,H,T), 282 (S,K,N,R,A,H,L,M,T), 283 (Q,K,L,P,R,W,Y,S), 287 (A,I,L,N,V,Y,K,R,T,D,C), 288 (A,C,I,S,T,V,Y,N,L,M), 291 (S,E,I,L,M,N,V,A,T), 297 (G,A,M,R,Y,C,F,K,T,D,N), 302 (E,K,L,G,T,V,D,Q,A), 304 (A,C,D,L,N,R,S,T,W,E,K,Y), 307 (K,A,C,G,I,M,N,Q,R,W,Y,H), and 312 (A,G,M,V,L,N,R,T,C), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
Thermolysin enzymes positions of the present invention that have at least 15% but less than 40% of the modifications tested as suitable modifications include positions 5, 9, 11, 19, 27, 31, 33, 37, 46, 64, 73, 76, 79, 80, 85, 89, 95, 98, 99, 107, 127, 129, 131, 137, 141, 145, 148, 151, 152, 155, 156, 160, 161, 164, 168, 171, 176, 180, 182, 187, 188, 205, 206, 207, 210, 212, 213, 220, 227, 234, 235, 236, 237, 242, 244, 246, 248, 249, 252, 255, 270, 274, 284, 294, 296, 306, 309, 310, 313, 314, and 315, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3. Suitable modifications include 5 (S,D,N,P,H,L), 9 (V,L,T,I), 11 (R,I,Y,K), 19 (N,L,Y,K,S), 27 (Y,W,A,M,V,C,L), 31 (Q,A,K,V,I,C,Y), 33 (N,S,T,K,A,C,L,M), 37 (N,D,Q,R,L,K), 46 (Y,L,H,N,C), 64 (A,H,Q,T,D,E), 73 (A,I,F,L,M,W), 76 (Y,H,L,M,Q,T), 79 (V,L,Q,T,A,N,S), 80 (T,I,D,A,L,N), 85 (K,E,A,L,N,R,S), 89 (N,L,M,H), 95 (G,A,D,H,M,N,S), 98 (A,C,E,H,R,Y,K,V), 99 (A,E,K,P,R,S), 107 (S,D,K,Y,A,G), 127 (G,C,D,E), 129 (T,I,R,E,Y,L,M), 131 (I,Y,W,L), 137 (I,P,A,E,T,V,L), 141 (A,S,C,G), 145 (T,A,C,E,G,M,N,Q), 148 (V,L,N,Y,M,A,Q), 151 (Y,K,G,H,S,W), 152 (T,S,L,M,G), 155 (L,C,I,M), 156 (I,M,T,L,Q), 160 (E,L,Y,Q), 161 (S,A,N,P,T), 164 (I,L,N,S,T,V,C,A), 168 (I,A,M,T,L), 171 (I,C,E,F,L,S,G), 176 (V,L,N,C), 180 (A,E,G,K,T,S), 182 (K,L,A,W), 187 (E,L,D), 188 (I,L,V), 205 (M,L,A,V,Q), 206 (S,A,C,K,L,M,R), 207 (D,A,H,N), 210 (K,I,L,V), 212 (G,Y,A,D,Q), 213 (D,N,S,L,A,G,W), 220 (R,K,V,A), 227 (N,D,L,Y,A), 234 (S,D,N,A,C), 235 (G,M,C,Q,S,A), 236 (I,M,A,C), 237 (I,N,F,M), 242 (Y,C,F,N,V), 244 (I,T,V,F,A,M,L), 246 (Q,E,N,T,L,C,D), 248 (G,A,E,S), 249 (T,K,M,N,L,Y,P), 252 (G,K,Y,A,S,T,W), 255 (V,L,P,A,Y,M,N), 270 (A,C,F,I,L,S,G), 274 (Y,F,H,A,C,Q,T,M), 284 (L,V,W,A,M,Y), 294 (D,A,V,Q,N), 296 (Y,N,L,R,H,W,M), 306 (V,A,S,F,I,L,T), 309 (A,G,S,T,V,C), 310 (F,A,C,W,M), 313 (V,T,A,G,L,I,C), 314 (G,A,E,H,M,S,W,Q), and 315 (V,A,C,I,M,L,T), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
Thermolysin enzymes positions of the present invention that have at least one modification but less than 15% of the modifications tested as suitable modifications include positions 3, 6, 7, 20, 23, 24, 44, 48, 50, 57, 63, 72, 75, 81, 92, 93, 94, 100, 102, 103, 104, 110, 117, 120, 134, 135, 136, 140, 144, 153, 173, 174, 175, 178, 183, 185, 189, 193, 201, 223, 230, 238, 239, 241, 247, 251, 260, 262, 269, and 285, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3. Suitable modifications include 3 (G,Y), 6 (T,C,V), 7 (V,L,I), 20 (I,L,V), 23 (T,F,W), 24 (Y,W), 44 (A,C), 48 (T,E,D), 50 (L,P), 57 (D,K), 63 (F,Y,C), 72 (D,F,W), 75 (Y,A), 81 (Y,F), 92 (S,L), 93 (Y,T,C), 94 (D,T), 100 (I,L,V), 102 (S,G,N), 103 (S,T), 104 (V,A), 110 (Y,L), 117 (G,H), 120 (M,L), 134 (S,A,P), 135 (G,A), 136 (G,A,S), 140 (V,D), 144 (L,T), 153 (A,T), 173 (G,A,C), 174 (T,C,A), 175 (L,H,S), 178 (F,H,Y), 183 (N,S), 185 (D,E), 189 (G,A), 193 (Y,F), 201 (S,C,A), 223 (G,D,K), 230 (V,A), 238 (N,L,M), 239 (K,A), 241 (A,L,S), 247 (G,A,S), 251 (Y,M), 260 (R,A,N), 262 (K,A), 269 (R,V,K), and 285 (R,K,Y), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
These amino acid positions can be considered useful positions for combinatorial modifications to a parent thermolysin enzyme. Thus, the invention includes thermolysin enzymes having one or more modifications at any of the above positions. Suitable modifications include 1 (I,V), 2 (T,C,I,M,P,Q,V), 127 (G,C), 128 (Q,C,E,F,I,L,V,Y), 180 (A,E,N), 181 (N,A,G,Q,S), 196 (G,L,Y), 197 (I,F), 198 (S,A,C,D,E,H,I,M,P,Q,T,V,Y), 211 (Y,A,C,E,F,H,I,Q,S,T,V,W), 224 (T,D,H,Y), 298 (S,A,C,E,F,G,K,M,N,P,Q,R,T,W,Y), 299 (T,A,C,D,F,G,H,I,K,L,M,N,P,Q,R,S,W), and 316 (K,A,D,E,H,M,N,P,Q,S,T,V,Y), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
The invention includes enzyme variants of thermolysin enzymes having one or more modifications from a parent thermolysin enzyme. The enzyme variants can be useful in a detergent composition by having a minimum performing index for wash performance, stability of the enzyme in detergent compositions and thermostability of the enzyme, while having at least one of these characteristics improved from a parent thermolysin enzyme.
Thermolysin enzymes positions of the present invention that have an improved detergent stability or thermostability compared to the parent thermolysin enzyme, and wherein the modification is at a position having a temperature factor greater than 1.5 times the observed variance above the mean main chain temperature factor for all residues in the amino acid sequence of thermolysin set forth in SEQ ID NO: 3 include positions 1, 2, 127, 128, 180, 181, 195, 196, 197, 198, 199, 211, 223, 224, 298, 299, 300, and 316, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
Stability variants of thermolysin can include modifications at a position having an increased temperature factor, based on crystallographic temperature factors which are a measure of the relative motion of individual atoms of a macromolecule. Temperature factors arise as a product of refinement of crystallographic models so that the calculated diffraction pattern given as individual intensities of crystal x-ray diffraction maxima best matches the observed pattern. The temperature factor can be refined as an attenuation factor to reflect that atoms with higher motion will have a diminishing effect of the overall macromolecule aggregate diffraction as a function of the scattering angle (theta), using the form −exp(−B sin2 θ/λ) where the B is the temperature factor (Blundell, T. L. and Johnson L. N., Protein Crystallography, Academic Press, 1976, pp 121). It is likely that regions with higher overall mobility might also represent points where the folded macromolecule is less stable and thus might be points where unfolding begins as the molecule is stressed by increasing temperature or denaturants. It would be further expected that these regions of higher overall mobility would be regions where the average temperature factors would be highest.
Regions calculated as consensus flexibility regions for thermolysin include the regions 1-2, 127-128, 180-181, 195-199, 211, 223-224, 298-300 and 316. Each of these regions can be used to modify thermolysin in order to achieve either thermostability or improved laundry performance. Combinable variants that confer either thermostability or improved laundry performance by modification of a position with a high temperature factor (high flexibility region), include positions 1, 2, 127, 128, 180, 181, 196, 197, 198, 211, 224, 298, 299, and 316. Suitable modifications include 1 (I,V), 2 (T,C,I,M,P,Q,V), 127 (G,C), 128 (Q,C,E,F,I,L,V,Y), 180 (A,E,N), 181 (N,A,G,Q,S), 196 (G,L,Y), 197 (I,F), 198 (S,A,C,D,E,H,I,M,P,Q,T,V,Y), 211 (Y,A,C,E,F,H,I,Q,S,T,V,W), 224 (T,D,H,Y), 298 (S,A,C,E,F,G,K,M,N,P,Q,R,T,W,Y), 299 (T,A,C,D,F,G,H,I,K,L,M,N,P,Q,R,S,W), 316 (K,A,D,E,H,M,N,P,Q,S,T,V,Y), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
In addition to combinable mutations, a second group of mutations for thermolysin is activity combinable mutations. Activity combinable mutations are ones that have PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba greater than or equal to 1.5, while not decreasing either detergent stability or thermostability PI values below 0.5. Activity combinable mutation positions include positions selected from the group consisting of 17, 19, 24, 25, 31, 33, 40, 48, 73, 79, 80, 81, 85, 86, 89, 94, 109, 117, 140, 141, 150, 151, 152, 153, 156, 158, 159, 160, 161, 168, 171, 174, 175, 176, 178, 180, 181, 182, 183, 189, 205, 206, 207, 210, 212, 213, 214, 218, 223, 224, 227, 235, 236, 237, 238, 239, 241, 244, 246, 248, 249, 250, 251, 252, 253, 254, 255, 258, 259, 260, 261, 262, 266, 268, 269, 270, 271, 272, 273, 274, 276, 278, 279, 280, 282, 283, 294, 295, 296, 297, 300, 302, 306, 310, and 312, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3. Activity combinable mutations include 17 (E,F,P), 19 (A,D,H,I,R,T,V), 24 (F,H), 25 (H), 31 (L), 33 (Q), 40 (C), 48 (A,R), 73 (Y), 79 (C), 80 (C,R), 81 (H), 85 (C,M,Y), 86 (V), 89 (K,R,T,V), 94 (E), 109 (D), 117 (A,K,R,T), 140 (S), 141 (T), 150 (E,M,W), 151 (A,C,E,I), 152 (D), 153 (V), 156 (H,R), 158 (F,G,I,V), 159 (F,I,K), 160 (S), 161 (Y), 168 (N), 171 (D), 174 (S,V), 175 (C,E,F,G,I), 176 (E,Q), 178 (C,M), 180 (L,W), 181 (Y), 182 (F,R), 183 (H,I,L,M,Q,R,T), 189 (C), 205 (C,F), 206 (F,H,I,T,V,Y), 207 (T), 210 (A,E,F,G,H,T), 212 (F,H,K,M,N,R,S,T), 213 (I,K,R,V,Y), 214 (Q), 218 (R), 223 (Y), 224 (I,R), 227 (C,E,G,K,Q,R,S,T,V), 235 (D,L,T), 236 (P), 237 (A,Q), 238 (A,C,D,E,R,S), 239 (C,G,H,L,Q,R,S,V,Y), 241 (E,F,G,I,T,V), 244 (Q), 246 (K,R), 248 (C,H), 249 (G,V), 250 (F,S), 251 (H), 252 (F,I,L), 253 (A,D,E,P), 254 (C,F,G,H,I,P), 255 (F,Q), 258 (F), 259 (I), 260 (C,D,I), 261 (K,R,T), 262 (C,F,H,L,P,R), 266 (W), 268 (F,R), 269 (P,T,W,Y), 270 (M,N,P,V), 271 (V), 272 (R), 273 (R), 274 (D,E), 276 (G,S), 278 (V), 279 (E), 280 (P,R,V), 282 (P), 283 (A,C,E,G,H,T,V), 294 (T), 295 (R), 296 (E,I), 297 (I,V), 300 (Q), 302 (W), 306 (Y), 310 (I,N), and 312 (Q), wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of thermolysin set forth in SEQ ID NO: 3.
The present invention provides novel polypeptides, which may be collectively referred to as “polypeptides of the invention.” Polypeptides of the invention include isolated, recombinant, substantially pure, or non-naturally occurring variant thermolysin enzyme polypeptides, including for example, variant thermolysin enzyme polypeptides, having enzymatic activity (e.g., thermolysin activity). In some embodiments, polypeptides of the invention are useful in cleaning applications and can be incorporated into cleaning compositions that are useful in methods of cleaning an item or a surface (e.g., of surface of an item) in need of cleaning.
In some embodiments, the thermolysin enzyme variant can be a variant of a parent thermolysin enzyme from the Genus Bacillus or Geobacillus. Various thermolysin enzymes have been found in the genus Bacillus or Geobacillus that have a high identity to each other and to the thermolysin enzyme from as shown in SEQ ID NO: 3. See, for example, Tables 4.1 and
In some embodiments, the thermolysin enzyme variant can be a variant having 50, 60, 70, 80, 90, 95, 96, 97, 98, 99 or 100% identity to a thermolysin enzyme from the genus Bacillus or Geobacillus. In various embodiments, the thermolysin enzyme variant can be a variant having 50, 60, 70, 80, 90, 95, 96, 97, 98, 99 or 100% identity to a thermolysin enzyme from any genus in Table 4.1. In various embodiments, the thermolysin enzyme variant can be a variant having 50, 60, 70, 80, 90, 95, 96, 97, 98, 99 or 100% identity to a thermolysin enzyme from any genus in Table 4.2.
In a particular embodiment, the invention is an enzyme derived from the genus Bacillus or Geobacillus. In a particular embodiment, the invention is an enzyme derived from a thermolysin enzyme from the species Geobacillus caldoproteolyticus.
Described are compositions and methods relating to thermolysin cloned from Geobacillus caldoproteolyticus. The compositions and methods are based, in part, on the observation that cloned and expressed thermolysin has proteolytic activity in the presence of a detergent composition. Thermolysin also demonstrates excellent stability in detergent compositions. These features of thermolysin makes it well suited for use in a variety of cleaning applications, where the enzyme can hydrolyze proteins in the presence of surfactants and other components found in detergent compositions.
In one aspect, the present compositions and methods provide a variant thermolysin polypeptide. The parent thermolysin polypeptide was isolated from (SEQ ID NO:4). The mature thermolysin polypeptide has the amino acid sequence of SEQ ID NO: 3. Similar, substantially identical thermolysin polypeptides may occur in nature, e.g., in other strains or isolates of G. caldoproteolyticus. These and other recombinant thermolysin polypeptides are encompassed by the present compositions and methods.
In some embodiments, the invention includes an isolated, recombinant, substantially pure, or non-naturally occurring variant thermolysin enzyme having thermolysin activity, which polypeptide comprises a polypeptide sequence having at least about 85%, at least about 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, at least about 99.5%, or 100% sequence identity to a parent thermolysin enzyme as provided herein.
In some embodiments, the variant polypeptide is a variant having a specified degree of amino acid sequence homology to the exemplified thermolysin polypeptide, e.g., at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or even at least 99% sequence homology to the amino acid sequence of SEQ ID NO: 3 or 4. Homology can be determined by amino acid sequence alignment, e.g., using a program such as BLAST, ALIGN, or CLUSTAL, as described herein.
Also provided is an isolated, recombinant, substantially pure, or non-naturally occurring sequence which encodes a variant thermolysin enzyme having thermolysin activity, said variant thermolysin enzyme (e.g., variant thermolysin) comprising an amino acid sequence which differs from the amino acid sequence of SEQ ID NO:4 by no more than 50, no more than 40, no more than 30, no more than 35, no more than 25, no more than 20, no more than 19, no more than 18, no more than 17, no more than 16, no more than 15, no more than 14, no more than 13, no more than 12, no more than 11, no more than 10, no more than 9, no more than 8, no more than 7, no more than 6, no more than 5, no more than 4, no more than 3, no more than 2, or no more than 1 amino acid residue(s), wherein amino acid positions of the variant thermolysin are numbered according to the numbering of corresponding amino acid positions in the amino acid sequence of thermolysin shown in SEQ ID NO: 3 as determined by alignment of the variant thermolysin enzyme amino acid sequence with the Geobacillus caldoproteolyticus thermolysin amino acid sequence.
As noted above, the variant thermolysin enzyme polypeptides of the invention have enzymatic activities (e.g., thermolysin activities) and thus are useful in cleaning applications, including but not limited to, methods for cleaning dishware items, tableware items, fabrics, and items having hard surfaces (e.g., the hard surface of a table, table top, wall, furniture item, floor, ceiling, etc.). Exemplary cleaning compositions comprising one or more variant thermolysin enzyme polypeptides of the invention are described infra. The enzymatic activity (e.g., thermolysin enzyme activity) of a variant thermolysin enzyme polypeptide of the invention can be determined readily using procedures well known to those of ordinary skill in the art. The Examples presented infra describe methods for evaluating the enzymatic activity, cleaning performance, detergent stability and/or thermostability. The performance of variant thermolysin enzymes of the invention in removing stains (e.g., a lipid stain), cleaning hard surfaces, or cleaning laundry, dishware or tableware item(s) can be readily determined using procedures well known in the art and/or by using procedures set forth in the Examples.
A polypeptide of the invention can be subject to various changes, such as one or more amino acid insertions, deletions, and/or substitutions, either conservative or non-conservative, including where such changes do not substantially alter the enzymatic activity of the polypeptide. Similarly, a nucleic acid of the invention can also be subject to various changes, such as one or more substitutions of one or more nucleic acids in one or more codons such that a particular codon encodes the same or a different amino acid, resulting in either a silent variation (e.g., mutation in a nucleotide sequence results in a silent mutation in the amino acid sequence, for example when the encoded amino acid is not altered by the nucleic acid mutation) or non-silent variation, one or more deletions of one or more nucleic acids (or codons) in the sequence, one or more additions or insertions of one or more nucleic acids (or codons) in the sequence, and/or cleavage of or one or more truncations of one or more nucleic acids (or codons) in the sequence. Many such changes in the nucleic acid sequence may not substantially alter the enzymatic activity of the resulting encoded variant thermolysin enzyme compared to the variant thermolysin enzyme encoded by the original nucleic acid sequence. A nucleic acid of the invention can also be modified to include one or more codons that provide for optimum expression in an expression system (e.g., bacterial expression system), while, if desired, said one or more codons still encode the same amino acid(s).
In some embodiments, the present invention provides a genus of polypeptides comprising variant thermolysin enzyme polypeptides having the desired enzymatic activity (e.g., thermolysin enzyme activity or cleaning performance activity) which comprise sequences having the amino acid substitutions described herein and also which comprise one or more additional amino acid substitutions, such as conservative and non-conservative substitutions, wherein the polypeptide exhibits, maintains, or approximately maintains the desired enzymatic activity (e.g., thermolysin enzyme activity or proteolytic activity, as reflected in the cleaning activity or performance of the variant thermolysin enzyme). Amino acid substitutions in accordance with the invention may include, but are not limited to, one or more non-conservative substitutions and/or one or more conservative amino acid substitutions. A conservative amino acid residue substitution typically involves exchanging a member within one functional class of amino acid residues for a residue that belongs to the same functional class (identical amino acid residues are considered functionally homologous or conserved in calculating percent functional homology). A conservative amino acid substitution typically involves the substitution of an amino acid in an amino acid sequence with a functionally similar amino acid. For example, alanine, glycine, serine, and threonine are functionally similar and thus may serve as conservative amino acid substitutions for one another. Aspartic acid and glutamic acid may serve as conservative substitutions for one another. Asparagine and glutamine may serve as conservative substitutions for one another. Arginine, lysine, and histidine may serve as conservative substitutions for one another. Isoleucine, leucine, methionine, and valine may serve as conservative substitutions for one another. Phenylalanine, tyrosine, and tryptophan may serve as conservative substitutions for one another.
Other conservative amino acid substitution groups can be envisioned. For example, amino acids can be grouped by similar function or chemical structure or composition (e.g., acidic, basic, aliphatic, aromatic, sulfur-containing). For instance, an aliphatic grouping may comprise: Glycine (G), Alanine (A), Valine (V), Leucine (L), Isoleucine (I). Other groups containing amino acids that are considered conservative substitutions for one another include: aromatic: Phenylalanine (F), Tyrosine (Y), Tryptophan (W); sulfur-containing: Methionine (M), Cysteine (C); Basic: Arginine (R), Lysine (K), Histidine (H); Acidic: Aspartic acid (D), Glutamic acid (E); non-polar uncharged residues, Cysteine (C), Methionine (M), and Proline (P); hydrophilic uncharged residues: Serine (S), Threonine (T), Asparagine (N), and Glutamine (Q). Additional groupings of amino acids are well-known to those of skill in the art and described in various standard textbooks. Listing of a polypeptide sequence herein, in conjunction with the above substitution groups, provides an express listing of all conservatively substituted polypeptide sequences.
More conservative substitutions exist within the amino acid residue classes described above, which also or alternatively can be suitable. Conservation groups for substitutions that are more conservative include: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, and asparagine-glutamine.
Conservatively substituted variations of a polypeptide sequence of the invention (e.g., variant proteases of the invention) include substitutions of a small percentage, sometimes less than 25%, 20%, 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, or 6% of the amino acids of the polypeptide sequence, or less than 5%, 4%, 3%, 2%, or 1%, or less than 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 amino acid substitution of the amino acids of the polypeptide sequence, with a conservatively selected amino acid of the same conservative substitution group.
As described elsewhere herein in greater detail and in the Examples provided herein, polypeptides of the invention may have cleaning abilities that may be compared to known proteases, including known metalloproteases.
In some embodiments, the protease variant comprises one or more mutations, and having a total net charge of −5, −4, −3, −2, −1, 0, 1, 2, 3, 4, or 5 relative to Geobacillus caldoproteolyticus thermolysin (SEQ ID NO: 3)
In some embodiments, the above high ionic strength thermolysin protease variants form part of a detergent composition that is diluted in water, typically within a laundry washing machine, to form a laundry detergent wash liquor, whose conductivity is from about 3 mS/cm to about 30 mS/cm, from about 3.5 mS/cm to about 20 mS/cm, or even from about 4 mS/cm to about 10 mS/cm.
The charge of the thermolysin protease variants is expressed relative to Geobacillus caldoproteolyticus thermolysin protease wild-type having the amino acid sequence of SEQ ID NO: 3. The amino acids that impart a single negative charge are D and E and those that impart a single positive charge are R, H and K. Any amino acid change versus SEQ ID NO:2 that changes a charge is used to calculate the charge of the thermolysin protease variant. For example, introducing a negative charge mutation from a wild-type neutral position will add a net charge of −1 to the thermolysin protease variant, whereas introducing a negative charge mutation (D or E) from a wild-type positive amino acid residue (R, H or K) will add a net charge of −2. Summing the charge changes from all the amino acid residues that are different for the protease variant versus Geobacillus caldoproteolyticus thermolysin protease wild-type having the amino acid sequence of SEQ ID NO: 3 gives the charge change of the protease variant. By correctly selecting the charge unexpectedly improved levels of thermolysin cleaning performance can be obtained. “Low conductivity laundry detergent solutions” are defined as having a conductivity of from about 0.1 mS/cm to about 3 mS/cm, from about 0.3 mS/cm to about 2.5 mS/cm, or even from about 0.5 mS/cm to about 2 mS/cm. “High conductivity laundry detergent solutions” are defined as having a conductivity of from about 3 mS/cm to about 30 mS/cm, from about 3.5 mS/cm to about 20 mS/cm, or even from about 4 mS/cm to about 10 mS/cm. It is intended that the above examples be non-limiting. Once mutations are combined to optimize thermolysin performance, the enzyme charge can also be balanced by mutations in further positions.
In some embodiments, the invention provides an isolated, recombinant, substantially pure, or non-naturally occurring variant protease (e.g., variant thermolysin) having proteolytic activity, said variant protease comprising an amino acid sequence which differs from the amino acid sequence shown in SEQ ID NO: 3 by no more than 50, no more than 45, no more than 40, no more than 35, no more than 30, no more than 25, no more than 20, no more than 19, no more than 18, no more than 17, no more than 16, no more than 15, no more than 14, no more than 13, no more than 12, no more than 11, no more than 10, no more than 9, or no more than 8 amino acid residues, wherein amino acid positions are numbered according to the numbering of corresponding amino acid positions in the amino acid sequence of Geobacillus caldoproteolyticus thermolysin shown in SEQ ID NO: 3, as determined by alignment of the variant protease amino acid sequence with the Geobacillus caldoproteolyticus thermolysin amino acid sequence.
In some embodiments, the invention provides an isolated, recombinant, substantially pure, or non-naturally occurring variant protease (e.g., variant thermolysin) having proteolytic activity, said variant protease comprising an amino acid sequence which differs from the amino acid sequence shown in SEQ ID NO:2 by no more than 50, no more than 45, no more than 40, no more than 35, no more than 30, no more than 25, no more than 20, no more than 19, no more than 18, no more than 17, no more than 16, no more than 15, no more than 14, no more than 13, no more than 12, no more than 11, no more than 10, no more than 9, no more than 6, no more than 5, no more than 4, no more than 3, no more than 2 amino acid residues, wherein amino acid positions are numbered according to the numbering of corresponding amino acid positions in the amino acid sequence of Geobacillus caldoproteolyticus thermolysin shown in SEQ ID NO: 3, as determined by alignment of the variant protease amino acid sequence with the Geobacillus caldoproteolyticus thermolysin amino acid sequence.
The invention provides isolated, non-naturally occurring, or recombinant nucleic acids (also referred to herein as “polynucleotides”), which may be collectively referred to as “nucleic acids of the invention” or “polynucleotides of the invention”, which encode polypeptides of the invention. Nucleic acids of the invention, including all described below, are useful in recombinant production (e.g., expression) of polypeptides of the invention, typically through expression of a plasmid expression vector comprising a sequence encoding the polypeptide of interest or fragment thereof. As discussed above, polypeptides include variant protease polypeptides, including variant thermolysin polypeptides having enzymatic activity (e.g., proteolytic activity) which are useful in cleaning applications and cleaning compositions for cleaning an item or a surface (e.g., surface of an item) in need of cleaning.
In some embodiments, the invention provides an isolated, recombinant, substantially pure, or non-naturally occurring nucleic acid comprising a nucleotide sequence encoding any polypeptide (including any fusion protein, etc.) of the invention described above in the section entitled “Polypeptides of the Invention” and elsewhere herein. The invention also provides an isolated, recombinant, substantially pure, or non-naturally-occurring nucleic acid comprising a nucleotide sequence encoding a combination of two or more of any polypeptides of the invention described above and elsewhere herein.
In some embodiments, the invention includes a polynucleotide encoding an isolated, recombinant, substantially pure, or non-naturally occurring variant thermolysin enzyme having thermolysin activity, which polypeptide comprises a polypeptide sequence having at least about 85%, at least about 86%, at least about 87%, at least about 88%, at least about 89%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, at least about 99%, at least about 99.5%, or 100% sequence identity to a parent thermolysin enzyme as provided herein.
In some embodiments, the variant polypeptide is a variant having a specified degree of amino acid sequence homology to the exemplified thermolysin polypeptide, e.g., at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or even at least 99% sequence homology to the amino acid sequence of SEQ ID NO: 3 or 4. Homology can be determined by amino acid sequence alignment, e.g., using a program such as BLAST, ALIGN, or CLUSTAL, as described herein.
Also provided is an isolated, recombinant, substantially pure, or non-naturally occurring nucleic acid comprising a polynucleotide sequence which encodes a variant protease having proteolytic activity, said variant protease (e.g., variant thermolysin) comprising an amino acid sequence which differs from the amino acid sequence of SEQ ID NO:2 by no more than 50, no more than 40, no more than 30, no more than 35, no more than 25, no more than 20, no more than 19, no more than 18, no more than 17, no more than 16, no more than 15, no more than 14, no more than 13, no more than 12, no more than 11, no more than 10, no more than 9, no more than 8, no more than 7, no more than 6, no more than 5, no more than 4, no more than 3, no more than 2, or no more than 1 amino acid residue(s), wherein amino acid positions of the variant thermolysin are numbered according to the numbering of corresponding amino acid positions in the amino acid sequence of Geobacillus caldoproteolyticus thermolysin shown in SEQ ID NO: 3 as determined by alignment of the variant protease amino acid sequence with the Geobacillus caldoproteolyticus thermolysin amino acid sequence.
The present invention provides nucleic acids encoding a thermolysin variant of Geobacillus or Bacillus thermolysin, wherein the thermolysin variant is a mature form having proteolytic activity and comprises an amino acid sequence comprising a combination of amino acid substitutions as listed throughout the specification, wherein the amino acid positions of the thermolysin variant are numbered by correspondence with the amino acid sequence of Geobacillus caldoproteolyticus thermolysin set forth as SEQ ID NO: 3.
Nucleic acids of the invention can be generated by using any suitable synthesis, manipulation, and/or isolation techniques, or combinations thereof. For example, a polynucleotide of the invention may be produced using standard nucleic acid synthesis techniques, such as solid-phase synthesis techniques that are well-known to those skilled in the art. In such techniques, fragments of up to 50 or more nucleotide bases are typically synthesized, then joined (e.g., by enzymatic or chemical ligation methods, or polymerase mediated recombination methods) to form essentially any desired continuous nucleic acid sequence. The synthesis of the nucleic acids of the invention can be also facilitated (or alternatively accomplished) by any suitable method known in the art, including but not limited to chemical synthesis using the classical phosphoramidite method (See e.g., Beaucage et al. Tetrahedron Letters 22:1859-69 [1981]); or the method described by Matthes et al. (See, Matthes et al., EMBO J. 3:801-805 [1984], as is typically practiced in automated synthetic methods. Nucleic acids of the invention also can be produced by using an automatic DNA synthesizer. Customized nucleic acids can be ordered from a variety of commercial sources (e.g., The Midland Certified Reagent Company, the Great American Gene Company, Operon Technologies Inc., and DNA2.0). Other techniques for synthesizing nucleic acids and related principles are known in the art (See e.g., Itakura et al., Ann. Rev. Biochem. 53:323 [1984]; and Itakura et al., Science 198:1056 [1984]).
As indicated above, recombinant DNA techniques useful in modification of nucleic acids are well known in the art. For example, techniques such as restriction endonuclease digestion, ligation, reverse transcription and cDNA production, and polymerase chain reaction (e.g., PCR) are known and readily employed by those of skill in the art. Nucleotides of the invention may also be obtained by screening cDNA libraries (e.g., cDNA libraries generated using mutagenesis techniques commonly used in the art, including those described herein) using one or more oligonucleotide probes that can hybridize to or PCR-amplify polynucleotides which encode a variant protease polypeptide(s) of the invention. Procedures for screening and isolating cDNA clones and PCR amplification procedures are well known to those of skill in the art and described in standard references known to those skilled in the art. Some nucleic acids of the invention can be obtained by altering a naturally occurring polynucleotide backbone (e.g., that encodes an enzyme or parent protease) by, for example, a known mutagenesis procedure (e.g., site-directed mutagenesis, site saturation mutagenesis, and in vitro recombination).
A variety of methods are known in the art that are suitable for generating modified polynucleotides of the invention that encode variant proteases of the invention, including, but not limited to, for example, site-saturation mutagenesis, scanning mutagenesis, insertional mutagenesis, deletion mutagenesis, random mutagenesis, site-directed mutagenesis, and directed-evolution, as well as various other recombinatorial approaches. Methods for making modified polynucleotides and proteins (e.g., variant proteases) include DNA shuffling methodologies, methods based on non-homologous recombination of genes, such as ITCHY (See, Ostermeier et al., 7:2139-44 [1999]), SCRACHY (See, Lutz et al. 98:11248-53 [2001]), SHIPREC (See, Sieber et al., 19:456-60 [2001]), and NRR (See, Bittker et al., 20:1024-9 [2001]; Bittker et al., 101:7011-6 [2004]), and methods that rely on the use of oligonucleotides to insert random and targeted mutations, deletions and/or insertions (See, Ness et al., 20:1251-5 [2002]; Coco et al., 20:1246-50 [2002]; Zha et al., 4:34-9 [2003]; Glaser et al., 149:3903-13 [1992]).
The present invention provides isolated or recombinant vectors comprising at least one polynucleotide of the invention described herein (e.g., a polynucleotide encoding a variant protease of the invention described herein), isolated or recombinant expression vectors or expression cassettes comprising at least one nucleic acid or polynucleotide of the invention, isolated, substantially pure, or recombinant DNA constructs comprising at least one nucleic acid or polynucleotide of the invention, isolated or recombinant cells comprising at least one polynucleotide of the invention, cell cultures comprising cells comprising at least one polynucleotide of the invention, cell cultures comprising at least one nucleic acid or polynucleotide of the invention, and compositions comprising one or more such vectors, nucleic acids, expression vectors, expression cassettes, DNA constructs, cells, cell cultures, or any combination or mixtures thereof.
In some embodiments, the invention provides recombinant cells comprising at least one vector (e.g., expression vector or DNA construct) of the invention which comprises at least one nucleic acid or polynucleotide of the invention. Some such recombinant cells are transformed or transfected with such at least one vector. Such cells are typically referred to as host cells. Some such cells comprise bacterial cells, including, but are not limited to Bacillus sp. cells, such as B. subtilis cells. The invention also provides recombinant cells (e.g., recombinant host cells) comprising at least one variant protease of the invention.
In some embodiments, the invention provides a vector comprising a nucleic acid or polynucleotide of the invention. In some embodiments, the vector is an expression vector or expression cassette in which a polynucleotide sequence of the invention which encodes a variant protease of the invention is operably linked to one or additional nucleic acid segments required for efficient gene expression (e.g., a promoter operably linked to the polynucleotide of the invention which encodes a variant protease of the invention). A vector may include a transcription terminator and/or a selection gene, such as an antibiotic resistance gene that enables continuous cultural maintenance of plasmid-infected host cells by growth in antimicrobial-containing media.
An expression vector may be derived from plasmid or viral DNA, or in alternative embodiments, contains elements of both. Exemplary vectors include, but are not limited to pXX, pC194, pJH101, pE194, pHP13 (See, Harwood and Cutting [eds.], Chapter 3, Molecular Biological Methods for Bacillus, John Wiley & Sons [1990]; suitable replicating plasmids for B. subtilis include those listed on p. 92; See also, Perego, Integrational Vectors for Genetic Manipulations in Bacillus subtilis, in Sonenshein et al., [eds.] Bacillus subtilis and Other Gram-Positive Bacteria: Biochemistry, Physiology and Molecular Genetics, American Society for Microbiology, Washington, D.C. [1993], pp. 615-624).
For expression and production of a protein of interest (e.g., variant protease) in a cell, at least one expression vector comprising at least one copy of a polynucleotide encoding the modified protease, and preferably comprising multiple copies, is transformed into the cell under conditions suitable for expression of the protease. In some embodiments of the present invention, a polynucleotide sequence encoding the variant protease (as well as other sequences included in the vector) is integrated into the genome of the host cell, while in other embodiments, a plasmid vector comprising a polynucleotide sequence encoding the variant protease remains as autonomous extra-chromosomal element within the cell. The invention provides both extrachromosomal nucleic acid elements as well as incoming nucleotide sequences that are integrated into the host cell genome. The vectors described herein are useful for production of the variant proteases of the invention. In some embodiments, a polynucleotide construct encoding the variant protease is present on an integrating vector that enables the integration and optionally the amplification of the polynucleotide encoding the variant protease into the bacterial chromosome. Examples of sites for integration are well known to those skilled in the art. In some embodiments, transcription of a polynucleotide encoding a variant protease of the invention is effectuated by a promoter that is the wild-type promoter for the selected precursor protease. In some other embodiments, the promoter is heterologous to the precursor protease, but is functional in the host cell. Specifically, examples of suitable promoters for use in bacterial host cells include, but are not limited to, for example, the amyE, amyQ, amyL, pstS, sacB, pSPAC, pAprE, pVeg, pHpaII promoters, the promoter of the B. stearothermophilus maltogenic amylase gene, the B. amyloliquefaciens (BAN) amylase gene, the B. subtilis alkaline protease gene, the B. clausii alkaline protease gene the B. pumilis xylosidase gene, the B. thuringiensis cryIIIA, and the B. licheniformis alpha-amylase gene. Additional promoters include, but are not limited to the A4 promoter, as well as phage Lambda PR or PL promoters, and the E. coli lac, trp or tac promoters.
Variant proteases of the present invention can be produced in host cells of any suitable Gram-positive microorganism, including bacteria and fungi. For example, in some embodiments, the variant protease is produced in host cells of fungal and/or bacterial origin. In some embodiments, the host cells are Bacillus sp., Streptomyces sp., Escherichia sp. or Aspergillus sp. In some embodiments, the variant proteases are produced by Bacillus sp. host cells. Examples of Bacillus sp. host cells that find use in the production of the variant proteases of the invention include, but are not limited to B. licheniformis, B. lentus, B. subtilis, B. amyloliquefaciens, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. coagulans, B. circulans, B. pumilis, B. thuringiensis, B. clausii, and B. megaterium, as well as other organisms within the genus Bacillus. In some embodiments, B. subtilis host cells are used for production of variant proteases. U.S. Pat. Nos. 5,264,366 and 4,760,025 (RE 34,606) describe various Bacillus host strains that can be used for producing variant proteases of the invention, although other suitable strains can be used.
Several industrial bacterial strains that can be used to produce variant proteases of the invention include non-recombinant (i.e., wild-type) Bacillus sp. strains, as well as variants of naturally-occurring strains and/or recombinant strains. In some embodiments, the host strain is a recombinant strain, wherein a polynucleotide encoding a polypeptide of interest has been introduced into the host. In some embodiments, the host strain is a B. subtilis host strain and particularly a recombinant Bacillus subtilis host strain. Numerous B. subtilis strains are known, including, but not limited to for example, 1A6 (ATCC 39085), 168 (1A01), SB19, W23, Ts85, B637, PB1753 through PB1758, PB3360, JH642, 1A243 (ATCC 39,087), ATCC 21332, ATCC 6051, MI113, DE100 (ATCC 39,094), GX4931, PBT 110, and PEP 211 strain (See e.g., Hoch et al., Genetics 73:215-228 [1973]; See also, U.S. Pat. Nos. 4,450,235 and 4,302,544, and EP 0134048, each of which is incorporated by reference in its entirety). The use of B. subtilis as an expression host cells is well known in the art (See e.g., Palva et al., Gene 19:81-87 [1982]; Fahnestock and Fischer, J. Bacteriol., 165:796-804 [1986]; and Wang et al., Gene 69:39-47 [1988]).
In some embodiments, the Bacillus host cell is a Bacillus sp. that includes a mutation or deletion in at least one of the following genes, degU, degS, degR and degQ. Preferably the mutation is in a degU gene, and more preferably the mutation is degU(Hy)32 (See e.g., Msadek et al., J. Bacteriol. 172:824-834 [1990]; and Olmos et al., Mol. Gen. Genet. 253:562-567 [1997]). One suitable host strain is a Bacillus subtilis carrying a degU32(Hy) mutation. In some embodiments, the Bacillus host comprises a mutation or deletion in scoC4 (See e.g., Caldwell et al., J. Bacteriol. 183:7329-7340 [2001]); spoIIE (See e.g., Arigoni et al., Mol. Microbiol. 31:1407-1415 [1999]); and/or oppA or other genes of the opp operon (See e.g., Perego et al., Mol. Microbiol. 5:173-185 [1991]). Indeed, it is contemplated that any mutation in the opp operon that causes the same phenotype as a mutation in the oppA gene will find use in some embodiments of the altered Bacillus strain of the invention. In some embodiments, these mutations occur alone, while in other embodiments, combinations of mutations are present. In some embodiments, an altered Bacillus host cell strain that can be used to produce a variant protease of the invention is a Bacillus host strain that already includes a mutation in one or more of the above-mentioned genes. In addition, Bacillus sp. host cells that comprise mutation(s) and/or deletions of endogenous protease genes find use. In some embodiments, the Bacillus host cell comprises a deletion of the aprE and the nprE genes. In other embodiments, the Bacillus sp. host cell comprises a deletion of 5 protease genes, while in other embodiments, the Bacillus sp. host cell comprises a deletion of 9 protease genes (See e.g., U.S. Pat. Appln. Pub. No. 2005/0202535, incorporated herein by reference).
Host cells are transformed with at least one nucleic acid encoding at least one variant protease of the invention using any suitable method known in the art. Whether the nucleic acid is incorporated into a vector or is used without the presence of plasmid DNA, it is typically introduced into a microorganism, in some embodiments, preferably an E. coli cell or a competent Bacillus cell. Methods for introducing a nucleic acid (e.g., DNA) into Bacillus cells or E. coli cells utilizing plasmid DNA constructs or vectors and transforming such plasmid DNA constructs or vectors into such cells are well known. In some embodiments, the plasmids are subsequently isolated from E. coli cells and transformed into Bacillus cells. However, it is not essential to use intervening microorganisms such as E. coli, and in some embodiments, a DNA construct or vector is directly introduced into a Bacillus host.
Those of skill in the art are well aware of suitable methods for introducing nucleic acid or polynucleotide sequences of the invention into Bacillus cells (See e.g., Ferrari et al., “Genetics,” in Harwood et al. [eds.], Bacillus, Plenum Publishing Corp. [1989], pp. 57-72; Saunders et al., J. Bacteriol. 157:718-726 [1984]; Hoch et al., J. Bacteriol. 93:1925-1937 [1967]; Mann et al., Current Microbiol. 13:131-135 [1986]; Holubova, Folia Microbiol. 30:97 [1985]; Chang et al., Mol. Gen. Genet. 168:11-115 [1979]; Vorobjeva et al., FEMS Microbiol. Lett. 7:261-263 [1980]; Smith et al., Appl. Env. Microbiol. 51:634 [1986]; Fisher et al., Arch. Microbiol. 139:213-217 [1981]; and McDonald, J. Gen. Microbiol. 130:203 [1984]). Indeed, such methods as transformation, including protoplast transformation and congression, transduction, and protoplast fusion are well known and suited for use in the present invention. Methods of transformation are used to introduce a DNA construct or vector comprising a nucleic acid encoding a variant protease of the present invention into a host cell. Methods known in the art to transform Bacillus cells include such methods as plasmid marker rescue transformation, which involves the uptake of a donor plasmid by competent cells carrying a partially homologous resident plasmid (See, Contente et al., Plasmid 2:555-571 [1979]; Haima et al., Mol. Gen. Genet. 223:185-191 [1990]; Weinrauch et al., J. Bacteriol. 154:1077-1087 [1983]; and Weinrauch et al., J. Bacteriol. 169:1205-1211 [1987]). In this method, the incoming donor plasmid recombines with the homologous region of the resident “helper” plasmid in a process that mimics chromosomal transformation.
In addition to commonly used methods, in some embodiments, host cells are directly transformed with a DNA construct or vector comprising a nucleic acid encoding a variant protease of the invention (i.e., an intermediate cell is not used to amplify, or otherwise process, the DNA construct or vector prior to introduction into the host cell). Introduction of the DNA construct or vector of the invention into the host cell includes those physical and chemical methods known in the art to introduce a nucleic acid sequence (e.g., DNA sequence) into a host cell without insertion into a plasmid or vector. Such methods include, but are not limited to calcium chloride precipitation, electroporation, naked DNA, liposomes and the like. In additional embodiments, DNA constructs or vector are co-transformed with a plasmid, without being inserted into the plasmid. In further embodiments, a selective marker is deleted from the altered Bacillus strain by methods known in the art (See, Stahl et al., J. Bacteriol. 158:411-418 [1984]; and Palmeros et al., Gene 247:255-264 [2000]).
In some embodiments, the transformed cells of the present invention are cultured in conventional nutrient media. The suitable specific culture conditions, such as temperature, pH and the like are known to those skilled in the art and are well described in the scientific literature. In some embodiments, the invention provides a culture (e.g., cell culture) comprising at least one variant protease or at least one nucleic acid of the invention. Also provided are compositions comprising at least one nucleic acid, vector, or DNA construct of the invention.
In some embodiments, host cells transformed with at least one polynucleotide sequence encoding at least one variant protease of the invention are cultured in a suitable nutrient medium under conditions permitting the expression of the present protease, after which the resulting protease is recovered from the culture. The medium used to culture the cells comprises any conventional medium suitable for growing the host cells, such as minimal or complex media containing appropriate supplements. Suitable media are available from commercial suppliers or may be prepared according to published recipes (See e.g., the catalogues of the American Type Culture Collection). In some embodiments, the protease produced by the cells is recovered from the culture medium by conventional procedures, including, but not limited to for example, separating the host cells from the medium by centrifugation or filtration, precipitating the proteinaceous components of the supernatant or filtrate by means of a salt (e.g., ammonium sulfate), chromatographic purification (e.g., ion exchange, gel filtration, affinity, etc.). Any method suitable for recovering or purifying a variant protease finds use in the present invention.
In some embodiments, a variant protease produced by a recombinant host cell is secreted into the culture medium. A nucleic acid sequence that encodes a purification facilitating domain may be used to facilitate purification of soluble proteins. A vector or DNA construct comprising a polynucleotide sequence encoding a variant protease may further comprise a nucleic acid sequence encoding a purification facilitating domain to facilitate purification of the variant protease (See e.g., Kroll et al., DNA Cell Biol. 12:441-53 [1993]). Such purification facilitating domains include, but are not limited to, for example, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals (See, Porath, Protein Expr. Purif. 3:263-281 [1992]), protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (e.g., protein A domains available from Immunex Corp., Seattle, Wash.). The inclusion of a cleavable linker sequence such as Factor XA or enterokinase (e.g., sequences available from Invitrogen, San Diego, Calif.) between the purification domain and the heterologous protein also find use to facilitate purification.
Assays for detecting and measuring the enzymatic activity of an enzyme, such as a variant protease of the invention, are well known. Various assays for detecting and measuring activity of proteases (e.g., variant proteases of the invention), are also known to those of ordinary skill in the art. In particular, assays are available for measuring protease activity that are based on the release of acid-soluble peptides from casein or hemoglobin, measured as absorbance at 280 nm or colorimetrically using the Folin method, well known to those skilled in the art. Other exemplary assays involve the solubilization of chromogenic substrates (See e.g., Ward, “Proteinases,” in Fogarty (ed.)., Microbial Enzymes and Biotechnology, Applied Science, London, [1983], pp. 251-317). Other exemplary assays include, but are not limited to succinyl-Ala-Ala-Pro-Phe-para nitroanilide assay (suc-AAPF-pNA) and the 2,4,6-trinitrobenzene sulfonate sodium salt assay (TNBS assay). Numerous additional references known to those in the art provide suitable methods (See e.g., Wells et al., Nucleic Acids Res. 11:7911-7925 [1983]; Christianson et al., Anal. Biochem. 223:119-129 [1994]; and Hsia et al., Anal Biochem. 242:221-227 [1999]).
A variety of methods can be used to determine the level of production of a mature protease (e.g., mature variant proteases of the present invention) in a host cell. Such methods include, but are not limited to, for example, methods that utilize either polyclonal or monoclonal antibodies specific for the protease. Exemplary methods include, but are not limited to enzyme-linked immunosorbent assays (ELISA), radioimmunoassays (RIA), fluorescent immunoassays (FIA), and fluorescent activated cell sorting (FACS). These and other assays are well known in the art (See e.g., Maddox et al., J. Exp. Med. 158:1211 [1983]).
In some other embodiments, the invention provides methods for making or producing a mature variant protease of the invention. A mature variant protease does not include a signal peptide or a propeptide sequence. Some methods comprise making or producing a variant protease of the invention in a recombinant bacterial host cell, such as for example, a Bacillus sp. cell (e.g., a B. subtilis cell). In some embodiments, the invention provides a method of producing a variant protease of the invention, the method comprising cultivating a recombinant host cell comprising a recombinant expression vector comprising a nucleic acid encoding a variant protease of the invention under conditions conducive to the production of the variant protease. Some such methods further comprise recovering the variant protease from the culture.
In some embodiments the invention provides methods of producing a variant protease of the invention, the methods comprising: (a) introducing a recombinant expression vector comprising a nucleic acid encoding a variant protease of the invention into a population of cells (e.g., bacterial cells, such as B. subtilis cells); and (b) culturing the cells in a culture medium under conditions conducive to produce the variant protease encoded by the expression vector. Some such methods further comprise: (c) isolating the variant protease from the cells or from the culture medium.
In some embodiments, the protease variants of the present invention can be used in compositions comprising an adjunct material and a protease variant, wherein the composition is a fabric and home care product.
In some embodiments, the fabric and home care product compositions comprising at least one thermolysin variant comprise one or more of the following ingredients (based on total composition weight): from about 0.0005 wt % to about 0.1 wt %, from about 0.001 wt % to about 0.05 wt %, or even from about 0.002 wt % to about 0.03 wt % of said thermolysin protease variant; and one or more of the following: from about 0.00003 wt % to about 0.1 wt % fabric hueing agent; from about 0.001 wt % to about 5 wt %, perfume capsules; from about 0.001 wt % to about 1 wt %, cold-water soluble brighteners; from about 0.00003 wt % to about 0.1 wt % bleach catalysts; from about 0.00003 wt % to about 0.1 wt % first wash lipases; from about 0.00003 wt % to about 0.1 wt % bacterial cleaning cellulases; and/or from about 0.05 wt % to about 20 wt % Guerbet nonionic surfactants.
In some embodiments, the fabric and home care product composition is a liquid laundry detergent, a dish washing detergent.
It is intended that the fabric and home care product is provided in any suitable form, including a fluid or solid. The fabric and home care product may be in the form of a unit dose pouch, especially when in the form of a liquid, and typically the fabric and home care product is at least partially, or even completely, enclosed by a water-soluble pouch. In addition, in some embodiments of the fabric and home care products comprising at least one protease variant, the fabric and home care product may have any combination of parameters and/or characteristics detailed above.
Unless otherwise noted, all component or composition levels provided herein are made in reference to the active level of that component or composition, and are exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources. Enzyme components weights are based on total active protein. All percentages and ratios are calculated by weight unless otherwise indicated. All percentages and ratios are calculated based on the total composition unless otherwise indicated. In the exemplified detergent compositions, the enzymes levels are expressed by pure enzyme by weight of the total composition and unless otherwise specified, the detergent ingredients are expressed by weight of the total compositions.
As indicated herein, in some embodiments, the cleaning compositions of the present invention further comprise adjunct materials including, but not limited to, surfactants, builders, bleaches, bleach activators, bleach catalysts, other enzymes, enzyme stabilizing systems, chelants, optical brighteners, soil release polymers, dye transfer agents, dispersants, suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes, photoactivators, fluorescers, fabric conditioners, hydrolyzable surfactants, preservatives, anti-oxidants, anti-shrinkage agents, anti-wrinkle agents, germicides, fungicides, color speckles, silvercare, anti-tarnish and/or anti-corrosion agents, alkalinity sources, solubilizing agents, carriers, processing aids, pigments, and pH control agents (See e.g., U.S. Pat. Nos. 6,610,642, 6,605,458, 5,705,464, 5,710,115, 5,698,504, 5,695,679, 5,686,014 and 5,646,101, all of which are incorporated herein by reference). Embodiments of specific cleaning composition materials are exemplified in detail below. In embodiments in which the cleaning adjunct materials are not compatible with the variant proteases of the present invention in the cleaning compositions, then suitable methods of keeping the cleaning adjunct materials and the protease(s) separated (i.e., not in contact with each other) until combination of the two components is appropriate are used. Such separation methods include any suitable method known in the art (e.g., gelcaps, encapsulation, tablets, physical separation, etc.).
The cleaning compositions of the present invention are advantageously employed for example, in laundry applications, hard surface cleaning, dishwashing applications, as well as cosmetic applications such as dentures, teeth, hair and skin. In addition, due to the unique advantages of increased effectiveness in lower temperature solutions, the enzymes of the present invention are ideally suited for laundry applications. Furthermore, the enzymes of the present invention find use in granular and liquid compositions.
The variant proteases of the present invention also find use in cleaning additive products. In some embodiments, low temperature solution cleaning applications find use. In some embodiments, the present invention provides cleaning additive products including at least one enzyme of the present invention is ideally suited for inclusion in a wash process when additional bleaching effectiveness is desired. Such instances include, but are not limited to low temperature solution cleaning applications. In some embodiments, the additive product is in its simplest form, one or more proteases. In some embodiments, the additive is packaged in dosage form for addition to a cleaning process. In some embodiments, the additive is packaged in dosage form for addition to a cleaning process where a source of peroxygen is employed and increased bleaching effectiveness is desired. Any suitable single dosage unit form finds use with the present invention, including but not limited to pills, tablets, gelcaps, or other single dosage units such as pre-measured powders or liquids. In some embodiments, filler(s) or carrier material(s) are included to increase the volume of such compositions. Suitable filler or carrier materials include, but are not limited to, various salts of sulfate, carbonate and silicate as well as talc, clay and the like. Suitable filler or carrier materials for liquid compositions include, but are not limited to water or low molecular weight primary and secondary alcohols including polyols and diols. Examples of such alcohols include, but are not limited to, methanol, ethanol, propanol and isopropanol. In some embodiments, the compositions contain from about 5% to about 90% of such materials. Acidic fillers find use to reduce pH. Alternatively, in some embodiments, the cleaning additive includes adjunct ingredients, as more fully described below.
The present cleaning compositions and cleaning additives require an effective amount of at least one of the protease variants provided herein, alone or in combination with other proteases and/or additional enzymes. The required level of enzyme is achieved by the addition of one or more protease variants of the present invention. Typically the present cleaning compositions comprise at least about 0.0001 weight percent, from about 0.0001 to about 10, from about 0.001 to about 1, or even from about 0.01 to about 0.1 weight percent of at least one of the variant proteases of the present invention.
The cleaning compositions herein are typically formulated such that, during use in aqueous cleaning operations, the wash water will have a pH of from about 5.0 to about 11.5 or even from about 7.5 to about 10.5. Liquid product formulations are typically formulated to have a neat pH from about 3.0 to about 9.0 or even from about 3 to about 5. Granular laundry products are typically formulated to have a pH from about 9 to about 11. Techniques for controlling pH at recommended usage levels include the use of buffers, alkalis, acids, etc., and are well known to those skilled in the art.
Suitable “low pH cleaning compositions” typically have a neat pH of from about 3 to about 5, and are typically free of surfactants that hydrolyze in such a pH environment. Such surfactants include sodium alkyl sulfate surfactants that comprise at least one ethylene oxide moiety or even from about 1 to about 16 moles of ethylene oxide. Such cleaning compositions typically comprise a sufficient amount of a pH modifier, such as sodium hydroxide, monoethanolamine or hydrochloric acid, to provide such cleaning composition with a neat pH of from about 3 to about 5. Such compositions typically comprise at least one acid stable enzyme. In some embodiments, the compositions are liquids, while in other embodiments, they are solids. The pH of such liquid compositions is typically measured as a neat pH. The pH of such solid compositions is measured as a 10% solids solution of said composition wherein the solvent is distilled water. In these embodiments, all pH measurements are taken at 20° C., unless otherwise indicated.
In some embodiments, when the variant protease(s) is/are employed in a granular composition or liquid, it is desirable for the variant protease to be in the form of an encapsulated particle to protect the variant protease from other components of the granular composition during storage. In addition, encapsulation is also a means of controlling the availability of the variant protease during the cleaning process. In some embodiments, encapsulation enhances the performance of the variant protease(s) and/or additional enzymes. In this regard, the variant proteases of the present invention are encapsulated with any suitable encapsulating material known in the art. In some embodiments, the encapsulating material typically encapsulates at least part of the catalyst for the variant protease(s) of the present invention. Typically, the encapsulating material is water-soluble and/or water-dispersible. In some embodiments, the encapsulating material has a glass transition temperature (Tg) of 0° C. or higher. Glass transition temperature is described in more detail in WO 97/11151. The encapsulating material is typically selected from consisting of carbohydrates, natural or synthetic gums, chitin, chitosan, cellulose and cellulose derivatives, silicates, phosphates, borates, polyvinyl alcohol, polyethylene glycol, paraffin waxes, and combinations thereof. When the encapsulating material is a carbohydrate, it is typically selected from monosaccharides, oligosaccharides, polysaccharides, and combinations thereof. In some typical embodiments, the encapsulating material is a starch (See e.g., EP 0 922 499; U.S. Pat. No. 4,977,252; U.S. Pat. No. 5,354,559, and U.S. Pat. No. 5,935,826). In some embodiments, the encapsulating material is a microsphere made from plastic such as thermoplastics, acrylonitrile, methacrylonitrile, polyacrylonitrile, polymethacrylonitrile and mixtures thereof; commercially available microspheres that find use include, but are not limited to those supplied by EXPANCEL® (Stockviksverken, Sweden), and PM 6545, PM 6550, PM 7220, PM 7228, EXTENDOSPHERES®, LUXSIL®, Q-CEL®, and SPHERICEL® (PQ Corp., Valley Forge, Pa.).
As described herein, the variant proteases of the present invention find particular use in the cleaning industry, including, but not limited to laundry and dish detergents. These applications place enzymes under various environmental stresses. The variant proteases of the present invention provide advantages over many currently used enzymes, due to their stability under various conditions.
Indeed, there are a variety of wash conditions including varying detergent formulations, wash water volumes, wash water temperatures, and lengths of wash time, to which proteases involved in washing are exposed. In addition, detergent formulations used in different geographical areas have different concentrations of their relevant components present in the wash water. For example, European detergents typically have about 4500-5000 ppm of detergent components in the wash water, while Japanese detergents typically have approximately 667 ppm of detergent components in the wash water. In North America, particularly the United States, detergents typically have about 975 ppm of detergent components present in the wash water.
A low detergent concentration system includes detergents where less than about 800 ppm of the detergent components are present in the wash water. Japanese detergents are typically considered low detergent concentration system as they have approximately 667 ppm of detergent components present in the wash water.
A medium detergent concentration includes detergents where between about 800 ppm and about 2000 ppm of the detergent components are present in the wash water. North American detergents are generally considered to be medium detergent concentration systems as they have approximately 975 ppm of detergent components present in the wash water. Brazil typically has approximately 1500 ppm of detergent components present in the wash water.
A high detergent concentration system includes detergents where greater than about 2000 ppm of the detergent components are present in the wash water. European detergents are generally considered to be high detergent concentration systems as they have approximately 4500-5000 ppm of detergent components in the wash water.
Latin American detergents are generally high suds phosphate builder detergents and the range of detergents used in Latin America can fall in both the medium and high detergent concentrations as they range from 1500 ppm to 6000 ppm of detergent components in the wash water. As mentioned above, Brazil typically has approximately 1500 ppm of detergent components present in the wash water. However, other high suds phosphate builder detergent geographies, not limited to other Latin American countries, may have high detergent concentration systems up to about 6000 ppm of detergent components present in the wash water.
In light of the foregoing, it is evident that concentrations of detergent compositions in typical wash solutions throughout the world varies from less than about 800 ppm of detergent composition (“low detergent concentration geographies”), for example about 667 ppm in Japan, to between about 800 ppm to about 2000 ppm (“medium detergent concentration geographies”), for example about 975 ppm in U.S. and about 1500 ppm in Brazil, to greater than about 2000 ppm (“high detergent concentration geographies”), for example about 4500 ppm to about 5000 ppm in Europe and about 6000 ppm in high suds phosphate builder geographies.
The concentrations of the typical wash solutions are determined empirically. For example, in the U.S., a typical washing machine holds a volume of about 64.4 L of wash solution. Accordingly, in order to obtain a concentration of about 975 ppm of detergent within the wash solution about 62.79 g of detergent composition must be added to the 64.4 L of wash solution. This amount is the typical amount measured into the wash water by the consumer using the measuring cup provided with the detergent.
As a further example, different geographies use different wash temperatures. The temperature of the wash water in Japan is typically less than that used in Europe. For example, the temperature of the wash water in North America and Japan is typically between about 10 and about 30° C. (e.g., about 20° C.), whereas the temperature of wash water in Europe is typically between about 30 and about 60° C. (e.g., about 40° C.). However, in the interest of saving energy, many consumers are switching to using cold water washing. In addition, in some further regions, cold water is typically used for laundry, as well as dish washing applications. In some embodiments, the “cold water washing” of the present invention utilizes “cold water detergent” suitable for washing at temperatures from about 10° C. to about 40° C., or from about 20° C. to about 30° C., or from about 15° C. to about 25° C., as well as all other combinations within the range of about 15° C. to about 35° C., and all ranges within 10° C. to 40° C.
As a further example, different geographies typically have different water hardness. Water hardness is usually described in terms of the grains per gallon mixed Ca2+/Mg2+. Hardness is a measure of the amount of calcium (Ca2+) and magnesium (Mg2+) in the water. Most water in the United States is hard, but the degree of hardness varies. Moderately hard (60-120 ppm) to hard (121-181 ppm) water has 60 to 181 parts per million (parts per million converted to grains per U.S. gallon is ppm # divided by 17.1 equals grains per gallon) of hardness minerals.
European water hardness is typically greater than about 10.5 (for example about 10.5 to about 20.0) grains per gallon mixed Ca2+/Mg2+, (e.g., about 15 grains per gallon mixed Ca2+/Mg2+). North American water hardness is typically greater than Japanese water hardness, but less than European water hardness. For example, North American water hardness can be between about 3 to about 10 grains, about 3 to about 8 grains or about 6 grains. Japanese water hardness is typically lower than North American water hardness, usually less than about 4, for example about 3 grains per gallon mixed Ca2+/Mg2+.
Accordingly, in some embodiments, the present invention provides variant proteases that show surprising wash performance in at least one set of wash conditions (e.g., water temperature, water hardness, and/or detergent concentration). In some embodiments, the variant proteases of the present invention are comparable in wash performance to other thermolysin proteases. In some embodiments of the present invention, the variant proteases provided herein exhibit enhanced oxidative stability, enhanced thermal stability, enhanced cleaning capabilities under various conditions, and/or enhanced chelator stability. In addition, the variant proteases of the present invention find use in cleaning compositions that do not include detergents, again either alone or in combination with builders and stabilizers.
In some embodiments of the present invention, the cleaning compositions comprise at least one variant protease of the present invention at a level from about 0.00001% to about 10% by weight of the composition and the balance (e.g., about 99.999% to about 90.0%) comprising cleaning adjunct materials by weight of composition. In some other embodiments of the present invention, the cleaning compositions of the present invention comprises at least one variant protease at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% by weight of the composition and the balance of the cleaning composition (e.g., about 99.9999% to about 90.0%, about 99.999% to about 98%, about 99.995% to about 99.5% by weight) comprising cleaning adjunct materials.
In some embodiments, the cleaning compositions of the present invention comprise one or more additional detergent enzymes, which provide cleaning performance and/or fabric care and/or dishwashing benefits. Examples of suitable enzymes include, but are not limited to, hemicellulases, cellulases, peroxidases, proteases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, pectate lyases, mannanases, keratinases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, β-glucanases, arabinosidases, hyaluronidases, chondroitinases, laccases, and amylases, or any combinations or mixtures thereof. In some embodiments, a combination of enzymes is used (i.e., a “cocktail”) comprising conventional applicable enzymes like protease, lipase, cutinase and/or cellulase in conjunction with amylase is used.
In addition to the protease variants provided herein, any other suitable protease finds use in the compositions of the present invention. Suitable proteases include those of animal, vegetable or microbial origin. In some embodiments, microbial proteases are used. In some embodiments, chemically or genetically modified mutants are included. In some embodiments, the protease is a serine protease, preferably an alkaline microbial protease or a trypsin-like protease. Examples of alkaline proteases include subtilisins, especially those derived from Bacillus (e.g., subtilisin, lentus, amyloliquefaciens, subtilisin Carlsberg, subtilisin 309, subtilisin 147 and subtilisin 168). Additional examples include those mutant proteases described in U.S. Pat. Nos. RE 34,606, 5,955,340, 5,700,676, 6,312,936, and 6,482,628, all of which are incorporated herein by reference. Additional protease examples include, but are not limited to trypsin (e.g., of porcine or bovine origin), and the Fusarium protease described in WO 89/06270. In some embodiments, commercially available protease enzymes that find use in the present invention include, but are not limited to MAXATASE®, MAXACAL™, MAXAPEM™, OPTICLEAN®, OPTIMASE®, PROPERASE®, PURAFECT®, PURAFECT® OXP, PURAMAX™, EXCELLASE™, and PURAFAST™ (Genencor); ALCALASE®, SAVINASE®, PRIMASE®, DURAZYM™, POLARZYME®, OVOZYME®, KANNASE®, LIQUANASE®, NEUTRASE®, RELASE® and ESPERASE® (Novozymes); BLAP™ and BLAP™ variants (Henkel Kommanditgesellschaft auf Aktien, Duesseldorf, Germany), and KAP (B. alkalophilus subtilisin; Kao Corp., Tokyo, Japan). Various proteases are described in WO95/23221, WO 92/21760, U.S. Pat. Publ. No. 2008/0090747, and U.S. Pat. Nos. 5,801,039, 5,340,735, 5,500,364, 5,855,625, U.S. Pat. Nos. RE 34,606, 5,955,340, 5,700,676, 6,312,936, and 6,482,628, and various other patents. In some further embodiments, metalloproteases find use in the present invention, including but not limited to the neutral metalloprotease described in WO 07/044993.
In addition, any suitable lipase finds use in the present invention. Suitable lipases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are encompassed by the present invention. Examples of useful lipases include Humicola lanuginosa lipase (See e.g., EP 258 068, and EP 305 216), Rhizomucor miehei lipase (See e.g., EP 238 023), Candida lipase, such as C. antarctica lipase (e.g., the C. antarctica lipase A or B; See e.g., EP 214 761), Pseudomonas lipases such as P. alcaligenes lipase and P. pseudoalcaligenes lipase (See e.g., EP 218 272), P. cepacia lipase (See e.g., EP 331 376), P. stutzeri lipase (See e.g., GB 1,372,034), P. fluorescens lipase, Bacillus lipase (e.g., B. subtilis lipase [Dartois et al., Biochem. Biophys. Acta 1131:253-260 [1993]); B. stearothermophilus lipase [See e.g., JP 64/744992]; and B. pumilus lipase [See e.g., WO 91/16422]).
Furthermore, a number of cloned lipases find use in some embodiments of the present invention, including but not limited to Penicillium camembertii lipase (See, Yamaguchi et al., Gene 103:61-67 [1991]), Geotricum candidum lipase (See, Schimada et al., J. Biochem., 106:383-388 [1989]), and various Rhizopus lipases such as R. delemar lipase (See, Hass et al., Gene 109:117-113 [1991]), a R. niveus lipase (Kugimiya et al., Biosci. Biotech. Biochem. 56:716-719 [1992]) and R. oryzae lipase.
Other types of thermolysin enzymes such as cutinases also find use in some embodiments of the present invention, including but not limited to the cutinase derived from Pseudomonas mendocina (See, WO 88/09367), and the cutinase derived from Fusarium solani pisi (See, WO 90/09446).
Additional suitable lipases include commercially available lipases such as M1 LIPASE™ LUMA FAST™, and LIPOMAX™ (Genencor); LIPEX®, LIPOLASE® and LIPOLASE® ULTRA (Novozymes); and LIPASE P™ “Amano” (Amano Pharmaceutical Co. Ltd., Japan).
In some embodiments of the present invention, the cleaning compositions of the present invention further comprise lipases at a level from about 0.00001% to about 10% of additional lipase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In some other embodiments of the present invention, the cleaning compositions of the present invention also comprise lipases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% lipase by weight of the composition.
In some embodiments of the present invention, any suitable amylase finds use in the present invention. In some embodiments, any amylase (e.g., alpha and/or beta) suitable for use in alkaline solutions also find use. Suitable amylases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Amylases that find use in the present invention, include, but are not limited to α-amylases obtained from B. licheniformis (See e.g., GB 1,296,839). Commercially available amylases that find use in the present invention include, but are not limited to DURAMYL®, TERMAMYL®, FUNGAMYL®, STAINZYME®, STAINZYME PLUS®, STAINZYME ULTRA®, and BAN™ (Novozymes), as well as POWERASE™, RAPIDASE® and MAXAMYL® P (Genencor).
In some embodiments of the present invention, the cleaning compositions of the present invention further comprise amylases at a level from about 0.00001% to about 10% of additional amylase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In some other embodiments of the present invention, the cleaning compositions of the present invention also comprise amylases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% amylase by weight of the composition.
In some further embodiments, any suitable cellulase finds used in the cleaning compositions of the present invention. Suitable cellulases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Suitable cellulases include, but are not limited to Humicola insolens cellulases (See e.g., U.S. Pat. No. 4,435,307). Especially suitable cellulases are the cellulases having color care benefits (See e.g., EP 0 495 257). Commercially available cellulases that find use in the present include, but are not limited to CELLUZYME®, CAREZYME® (Novozymes), and KAC-500(B)™ (Kao Corporation). In some embodiments, cellulases are incorporated as portions or fragments of mature wild-type or variant cellulases, wherein a portion of the N-terminus is deleted (See e.g., U.S. Pat. No. 5,874,276). In some embodiments, the cleaning compositions of the present invention further comprise cellulases at a level from about 0.00001% to about 10% of additional cellulase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In some other embodiments of the present invention, the cleaning compositions of the present invention also comprise cellulases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% cellulase by weight of the composition.
Any mannanase suitable for use in detergent compositions also finds use in the present invention. Suitable mannanases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Various mannanases are known which find use in the present invention (See e.g., U.S. Pat. No. 6,566,114, U.S. Pat. No. 6,602,842, and U.S. Pat. No. 6,440,991, all of which are incorporated herein by reference). In some embodiments, the cleaning compositions of the present invention further comprise mannanases at a level from about 0.00001% to about 10% of additional mannanase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In some embodiments of the present invention, the cleaning compositions of the present invention also comprise mannanases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% mannanase by weight of the composition.
In some embodiments, peroxidases are used in combination with hydrogen peroxide or a source thereof (e.g., a percarbonate, perborate or persulfate) in the compositions of the present invention. In some alternative embodiments, oxidases are used in combination with oxygen. Both types of enzymes are used for “solution bleaching” (i.e., to prevent transfer of a textile dye from a dyed fabric to another fabric when the fabrics are washed together in a wash liquor), preferably together with an enhancing agent (See e.g., WO 94/12621 and WO 95/01426). Suitable peroxidases/oxidases include, but are not limited to those of plant, bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. In some embodiments, the cleaning compositions of the present invention further comprise peroxidase and/or oxidase enzymes at a level from about 0.00001% to about 10% of additional peroxidase and/or oxidase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In some other embodiments of the present invention, the cleaning compositions of the present invention also comprise, peroxidase and/or oxidase enzymes at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% peroxidase and/or oxidase enzymes by weight of the composition.
In some embodiments, additional enzymes find use, including but not limited to perhydrolases (See e.g., WO 05/056782). In addition, in some embodiments, mixtures of the above mentioned enzymes are encompassed herein, in particular one or more additional protease, amylase, lipase, mannanase, and/or at least one cellulase. Indeed, it is contemplated that various mixtures of these enzymes will find use in the present invention. It is also contemplated that the varying levels of the variant protease(s) and one or more additional enzymes may both independently range to about 10%, the balance of the cleaning composition being cleaning adjunct materials. The specific selection of cleaning adjunct materials are readily made by considering the surface, item, or fabric to be cleaned, and the desired form of the composition for the cleaning conditions during use (e.g., through the wash detergent use).
Examples of suitable cleaning adjunct materials include, but are not limited to, surfactants, builders, bleaches, bleach activators, bleach catalysts, other enzymes, enzyme stabilizing systems, chelants, optical brighteners, soil release polymers, dye transfer agents, dye transfer inhibiting agents, catalytic materials, hydrogen peroxide, sources of hydrogen peroxide, preformed peracids, polymeric dispersing agents, clay soil removal agents, structure elasticizing agents, dispersants, suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes, photoactivators, fluorescers, fabric conditioners, fabric softeners, carriers, hydrotropes, processing aids, solvents, pigments, hydrolyzable surfactants, preservatives, anti-oxidants, anti-shrinkage agents, anti-wrinkle agents, germicides, fungicides, color speckles, silvercare, anti-tarnish and/or anti-corrosion agents, alkalinity sources, solubilizing agents, carriers, processing aids, pigments, and pH control agents (See e.g., U.S. Pat. Nos. 6,610,642, 6,605,458, 5,705,464, 5,710,115, 5,698,504, 5,695,679, 5,686,014 and 5,646,101, all of which are incorporated herein by reference). Embodiments of specific cleaning composition materials are exemplified in detail below. In embodiments in which the cleaning adjunct materials are not compatible with the variant proteases of the present invention in the cleaning compositions, then suitable methods of keeping the cleaning adjunct materials and the protease(s) separated (i.e., not in contact with each other) until combination of the two components is appropriate are used. Such separation methods include any suitable method known in the art (e.g., gelcaps, encapsulation, tablets, physical separation, etc.).
In some embodiments, an effective amount of one or more variant protease(s) provided herein is included in compositions useful for cleaning a variety of surfaces in need of proteinaceous stain removal. Such cleaning compositions include cleaning compositions for such applications as cleaning hard surfaces, fabrics, and dishes. Indeed, in some embodiments, the present invention provides fabric cleaning compositions, while in other embodiments, the present invention provides non-fabric cleaning compositions. Notably, the present invention also provides cleaning compositions suitable for personal care, including oral care (including dentrifices, toothpastes, mouthwashes, etc., as well as denture cleaning compositions), skin, and hair cleaning compositions. It is intended that the present invention encompass detergent compositions in any form (i.e., liquid, granular, bar, semi-solid, gels, emulsions, tablets, capsules, etc.).
By way of example, several cleaning compositions wherein the variant proteases of the present invention find use are described in greater detail below. In some embodiments in which the cleaning compositions of the present invention are formulated as compositions suitable for use in laundry machine washing method(s), the compositions of the present invention preferably contain at least one surfactant and at least one builder compound, as well as one or more cleaning adjunct materials preferably selected from organic polymeric compounds, bleaching agents, additional enzymes, suds suppressors, dispersants, lime-soap dispersants, soil suspension and anti-redeposition agents and corrosion inhibitors. In some embodiments, laundry compositions also contain softening agents (i.e., as additional cleaning adjunct materials). The compositions of the present invention also find use detergent additive products in solid or liquid form. Such additive products are intended to supplement and/or boost the performance of conventional detergent compositions and can be added at any stage of the cleaning process. In some embodiments, the density of the laundry detergent compositions herein ranges from about 400 to about 1200 g/liter, while in other embodiments, it ranges from about 500 to about 950 g/liter of composition measured at 20° C.
In embodiments formulated as compositions for use in manual dishwashing methods, the compositions of the invention preferably contain at least one surfactant and preferably at least one additional cleaning adjunct material selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.
In some embodiments, various cleaning compositions such as those provided in U.S. Pat. No. 6,605,458, find use with the variant proteases of the present invention. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a compact granular fabric cleaning composition, while in other embodiments, the composition is a granular fabric cleaning composition useful in the laundering of colored fabrics, in further embodiments, the composition is a granular fabric cleaning composition which provides softening through the wash capacity, in additional embodiments, the composition is a heavy duty liquid fabric cleaning composition. In some embodiments, the compositions comprising at least one variant protease of the present invention are fabric cleaning compositions such as those described in U.S. Pat. Nos. 6,610,642 and 6,376,450. In addition, the variant proteases of the present invention find use in granular laundry detergent compositions of particular utility under European or Japanese washing conditions (See e.g., U.S. Pat. No. 6,610,642).
In some alternative embodiments, the present invention provides hard surface cleaning compositions comprising at least one variant protease provided herein. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a hard surface cleaning composition such as those described in U.S. Pat. Nos. 6,610,642, 6,376,450, and 6,376,450.
In yet further embodiments, the present invention provides dishwashing compositions comprising at least one variant protease provided herein. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a hard surface cleaning composition such as those in U.S. Pat. Nos. 6,610,642 and 6,376,450. In some still further embodiments, the present invention provides dishwashing compositions comprising at least one variant protease provided herein. In some further embodiments, the compositions comprising at least one variant protease of the present invention comprise oral care compositions such as those in U.S. Pat. Nos. 6,376,450, and 6,376,450. The formulations and descriptions of the compounds and cleaning adjunct materials contained in the aforementioned U.S. Pat. Nos. 6,376,450, 6,605,458, 6,605,458, and 6,610,642, find use with the variant proteases provided herein.
The cleaning compositions of the present invention are formulated into any suitable form and prepared by any process chosen by the formulator, non-limiting examples of which are described in U.S. Pat. Nos. 5,879,584, 5,691,297, 5,574,005, 5,569,645, 5,565,422, 5,516,448, 5,489,392, and 5,486,303, all of which are incorporated herein by reference. When a low pH cleaning composition is desired, the pH of such composition is adjusted via the addition of a material such as monoethanolamine or an acidic material such as HCl.
While not essential for the purposes of the present invention, the non-limiting list of adjuncts illustrated hereinafter are suitable for use in the instant cleaning compositions. In some embodiments, these adjuncts are incorporated for example, to assist or enhance cleaning performance, for treatment of the substrate to be cleaned, or to modify the aesthetics of the cleaning composition as is the case with perfumes, colorants, dyes or the like. It is understood that such adjuncts are in addition to the variant proteases of the present invention. The precise nature of these additional components, and levels of incorporation thereof, will depend on the physical form of the composition and the nature of the cleaning operation for which it is to be used. Suitable adjunct materials include, but are not limited to, surfactants, builders, chelating agents, dye transfer inhibiting agents, deposition aids, dispersants, additional enzymes, and enzyme stabilizers, catalytic materials, bleach activators, bleach boosters, hydrogen peroxide, sources of hydrogen peroxide, preformed peracids, polymeric dispersing agents, clay soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, perfumes, structure elasticizing agents, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. In addition to the disclosure below, suitable examples of such other adjuncts and levels of use are found in U.S. Pat. Nos. 5,576,282, 6,306,812, and 6,326,348, incorporated by reference. The aforementioned adjunct ingredients may constitute the balance of the cleaning compositions of the present invention.
In some embodiments, the cleaning compositions according to the present invention comprise at least one surfactant and/or a surfactant system wherein the surfactant is selected from nonionic surfactants, anionic surfactants, cationic surfactants, ampholytic surfactants, zwitterionic surfactants, semi-polar nonionic surfactants and mixtures thereof. In some low pH cleaning composition embodiments (e.g., compositions having a neat pH of from about 3 to about 5), the composition typically does not contain alkyl ethoxylated sulfate, as it is believed that such surfactant may be hydrolyzed by such compositions the acidic contents. In some embodiments, the surfactant is present at a level of from about 0.1% to about 60%, while in alternative embodiments the level is from about 1% to about 50%, while in still further embodiments the level is from about 5% to about 40%, by weight of the cleaning composition.
In some embodiments, the cleaning compositions of the present invention comprise one or more detergent builders or builder systems. In some embodiments incorporating at least one builder, the cleaning compositions comprise at least about 1%, from about 3% to about 60% or even from about 5% to about 40% builder by weight of the cleaning composition. Builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates, alkali metal silicates, alkaline earth and alkali metal carbonates, aluminosilicates, polycarboxylate compounds, ether hydroxypolycarboxylates, copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1,3,5-trihydroxy benzene-2,4,6-trisulphonic acid, and carboxymethyloxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, citric acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof. Indeed, it is contemplated that any suitable builder will find use in various embodiments of the present invention.
In some embodiments, the builders form water-soluble hardness ion complexes (e.g., sequestering builders), such as citrates and polyphosphates (e.g., sodium tripolyphosphate and sodium tripolyphospate hexahydrate, potassium tripolyphosphate, and mixed sodium and potassium tripolyphosphate, etc.). It is contemplated that any suitable builder will find use in the present invention, including those known in the art (See e.g., EP 2 100 949).
In some embodiments, the cleaning compositions of the present invention contain at least one chelating agent. Suitable chelating agents include, but are not limited to copper, iron and/or manganese chelating agents and mixtures thereof. In embodiments in which at least one chelating agent is used, the cleaning compositions of the present invention comprise from about 0.1% to about 15% or even from about 3.0% to about 10% chelating agent by weight of the subject cleaning composition.
In some still further embodiments, the cleaning compositions provided herein contain at least one deposition aid. Suitable deposition aids include, but are not limited to, polyethylene glycol, polypropylene glycol, polycarboxylate, soil release polymers such as polytelephthalic acid, clays such as kaolinite, montmorillonite, atapulgite, illite, bentonite, halloysite, and mixtures thereof.
As indicated herein, in some embodiments, anti-redeposition agents find use in some embodiments of the present invention. In some embodiments, non-ionic surfactants find use. For example, in automatic dishwashing embodiments, non-ionic surfactants find use for surface modification purposes, in particular for sheeting, to avoid filming and spotting and to improve shine. These non-ionic surfactants also find use in preventing the re-deposition of soils. In some embodiments, the anti-redeposition agent is a non-ionic surfactant as known in the art (See e.g., EP 2 100 949).
In some embodiments, the cleaning compositions of the present invention include one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof. In embodiments in which at least one dye transfer inhibiting agent is used, the cleaning compositions of the present invention comprise from about 0.0001% to about 10%, from about 0.01% to about 5%, or even from about 0.1% to about 3% by weight of the cleaning composition.
In some embodiments, silicates are included within the compositions of the present invention. In some such embodiments, sodium silicates (e.g., sodium disilicate, sodium metasilicate, and crystalline phyllosilicates) find use. In some embodiments, silicates are present at a level of from about 1% to about 20%. In some embodiments, silicates are present at a level of from about 5% to about 15% by weight of the composition.
In some still additional embodiments, the cleaning compositions of the present invention also contain dispersants. Suitable water-soluble organic materials include, but are not limited to the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.
In some further embodiments, the enzymes used in the cleaning compositions are stabilized by any suitable technique. In some embodiments, the enzymes employed herein are stabilized by the presence of water-soluble sources of calcium and/or magnesium ions in the finished compositions that provide such ions to the enzymes. In some embodiments, the enzyme stabilizers include oligosaccharides, polysaccharides, and inorganic divalent metal salts, including alkaline earth metals, such as calcium salts. It is contemplated that various techniques for enzyme stabilization will find use in the present invention. For example, in some embodiments, the enzymes employed herein are stabilized by the presence of water-soluble sources of zinc (II), calcium (II) and/or magnesium (II) ions in the finished compositions that provide such ions to the enzymes, as well as other metal ions (e.g., barium (II), scandium (II), iron (II), manganese (II), aluminum (III), Tin (II), cobalt (II), copper (II), nickel (II), and oxovanadium (IV). Chlorides and sulfates also find use in some embodiments of the present invention. Examples of suitable oligosaccharides and polysaccharides (e.g., dextrins) are known in the art (See e.g., WO 07/145964). In some embodiments, reversible protease inhibitors also find use, such as boron-containing compounds (e.g., borate, 4-formyl phenyl boronic acid) and/or a tripeptide aldehyde find use to further improve stability, as desired.
In some embodiments, bleaches, bleach activators and/or bleach catalysts are present in the compositions of the present invention. In some embodiments, the cleaning compositions of the present invention comprise inorganic and/or organic bleaching compound(s). Inorganic bleaches include, but are not limited to perhydrate salts (e.g., perborate, percarbonate, perphosphate, persulfate, and persilicate salts). In some embodiments, inorganic perhydrate salts are alkali metal salts. In some embodiments, inorganic perhydrate salts are included as the crystalline solid, without additional protection, although in some other embodiments, the salt is coated. Any suitable salt known in the art finds use in the present invention (See e.g., EP 2 100 949).
In some embodiments, bleach activators are used in the compositions of the present invention. Bleach activators are typically organic peracid precursors that enhance the bleaching action in the course of cleaning at temperatures of 60° C. and below. Bleach activators suitable for use herein include compounds which, under perhydrolysis conditions, give aliphatic peroxoycarboxylic acids having preferably from about 1 to about 10 carbon atoms, in particular from about 2 to about 4 carbon atoms, and/or optionally substituted perbenzoic acid. Additional bleach activators are known in the art and find use in the present invention (See e.g., EP 2 100 949).
In addition, in some embodiments and as further described herein, the cleaning compositions of the present invention further comprise at least one bleach catalyst. In some embodiments, the manganese triazacyclononane and related complexes find use, as well as cobalt, copper, manganese, and iron complexes. Additional bleach catalysts find use in the present invention (See e.g., U.S. Pat. Nos. 4,246,612, 5,227,084, 4,810,410, WO 99/06521, and EP 2 100 949).
In some embodiments, the cleaning compositions of the present invention contain one or more catalytic metal complexes. In some embodiments, a metal-containing bleach catalyst finds use. In some embodiments, the metal bleach catalyst comprises a catalyst system comprising a transition metal cation of defined bleach catalytic activity, (e.g., copper, iron, titanium, ruthenium, tungsten, molybdenum, or manganese cations), an auxiliary metal cation having little or no bleach catalytic activity (e.g., zinc or aluminum cations), and a sequestrate having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra (methylenephosphonic acid) and water-soluble salts thereof are used (See e.g., U.S. Pat. No. 4,430,243). In some embodiments, the cleaning compositions of the present invention are catalyzed by means of a manganese compound. Such compounds and levels of use are well known in the art (See e.g., U.S. Pat. No. 5,576,282). In additional embodiments, cobalt bleach catalysts find use in the cleaning compositions of the present invention. Various cobalt bleach catalysts are known in the art (See e.g., U.S. Pat. Nos. 5,597,936 and 5,595,967) and are readily prepared by known procedures.
In some additional embodiments, the cleaning compositions of the present invention include a transition metal complex of a macropolycyclic rigid ligand (MRL). As a practical matter, and not by way of limitation, in some embodiments, the compositions and cleaning processes provided by the present invention are adjusted to provide on the order of at least one part per hundred million of the active MRL species in the aqueous washing medium, and in some embodiments, provide from about 0.005 ppm to about 25 ppm, more preferably from about 0.05 ppm to about 10 ppm, and most preferably from about 0.1 ppm to about 5 ppm, of the MRL in the wash liquor.
In some embodiments, transition-metals in the instant transition-metal bleach catalyst include, but are not limited to manganese, iron and chromium. MRLs also include, but are not limited to special ultra-rigid ligands that are cross-bridged (e.g., 5,12-diethyl-1,5,8,12-tetraazabicyclo[6.6.2]hexadecane). Suitable transition metal MRLs are readily prepared by known procedures (See e.g., WO 2000/32601, and U.S. Pat. No. 6,225,464).
In some embodiments, the cleaning compositions of the present invention comprise metal care agents. Metal care agents find use in preventing and/or reducing the tarnishing, corrosion, and/or oxidation of metals, including aluminum, stainless steel, and non-ferrous metals (e.g., silver and copper). Suitable metal care agents include those described in EP 2 100 949, WO 9426860 and WO 94/26859). In some embodiments, the metal care agent is a zinc salt. In some further embodiments, the cleaning compositions of the present invention comprise from about 0.1% to about 5% by weight of one or more metal care agent.
In some embodiments, the cleaning composition is a high density liquid (HDL) composition having a variant thermolysin protease. The HDL liquid laundry detergent can comprise a detersive surfactant (10%-40%) comprising anionic detersive surfactant (selected from a group of linear or branched or random chain, substituted or unsubstituted alkyl sulphates, alkyl sulphonates, alkyl alkoxylated sulphate, alkyl phosphates, alkyl phosphonates, alkyl carboxylates, and/or mixtures thereof); and optionally non-ionic surfactant (selected from a group of linear or branched or random chain, substituted or unsubstituted alkyl alkoxylated alcohol, for example a C8-C18 alkyl ethoxylated alcohol and/or C6-C12 alkyl phenol alkoxylates), optionally wherein the weight ratio of anionic detersive surfactant (with a hydrophilic index (HIc) of from 6.0 to 9) to non-ionic detersive surfactant is greater than 1:1.
The composition can comprise optionally, a surfactancy boosting polymer consisting of amphiphilic alkoxylated grease cleaning polymers (selected from a group of alkoxylated polymers having branched hydrophilic and hydrophobic properties, such as alkoxylated polyalkylenimines in the range of 0.05 wt %-10 wt %) and/or random graft polymers (typically comprising of hydrophilic backbone comprising monomers selected from the group consisting of: unsaturated C1-C6 carboxylic acids, ethers, alcohols, aldehydes, ketones, esters, sugar units, alkoxy units, maleic anhydride, saturated polyalcohols such as glycerol, and mixtures thereof; and hydrophobic side chain(s) selected from the group consisting of: C4-C25 alkyl group, polypropylene, polybutylene, vinyl ester of a saturated C1-C6 mono-carboxylic acid, C1-C6 alkyl ester of acrylic or methacrylic acid, and mixtures thereof.
The composition can comprise additional polymers such as soil release polymers (include anionically end-capped polyesters, for example SRP1, polymers comprising at least one monomer unit selected from saccharide, dicarboxylic acid, polyol and combinations thereof, in random or block configuration, ethylene terephthalate-based polymers and co-polymers thereof in random or block configuration, for example Repel-o-tex SF, SF-2 and SRP6, Texcare SRA100, SRA300, SRN100, SRN170, SRN240, SRN300 and SRN325, Marloquest SL), anti-redeposition polymers (0.1 wt % to 10 wt %, include carboxylate polymers, such as polymers comprising at least one monomer selected from acrylic acid, maleic acid (or maleic anhydride), fumaric acid, itaconic acid, aconitic acid, mesaconic acid, citraconic acid, methylenemalonic acid, and any mixture thereof, vinylpyrrolidone homopolymer, and/or polyethylene glycol, molecular weight in the range of from 500 to 100,000 Da); cellulosic polymer (including those selected from alkyl cellulose, alkyl alkoxyalkyl cellulose, carboxyalkyl cellulose, alkyl carboxyalkyl cellulose examples of which include carboxymethyl cellulose, methyl cellulose, methyl hydroxyethyl cellulose, methyl carboxymethyl cellulose, and mixtures thereof) and polymeric carboxylate (such as maleate/acrylate random copolymer or polyacrylate homopolymer).
The composition can further comprise saturated or unsaturated fatty acid, preferably saturated or unsaturated C12-C24 fatty acid (0 wt % to 10 wt %); deposition aids (examples for which include polysaccharides, preferably cellulosic polymers, poly diallyl dimethyl ammonium halides (DADMAC), and co-polymers of DAD MAC with vinyl pyrrolidone, acrylamides, imidazoles, imidazolinium halides, and mixtures thereof, in random or block configuration, cationic guar gum, cationic cellulose such as cationic hydoxyethyl cellulose, cationic starch, cationic polyacylamides, and mixtures thereof.
The composition can further comprise dye transfer inhibiting agents examples of which include manganese phthalocyanine, peroxidases, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles and/or mixtures thereof; chelating agents examples of which include ethylene-diamine-tetraacetic acid (EDTA); diethylene triamine penta methylene phosphonic acid (DTPMP); hydroxy-ethane diphosphonic acid (HEDP); ethylenediamine N,N′-disuccinic acid (EDDS); methyl glycine diacetic acid (MGDA); diethylene triamine penta acetic acid (DTPA); propylene diamine tetracetic acid (PDT A); 2-hydroxypyridine-N-oxide (HPNO); or methyl glycine diacetic acid (MGDA); glutamic acid N,N-diacetic acid (N,N-dicarboxymethyl glutamic acid tetrasodium salt (GLDA); nitrilotriacetic acid (NTA); 4,5-dihydroxy-m-benzenedisulfonic acid; citric acid and any salts thereof; N-hydroxyethylethylenediaminetri-acetic acid (HEDTA), triethylenetetraaminehexaacetic acid (TTHA), N-hydroxyethyliminodiacetic acid (HEIDA), dihydroxyethylglycine (DHEG), ethylenediaminetetrapropionic acid (EDTP) and derivatives thereof.
The composition can further comprise enzymes (0.01 wt % active enzyme to 0.03 wt % active enzyme) selected from a group of proteases; amylases; lipases; cellulases; choline oxidases; peroxidases/oxidases; pectate lyases; mannanases; cutinases; laccases; phospholipases; lysophospholipases; acyltransferase; perhydrolase; arylesterase and any mixture thereof. The composition may comprise an enzyme stabilizer (examples of which include polyols such as propylene glycol or glycerol, sugar or sugar alcohol, lactic acid, reversible protease inhibitor, boric acid, or a boric acid derivative, e.g., an aromatic borate ester, or a phenyl boronic acid derivative such as 4-formylphenyl boronic acid).
The composition can further comprise silicone or fatty-acid based suds suppressors; hueing dyes, calcium and magnesium cations, visual signaling ingredients, anti-foam (0.001 wt % to about 4.0 wt %), and/or structurant/thickener (0.01 wt % to 5 wt %, selected from the group consisting of diglycerides and triglycerides, ethylene glycol distearate, microcrystalline cellulose, cellulose based materials, microfiber cellulose, biopolymers, xanthan gum, gellan gum, and mixtures thereof).
Suitable detersive surfactants also include cationic detersive surfactants (selected from a group of alkyl pyridinium compounds, alkyl quarternary ammonium compounds, alkyl quarternary phosphonium compounds, alkyl ternary sulphonium compounds, and/or mixtures thereof); zwitterionic and/or amphoteric detersive surfactants (selected from a group of alkanolamine sulpho-betaines); ampholytic surfactants; semi-polar non-ionic surfactants and mixtures thereof.
The composition can be any liquid form, for example a liquid or gel form, or any combination thereof. The composition may be in any unit dose form, for example a pouch.
In some embodiments, the cleaning composition is a high density powder (HDD) composition having a variant thermolysin protease. The HDD powder laundry detergent can comprise a detersive surfactant including anionic detersive surfactants (selected from a group of linear or branched or random chain, substituted or unsubstituted alkyl sulphates, alkyl sulphonates, alkyl alkoxylated sulphate, alkyl phosphates, alkyl phosphonates, alkyl carboxylates and/or mixtures thereof), non-ionic detersive surfactant (selected from a group of linear or branched or random chain, substituted or unsubstituted C8-C18 alkyl ethoxylates, and/or C6-C12 alkyl phenol alkoxylates), cationic detersive surfactants (selected from a group of alkyl pyridinium compounds, alkyl quaternary ammonium compounds, alkyl quaternary phosphonium compounds, alkyl ternary sulphonium compounds, and mixtures thereof), zwitterionic and/or amphoteric detersive surfactants (selected from a group of alkanolamine sulpho-betaines); ampholytic surfactants; semi-polar non-ionic surfactants and mixtures thereof; builders (phosphate free builders [for example zeolite builders examples of which include zeolite A, zeolite X, zeolite P and zeolite MAP in the range of 0 wt % to less than 10 wt %]; phosphate builders [examples of which include sodium tri-polyphosphate in the range of 0 wt % to less than 10 wt %]; citric acid, citrate salts and nitrilotriacetic acid or salt thereof in the range of less than 15 wt %); silicate salt (sodium or potassium silicate or sodium meta-silicate in the range of 0 wt % to less than 10 wt %, or layered silicate (SKS-6)); carbonate salt (sodium carbonate and/or sodium bicarbonate in the range of 0 wt % to less than 10 wt %); and bleaching agents (photobleaches, examples of which include sulfonated zinc phthalocyanines, sulfonated aluminum phthalocyanines, xanthenes dyes, and mixtures thereof; hydrophobic or hydrophilic bleach activators (examples of which include dodecanoyl oxybenzene sulfonate, decanoyl oxybenzene sulfonate, decanoyl oxybenzoic acid or salts thereof, 3,5,5-trimethy hexanoyl oxybenzene sulfonate, tetraacetyl ethylene diamine-TAED, and nonanoyloxybenzene sulfonate-NOBS, nitrile quats, and mixtures thereof; hydrogen peroxide; sources of hydrogen peroxide (inorganic perhydrate salts examples of which include mono or tetra hydrate sodium salt of perborate, percarbonate, persulfate, perphosphate, or persilicate); preformed hydrophilic and/or hydrophobic peracids (selected from a group consisting of percarboxylic acids and salts, percarbonic acids and salts, perimidic acids and salts, peroxymonosulfuric acids and salts) & mixtures thereof and/or bleach catalyst (such as imine bleach boosters examples of which include iminium cations and polyions; iminium zwitterions; modified amines; modified amine oxides; N-sulphonyl imines; N-phosphonyl imines; N-acyl imines; thiadiazole dioxides; perfluoroimines; cyclic sugar ketones and mixtures thereof; metal-containing bleach catalyst for example copper, iron, titanium, ruthenium, tungsten, molybdenum, or manganese cations along with an auxiliary metal cations such as zinc or aluminum and a sequestrate such as ethylenediaminetetraacetic acid, ethylenediaminetetra(methylenephosphonic acid) and water-soluble salts thereof).
The composition can further comprise enzymes selected from a group of proteases; amylases; lipases; cellulases; choline oxidases; peroxidases/oxidases; pectate lyases; mannanases; cutinases; laccases; phospholipases; lysophospholipases; acyltransferase; perhydrolase; arylesterase and any mixture thereof.
The composition can further comprise additional detergent ingredients including perfume microcapsules, starch encapsulated perfume accord, hueing agents, additional polymers including fabric integrity and cationic polymers, dye lock ingredients, fabric-softening agents, brighteners (for example C.I. Fluorescent brighteners), flocculating agents, chelating agents, alkoxylated polyamines, fabric deposition aids, and/or cyclodextrin.
In some embodiments, the cleaning composition is an automatic dishwashing (ADW) detergent composition having a variant thermolysin protease. The ADW detergent can comprise two or more non-ionic surfactants selected from a group of ethoxylated non-ionic surfactants, alcohol alkoxylated surfactants, epoxy-capped poly(oxyalkylated) alcohols, or amine oxide surfactants present in amounts from 0 to 10% by weight; builders in the range of 5-60% comprising either phosphate (mono-phosphates, di-phosphates, tri-polyphosphates or oligomeric-poylphosphates, preferred sodium tripolyphosphate-STPP or phosphate-free builders [amino acid based compounds, examples of which include MGDA (methyl-glycine-diacetic acid), and salts and derivatives thereof, GLDA (glutamic-N,Ndiacetic acid) and salts and derivatives thereof, IDS (iminodisuccinic acid) and salts and derivatives thereof, carboxy methyl inulin and salts and derivatives thereof and mixtures thereof, nitrilotriacetic acid (NTA), diethylene triamine penta acetic acid (DTPA), B-alaninediacetic acid (B-ADA) and their salts], homopolymers and copolymers of poly-carboxylic acids and their partially or completely neutralized salts, monomeric polycarboxylic acids and hydroxycarboxylic acids and their salts in the range of 0.5% to 50% by weight; sulfonated/carboxylated polymers (provide dimensional stability to the product) in the range of about 0.1% to about 50% by weight; drying aids in the range of about 0.1% to about 10% by weight (selected from polyesters, especially anionic polyesters optionally together with further monomers with 3 to 6 functionalities which are conducive to polycondensation, specifically acid, alcohol or ester functionalities, polycarbonate-, polyurethane- and/or polyurea-polyorganosiloxane compounds or precursor compounds thereof of the reactive cyclic carbonate and urea type); silicates in the range from about 1% to about 20% by weight (sodium or potassium silicates for example sodium disilicate, sodium meta-silicate and crystalline phyllosilicates); bleach-inorganic (for example perhydrate salts such as perborate, percarbonate, perphosphate, persulfate and persilicate salts) and organic (for example organic peroxyacids including diacyl and tetraacylperoxides, especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid, and diperoxyhexadecanedioc acid); bleach activators-organic peracid precursors in the range from about 0.1% to about 10% by weight; bleach catalysts (selected from manganese triazacyclononane and related complexes, Co, Cu, Mn and Fe bispyridylamine and related complexes, and pentamine acetate cobalt(III) and related complexes); metal care agents in the range from about 0.1% to 5% by weight (selected from benzatriazoles, metal salts and complexes, and/or silicates); enzymes in the range from about 0.01 to 5.0 mg of active enzyme per gram of automatic dishwashing detergent composition (selected from a group of proteases; amylases; lipases; cellulases; choline oxidases; peroxidases/oxidases; pectate lyases; mannanases; cutinases; laccases; phospholipases; lysophospholipases; acyltransferase; perhydrolase; arylesterase and any mixture thereof); and enzyme stabilizer components (selected from oligosaccharides, polysaccharides and inorganic divalent metal salts).
The tables below show representative detergent composition useful as compositions having a variant thermolysis variant of the present invention.
1Random graft copolymer is a polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains. The molecular weight of the polyethylene oxide backbone is about 6000 and the weight ratio of the polyethylene oxide to polyvinyl acetate is about 40 to 60 and no more than 1 grafting point per 50 ethylene oxide units.
2 Polyethylenimine (MW = 600) with 20 ethoxylate groups per —NH.
3 Amphiphilic alkoxylated grease cleaning polymer is a polyethylenimine (MW = 600) with 24 ethoxylate groups per —NH and 16 propoxylate groups per —NH
17%
1Random graft copolymer is a polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains. The molecular weight of the polyethylene oxide backbone is about 6000 and the weight ratio of the polyethylene oxide to polyvinyl acetate is about 40 to 60 and no more than 1 grafting point per 50 ethylene oxide units.
2Polyethylenimine (MW = 600) with 20 ethoxylate groups per —NH.
3Amphiphilic alkoxylated grease cleaning polymer is a polyethylenimine (MW = 600) with 24 ethoxylate groups per —NH and 16 propoxylate groups per —NH
5Ethoxylated thiophene Hueing Dye is as described in U.S. Pat. No. 7,208,459 B2.
4Reversible Protease inhibitor of structure:
1Random graft copolymer is a polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains. The molecular weight of the polyethylene oxide backbone is about 6000 and the weight ratio of the polyethylene oxide to polyvinyl acetate is about 40 to 60 and no more than 1 grafting point per 50 ethylene oxide units.
3Amphiphilic alkoxylated grease cleaning polymer is a polyethylenimine (MW = 600) with 24 ethoxylate groups per —NH and 16 propoxylate groups per —NH
5Ethoxylated thiophene Hueing Dye is as described in U.S. Pat. No. 7,208,459 B2.
5Ethoxylated thiophene Hueing Dye is as described in U.S. Pat. No. 7,208,459 B2.
5Ethoxylated thiophene Hueing Dye is as described in U.S. Pat. No. 7,208,459 B2.
1Polyethylenimine (MW = 600) with 20 ethoxylate groups per —NH.
1Random graft copolymer is a polyvinyl acetate grafted polyethylene oxide copolymer having a polyethylene oxide backbone and multiple polyvinyl acetate side chains. The molecular weight of the polyethylene oxide backbone is about 6000 and the weight ratio of the polyethylene oxide to polyvinyl acetate is about 40 to 60 and no more than 1 grafting point per 50 ethylene oxide units.
2 Polyethylenimine (MW = 600) with 20 ethoxylate groups per —NH.
3 Amphiphilic alkoxylated grease cleaning polymer is a polyethylenimine (MW = 600) with 24 ethoxylate groups per —NH and 16 propoxylate groups per —NH
0-40.0%
0-8%
1Copolymer comprising
2Nonionic surfactant of the general formula R1—CH(OH)CH20-(AO)w-(A′0)x-(A″0)y-(A′″0)z-R2, in which R1 denotes a straight-chain or branched, saturated or mono- or polyunsaturated C6-24 alkyl or alkenyl residue; R2 denotes a linear or branched hydrocarbon residue with 2 to 26 carbon atoms; A, A′, A″ and A′″ mutually independently denote a residue from the group comprising —CH2CH2, —CH2CH2—CH2, —CH2CH2—CH(CH3), CH2—CH2—CH2CH2, —CH2—CH—(CH3)—CH2—, —CH2—CH(CH2—CH3), w, x, y and z denote values between 0.5 and 120, wherein x, y and/or z may also be 0.
0-0.4
15-40
10-30
12-50
15-40
1-18
5-50
10-30
0-20
As indicated above, the cleaning compositions of the present invention are formulated into any suitable form and prepared by any process chosen by the formulator, non-limiting examples of which are described in U.S. Pat. Nos. 5,879,584, 5,691,297, 5,574,005, 5,569,645, 5,516,448, 5,489,392, and 5,486,303, all of which are incorporated herein by reference. In some embodiments in which a low pH cleaning composition is desired, the pH of such composition is adjusted via the addition of an acidic material such as HCl.
The cleaning compositions disclosed herein of find use in cleaning a situs (e.g., a surface, item, dishware, or fabric). Typically, at least a portion of the situs is contacted with an embodiment of the present cleaning composition, in neat form or diluted in a wash liquor, and then the situs is optionally washed and/or rinsed. For purposes of the present invention, “washing” includes but is not limited to, scrubbing, and mechanical agitation. In some embodiments, the cleaning compositions are typically employed at concentrations of from about 500 ppm to about 15,000 ppm in solution. When the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C. and, when the situs comprises a fabric, the water to fabric mass ratio is typically from about 1:1 to about 30:1.
The cleaning compositions of the present invention are formulated into any suitable form and prepared by any suitable process chosen by the formulator, (See e.g., U.S. Pat. Nos. 5,879,584, 5,691,297, 5,574,005, 5,569,645, 5,565,422, 5,516,448, 5,489,392, 5,486,303, 4,515,705, 4,537,706, 4,515,707, 4,550,862, 4,561,998, 4,597,898, 4,968,451, 5,565,145, 5,929,022, 6,294,514 and 6,376,445).
In some embodiments, the cleaning compositions of the present invention are provided in unit dose form, including tablets, capsules, sachets, pouches, and multi-compartment pouches. In some embodiments, the unit dose format is designed to provide controlled release of the ingredients within a multi-compartment pouch (or other unit dose format). Suitable unit dose and controlled release formats are known in the art (See e.g., EP 2 100 949, WO 02/102955, U.S. Pat. Nos. 4,765,916 and 4,972,017, and WO 04/111178 for materials suitable for use in unit dose and controlled release formats). In some embodiments, the unit dose form is provided by tablets wrapped with a water-soluble film or water-soluble pouches. Various formats for unit doses are provided in EP 2 100 947, and are known in the art.
In some embodiments, the cleaning compositions of the present invention find use in cleaning surfaces (e.g., dishware), laundry, hard surfaces, contact lenses, etc. In some embodiments, at least a portion of the surface is contacted with at least one embodiment of the cleaning compositions of the present invention, in neat form or diluted in a wash liquor, and then the surface is optionally washed and/or rinsed. For purposes of the present invention, “washing” includes, but is not limited to, scrubbing, and mechanical washing. In some embodiments, the cleaning compositions of the present invention are used at concentrations of from about 500 ppm to about 15,000 ppm in solution. In some embodiments in which the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C.
The present invention provides methods for cleaning or washing an item or surface (e.g., hard surface) in need of cleaning, including, but not limited to methods for cleaning or washing a dishware item, a tableware item, a fabric item, a laundry item, personal care item, etc., or the like, and methods for cleaning or washing a hard or soft surface (e.g., a hard surface of an item).
In some embodiments, the present invention provides a method for cleaning an item, object, or surface in need of cleaning, the method comprising contacting the item or surface (or a portion of the item or surface desired to be cleaned) with at least one variant thermolysin protease of the present invention or a composition of the present invention for a sufficient time and/or under conditions suitable and/or effective to clean the item, object, or surface to a desired degree. Some such methods further comprise rinsing the item, object, or surface with water. For some such methods, the cleaning composition is a dishwashing detergent composition and the item or object to be cleaned is a dishware item or tableware item. As used herein, a “dishware item” is an item generally used in serving or eating food. A dishware item can be, but is not limited to for example, a dish, plate, cup, bowl, etc., and the like. As used herein, “tableware” is a broader term that includes, but is not limited to for example, dishes, cutlery, knives, forks, spoons, chopsticks, glassware, pitchers, sauce boats, drinking vessels, serving items, etc. It is intended that “tableware item” includes any of these or similar items for serving or eating food. For some such methods, the cleaning composition is an automatic dishwashing detergent composition or a hand dishwashing detergent composition and the item or object to be cleaned is a dishware or tableware item. For some such methods, the cleaning composition is a laundry detergent composition (e.g., a power laundry detergent composition or a liquid laundry detergent composition), and the item to be cleaned is a fabric item. In some other embodiments, the cleaning composition is a laundry pre-treatment composition.
In some embodiments, the present invention provides methods for cleaning or washing a fabric item optionally in need of cleaning or washing, respectively. In some embodiments, the methods comprise providing a composition comprising the variant protease, including but not limited to fabric or laundry cleaning composition, and a fabric item or laundry item in need of cleaning, and contacting the fabric item or laundry item (or a portion of the item desired to be cleaned) with the composition under conditions sufficient or effective to clean or wash the fabric or laundry item to a desired degree.
In some embodiments, the present invention provides a method for cleaning or washing an item or surface (e.g., hard surface) optionally in need of cleaning, the method comprising providing an item or surface to be cleaned or washed and contacting the item or surface (or a portion of the item or surface desired to be cleaned or washed) with at least one thermolysin variant of the invention or a composition of the invention comprising at least one such thermolysin variant for a sufficient time and/or under conditions sufficient or effective to clean or wash the item or surface to a desired degree. Such compositions include, but are not limited to for example, a cleaning composition or detergent composition of the invention (e.g., a hand dishwashing detergent composition, hand dishwashing cleaning composition, laundry detergent or fabric detergent or laundry or fabric cleaning composition, liquid laundry detergent, liquid laundry cleaning composition, powder laundry detergent composition, powder laundry cleaning composition, automatic dishwashing detergent composition, laundry booster cleaning or detergent composition, laundry cleaning additive, and laundry pre-spotter composition, etc.). In some embodiments, the method is repeated one or more times, particularly if additional cleaning or washing is desired. For example, in some instance, the method optionally further comprises allowing the item or surface to remain in contact with the at least one variant protease or composition for a period of time sufficient or effective to clean or wash the item or surface to the desired degree. In some embodiments, the methods further comprise rinsing the item or surface with water and/or another liquid. In some embodiments, the methods further comprise contacting the item or surface with at least one variant protease of the invention or a composition of the invention again and allowing the item or surface to remain in contact with the at least one variant protease or composition for a period of time sufficient to clean or wash the item or surface to the desired degree. In some embodiments, the cleaning composition is a dishwashing detergent composition and the item to be cleaned is a dishware or tableware item. In some embodiments of the present methods, the cleaning composition is an automatic dishwashing detergent composition or a hand dishwashing detergent composition and the item to be cleaned is a dishware or tableware item. In some embodiments of the methods, the cleaning composition is a laundry detergent composition and the item to be cleaned is a fabric item.
The present invention also provides methods of cleaning a tableware or dishware item in an automatic dishwashing machine, the method comprising providing an automatic dishwashing machine, placing an amount of an automatic dishwashing composition comprising at least one thermolysin variant of the present invention or a composition of the invention sufficient to clean the tableware or dishware item in the machine (e.g., by placing the composition in an appropriate or provided detergent compartment or dispenser in the machine), putting a dishware or tableware item in the machine, and operating the machine so as to clean the tableware or dishware item (e.g., as per the manufacturer's instructions). In some embodiments, the methods include any automatic dishwashing composition described herein, which comprises, but is not limited to at least one thermolysin variant provided herein. The amount of automatic dishwashing composition to be used can be readily determined according to the manufacturer's instructions or suggestions and any form of automatic dishwashing composition comprising at least one variant protease of the invention (e.g., liquid, powder, solid, gel, tablet, etc.), including any described herein, may be employed.
The present invention also provides methods for cleaning a surface, item or object optionally in need of cleaning, the method comprises contacting the item or surface (or a portion of the item or surface desired to be cleaned) with at least one variant thermolysin of the present invention or a cleaning composition of the invention in neat form or diluted in a wash liquor for a sufficient time and/or under conditions sufficient or effective to clean or wash the item or surface to a desired degree. The surface, item, or object may then be (optionally) washed and/or rinsed if desired. For purposes of the present invention, “washing” includes, but is not limited to for example, scrubbing and mechanical agitation. In some embodiments, the cleaning compositions are employed at concentrations of from about 500 ppm to about 15,000 ppm in solution (e.g., aqueous solution). When the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C. and when the surface, item or object comprises a fabric, the water to fabric mass ratio is typically from about 1:1 to about 30:1.
The present invention also provides methods of cleaning a laundry or fabric item in an washing machine, the method comprising providing an washing machine, placing an amount of a laundry detergent composition comprising at least one variant thermolysin of the invention sufficient to clean the laundry or fabric item in the machine (e.g., by placing the composition in an appropriate or provided detergent compartment or dispenser in the machine), placing the laundry or fabric item in the machine, and operating the machine so as to clean the laundry or fabric item (e.g., as per the manufacturer's instructions). The methods of the present invention include any laundry washing detergent composition described herein, comprising but not limited to at least one of any variant thermolysin provided herein. The amount of laundry detergent composition to be used can be readily determined according to manufacturer's instructions or suggestions and any form of laundry detergent composition comprising at least one variant protease of the invention (e.g., solid, powder, liquid, tablet, gel, etc.), including any described herein, may be employed.
The following assays are standard assays used in the examples described below. Occasionally specific protocols call for deviations from these standard assays. In those cases, deviations from these standard assay protocols below are identified in the examples.
The performance index (PI) compares the performance of the variant (measured value) and the standard enzyme (theoretical value) at the same protein concentration. In addition, the theoretical values can be calculated, using the parameters of the Langmuir equation of the standard enzyme. A performance index (PI) that is greater than 1 (PI>1) indicates improved performance by a variant as compared to the standard (e.g., Thermolysin), while a PI of 1 (PI=1) identifies a variant that performs the same as the standard, and a PI that is less than 1 (PI<1) identifies a variant that performs worse than the standard.
In order to determine the protease activity of the Thermolysin metalloprotease and thermolysin metalloprotease variants, the hydrolysis of 2-Aminobenzoyl-L-alanylglycyl-L-leucyl-L-alanino-4-nitrobenzylamide (Abz-AGLA-Nba) is measured.
The reagent solutions used are:
To prepare a 2.4 mM Abz-AGLA-Nba working solution, 1 mL of Abz-AGLA-Nba stock solution is added to 19 mL of MES buffer and mixed thoroughly for at least 10 seconds. The solution is kept at room temperature shielded from light.
To prepare the protease solutions, filtered culture supernatants of Thermolysin variants are diluted 50-fold in the enzyme dilution buffer.
The assay is performed in disposable black polystyrene flat-bottom 96-well micro plates suitable for fluorescence reading (e.g., Greiner 655076). First, 195 μL of 2.4 mM Abz-AGLA-Nba working solution is added to each well of the 96-well micro assay plates, followed by the addition of 5 μL of diluted protease samples. The solutions are mixed for 5 seconds and the fluorescence change is measured in kinetic mode (9 readings in 180 seconds, excitation wavelength 350 nm, emission wavelength 415 nm, no cut-off filter) at 25° C. using a micro plate spectrofluorometer (SpectraMAX Gemini EM, Molecular Devices). The rate of fluorescence change in RFU/sec (RFU=relative fluorescence units) provides a measure of protease activity.
The thermostability of the Thermolysin variants relative to the wild-type Thermolysin enzyme having the amino acid sequence of SEQ ID NO: 3 is determined by incubating the protease samples under defined conditions in either HEPES buffer, or a detergent solution. The temperature of the incubation is chosen such that the remaining activity of wild-type Thermolysin after the incubation is equal to approximately 30% of the initial activity. The initial and residual Thermolysin activities are determined using the Abz-AGLA-Nba assay described above in section B.
The reagent solutions used for this set of assays are:
1. 2.4 mM Abz-AGLA-Nba working solution (see section B, above)
2. Dilution buffer: 10 mM NaCl, 0.1 mM CaCl2, 0.005% (v/v) TWEEN®80
3. HEPES buffer: 10 mM HEPES, 0.1 mM CaCl2, 0.005% (v/v) TWEEN®-80, pH 7.15
4. AT formula pH 8 detergent (2.5 g/L in 21° GH water)
5. Sun All-in-1 Turbo Gel pH 6.3 (3 g/L in 21° GH water)
6. Filtered culture supernatants of Thermolysin variants
The equipment used for this set of assays includes a Biomek FX Robot (Beckman Coulter), a SpectraMAX Gemini EM micro plate spectrofluorometer (Molecular Devices) and Tetrad2 Peltier Thermal cycler (Bio-Rad).
Culture supernatants of Thermolysin variants are diluted to ˜1 μg/ml in HEPES buffer, and 50 μl/well of diluted enzyme sample is transferred to a 96-well PCR plate. The initial activity of the enzyme samples is measured using the Abz-AGLA-Nba assay as described in section B above, by transferring 5 μL of enzyme sample to a black 96-well assay micro plate (e.g., Greiner 655076) containing 195 μL of 2.4 mM Abz-AGLA-Nba substrate solution. The PCR plate containing the remaining 45 μl/well of the enzyme samples is sealed with an adhesive foil seal (Bio-Rad B-seal), placed in the Tetrad2 thermal cycler and incubated for 15 min at 83° C. After incubation, the samples in the PCR plate are cooled to room temperature and residual activity of the enzyme samples is measured using Abz-AGLA-Nba assay as described in section B above, by transferring 5 μL of enzyme sample to a black 96-well assay micro plate (e.g., Greiner 655076) containing 195 μL of 2.4 mM Abz-AGLA-Nba substrate solution. The thermostability activity ratio is calculated based on enzyme activity after the heat incubation divided by enzyme activity before the heat incubation, and is expressed as percentage remaining activity. The performance index for thermostability is determined by comparing the activity ratio of the variant enzyme with that of the similarly treated wild-type Thermolysin enzyme having the amino acid sequence of SEQ ID NO: 3.
The detergent stability of the Thermolysin variants is monitored by incubating the variants under stress conditions in a 0.3% (w/v) solution of the liquid automatic dish detergent known commercially as Sun All-in-1 Turbo Gel (Unilever, The Netherlands) and in a 0.25% (w/v) solution of the AT formula pH 8 detergent (described in section E) at elevated temperature. Heat inactivation of enzyme present in the commercially available Sun All-in-1 Turbo Gel detergent is performed by incubating a 10% detergent solution at 80° C. for 2 hours. At the end of the incubation, the measured pH value is 6.3.
Culture supernatants of Thermolysin variants are diluted to ˜1 μg/ml in the detergent solution, and 50 μl/well of diluted enzyme sample is transferred to a 96-well PCR plate. The PCR plate is sealed with an adhesive foil seal (Bio-Rad-B seal), placed in the Tetrad2 thermal cycler and incubated for 15 min. The temperature of the incubation is chosen such that the remaining activity of wild-type Thermolysin after the incubation is equal to approximately 30% of the initial activity. The samples in the heat-inactivated Sun All-in-1 Turbo Gel are incubated at 81° C. for 15 min, the samples in the AT formula pH 8 detergent are incubated at 69° C. for 15 min. After incubation, the samples in the PCR plate are cooled to room temperature and residual activity of the enzyme samples is measured using Abz-AGLA-Nba assay as described in section B above, by transferring 5 μL of enzyme sample to a black 96-well assay micro plate (e.g., Greiner 655076) containing 195 μL of 2.4 mM Abz-AGLA-Nba substrate solution.
The detergent activity ratio is calculated based on enzyme activity in the detergent solution after the heat incubation divided by enzyme activity in HEPES buffer before the heat incubation, and is expressed as percentage remaining activity.
The performance index for detergent stability is determined by comparing the activity ratio of the variant enzyme, with that of the similarly treated wild-type Thermolysin enzyme having the amino acid sequence of SEQ ID NO: 3.
The cleaning performance of the Thermolysin variants is tested using a microswatch assay on polyacryl swatches pre-stained with egg yolk and pigment (Center for Testmaterials, CFT, The Netherlands), in a 96-well micro plate format. The principle of this protease wash-performance assay is based on the liberation of egg yolk particles and a carbon black dye due to the hydrolysis of egg yolk incorporated on a microswatch. The absorbance at 405 nm of the wash liquid is measured, providing a measure of protease activity in the sample analysed (at the desired conditions: pH, temperature, detergent).
Reagent and Solutions Used:
1. PAS-38 microswatches (egg yolk on polyacryl fabric, aged and colored with carbon black dye; CFT-Vlaardingen, The Netherlands)
2. Citrate based detergent, pH8, with and without PAP (AT formulation, see section E)
3. The heat-inactivated commercially available liquid detergent Sun All-in-1 Turbo Gel
4. 100 mM CAPS buffer pH 10.2 (Rinse buffer)
5. Dilution buffer with propylene glycol: 10 mM NaCl, 0.1 mM CaCl2, 0.005% TWEEN®80 solution, 10% propylene glycol
Detergents and Conditions:
The protease samples (filtered supernatants of bacterial cultures grown in MTP plates) are tested at appropriate concentrations under several conditions.
AT formula pH 6 detergent, 50° C.; final protease concentration in assay ˜0.3 μg/ml
AT formula pH 8 detergent, 50° C.; final protease concentration in assay ˜0.2 μg/ml
AT formula pH 8 detergent+PAP, 50° C.; final protease concentration in assay ˜0.15 μg/ml
Sun All-in-1 Turbo Gel, pH 6.3 detergent, 50° C.; final protease concentration in assay ˜0.5 μg/ml
PAS-38 swatches are cut into 5 mm diameter pieces and placed in each well of a 96 well microplate. Culture supernatant samples are diluted in dilution buffer to approximately 10 μg/ml. Using a Biomek FX pipetting robot, detergent solution and diluted enzyme samples are added to a 96-well microplate containing PAS-38 microswatches to a final volume of 180 μl/well. The MTP is sealed with an adhesive seal, placed in the iEMS incubator/shaker (Thermo Scientific) and incubated for 30 minutes at 50° C. with shaking at 1150 RPM. After the incubation, 100 μL of wash liquid from each well is transferred to a new MTP, and the absorbance at 405 nm is measured using a SpectraMAX microplate spectrophotometer (Molecular Devices). This value is referred to as the “initial performance liquid”. The remaining wash liquid from the microswatch plate is discarded and the microswatches are subsequently rinsed once with 200 μL of water. Finally, 180 μL of 0.1 M CAPS buffer is added to each well and the MTP is incubated for an additional period of 10 minutes in the iEMS incubator/shaker at 50° C. with shaking at 1150 RPM. Following this incubation step, again 100 μL of liquid is transferred to a new MTP and the absorbance at 405 nm is measured using a SpectraMAX microplate spectrophotometer (Molecular Devices). This value is referred to as “rinse liquid”. The two measurements (the “initial performance liquid” and the “rinse liquid”) are added together and represent the “total performance”. Control wells containing a microswatch, detergent but no enzyme are included for background subtraction.
The obtained absorbance value is corrected for the blank value (obtained after incubation of microswatches in the absence of enzyme), and the resulting absorbance is a measure of hydrolytic activity. A performance index (PI) is calculated for each sample. For the PI calculation for the wash performance indices, a Langmuir curve fit based on wild type Thermolysin is used. Using the protein concentration of the variants, the expected performance based on the curve fit is calculated. The observed performance is divided by the calculated performance and this value is then divided by the performance of the wild type Thermolysin enzyme having the amino acid sequence of SEQ ID NO: 3.
Two detergents are used:
1. Sun ALL-in-1 Turbo Gel (Unilever, The Netherlands) purchased commercially in 2010.
2. AT formula, ingredients listed below in Table 1.1
Protein determination of Thermolysin variants from culture supernatants is performed using an Agilent 1200 HPLC system. A calibration curve (18 ppm-400 ppm) using purified wild-type Thermolysin protein (concentration determined using A222 absorbance) is prepared in dilution buffer (10 mM NaCl, 0.1 mM CaCl2, 0.005% TWEEN®-80 solution, 10% propylene glycol). All samples are transferred to 96-well microplates, pretreated with hydrochloric acid (0.3 M final concentration) and incubated at 4° C. for 5 minutes. Prior to loading the samples using an auto-sampler to a size-exclusion column BioSuite 250 4 μm UHR, 4.6×300 mm (Waters Corporation, Milford, Mass.), the samples are treated with sodium dodecyl sulphate (SDS) to a final concentration of 2% (w/v). The samples are eluted from the column using 25 mM sodium phosphate, pH 6 containing 2% (w/v) SDS. The flow rate is 0.4 mL/min with a 14 min run. The absorption of the samples is measured at 222 nm using an UV-detector and the protein concentration determined based on the calibration curve.
The performance index is determined by comparing the expression of the variant enzyme with that of the Bacillus thermoproteolyticus Thermolysin enzyme having the amino acid sequence of SEQ ID NO: 3.
Thermolysin-like proteases (TLPs) are members of the peptidase family M4 of which thermolysin (TLN; EC 3.4.24.27) is the prototype. The amino acid sequence of thermolysin, (EC 3.4.24.27) the neutral metallo endo-peptidase secreted from Bacillus thermoproteolyticus was first reported by Titani et al (Titani et al, (1972), Amino-acid sequence of thermolysin. Nature New Biol. 238:35-37). Subsequently, the gene for this enzyme was cloned by O'Donohue et al (O'Donohue, M. J (1994) Cloning and expression in Bacillus subtilis of the npr gene from Bacillus thermoproteolyticus Rokko coding for the thermostable metalloprotease thermolysin. Biochem. J. 300:599-603) and the sequence set forth as UniProtKB/Swiss-Prot Accession No. P00800 (SEQ ID NO:4). The only differences between the protein sequences reported by Titani et al and O'Donohue et al are the confirmation of Asn at position 37 (instead of Asp) and Gln at position 119 (instead of Glu).
The full-length thermolysin protein of Bacillus thermoproteolyticus (O'Donohue, M. J (1994) Biochem. J. 300:599-603) (shown here in SEQ ID NO:4) is greater than 99% identical to: the thermolysin of Geobacillus caldoproteolyticus (Chen et al (2004). Extremophiles 8:489-498, and described in WO2009058303) to the product of the nprS gene of Bacillus stearothermophilus (Nishiya, Y. and Imanaka, T. (1990) J. Bacteriol. 172:4861-4869), and to the Bacillus stearothermophilus nprM (M. Kubo and T. Imanaka, J. Gen. Microbiol. 134:1883-1892, 1988). As such the terms “thermolysin,” “stearolysin”, “bacillolysin,” “proteinase-T”, “PrT”, “Thermolysin-like protease”, and “TLPs”, are used interchangeably herein to refer to the neutral metalloprotease enzyme of Bacillus thermoproteolyticus. The only sequence difference between full-length thermolysin protein of Bacillus thermoproteolyticus (SEQ ID NO:4) and thermolysin of Geobacillus caldoproteolyticus (SEQ ID NO:5), is the presence of Ala at position 115 (within the pro-region) instead of Ser, the result of a change of one nucleotide in the codon for that position. (TCG to GCG).
The pHPLT-ProteinaseT plasmid was provided to BaseClear (Leiden, The Netherlands) for the generation of Site Evaluation Libraries (SELs).This plasmid encodes the Geobacillus caldoproteolyticus thermolysin protein coding sequence. The full-length protein sequence (SEQ ID NO:2) differs in one amino acid within the pro-region of the molecule originally cloned (SEQ ID NO:5) but both produce identical 316 amino acid mature proteins. The amino acid sequence of the mature Thermolysin protein is shown in SEQ ID NO: 3. BaseClear generated positional libraries at each of the sites in the Thermolysin mature protein.
This B. subtilis expression plasmid, pHPLT-ProteinaseT, contains the Thermolysin expression cassette shown below, the B. licheniformis LAT promoter (Plat), and additional elements from pUB 110 (McKenzie et al., Plasmid, 15:93-103, 1986) including a replicase gene (reppUB), a neomycin/kanamycin resistance gene (neo) and a bleomycin resistance marker (bleo) (FIG. 4 in U.S. Pat. No. 6,566,112). The pHPLT-ProteinaseT plasmid map is provided in
SEQ ID NO:1 sets forth the nucleotide sequence of Thermolysin gene from expression plasmid pHPLT-ProteinaseT (the native signal sequence is shown in lower case letters, native propeptide in lower case, underlined text, and mature sequence in uppercase letters):
tacatggaaccaacaatttcaaaccectcaattcatctccggtgatctg
ctgaaagtgaatggcacatccccagaagaactcgtctatcaatatgaga
aaaaaacgaaaacaagataaatttcatgaaaacgctaaggatactctac
aattgaaagaaaagaaaaatgataaccaggattacgatatgcacttcca
acaaacgtataaagggattcctgtgtttggagcagtagtaactgcgcac
gtgaaagatggcacgctgacggcgctatcagggacactgattccgaatt
tggacacgaaaggatccttaaaaagcgggaagaaattgagtgagaaaca
agcgcgtgacattgctgaaaaagatttagtggcaaatgtaacaaaggaa
gtaccggaatatgaacagggaaaagacaccgagtttgttgtttatgtca
atggggacgaggcttctttagcgtacgttgtcaatttaaactttttaac
tcctgaaccaggaaactggctgtatatcattgatgccgtagacggaaaa
attttaaataaatttaaccaacttgacgccgcaaaaccaggtgacgtca
agtcgATAACAGGAACATCAACTGTCGGAGTGGGAAGAGGAGTACTTGG
SEQ ID NO:2 sets forth the amino acid sequence of Thermolysin from expression plasmid pHPLT-ProteinaseT (the native signal sequence is shown in lower case letters, native propeptide in lower case, underlined text, and mature sequence in uppercase letters).
lkvngtspeelvyqyveknenkfkfhenakdtlqlkekkndnlgftfmh
fqqtykgipvfgavvtahvkdgtltalsgtlipnldtkgslksgkklse
kqardiaekdlvanvtkevpeyeqgkdtefvvyvngdeaslayvvnlnf
ltpepgnwlyiidavdgkilnkfnqldaakpgdyksITGTSTVGVGRGV
SEQ ID NO: 3 sets forth the amino acid sequence of the Thermolysin mature protein produced from pHPLT-ProteinaseT plasmid (316 residues):
SEQ ID NO:4 sets forth the full-length amino acid sequence of the thermolysin from Bacillus thermoproteolyticus UniProtKB/Swiss-Prot Accession No. P00800
lkvngtspeelvyqyveknenkfkfhenakdtlqlkekkndnlgftfmr
fqqtykgipvfgavvtshvkdgtltalsgtlipnldtkgslksgkklse
kqardiaekdlvanvtkevpeyeqgkdtefvvyvngdeaslayvvnlnf
ltpepgnwlyiidavdgkilnkfnqldaakpgdyksITGTSTVGVGRGV
SEQ ID NO:5 sets forth the full-length amino acid sequence of the thermolysin from Geobacillus caldoproteolyticus (Chen et al (2004). Extremophiles 8:489-498, and described in WO2009058303).
lkvngtspeelvyqyveknenkfkfhenakdtlqlkekkndnlgftfmr
fqqtykgipvfgavvtahvkdgtltalsgtlipnldtkgslksgkklse
kqardiaekdlvanvtkevpeyeqgkdtefvvyvngdeaslayvvnlnf
ltpepgnwlyiidavdgkilnkfnqldaakpgdyksITGTSTVGVGRGV
The positional libraries for each of the 316 residues were constructed by BaseClear BV (Leiden, The Netherlands). The libraries consisted of transformed B. subtilis cells containing expression plasmids encoding Thermolysin variant sequences at the 316 positions of the mature protein. Each variant was confirmed by DNA sequencing analysis prior to protein activity evaluation. Individual clones were cultured as described below to obtain the different Thermolysin variants for functional characterization.
The B. subtilis transformants containing Thermolysin variants were cultured in 96 well plates for 16 hours in Tryptic Soy Broth (TSB) with 10 μg/ml neomycin, and 10 μl of this pre-culture was added to Corning 3599 MTP's filled with 190 μl of cultivation media (described below) supplemented with 10 μg/ml Neomycin. The plates were incubated for 22-26 hours at 37° C. at 80% humidity with constant rotational mixing at 300 rpm. Cells were harvested by centrifugation at 2500 rpm for 10 minutes and filtered through Millipore Multiscreen filter plate using a Millipore vacuum system. After harvesting, propylene glycol was added to the culture supernatants to a final concentration of 10%, and these samples were used for assays. The cultivation media was an enriched semi-defined media based on phosphate buffer, glucose and maltodextrin as the main carbon sources, and supplemented with 0.2% soytone and 0.14% yeast extract for robust cell growth.
Productive positions are described as those positions within a molecule that are most useful for making combinatorial variants exhibiting an improved characteristic, where the position itself allows for at least one combinable mutation. Combinable mutations can be described as those substitutions in a molecule that can be used to make combinatorial variants. Combinable mutations are ones that improve at least one desired property of the molecule, while not significantly decreasing either: expression, activity, or stability.
Combinable mutations are ones that improve at least one desired property of the molecule, while not significantly decreasing either: expression, activity, or stability. Combinable mutations in Thermolysin were determined using performance index (PI) values resulting from the assays described in Example 1: Abz-AGLA-Nba protease assay (activity), PAS-38 microswatch assay (activity), detergent stability and thermostability assays, and protein determination (expression).
In addition to Combinable mutations, a second group of mutations for thermolysis is Activity Combinable mutations. Activity Combinable mutations are ones that improve at least one activity property of the molecule, with a performance index greater than or equal to 1.5, while not decreasing either expression or stability PI values below 0.5.
Combinable mutations have been grouped according to the following criteria (summarized on Table 3.1):
A variant where the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.9, and in addition have a PI for any one of these tests that is greater than or equal to 1.0 (Group A)
A variant where the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.8, and in addition have a PI for any one of these tests that is greater than or equal to 1.2 (Group B)
A variant where the minimum performance indices (PI) relative to Thermolysin parent for PAS-38 microswatch cleaning at pH6 or pH8, activity on Abz-AGLA-Nba, detergent stability and thermostability are greater than or equal to 0.5, and in addition have a PI for any one of these tests that is greater than or equal to 1.5 (Group C)
Groups A, B, and C further contain amino acid positions that have differing degrees of tolerance for multiple substitutions. To identify productive positions, we measure the degree of substitutions tolerated at each position, and assign a Productivity Score to each position. The Productivity Score was assigned according to the percentage of substitutions (calculated based on all the tested variants) within each position that fall within groups A, B, or C, using the criteria set forth below.
Productive positions are defined as the positions which have shown a certain degree of tolerance for multiple substitutions, while at the same time meeting a set of criteria for combinability as set forth below.
The criteria to determine the Productivity Score for productive positions are as follows:
Positions where less than 15% of the substitutions at a given position fall within groups A, B, or C are given a Productivity Score of “1”.
Positions where less than 40%, but greater than, or equal to 15% of the substitutions at a given position fall within groups A, B, or C are given a Productivity Score of “2”.
Positions where less than 75%, but greater than, or equal to 40% of the substitutions at a given position fall within groups A, B, or C are given a Productivity Score of “3”.
Positions where 75% or more of the substitutions at a given position fall within groups A, B, or C are given a Productivity Score of “4”.
These amino acid substitutions are further assigned a Suitability Score based on the group(s) (A, B, C) where the substitution appears, and where a higher suitability score represents a substitution more suitable for use in making combinatorial variants. Suitability scores are defined in Table 3.2.
Table 3.2 defines each Suitability Score as it relates to groups of combinable mutations and 5 productive positions.
Table 3.3 shows the shows the productive positions in Thermolysin that fall within the previously described Productivity Score of “4” and the substitutions within those positions that are combinable. Position numbering based on mature Thermolysin protein listed in SEQ ID NO: 3.
Table 3.4 shows the shows the productive positions in Thermolysin that fall within the previously described Productivity Score of “3” and the substitutions within those positions that are combinable. Position numbering based on mature Thermolysin protein listed in SEQ ID NO: 3.
Table 3.5 shows the shows the productive positions in Thermolysin that fall within the previously described Productivity Score of “2” and the substitutions within those positions that are combinable. Position numbering based on mature Thermolysin protein listed in SEQ ID NO: 3.
Table 3.6 shows the shows the productive positions in Thermolysin that fall within the previously described Productivity Score of “1” and the substitutions within those positions that are combinable. Position numbering based on mature Thermolysin protein listed in SEQ ID NO: 3.
As shown in Example 3, combinable mutations in thermolysin were determined using performance index (PI) values resulting from the assays described in Example 1.
Combinable mutations were assigned to groups A, B or C according to criteria set forth in Example 3. These substitutions are further assigned a Suitability Score based on the group(s) (A, B, C) where the substitution appears, and where a higher suitability score represents a substitution more suitable for use in making combinatorial variants. Suitability scores are defined in Table 4.1. Suitability scores for individual substitutions of thermolysin that fit the above criteria are reported below.
Table 4.1 defines each Suitability Score as it relates to groups of combinable mutations and productive positions.
Variants with suitability score +++++:
I001L, T002A, T002C, T002I, T002K, T002M, T004K, T004L, T004M, T004Y, Q017L, N037K, F040K, F040L, K045A, K045G, K045M, T049E, T049M, T049Y, L050P, S053C, S053L, A056M, A058E, A058L, Q061L, F063C, A064D, A064E, S065A, S065D, S065E, S065P, S065Y, V087C, V087K, V087L, V087M, V087N, V087Q, V087W, V087Y, N096K, N096L, N096Y, R101H, Q108L, Q108M, G109E, G109M, G109R, G109W, S118A, S118D, S118M, S118Q, S118R, S118T, S118V, Q128A, Q128L, Q128Y, I131L, I137L, T149N, G154A, G154H, G154K, G154M, G154Y, L155M, I164A, N181S, G196A, G196W, I197C, S198A, S198K, G199A, G199Y, A209C, A209M, H216A, Y217C, Y217L, T222K, N227A, I244L, Q246D, V256N, L263A, L263M, T272K, Q273N, Y274M, P277A, P277D, P277Y, L284A, L284M, L284Y, A286K, A286L, A286M, A286N, A286Y, A287C, A288L, A288M, V289A, S291A, S291T, T293A, T293I, T293K, T293L, T293M, T293Y, L295A, L295K, L295M, L295W, Y296M, G297N, S298A, S298G, S298K, S298M, S298R, T299A, T299K, S300D, S300N, Q301K, E302A, V303A, V303P, V303Y, A304E, A304K, A304Y, S305A, S305K, S305M, V306L, V306T, A309C, F310M, D311A, D311K, D311L, D311M, D311V, D311W, D311Y, and A312C
Variants with suitability score ++++:
T002Q, T004V, V007I, V009I, R011K, I020L, I020V, S025A, S025C, S025K, S025M, S025R, T026C, T026D, Y027C, Y027L, N037L, F040A, A044C, K045F, K045H, K045Q, K045Y, Y046C, R047D, R047E, R047G, R047L, R047M, R047Q, R047T, T049L, T049N, T049Q, T049V, S053A, S053N, S053V, A056E, Q061C, Q061I, A064T, S065L, S065T, S065W, A073F, A073L, A073M, A073W, H074C, H074F, H074M, H074N, H074Q, H074W, T080L, T080N, K085S, N086D, V087R, V087T, L091A, L091N, L091R, L091W, L091Y, S092L, Y093C, N096G, N096H, N096Q, N096R, N096S, N096W, N097E, N097M, A099R, A099S, R101C, R101L, R101S, S102N, S107G, Q108I, Q108K, Q108N, G109S, S118E, M120L, Q128I, Q128K, T129L, T129M, I131W, S134P, G136S, I137E, I137T, I137V, V140D, V148A, V148Q, T149D, T149S, T152G, G154C, G154N, L155I, N159S, N159Y, I164C, I168L, I171G, Y179F, A180S, G189A, Y193F, G196H, G196L, G196Y, I197F, S198M, S198N, S198R, S198W, S201A, A209G, A209I, A209K, A209P, A209R, A209Y, Y211E, Y211R, P214A, P214R, Y217A, Y217F, Y217M, Y217N, K219A, K219E, K219R, K219S, R220A, Y221A, Y221F, Y221G, Y221M, T222A, T222M, Q225C, Q225E, Q225K, Q225L, Q225S, I232L, I232R, I232S, I232T, I232V, I232Y, S234A, S234C, G235A, I236C, I244A, I244M, Q246C, V256S, G257K, G257R, I258A, I258C, I258K, I258Q, I258V, G259N, G259S, G259T, L263H, L263K, L263N, L263V, G264A, G264N, G264P, G264Q, G264S, G264T, K265N, I266C, I266M, I266T, I266V, F267A, F267C, F267H, F267I, F267K, F267L, F267M, F267T, F267Y, R269K, A270G, L271H, T272A, Q273E, Q273G, L275C, L275Q, L275S, L275T, T276A, T276L, T276V, T276Y, P277E, P277F, P277G, P277H, P277N, P277R, P277V, P277W, S279G, R285Y, A286C, A286Q, A286R, A286T, A288N, V289L, V289M, V289Y, Q290A, Q290H, Q290N, S291V, T293N, T293V, T293W, D294N, L295F, L295G, Y296W, G297D, S298E, S298N, S298P, T299N, S300A, S300G, S300T, Q301M, Q301S, Q301T, Q301V, E302D, E302Q, V303G, V303K, V303L, V303R, V303W, A304R, A304S, A304T, A304W, S305H, S305T, S305V, V306I, Q308A, Q308L, F310C, F310W, D311F, D311G, D311I, D311Q, D311S, D311T, V313C, G314Q, V315L, V315T, K316A, and K316M
Variants with suitability score +++:
I001K, I001M, I001V, T002F, T002L, T002P, T002S, T002V, T002W, T002Y, T004E, S005D, S005N, S005P, T006C, R011I, Q017I, Q017W, Q017Y, S025D, S025F, T026K, T026L, T026R, T026V, T026Y, Y027W, Q031A, Q031K, Q031V, N033S, N033T, N037D, N037Q, N037R, F040E, F040G, F040M, F040Q, F040S, F040Y, K045E, K045L, K045S, Y046L, R047A, R047C, R047H, R047K, R047N, T048E, T049A, T049D, T049F, T049H, T049I, T049S, S053F, S053H, S053I, S053M, S053Q, S053T, S053W, A056K, A056Q, A056V, A056W, Q061M, S065I, S065M, S065Q, S065V, D072F, H074E, H074L, Y076H, Y076L, Y076M, Y076Q, V079L, V079Q, V079T, T080I, Y081F, K085E, N086L, N086S, V087D, V087E, V087G, V087I, V087S, L091D, L091E, L091F, L091K, L091M, L091P, L091Q, L091S, Y093T, G095A, G095D, G095H, G095M, G095N, G095S, N096C, N096D, N096I, N096V, N097K, A098C, A098E, A098H, A098R, A099E, A099K, A099P, S107D, Q108C, Q108E, Q108F, Q108H, G127C, G127D, G127E, Q128C, Q128D, Q128E, Q128R, Q128S, T129I, T129R, S134A, I137P, A141S, T145A, T145C, T145E, T145G, T145M, T145N, T145Q, V148L, V148N, V148Y, T149M, T149V, Y151K, T152S, A153T, G154L, G154Q, G154S, G154T, L155C, Q158A, Q158K, Q158M, Q158N, N159R, N159W, S161A, S161N, S161P, S161T, I164L, I164N, I164S, I164T, I164V, I171C, I171E, I171F, I171L, I171S, F172G, F172L, F172M, F172Q, F172S, F172V, F172W, F172Y, G173A, G173C, T174C, V176L, V176N, N181L, G196D, G196E, G196T, I197D, I197K, I197L, I197T, I197V, I197W, I197Y, S198C, S198E, S198F, S198G, S198H, S198I, S198P, S198Q, S198T, S198V, G199C, G199E, G199F, G199H, G199Q, G199S, G199T, G199W, M205L, A209D, A209E, A209L, A209S, A209T, A209V, Y211A, Y211C, Y211D, Y211F, Y211G, Y211H, Y211I, Y211L, Y211N, Y211Q, Y211S, Y211T, D213N, D213S, P214C, P214G, P214K, P214S, H216C, H216E, H216S, H216T, Y217Q, Y217S, Y217T, Y217V, Y217W, S218K, S218L, S218Y, K219D, K219F, K219G, K219H, K219I, K219M, K219N, K219Q, K219T, R220K, R220V, Y221K, Y221N, Y221Q, Y221R, Y221S, Y221T, Y221V, T222C, T222D, T222L, T222Y, T224K, T224M, Q225D, Q225G, Q225H, Q225I, Q225P, Q225V, Q225W, I232C, I232E, I232F, I232K, I232M, I232N, I232Q, I232W, S234D, G235M, I236M, Y242C, Y242F, Y242N, Y242V, I244T, I244V, Q246E, Q246N, Q246T, G247A, G247S, T249K, T249M, T249N, H250A, H250C, G252K, G252Y, V253N, V253T, S254A, S254M, S254R, S254Y, V255L, V255P, V256L, V256T, G257C, G257D, G257E, G257L, G257N, G257P, G257Q, G257S, G257T, G257Y, I258E, I258L, I258M, I258N, G259A, G259C, G259E, G259F, G259H, G259L, G259M, G259W, D261A, D261N, L263C, L263I, L263Q, L263T, K265A, K265C, K265D, K265M, K265P, K265Q, K265S, I266A, I266F, I266L, I266S, F267E, F267G, F267N, F267S, F267V, F267W, Y268M, Y268Q, Y268V, A270C, A270F, A270I, A270L, A270S, L271A, L271D, L271F, L271I, T272E, T272L, T272V, T272W, Q273A, Q273H, Q273Y, Y274F, Y274H, L275I, L275M, L275V, T276C, T276F, T276I, T276P, T276Q, T276W, P277Q, P277S, P277T, T278G, S279A, S279D, S279I, S279L, S279M, S279N, S279Q, S279T, N280A, N280C, N280D, N280E, S282K, S282N, L284V, L284W, R285K, A286D, A286E, A286F, A286G, A286H, A286I, A286S, A287I, A287L, A287N, A287V, A287Y, A288C, A288I, A288S, A288T, A288V, V289C, V289E, V289F, V289G, V289I, V289N, V289S, V289W, Q290C, Q290D, Q290F, Q290G, Q290L, Q290W, S291E, T293C, T293E, T293F, T293G, T293H, T293Q, T293S, L295C, L295I, L295N, Y296N, G297A, G297M, G297R, G297Y, S298C, S298T, S298W, S298Y, T299C, T299F, T299L, T299M, T299R, T299W, S300C, S300K, S300M, S300R, S300Y, Q301E, Q301H, Q301P, Q301R, V303C, V303H, A304C, A304D, A304L, A304N, S305G, S305I, S305L, S305N, S305W, S305Y, V306A, V306S, K307A, K307C, K307G, K307I, K307M, K307N, K307Q, K307R, K307W, K307Y, Q308C, Q308D, Q308F, Q308G, Q308I, Q308M, A309G, A309S, D311C, D311E, A312G, A312M, A312V, V313T, G314A, G314E, G314H, G314M, G314S, G314W, V315A, V315C, V315I, V315M, K316D, K316E, K316F, K316G, K316H, K316L, K316N, K316P, K316Q, K316R, K316S, K316V, K316W, and K316Y
Variants with suitability score ++:
I001C, T004R, T006V, Q017T, N019K, N019S, T023F, T023W, Y024W, T026F, T026G, T026H, T026I, T026M, Y027M, Y027V, Q031C, Q031Y, N033A, N033C, N033L, N033M, Y046H, Y046N, T048D, T049W, A058C, A058V, Q061F, Q061V, A064H, A064Q, D072W, A073I, H074V, Y076T, V079S, T080A, K085A, K085L, K085N, K085R, N086A, N086C, N086E, N086F, N086G, N086K, N089H, N096F, N096T, N097C, N097R, N097S, N097Y, A098K, A098V, HOW, I100V, R101T, S102G, S103T, S107A, Q108D, G117H, S118G, Q128V, T129Y, G136A, A141G, L144T, V148M, D150S, Y151G, Y151H, Y151S, Y151W, G154D, G154I, G154W, I156L, I156Q, Q158S, N159A, N159C, N159G, N159M, N159T, E160Q, I168A, I168M, I168T, F172D, F172H, L175S, V176C, F178H, F178Y, Y179A, Y179D, Y179H, Y179M, Y179N, Y179Q, Y179S, Y179T, Y179W, A180E, A180G, A180K, A180T, N181G, N181K, N181M, N181T, K182A, K182W, N183S, D185E, E187D, I188V, G196K, G196R, G196V, I197E, I197Q, I197R, G199L, S201C, M205Q, S206M, S206R, D207H, D207N, K210I, K210L, K210V, G212A, G212D, G212Q, D213A, D213G, D213W, P214N, Y217G, S218G, S218T, S218V, T222I, T222V, G223D, G223K, T224E, T224H, Q225A, Q225M, Q225R, V230A, I232G, S234N, G235C, G235Q, G235S, I237F, I237M, I244F, G248A, G248E, G248S, T249P, Y251M, G252A, G252S, G252T, G252W, V253M, V253Q, S254N, S254V, S254W, V255M, V255N, V256A, V256D, V256F, V256G, V256H, V256R, I258R, I258S, G259K, G259R, R260A, R260N, D261G, D261H, D261I, D261S, G264C, G264R, K265G, K265I, K265L, K265R, Y268K, L271N, L271Y, T272C, T272F, T272N, T272Q, Y274C, Y274Q, Y274T, T276H, T278C, T278H, T278M, T278N, T278Q, T278S, N280H, N280T, S282A, S282H, S282L, S282M, S282T, Q283S, A286P, A287D, A288Y, V289R, V289T, Q290R, Q290T, Q290V, D294Q, L295T, L295V, Y296H, G297C, G297F, G297K, G297T, T299D, T299Q, S300H, S300P, S300V, S300W, Q301C, Q301F, Q301G, Q301W, E302G, E302T, E302V, S305Q, V306F, K307H, Q308R, Q308V, Q308W, Q308Y, A309T, A309V, A312T, and V313I
Variants with suitability +:
I001A, I001H, I001W, I001Y, G003Y, T004A, T004N, S005H, S005L, V007L, V009L, V009T, R011Y, Q017C, Q017R, Q017V, N019L, N019Y, T026W, Y027A, Q031I, N033K, F040W, S053K, S053R, A056H, A056I, A056Y, D057K, A058N, A058Y, Q061R, Q061W, F063Y, Y075A, V079A, V079N, T080D, N086Y, V087P, N089L, N089M, D094T, A098Y, V104A, S107K, S107Y, Q108A, G109A, G109L, Y110L, S118C, T129E, I131Y, G135A, I137A, A141C, T149A, T149L, D150A, D150F, D150K, D150N, D150Q, D150T, D150V, T152L, T152M, I156M, I156T, Q158L, Q158R, Q158Y, E160L, E160Y, T174A, L175H, N181A, K182L, E187L, I188L, I197A, I197H, I197N, M205A, M205V, S206A, S206C, S206K, S206L, D207A, G212Y, D213L, H216R, S218F, T224F, T224L, T224P, T224Q, T224V, T224Y, N227D, N227L, N227Y, I236A, I237N, N238L, N238M, K239A, A241L, A241S, Q246L, T249L, T249Y, H250K, H250M, H250N, H250P, H250Q, H250R, H250V, H250Y, V253I, V253R, V253Y, S254K, S254L, V255A, V255Y, V256K, D261P, D261V, D261W, K262A, Y268A, Y268S, R269V, T272P, T272Y, Q273C, Q273S, Q273W, Y274A, T278K, T278R, T278Y, N280G, N280Q, S282R, Q283K, Q283L, Q283P, Q283R, Q283W, Q283Y, A287K, A287R, A287T, Q290Y, S291I, S291L, S291M, S291N, D294A, D294V, Y296L, Y296R, T299P, S300I, S300L, Q301L, E302K, E302L, F310A, A312L, A312N, A312R, V313A, V313G, and V313L
Further listed are selected productive position variants of Thermolysin. Position numbering is based on mature Thermolysin protein listed in SEQ ID NO: 3. T002I, T002M, T048E, A058L, F063C, V087L, N096H, Q128Y, Y151R, A180E, S198A, I244T, Q273N, P277R, T278R, Q283E, T293L, T293N, L295F, S298A, Q301I, N019D, S025A, T026R, T049K, T049Q, F063L, S065A, S065T, L091M, N096Q, N096R, N096Y, N097K, R101M, G109A, S118A, I131L, V140D, Q158A, N159E, N159K, L175V, A180R, G196H, G196T, G196Y, K219S, Q225E, I232R, I244L, Q246D, D261N, P277G, T293Y, S300G, Q301F, Q301M, V303R, S305A, D311A.
Thermolysin of Bacillus thermoproteolyticus is classified under Family M4 (M for metalloprotease) in the MEROPS protease database (http://merops.sanger.ac.uk). Thermolysin is the prototype for the M4 family (thermolysin family) of metalloproteases and the type-example of clan MA. It is further classified into subbclan MA(E) also known as Glu-Zincins, because the third zinc ligand is a glutamate. Thermolysin of Bacillus thermoproteolyticus was assigned Merops accession number MER001026.
The MEROPS database uses a hierarchical, structure-based classification of the peptidases (proteases). In this, each peptidase is assigned to a Family on the basis of statistically significant similarities in amino acid sequence, and families that are thought to be homologous are grouped together in a Clan. The classification of peptidases by molecular structure and homology was developed in the 1990s because it depends on the availability of data for amino acid sequences and three-dimensional structures in quantities that were realized then. In 1993, Rawlings & Barrett described a system in which individual peptidases were assigned to families, and the families were grouped in clans (Rawlings, N. D. & Barrett, A. J. (1993) Evolutionary families of peptidases. Biochem J 290, 205-218).
All peptidases in the M4 family bind a single, catalytic zinc ion. As in many other families of metallopeptidases, there is an HEXXH motif, in which the histidines are zinc ligands and the glutamate is an active site residue. Most members of this family are endopeptidases active at neutral pH and are almost exclusively from bacteria, and thermostability has been attributed to binding of calcium ions. Proteins and peptides are degraded with a preference for cleavage of Xaa+Yaa, in which Xaa is a hydrophobic residue and Yaa is Leu, Phe, Ile, or Val. Thermolysin has a two-domain structure with the active site between the domains. The N-terminal domain includes a distinctive six-strand beta sheet with two helices, one of which carries the HEXXH zinc-binding motif. The C-terminal domain, which is unique for the family, is predominantly helical and carries the third zinc ligand.
A BLAST search for homologs of mature thermolysin protein (SEQ ID NO: 3) within MEROPS (version 9.5) yielded the results shown below (Table 5.1). Each enzyme is listed by MEROPS database unique accession number, gene origin and shows percent identity calculated by the program.
Further analysis of members of the various families in the MEROPS database can be performed, such as the generation of phylogenetic trees. The architecture for the 424 members of the Family M4 phylogenetic tree (http://merops.sanger.ac.uk/cgi-bin/famwrap/famcards/trees/m4_tree.htm) is provided below (
1 Stigmatella aurantiaca) family M4 unassigned peptidases (MER086404)
2 (Stigmatella aurantiaca) family M4 unassigned peptidases (MER086488)
3 (Myxococcus xanthus) family M4 unassigned peptidases (MER068045)
4 (Pseudoalteromonas tunicata) family M4 unassigned peptidases (MER063156)
5 M04.017 (Streptomyces avermitilis) griselysin (MER028561)
6 M04.017 (Streptomyces sviceus) griselysin (MER144000)
7 M04.017 (Streptomyces viridochromogenes) griselysin (MER229668)
8 M04.017 (Streptomyces coelicolor) griselysin (MER012275)
9 M04.017 (Streptomyces scabiei) griselysin (MER200776)
10 M04.017 (Kribbella flavida) griselysin (MER076577)
11 M04.017 (Janibacter sp. HTCC2649) griselysin (MER119370)
12 M04.017 (Nocardioides sp. JS614) griselysin (MER075575)
13 M04.017 (Stigmatella aurantiaca) griselysin (MER086497)
14 M04.017 (Xanthomonas campestris) griselysin (MER070193)
15 M04.017 (Xanthomonas axonopodis) griselysin (XAC0465 protein) (MER019560)
16 M04.017 (Xanthomonas oryzae) griselysin (MER113870)
17 M04.017 (Micromonospora sp. L5) griselysin (MER230635)
18 M04.017 (Streptomyces avermitilis) griselysin (SAV1037 protein) (MER028563)
19 M04.017 (Streptomyces sviceus) griselysin (MER187827)
20 M04.017 (Streptomyces pristinaespiralis) griselysin (MER137080)
21 M04.017 (Streptomyces sp. SPB74) griselysin (MER163965)
22 M04.017 (Streptomyces albus) griselysin (MER187823)
23 M04.017 (Streptomyces avermitilis) griselysin (SAV2795 protein) (MER028566)
24 M04.017 (Streptomyces sviceus) griselysin (MER137175)
25 M04.017 (Streptomyces ghanaensis) griselysin (MER187817)
26 M04.017 (Streptomyces coelicolor) griselysin (MER019351)
27 M04.017 (Streptomyces scabiei) griselysin (MER200969)
28 M04.017 (Streptomyces sp. SPB74) griselysin (MER137964)
29 M04.017 (Streptomyces sviceus) griselysin (MER187826)
30 M04.017 (Streptomyces avermitilis) griselysin (MER028567)
31 M04.017 (Streptomyces septatus) griselysin (MER108931)
32 M04.017 (Streptomyces scabiei) griselysin (MER200878)
33 M04.017 (Streptomyces sp. Mg1) griselysin (MER180683)
34 M04.017 (Streptomyces sviceus) griselysin (MER187825)
35 M04.017 (Streptomyces coelicolor) griselysin (MER011085)
36 M04.017 (Streptomyces scabiei) griselysin (MER200968)
37 M04.017 (Streptomyces ghanaensis) griselysin (MER187816)
38 M04.017 (Streptomyces griseus) griselysin (MER004744)
39 M04.017 (Streptomyces filamentosus) griselysin (MER187821)
40 M04.017 (Streptomyces avermitilis) griselysin (MER028565)
41 M04.017 (Streptomyces sp. Mg1) griselysin (MER163416)
42 M04.017 (Streptomyces griseus) griselysin (MER121393)
43 M04.017 (Streptomyces filamentosus) griselysin (MER187820)
44 M04.017 (Streptomyces sp. TH-3) griselysin (MER169964)
45 M04.017 (Janibacter sp. HTCC2649) griselysin (MER109443)
46 M04.017 (Janibacter sp. HTCC2649) griselysin (MER109417)
47 M04.017 (Kribbella flavida) griselysin (MER096497)
48 M04.017 (Streptomyces avermitilis) griselysin (MER028564)
49 M04.022 (Burkholderia pseudomallei) ZmpA peptidase (MER029961)
50 M04.022 (Burkholderia mallei) ZmpA peptidase (MER040142)
51 M04.022 (Burkholderia thailandensis) ZmpA peptidase (MER058477)
52 M04.022 (Burkholderia oklahomensis) ZmpA peptidase (MER187766)
53 M04.022 (Burkholderia cenocepacia) ZmpA peptidase (MER050804)
54 M04.022 (Burkholderia cepacia) ZmpA peptidase (MER028622)
55 M04.022 (Burkholderia ambifaria) ZmpA peptidase (MER055697)
56 M04.022 (Burkholderia sp. 383) ZmpA peptidase (MER056816)
57 M04.022 (Burkholderia ubonensis) ZmpA peptidase. (MER166266)
58 (Dehalococcoides sp. VS) M4 unassigned peptidases (MER109883)
59 (unidentified eubacterium SCB49) M4 unassigned peptidases (MER137229)
60 (Croceibacter atlanticus) M4 unassigned peptidases (MER118340)
61 (Flavobacterium johnsoniae) M4 unassigned peptidases (MER062832)
62 (Flavobacterium columnare) M4 unassigned peptidases (MER091620)
63 (Croceibacter atlanticus) M4 unassigned peptidases (MER109847)
64 (Chryseobacterium gleum) M4 unassigned peptidases (MER187776)
65 (Kordia algicida) M4 unassigned peptidases (MER166403)
66 (Microscilla marina) M4 unassigned peptidases (MER091624)
67 (Croceibacter atlanticus) M4 unassigned peptidases (MER117388)
68 (Croceibacter atlanticus) M4 unassigned peptidases (MER138802)
69 (Paenibacillus larvae) M4 unassigned peptidases (MER187765)
70 M04.001 (Paenibacillus larvae) thermolysin (MER168882)
71 (Paenibacillus polvmyxa) M4 unassigned peptidases (MER001033)
72 M04.001 (Brevibacillus brevis) thermolysin (MER001028)
73 M04.001 (Brevibacillus brevis) thermolysin (npr protein) (MER169677)
74 M04.001 (Bacillus pseudomycoides) thermolysin (MER187790)
75 M04.001 (Bacillus mycoides) thermolysin (MER187794)
76 M04.001 (Bacillus cereus) thermolysin (MER061817)
77 M04.001 (Bacillus cereus) thermolysin (MER187808)
78 M04.001 (Bacillus weihenstephanensis) thermolysin (MER109389)
79 M04.001 (Bacillus mycoides) thermolysin (MER187798)
80 M04.001 (Bacillus cereus) thermolysin (MER001030)
81 M04.001 (Bacillus thuringiensis) thermolysin (MER003181)
82 M04.001 (Bacillus pseudomycoides) thermolysin (MER176709)
83 M04.001 (Lactobacillus sp.) thermolysin (MER001354)
84 M04.001 (Bacillus anthracis) thermolysin (MER021824)
85 M04.001 (Bacillus megaterium) thermolysin (MER001031)
86 M04.001 (Bacillus sp. SG-1) thermolysin (MER109427)
87 M04.001 (Bacillus caldolyticus) thermolysin (MER001034)
88 M04.018 (Geobacillus stearothermophilus) stearolysin (MER001025)
89 M04.001 (Geobacillus sp. Y412MC52) thermolysin (MER234417)
90 M04.001 (Alicyclobacillus acidocaldarius) thermolysin (MER001353)
91 M04.001 (Bacillus sp.) thermolysin (MER001927)
92 M04.001 (Geobacillus sp. Y412MC61) thermolysin (MER168133)
93 M04.001 (Geobacillus sp. C56-T3) thermolysin (MER212338)
94 M04.001 (Geobacillus kaustophilus) thermolysin (MER040474)
95 M04.001 (Bacillus thermoproteolyticus) thermolysin (MER001026)
96 M04.001 (Geobacillus stearothermophilus) thermolysin (MER001027)
97 M04.018 (Bacillus sp. SG-1) stearolysin (MER109364)
98 M04.001 (Exiguobacterium sibiricum) thermolysin (MER091675)
99 M04.001 (Exiguobacterium sp. AT1b) thermolysin (MER124526)
100 M04.001 (Bacillus mycoides) thermolysin (MER187797)
101 M04.001 (Bacillus pseudomycoides) thermolysin (MER187793)
102 (Bacillus thuringiensis) M4 unassigned peptidases (MER187787)
103 M04.012 (Bacillus thuringiensis) neutral peptidase B (MER039810)
104 M04.012 (Bacillus cereus) neutral peptidase B (MER028887)
105 M04.012 (Bacillus weihenstephanensis) neutral peptidase B (MER084215)
106 M04.012 (Bacillus mycoides) neutral peptidase B (MER187800)
107 M04.012 (Bacillus cereus) neutral peptidase B (MER151875)
108 M04.012 (Bacillus anthracis) neutral peptidase B (MER021804)
109 M04.012 (Bacillus pseudomycoides) neutral peptidase B (MER187792)
110 M04.012 (Bacillus mycoides) neutral peptidase B (MER187796)
111 (Bacillus cereus) M4 unassigned peptidases (MER084165)
112 M04.012 (Bacillus cereus) neutral peptidase B (MER187810)
113 M04.012 (Bacillus cereus) neutral peptidase B (MER187806)
114 M04.012 (Bacillus thuringiensis) neutral peptidase B (MER187779)
115 M04.012 (Oceanobacillus iheyensis) neutral peptidase B (MER022038)
116 M04.012 (Bacillus subtilis) neutral peptidase B (MER001029)
117 (Herpetosiphon aurantiacus) M4 unassigned peptidases (MER091650)
118 (Bacillus cereus) M4 unassigned peptidases (MER187809)
119 M04.009 (Staphylococcus epidermidis) aureolysin (MER001869)
120 M04.009 (Staphylococcus capitis) aureolysin (MER178903)
121 M04.009 (Staphylococcus aureus) aureolysin (MER004711)
122 M04.009 (Macrococcus caseolyticus) aureolysin (MER155135)
123 M04.009 (Staphylococcus pseudintermedius) aureolysin (MER179736)
124 M04.009 (Staphylococcus warneri) aureolysin (MER187814)
125 M04.009 (Staphylococcus chromogens) aureolysin (MER011075)
126 M04.009 (Staphylococcus saprophyticus) aureolysin (MER057051)
127 (Bacillus cereus) M4 unassigned peptidases (MER050323)
128 (Bacillus thuringiensis M4 unassigned peptidases (MER187780)
129 (Bacillus cereus) unassigned peptidases (MER062591)
130 (Bacillus cereus) M4 unassigned peptidases (MER187770)
131 (Bacillus thuringiensis) M4 unassigned peptidases (MER080987)
132 (Bacillus cereus M4 unassigned peptidases (MER187805)
133 (Bacillus thuringiensis) M4 unassigned peptidases (MER187789)
134 (Bacillus vietnamensis) M4 unassigned peptidases (MER038281)
135 (Bacillus sp. NRRL B-14911) M4 unassigned peptidases (MER062589)
136 (Bacillus sp. SG-1) M4 unassigned peptidases (MER109478)
137 (Bacillus coahuilensis) M4 unassigned peptidases (MER187771)
138 M04.021 (Thermoactinomyces sp. 27a) neutral peptidase (MER029719)
139 M04.014 (Bacillus subtilis) bacillolysin (MER080014)
140 M04.014 (Bacillus sp. RH219) bacillolysin (MER080743)
141 M04.014 (Bacillus sp. B16) bacillolysin (MER054676)
142 M04.014 (Brevibacillus laterosporus) bacillolysin (MER048471)
143 M04.014 (Bacillus amyloliquefaciens) bacillolysin (MER001035)
144 M04.014 (Bacillus sp.) bacillolysin (MER001038)
145 M04.014 (Bacillus pumilus) bacillolysin (MER091634)
146 M04.014 (Bacillus subtilis) bacillolysin (MER001032)
147 (Clostridium acetobutylicum) family M4 unassigned peptidases (MER014937)
148 M04.011 (Clostridium perfringens) lambda toxin (MER002103)
149 M04.011 (Clostridium acetobutylicum) lambda toxin (MER014941)
150 (Clostridium histolyticum) M4 unassigned peptidases (MER003790)
151 (Chloroflexus aurantiacus) family M4 unassigned peptidases (MER001453)
152 (Chloroflexus sp. Y-400-fl) family M4 unassigned peptidases (MER155497)
153 M04.008 (Listeria innocua) Mpl peptidase (Listeria sp.) (MER229925)
154 M04.008 (Listeria monocytogenes) Mpl peptidase (MER001047)
155 M04.008 (Listeria ivanovii) Mpl peptidase (MER045739)
156 M04.008 (Listeria seeligeri) Mpl peptidase (MER045740)
157 (Plesiocystis pacifica) M4 unassigned peptidases (MER160603)
158 (Stigmatella aurantiaca) M4 unassigned peptidases (MER091643)
159 (Stigmatella aurantiaca) M4 unassigned peptidases (MER091640)
160 (Myxococcus xanthus) M4 unassigned peptidases (MER068475)
161 Myxococcus xanthus) M4 unassigned peptidases (MER017624)
162 (Shewanella halifaxensis) M4 unassigned peptidases (MER117663)
163 (Shewanella violacea) M4 unassigned peptidases (MER203088)
164 (Haliscomenobacter hydrossis) M4 unassigned peptidases (MER248570)
165 (Cytophaga hutchinsonii) M4 unassigned peptidases (MER023927)
166 (Vibrio mimicus) M4 unassigned peptidases (MER229315)
167 (Vibrio vulnificus) M4 unassigned peptidases (MER025442)
168 (Bacillus cereus) M4 unassigned peptidases (MER187802)
169 (Bacillus cereus) M4 unassigned peptidases (MER091678)
170 (Bacillus anthracis) M4 unassigned peptidases (MER019065)
171 (Bacillus cereus) M4 unassigned peptidases (MER054507)
172 (Bacillus thuringiensis) M4 unassigned peptidases (MER039813)
173 (Bacillus cereus) M4 unassigned peptidases (MER187804)
174 (Bacillus thuringiensis) M4 unassigned peptidases (MER091674)
175 (Bacillus cereus) M4 unassigned peptidases (MER028889)
176 (Bacillus thuringiensis) M4 unassigned peptidases (MER039811)
177 (Bacillus cereus) M4 unassigned peptidases (MER028890)
178 (Bacillus anthracis) M4 unassigned peptidases (MER020840)
179 (Bacillus mycoides) M4 unassigned peptidases (MER187799)
180 (Bacillus weihenstephanensis) M4 unassigned peptidases (MER109684)
181 (Bacillus pseudomycoides) M4 unassigned peptidases (MER187791)
182 (Bacillus mycoides) M4 unassigned peptidases (MER187795)
183 (Bacillus mycoides) M4 unassigned peptidases (MER187801)
184 (Bacillus thuringiensis) M4 unassigned peptidases (MER039814)
185 (Bacillus cereus) M4 unassigned peptidases (MER028888)
186 (Bacillus anthracia) M4 unassigned peptidases (MER020835)
187 (Hahella chejuensis) M4 unassigned peptidases (MER058667)
188 (Clostridium botulinum) M4 unassigned peptidases (npr protein) (MER088299)
189 (Clostridium botulinum) M4 unassigned peptidases (npr-1 protein) (MER079342)
190 (Clostridium sporogenes) M4 unassigned peptidases (MER137542)
191 (Clostridium botulinum) family M4 unassigned peptidases (npr protein) (MER187767)
192 (Clostridium botulinum) M4 unassigned peptidases (npr—1 protein) (MER187754)
193 (Clostridium botulinum) M4 unassigned peptidases (MER187753)
194 (Clostridium botulinum) M4 unassigned peptidases (MER079338)
195 (Clostridium sporogenes) M4 unassigned peptidases (MER144884)
196 (Clostridium botulinum) M4 unassigned peptidases (npr protein) (MER079341)
197 (Clostridium sporogenes) M4 unassigned peptidases (MER187769)
198 (Clostridium botulinum) M4 unassigned peptidases (npr—2 protein) (MER187755)
199 (Clostridium botulinum) M4 unassigned peptidases (MER079340)
200 (Clostridium botulinum) M4 unassigned peptidases (npr-4 protein) (MER095317)
201 (Clostridium botulinum) M4 unassigned peptidases (npr-4 protein) (MER094802)
202 (Clostridium botulinum) M4 unassigned peptidases (npr protein) (MER094801)
203 (Clostridium sporogenes) M4 unassigned peptidases (MER136684)
204 (Clostridium botulinum) M4 unassigned peptidases (npr protein) (MER079339)
205 (Clostridium sporogenes) M4 unassigned peptidases (MER178275)
206 (Methanosarcina acetivorans) M4 unassigned peptidases (MER017697)
207 (Streptomyces ghanaensis) M4 unassigned peptidases (MER187818)
208 (Streptomyces coelicolor) family M4 unassigned peptidases (MER011082)
209 (Streptomyces scabiei) family M4 unassigned peptidases (MER200705)
210 (Streptomyces avermitilis) family M4 unassigned peptidases (MER028562)
211 (Streptomyces sviceus) family M4 unassigned peptidases (MER137373)
212 (Streptomyces sp. Mg1) family M4 unassigned peptidases (MER137463)
213 (Streptomyces griseus) family M4 unassigned peptidases (MER121447)
214 (Streptomyces filamentosus) family M4 unassigned peptidases (MER187819)
215 (Streptomyces pristinaespiralis) family M4 unassigned peptidases (MER140364)
216 (Streptomyces albus) family M4 unassigned peptidases (MER187822)
217 (Streptomyces sp. SPB74) family M4 unassigned peptidases (MER163861)
218 http://merops.sanger.ac.uk/cgi-bin/pepsum?id=M04.UPW (Streptomyces clavuligerus) family M4 unassigned peptidases (MER187824)
219 (Arthrobacter chlorophenolicus) family M4 unassigned peptidases (MER126758)
220 (Arthrobacter phenanthrenivorans) family M4 unassigned peptidases (MER240183)
221 (Arthrobacter sp. FB24) family M4 unassigned peptidases (MER050759)
222 (Arthrobacter aurescens) family M4 unassigned peptidases (MER075195)
223 (marine actinobacterium PHSC20C1) family M4 unassigned peptidases
224 (Brachybacterium faecium) family M4 unassigned peptidases (MER127552)
225 (Clavibacter michiganensis) family M4 unassigned peptidases (MER121216)
226 (Clavibacter michiganensis) family M4 unassigned peptidases (MER115299)
227 (Microbacterium testaceum) family M4 unassigned peptidases (MER247399)
228 (Intrasporangium calvum) family M4 unassigned peptidases (MER231738)
229 (Janibacter sp. HTCC2649) family M4 unassigned peptidases (MER115301)
230 (Frankia alni) family M4 unassigned peptidases (MER091651)
231 (Frankia sp. CcI3) family M4 unassigned peptidases (MER051510)
232 (Frankia sp. EAN1pec) family M4 unassigned peptidases (MER051747)
233 (Meiothermus silvanus) family M4 unassigned peptidases (MER038269)
234 (Pseudomonas fluorescens) family M4 unassigned peptidases (MER187756)
235 (Myxococcus xanthus) family M4 unassigned peptidases (MER068095)
236 (Burkholderia sp. CCGE1002) family M4 unassigned peptidases (MER203878)
237 (Ricinus communis) family M4 unassigned peptidases (MER162821)
238 (Catenulispora acidiphila) family M4 unassigned peptidases (MER132795)
239 (Brevibacterium linens) family M4 unassigned peptidases (MER115300)
240 (Anabaena variabilis) family M4 unassigned peptidases (MER054976)
241 (Nostoc sp. PCC 7120) family M4 unassigned peptidases (MER016719)
242 (Nostoc punctiforme) family M4 unassigned peptidases (MER024259)
243 (Xanthomonas axonopodis) family M4 unassigned peptidases (MER019561)
244 (Xanthomonas campestris) family M4 unassigned peptidases (MER070175)
245 (Xanthomonas oryzae) family M4 unassigned peptidases (MER027496)
246 (Xanthomonas campestris) family M4 unassigned peptidases (MER019416)
247 (Thermomonospora curvata) family M4 unassigned peptidases (MER129229)
248 (Halomonas elongata) family M4 unassigned peptidases (MER223548)
249 (Chromohalobacter salexigens) family M4 unassigned peptidases (MER050897)
250 (Bordetella parapertussis) family M4 unassigned peptidases (MER030706)
251 (Bordetella bronchiseptica) family M4 unassigned peptidases (MER030781)
252 (Bordetella petrii) family M4 unassigned peptidases (MER114690)
253 (Variovorax paradoxus) family M4 unassigned peptidases (MER187757)
254 (Variovorax paradoxus) family M4 unassigned peptidases (MER235281)
255 (Pseudomonas brassicacearum) family M4 unassigned peptidases (MER244770)
256 (Pseudomonas fulva) family M4 unassigned peptidases (MER249215)
257 (Pseudomonas stutzeri) family M4 unassigned peptidases (MER094699)
258 (Dickeya dadantii) family M4 unassigned peptidases (MER223843)
259 (Dickeya dadantii) family M4 unassigned peptidases (MER193415)
260 (Dickeya zeae) family M4 unassigned peptidases (MER187758)
261 (Pectobacterium carotovorum) family M4 unassigned peptidases (MER001045)
262 (Pectobacterium wasabiae) family M4 unassigned peptidases (MER187830)
263 (Dickeya dadantii) family M4 unassigned peptidases (MER182707)
264 M04.023 (Citrobacter rodentium) zpx peptidase (MER196184)
265 M04.023 (Enterobacter cancerogenus) zpx peptidase (MER187772)
266 M04.023 (Salmonella enterica) zpx peptidase (MER108712)
267 M04.023 (Enterobacter sakazakii) zpx peptidase (zpx protein) (MER091601)
268 M04.023 (Erwinia amylovora) zpx peptidase (prt1 protein) (MER202074)
269 M04.025 (Erwinia billingiae) protealysin (mpr protein) (MER220902)
270 M04.025 (Pantoea sp. At-9b) protealysin (MER232022)
271 M04.025 (Pantoea ananatis) protealysin (MER202817)
272 M04.025 (Rahnella sp. Y9602) protealysin (MER237139)
273 M04.025 (Serratia grimesii) protealysin (MER115298)
274 M04.025 (Serratia sp. A2) protealysin (MER119664)
275 M04.025 (Serratia proteamaculans) protealysin (MER059439)
276 M04.025 (Serratia sp. AS9) protealysin (MER249825)
277 M04.025 (Serratia sp. AS12) protealysin (MER249807)
278 (Geodermatophilus obscures) family M4 unassigned peptidases (MER132589)
279 (Gemmata obscuriglobus) family M4 unassigned peptidases (MER187768)
280 (Nocardioides sp. JS614) family M4 unassigned peptidases (MER049523)
281 M04.024 (Xenorhabdus bovienii) PrtS peptidase (Photorhabdus luminescens) (MER200616)
282 M04.024 (Xenorhabdus nematophila) PrtS peptidase (MER219816)
283 M04.024 (Xenorhabdus nematophila) PrtS peptidase (MER219815)
284 M04.024 (Photorhabdus asymbiotica) PrtS peptidase (MER187759)
285 M04.024 (Photorhabdus luminescens) PrtS peptidase (MER033481)
286 M04.024 (Photorhabdus sp. Az29) PrtS peptidase (MER115297)
287 (Aspergillus terreus) family M4 unassigned peptidases (MER091644)
288 (Neosartorya fischeri) family M4 unassigned peptidases (MER091615)
289 (Pyrenophora tritici-repentis) family M4 unassigned peptidases (MER138903)
290 (Saccharopolyspora erythraea) family M4 unassigned peptidases (MER088688)
291 (Nectria haematococca) family M4 unassigned peptidases (MER243771)
292 (Gibberella zeae) family M4 unassigned peptidases (MER064838)
293 (Metarhizium anisopliae) family M4 unassigned peptidases (MER243770)
294 (Metarhizium acridum) family M4 unassigned peptidases (MER243769)
295 (Waddlia chondrophila) family M4 unassigned peptidases (MER211844)
296 (Pseudomonas savastanoi) family M4 unassigned peptidases (MER232822)
297 (Pseudomonas syringae) family M4 unassigned peptidases (MER052672)
298 (Pseudomonas coronafaciens) family M4 unassigned peptidases (MER187813)
299 (Cyanothece sp. ATCC 51142) family M4 unassigned peptidases (MER103362)
300 (Bacillus thuringiensis) family M4 unassigned peptidases (MER187783)
301 (Bacillus cereus) family M4 unassigned peptidases (MER178978)
302 (Bacillus cereus) family M4 unassigned peptidases (MER187811)
303 (Bacillus thuringiensis) family M4 unassigned peptidases (MER187778)
304 (Bacillus cereus) family M4 unassigned peptidases (MER187807)
305 (Methanosarcina acetivorans) family M4 unassigned peptidases (MER017698)
306 (Bacillus thuringiensis) family M4 unassigned peptidases (MER187784)
307 (Bacillus thuringiensis) family M4 unassigned peptidases (MER187788)
308 (Cellulophaga algicola) family M4 unassigned peptidases (MER235562)
309 (Aspergillus niger) family M4 unassigned peptidases (MER091631)
310 (Providencia rustigianii) family M4 unassigned peptidases (MER187773)
311 (Providencia alcalifaciens) family M4 unassigned peptidases (MER187774)
312 (Providencia rettgeri) family M4 unassigned peptidases (MER187775)
313 (Providencia stuartii) family M4 unassigned peptidases (MER122839)
314 (Mycobacterium abscessus) family M4 unassigned peptidases (MER117364)
315 (Mycobacterium abscessus) family M4 unassigned peptidases (MER117363)
316 (Bradyrhizobium japonicum) family M4 unassigned peptidases (MER026988)
317 (Agrobacterium vitis) family M4 unassigned peptidases (MER162454)
318 (Mucilaginibacter paludis) family M4 unassigned peptidases (MER229316)
319 (Serratia marcescens) family M4 unassigned peptidases (MER001046)
320 (Streptomyces ghanaensis) family M4 unassigned peptidases (MER187815)
321 (Sorangium cellulosum) family M4 unassigned peptidases (MER114292)
322 (Streptomyces filamentosus) family M4 unassigned peptidases (MER091679)
323 (Streptomyces avermitilis) family M4 unassigned peptidases (MER028519)
324 (Streptosporangium roseum) family M4 unassigned peptidases (MER187812)
325 M04.007 (Enterococcus faecium) coccolysin (MER187749)
326 M04.007 (Enterococcus faecalis) coccolysin (MER002810)
327 (Renibacterium salmoninarum) family M4 unassigned peptidases (MER002083)
328 (Kribbella flavida) family M4 unassigned peptidases (MER079366)
329 (Herpetosiphon aurantiacus) family M4 unassigned peptidases (MER085851)
330 M04.016 (Aeromonas jandaei) PA peptidase (Aeromonas-type) (MER079815)
331 M04.016 (Aeromonas eucrenophila) PA peptidase (Aeromonas-type) (MER079803)
332 M04.016 (Aeromonas punctata) PA peptidase (Aeromonas-type) (MER029943)
333 M04.016 (Aeromonas encheleia) PA peptidase (MER079817)
334 M04.016 (Aeromonas bestiarum) PA peptidase (MER079816)
335 M04.016 (Aeromonas media) PA peptidase (MER079802)
336 M04.016 (Aeromonas salmonicida) PA peptidase (MER079819)
337 M04.016 (Aeromonas punctata) PA peptidase (MER030073)
338 M04.016 (Aeromonas encheleia) PA peptidase (MER079804)
339 M04.016 (Aeromonas popoffii) PA peptidase (MER079805)
340 M04.016 (Aeromonas hydrophila) PA peptidase (MER011853)
341 M04.016 (Aeromonas sp. CDC 2478-85) PA peptidase (MER079818)
342 M04.016 (Aeromonas schubertii) PA peptidase (Aeromonas-type) (MER079806)
343 (Aeromonas veronii) M4 unassigned peptidases (MER055154)
344 (Aeromonas sobria) M4 unassigned peptidases (MER079820)
345 (Reinekea sp. MED297) family M4 unassigned peptidases (MER083727)
346 (Shewanella denitrificans) family M4 unassigned peptidases (MER050231)
347 (Shewanella baltica) family M4 unassigned peptidases (MER048895)
348 (Shewanella amazonensis) family M4 unassigned peptidases (MER048811)
349 (Shewanella woodyi) family M4 unassigned peptidases (MER087265)
350 (Chromobacterium violaceum) family M4 unassigned peptidases (MER027350)
351 (Pseudoalteromonas sp. SB-B1) family M4 unassigned peptidases (MER140592)
352 (Pseudoalteromonas sp. SM9913) family M4 unassigned peptidases (MER091617)
353 (Pseudoalteromonas sp. A28) family M4 unassigned peptidases (MER019098)
354 (Antarctic bacterium str. 643) family M4 unassigned peptidases (MER012255)
355 (Pseudoalteromonas sp. SM495) family M4 unassigned peptidases (MER187748)
356 (Pseudoalteromonas piscicida) family M4 unassigned peptidases (MER019099)
357 (Pseudoalteromonas ruthenica) family M4 unassigned peptidases (MER187751)
358 (Pseudoalteromonas tunicata) family M4 unassigned peptidases (MER108855)
359 (Moritella viscosa) family M4 unassigned peptidases (MER139442)
360 (Haliangium ochraceum) family M4 unassigned peptidases (MER114761)
361 (Haliangium ochraceum) family M4 unassigned peptidases (MER124450)
362 (Kangiella koreensis) family M4 unassigned peptidases (MER065613)
363 M04.003 (Marinomonas sp. MED121) vibriolysin (MER139826)
364 (Vibrio splendidus) family M4 unassigned peptidases (MER122486)
365 (Vibrionales bacterium SWAT-3) family M4 unassigned peptidases (MER139254)
366 (Vibrio tubiashii) family M4 unassigned peptidases (MER187750)
367 (Vibrio harveyi) family M4 unassigned peptidases (MER091688)
368 (Vibrio campbellii) family M4 unassigned peptidases (MER139568)
369 (Shewanella sp. MR-7) family M4 unassigned peptidases (MER072768)
370 (Shewanella sp. MR-4) family M4 unassigned peptidases (MER073030)
371 (Shewanella sp. ANA-3) family M4 unassigned peptidases (MER073381)
372 (Shewanella amazonensis) family M4 unassigned peptidases (MER049928)
373 (Shewanella woodyi) family M4 unassigned peptidases (MER087209)
374 (Vibrio parahaemolyticus) family M4 unassigned peptidases (MER027936)
375 (Vibrio sp. Ex25) family M4 unassigned peptidases (MER139749)
376 (Vibrio harveyi) family M4 unassigned peptidases (MER109271)
377 (Hahella chejuensis) family M4 unassigned peptidases (MER080002)
378 M04.003 (Moritella sp. PE36) vibriolysin (MER113768)
379 (uncultured bacterium pTW3) family M4 unassigned peptidases (MER164961)
380 (uncultured bacterium pTW2) family M4 unassigned peptidases (MER164951)
381 M04.005 (Pseudomonas aeruginosa) pseudolysin (MER001024)
382 M04.003 (Vibrio tubiashii) vibriolysin (MER139044)
383 M04.003 (Vibrio proteolyticus) vibriolysin (MER001043)
384 M04.003 (Listonella anguillarum) vibriolysin (MER120583)
385 M04.003 (Vibrio anguillarum) vibriolysin (MER001044)
386 M04.003 (Listonella anguillarum) vibriolysin (MER120671)
387 M04.003 (Vibrio aestuarianus) vibriolysin (MER113809)
388 M04.003 (Vibrio vulnificus) vibriolysin (MER003353)
389 M04.010 (Vibrio splendidus) vimelysin (MER091636)
390 M04.010 (Vibrio sp. MED222) vimelysin (MER113711)
391 M04.010 (Vibrio sp. T-1800) vimelysin (MER029796)
392 M04.010 (Vibrionales bacterium SWAT-3) vimelysin (MER109237)
393 M04.003 (Vibrio cholerae) vibriolysin (MER001041)
394 M04.003 (Vibrio mimicus) vibriolysin (MER122299)
395 M04.003 (Vibrio fluvialis) vibriolysin (MER019097)
396 M04.003 (Salinivibrio sp. AF-2004) vibriolysin (MER091639)
397 M04.010 (Photobacterium sp. SKA34) vimelysin (MER110034)
398 M04.010 (Vibrio angustum) vimelysin (MER109056)
399 M04.010 (Photobacterium angustum) vimelysin (MER187763)
400 M04.010 (Vibrio angustum) vimelysin (MER109302)
401 (Moritella sp. PE36) family M4 unassigned peptidases (MER109180)
402 (Alteromonadales bacterium TW-7) family M4 unassigned peptidases (MER091610)
403 (Shewanella violacea) family M4 unassigned peptidases (MER203253)
404 (Vibrio campbellii) family M4 unassigned peptidases (MER168125)
405 (Legionella longbeachae) family M4 unassigned peptidases (MER198565)
406 M04.020 (Vibrio sp. AND4) pap6 peptidase (MER187764)
407 M04.020 (Vibrio campbellii) pap6 peptidase (MER118605)
408 M04.020 (Vibrio harveyi) pap6 peptidase (MER020240)
409 (Vibrio splendidus) family M4 unassigned peptidases (MER139945)
410 M04.006 (Legionella pneumophila) Msp peptidase (Legionella-type) (MER001039)
411 M04.006 (Legionella drancourtii) Msp peptidase (Legionella-type) (MER187828)
412 M04.006 (Legionella longbeachae) Msp peptidase (Legionella-type) (MER002394)
413 (Legionella pneumophila) family M4 unassigned peptidases (MER040780)
414 (Legionella drancourtii) family M4 unassigned peptidases (MER187829)
415 (Legionella longbeachae) family M4 unassigned peptidases (MER198471)
416 (Legionella pneumophila) family M4 unassigned peptidases (MER040782)
417 (Legionella pneumophila) family M4 unassigned peptidases (MER040781)
418 M04.019 (Pseudoalteromonas piscicida) MprIII (MER024591)
419 (Teredinibacter turnerae) M4 unassigned peptidases (MER187760)
420 (Reinekea sp. MED297) family M4 unassigned peptidases (MER083722)
421 (Reinekea blandensis) family M4 unassigned peptidases (MER187762)
422 (Reinekea sp. MED297) family M4 unassigned peptidases (MER117392)
423 (Alteromonas sp. SN2) family M4 unassigned peptidases (MER247991)
424 (Hydrogenivirga sp. 128-5-R1-1) family M4 unassigned peptidases (MER142070)
A protein BLAST analysis (Altschul S F, Madden T L, Schäffer AaA, Zhang J, Zhang Z, Miller W, Lipman D J. (1997) Nucleic Acids Res. 25:3389-402) run within Genome Quest (www.genomequest.com) against patent and public domain databases, using the sequence of Thermolysin (SEQ ID NO: 3) as query yielded the results shown below (Table 5.2). BLAST is GenomeQuest's implementation of the NCBI BLAST2 algorithm and finds the most relevant sequences in terms of biological similarity. The sequence search has the following default BLAST parameters for protein searches: Word size: 3, E-value cutoff: 10, Scoring Matrix: BLOSUM62, Gap Opening: 11, Gap extension: 2
Bacillus
stearothermophilus
Bacillus
thermoproteolyticus
Geobacillus
stearothermophilus
Bacillus
thermoproteolyticus
Bacillus
thermoproteolyticus
Bacillus
Thermoproteolyticus
Bacillus caldolyticus
Bacillus sp.
Bacillus caldolyticus
Geobacillus
stearothermophilus
Geobacillus
kaustophilus
Bacillus Cereus,
Bacillus cereus
Bacillus
thuringiensis serovar
Bacillus
thuringiensis
Bacillus
thuringiensis
Bacillus
thuringiensis
Bacillus cereus
Lactobacillus sp.
Lactobacillus sp.
Exiguobacterium
sibiricum 255-15
Exiguobacterium sp.
Brevibacillus brevis
Paenibacillus
mucilaginosus
Brevibacillus brevis
Bacillus
thuringiensis
Bacillus
vietnamensis
Paenibacillus
polymyxa E681
Bacillus sp.
Paenibacillus
polymyxa SC2
Thermoactinomyces
Bacillus polymyxa
Paenibacillus
polymyxa
Bacillus cereus
Bacillus cereus
Bacillus
weihenstephanensis
Bacillus subtilis
Bacillus cytotoxicus
polymyxa E681]
Bacillus cereus
Bacillus anthracis
Bacillus subtilis
Bacillus
amyloliquefaciens
Brevibacillus
laterosporus
Clostridium
acetobutylicum EA
Bacillus subtilis
Staphylococcus
epidermis
Macrococcus
caseolyticus
Bacillus
amyloliquefaciens
Bacillus subtilis
Bacillus atrophaeus
Staphylococcus
aureus
Staphylococcus
Aureus
Staphylococcus
aureus
Staphylococcus
aureus
Bacillus
amyloliquefaciens
Bacillus
amyloliquefaciens
Bacillus
amyloliquefaciens
Bacillus
amyloliquefaciens
Bacillus
amyloliquefaciens
Bacillus
amyloliquefaciens
Crystallographic temperature factors are a measure of the relative motion of individual atoms of a macromolecule. These temperature factors arise as a product of refinement of the model so that the calculated diffraction pattern given as individual intensities of crystal x-ray diffraction maxima best matches the observed pattern. The temperature factor is refined as an attenuation factor to reflect that atoms with higher motion will have a diminishing effect of the overall macromolecule aggregate diffraction as a function of the scattering angle (theta), using the form −exp(−B sin2 θ/λ) where the B is the temperature factor (Blundell, T. L. and Johnson L. N., Protein Crystallography, Academic Press, 1976, pp 121).
It is likely that regions with higher overall mobility might also represent points where the folded macromolecule is less stable and thus might be points where unfolding begins as the molecule is stressed by increasing temperature or denaturants. It would be further expected that these regions of higher overall mobility would be regions where the average temperature factors would be highest.
The crystallographic structure of Bacillus thermoproteolyticus Thermolysin protein has been determined by a number of independent laboratories. Three independent models of the protein were selected from the Protein Data Bank with entry identifications of 8TLN, 2TLX and 3DO1. We looked for regions of overall mobility by screening regions in the crystal structure where the temperature factors for the main chain are the highest and specifically where the average main chain temperature factor exceeds at least 1.5 times the observed variance from the mean. Tables 6a-6c list the residues for which the average main chain temperature factor has a z-score greater than 1.5 compared to the variance observed for the average main chain temperature factor for the overall molecule in a given crystallographic model. In these three structures, the same regions are found to exhibit temperature factors that are greater than 1.5 times the observed variance above the mean main chain temperature factor for all residues in Thermolysin. These regions represent consensus flexibility regions and include the following residues:
1-2 (N-terminal residues), 127-128, 180-181, 195-199, 211, 223-224, 298-300, and 316 (C-terminal residue).
All sites in Thermolysin were screened by making as many possible single substitutions of amino acids in the molecule. Several variants that confer either thermostability or improved laundry performance at elevated temperatures in different laundry detergent formulations were found occurring at a site corresponding to one of these consensus flexibility regions. Representative substitutions in the consensus flexibility regions that confer improved laundry performance in Sun All-in-1 Turbo Gel or AT formula pH 8 detergent or improved thermostability are listed in Table 6.2. The working hypothesis is that these flexible regions are the initial sites of protein unfolding. Based on this hypothesis, combinations of variants from different consensus flexibility regions might be predicted to provide more stabilization. Simultaneous stabilization of several flexible regions selected from those shown in Table 2 would result in a substantially more stable molecule.
This application claims benefit of priority from U.S. provisional patent application Ser. No. 61/722,660 filed on 5 Nov. 2012, and is incorporated herein by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US13/68590 | 11/5/2013 | WO | 00 |
Number | Date | Country | |
---|---|---|---|
61722660 | Nov 2012 | US |