Patent Application
20180187179
The present invention relates to variants of chymosin with improved properties.
Chymosin (EC 3.4.23.4) and pepsin (EC 3.4.23.1), the milk clotting enzymes of the mammalian stomach, are aspartic proteases belonging to a broad class of peptidases.
When produced in the gastric mucosal cells, chymosin and pepsin occur as en-zymatically inactive pre-prochymosin and pre-pepsinogen, respectively. When chymosin is excreted, an N-terminal peptide fragment, the pre-fragment (signal peptide) is cleaved off to give prochymosin including a pro-fragment. Prochymosin is a substantially inactive form of the enzyme which, however, becomes activated under acidic conditions to the active chymosin by autocatalytic removal of the pro-fragment. This activation occurs in vivo in the gastric lumen under appropriate pH conditions or in vitro under acidic conditions.
The structural and functional characteristics of bovine, i.e. Bos taurus, preprochymosin, prochymosin and chymosin have been studied extensively. The pre-part of the bovine pre-prochymosin molecule comprises 16 aa residues and the pro-part of the corresponding prochymosin has a length of 42 aa residues. The active bovine chymosin comprises 323 aa.
Chymosin is produced naturally in mammalian species such as bovines, camels, caprines, buffaloes, sheep, pigs, humans, monkeys and rats.
Bovine and camel chymosin has for a number of years been commercially available to the dairy industry.
Enzymatic coagulation of milk by milk-clotting enzymes, such as chymosin and pepsin, is one of the most important processes in the manufacture of cheeses. Enzymatic milk coagulation is a two-phase process: a first phase where a proteolytic enzyme, chymosin or pepsin, attacks K-casein, resulting in a metastable state of the casein micelle structure and a second phase, where the milk subsequently coagulates and forms a coagulum (reference 1). Besides facilitating coagulation of milk by cleaving κ-casein, chymosins cleave β-casein (β-casein), primarily between Leu192 and Tyr193, resulting in the formation of a β(193-209) peptide. Further proteolysis of β(193-209) and formation of short hydrophobic peptides may result in an undesirable bitter flavor of the product.
WO02/36752A2 (Chr. Hansen) describes recombinant production of camel chymosin.
WO2013/174840A1 (Chr. Hansen) describes mutants/variants of bovine and camel chymosin.
WO2013/164479A2 (DSM) describes mutants of bovine chymosin.
The references listed immediately below may in the present context be seen as references describing mutants of chymosin:
None of the prior art references mentioned above describe directly and unambiguously any of the chymosin variants with lowered β-casein cleavage frequency at similar clotting activity compared to the parent from which the variant is derived, as described below.
The problem to be solved by the present invention is to provide variants of chymosin which, when compared to the parent polypeptide, has a lower lowered βcasein cleavage frequency while substantially maintaining its clotting efficiency.
Accordingly, the present invention provides isolated chymosin polypeptide variants characterized in that:
The isolated chymosin polypeptide variant of present invention may be derived from a parent polypeptide has at least 80%, such as at least e.g. 85%, 95%, 97%, 98%, 99%, 100% sequence identity with the polypeptide of SEQ ID NO:4 (camel chymosin).
In a related aspect, the isolated chymosin polypeptide variant of present invention has at least 70%, such as at least e.g. 75%, 80%, 90%, 100%, 110%, 120%, 130% or 150% of the specific clotting activity of isolated camel chymosin polypeptide characterized by SEQ ID NO:4.
In yet a related aspect, the isolated chymosin polypeptide variant of present invention preferably has at least has less than 50%, such as e.g. less than 40%, less than 30%, less than 20%, less than 15%, less than 10% or less than 6% of the unspecific proteolytic activity (P) of isolated camel chymosin polypeptide characterized by SEQ ID NO:4.
In a further related aspect, the isolated chymosin polypeptide variant of present invention has at least has a C/P ratio of at least 300%, 400%, 500%, 600%, 700%, 800%, 1000%, 1200%, 1400% or 1600% of the C/P ratio of isolated camel chymosin polypeptide characterized by SEQ ID NO:4.
The isolated chymosin polypeptide variant of present invention may comprise one or more amino acid substitutions, deletions or insertions, wherein the one or more substitution, deletion or insertion is specified in relation to the amino acid sequence of SEQ ID NO:4: Y11, L130, S132, V32, S226, R266, L12, V221, S255, S277, L222, L253, M157, V260, S271, H76, K19, V183, S164, I263, V51, T239, Y307, R67, G251, R61, Q288, E83, D59, V309, S273, G251, S154, Y21, V203, L180, E294, G289, L215, D144, I303, L105, T284, Y127, V248, K321, V205, E262, K231, R316, M256, D158, D59, N249, L166, R242 or I96, and more specifically such as e.g. Y11I, Y11V, L130I, S132A, V32L, S226T, R266V, L12M, V221M, S255Y, S277N, L222I, L253I, M157L, V260T, S271P, H76Q, K19T, V183I, S164G, I263L, V51L, T239S, Y307F, R67Q, G251D, R61Q, Q288E, E83S, D59N, V309I, S273Y, G251W, S154A, Y21S, V203A, L180I, E294Q, G289S, L215V, D144Q, I303L, L105E, T284S, Y127F, V248I, K321P, V205I, E262T, K231N, R316L, M256L, D158S, D59N, N249E, L166V, R242E and/or I96L.
The present invention further provides methods of making the isolated chymosin polypeptide variants of present invention, methods of making a food or feed product using the isolated chymosin polypeptide variants, food and feed products comprising these variants as well as the use of the variants for making food and feed products.
In a related alternative aspect, the invention relates to methods for making an isolated chymosin polypeptide with decreased comprising the following steps:
Y11, L130, S132, V32, S226, R266, L12, V221, S255, S277, L222, L253, M157, V260, S271, H76, K19, V183, S164, I263, V51, T239, Y307, R67, G251, R61, Q288, E83, D59, V309, S273, G251, S154, Y21, V203, L180, E294, G289, L215, D144, I303, L105, T284, Y127, V248, K321, V205, E262, K231, R316, M256, D158, D59, N249, L166, R242 or I96 in SEQ ID NO:4;
The isolated chymosin produced by the methods above, may comprise one or more of the following substitutions:
Y11I, Y11V, L130I, S132A, V32L, S226T, R266V, L12M, V221M, S255Y, S277N, L222I, L253I, M157L, V260T, S271P, H76Q, K19T, V183I, S164G, I263L, V51L, T239S, Y307F, R67Q, G251D, R61Q, Q288E, E83S, D59N, V309I, S273Y, G251W, S154A, Y21S, V203A, L180I, E294Q, G289S, L215V, D144Q, I303L, L105E, T284S, Y127F, V248I, K321P, V205I, E262T, K231N, R316L, M256L, D158S, D59N, N249E, L166V, R242E and/or I96L.
In a related aspect the isolated chymosin polypeptide variant of present invention and the variant produced by the methods above may comprise a combination of substitutions and wherein each substitution is specified in relation to the amino acid sequence of SEQ ID NO:4:
I96+G163+V221; R67+H76+S132+V248+S271; R67+L130+M157; V136+V221+L222+S226; S132+R254+V259+Y307; V32+I96+S277; L130+M142+I200+V259+E294; L130+S132+V32; L130+G163+Y307;R61+L166+T239; L130+T239+S277+L295; D98+H146+V203+I263+S271; S132+V221+S255+S273+V317; H76+L222+G251;H76+K231+G244; Y127+S132+D158;V221+V248+L253+L295;V32+R61+H146; V32+E294+R316+V317; H76+I96+D158; D98+M157+V183; S226+G244+I263+G289;G70+L130+Y268; D59+V248+L222+V248; R67+G7O+H146+Q188+S226; 574+H76+M142+M157+G163; R61+5226+T239+V248+G251;V32+L130+R145+L222+D279; D59+L222+G251+E83+Q162; D59+L222+G251+F17+Y21; D59+L222+G251+H76+5164;D59+L222+G251+K62+M165;D59+L222+G251+Q162+V155;D59+L222+G251+S273+L166;D59+L222+G251+Y268+V198;D59+L222+G251+5273+F66;D59+L222+G251+M165+L166;D59+L222+G251+H76+M165;D59+L222+G251+F17+5273; D59+L222+G251+L166+I45; D59+L222+G251+L180+T284; D59+L222+G251+V32+L12+T284; D59+L222+G251+Y21+L166; D59+L222+G251+V155+E262+V32; D59+L222+G251+L105+S164; D59+L222+G251+Y21+L215+L105; D59+L222+G251+I96+T177+K321; D59+L222+G251+F17+T284+V203; D59+L222+G251+V32+K321+V260; D59+L222+G251+V198+V32+E83; D59+L222+G251+I96+V203+V309; D59+L222+G251+Y268+L215+V32; D59+L222+G251+H76+L105+V260; D59+L222+G251+Y21+H76+Y268; D59+L222+G251+S164+R266+I96; D59+L222+G251+H181+F66+V32; D59+L222+G251+H181+R266+D267; D59+L222+G251+Y268+L12+D267; D59+L222+G251+L166+E262+T177; D59+L222+G251+F66+Q288+I96; D59+L222+G251+V203+R266+F223; D59+L222+G251+1303+S154+V260; D59+L222+G251+Y21+T284+I96; D59+L222+G251+Q288+K19+T177; D59+L222+G251+K62+Y268+K19; L12+Y21+D59+H76+M165+V198+L222+G251+Q288; L12+Y21+D59+H76+M165+L222+G251+S273; L12+D59+H76+M165+V198+L222+G251+S273+K321; L12+D59+H76+S154+M165+V203+L222+G251+V309; L12+D59+H76Q+D98+L222; L12+K19+V32+D59+H76+D144+M165+L222+G251; L12+Y21+D59+H76+M165+V203+L222+G251+E262; L12+V51+H76+M165+G251; L12+D59+F66+H76+M165+L180+L222+G251+V309; L12+D59+H76+S154+M165+L222+G251+Q288; L12+D59+H76+D98+M165+L222+G251+E262+Q288; L12+V51+D59+H76+L166+L222+G251; L12+D59+H76+D144+M165+V203+L222; L12+D59+144+M165+L166+L222+G251; L12+K19+D59+H76+S154+M165+V198+L222+G251; L12+H76+D98+M165+L222+G251; L12+V32+D59+H76+M165+L180+V198+L222+G251; L12+D59+H76+S154+M165+S273; L12+V51+D59+F66Y+H76Q+M165E+V203A+L222I+G251W; L12+V32+H76+M165+L222+E262;L12+N50+D59+H76+M165+G251+E262; V51+D59+H76+M165+L180+L222+G251+E262; L12+D59+H76+M165+G251+Q288+V309+K321; L12+N50+D59+V203+L222+G251; L12+D59+H76+L180+L222+G251+K321; L12+Y21+D59+M165+L222+K321; D59+H76+M165+L166+V198+L222; L12+K19+N50+D59+H76+M165+L222+Q288; L12+Y21+N5O+D59+F66+H76+D144+M165+L222+G251; H76+S132+S164+L222+N249+G251; Y21+D59+H76+S164+L166+N249+G251+S273; D59+H76+S164+L222+R242+S273+V309; D59+H76+L130+L166+L222+N249+G251+S273; Y21+D59+S164+L222+R242+G251+S273+V309; K19+Y21+D59+H76+S132+S164+L222+G251+S273; D59+H76+I96+L130+S164+L222+R242+G251; H76+S164+L166+L222+S226+S273; K19+D59+I96+S164+L222+G251; Y21+H76+S164+L222+R242+G251+S273; H76+I96+S164+L222+R242+G251+S273; H76+S164+L222+N249+G251+S273+V309; K19+D59+H76+S164+L222+N249+S273; Y21+D59+H76+S164+L222+S226+G251+S273+V309; H76+S164+L166+L222+R242+G251+S273; D59+H76+I96+S164+L222+S226+N249+G251+S273; D59+H76+L130+S164+L166+L222+G251+S273+V309; D59+S132+S164+L222+R242+N249+G251+S273; H76+I96+S164+G251+S273+V309; D59+H76+L130+S164+G251+V309; K19+D59+S164+L166+L222+S226+G251+S273; D59+H76+I96+S132+S164+L222+S226+G251+S273; K19+D59+H76+I96+S164+L166+L222+G251+S273; K19+D59+H76+L130+5164+L222+5226+G251+5273; K19+D59+H76+5132+L222+G251+5273+V309; H76+L130+L222+5226+G251+5273; K19+Y21+D59+H76+L130+5164+L222+5273; Y21+D59+H76+I96+S164+L222+N249+G251+S273; K19+D59+H76+5164+R242+N249+G251+5273; D59+H76+S164+L222+S226+R242; D59+H76+I96+S132+S164+L166+L222+G251+S273; D59+H76+S132+S164+L166+S273; Y21+D59+5164+L222+5226+N249+G251+5273; D59+H76+L130+5132+5164+L222+R242+G251+5273; D59+H76+S164+L166+L222+N249+G251+S273+V309; D59+H76+I96+S164+L222+S226+G251+S273+V309; K19+D59+H76+L166+L222+R242+G251+S273; Y21+D59+H76+I96+L222+S273; D59+H76+I96+L130+S164+L222+N249+G251+S273; L130+S164+L222+S273; K19+Y21+H76+S164+L222+G251+S273; Y21+D59+H76+L130+S132+S164+L222+G251+S273; D59+H76+S226+R242+G251+S273; K19+D59+I96+S164+L222+G251; Y11+K19+D59+I96+L222+R242+G251; K19+D59+I96+S164+G251; K19+I96+S164+L166+L222+R242; K19+D59+I96+S164+L166+L222+R242+G251+L253; D59+196+S164+L222+R242+L253+I263; K19+D59+E83+196+L222+G251+I263; Y11+K19+D59+S164+L222+G251+I263; K19+D59+I96+S164+L166+G251+L253; K19+I96+S164+L222+N249+G251+L253; K19+I96+L222+R242+L253; K19+E83+I96+S164+L222+R242+G251+L253; D59+E83+I96+S164+L222+G251; K19+D59+I96+S164+L222+R242+N249+G251; K19+I96+S164+L166+L222+N249+I263; D59+I96+L166+L222+R242+G251; K19+D59+E83+S164+L166+L222+R242+G251; Y11+K19+D59+E83+I96+S164+L222+N249; K19+E83+I96+S164+L222+R242+L253; K19+D59+I96+S164+L166+L222+R242+N249; Y11+K19+D59+I96+S164+L166+L222+R242+G251+L253; K19+I96+S164+L222+R242+I263; Y11+D59+I96+S164+L222+G251+L253; K19+D59+196+S164+L166+L222+R242+I263; Y11+K19+D59+I96+S164+L166+L222+G251; K19+196+S164+L166+L222+R242+N249+G251+I263; K19+I96+S164+R242+L253; K19+D59+E83+I96+S164+L222+G251; K19+D59+I96+S164+L222+N249+G251+I263; K19+D59+I96+S164+L222+N249+G251+L253+I263; Y11+K19+I96+S164+L222+R242+G251; I96+S164+L222+R242+N249+G251+1263; K19+D59+196+S164+L166+L222+R242+G251+1263; K19+D59+I96+5164+L222+R242+N249+L253; H76+I96+5164+L222+R242+G251+5273; K19+E83+I96+S164+L222+R242+N249+G251+L253; I96+S164+L166+L222+R242+N249+1263; Y11+K19+E83+I96+S164+L166+L222+R242+G251; Y11+K19+I96+S164+L166+L222+R242; Y11+E83+196+5164+L222+R242+G251+L253+I263; Y11+I96+S164+L222+R242+N249+L253+1263; K19+196+S164+L166+L222+R242+N249+I263; Y11+E83+196+5164+L222+R242+L253+I263; K19+E83+I96+S164+L166+L222+R242+N249+G251+L253; I96+5164+L222+R242+G251+5274; H76+I96+5164+L222+R242+G251; I96+5164+L222+R242+G251; V32+N100+N291; V221+N100+N291; D290+N100+N291; V136+N100+N291; E240+N100+N291; R242+N100+N291; G289+N100+N291; N292+N100+N291; L295+N100+N291; V136+N100+N291; D290+N100+N291; F119+N100+N291; Q280+N100+N291; F282+N100+N291; R254+N100+N291; R242+N100+N291; V203+N100+N291; N249+N100+N291; H56+N100+N291; 574+N100+N291; A131+N100+N291; Y190+N100+N291; I297+N100+N291; H76+N100+N291; 5273+N100+N291; K19+N100+N291; D59+N100+N291; L222+N100+N291; V309+N100+N291; I96+N100+N291; Y21+N100+N291; L130+N100+N291; S132+N100+N291; S226+N100+N291; G251+N100+N291; Y243+N100+N291; S273+N100+N291; R242+Q280+N100+N291; R242+N252+N100+N291; N252+Q280+N100+N291; Y243+Q280+N100+N291; Y243+N252+N100+N291; R254+Q280+N100+N291; S273+Q280+N100+N291; R242+G251+N100+N291; R242+G251+Q280+N100+N291; R242+S273+Q280+N100+N291; N252+S273+Q280+N100+N291; G251+S273+Q280+N100+N291; R242+R254+Q280+N100+N291; R242+R254+S273+Q280+N100+N291; Y243+R254+S273+N100+N291; V223+N252+N291; E290+N252+N291; A117+N252+N291; I136+N252+N291; Q242+N252+N291; Q278+N252+N291; S289+N252+N291; Q294+N252+N291; D249+N252+N291; D251+N252+N291; G244+N252+N291; Q56+N252+N291; L32+N252+N291; K71+N252+N291; P72+N252+N291; Q83+N252+N291; V113+N252+N291; E133+N252+N291; Y134+N252+N291; K71+N252+N291; Y11+N100+N291; Y11+D290+N100+N291; L12+N100+N291; D13+N100+N291; D13+N100+N291; R67+N100+L130+M157+V248+N291; N100+L130+S132+M157+K231; R67+196+L130+M157+L222+M256; R67+L130+S132+M157+R242+V248; R67+N100+M157+R242+M256; R67+G70+M157+R242+V248; V32+R67+M157+L222+R242; Y11+R67+M157+V248+M256; R67+V136+M157+L222+V248; L130+M157+V248+M256+N291; R67+196+L130+M157+K231+R242; V32+R67+L130+M157+L222+K231; L130+V136+M157+L222+N292; R67+G70+M157+L222+N291; V32+R67+L130+K231+N292; Y11+R67+N100+L130+V136+M157; R67+L130+L222+R242+M256; R67+M157+L222+V248+N292; V32+R67+M157+M256+N291; R67+L130+S132+M157+L222+N292; R67+N100+L130+M157+K231+N291; R67+L130+K231+V248+N291; Y11+R67+L130+M157+L222+K231; I45+L130+M157+K231+R242; V32+R67+V136+M157+N291; R67+N100+L130+D158+V248; I45+R67+L130+M157+L222+K231; V32+R67+L130+S132+M157+V248; Y11+R67+L130+M157+N291+N292; R67+N100+L130+M157+L222+K231; 145+R67+G70+L130+S132; I45+R67+L130+V248+N292; Y11+R67+L130+M157+L222+R242; R67+N100+D158+L130+M157+L222; R67+L130+V136+M157+K231+V248; I45+R67+L130+L222+N291; R67+G70+L130+M157+K231+M256; V32+R67+L130+M157+D158+V248; R67+L130+M157+D158+R242+N291; R67+L130+M157+D158+K231+N292; R67+L130+V248+M256+N292; V32+R67+I96+L130+M157+V248; R67+I96+N100+L130+M157+N292; V32+R67+G70+N100+M157; V32+R67+L130+M157+K231+M256; R67+I96+M157+L222+K231; R67+M157+L222+K231+V248; R67+L130+M157+R242+M256+N292; R67+L222+K231+V248; R67+S132+L222+K231+R242+V248; Y11+K19+D59+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+G251; Y11+K19+D59+I96+L166+L222+R242+N249+G251+L253; Y11+K19+D59+I96+S164+L166+R242; Y11+K19+D59+I96+S164+L222+R242+G251; Y11+K19+D59+I96+S164+L166+R242+N249+G251+L253; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251+L253; Y11+K19+D59+L166+L222+R242+N249+G251+L253; Y11+K19+D59+I96+S164+L166+L222+R242+N249; Y11+K19+D59+S164+L166+L222+R242+G251; Y11+K19+D59+I96+S164+R242+G251; Y11+D59+I96+S164+L166+L222+R242+G251+L253; Y11+D59+I96+S164+L166+L222+R242+G251; Y11+D59+I96+S164+L166+L222+R242+G251+L253; Y11+K19+D59+I96+S164+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+L253; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+I96+S164+L166+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+G251; Y11+K19+D59+I96+S164+L222+R242+N249+G251; Y11+K19+L222+R242+N249+G251; Y11+K19+I96+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242+N249; Y11+K19+D59+I96+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242; Y11+K19+D59+I96+S164+L166+R242+G251; Y11+K19+D59+S164+L166+L222+R242+G251; Y11+I96+L222+R242+N249+G251; Y11+I96+S164+L222+R242; Y11+K19+I96+L166+L222+R242+G251; Y11+D59+I96+S164+L222+R242+G251; Y11+D59+I96+S164+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242+N249+G251; Y11+D59+I96+S164+L166+L222+R242+G251; Y11+K19+D59+I96+L222+R242+G251; Y11+K19+S164+L166+L222+R242+N249+G251; Y11+D59+I96+S164+L166+L222+R242+N249+G251, such as e.g.: I96L+G163E+V221M; R67Q+H76Q+S132A+V248I+S271P; R67Q+L130I+M157L; V136I+V221M+L222I+S226T; S132A+R254S+V259I+Y307F; V32L+I96L+S277N; L130I+M142I+I200V+V259I+E294Q; L130I+G163E+Y307F; R61S+L166V+T239S; L130I+T239S+S277N+L295K; L130I+S132A+V32L; D98V+H146R+V203A+I263L+S271P; S132A+V221M+S255Y+S273Y+V317L; H76Q+L222I+G251W; H76Q+K231N+G244D; Y127F+S132A+D158S; V221M+V248I+L253I+L295K; V32L+R61Q+H146R; V32L+E294Q+R316L+V317L; H76Q+I96L+D158S; D98V+M157L+V183I; S226T+G244D+I263L+G289S; G70D+L130I+Y268F; D59N+V248I+L222I+V248I; R67Q+G70N+H146R+Q188E+S226T; S74F+H76Q+M142I+M157L+G163E; R61Q+S226T+T239S+V248I+G251W; V32L+L130I+R145Q+L222I+D279E; D59N+L222I+G251D+E83S+Q162S; D59N+L222I+G251W+F17Y+Y21S; D59N+L222I+G251D+H76Q+S164G; D59N+L222I+G251D+K62Q+M165E; D59N+L222I+G251D+Q162S+V155F; D59N+L222I+G251D+S273Y+L166V; D59N+L222I+G251D+Y268F+V198I; D59N+L222I+G251D+S273Y+F66Y; D59N+L222I+G251D+M165E+L166V; D59N+L222I+G251D+H76Q+M165E; D59N+L222I+G251D+F17Y+S273Y; D59N+L222I+G251D+L166V+145V; D59N+L222I+G251W+L180I+T284S; D59N+L222I+G251D+V32L+L12M+T284S; D59N+L222I+G251D+Y21S+L166V; D59N+L222I+G251D+V155F+E262T+V32L; D59N+L222I+G251D+L105E+S164G; D59N+L222I+G251D+Y21S+L215V+L105E; D59N+L222I+G251D+196L+T177S+K321P; D59N+L222I+G251D+F17Y+T284S+V203A; D59N+L222I+G251D+V32L+K321P+V260T; D59N+L222I+G251D+V1981+V32L+E83S; D59N+L222I+G251D+196L+V203A+V3091; D59N+L222I+G251D+Y268F+L215V+V32L; D59N+L222I+G251D+H76Q+L105E+V260T; D59N+L222I+G251D+Y21S+H76Q+Y268F; D59N+L222I+G251D+S164G+R266V+196L; D59N+L222I+G251D+H181N+F66Y+V32L; D59N+L222I+G251D+H181N+R2661+D267Q; D59N+L222I+G251D+Y268F+L12M+D267Q; D59N+L222I+G251D+L166V+E262T+T177S; D59N+L222I+G251D+F66Y+Q288E+196L; D59N+L222I+G251D+V203A+R266V+F223A; D59N+L222I+G251D+1303L+S154A+V260T; D59N+L222I+G251D+Y21S+T284S+196L; D59N+L222I+G251D+Q288E+K19T+T177S; D59N+L222I+G251D+K62Q+Y268F+K19T L12M+Y21S+D59N+H76Q+M165E+V198I+L222I+G251D+Q288E; L12M+Y21S+D59N+H76Q+M165E+L222I+G251W+S273Y; L12M+D59N+H76Q+M165E+V198I+L222I+G251D+S273Y+K321P; L12M+D59N+H76Q+S154A+M165E+V203A+L222I+G251D+V309I; L12M+D59N+H76Q+D98V+L222I; L12M+K19T+V32L+D59N+H76Q+D144Q+M165E+L222I+G251D; L12M+Y21S+D59N+H76Q+M165E+V203A+L222I+G251D+E262T; L12M+V51L+H76Q+M165E+G251D; L12M+D59N+F66Y+H76Q+M165E+L180I+L222I+G251D+V309I; L12M+D59N+H76Q+S154A+M165E+L222I+G251W+Q288E; L12M+D59N+H76Q+D98V+M165E+L222I+G251D+E262T+Q288E; L12M+V51L+D59N+H76Q+L166V+L222I+G251D; L12M+D59N+H76Q+D144Q+M165E+V203A+L222I; L12M+D59N+144Q+M165E+L166V+L222I+G251D; L12M+K19T+D59N+H76Q+S154A+M165E+V198I+L222I+G251D; L12M+H76Q+D98V+M165E+L222I+G251W; L12M+V32L+D59N+H76Q+M165E+L180I+V198I+L222I+G251D; L12M+D59N+H76Q+S154A+M165E+S273Y; L12M+V51L+D59N+F66Y+H76Q+M165E+V203A+L222I+G251W; L12M+V32L+H76Q+M165E+L222I+E262T; L12M+N50D+D59N+H76Q+M165E+G251W+E262T; V51L+D59N+H76Q+M165E+L180I+L222I+G251D+E262T; L12M+D59N+H76Q+M165E+G251D+Q288E+V309I+K321P; L12M+N50D+D59N+V203A+L222I+G251D; L12M+D59N+H76Q+L180I+L222I+G251W+K321P; L12M+Y21S+D59N+M165E+L222I+K321P; D59N+H76Q+M165E+L166V+V198I+L222I; L12M+K19T+N50D+D59N+H76Q+M165E+L222I+Q288E; L12M+Y21S+N50D+D59N+F66Y+H76Q+D144Q+M165E+L222I+G251D; H76Q+S132A+S164G+L222I+N249D+G251D; Y21S+D59N+H76Q+S164G+L166V+N249D+G251D+S273Y; D59N+H76Q+S164G+L222I+R242E+S273Y+V309I; D59N+H76Q+L130I+L166V+L222I+N249D+G251D+S273Y; Y21S+D59N+S164G+L222I+R242E+G251D+S273Y+V309I; K19T+Y21S+D59N+H76Q+S132A+S164G+L222I+G251D+S273Y; D59N+H76Q+196L+L130I+S164G+L222I+R242E+G251D; H76Q+S164G+L166V+L222I+S226T+S273Y; K19T+D59N+196L+S164G+L222I+G251D; Y21S+H76Q+S164G+L222I+R242E+G251D+S273Y; H76Q+196L+S164G+L222I+R242E+G251D+S273Y; H76Q+S164G+L2221+N249D+G251D+S273Y+V309I; K19T+D59N+H76Q+S164G+L222I+N249D+S273Y; Y21S+D59N+H76Q+S164G+L222I+S226T+G251D+S273Y+V309I; H76Q+S164G+L166V+L222I+R242E+G251D+S273Y; D59N+H76Q+196L+S164G+L222I+S226T+N249D+G251D+S273Y; D59N+H76Q+L130I+S164G+L166V+L222I+G251D+S273Y+V309I; D59N+S132A+S164G+L222I+R242E+N249D+G251D+S273Y; H76Q+196L+S164G+G251D+S273Y+V309I; D59N+H76Q+L130I+S164G+G251D+V309I; K19T+D59N+S164G+L166V+L222I+S226T+G251D+S273Y; D59N+H76Q+196L+S132A+S164G+L222I+S226T+G251D+S273Y; K19T+D59N+H76Q+196L+S164G+L166V+L222I+G251D+S273Y; K19T+D59N+H76Q+L130I+S164G+L222I+S226T+G251D+S273Y; K19T+D59N+H76Q+S132A+L222I+G251D+S273Y+V309I; H76Q+L130I+L222I+S226T+G251D+S273Y; K19T+Y21S+D59N+H76Q+L130I+S164G+L222I+S273Y; Y21S+D59N+H76Q+196L+S164G+L222I+N249D+G251D+S273Y; K19T+D59N+H76Q+S164G+R242E+N249D+G251D+S273Y; D59N+H76Q+S164G+L222I+S226T+R242E; D59N+H76Q+196L+S132A+S164G+L166V+L222I+G251D+S273Y; D59N+H76Q+S132A+S164G+L166V+S273Y; Y21S+D59N+S164G+L222I+S226T+N249D+G251D+S273Y; D59N+H76Q+L130I+S132A+S164G+L222I+R242E+G251D+S273Y; D59N+H76Q+S164G+L166V+L222I+N249D+G251D+S273Y+V309I; D59N+H76Q+196L+S164G+L222I+S226T+G251D+S273Y+V309I; K19T+D59N+G251D+S273; H76Q+L166V+L222I+R242E+G251D+S273Y; Y21S+D59N+H76Q+196L+L222I+S273Y; D59N+H76Q+I96L+L130I+S164G+L222I+N249D+G251D+S273Y; L130I+S164G+L222I+S273Y; K19T+Y21S+H76Q+S164G+L222I+G251D+S273Y; Y21S+D59N+H76Q+L130I+S132A+S164G+L222I+G251D+S273Y; D59N+H76Q+S226T+R242E+G251D+S273Y; K19T+D59N+196L+S164G+L222I+G251D; Y11I+K19T+D59N+196V+L222I+R242D+G251D; K19S+D59N+I96V+S164G+G251D;K19S+I96L+S164G+L166V+L222I+R242E; K19T+D59N+I96L+S164G+L166V+L222I+R242D+G251D+L253I; D59N+I96L+S164G+L222I+R242E+L253I+I263L; K19T+D59N+E83T+I96L+L222I+G251D+I263L; Y11I+K19T+D59N+S164G+L222I+G251D+I263V; K19T+D59N+I96L+S164G+L166I+G251D+L253V; K19T+196V+S164G+L2221+N249D+G251D+L253I; K19T+196L+L222I+R242E+L253I; K19T+E83S+196L+S164G+L2221+R242E+G251D+L2531; D59N+E83T+I96L+S164N+L222V+G251D; K19S+D59N+I96L+S164G+L222I+R242E+N249E+G251D; K19T+I96L+S164G+L166V+L222I+N249D+I263L; D59N+I96L+L166V+L222I+R242E+G251D; K19T+D59N+E83T+S164G+L166V+L222I+R242D+G251D; Y11I+K19T+D59N+E83S+I96L+S164G+L222I+N249D; K19T+E83T+I96L+S164G+L222I+R242E+L253V; K19T+D59N+I96L+S164G+L166I+L222I+R242E+N249D; Y11V+K19T+D59N+I96L+S164G+L166V+L222I+R242E+G251D+L253I; K19T+I96L+S164N+L222I+R242E+I263L; Y11V+D59N+I96L+S164G+L222I+G251D+L253V; K19T+D59N+I96V+S164G+L166V+L222I+R242E+I263L; Y11V+K19T+D59N+I96L+S164N+L166I+L222I+G251D; K19T+I96L+S164G+L166V+L222I+R242E+N249D+G251D+I263V; K19T+I96L+S164G+R242E+L253I; K19S+D59N+E83S+I96L+S164N+L222I+G251D; K19T+D59N+I96L+S164G+L222V+N249E+G251D+I263V; K19T+D59N+I96L+S164G+L222I+N249E+G251D+L253V+I263L; Y11I+K19T+I96L+S164G+L222V+R242E+G251D; I96L+S164G+L222I+R242E+N249D+G251D+I263L; K19T+D59N+196L+S164G+L166I+L222I+R242D+G251D+I263V; K19T+D59N+196L+S164G+L222V+R242E+N249D+L253I; H76Q+I96L+5164G+L222I+R242E+G251D+S273Y; K19T+E83S+I96L+S164G+L222I+R242E+N249D+G251D+L253I; I96L+S164G+L166V+L222I+R242E+N249D+I263L; Y11V+K19T+E83S+I96L+S164G+L166V+L222I+R242E+G251D; Y11V+K19T+I96L+S164G+L166V+L222I+R242E; Y11V+E83S+I96L+S164G+L222I+R242E+G251D+L253I+I263L; Y11V+I96L+S164G+L222I+R242E+N249D+L253I+I263L; K19T+I96L+S164G+L166V+L222I+R242E+N249D+I263L; Y11V+E83S+I96L+S164G+L222I+R242E+L253I+I263L; K19T+E83S+I96L+S164G+L166V+L222I+R242E+N249D+G251D+L253I; I96L+S164G+L222I+R242E+G251D+S274Y; H76Q+I96L+S164G+L222I+R242E+G251D; I96L+S164G+L222I+R242E+G251D; V32L+N100Q+N291Q; V221K+N100Q+N291Q; D290E+N100Q+N291Q; V136I+N100Q+N291Q; E240Q+N100Q+N291Q; R242Q+N100Q+N291Q; G289S+N100Q+N291Q; N292H+N100Q+N291Q; L295K+N100Q+N291Q; V136E+N100Q+N291Q; D290L+N100Q+N291Q; F119Y+N100Q+N291Q; Q280E+N100Q+N291Q; F282E+N100Q+N291Q; R254S+N100Q+N291Q: R242E+N100Q+N291Q; V203R+N100Q+N291Q; N249R+N100Q+N291Q; H56K+N100Q+N291Q; S74D+N100Q+N219Q; A131D+N100Q+N291Q; Y190A+N100Q+N291Q; I297A+N100Q+N291Q; H76Q+N100Q+N291Q; S273Y+N100Q+N291Q; K19T+N100Q+N291Q; D59N+N100Q+N291Q; L222I+N100Q+N291Q; V309I+N100Q+N291Q; I96L+N100Q+N291Q; Y21S+N100Q+N291Q; L130I+N100Q+N291Q; S132A+N100Q+N291Q; S226T+N100Q+N291Q; G251D+N100Q+N291Q; Y243E+N100Q+N291Q; S273D+N100Q+N291Q; R242E+Q280E+N100Q+N291Q: R242E+N252D+N100Q+N291Q; N252D+Q280E+N100Q+N291Q; Y243E+Q280E+N100Q+N291Q; Y243E+N252D+N100Q+N291Q; R254E+Q280E+N100Q+N291Q; S273D+Q280E+N100Q+N291Q; R242E+G251D+N100Q+N291Q; R242E+G251D+Q280E+N100Q+N291Q; R242E+S273D+Q280E+N100Q+N291Q; N252D+S273D+Q280E+N100Q+N291Q; G251D+S273D+Q280E+N100Q+N291Q; R242E+R254E+Q280E+N100Q+N291Q; R242E+R254E+S273D+Q280E +N100Q+N291Q; Y243E+R254E+S273D+N100Q+N291Q; V223F+N252Q+N291Q; E290D+N252Q+N291Q; A117S+N252Q+N291Q; I136V+N252Q+N291Q; Q242R+N252Q+N291Q; Q278K+N252Q+N291Q; S289G+N252Q+N291Q; Q294E+N252Q+N291Q; D249N+N252Q+N291Q; D251G+N252Q+N291Q; G244D+N252Q+N291Q; Q56H+N252Q+N291Q; L 32I+N252Q+N291Q; K71E+N252Q+N291Q; P72T+N252Q+N291Q; Q83T+N252Q+N291Q; V113F+N252Q+N291Q; E133S+N252Q+N291Q; Y134G+N252Q+N291Q; K71A+N252Q+N291Q; Y11H+N100Q+N291Q; Y11K+N100Q+N291Q; Y11R+N100Q+N291Q; Y11H+D290E+N100Q+N291Q; Y11R+D290E+N100Q+N291Q; Y11F+N100Q+N291Q; Y11I+N100Q+N291Q; Y11L+N100Q+N291Q; L12F+N100Q+N291Q; L12I+N100Q+N291Q; D13N+N100Q+N291Q; D13Q+N100Q+N291Q; D13S+N100Q+N291Q; D13T+N100Q+N291Q; D13F+N100Q+N291Q; D13L+N100Q+N291Q; D13V+N100Q+N291Q; D13Y+N100Q+N291Q R67Q+N100Q+L130I+M157L+V248I+N291Q; N100Q+L130I+S132A+M157L+K231N; R67Q+I96L+L130I+M157L+L222I+M256L; R67Q+L130I+S132A+M157L+R242E+V248I; R67Q+N100Q+M157L+R242E+M256L; R67Q+G70D+M157L+R242E+V2481; V32L+R67Q+M157L+L222I+R242E; Y11V+R67Q+M157L+V248I+M256L; R67Q+V136I+M157L+L222I+V248I; L130I+M157L+V248I+M256L+N291Q; R67Q+I96L+L130I+M157L+K231N+R242E; V32L+R67Q+L130I+M157L+L222I+K231N; L130I+V136I+M157L+L222I+N292H; R67Q+G70D+M157L+L222I+N291Q; V32L+R67Q+L130I+K231N+N292H; Y11V+R67Q+N100Q+L130I+V136I+M157L; R67Q+L130I+L222I+R242E+M256L; R67Q+M157L+L222I+V248I+N292H; V32L+R67Q+M157L+M256L+N291Q; R67Q+L130I+S132A+M157L+L222I+N292H; R67Q+N100Q+L130I+M157L+K231N+N291Q; R67Q+L130I+K231N+V248I+N291Q; Y11V+R67Q+L130I+M157L+L222I+K231N; I145V+L130I+M157L+K231N+R242E; V32L+R67Q+V136I+M157L+N291Q; R67Q+N100Q+L130I+D158S+V248I; I45V+R67Q+L130I+M157L+L222I+K231N; V32L+R67Q+L130I+S132A+M157L+V248I; Y11V+R67Q+L130I+M157L+N291Q+N292H; R67Q+N100Q+L130I+M157L+L222I+K231N; I45V+R67Q+G70D+L130I+S132A; I45V+R67Q+L130I+V248I+N292H; Y11V+R67Q+L130I+M157L+L222I+R242E; R67Q+N100Q+D158S+L130I+M157L+L222I; R67Q+L130I+V136I+M157L+K231N+V248I; I45V+R67Q+L130I+L222I+N291Q; R67Q+G70D+L130I+M157L+K231N+M256L; V32L+R67Q+L130I+M157L+D158S+V248I; R67Q+L130I+M157L+D158S+R242E+N291Q; R67Q+L130I+M157L+D158S+K231N+N292H; R67Q+L130I+V248I+M256L+N292H; V32L+R67Q+I96L+L130I+M157L+V248I; R67Q+I96L+N100Q+L130I+M157L+N292H; V32L+R67Q+G70D+N100Q+M157L; V32L+R67Q+L130I+M157L+K231N+M256L; R67Q+I96L+M157L+L222I+K231N; R67Q+M157L+L222I+K231N+V248I; R67Q+L130I+M157L+R242E+M256L+N292H; R67Q+L222I+K231N+V248I; R67Q+S132A+L222I+K231N+R242E+V248I; Y11V+K19T+D59N+S164G+L166V+L222I+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L166I+L222I+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L166V+L222I+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L166I+L222I+R242E+G251D; Y11V+K19T+D59N+I96L+L166V+L222V+R242E+N249E+G251D+L253I; Y11V+K19T+D59N+I96L+S164G+L166V+R242E; Y11V+K19T+D59N+I96L+S164G+L222V+R242E+G251D; Y11V+K19T+D59N+I96L+S164G+L166I+R242E+N249E+G251D+L253I; Y11V+K19T+D59N+I96L+S164G+L166V+L222V+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L166I+L222V+R242E+N249E+G251D+L253I; Y11V+K19T+D59N+L166V+L222I+R242E+N249E+G251D+L253I; Y11V+K19T+D59N+I96L+S164G+L166V+L222I+R242E+N249E; Y11V+K19T+D59N+S164G+L166I+L222I+R242E+G251D; Y11V+K19T+D59N+I96L+S164G+R242E+G251D; Y11V+D59N+I96L+S164G+L166I+L222V+R242E+G251D+L253I; Y11V+D59N+I96L+S164G+L166I+L222I+R242E+G251D; Y11I+D59N+I96L+S164G+L166V+L222I+R242E+G251D+L253I; Y11V+K19T+D59N+I96L+S164G+L222I+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L166I+L222V+R242E+G251D; Y11V+K19T+D59N+I96L+S164G+L166V+L222V+R242E+N249E+L253I; Y11V+K19T+D59N+I96L+S164G+L166I+L222V+R242E+N249E+G251D; Y11I+K19T+I96L+S164G+L166V+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L166V+L222V+R242E+G251D; Y11V+K19T+D59N+I96L+S164G+L222V+R242E+N249E+G251D; Y11I+K19T+L222V+R242E+N249E+G251D; Y11V+K19T+I96L+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L166V+L222V+R242E+N249E+G251D; Y11V+K19T+I96L+S164G+L166V+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L166I+L222V+R242E+N249E+G251D; Y11I+I96L+S164G+L166V+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L222V+R242E+N249E; Y11I+K19T+D59N+I96L+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L222I+R242E; Y11I+K19T+D59N+I96L+S164G+L166V+R242E+G251D; Y11I+K19T+D59N+5164G+L166I+L222V+R242E+G251D; Y11I+I96L+L222V+R242E+N249E+G251D; Y11I+I96L+5164G+L222I+R242E; Y11V+K19T+I96L+L166V+L222V+R242E+G251D; Y11I+D59N+I96L+5164G+L222I+R242E+G251D; Y11I+D59N+I96L+S164G+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L222I+R242E+N249E+G251D; Y11I+D59N+I96L+5164G+L166V+L222V+R242E+G251D; Y11V+K19T+D59N+I96L+L222V+R242E+G251D; Y11I+K19T+5164G+L166I+L222V+R242E+N249E+G251D or Y11I+D59N+I96L+S164G+L166V+L222V+R242E+N249E+G251D.
An alternative aspect relates to methods for making a food or feed product comprising adding an effective amount of the isolated chymosin polypeptide variant of present invention to the food or feed ingredient(s) and carrying our further manufacturing steps to obtain the food or feed product, such as e.g. a milk-based product and optionally more specifically methods for making cheese such as e.g. Pasta filata, Cheddar, Continental type cheeses, soft Cheese or White Brine Cheese.
Accordingly, present invention relates to a food or feed product comprising a chymosin polypetide variant as described herein.
The polypeptide variant of present invention may also be used to reduce bitterness in cheese and other dairy products as e.g. yohurt.
In cheese ripening, chymosin cleaves β-casein primarily between Leu192 and Tyr193 (references 2,3). The resulting peptide β(193-209) will be further degraded by proteases to short hydrophobic peptides that taste bitter (reference 4). Since bitterness in dairy applications is most often considered an undesirable feature, it is desirable to develop chymosin variants with lower β-casein cleavage frequency.
Based on intelligent design and a comparative analysis of different variants the present inventors identified a number of amino acid positions that are herein important in the sense that by making a variant in one or more of these positions one may get an improved chymosin variant with a lower β-casein cleavage frequency.
The amino acid numbering as used herein to specify a variant or mutation is done on the mature peptide numbering. For clarification, the mature polypeptide of SEQ ID NO:2 corresponds to SEQ ID NO:4.
As known in the art—different natural wildtype chymosin polypeptide sequences obtained from different mammalian species (such as e.g. bovines, camels, sheep, pigs, or rats) are having a relatively high sequence similarity/identity.
In
In view of this relatively close sequence relationship—it is believed that the 3D structures of different natural wildtype chymosins are also relatively similar.
In the present context—a natural obtained wildtype chymosin (such as bovine chymosin or camel chymosin) may herein be an example of a parent polypeptide i.e. a parent polypeptide to which an alteration is made to produce a variant chymosin polypeptide of the present invention.
Without being limited to theory—it is believed that the herein discussed chymosin related amino acid positions are of general importance in any herein relevant chymosin enzyme of interest (e.g. chymosins of e.g. bovines, camels, sheep, pigs, rats etc)—in the sense that by making a variant in one or more of these positions one may get an improved chymosin variant in general (e.g. an improved bovine, camel, sheep, pig or rat chymosin variant).
As discussed herein—as a reference sequence for determining the amino acid position of a parent chymosin polypeptide of interest (e.g. camel, sheep, bovine etc) is herein used the public known mature Camelius dromedarius chymosin sequence of SEQ ID NO:2 herein. It may herein alternatively be termed camel chymosin. The sequence is also shown in
In the present context it is believed that a parent chymosin polypeptide (e.g. from sheep or rat) that has at least 65% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin) may herein be seen as sufficient structural related to e.g. bovine or camel chymosin in order to be improved by making a variant in any of the amino acid positions as described herein.
Embodiments of the present invention are described below.
All definitions of herein relevant terms are in accordance of what would be understood by the skilled person in relation to the herein relevant technical context.
The term “β-cleavage” or “cleavage of β-casein” means any enzymatic cleavage of β-casein. Such as e.g. cleavage between Leu192 and Tyr193, resulting in the formation of β(193-209) peptide. In one aspect β-cleavage is determined by quantifying the β(193-209) peptide obtained by incubating skim milk with the chymosin variant polypeptide or the camel chymosin, wherein quantification is carried out by RP-HPLC coupled to an ESI-Q-TOF mass spectrometer. Full details of a preferred method of determining β-casein cleavage are described in the Examples.
The term “chymosin” relates to an enzyme of the EC 3.4.23.4 class. Chymosin has a high specificity and predominantly clots milk by cleavage of a single 104-Ser-Phe-|-Met-Ala-108 bond in κ-chain of casein. As a side-activity, chymosin also cleaves β-casein primarily between Leu192 and Tyr193 (references 2,3). The resulting peptide β(193-209) will be further degraded by proteases to short hydrophobic peptides that taste bitter (reference 4). An alternative name of chymosin used in the art is rennin.
The term “chymosin activity” relates to chymosin activity of a chymosin enzyme as understood by the skilled person in the present context. The skilled person knows how to determine herein relevant chymosin activity.
The term “specific clotting activity” describes the milk clotting activity of a chymosin polypeptide and can be determined according to assays well known in the art. A preferred method for determining the specific clotting activity in terms of IMCU/mg of protein is the standard method developed by the International Dairy Federation (IDF method), which comprises steps, wherein milk clotting activity is determined from the time needed for a visible flocculation of a milk substrate and the clotting time of a sample is compared to that of a reference standard having known milk-clotting activity and the same enzyme composition by IDF Standard 110B as the sample. Samples and reference standards are measured under identical chemical and physical conditions. Full details of a the IDF method are described in the Examples.
As known in the art—the herein relevant so-called C/P ratio is determined by dividing the specific clotting activity (C) with the proteolytic activity (P). As known in the art—a higher C/P ratio implies generally that the loss of protein during e.g. cheese manufacturing due to non-specific protein degradation is reduced, i.e. the yield of cheese is improved.
The term “isolated variant” means a variant that is modified by the act of man. In one aspect, the variant is at least 1% pure, e.g., at least 5% pure, at least 10% pure, at least 20% pure, at least 40% pure, at least 60% pure, at least 80% pure, and at least 90% pure, as determined by SDS PAGE.
The amino acid numbering as used herein to specify chymosin polypeptide variants of the present invention is done on the mature peptide numbering. In the sequence listing provided with the present application:
SEQ ID NO:1 represents the complete polypeptide sequence of bovine preprochmyosin;
SEQ ID NO:2 represents the complete polypeptide sequence of camel preprochmyosin;
SEQ ID NO:3 represents the polypeptide sequence of mature bovine chymosin;
SEQ ID NO:4 represents the polypeptide sequence of mature camel chymosin.
In other words, SEQ ID NOs:3 and 4 correspond to amino acids 59 to 381 of SEQ ID NOs:1 and 2, respectively. All of the specific substitutions identified herein are identified in relation to the position of the mature chymosin sequence, i.e. in relation to the amino acid numbering of SEQ ID NOs:3 or 4. Insofar as the position is identified in relation to the amino acid numbering of SEQ ID NOs:1 or 2 one has to subtract 58 residues to identify the position in SEQ ID NOs:3 or 4 and vice versa.
The term “mature polypeptide” means a peptide in its final form following translation and any post-translational modifications, such as N terminal processing, C terminal truncation, glycosylation, phosphorylation, etc. In the present context may a herein relevant mature chymosin polypeptide be seen as the active chymosin polypeptide sequence - i.e. without the pre-part and/or pro-part sequences. Herein relevant examples of a mature polypeptide are e.g. the mature polypeptide of SEQ ID NO: 1 (bovine chymosin), which is from amino acid position 59 to amino acid position 381 of SEQ ID NO: 1 or the mature polypeptide of SEQ ID NO:2 (camel chymosin), which is from amino acid position 59 to amino acid position 381 of SEQ ID NO:2.
The term “parent”, “parent polypeptide” or “parent polypeptide having chymosin activity” means a polypeptide to which an alteration is made to produce the enzyme variants of the present invention. The parent may be a naturally occurring (wild-type) polypeptide or a variant thereof. In a preferred embodiment of present invention, the parent polypeptide has at least 80%, such as at least e.g. 85%, 95%, 97%, 98%, 99% or 100% sequence identity with the polypeptide of SEQ ID NO:4 (camel chymosin).
The term “Sequence Identity” relates to the relatedness between two amino acid sequences or between two nucleotide sequences.
For purposes of the present invention, the degree of sequence identity between two amino acid sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, Trends Genet. 16: 276-277), preferably version 3.0.0 or later. The optional parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EBLOSUM62 (EMBOSS version of BLOSUM62) substitution matrix. The output of Needle labeled “longest identity” (obtained using the—nobrief option) is used as the percent identity and is calculated as follows:
(Identical Residues×100)/(Length of Alignment—Total Number of Gaps in Alignment)
For purposes of the present invention, the degree of sequence identity between two deoxyribonucleotide sequences is determined using the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, supra) as implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, supra), preferably version 3.0.0 or later. The optional parameters used are gap open penalty of 10, gap extension penalty of 0.5, and the EDNAFULL (EMBOSS version of NCBI NUC4.4) substitution matrix. The output of Needle labeled “longest identity” (obtained using the—nobrief option) is used as the percent identity and is calculated as follows: (Identical Deoxyribonucleotides×100)/(Length of Alignment—Total Number of Gaps in Alignment).
The term “variant” means a peptide having chymosin activity comprising an alteration, i.e., a substitution, insertion, and/or deletion, at one or more (several) positions. A substitution means a replacement of an amino acid occupying a position with a different amino acid; a deletion means removal of an amino acid occupying a position; and an insertion means adding 1-3 amino acids adjacent to an amino acid occupying a position.
The amino acid may be natural or unnatural amino acids—for instance, substitution with e.g. a particularly D-isomers (or D-forms) of e.g. D-alanine could theoretically be possible.
The term “wild-type” peptide refers to a nucleotide sequence or peptide sequence as it occurs in nature, i.e. nucleotide sequence or peptide sequence which hasn't been subject to targeted mutations by the act of man.
In relation to the chymosin sequences shown in
As understood by the skilled person in the present context—herein relevant sequence identity percentages of mature polypeptide sequences of e.g. sheep, C._bactrianus, camel, pig or rat chymosin with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin—i.e. amino acid positions 59 to 381 of SEQ ID NO: 1) are relatively similar to above mentioned sequence identity percentages.
3D structure of camel chymosin (PDB: 4AA9) with a model of bound β-casein shown in purple. The β-casein is placed in the chymosin substrate binding cleft with the scissile bond between residues 192 and 193. Camel chymosin residues V32, L130, and S132 are highlighted in green.
3D structure of camel chymosin (PDB: 4AA9). Camel chymosin residues V32 and L12 are highlighted in green.
As discussed above—as a reference sequence for determining the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.) is herein used the public known camel chymosin sequence disclosed as SEQ ID NO:2 herein.
The amino acid sequence of another chymosin polypeptide is aligned with the polypeptide disclosed in SEQ ID NO: 1, and based on the alignment, the amino acid position number corresponding to any amino acid residue in the polypeptide disclosed in SEQ ID NO: 1 is determined using the ClustalW algorithm as described in working Example 1 herein.
Based on above well-known computer programs—it is routine work for the skilled person to determine the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.).
In
Just as an example—in
In describing the variants of the present invention, the nomenclature described below is adapted for ease of reference. The accepted IUPAC single letter or three letter amino acid abbreviations are employed.
The specific variants discussed in this “nomenclature” section below may not be herein relevant variants of the present invention—i.e. this “nomenclature” section is just to describe the herein relevant used nomenclature as such. As indicated above, the amino acid numbering used to specify chymosin polypetide variants of the present invention is based on the position of the amino acid in the mature chymosin polypeptide sequence.
Substitutions. For an amino acid substitution, the following nomenclature is used: Original amino acid, position, substituted amino acid.
Accordingly, a theoretical substitution of threonine with alanine at position 226 is designated as “Thr226Ala” or “T226A”. Multiple mutations are separated by addition marks (“+”), e.g., “Gly205Arg +Ser411Phe” or “G205R +S411F”, representing substitutions at positions 205 and 411 of glycine (G) with arginine (R) and serine (S) with phenylalanine (F), respectively. A substitution e.g. designated “226A” refers to a substitution of a parent amino acid (e.g. T, Q, S or another parent amino acid) with alanine at position 226. Likewise, a substitution designated “A226” or “A226X” refers to a substitution of an alanine in position 226 with another unspecified amino acid.
Deletions. For an amino acid deletion, the following nomenclature is used: Original amino acid, position, *. Accordingly, the deletion of glycine at position 195 is designated as “Gly195*” or “G195*”. Multiple deletions are separated by addition marks (“+”), e.g., “Gly195*+Ser411*” or “G195*+S411*”.
Insertions. For an amino acid insertion, the following nomenclature is used: Original amino acid, position, original amino acid, inserted amino acid. Accordingly the insertion of lysine after glycine at position 195 is designated “Glyl95GlyLys” or “G195GK”. An insertion of multiple amino acids is designated [Original amino acid, position, original amino acid, inserted amino acid #1, inserted amino acid #2; etc.]. For example, the insertion of lysine and alanine after glycine at position 195 is indicated as “Gly195GlyLysAla” or “G195GKA”.
In such cases the inserted amino acid residue(s) are numbered by the addition of lower case letters to the position number of the amino acid residue preceding the inserted amino acid residue(s). In the above example, the sequence would thus be:
Multiple alterations. Variants comprising multiple alterations are separated by addition marks (“+”), e.g., “Arg170Tyr+Gly195Glu” or “R170Y+G195E” representing a substitution of tyrosine and glutamic acid for arginine and glycine at positions 170 and 195, respectively.
Different substitutions. Where different substitutions can be introduced at a position, the different substitutions are separated by a comma, e.g., “Arg170Tyr,Glu” or “R170Y,E” represents a substitution of arginine with tyrosine or glutamic acid at position 170. Thus, “Tyr167Gly,Ala +Arg170Gly,Ala” or “Y167G,A +R170G,A” designates the following variants:
“Tyr167Gly+Arg170Gly”, “Tyr167Gly+Arg170Ala”, “Tyr167Ala+Arg170Gly”, and “Tyr167Ala+Arg170Ala”.
Preferred variants:
As outlined in the Examples below, the inventors have made a number of preferred chymosin polypeptide variants that cleave β-casein with a lower frequency than the corresponding parent polypeptide while at least maintaining its clotting activity.
Preferred variants with reduced β-casein cleavage frequency:
The isolated chymosin polypeptide variants of the present invention have a specific clotting activity (IMCU/mg total protein) that is at least 80% of the specific clotting activity of isolated camel chymosin polypeptide characterized by SEQ ID NO:4, including a specific clotting activity (IMCU/mg total protein) that is at least 85%, at least 90%, at least 95% or at least 97% of the specific clotting activity of isolated camel chymosin polypeptide characterized by SEQ ID NO:4.
The isolated chymosin polypeptide variant of present invention may be derived from a parent polypeptide has at least 80%, such as at least e.g. 80%, 85%, 95%, 97%, 98%, 99% sequence identity with the polypeptide of SEQ ID NO:4 (camel chymosin).
The isolated chymosin polypeptide variant of present invention may comprise one or more amino acid substitutions, deletions or insertions, wherein the one or more substitution, deletion or insertion is specified in relation to the amino acid sequence of SEQ ID NO:4: Y11, L130, S132, V32, S226, R266, L12, V221, S255, S277, L222, L253, M157, V260, S271, H76, K19, V183, S164, I263, V51, T239, Y307, R67, G251, R61, Q288, E83, D59, V309, S273, G251, S154, Y21, V203, L180, E294, G289, L215, D144, I303, L105, T284, Y127, V248, K321, V205, E262, K231, R316, M256, D158, D59, N249, L166, R242 or I96 such as e.g. Y11I, Y11V, L130I, S132A, V32L, S226T, R266V, L12M, V221M, S255Y, S277N, L222I, L253I, M157L, V260T, S271P, H76Q, K19T, V183I, S164G, I263L, V51L, T239S, Y307F, R67Q, G251D, R61Q, Q288E, E83S, D59N, V309I, S273Y, G251W, S154A, Y21S, V203A, L180I, E294Q, G289S, L215V, D144Q, I303L, L105E, T284S, Y127F, V248I, K321P, V205I, E262T, K231N, R316L, M256L, D158S, D59N, N249E, L166V, R242E and/or I96L.
In a related aspect, the isolated chymosin polypeptide variant of present invention may comprise a combination of substitutions, wherein the combination of substitutions is selected from a list comprising:
Y11+K19+D59+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242+G251; Y11+K19+D59+I96+S164+L166+R242+N249+G251+L253; Y11+K19+I96+S164+L166+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242+N249+G251; Y11+K19+I96+S164+L166+L222+R242+N249+G251; Y11+K19+D59+I96+S164+L222+R242+N249; Y11+K19+D59+I96+S164+L166+R242+G251; Y11+I96+S164+L222+R242; Y11+D59+I96+S164+L222+R242+G251 or Y11I+K19+D59+I96+S164+ +R242+N249+G251 such as e.g. Y11I+K19T+D59N+I96L+S164G+L166V+L222I+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L222V+R242E+G251D; Y11V+K19T+D59N+I96L+S164G+L166I+R242E+N249E+G251D+L253I; Y11I+K19T+I96L+S164G+L166V+R242E+N249E+G251D; Y11V+K19T+D59N+I96L+S164G+L222V+R242E+N249E+G251D; Y11V+K19T+I96L+S164G+L166V+L222V+R242E+N249E+G251D; Y11I+K19T+D59N+I96L+S164G+L222V+R242E+N249E; Y11I+K19T+D59N+I96L+S164G+L166V+R242E+G251D; Y11I+I96L+S164G+L222I+R242E; Y11I+D59N+I96L+S164G+L222I+R242E+G251D or Y11I+K19T+D59N+I96L+S164G+L222I+R242E+N249E+G251D and wherein each substitution is specified in relation to the amino acid sequence of SEQ ID NO:4.
In a related aspect, the variant may comprise alterations in one or more specified positions compared to a parent polypeptide having chymosin activity, wherein in the alteration is comprising a substitution, a deletion or an insertion in at least one amino acid position corresponding to any of positions 11, 130, 132, 32, 226, 266, 12, 221, 255, 277, 222, 253, 157, 260, 271, 76, 19, 183, 164, 263, 51, 239, 307, 67, 251, 61, 288, 83, 59, 309, 273, 251, 154, 21, 203, 180, 294, 289, 215, 144, 303, 105, 284, 127, 248, 321, 205, 262, 231, 316, 256, 158, 59, 249, 166, 242 or 96, wherein the amino acid position of the parent polypeptide is determined by an alignment of the parent polypeptide with the mature polypeptide of SEQ ID NO:2 (camel chymosin) and the parent polypeptide has at least 65% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin), which is from amino acid position 59 to amino acid position 381 of SEQ ID NO:2, wherein the isolated chymosin polypeptide variant cleaves β-casein with a lower frequency than the corresponding parent polypeptide.
In a preferred embodiment the parent polypeptide has at least 80%, such as at least e.g. 85%, 95%, 97%, 98%, 99% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin).
Preferably, an isolated chymosin polypeptide variant as described herein is a variant, wherein the variant has a lower β-casein cleavage frequency as compared to the parent peptide from which the variant is derived.
More preferably, an isolated chymosin polypeptide variant as described herein is a variant, wherein the variant has
As discussed above—as a reference sequence for determining the amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.) is herein used the mature peptide of the publicly known camel chymosin sequence disclosed as SEQ ID NO:2 herein.
As discussed above—based on e.g. the computer sequence alignment programs discussed herein—it is routine work for the skilled person to determine the here—in relevant amino acid position of a herein relevant chymosin polypeptide of interest (e.g. camel, sheep, bovine etc.).
The term “the parent polypeptide has at least 65% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin)” may be seen as relating to a sequence based limitation of the parent chymosin polypeptide used to make a herein relevant variant thereof.
In a preferred embodiment—the parent polypeptide has at least 92% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin), more preferably the parent polypeptide has at least 95% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin) and even more preferably the parent polypeptide has at least 97% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin). It may be preferred that the parent polypeptide is the mature polypeptide of SEQ ID NO:2 (Camel chymosin).
As understood by the skilled person in the present context—a herein relevant parent polypeptide having chymosin activity may already e.g. be a variant of e.g. a corresponding wildtype chymosin.
Said in other words, a herein relevant isolated chymosin polypeptide variant may comprise alterations (e.g. substitutions) in other positions than the positions claimed herein.
In relation to the chymosin sequences shown in
As understood by the skilled person in the present context—herein relevant sequence identity percentages of e.g. mature sheep, C._bactrianus, camel, pig or rat chymosin with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin—i.e. amino acid positions 59 to 381 of SEQ ID NO: 1) are relatively similar to above mentioned sequence identity percentages.
Preferably, an isolated bovine chymosin polypeptide variant as described herein is a variant, wherein the variant has a chymosin activity giving a lower β-casein cleavage frequency as compared to the β-casein cleavage frequency of camel chymosin comprising the mature polypeptide of SEQ ID NO:2.
As discussed above—in working examples herein were made variants using the polypeptide of SEQ ID NO:2 (camel chymosin) as parent polypeptide—such variant may herein be termed camel chymosin variant.
As understood by the skilled person in the present context—an isolated chymosin variant may comprise alterations (e.g. substitutions) in other amino acid positions than given above.
For instance, a camel chymosin variant with e.g. 5-10 alterations (e.g. substitutions) as compared to wildtype camel chymosin polypeptide of SEQ ID NO:2 will still be a parent polypeptide that has at least 95% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin).
It may be preferred that the isolated camel chymosin variant comprises less than 30 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO:2 (camel chymosin) or it may be preferred that the isolated camel chymosin variant comprises less than 20 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO:2 (camel chymosin) or it may be preferred that the isolated camel chymosin variant comprises less than 10 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO:2 (camel chymosin) or it may be preferred that the isolated camel chymosin variant comprises less than 5 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO:2 (camel chymosin).
As understood by the skilled person in the present context—the term “the isolated variant polypeptide has less than 100% sequence identity with the mature polypeptide of SEQ ID NO:2 (camel chymosin)” above relates to that the herein described isolated camel chymosin variant shall not have a polypeptide sequence that is 100% identical to the public known wildtype camel chymosin sequence of SEQ ID NO:2.
A preferred embodiment relates to an isolated camel chymosin polypeptide variant, wherein the alteration comprises a substitution, a deletion or an insertion in at least one amino acid position corresponding to any of positions claimed herein.
It may be preferred that at least one alteration is a substitution—i.e. a herein relevant preferred embodiment relates to an isolated chymosin polypeptide variant, wherein the alteration is comprising a substitution in at least one amino acid position corresponding to any of positions claimed herein.
Preferred parent polypeptide having chymosin activity:
Preferably, the parent polypeptide has at least 80%, such as e.g. 85%, 90%, 95%, 97%, 98%, or 99% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) and/or SEQ ID NO:2 (camel chymosin).
Just as an example—a herein suitable relevant parent polypeptide could e.g. be bovine chymosin A—as known in the art bovine chymosin A may only have one amino acid difference as compared to bovine chymosin B of SEQ ID NO: 1 herein.
In a preferred embodiment—the parent polypeptide has at least 90% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin), more preferably the parent polypeptide has at least 95% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) and even more preferably the parent polypeptide has at least 97% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin). It may be preferred that the parent polypeptide is the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).
As understood by the skilled person in the present context—a herein relevant parent polypeptide having chymosin activity may already e.g. be a variant of e.g. a corresponding wildtype chymosin.
For instance, a bovine chymosin variant with e.g. 5-10 alterations (e.g. substitutions) as compared to mature wildtype bovine chymosin polypeptide of SEQ ID NO: 1 will still be a parent polypeptide that has at least 95% sequence identity with the mature polypeptide of SEQ ID NO: 1 (Bovine chymosin).
Said in other words and in general—a herein relevant isolated chymosin polypeptide variant may comprise alterations (e.g. substitutions) in other positions than the positions claimed herein.
As understood by the skilled person in the present context—a parent polypeptide that has at least 90% sequence identity with the mature polypeptide of SEQ ID NO:2 (Camel) is still within the SEQ ID NO: 1 (Bovine) based sequence identity requirement i.e. it will be a parent polypeptide that has at least 65% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).
In a preferred embodiment—the parent polypeptide has at least 92% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin), more preferably the parent polypeptide has at least 95% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) and even more preferably the parent polypeptide has at least 97% sequence identity with the mature polypeptide of SEQ ID NO: 1 (bovine chymosin). It may be preferred that the parent polypeptide is the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).
As understood by the skilled person in the present context—an isolated chymosin variant may comprise alterations (e.g. substitutions) in other amino acid positions than given above.
For instance, a bovine chymosin variant with e.g. 5-10 alterations (e.g. substitutions) as compared to wildtype bovine chymosin polypeptide of SEQ ID NO: 1 will still be a parent polypeptide that has at least 95% sequence identity with the mature polypeptide of SEQ ID NO: 1 (Bovine chymosin).
It may be preferred that the isolated bovine chymosin variant comprises less than 30 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) or it may be preferred that the isolated bovine chymosin variant comprises less than 20 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) or it may be preferred that the isolated bovine chymosin variant comprises less than 10 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO: 1 (bovine chymosin) or it may be preferred that the isolated bovine chymosin variant comprises less than 5 amino acid alterations (e.g. substitutions) as compared to the mature polypeptide of SEQ ID NO: 1 (bovine chymosin).
The camel chymosin polypeptide of SEQ ID NO:2 has 84% sequence identity with the bovine polypeptide of SEQ ID NO: 1 (i.e. the complete SEQ ID NO: 1 from position 1 to 381, which includes pre and pro sequence).
As discussed above—as known in the art, the skilled person may, based on his common general knowledge, routinely produce and purify chymosin and chymosin variants.
Said in other words, once the skilled person is in possession of a herein relevant parent polypeptide having chymosin activity of interest (e.g. from bovines, camels, sheep, pigs, or rats) it is routine work for the skilled person to make a variant of such a parent chymosin of interest.
An example of a suitable method to produce and isolate a chymosin (variant or parent) may be by well-known e.g. fungal recombinant expression/production based technology as e.g. described in WO02/36752A2 (Chr. Hansen).
It is also routine work for the skilled person to make alteration at one or more positions in a parent polypeptide having chymosin activity, wherein the alteration is comprising a substitution, a deletion or an insertion in at least one amino acid position.
As known to the skilled person this may e.g. be done by so-called site directed mutagenesis and recombinant expression/production based technology.
It is also routine work for the skilled person to determine if a herein relevant parent polypeptide (e.g. camel or bovine wildtype chymosin) and/or a herein relevant variant has chymosin activity or not. As known in the art chymosin specificity may be determined by the so-called C/P ratio, which is determined by dividing the specific clotting activity (C) with the proteolytic activity (P).
As known in the art—a higher C/P ratio implies generally that the loss of protein during e.g. cheese manufacturing due to non-specific protein degradation is reduced, i.e. the yield of cheese is improved.
As also known in the art, β-casein cleavage and β-casein (including β(193-209)) formation may be determined using standard methods available to the person skilled in the art.
As discussed above—an isolated chymosin polypeptide variant as described herein may be used according to the art—e.g. to make a milk based product of interest (such as e.g. a cheese product).
As discussed above—an aspect of the invention relates to a method for making a food or feed product comprising adding an effective amount of the isolated chymosin polypeptide variant as described herein to the food or feed ingredient(s) and carrying our further manufacturing steps to obtain the food or feed product.
Preferably, the food or feed product is a milk based product and wherein the method comprises adding an effective amount of the isolated chymosin polypeptide variant as described herein to milk and carrying our further manufacturing steps to obtain the milk based product.
For example, the chymosin polypeptide variant of the present invention may be added to a milk-based product after fermentation of the milk. In one aspect the chymosin polypeptide variant of the present invention is added for coagulation of a fermented milk product as part of a method of producing cheese.
The milk may e.g. be soy milk, sheep milk, goat milk, buffalo milk, yak milk, lama milk, camel milk or cow milk.
The milk based product may e.g. be a fermented milk product such as a quark or a cheese.
The present invention also provides food and feed products comprising a chymosin polypetide variant of the present invention or a chymosin polypeptide variant obtainable according to a method of the present invention. The food and feed product is preferably a fermented food product, such as a fermented milk product, including cheese and quark.
In yet a related aspect, the present invention relates to a method for making a food or feed product comprising adding an effective amount of the isolated chymosin polypeptide variant according to the invention. Preferably, the food or feed product is a milk-based product.
The chymosin polypetide variant of present invention may also be used in a process for making cheese, such as e.g. to reduce bitterness in cheese.
Chymosin protein sequences were aligned using the ClustalW algorithm as provided by the EBI (EBI, tools, multiple sequence alignment, CLUSTALW″, http://www.ebi.ac.uk/Tools/msa/clustalw2/) and as described in Larkin M A, Blackshields G, Brown N P, Chenna R, McGettigan P A, McWilliam H, Valentin F, Wallace I M, Wilm A, Lopez R, Thompson J D, Gibson T J, Higgins D G (2007). Bio-informatics 23(21), 2947-2948.
ClustalW2 settings for multiple sequence alignments were Protein weight Matrix=BLOSUM, GAP open=10, GAP EXTENSION=0.05, GAP DISTANCES=8, No End Gaps, ITERATION=none, NUMITER=1, CLUSTERING=NJ
As a reference sequence the bovine chymosin B preprochymosin was used (Gen-bank accession number P00794—disclosed herein as SEQ ID NO: 1), where the N-terminal Methionin has number 1 (MRCL) and the C-terminal Isoleucin (in the protein sequence . . . LAKAI) has number 381.
Chymosin variants were designed using different strategies.
When there is referred to camel chymosin there is referred to camel chymosin comprising the mature polypeptide of SEQ ID NO:2 herein.
Camel chymosin of SEQ ID NO:2 may be seen as a herein relevant parent polypeptide having chymosin activity used to make camel chymosin variants thereof.
When there is referred to bovine chymosin there is referred to bovine chymosin comprising the polypeptide of SEQ ID NO: 1 herein.
Bovine chymosin of SEQ ID NO: 1 may be seen as a relevant parent polypeptide having chymosin activity used to make bovine chymosin variants thereof.
Variants 1 to 269 and 367 to 461 of camel chymosin were designed based on an alignment of a large set of public known aspartic protease sequences having an identity of 25% or more compared to bovine chymosin B.
Variations were generally introduced in regions with a high level of amino acid variation between species, while conserved regions were not changed. Amino acid substitutions were chosen based on phylogenetic, structural and experimental information to identify changes with high probability to show beneficial effects on β-casein cleavage. Multiple variations were introduced in each variant construct, ensuring that each single mutation was present in multiple variant constructs to minimize the effect of covariation between various substitutions. Machine learning and statistical analysis of experimental data were used to determine the relative contributions of the amino acid substitutions to measured coagulant performance of the chymosin variants (references 14, 15).
Variants 271 to 366 were designed based on detailed structural analysis of bovine chymosin (PDB code: 4AA8) and camel chymosin (PDB code: 4AA9). Variations were chosen based on the chemical nature of the respective amino acid side chains and their expected impact on either casein substrate binding or general enzyme properties. Most of the amino acid substitutions in variants 271 to 346 were made in sequence positions either within or in close structural proximity to the substrate binding cleft, or in secondary structural elements that get into contact with the bound casein substrate. Furthermore, changes were made in positions on the protein surface that alter the charge profile of these regions (reference 5) and are therefore expected to have an impact on enzyme performance. Variants 347 to 366 were made based on the different structural conformation of the N-terminal sequence in bovine and camel chymosin. Amino acid substitutions were made in positions within the substrate binding cleft that interact with the N-terminus in camel chymosin.
All chymosin variants were synthesized as synthetic genes and cloned into a fungal expression vector such as e.g. pGAMpR-C (described in WO02/36752A2)
The vectors were transformed into E. coli and plasmid DNA was purified using standard molecular biology protocols, known to the person skilled in the art.
The variant plasmids were individually transformed into an Aspergillus niger or Aspergillus nidulans strain and protein was produced essentially as described in WO02/36752A2 and purified using standard chromatography techniques.
As known in the art—the skilled person may, based on his common general knowledge, produce and purify chymosin and chymosin variants—such as herein described bovine and camel chymosin variants.
Milk clotting activity was determined using the REMCAT method, which is the standard method developed by the International Dairy Federation (IDF method) Milk clotting activity is determined from the time needed for a visible flocculation of a standard milk substrate prepared from a low-heat, low fat milk powder with a calcium chloride solution of 0.5 g per liter (pH 6.5). The clotting time of a rennet sample is compared to that of a reference standard having known milk-clotting activity and having the same enzyme composition by IDF Standard 110B as the sample. Samples and reference standards were measured under identical chemical and physical conditions. Variant samples were adjusted to approximately 3 IMCU/ml using an 84 mM acetic acid buffer pH 5.5. Hereafter, 200 μl enzyme preparation was added to 10 ml preheated milk (32° C.) in a glass test tube placed in a water bath, capable of maintaining a constant temperature of 32° C. ±1° C. under constant stirring. Alternatively, 20 μL enzyme preparation was added to 1 mL preheated milk as described above.
The total milk-clotting activity (strength) of a rennet was calculated in International Milk-Clotting Units (IMCU) per ml relative to a standard having the same enzyme composition as the sample according to the formula:
Sstandard: The milk-clotting activity of the international reference standard for rennet.
Tstandard: Clotting time in seconds obtained for the standard dilution.
Dsample: Dilution factor for the sample
Dstandard: Dilution factor for the standard
Tsample: Clotting time in seconds obtained for the diluted rennet sample from addition of enzyme to time of flocculation
For clotting activity determination of library 1,3, 4 and 6 variants as well as variants by structural design, the μIMCU method was used instead of the REMCAT method. As compared to REMCAT, flocculation time of chymosin variants in the μIMCU assay was determined by OD measurements in 96-well microtiter plates at 800 nm in a UV/VIS plate reader. A standard curve of various dilutions of a reference standard with known clotting strength was recorded on each plate. Samples were prepared by diluting enzyme in 84 mM acetate buffer, 0.1% triton X-100, pH 5.5. Reaction at 32° C. was started by adding 250 μL of a standard milk substrate containing 4% (w/w) low-heat, low fat milk powder and 7.5% (w/w) calcium chloride (pH ,'z-', 6.5) to 25 uL enzyme sample. Milk clotting activity of chymosin variants in International Milk-Clotting Units (IMCU) per ml was determined based on sample flocculation time relative to the standard curve.
Total protein content was determined using the Pierce BCA Protein Assay Kit from Thermo Scientific following the instructions of the providers.
Specific clotting activity (IMCU/mg total protein) was determined by dividing the clotting activity (IMCU/ml) by the total protein content (mg total protein per ml).
Chymosin mediated proteolysis of milk proteins was characterized by determining. ing profiles of water soluble peptides extracted at pH 4.6. A culture free cheese model made in 96 well plates was used for the study. In brief, 750 μl skim milk from Øllingege,rng g{circle around (a)}rd, Denmark added glucono-delta-lactone (GDL) and calcium chloride was aliquoted into the wells of a 96 deep well plate. After 10 min from addition of GDL to the milk, variants of chymosin were added to individual wells of the plate to a final activity of 0.05 IMCU/ml. The formed coagulum was cut after 30 min from addition of rennet by thoroughly stirring the coagulum with a pipette tip; a new tip was used for each well. Subsequently, the plate was left for another 60 min before curd and whey was separated by centrifugation of the plate for 10 min at 2500 g. The milk was kept at 30° C. during renneting, cutting and syneresis. Finally, whey was decanted from the plate and the pellet of rennet curd left in the plate was stored for 4 days at room temperature. Peptides were extracted by adding 500 μl of 0.5 M tri-sodium citrate to each well and gentle shaking the plate for 24 hours at 37° C. The now fully dissolved rennet curd was then precipitated by adding hydrochloric acid to a final pH of 4.4-4.5. The plate was spun down in a centrifuge and the supernatant recovered for further analysis of pH 4.5 soluble peptides.
Profiles of pH 4.5 soluble peptides were determined using RP-HPLC coupled to an ESI-Q-TOF mass spectrometer. The analysis was performed by using a liquid chromatography system (Agilent 1290 infinity, Agilent Technologies A/S, Santa Clara, Calif., USA) coupled to a mass spectrometer (G6540A Q-TOF, Agilent Technologies A/S, Santa Clara, Calif., USA). The column in the LC system was Ascentis Express Peptide ES-C18m, 2.7 μm, 100×2.1mm (Supelco, Sigma-Aldrich, St. Louis, USA). The mobile phase consisted of eluent A (0.1% formic acid in water) and eluent B (Acetonitrile: 0.1% formic acid in water, 9:1). After equilibration of the column with 2% B, a sample volume of 10 μL was injected. The peptides were separated by gradient elution generated by increasing eluent B from 2% to 50% over 15 column volumes. The flow rate was 0.44 mL/min. Peptides were detected by continuously measuring the UV absorbance at 214 nm. By running MS scans from 100 to 2000 m/z the mass spectra were collected. MS/MS analysis was performed on the two most intense ions from each scan. A MIX sample consisting of equal volume of all samples analyzed was prepared and this sample was analyzed for each 12 samples. MS data were converted from the Agilent .d format to .mzml files using MSConvert ver. 3.0.6618. All further data analysis was done using R 3.1.3. Peptides were identified from MS/MS spectra using R package ‘MSGFplus’ version 1.05. Search database for peptide identification were limited to the bovine milk proteins: αs1-casein, αs2-casein, β-casein, κ-casein, β-lactoglobulin, α-lactalbumin, lactoperoixdase and lactoferrin. Serine phosphorylation and methionine oxidation were included as variable modifications. R package ‘xcms’ v. 1.42.0 was used for detecting and grouping peaks across samples in a sample set according to Smith et al. (2006). Massifquant method was used for peak detection and grouping of peaks was based on the density method. Identity was assigned to grouped peaks resulting in quantitative tables of identified peptides including β-casein 193-209.
A statistical machine-learning approach and PCA-based analysis was used to determine the effects of all single mutations present in the variants of multi-substitution libraries 1-3, 4 and 6 on cleavage of β-casein at position 192/193.
Variants of camel chymosin, each having multiple substitutions compared to wild type, were generated and analyzed as described above. All variants have an amino acid sequence identical to camel chymosin (mature polypeptide of SEQ ID NO:2), except for the variations mentioned in the table. Both bovine and camel chymosin were included as references.
Clotting activities were determined using the μIMCU method.
9
R67Q
H76Q
S132A
V248I
S271P
41
16
R67Q
L130I
M157L
48
26
V32L
I96L
S277N
25
39
L130I
G163E
Y307F
51
47
S132A
V221M
S255Y
S273Y
V317L
19
51
Y127F
S132A
D158S
35
60
V32L
R61Q
H146R
22
68
V32L
E294Q
R316L
V317L
27
78
S226T
G244D
I263L
G289S
51
84
G70D
L130I
Y268F
49
95
V32L
L130I
R145Q
L222I
D279E
5
In Table 1 are shown camel chymosin variants with data on cleavage of β-casein at position 192/193. Since all enzyme variants were used at a normalized concentration of 0.05 IMCU/mL in the experiments, low β-casein cleavage indicates high specificity of the respective variant for κ-casein 104/105 over β-casein 192/193 cleavage, rather than low general enzymatic activity.
Variants with half or less than wild type proteolytic activity on β-casein are high-lighted in bold (variants 9, 16, 26, 39, 47, 51, 60, 68, 78, 84, 95). In those, mutations V32L, L130I, and S132A are overrepresented, compared to the mutational pattern present in the entire variant set shown. Four out of six variants with mutation V32L, four out of six variants with mutation L130I, and three out of five variants with mutation S132A show β-casein 192/193 cleavage equal or less than 50% of wild type camel chymosin.
In the three-dimensional structure of camel chymosin, position V32 is interacting with the P1 residue of the substrate peptide sequence (
Another set of camel chymosin variants, each having multiple substitutions compared to wild type, were generated and analyzed as described. All variants have an amino acid sequence identical to camel chymosin, except for the variations mentioned in the table. Both bovine and camel chymosin were included as references. Clotting activities were determined using the REMCAT method.
In Tab. 2 are shown camel chymosin variants with data on cleavage of β-casein at position 192/193. Since all enzyme variants were used at a normalized concentration of 0.05 IMCU/mL in the experiments, low β-casein cleavage indicates high specificity of the respective variant for κ-casein 104/105 over β-casein 192/193 cleavage, rather than low general enzymatic activity.
Variants with less than 25% wild type proteolytic activity on β-casein are high-lighted in bold (variants 110, 112, 122, 125, 132). In those, mutation V32L is overrepresented, compared to the mutational pattern present in the entire variant set shown. Five out of six variants with mutation V32L show β-casein 192/193 cleavage equal or less than 25% of wild type camel chymosin. These results support the findings and conclusions of the previous variant set.
A third set of camel chymosin variants, each having multiple substitutions compared to wild type, were generated and analyzed as described. All variants have an amino acid sequence identical to camel chymosin, except for the variations mentioned in the table. Both bovine and camel chymosin were included as references. Clotting activities were determined using the μIMCU method.
In Tab. 3 are shown camel chymosin variants with data on cleavage of β-casein at position 192/193. Since all enzyme variants were used at a normalized concentration of 0.05 IMCU/mL in the experiments, low β-casein cleavage indicates high specificity of the respective variant for κ-casein 104/105 over β-casein 192/193 cleavage, rather than low general enzymatic activity.
Variants with less than 10% wild type proteolytic activity on β-casein are high-lighted in bold (variants 150, 161, 165). In those, mutation V32L is overrepresented, compared to the mutational pattern present in the entire variant set shown. All three variants with mutation V32L show β-casein 192/193 cleavage less than 10% of wild type camel chymosin.
Only one variant from this variant set (variant 176) is showing higher than 50% β-casein 192/193 cleavage compared to wild type camel chymosin. This is also the only variant from this set lacking mutation L12M.
Position L12 is located in the sequence stretch close to the N-terminus of camel chymosin that is bound in the substrate binding cleft of the enzyme (
A statistical analysis of the positional and mutational effects on β-casein cleavage was performed based on the proteolytic data of libraries 1-3. The most beneficial mutations for decreased β-casein cleavage are shown in table 4.
Based on the obtained results it is concluded that mutations shown in table 4 reduce β-casein 192/193 cleavage, with the above described mutations L130I, S132A, V32L, and L12M being amongst the mutations with the strongest impact (highlighted in bold in table 4).
Since the mutations shown in table 4 cause less generation of the C-terminal fragment of β-casein, 13(193-209), they represent preferred mutations in chymosin variants for making cheese with less bitter taste due to reduced cleavage of β-casein.
Another set of camel chymosin variants, each having multiple substitutions compared to wild type, were generated and analyzed as described above. All variants have an amino acid sequence identical to camel chymosin (mature polypeptide of SEQ ID NO:2), except for the variations mentioned in the table. Camel chymosin (CHY-MAX M) is included as reference.
Clotting activities were determined using the μIMCU method.
In table 5 are shown camel chymosin variants with data on cleavage of β-casein 192/193. All variants reveal between 44% and 93% reduced proteolytic activity compared to wild type camel chymosin.
A statistical analysis of the positional and mutational effects on β-casein cleavage was performed based on the proteolytic data of library 4 variants. The most beneficial mutations for decreased 13-casein cleavage are shown in table 6.
Based on the obtained results it is concluded that mutations shown in table 6 reduce β-casein 192/193 cleavage.
Since these mutations cause less generation of the C-terminal fragment of β-casein, B(193-209), they represent preferred mutations in chymosin variants for making cheese with less bitter taste due to reduced cleavage of β-casein.
Another set of camel chymosin variants, each having multiple substitutions compared to wild type, were generated and analyzed as described above. All variants have an amino acid sequence identical to camel chymosin (mature polypeptide of SEQ ID NO:2), except for the variations mentioned in the table. Camel chymosin (CHY-MAX M) is included as reference.
Clotting activities were determined using the REMCAT method.
In Table 7 are shown camel chymosin variants with data on cleavage of β-casein 192/193. Out of 47 variants, 46 reveal between 16% and 83% reduced proteolytic activity compared to wild type camel chymosin.
A statistical analysis of the positional and mutational effects on β-casein cleavage was performed based on the proteolytic data of library 5 variants. The most beneficial mutations for decreased 8-casein cleavage are shown in table 8.
Based on the obtained results it is concluded that mutations shown in table 8 reduce β-casein 192/193 cleavage.
Since these mutations cause less generation of the C-terminal fragment of β-casein, β(193-209), they represent preferred mutations in chymosin variants for making cheese with less bitter taste due to reduced cleavage of β-casein.
Variants of camel chymosin (SEQ ID NO:2) were made with amino acid changes in positions determined by protein structural analysis (Tab. 9). Mutations N100Q and N291Q were introduced into both N-glycosylation sites of these variants and the reference camel chymosin (CamUGly) to yield non-glycosylated, homogeneous protein samples.
Clotting activities were determined using the μIMCU method.
Based on the results shown in table 9 it is concluded that mutations K19T, Y21S, V32L, D59N, H76Q, I96L, L130I, S132A, Y190A, L222I, S226T, D290E, D290L, R242E, R242Q, Y243E, G251D, R254S, S273D, S273Y, Q280E, F282E, G289S, and V3091 reduce cleavage of β-casein 192/193 by more than 10%.
Since these mutations cause less generation of the C-terminal fragment of β-casein, β(193-209), they represent preferred mutations in chymosin variants for making cheese with less bitter taste due to reduced cleavage of β-casein.
Ten out of 24 variants with decreased cleavage of β-casein 192/193 shown in table 9 bear mutations (V32L, H76Q, L130I, S132A, Y190A, L222I, S226T, G289S, D290E, D290L) within or in structural proximity to the substrate binding cleft (
Nine out of 24 variants with decreased cleavage of β-casein 192/193 shown in table 9 bear mutations (R242E, R242Q, Y243E, G251D, R254S, S273D, S273Y, Q280E, F282E) in a distinct region on the protein surface that is located in proximity to the binding cleft as seen in
More variants of camel chymosin (SEQ ID NO:2) were made with combinations of mutations that introduce negative charges into the surface region described above (R242E, Y243E, G251D, N252D, R254E, S273D, Q280E). Mutations N100Q and N291Q were introduced into both N-glycosylation sites of these variants and the reference camel chymosin (CamUGly) to yield non-glycosylated, homogeneous protein samples (Tab. 10).
Clotting activities were determined using the pIMCU method.
All variants shown in table 10 reveal decreased β-casein cleavage compared to non-glycosylated camel chymosin. It is concluded that the inhibition of β-casein cleavage by introducing negative charges into the P10-P4 interacting region on the chymosin structure can be further enhanced by combinations of the respective mutations.
Variants of bovine chymosin (SEQ ID NO:1) were made with amino acid changes in positions determined by protein structural analysis (Tab. 11). Mutations N252Q and N291Q were introduced into both N-glycosylation sites of these variants and the reference bovine chymosin (BovUGly) to yield non-glycosylated homogeneous protein samples.
Clotting activities were determined using the μIMCU method.
Except I136V, all mutations caused increased cleavage of β-casein 192/193 in the variants shown in table 11. Notably, while substitutions I136V, Q242R, D251G, S289G, and E290D increased β-casein cleavage of bovine chymosin, decreased β-casein cleavage was observed by the respective reverse mutations V136I, R242Q, G251D, G289S, and D290E in camel chymosin (Tab. 9). A similar effect is seen in position 32. While V32L caused decreased β-casein cleavage of camel chymosin, mutation of L32 to I a β branched hydrophobic amino acid with structural similarity to V—resulted in increased β-casein cleavage of bovine chymosin. This demonstrates that these amino acid changes exert similar effects on chymosin specificity across species.
Variants of camel chymosin (SEQ ID NO:2) were made with amino acid changes in positions determined by protein structural analysis of the molecular interactions of the N-terminal sequence Y11-D13 within the substrate binding cleft (Tab. 12). Mutations N100Q and N291Q were introduced into both N-glycosylation sites of these variants and the reference camel chymosin (CamUGly) to yield non-glycosylated, homogeneous protein samples.
Clotting activities were determined using the μIMCU method.
Analysis of the camel chymosin structure guided variations in the N-terminal sequence Y11-D13 as well as in position D290, a potential interaction partner of Y11 (
Another set of camel chymosin variants, each having multiple substitutions compared to wild type, were generated and analyzed as described above. All variants have an amino acid sequence identical to camel chymosin (mature polypeptide of SEQ ID NO:2), except for the variations mentioned in the table. Camel chymosin (CHY-MAX M) is included as reference.
Clotting activities were determined using the pIMCU method.
In Table 13 are shown camel chymosin variants with data on cleavage of β-casein 192/193. All 50 variants reveal between 19% and 97% reduced proteolytic activity compared to wild type camel chymosin.
A statistical analysis of the positional and mutational effects on β-casein cleavage was performed based on the proteolytic data of library 6 variants. The most beneficial mutations for decreased β-casein cleavage are shown in Table 14.
Based on the obtained results it is concluded that mutations shown in Table 14 reduce β-casein 192/193 cleavage.
Since these mutations cause less generation of the C-terminal fragment of β-casein, β(193-209), they represent preferred mutations in chymosin variants for making cheese with less bitter taste due to reduced cleavage of β-casein.
Another set of camel chymosin variants, each having multiple substitutions compared to the wild type, were generated and analyzed as described above. All variants have an amino acid sequence identical to camel chymosin (mature polypeptide of SEQ ID NO:2), except for the variations mentioned in the table. Camel chymosin (CHY-MAX M) is included as reference.
Clotting activities were determined using the μIMCU method.
In Table 15 are shown camel chymosin variants with data on cleavage of β-casein 192/193. All 45 variants show reduced proteolytic activity compared to wild type camel chymosin.
Blundell, N. Andreeva, J. Mol. Biol. 1991, 221, 1295-1309.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15173099.1 | Jun 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/064414 | 6/22/2016 | WO | 00 |
