Patent Application
20120322715
The present invention relates to a composition which comprises a serine hydrolase acting on ester bonds and which does not comprise a protease.
Serine hydrolases acting on ester bonds such as lipases for industrial use may be supplied in a liquid or granule formulation for use, e.g., in liquid or granular detergents. The formulation is typically free of protease and/or free of surfactant, and it is generally desirable to improve the storage stability of the serine hydrolase in the formulation.
WO 2009/118375 discloses that in a liquid detergent containing a protease and a lipase, the storage stability of the lipase can be improved by the addition of a peptide aldehyde due to inhibition of the protease.
The inventors have found that the storage stability of a serine hydrolase acting on ester bonds in a formulation without a protease can be improved by incorporating a serine protease inhibitor. Without wishing to be bound by theory, the inventors believe that the structure of the serine hydrolase is stabilized by incorporating a serine protease inhibitor in the active site.
Accordingly, the invention provides a composition which comprises a serine hydrolase acting on ester bonds and a serine protease inhibitor, and which does not comprise a protease.
Serine hydrolase acting on ester bonds
The serine hydrolase is an enzyme in the serine hydrolase superfamily. It acts on ester bonds and belongs to enzyme class EC 3.1. It may be a lipase (EC 3.1.1.3), a phospholipase A2 (EC 3.1.1.4), a carboxylesterase (EC 3.1.1.1), an acetylcholinesterase (EC 3.1.1.7), or a thioester hydrolase (EC 3.1.2).
The lipase may be Thermomyces lanuginosus lipase (TLL, shown as SEQ ID NO: 2 in WO 2009/109500), Candida antarctica lipase A (CALA, shown as SEQ ID NO: 1 in WO 2008/040739), Candida antarctica lipase B (CALB, having the amino acid sequence described in J. Uppenberg et al., Structure, 1994, 2:293-308), Rhizomucor miehei lipase, Aspergillus niger lipase, Candida rugosa lipase (SWISSPROT:P20261), Penicillium roqueforti lipase, Rhizopus niveus lipase (SWISPROT:P61872), Rhizopus oryzae lipase, Alcaligenes sp. lipase, Achromobacter sp. lipase, Burkholderia cepacia lipase, Pseudomonas stutzeri lipase, or it may be a variant which has an amino sequence with at least 80% identity to one of these, particularly at least 85%, at least 90%, at least 95% or at least 98% identity.
Examples of TLL homologues are described in WO 1992/005249 (NZ 3520, Lipolase Ultra), WO0060063, WO9707202, WO0032758, WO02055679, WO04099400, WO07087508 and WO 2009/109500. Commercial lipases include the following products of Novozymes A/S: Novozym™ 435, Novozym 735, Lipozyme∩ RM, Novozym 388, Lipolase Ultra™, Lipex™, Lipoprime™, Resinase™ HT, Lipolase™, Resinase™, Lipopan™, Lipoclean™ and Lipolex™. Commercial lipases also include the following products of Amano Enzyme, Danisco, DSM, Meito Sangyo: Lipase A, LipaseG, Lipase AY, Lipase R, Newlase™ F, Grindamyl™, Powerbake™ BakeZyme L, BakeZyme PH, Panamore, Panamore Golden, Panamore Spring, Lipase MY, Lipase OF, Lipase PL, Lipase QL, Lipase AL, Lipase SL, Lipase TL, and Lipase UL.
The phospholipase A2 may be of animal origin, e.g. pancreatic such as porcine pancreatic or bovine pancreatic. The phospholipase A2 may also be derived from other eukaryotic organisms such as Tuber, Verticillium, Neurospora, Aspergillus, Helicosporum or Fusarium, particularly T. borchii, T. albidum, V. dahliae, V. tenerum, N. crassa, A. oryzae, Helicosporium sp. HN1 or F. venenatum, or it may be a variant having a sequence identity of at least 80%, 85%, 90% or 95% to one of those mentioned, e.g. as described in WO04097012.
The serine protease inhibitor is selected from inhibitors to proteases from the serine hydrolase superfamily. In particular, the serine protease inhibitor may be a peptide aldehyde or a boronic acid derivative.
The inhibitor may have an inhibition constant to a serine protease Ki (M, mol/L) of 1E-12-1E-03; more preferred 1E-11-1E-04; even more preferred: 1E-10-1E-05; even more preferred 1E-10-1E-06; most preferred 1E-09-1E-07.
The serine protease inhibitor has the general formula A4-A3-A2-A1, where
The serine protease inhibitor may be a peptide aldehyde or an aldehyde analogue having the formula B2-B1-B0-R wherein:
a) R is hydrogen, CH3, CX3, CHX2, or CH2X, wherein X is a halogen atom; a phosphonate or a boronic acid (B(OH)2).
b) B0 is a single amino acid residue;
c) B1 is 1-2 amino acid residues; and
d) B2 consists of one or more amino acid residues (preferably one or two), optionally comprising an N-terminal protection group or an N-terminal protection group attached to B1 (preferred if B1 is a dipeptide).
In the above formula, B° may be an L or D-amino acid with an optionally substituted aliphatic or aromatic side chain, preferably D- or L-Tyr (p-tyrosine), m-tyrosine, 3,4-dihydroxyphenylalanine, Leu, Phe, Val, Gly, Met, Trp, Ile, Nva or Nle. If R is boronic acid or a phosphonate then B0 is an amino acid residue without double-bound oxygen on the C-terminal carbon.
B1 may be 1-2 amino acid residues, preferably 2, with a small optionally substituted aliphatic side chain, preferably selected from Ala, Cys, Gly, Leu, Arg, Pro, Ser, Ile, Thr, Val, Nva, or Nle, most preferred selected from Ala, Gly, Leu, Nva or Nle. The most preferred combinations are, Gly-Ala, Ala-Ala, Gly-Gly, and Gly-Leu. B2 may be an N-capping group known from protein chemistry, preferably selected from benzyloxycarbonyl (Cbz), p-methoxybenzyl carbonyl (MOZ), benzyl (Bn), benzoyl (Bz), p-methoxybenzyl (PMB), p-methoxyphenyl (PMP), formyl, acetyl, methyloxy, methyloxycarbonyl/methyl carbamate, or methyl urea, or B2 may be anyl-2 amino acid residues without specifying structure optionally comprising a protection group as described above.
More particularly, the peptide aldehyde may be Z-GGY-H, Z-GGF-H, Z-GGG-H, Z-GAG-H, Z-RAY-H, Ac-GAY-H, Z-GAY-H, Z-GAL-H, Z-GAF-H, Z-GAV-H, Z-RVY-H, Z-LVY-H, Ac-LGAY-H, Ac-FGAY-H, Ac-YGAY-H, Ac-FGVY-H, Ac-FGAM-H, Ac-WLVY-H, MeO-CO-VAL-H, MeO-CO-LLY-H, MeOCO-FGAL-H, MeO-FGAF-H, MeNCO-FGAL-H Z-VAL-CF3, Ac-NHCH(CH2CH(CH3))-B(OH)2, Ac-NHCH(CH2Ph)-B(OH)2, MeOCO-FGA-NHCH(Ph)CH2-B(OH)2, Z-GA-N(CH3)CH(Ph)CH2-B(OH)2- wherein Z is benzyloxycarbonyl, Me is methyl and Ac is acetyl.
Alternatively, the serine protease inhibitor may be a peptide aldehyde with the formula: P-O-(A1-X′)n-An+1-Q
wherein Q is hydrogen, CH3, CX3, CHX2, or CH2X, wherein X is a halogen atom;
wherein one X′ is the “double N-capping group” CO, CO-CO, CS, CS-CS or CS-CO, most preferred ureido/“urea” (CO), and the other X'es are nothing,
wherein n=1-10, preferably 2-5, most preferably 2,
wherein each of A1 and An+1 is an amino acid residue having the structure:
—NH—CR—CO— for a residue to the right of X═—CO—, or
—CO—CR—NH— for a residue to the left of X═—CO—
wherein R is H— or an optionally substituted alkyl or alkylaryl group which may optionally include a hetero atom and may optionally be linked to the N atom. Preferred amino acids at the C-terminal (An+1) are L or D-amino acids with an optionally substituted aliphatic or aromatic side chain, preferably D- or L-Tyr (p-tyrosine), m-tyrosine, 3,4-dihydroxyphenylalanine, Leu, Phe, Val, Gly, Met, Trp, Ile, Nva or Nle. Preferred amino acid residues Ai (i<=n) to the right of X═—CO are those with small optionally substituted aliphatic side chain, preferably selected from Ala, Cys, Gly, Leu, Arg, Pro, Ser, Ile, Thr, Val, Nva, or Nle,
wherein P is hydrogen or any C-terminal protection group.
Examples of such peptide aldehydes include α-MAPI, β-MAPI, F-urea-RVY-H, F-urea-GGY-H, F-urea-GGF-H, F-urea-GAF-H, F-urea-GAY-H, F-urea-GAL-H, F-urea-GA-Nva-H, F-urea-GA-Nle-H, Y-urea-RVY-H, Y-urea-GAY-H, F-CS-RVF-H, F-CS-RVY-H, F-CS-GAY-H, Antipain, GE20372A, GE20372B, Chymostatin A, Chymostatin B, and Chymostatin C. Further examples of peptide aldehydes are disclosed in WO 2009/118375 and PCT/EP2009/053580, WO 94/04651, WO 98/13459, WO 98/13461, WO 98/13462, WO 2007/145963, (P&G) hereby incorporated by reference.
As another alternative, the serine protease inhibitor may be a borate such as borax. It may also be a boronic acid derivative having the formula B(OH)2—C6H4—R wherein —C6H4-has bonds attached in the m- or p-position, and R is selected from the group consisting of CHO, COOH, C1-C6 alkyl substituted CO-C1-C6 alkyl, C1-C6 alkenyl and substituted C1-C6 alkenyl, X (halogen), most preferred is 4-formyl phenylboronic acid (4-FPBA) and borax.
As another alternative the serine protease inhibitor may be an aliphatic aldehyde, phosphonate or boronic acid with the structure:
D2-D1-W
Examples of such inhibitors are Z—NH—(CH2)7—CHO, Z—NH—(CH2)6—CH(CH2Ph)-CHO and Z—NH—(CH2)6—CH(CH2C6H4-pOH)—CHO.
Further examples of inhibitors are described in WO 95/25791, WO9813459, WO9813461, WO9813462, WO2007145963 and WO2007141736.
The composition comprises a serine hydrolase acting on ester bonds and a serine protease inhibitor, and it does not contain a protease. It may be in granular or liquid form. It may be a detergent, or a non-detergent, i.e. a serine hydrolase formulation without a surfactant.
For a non-detergent composition, the serine hydrolase acting on ester bonds may be a lipase present in an amount of 5-40 mg of enzyme protein per g, more preferred 10-30 mg enzyme protein/g. If the serine protease inhibitor is a peptide aldehyde or analogue it may be present in an amount of 0.01%-1%, more preferred 0.02%-0.5% or at a molar ratio of inhibitor:lipase of 0.5:1 to 20:1, more preferred 1:10 and even more preferred 1:5. If the serine protease inhibitor is a boric acid derivative (ex borax or substituted/unsubstituted phenylboronic acid derivatives) the inhibitor is present in an amount of 0.5-20%; more preferred 1%-10%. Other ingredients in a non-detergent liquid compositions may be—but not limited to—polyols or mixtures of polyols (ex sorbitol, glycerol, monopropylene glycol, etc.) in 1-60%, small amounts of non-ionic surfactants (ex softanol) 0-5%, calcium ions 0.001%-0.5%, water, and preservatives (ex proxel, 2-phenoxyethanol, etc).
The serine protease inhibitor may be used to stabilized a lipase in a particle for triggered release of a rinse benefit agent comprising a lipase substrate, e.g. as described in WO2009/118329.
For a liquid or granular detergent, the non-detergent composition described above may be added in an amount of 0.01%-5%, more preferred 0.1-2.5%, or the enzyme a and the protease inhibitor may be added separately. The serine hydrolase acting on ester bonds may be a lipase present in an amount of 0.1-2 mg enzyme protein per g detergent. If the serine protease inhibitor is a peptide aldehyde or analogue it may be present in an amount of 0.01 ppm-0.02%, more preferred 0.5 ppm-0.01%, even more preferred 0.8 ppm-40 ppm, or at a molar ratio of inhibitor:lipase of 0.5:1 to 20:1, more preferred up to 10:1 and even more preferred up to 5:1. If the serine protease inhibitor is a boric acid derivative (ex borax or substituted/unsubstituted phenylboronic acid derivatives) the inhibitor is present in an amount of 0.1 ppm-3%, more preferred 1 ppm-1%, even more preferred 5 ppm-0.5%, most preferred 30 ppm-0.2%. Other ingredients may include chelating agents, solvents, colorants, and perfumes. If the detergent is a liquid, then pH is between 5-10, more preferred between 7-10 or 7-9.
The liquid detergent may be aqueous, typically containing 5-95% water, e.g. 5-15% or 20-70% water and 0-20% organic solvent (hereinafter, percentages by weight).
The detergent comprises a surfactant which may be anionic, non-ionic, cationic, amphoteric or a mixture of these types. The detergent will usually contain 5-30% anionic surfactant such as linear alkyl benzene sulphonate (LAS), alpha-olefin sulphonate (AOS), alcohol ethoxy sulphate (AES) or soap. It may also contain 3-20% anionic surfactant such as nonyl phenol ethoxylate or alcohol ethoxylate.
The pH (measured in aqueous detergent solution) will usually be neutral or alkaline, e.g. The detergent may contain 1-40% of a detergent builder such as zeolite, phosphate, phosphonate, citrate, NTA, MGDA, GLDA, EDTA or DTPA, or it may be unbuilt (i.e. essentially free of a detergent builder). It may also contain other conventional detergent ingredients, e.g. fabric conditioners, foam boosters, bactericides, optical brighteners and perfumes.
The detergent composition may be a fabric cleaning compositions, hard surface cleansing compositions, light duty cleaning compositions including dish cleansing compositions and automatic dishwasher detergent compositions.
The liquid detergent composition may comprise from about 0.0001% to about 10%, more particularly from about 0.00015% to about 1%, and most particularly from about 0.001% to about 0.1% of the inhibitor
Thus, a stabilized liquid enzyme formulation typically contains 0.5-20% by weight, particularly 1-10% by weight, of enzyme protein (total of protease and optional second enzyme) and 0.01%-10% of the inhibitor, more particularly 0.05-5% by weight and most particularly 0.1%-2% by weight of the inhibitor.
A liquid detergent formulation will typically contain 0.04-400 micromolar enzyme (or 1-10000 mg EP/L), more particularly 0.16-160 micromolar enzyme (4-4400 mg EP/L) and most particularly 0.8-80 (20-2200 mg EP/L) and about 1-20 times more of the inhibitor, most particularly about 1-10 times more of the inhibitor.
The liquid detergent composition may contain water and other solvents as carriers. Low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and iso-propanol are suitable. Monohydric alcohols are preferred for solubilizing surfactants, but polyols such as those containing from about 2 to about 6 carbon atoms and from about 2 to about 6 hydroxy groups (e.g., 1,3-propanediol, ethylene glycol, glycerol, and 1,2-propanediol) can also be used. The compositions may contain from about 5-90%, 10-50% 2-50%; 2-25% of such carriers.
The detergent compositions herein will preferably be formulated such that during use in aqueous cleaning operations, the wash water will have a pH between about 6.8 and about 11. Finished products are typically formulated at this range. Techniques for controlling pH at recommended usage levels include the use of, for example, buffers, alkalis, and acids. Such techniques are well known to those skilled in the art.
When formulating the hard surface cleaning compositions and fabric cleaning compositions of the present invention, the formulator may wish to employ various builders at levels from about 5% to about 50% by weight. Typical builders include the 1-10 micron zeolites, polycarboxylates such as citrate and oxydisuccinates, layered silicates, phosphates, and the like. Other conventional builders are listed in standard formularies. The invention is particularly applicable to the formulation of liquid detergents where enzyme stability problems are pronounced.
The detergent may in particular be formulated for laundry, dishwashing or hard surface cleaning, e.g. for floor cleaning, carwash, industrial and institutional laundry, or washing of wool and silk textiles. The detergent may be formulated as described in US2006247150, WO2005040320, US2005020466, US2009217463, WO2008010920, WO2007087259, WO9600277, WO9511292, EP430315, DE10023580, WO9617052, WO2009107091, WO2008010920, WO2007087259, WO9600277, JP2006131659, JP2004204084 JP2004203918, WO2009060966, WO2006050308 and JP63260997.
The serine protease inhibitor may be used to stabilize the serine hydrolase acting on ester bonds in the absence of a protease. Thus, the inhibitor may be used in the manufacture of the serine hydrolase, e.g. by adding it during fermentation, recovery or during formulation of the serine hydrolase acting on ester bonds, e.g. as described in WO95/25791. The inhibitor may also be used in a lipid-based drug delivery system containing phospholipase A2, e.g. as described in WO200158910.
Lipoclean formulations, per se (LCLU/g) residual activities: The Lipase was formulated from crude concentrate with standard formulation ingredients (sorbitol and glycerol) with and without the serine protease inhibitor (2% enzyme protein, 0.08% Z-GAY-H added with a 1% DMSO solution). The solution was split into separate vials which were incubated at different temperature and times and compared in activity with a frozen reference sample frozen directly after mixing. The lipase activity was measured by ester bond hydrolysis in the substrate PNP-Palmitate (C:16) and releases PNP which is yellow and can be detected at 405 nm.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10150333.2 | Jan 2010 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2011/050065 | 1/4/2011 | WO | 00 | 7/3/2012 |
