Perhydrolase for enzymatic peracid production
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IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C12P-007/14
C12N-009/14
C12N-015/00
C12N-001/21
출원번호
US-0571702
(2009-10-01)
등록번호
US-8222012
(2012-07-17)
발명자
/ 주소
DiCosimo, Robert
Gavagan, John Edward
Payne, Mark Scott
출원인 / 주소
E. I. du Pont de Nemours and Company
인용정보
피인용 횟수 :
5인용 특허 :
38
초록▼
A process is provided for rapidly producing target concentrations of peroxycarboxylic acids from carboxylic acid esters. More specifically, carboxylic acid esters are reacted with a source of peroxygen, such as hydrogen peroxide, in the presence of an enzyme catalyst comprising an enzyme having iden
A process is provided for rapidly producing target concentrations of peroxycarboxylic acids from carboxylic acid esters. More specifically, carboxylic acid esters are reacted with a source of peroxygen, such as hydrogen peroxide, in the presence of an enzyme catalyst comprising an enzyme having identity to an acetyl xylan esterase from Lactococcus lactis having perhydrolysis activity. The polypeptide is an enzyme structurally classified as a member of the carbohydrate esterase family 7 (CE-7). The peroxycarboxylic acids produced by the present process can be used in disinfecting, bleaching, and other laundry care applications. Compositions comprising the reaction components and the peroxycarboxylic acids produced by the process are also provided.
대표청구항▼
1. A process for producing a target concentration of peroxycarboxylic acid comprising: (a) selecting a set of reaction components comprising: (1) at least one substrate selected from the group consisting of: (i) esters having the structure [X]mR5 whereinX=an ester group of the formula R5—C(O)O;R6═C1
1. A process for producing a target concentration of peroxycarboxylic acid comprising: (a) selecting a set of reaction components comprising: (1) at least one substrate selected from the group consisting of: (i) esters having the structure [X]mR5 whereinX=an ester group of the formula R5—C(O)O;R6═C1 to C7 linear, branched or cyclic hydrocarbyl moiety, optionally substituted with hydroxyl groups or C1 to C4 alkoxy groups, wherein R6 optionally comprises one or more ether linkages for R6═C2 to C7;R5=a C1 to C6 linear, branched, or cyclic hydrocarbyl moiety optionally substituted with hydroxyl groups; wherein each carbon atom in R5 individually comprises no more than one hydroxyl group or no more than one ester group;wherein R5 optionally comprises one or more ether linkages;m=1 to the number of carbon atoms in R5; andwherein said esters have solubility in water of at least 5 ppm at 25° C.;(ii) glycerides having the structure wherein R1═C1 to C7 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R3 and R4 are individually H or R1C(O); and(iii) acetylated saccharides selected from the group consisting of acetylated monosaccharides, acetylated disaccharides, and acetylated polysaccharides;(2) a source of peroxygen; and(3) an enzyme catalyst having perhydrolysis activity, wherein said enzyme catalyst comprises an enzyme having a signature motif that aligns with a reference sequence SEQ ID NO:2 using CLUSTALW, said signature motif comprising: (i) an RGQ motif at amino acid positions 118-120 of SEQ ID NO:2;(ii) a GXSQG motif at amino acid positions 179-183 of SEQ ID NO:2; and(iii) an HE motif at amino acid positions 298-299 of SEQ ID NO:2;wherein said enzyme has at least 95% amino acid identity to SEQ ID NO:4; and(b) combining the reaction components under aqueous reactions to form a reaction mixture; whereby reaction products are formed comprising enzymatically-produced peroxycarboxylic acid; wherein (1) the pH of the reaction mixture remains in the range of from about 6.0 to about 9.0; and(2) the concentration of peroxycarboxylic acid produced one minute after combining the reaction components is not exceeded by more than 100% at a reaction time equal to or greater than five minutes after combining the reaction components. 2. The process of claim 1 wherein the concentration of peroxycarboxylic acid produced one minute after combining the reaction components is not exceeded by more than 100% at a reaction time equal to or greater than 30 minutes after combining the reaction components. 3. The process of claim 1 wherein the concentration of peroxycarboxylic acid produced one minute after combining the reaction components is not exceeded by more than 50% at a reaction time equal to or greater than five minutes after combining the reaction components. 4. The process of claim 3 wherein the concentration of peroxycarboxylic acid produced one minute after combining the reaction components is not exceeded by more than 20% at a reaction time equal to or greater than five minutes after combining the reaction components. 5. The process of claim 1 wherein the total amount of peroxycarboxylic acid produced by the process is not limited by the amount of substrate or the amount of peroxygen in the reaction mixture. 6. The process of claim 1 wherein the pH of the reaction mixture ranges from about 6.5 to about 8.5. 7. The process of claim 6 wherein the pH of the reaction mixture ranges from about 7.0 to about 8.0. 8. The process of claim 1 wherein the reaction mixture comprises at least one buffer. 9. The process of claim 8 wherein the at least one buffer is selected from the group consisting of sodium bicarbonate, potassium bicarbonate, mixtures of sodium bicarbonate and potassium bicarbonate, sodium phosphate, potassium phosphate, and mixtures of sodium phosphate and potassium phosphate. 10. The process of claim 1 wherein the substrate is selected from the group consisting of: monoacetin; diacetin; triacetin; monopropionin; dipropionin; tripropionin; monobutyrin; dibutyrin; tributyrin; glucose pentaacetate; xylose tetraacetate; acetylated xylan; acetylated xylan fragments; β-D-ribofuranose-1,2,3,5-tetraacetate; tri-O-acetyl-D-galactal; tri-O-acetyl-glucal; monoesters or diesters of 1,2-ethanediol; 1,2-propanediol; 1,3-propanediol; 1,2-butanediol; 1,3-butanediol; 2,3-butanediol; 1,4-butanediol; 1,2-pentanediol; 2,5-pentanediol; 1,6-pentanediol; 1,2-hexanediol; 2,5-hexanediol; 1,6-hexanediol; propylene glycol diacetate; ethylene glycol diacetate; and mixtures thereof. 11. The process of claim 1 wherein the peroxycarboxylic acid produced is peracetic acid, perpropionic acid, perbutyric acid, perlactic acid, perglycolic acid, permethoxyacetic acid, per-β-hydroxybutyric acid, or mixtures thereof. 12. The process of claim 1 wherein the enzyme catalyst is in the form of a microbial cell, a permeabilized microbial cell, a microbial cell extract, a partially purified enzyme, or a purified enzyme. 13. The process of claim 1 wherein the enzyme catalyst lacks catalase activity. 14. The process of claim 1 further comprising the step of: (c) contacting a surface or inanimate object with the peroxycarboxylic acid produced in step (b) whereby said surface or said inanimate object is disinfected, destained, deordorized or bleached. 15. The process of claim 1 further comprising the step of: (c) contacting a textile with peroxycarboxylic acid produced in step (b), whereby the textile receives a benefit. 16. The process of claim 15 wherein the benefit is selected from the group consisting of a disinfecting, bleaching, destaining, deodorizing, and any combination thereof. 17. A process for producing a target concentration of peroxycarboxylic acid comprising: (a) selecting a set of reaction components comprising: (1) at least one substrate selected from the group consisting of: (i) esters having the structure [X]mR5 whereinX=an ester group of the formula R6—C(O)O;R6═C1 to C7 linear, branched or cyclic hydrocarbyl moiety, optionally substituted with hydroxyl groups or C1 to C4 alkoxy groups, wherein R6 optionally comprises one or more ether linkages for R6═C2 to C7;R5=a C1 to C6 linear, branched, or cyclic hydrocarbyl moiety optionally substituted with hydroxyl groups; wherein each carbon atom in R5 individually comprises no more than one hydroxyl group or no more than one ester group;wherein R5 optionally comprises one or more ether linkages;m=1 to the number of carbon atoms in R5; and wherein said esters have solubility in water of at least 5 ppm at 25° C.;(ii) glycerides having the structure wherein R1═C1 to C7 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R3 and R4 are individually H or R1C(O); and(iii) acetylated saccharides selected from the group consisting of acetylated monosaccharides, acetylated disaccharides, and acetylated polysaccharides;(2) a source of peroxygen; and(3) an enzyme catalyst having perhydrolysis activity, wherein said enzyme catalyst comprises an enzyme having a signature motif that aligns with a reference sequence SEQ ID NO:2 using CLUSTALW, said signature motif comprising: (i) an RGQ motif at amino acid positions 118-120 of SEQ ID NO:2;(ii) a GXSQG motif at amino acid positions 179-183 of SEQ ID NO:2; and(iii) an HE motif at amino acid positions 298-299 of SEQ ID NO:2;wherein said enzyme has at least 95% amino acid identity to SEQ ID NO:4; and(b) combining the selected set of reaction components under aqueous reaction conditions to form a reaction mixture; whereby reaction products are formed comprising enzymatically-produced peroxycarboxylic acid; wherein (1) the pH of the aqueous reaction mixture remains in the range of from about 6.0 to about 9.0; and(2) the concentration of peroxycarboxylic acid produced five minutes after combining the reaction components is not exceeded by more than 100% at a reaction time equal to or greater than 30 minutes after combining the reaction components. 18. The process of claim 17 wherein concentration of peroxycarboxylic acid produced five minutes after combining the reaction components is not exceeded by more than 50% at a reaction time equal to or greater than 30 minutes after combining the reaction components. 19. The process of claim 18 wherein the concentration of peroxycarboxylic acid produced five minutes after combining the reaction components is not exceeded by more than 20% at a reaction time equal to or greater than 30 minutes after combining the reaction components. 20. A composition comprising: (a) a set of reaction components comprising: (1) at least one substrate selected from the group consisting of: (i) esters having the structure [X]mR5 whereinX=an ester group of the formula R6—C(O)O;R6═C1 to C7 linear, branched or cyclic hydrocarbyl moiety, optionally substituted with hydroxyl groups or C1 to C4 alkoxy groups, wherein R6 optionally comprises one or more ether linkages for R6═C2 to C7;R5=a C1 to C6 linear, branched, or cyclic hydrocarbyl moiety optionally substituted with hydroxyl groups; wherein each carbon atom in R5 individually comprises no more than one hydroxyl group or no more than one ester group;wherein R5 optionally comprises one or more ether linkages;m=1 to the number of carbon atoms in R5; andwherein said esters have solubility in water of at least 5 ppm at 25° C.;(ii) glycerides having the structure wherein R1═C1 to C7 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R3 and R4 are individually H or R1C(O); and(iii) acetylated saccharides selected from the group consisting of acetylated monosaccharides, acetylated disaccharides, and acetylated polysaccharides;(2) a source of peroxygen; and(3) an enzyme catalyst having perhydrolysis activity, wherein said enzyme catalyst comprises an enzyme having a signature motif that aligns with a reference sequence SEQ ID NO:2 using CLUSTALW, said signature motif comprising: (i) an RGQ motif at amino acid positions 118-120 of SEQ ID NO:2;(ii) a GXSQG motif at amino acid positions 179-183 of SEQ ID NO:2; and(iii) an HE motif at amino acid positions 298-299 of SEQ ID NO:2;wherein said enzyme also has at least 95% amino acid identity to SEQ ID NO:4; and(b) at least one peroxycarboxylic acid formed upon combining the set of reaction components of (a). 21. The composition of claim 20 wherein the enzyme catalyst comprises an enzyme having amino acid sequence SEQ ID NO:4. 22. A kit comprising: (a) a first compartment comprising (1) an enzyme catalyst comprising an enzyme having at least 95% amino acid identity to SEQ ID NO: 4;(2) at least one substrate selected from the group consisting of: (i) esters having the structure [X]mR5 whereinX=an ester group of the formula R5—C(O)O;R6═C1 to C7 linear, branched or cyclic hydrocarbyl moiety, optionally substituted with hydroxyl groups or C1 to C4 alkoxy groups, wherein R6 optionally comprises one or more ether linkages for R6═C2 to C7;R5=a C1 to C6 linear, branched, or cyclic hydrocarbyl moiety optionally substituted with hydroxyl groups; wherein each carbon atom in R5 individually comprises no more than one hydroxyl group or no more than one ester group;wherein R5 optionally comprises one or more ether linkages;m=1 to the number of carbon atoms in R5; and wherein said esters have solubility in water of at least 5 ppm at 25° C.;(ii) glycerides having the structure wherein R1═C1 to C7 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R3 and R4 are individually H or R1C(O); and(iii) acetylated saccharides selected from the group consisting of acetylated monosaccharides, acetylated disaccharides, and acetylated polysaccharides; and(3) an optional buffer; and(b) a second compartment comprising (1) a source of peroxygen;(2) a peroxide stabilizer; and(3) an optional buffer.
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