Method for the enzyme-catalysed hydrolysis of polyacrylic acid esters, and esterases used therefor

Patent metadata

Field	Value
Publication number	US-2016168602-A1
Application number	US-201615013299-A
Country	US
Kind code	A1
Filing date	Feb 2, 2016
Priority date	Jul 18, 2008
Publication date	Jun 16, 2016
Grant date	—

Abstract

The invention relates to a method for the enzyme-catalysed hydrolysis of polyacrylic acid esters. According to the method, at least one polyacrylic acid ester is provided and incubated with at least one enzyme selected from enzymes (EC 3.1) acting on ester bindings, until the ester groups contained in the polyacrylic acid ester are partially or fully hydrolytically split, and optionally the modified polymer obtained thereby is isolated. The invention also relates to the enzymes used and mutants thereof, nucleic acids coding for the enzymes, vectors comprising the nucleic acids, micro-organisms comprising the vectors, and the use of the enzymes, the vectors or the micro-organisms for carrying out a method for the enzyme-catalysed hydrolysis of polyacrylic acid esters. The present application also relates to polymer reaction products that can be obtained by the method, and methods for producing esterases.

First claim

1 . A functional esterase mutant of the esterase of SEQ ID NO: 1, wherein said functional esterase mutant has:
i) comparable or increased activity with respect to the hydrolysis of polyacrylic acid esters relative to the esterase of SEQ ID NO: 1; ii) increased stability relative to SEQ ID NO: 1; and/or iii) increased hydrolytic activity against at least one of polyacrylic acid methyl esters or polyacrylic acid butyl relative to the esterase of SEQ ID NO: 1; and wherein said functional esterase mutant is: a) a mutant of the esterase of SEQ ID NO: 1 and comprises a mutation in one or more of the amino acid residues selected from Ser17, Gly132, Trp134, Arg155, Glu251, Ala311 and Glu316; b) a mutant of the esterase of SEQ ID NO: 1 and comprises at least one of the mutations selected from Ser17Leu, Gly132Ser, Glu251Gly, Ala311Val and Glu316Lys, c) a mutant of the esterase of SEQ ID NO: 1 and comprises at least one of the mutations selected from Pro8Leu, Gly132Ser, Trp134Arg, Arg155Cys, Glu251Gly, Ala311Val and Glu316Lys; or d) a mutant of the esterase of SEQ ID NO: 1 and comprises the amino acid sequence of SEQ ID NO: 37 or SEQ ID NO: 38.

2 . A method for the enzyme-catalyzed hydrolysis of polyacrylic acid esters, the method comprising:
a) preparing a polyacrylic acid ester, b) incubating the polyacrylic acid ester with the functional esterase mutant of claim 1 , whereby at least one ester group of the polyacrylic acid ester is hydrolytically cleaved; and c) optionally, isolating the modified polymer.

3 . The method of claim 2 , wherein the polyacrylic acid ester is a homopolymer or a copolymer.

4 . The method of claim 2 , wherein the polyacrylic acid ester is an alternating copolymer, a random copolymer, a gradient copolymer, a block copolymer or a graft copolymer.

5 . The method of claim 2 , wherein the modified polymer comprises monomer building blocks of general formula I
R 1 R 2 C═CR 3 —COOR 4   (I)
wherein R 1 , R 2 and R 3 may be identical or different and are selected from the group consisting of H, a linear C 1 -C 20 hydrocarbyl residue and a branched C 3 -C 20 hydrocarbyl residue, and R 4 is selected from the group consisting of H, a linear C 1 -C 20 hydrocarbyl residue, a branched C 3 -C 20 hydrocarbyl residue and a cyclic C 3 -C 20 hydrocarbyl residue, the hydrocarbyl residue optionally is substituted with one or more identical or different groups, selected from hydroxyl, amino, epoxide, thiol groups and halogen atoms, and in the polymer, in at least one monomer building block of formula I, R 4 is not H.

6 . The method of claim 5 , wherein the polyacrylic acid ester contains, additionally to the monomers of formula I, at least one further monomer component different therefrom, in a molar proportion from 0 to 15 mol. %, which is preferably selected from N-vinylformamide, methacrylic acid, methacrylic acid ester, itaconic acid, itaconic acid ester, vinylphosphonic acid, vinylsulfonic acid, vinyl alcohol, N-vinylimidazole, N-vinylformamide, styrene, maleic acid, maleic acid ester, ethylene and/or propylene, and acrylamide and substituted acrylamides, where the substituent is selected from a linear C 1 -C 20 hydrocarbyl residue, a branched C 3 -C 20 hydrocarbyl residue and a cyclic C 3 -C 20 hydrocarbyl residue, the hydrocarbyl residue optionally being substituted with one or more identical or different groups, which are selected from hydroxyl, amino, epoxide, thiol groups and halogen atoms.

7 . A functional esterase mutant of the esterase of SEQ ID NO: 2, wherein said functional esterase mutant has:
i) comparable or increased activity with respect to the hydrolysis of polyacrylic acid esters relative to the esterase of SEQ ID NO: 2; ii) increased stability relative to SEQ ID NO: 2; and/or iii) increased hydrolytic activity against at least one of polyacrylic acid methyl esters or polyacrylic acid butyl relative to the esterase of SEQ ID NO: 2; and wherein said functional esterase mutant is: a) a mutant of the esterase of SEQ ID NO: 2 and comprises a mutation in one or more of the amino acid residues selected from Phe138, Val150, Leu160, Thr188 and Leu193; or b) a mutant of the esterase of SEQ ID NO: 2 and comprises one of the following mutations or combinations of mutations: (a) Phe138Ala; (b) Phe138Ala, Thr188Ser; (c) Phe138Ala, Leu160Ala, Thr188Ser; (d) Leu193Ala; (e) Leu193Ala, Phe138Ala, Thr188Ser, Val150Ala; (f) Leu193Ala, Phe138Ala, Thr188Ser; (g) Leu193Ala, Phe138Ala, Thr188Ser, Leu160Ala, Val150Ala; (h) Val150Ala; (i) Val150Ala, Thr188Ser; (j) Leu193Ala, Phe138Val; (k) Leu193Ala, Phe138Val, Thr188Ser, Val150Ala; (1) Leu193Ala, Thr188Ser; (m) Leu193Ala, Phe138Val, Thr188Ser; (n) Leu193Ala, Phe138Val, Thr188Ser, Leu160Ala; (o) Phe138Val, Val150Ala, Thr188Ser; (p) Phe138Val; or (q) Phe138Val, Thr188Ser.

8 . A method for the enzyme-catalyzed hydrolysis of polyacrylic acid esters, the method comprising:
a) preparing a polyacrylic acid ester, b) incubating the polyacrylic acid ester with the functional esterase mutant of claim 7 , whereby at least one ester group of the polyacrylic acid ester is hydrolytically cleaved; and c) optionally, isolating the modified polymer.

9 . The method of claim 8 , wherein the polyacrylic acid ester is a homopolymer or a copolymer.

10 . The method of claim 8 , wherein the polyacrylic acid ester is an alternating copolymer, a random copolymer, a gradient copolymer, a block copolymer or a graft copolymer.

11 . The method of claim 8 , wherein the modified polymer comprises monomer building blocks of general formula I
R 1 R 2 C═CR 3 —COOR 4   (1)
wherein R 1 , R 2 and R 3 may be identical or different and are selected from the group consisting of H, a linear C 1 -C 20 hydrocarbyl residue and a branched C 3 -C 20 hydrocarbyl residue, and R 4 is selected from the group consisting of H, a linear C 1 -C 20 hydrocarbyl residue, a branched C 3 -C 20 hydrocarbyl residue and a cyclic C 3 -C 20 hydrocarbyl residue, the hydrocarbyl residue optionally is substituted with one or more identical or different groups, selected from hydroxyl, amino, epoxide, thiol groups and halogen atoms, and in the polymer, in at least one monomer building block of formula I, R 4 is not H.

12 . The method of claim 11 , wherein the polyacrylic acid ester contains, additionally to the monomers of formula I, at least one further monomer component different therefrom, in a molar proportion from 0 to 15 mol. %, which is preferably selected from N-vinylformamide, methacrylic acid, methacrylic acid ester, itaconic acid, itaconic acid ester, vinylphosphonic acid, vinylsulfonic acid, vinyl alcohol, N-vinylimidazole, N-vinylformamide, styrene, maleic acid, maleic acid ester, ethylene and/or propylene, and acrylamide and substituted acrylamides, where the substituent is selected from a linear C 1 -C 20 hydrocarbyl residue, a branched C 3 -C 20 hydrocarbyl residue and a cyclic C 3 -C 20 hydrocarbyl residue, the hydrocarbyl residue optionally being substituted with one or more identical or different groups, which are selected from hydroxyl, amino, epoxide, thiol groups and halogen atoms.

Assignees

• Basf Se

Inventors

• Hauer Bernhard
• HÖFFKEN Hans Wolfgang
• Kvarnström Branneby Cecilia
• Schwab Helmut
• Feichtenhofer Sabine
• Buchebner Marlene
• Pohn Brigitte

Classifications

• C12N9/16 Primary

  acting on ester bonds (3.1) · CPC title

• C12P7/62 Primary

  Carboxylic acid esters · CPC title

• C12N9/18

  Carboxylic ester hydrolases {(3.1.1)} · CPC title

• C08F8/12

  Hydrolysis · CPC title

• C12Y301/01001

  Carboxylesterase (3.1.1.1) · CPC title