IP Library Granted Patent US 7,572,608
Granted Patent B2
US 7,572,608 · App. 10/548,271 · Granted Aug 11, 2009

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Quick Facts
Patent No.
US 7,572,608
App. No.
10/548,271
Granted
Aug 11, 2009
Kind
B2
Abstract

The invention relates to R-hydroxynitrillyases from the family of Rosaceae that are characterized by an improved substrate tolerance and increased stability. In the active center of the R-hydroxynitrillyases either a) an alanine group is substituted by glycine, valine, leucine, isoleucine, or phenylalanine or b) a phenylalanine group is substituted by alanine, glycine valine, leucine or isoleucine, or c) a leucine group is substituted by alanine, glycine, valine, isoleucine or phenylalanine, or d) an isoleucine group is substituted by alanine, glycine, valine, leucine or phenylalanine. The invention also relates to the use of these lyases in the production of enantiomer-pure R- or S-cyanohydrines.

Claims (11)

1. An R-hydroxynitrile (R-HNL) lyase comprising the amino acid sequence of SEQ ID NO: 27.

2. A process for preparing enantiopure R-cyanohydrin comprising:

(a) contacting a substrate in the presence of a cyanide ion with the R-hydroxynitrile lyase of claim 1 in a reaction mixture, and

(b) recovering enantiopure R-cyanohydrin from the reaction mixture.

3. A process for preparing enantiopure R-cyanohydrins comprising contacting aliphatic, aromatic or heteroaromatic aldehydes or ketones in the presence of a cyanide ion with the R-hydroxynitrile lyase of claim 1 at a pH from 1.8 to 7.

4. The R-hydroxynitrile lyase of claim 1 which is obtained by expressing the nucleic acid encoding the R-hydroxvnitrile lyase of claim 1 in a microorganism.

5. The R-hydroxynitrile lyase of claim 4 , wherein said recombinant R-hydroxynitrile lyase is produced in a microorganism selected from the group consisting of Pichia pastoris, Saccharomyces cerevisiae, Escherichia coli, Bacillus subtilis, Kluyveromyces lactis, Aspergillus niger, Penicillium chrysogenum, Pichia methanolica, Pichia polymorpha, Pichia anomala , and Schizosaccharomyces pombe.

6. The R-hydroxynitrile lyase of claim 1 which is obtained by site-specific mutagenesis.

7. A process for preparing enantiopure R-cyanohydrin comprising contacting 2-chlorobenzaldehyde or 3-chlorobenzaldehyde in the presence of a cyanide ion with the R-hydroxynitrile lyase of claim 1 at a pH from 1.8 to 7.

8. The process according to claim 2 wherein said contacting occurs at a temperature from −5° C. to +45° C.

9. The process according to claim 7 wherein said contacting occurs at a temperature from −5° C. to +45° C.

Assignments (4)
RELEASE (REEL 032424 / FRAME 0001) Recorded Sep 28, 2017
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG
Reel/Frame 044037/0879 →
NOTICE OF SUCCESSION OF AGENCY FOR PATENT SECURITY INTEREST PREVIOUSLY RECORDED AT REEL/FRAME (032424/0001) Recorded Jul 12, 2017
From: UBS AG, STAMFORD BRANCH, AS PRIOR AGENT
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS SUCCESSOR AGENT
Reel/Frame 043165/0987 →
SECURITY INTEREST Recorded Mar 11, 2014
From: DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 032424/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2005
From: SKRANC, WOLFGANG; GLIEDER, ANTON; GRUBER, KARL; WEIS, ROLAND; LUITEN, RUUD
To: DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG
Reel/Frame 017652/0183 →