Method for producing L-amino acid

Patent metadata

Field	Value
Publication number	US-9464306-B2
Application number	US-200913126534-A
Country	US
Kind code	B2
Filing date	Oct 28, 2009
Priority date	Oct 29, 2008
Publication date	Oct 11, 2016
Grant date	Oct 11, 2016

Abstract

The present invention relates to a method for producing an L-amino acid by reacting an enantiomeric mixture of an N-succinyl amino acid with L-succinylase in the presence of N-acylamino acid racemase to specifically hydrolyze the L-form. In particular, the present invention relates to a method for producing an L-amino acid in high yield by using an N-succinyl amino acid whose dissolved concentration is particularly low as a raw material to perform a reaction while precipitating the produced L-amino acid out of the reaction system. The present invention enables efficient production of an L-amino acid having high optical purity, particularly an L-amino acid useful as a raw material for products such as pharmaceutical products and agricultural chemicals.

First claim

The invention claimed is:

1. A method for producing an L-amino acid by hydrolyzing a succinyl group of an N-succinyl amino acid in an L-form selective manner with L-succinylase, while racemizing an enantiomeric mixture of the N-succinyl amino acid with N-acylamino acid racemase,
the reaction being performed with precipitating the produced L-amino acid.

2. The method according to claim 1 ,
wherein the L-amino acid has a dissolved concentration of 1% by weight or lower.

3. The method according to claim 1 ,
wherein the N-succinyl amino acid is represented by formula (I):

wherein R represents an optionally substituted C1 to C20 alkyl group, an optionally substituted C2 to C20 alkenyl group, an optionally substituted C2 to C20 alkynyl group, an optionally substituted C4 to C20 aryl group, or an optionally substituted C5 to C20 aralkyl group; and
the L-amino acid is represented by formula (II):

wherein R is the same as defined above.

4. The method according to claim 3 ,
wherein R in formula (I) and formula (II) is a 4-bromobenzyl group, a 3-fluorobenzyl group, a naothylmethyl group, an indanyl group, or a 6-heptenyl group.

5. The method according to any one of the claims 1 to 4 ,
wherein the enantiomeric mixture of the N-succinyl amino acid is racemized by a N-acylamino acid racemase obtained from a microorganism of the genus Geobacillus or Thermus , and the succinyl group of the N-succinyl amino acid is hydrolyzed by a L-succinylase obtained from a microorganism of the genus Geobacillus.

6. The method according to claim 5 ,
wherein the N-acylamino acid racemase is obtained from Geobacillus kaustophilus or Thermus thermophilus , and the L-succinylase is obtained from Geobacillus kaustophilus.

7. The method according to claim 6 ,
wherein the N-acylamino acid racemase is obtained from Geobacillus kaustophilus NBRC 102445 or Thermus thermophiles HB8, and the L-succinylase is obtained from Geobacillus kaustophilus NBRC 102445.

8. The method according to any one of claims 1 to 4 ,
wherein a transformant transformed by a vector that contains DNA encoding a N-acylamino acid racemase and DNA encoding a L-succinylase is used for hydrolyzing the succinyl group of the N-succinyl amino acid and racemizing the enantiomeric mixture of the N-succinyl amino acid.

Assignees

• Nojiri Masutoshi
• Nishiyama Tozo
• Taoka Naoaki
• Kaneka Corp

Inventors

• Nojiri Masutoshi
• Nishiyama Tozo
• Taoka Naoaki

Classifications

• C12P13/04 Primary

  Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title

• C12N9/90

  Isomerases (5.) · CPC title

• C07C227/30

  Preparation of optical isomers · CPC title

• C12N9/104

  Aminoacyltransferases (2.3.2) · CPC title

• C12P13/222

  Phenylalanine · CPC title