Production of aromatic D-amino acids from α-keto acids and ammonia by coupling of four enzyme reactions

被引:36
|
作者
Bae, HS
Lee, SG
Hong, SP
Kwak, MS
Esaki, N
Soda, K
Sung, MH
机构
[1] KRIBB, Microbial Convers Res Unit, Taejon 305600, South Korea
[2] Kyoto Univ, Inst Chem Res, Microbial Biochem Lab, Kyoto 611, Japan
[3] Kansai Univ, Dept Biotechnol, Suita, Osaka 564, Japan
关键词
aromatic D-amino acid; D-amino acid aminotransferase; glutamate racemase; alpha-keto acid; multi-enzyme system;
D O I
10.1016/S1381-1177(98)00073-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A multi-enzyme system composed of glutamate racemase, thermostable D-amino acid aminotransferase, glutamate dehydrogenase and formate dehydrogenase was employed for the production of aromatic D-amino acids, D-phenylalanine and D-tyrosine, from the corresponding alpha-keto acids, phenylpyruvate and hydroxyphenylpyruvate, respectively. The optimal concentration of ammonium formate for the production of these D-amino acids was found in the range of 0.25-1.0 M. The optimal concentration of alpha-keto acid was determined to be 50 mM, above which the productivity greatly decreased. To keep the concentration of alpha-keto acid around this concentration, alpha-keto acid was intermittently fed into the multi-enzyme system during the production period. By running the multi-enzyme system for 35 h, 48 gl(-1) of D-phenylalanine and 60 gl(-1) of D-tyrosine were produced with 100% of optical purity from the equimolar amounts of phenylpyruvate and hydroxyphenylpyruvate, respectively. The production levels of both aromatic D-amino acids were demonstrated to be dependent on the stability of glutamate racemase. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:241 / 247
页数:7
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