Isobe Kimiyasu, Tamauchi Hiroshi, Fuhshuku Ken-Ichi, Nagasawa Shouko, Asano Yasuhisa
Department of Biological Chemistry and Food Science, Faculty of Agriculture, Iwate University, 3-18-8 Ueda, Morioka 020-8550, Japan.
Enzyme Res. 2010 Aug 5;2010:567210. doi: 10.4061/2010/567210.
A simple enzymatic method for production of a wide variety of D-amino acids was developed by kinetic resolution of DL-amino acids using L-amino acid oxidase (L-AAO) with broad substrate specificity from Rhodococcus sp. AIU Z-35-1. The optimum pH of the L-AAO reaction was classified into three groups depending on the L-amino acids as substrate, and their respective activities between pH 5.5 and 8.5 accounted for more than 60% of the optimum activity. The enzyme was stable in the range from pH 6.0 to 8.0, and approximately 80% of the enzyme activity remained after incubation at 40°C for 60 min at pH 7.0. D-Amino acids such as D-citrulline, D-glutamine, D-homoserine or D-arginine, which are not produced by D-aminoacylases or D-hydantoinases, were produced from the racemic mixture within a 24-hr reaction at 30°C and pH 7.0. Thus, the present method using L-AAO was versatile for production of a wide variety of D-amino acids.
利用来自红球菌属AIU Z-35-1的具有广泛底物特异性的L-氨基酸氧化酶(L-AAO),通过对DL-氨基酸进行动力学拆分,开发了一种简单的酶法来生产多种D-氨基酸。根据作为底物的L-氨基酸,L-AAO反应的最佳pH分为三组,在pH 5.5至8.5之间它们各自的活性占最佳活性的60%以上。该酶在pH 6.0至8.0范围内稳定,在pH 7.0下于4℃孵育60分钟后,约80%的酶活性仍然保留。在30℃和pH 7.0下进行24小时反应,从外消旋混合物中产生了D-瓜氨酸、D-谷氨酰胺、D-高丝氨酸或D-精氨酸等D-氨基酸,这些氨基酸不是由D-氨基酸酰化酶或D-海因酶产生的。因此,使用L-AAO的本方法对于生产多种D-氨基酸具有通用性。