화학공학소재연구정보센터
Biotechnology Letters, Vol.21, No.8, 711-713, 1999
Simultaneous recognition of two chiral centers in alpha,beta-diastereomeric amino acids by an N-carbamoyl-L-alpha-amino acid amidohydrolase from Alcaligenes xylosoxidans
Cells of Alcaligenes xylosoxidans containing N-carbamoyl-L-alpha-amino acid amidohydrolase strictly distinguished the configuration of not only the alpha-carbon but also the beta-carbon of N-carbamoyl-beta-methylphenylalanine, and produced threo-L-beta-methylphenylalanine specifically from a mixture of the four stereoisomers.