Ikenaka Y, Nanba H, Yamada Y, Yajima K, Takano M, Takahashi S
Fine Chemicals Research Laboratories, Kaneka Corporation, Hyogo, Japan.
Biosci Biotechnol Biochem. 1998 May;62(5):882-6. doi: 10.1271/bbb.62.882.
For the production of D-amino acids, thermotolerant bacteria producing N-carbamyl-D-amino acid amidohydrolase were isolated from soil by enrichment culture at 45 degrees C with N-carbamyl-D-amino acids as the sole nitrogen source. The enzyme activities and substrate specificities of these strains were examined by the resting cells reaction. One of the enzymes, produced by Pseudomonas sp. strain KNK003A, was purified and characterized, and the amino acids of its N-terminal region were sequenced. A DNA fragment containing the gene for a thermostable N-carbamyl-D-amino acid amidohydrolase was then cloned into Escherichia coli. The gene encoded a peptide of 312 amino acids, with a calculated molecular weight of 35,000. The similarity of the deduced amino acid sequences of this enzyme and a related enzyme from a mesophile, Agrobacterium sp. strain KNK712, was 60%. A database was searched for similar sequences.
为了生产D-氨基酸,以N-氨甲酰-D-氨基酸作为唯一氮源,通过在45℃下进行富集培养,从土壤中分离出了产N-氨甲酰-D-氨基酸酰胺水解酶的耐热细菌。通过静息细胞反应检测了这些菌株的酶活性和底物特异性。对其中一种由假单胞菌属菌株KNK003A产生的酶进行了纯化和特性鉴定,并对其N端区域的氨基酸进行了测序。然后将包含耐热N-氨甲酰-D-氨基酸酰胺水解酶基因的DNA片段克隆到大肠杆菌中。该基因编码一个由312个氨基酸组成的肽段,计算分子量为35000。该酶推导的氨基酸序列与来自嗜温菌土壤杆菌属菌株KNK712的相关酶的相似性为60%。在数据库中搜索了相似序列。