The molecular cloning and sequencing of the nitrilase gene of Rhodococcus rhodochrous PA‐34

T. Bhalla, M. Aoshima, S. Misawa, R. Muramatsu, K. Furuhashi
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引用次数: 17

Abstract

The nitrilase of Rhodococcus rhodochrous PA-34 catalyzes the production of optically active amino acids from aminonitriles. The amino acid sequence of the NH 2 terminus of the purified nitrilase was determined for the preparation of a synthetic oligonucleotide as a southern hybridization probe. A 9.5-kbp Pst I-fragment, which hybridized with the oligonucleotide probe, was isolated from R. rhodochrous PA-34 genomic libraries constructed in pUC 19. Nucleotide sequence analysis revealed that the nitrilase gene codes for a putative polypeptide of 380 amino acids which correspond to a relative molecular weight of 41,723.
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Rhodococcus rhodochrous PA‐34硝化酶基因的克隆与测序
Rhodococcus rhodochrous PA-34的腈酶催化氨基腈生成光学活性氨基酸。测定纯化的腈酶nh2末端的氨基酸序列,制备合成的寡核苷酸作为南杂交探针。从pUC 19构建的R. rhodochrous PA-34基因组文库中分离到一个9.5 kbp的Pst - 1片段,并与寡核苷酸探针杂交。核苷酸序列分析表明,该基因编码的推测多肽有380个氨基酸,相对分子量为41723。
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