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Acinetobacter cyclohexanone monooxygenase: gene cloning and sequence determination.

机译:不动杆菌环己酮单加氧酶:基因克隆和序列测定。

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摘要

The gene coding for cyclohexanone monooxygenase from Acinetobacter sp. strain NCIB 9871 was isolated by immunological screening methods. We located and determined the nucleotide sequence of the gene. The structural gene is 1,626 nucleotides long and codes for a polypeptide of 542 amino acids; 389 nucleotides 5' and 108 nucleotides 3' of the coding region are also reported. The complete amino acid sequence of the enzyme was derived by translation of the nucleotide sequence. From a comparison of the amino acid sequence with consensus sequences of nucleotide-binding folds, we identified a potential flavin-binding site at the NH2 terminus of the enzyme (residues 6 to 18) and a potential nicotinamide-binding site extending from residue 176 to residue 208 of the protein. An overproduction system for the gene to facilitate genetic manipulations was also constructed by using the tac promoter vector pKK223-3 in Escherichia coli.
机译:不动杆菌属中编码环己酮单加氧酶的基因。通过免疫筛选方法分离出NCIB 9871菌株。我们找到并确定了该基因的核苷酸序列。结构基因长1,626个核苷酸,编码542个氨基酸的多肽。还报道了编码区的389个核苷酸5'和108个核苷酸3'。该酶的完整氨基酸序列通过核苷酸序列的翻译而获得。通过比较氨基酸序列与核苷酸结合折叠的共有序列,我们确定了该酶在NH2末端的潜在黄素结合位点(残基6至18)和从残基176延伸至残基的潜在烟酰胺结合位点。蛋白质的残基208。还通过在大肠杆菌中使用tac启动子载体pKK223-3构建了该基因的过量生产系统,以促进遗传操作。

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