Chen Y C, Peoples O P, Walsh C T
Department of Biology and Chemistry, Massachusetts Institute of Technology, Cambridge 02139.
J Bacteriol. 1988 Feb;170(2):781-9. doi: 10.1128/jb.170.2.781-789.1988.
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.
通过免疫筛选方法分离出了不动杆菌属菌株NCIB 9871中环己酮单加氧酶的编码基因。我们确定了该基因的位置并测定了其核苷酸序列。结构基因长1626个核苷酸,编码一个由542个氨基酸组成的多肽;还报道了编码区5'端的389个核苷酸和3'端的108个核苷酸。通过核苷酸序列的翻译得出了该酶完整的氨基酸序列。通过将氨基酸序列与核苷酸结合折叠的共有序列进行比较,我们在酶的NH2末端(第6至18位残基)鉴定出一个潜在的黄素结合位点,以及一个从蛋白质的第176位残基延伸至第208位残基的潜在烟酰胺结合位点。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表达系统,以促进基因操作。