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来自大肠杆菌的磷酸转乙酰酶编码基因的克隆。

Cloning of a gene coding for phosphotransacetylase from Escherichia coli.

作者信息

Yamamoto-Otake H, Matsuyama A, Nakano E

机构信息

Research and Development Division, Kikkoman Corporation, Chiba, Japan.

出版信息

Appl Microbiol Biotechnol. 1990 Sep;33(6):680-2. doi: 10.1007/BF00604937.

Abstract

A phosphotransacetylase gene (pta) has been cloned from a genomic DNA library of Escherichia coli 1100, a derivative of strain K-12. The phosphotransacetylase activities of pta+ plasmid-containing strains were amplified about 150-fold under control of the lac promoter. The molecular weight of the phosphotransacetylase was estimated to be about 81,000 by sodium dodecyl sulphate-polyacrylamide gel electrophoresis. The pta gene was found to be downstream of ackA by a combination of restriction analysis and plasmid subcloning. It is located about 13 kb upstream of the purF-folC-hisT region of the chromosome.

摘要

已从K-12菌株的衍生物大肠杆菌1100的基因组DNA文库中克隆出磷酸转乙酰酶基因(pta)。含pta⁺质粒的菌株中磷酸转乙酰酶的活性在乳糖启动子的控制下扩增了约150倍。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳估计磷酸转乙酰酶的分子量约为81,000。通过限制性分析和质粒亚克隆相结合的方法发现pta基因位于ackA的下游。它位于染色体上purF-folC-hisT区域上游约13 kb处。

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