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大肠杆菌K12的glpT转录受厌氧状态和fnr的调控。

Transcription of glpT of Escherichia coli K12 is regulated by anaerobiosis and fnr.

作者信息

Wong K K, Kwan H S

机构信息

Department of Biology, Chinese University of Hong Kong, Shatin.

出版信息

FEMS Microbiol Lett. 1992 Jul 1;73(1-2):15-8. doi: 10.1016/0378-1097(92)90574-8.

Abstract

The transcriptional expression of the sn-glycerol 3-phosphate transport gene, glpT, was studied with a glpT-lac fusion contained on a low-copy-number plasmid pFZY1. The fusion was isolated during a 'shot gun' cloning of promoters expressed under anaerobic growth conditions. It was shown that glpT was induced six-fold by anaerobiosis. Furthermore, aerobic expression of glpT was induced by the substrate glycerol 3-phosphate, while the anaerobic expression of glpT was decreased by nitrate, glucose and a fnr mutation. However, nitrate repression on glpT expression was relieved if the upstream region from -290 of the transcription site was removed.

摘要

利用低拷贝数质粒pFZY1上携带的glpT-lac融合基因,研究了sn-甘油-3-磷酸转运基因glpT的转录表达。该融合基因是在厌氧生长条件下表达的启动子的“鸟枪法”克隆过程中分离得到的。结果表明,厌氧可使glpT的表达诱导6倍。此外,底物甘油-3-磷酸可诱导glpT的需氧表达,而硝酸盐、葡萄糖和fnr突变则可降低glpT的厌氧表达。然而,如果去除转录位点-290上游区域,则可解除硝酸盐对glpT表达的抑制作用。

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