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大肠杆菌中FNR依赖的nirB启动子核苷酸序列的突变分析。

Mutational analysis of the nucleotide sequence at the FNR-dependent nirB promoter in Escherichia coli.

作者信息

Jayaraman P S, Cole J A, Busby S J

机构信息

University of Birmingham, Department of Biochemistry, UK.

出版信息

Nucleic Acids Res. 1989 Jan 11;17(1):135-45. doi: 10.1093/nar/17.1.135.

Abstract

During anaerobic growth of E. coli, the FNR protein activates transcription initiation at the nirB promoter. After chemical synthesis using deliberately contaminated nucleotides, we isolated a series of recombinant plasmids with single point mutations or one base pair deletions in the nirB promoter. The effects of these alterations on the anaerobic induction of promoter activity were measured. Mutations that abolish anaerobic induction identify the -10 hexamer sequence whilst changes that allow reduced induction suggest positions involved in FNR binding. Comparison of the nucleotide sequence of the nirB promoter with other promoters that are regulated by FNR show clear homologies, suggesting consensus sequences for FNR binding sites, and confirming that some of the point mutations described here do indeed act by weakening FNR binding.

摘要

在大肠杆菌厌氧生长期间,FNR蛋白激活nirB启动子处的转录起始。在使用故意污染的核苷酸进行化学合成后,我们分离出了一系列在nirB启动子中具有单点突变或一个碱基对缺失的重组质粒。测量了这些改变对启动子活性厌氧诱导的影响。消除厌氧诱导的突变确定了-10六聚体序列,而允许诱导降低的变化表明了参与FNR结合的位置。将nirB启动子的核苷酸序列与其他受FNR调控的启动子进行比较,显示出明显的同源性,表明了FNR结合位点的共有序列,并证实了此处描述的一些点突变确实是通过削弱FNR结合而起作用的。

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