Suppr超能文献

在严谨反应中发生改变的大肠杆菌rnpB启动子突变体。

Escherichia coli rnpB promoter mutants altered in stringent response.

作者信息

Jung Y H, Lee Y

机构信息

Department of Chemistry, Korea Advanced Institute of Science and Technology, Taejon.

出版信息

Biochem Biophys Res Commun. 1997 Jan 23;230(3):582-6. doi: 10.1006/bbrc.1996.6005.

Abstract

The promoter of the rnpB gene (encoding the RNA component of Escherichia coli RNase P) shares a consensus discriminator sequence, located between the -10 hexamer sequence and the transcription start site, with other promoters whose activities are repressed upon stringent condition. Under stringent conditions induced by seryl-tRNA starvation the transcription of the rnpB gene was repressed in wild type E. coli but not in a relaxed strain carrying a relA- mutation. Site-directed mutagenesis was carried out to examine sequences of the rnpB promoter necessary for stringent control. The results indicate that the discriminator region is responsible for the transcription repression of the rnpB gene during the stringent response and that both the content and position of GC pairs in the region determine the strength of negative stringent signals.

摘要

rnpB基因(编码大肠杆菌核糖核酸酶P的RNA组分)的启动子与其他在严格条件下活性受到抑制的启动子共有一个共有鉴别序列,该序列位于-10六聚体序列与转录起始位点之间。在丝氨酰tRNA饥饿诱导的严格条件下,野生型大肠杆菌中rnpB基因的转录受到抑制,但在携带relA-突变的松弛型菌株中则不受抑制。进行了定点诱变以检查严格控制所需的rnpB启动子序列。结果表明,鉴别区负责严格应答期间rnpB基因的转录抑制,并且该区域中GC对的含量和位置都决定了负性严格信号的强度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验