Suppr超能文献

荚膜红细菌中替代σ因子RpoN的结构与表达;自激活的nifU2-rpoN超级操纵子的生理相关性

Structure and expression of the alternative sigma factor, RpoN, in Rhodobacter capsulatus; physiological relevance of an autoactivated nifU2-rpoN superoperon.

作者信息

Cullen P J, Foster-Hartnett D, Gabbert K K, Kranz R G

机构信息

Department of Biology, Washington University, St. Louis, Missouri 63130.

出版信息

Mol Microbiol. 1994 Jan;11(1):51-65. doi: 10.1111/j.1365-2958.1994.tb00289.x.

Abstract

The alternative sigma factor, RpoN (sigma 54) is responsible for recruiting core RNA polymerase to the promoters of genes required for diverse physiological functions in a variety of eubacterial species. The RpoN protein in Rhodobacter capsulatus is a putative sigma factor specific for nitrogen fixation (nif) genes. Insertional mutagenesis was used to define regions important for the function of the R. capsulatus RpoN protein. Insertions of four amino acids in the predicted helixturn-helix or in the highly conserved C-terminal eight amino acid residues (previously termed the RpoN box), and an in-frame deletion of the glutamine-rich N-terminus completely inactivated the R. capsulatus RpoN protein. Two separate insertions in the second hydrophobic heptad repeat, a putative leucine zipper, resulted in a partially functional RpoN protein. Eight other linkers in the rpoN open reading frame (ORF) resulted in a completely or partially functional RpoN protein. The rpoN gene in R. capsulatus is downstream from the nifHDKU2 genes, in a nifU2-rpoN operon. Results of genetic experiments on the nifU2-rpoN locus show that the rpoN gene is organized in a nifU2-rpoN superoperon. A primary promoter directly upstream of the rpoN ORF is responsible for the initial expression of rpoN. Deletion analysis and insertional mutagenesis were used to define the primary promoter to 50 bp, between 37 and 87 nucleotides upstream of the predicted rpoN translational start site. This primary promoter is expressed constitutively with respect to nitrogen, and it is necessary and sufficient for growth under nitrogen-limiting conditions typically used in the laboratory. A secondary promoter upstream of nifU2 is autoactivated by RpoN and NifA to increase the expression of rpoN, which ultimately results in higher expression of RpoN-dependent genes. Moreover, rpoN expression from this secondary promoter is physiologically beneficial under certain stressful conditions, such as nitrogen-limiting environments that contain high salt (> 50 mM NaCl) or low iron (< 400 nM FeSO4).

摘要

替代σ因子RpoN(σ54)负责将核心RNA聚合酶招募到多种真细菌物种中各种生理功能所需基因的启动子上。荚膜红细菌中的RpoN蛋白是一种假定的对固氮(nif)基因具有特异性的σ因子。采用插入诱变来确定对荚膜红细菌RpoN蛋白功能重要的区域。在预测的螺旋-转角-螺旋结构域或高度保守的C端八个氨基酸残基(以前称为RpoN框)中插入四个氨基酸,以及富含谷氨酰胺的N端的框内缺失,完全使荚膜红细菌RpoN蛋白失活。在第二个疏水七肽重复序列(一种假定的亮氨酸拉链)中的两个单独插入导致了部分功能性的RpoN蛋白。rpoN开放阅读框(ORF)中的其他八个接头导致了完全或部分功能性的RpoN蛋白。荚膜红细菌中的rpoN基因位于nifHDKU2基因的下游,在一个nifU2-rpoN操纵子中。对nifU2-rpoN位点的遗传实验结果表明,rpoN基因组织在一个nifU2-rpoN超级操纵子中。rpoN ORF直接上游的一个主要启动子负责rpoN的初始表达。采用缺失分析和插入诱变将主要启动子定位到50 bp,位于预测的rpoN翻译起始位点上游37至87个核苷酸之间。这个主要启动子在氮方面是组成型表达的,并且对于实验室通常使用的氮限制条件下的生长是必要且充分的。nifU2上游的一个次要启动子被RpoN和NifA自动激活,以增加rpoN的表达,最终导致RpoN依赖性基因的更高表达。此外,在某些应激条件下,例如含有高盐(>50 mM NaCl)或低铁(<400 nM FeSO4)的氮限制环境中,来自这个次要启动子的rpoN表达在生理上是有益的。

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