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大肠杆菌硝酸还原酶(narGHJI)操纵子由NarL和Fnr激活需要整合宿主因子。

Activation of the Escherichia coli nitrate reductase (narGHJI) operon by NarL and Fnr requires integration host factor.

作者信息

Schröder I, Darie S, Gunsalus R P

机构信息

Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024.

出版信息

J Biol Chem. 1993 Jan 15;268(2):771-4.

PMID:8419352
Abstract

Integration host factor protein (IHF) was shown to be required for Fnr- and NarL-dependent activation of the nitrate reductase (narGHJI) operon of Escherichia coli in response to nitrate availability and anaerobiosis. Using a narG-lacZ reporter fusion to evaluate narGHJI expression in vivo both the nitrate and anaerobic dependent controls were severely impaired in a himA mutant compared with the wild type strain. IHF was also required for Fnr-independent anaerobic control of narGHJI expression. In vitro, purified IHF protein was shown to bind to a narG promoter fragment with an apparent dissociation value of 5 nM by use of a gel shift assay. DNase I footprinting studies revealed that IHF protects a 37-base pair region centered 125 base pairs 5' of the narG transcription site. These studies suggest that the IHF protein performs a DNA bending function at the narG promoter to allow nitrate-dependent activation by the NarL regulatory protein, and second, it enhances the Fnr-dependent expression from the narG promoter under anaerobic cell growth conditions. A model whereby three transcriptional activators, NarL, IHF, and Fnr, induce expression of a sigma 70-dependent promoter for the narGHJI operon is discussed.

摘要

整合宿主因子蛋白(IHF)被证明是大肠杆菌硝酸盐还原酶(narGHJI)操纵子响应硝酸盐可用性和厌氧状态时,Fnr和NarL依赖性激活所必需的。使用narG-lacZ报告基因融合来评估体内narGHJI的表达,与野生型菌株相比,himA突变体中硝酸盐和厌氧依赖性控制均严重受损。IHF也是narGHJI表达的Fnr非依赖性厌氧控制所必需的。在体外,通过凝胶迁移试验表明,纯化的IHF蛋白与narG启动子片段结合,其表观解离值为5 nM。DNase I足迹研究表明,IHF保护一个以narG转录位点5'端125个碱基对为中心的37个碱基对区域。这些研究表明,IHF蛋白在narG启动子处执行DNA弯曲功能,以允许NarL调节蛋白进行硝酸盐依赖性激活,其次,它在厌氧细胞生长条件下增强了narG启动子的Fnr依赖性表达。本文讨论了一种模型,其中三种转录激活因子NarL、IHF和Fnr诱导narGHJI操纵子的σ70依赖性启动子的表达。

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