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类H-NS蛋白HvrA通过与特定的固氮基因启动子结合来调控光合紫色细菌荚膜红细菌中固氮基因的表达。

The H-NS-like protein HvrA modulates expression of nitrogen fixation genes in the phototrophic purple bacterium Rhodobacter capsulatus by binding to selected nif promoters.

作者信息

Raabe Karsten, Drepper Thomas, Riedel Kai Uwe, Masepohl Bernd, Klipp Werner

机构信息

Ruhr-Universität Bochum, Fakultät für Biologie, Lehrstuhl für Biologie der Mikroorganismen, 44780, Bochum, Germany.

出版信息

FEMS Microbiol Lett. 2002 Nov 5;216(2):151-8. doi: 10.1111/j.1574-6968.2002.tb11429.x.

Abstract

Genetic analyses based on chromosomal lac fusions to nitrogen fixation (nif) genes demonstrated that NifA-dependent transcriptional activation of expression of Rhodobacter capsulatus nifH and nifB1 was negatively modulated by HvrA, whereas regulation of rpoN, nifA1, and nifA2 was independent of HvrA. Expression of hvrA itself was not influenced by a mutation in ntrC, which is absolutely essential for N(2) fixation. Furthermore, HvrA accumulated to comparable levels in the presence and absence of ammonium, suggesting that the amount of HvrA in the cells does not differ under nitrogenase-repressing or -derepressing conditions. In addition, competitive gel retardation studies with HvrA-His(6) purified from R. capsulatus were carried out, demonstrating preferential binding of HvrA to the nifH promoter region.

摘要

基于与固氮(nif)基因的染色体lac融合的遗传分析表明,荚膜红细菌nifH和nifB1表达的NifA依赖性转录激活受到HvrA的负调控,而rpoN、nifA1和nifA2的调控则独立于HvrA。hvrA自身的表达不受ntrC突变的影响,ntrC对固氮绝对必要。此外,无论有无铵存在,HvrA积累到相当的水平,这表明在固氮酶抑制或去抑制条件下细胞中HvrA的量没有差异。另外,利用从荚膜红细菌纯化的HvrA-His(6)进行了竞争性凝胶阻滞研究,证明HvrA优先结合到nifH启动子区域。

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