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Identification and functional characterization of NifA variants that are independent of GlnB activation in the photosynthetic bacterium Rhodospirillum rubrum

机译:NiFa变体的鉴定和功能表征,其与光合菌罗姆摩勒姆肾上腺素中的GLNB活化无关

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摘要

The activity of NifA, the transcriptional activator of the nitrogen fixation (nif) gene, is tightly regulated in response to ammonium and oxygen. However, the mechanisms for the regulation of NifA activity are quite different among various nitrogen-fixing bacteria. Unlike the well-studied NifL–NifA regulatory systems in Klebsiella pneumoniae and Azotobacter vinelandii, in Rhodospirillum rubrum NifA is activated by a direct protein–protein interaction with the uridylylated form of GlnB, which in turn causes a conformational change in NifA. We report the identification of several substitutions in the N-terminal GAF domain of R. rubrum NifA that allow NifA to be activated in the absence of GlnB. Presumably these substitutions cause conformational changes in NifA necessary for activation, without interaction with GlnB. We also found that wild-type NifA can be activated in a GlnB-independent manner under certain growth conditions, suggesting that some other effector(s) can also activate NifA. An attempt to use Tn5 mutagenesis to obtain mutants that altered the pool of these presumptive effector(s) failed, though much rarer spontaneous mutations in nifA were detected. This suggests that the necessary alteration of the pool of effector(s) for NifA activation cannot be obtained by knockout mutations.
机译:NiFa的活性是氮固定(NIF)基因的转录激活剂,响应于铵和氧气而紧密调节。然而,在各种氮素固定细菌中,调节NiFa活性的机制在各种氮气纤细胞膜中是完全不同的。与富裕的NiFl-NiFa调节系统不同于Klebsiella肺炎和vinelancii,在Rhodospirillum rubrum NiFa中,通过与GLNB的尿苷化形式的直接蛋白质 - 蛋白质相互作用来激活,这反过来导致NIFA的构象变化。我们报告鉴定R. Rubrum NiFa的N-末端GAF结构域中的几种取代,其允许NIFA在没有GLNB的情况下被激活。据推测,这些取代导致激活所需NIFA的构象变化,而不与GLNB相互作用。我们还发现,在某些生长条件下,野生型NiFa可以以GLNB的方式以独立于GLNB的方式激活,表明一些其他效应器也可以激活NIFA。试图使用TN5诱变获得改变这些推测效应器的池的突变体失败,但是检测到NIFA中的许多自发性突变。这表明不能通过敲除突变获得对NiFa活化的效应池的必要变化。

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