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The NnaR orphan response regulator is essential for the utilization of nitrate and nitrite as sole nitrogen sources in mycobacteria

机译:NnaR孤儿应答调节剂对于利用硝酸盐和亚硝酸盐作为分枝杆菌中唯一的氮源至关重要

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摘要

Nitrogen is an essential component of biological molecules and an indispensable microelement required for the growth of cells. Nitrogen metabolism of Mycobacterium smegmatis is regulated by a number of transcription factors, with the glnR gene product playing a major role. Under nitrogen-depletion conditions, GlnR controls the expression of many genes involved in nitrogen assimilation, including the msmeg_0432 gene encoding NnaR, the homologue of a nitriteitrate transport regulator from Streptomyces coelicolor. In the present study, the role of NnaR in the nitrogen metabolism of M. smegmatis was evaluated. The ∆glnR and ∆nnaR mutant strains were generated and cultured under nitrogen-depletion conditions. Total RNA profiling was used to investigate the potential role of NnaR in the GlnR regulon under nitrogen-depletion and in nitrogen-rich media. We found that disruption of MSMEG_0432 affected the expression of genes involved in nitriteitrate uptake, and its removal rendered mycobacteria unable to assimilate nitrogen from those sources, leading to cell death. RNA-Seq results were validated using quantitative real-time polymerase chain reaction (qRT-PCR) and electrophoretic mobility shift assays (EMSAs). The ability of mutants to grow on various nitrogen sources was evaluated using the BIOLOG Phenotype screening platform and confirmed on minimal Sauton’s medium containing various sources of nitrogen. The ∆glnR mutant was not able to convert nitrates to nitrites. Interestingly, NnaR required active GlnR to prevent nitrogen starvation, and both proteins cooperated in the regulation of gene expression associated with nitrateitrite assimilation. The ∆nnaR mutant was able to convert nitrates to nitrites, but it could not assimilate the products of this conversion. Importantly, NnaR was the key regulator of the expression of the truncated haemoglobin trHbN, which is required to improve the survival of bacteria under nitrosative stress.
机译:氮是生物分子的基本组成部分,是细胞生长所必需的微量元素。耻垢分枝杆菌的氮代谢受多种转录因子调控,其中glnR基因产物起主要作用。在氮耗竭的条件下,GlnR控制着许多与氮同化有关的基因的表达,包括编码NnaR的msmeg_0432基因,NnaR是天蓝链霉菌的亚硝酸盐/硝酸盐转运调节物的同源物。在本研究中,评估了NnaR在耻垢分枝杆菌氮代谢中的作用。产生了ΔglnR和ΔnnaR突变株,并在氮耗尽条件下进行了培养。使用总RNA谱分析来研究NnaR在缺氮和富氮培养基中在GlnR调节子中的潜在作用。我们发现,破坏MSMEG_0432会影响涉及亚硝酸盐/硝酸盐吸收的基因的表达,并且将其去除会使分枝杆菌无法吸收这些来源的氮,从而导致细胞死亡。使用定量实时聚合酶链反应(qRT-PCR)和电泳迁移率变动分析(EMSA)验证了RNA-Seq结果。使用BIOLOG表型筛选平台评估了突变体在各种氮源上的生长能力,并在含有各种氮源的Sauton培养基中进行了确认。 ΔglnR突变体无法将硝酸盐转化为亚硝酸盐。有趣的是,NnaR需要活性GlnR来防止氮饥饿,并且这两种蛋白在与硝酸盐/亚硝酸盐同化相关的基因表达的调控中协同作用。 ΔnnaR突变体能够将硝酸盐转化为亚硝酸盐,但不能吸收这种转化的产物。重要的是,NnaR是截短的血红蛋白trHbN表达的关键调节子,这是提高亚硝化胁迫下细菌存活所必需的。

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