首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Integrated stress response of Escherichia coli to methylglyoxal: transcriptional readthrough from the nemRA operon enhances protection through increased expression of glyoxalase I
【2h】

Integrated stress response of Escherichia coli to methylglyoxal: transcriptional readthrough from the nemRA operon enhances protection through increased expression of glyoxalase I

机译:大肠杆菌对甲基乙二醛的综合应激反应:nemRA操纵子的转录通读通过增加乙二醛酶I的表达来增强保护

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Methylglyoxal (MG) elicits activation of K+ efflux systems to protect cells against the toxicity of the electrophile. ChIP-chip targeting RNA polymerase, supported by a range of other biochemical measurements and mutant creation, was used to identify genes transcribed in response to MG and which complement this rapid response. The SOS DNA repair regulon is induced at cytotoxic levels of MG, even when exposure to MG is transient. Glyoxalase I alone among the core MG protective systems is induced in response to MG exposure. Increased expression is an indirect consequence of induction of the upstream nemRA operon, encoding an enzyme system that itself does not contribute to MG detoxification. Moreover, this induction, via nemRA only occurs when cells are exposed to growth inhibitory concentrations of MG. We show that the kdpFABCDE genes are induced and that this expression occurs as a result of depletion of cytoplasmic K+ consequent upon activation of the KefGB K+ efflux system. Finally, our analysis suggests that the transcriptional changes in response to MG are a culmination of the damage to DNA and proteins, but that some integrate specific functions, such as DNA repair, to augment the allosteric activation of the main protective system, KefGB.
机译:甲基乙二醛(MG)引起K + 外排系统的激活,从而保护细胞免受亲电试剂的毒性。 ChIP芯片靶向RNA聚合酶,得到一系列其他生化测量和突变体创建的支持,被用于鉴定响应MG转录的基因,这些基因补充了这种快速反应。 SOS DNA修复调节因子在MG的细胞毒性水平下被诱导,即使在短暂暴露于MG的情况下也是如此。 MG核心保护系统中单独的乙二醛酶I响应MG暴露而被诱导。表达增加是诱导上游nemRA操纵子的间接结果,该操纵子编码本身并不有助于MG解毒的酶系统。而且,仅当细胞暴露于生长抑制浓度的MG时,才通过nemRA进行诱导。我们表明,kdpFABCDE基因被诱导,并且该表达是由于激活KefGB K + 外排系统后细胞质K + 耗尽而发生的。最后,我们的分析表明,对MG的转录变化是对DNA和蛋白质破坏的最终结果,但其中一些整合了特定功能,例如DNA修复,以增强主要保护系统KefGB的变构活化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号