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Investigating AmrZ-mediated activation of Pseudomonas aeruginosa twitching motility and alginate production.

机译:研究AmrZ介导的铜绿假单胞菌抽动运动和藻酸盐产生的激活。

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摘要

The Gram negative bacterium Pseudomonas aeruginosa is ubiquitous in the natural environment and responsible for various human infections. Successful P. aeruginosa infections require many virulence factors such as flagella, type IV pilus and alginate, whose expression is under tight control by transcription factors such as AmrZ. AmrZ activates type IV pilus-mediated twitching motility and alginate production while repressing the flagella machinery. However, molecular mechanisms of AmrZ-mediated activation of twitching motility and the alginate biosynthesis operon promoter ( algD promoter) remain elusive and are the emphases of this study.;Specifically, DNA microarray analyses were performed in order to identify AmrZ-dependent gene(s) that is required for twitching motility. The AmrZ regulon contains 112 genes, many of which are involved in virulence. However, this regulon does not contain a gene that is known to be necessary for twitching motility. In addition, we used multiple biochemical methods to show that AmrZ tetramerizes via its C-terminal domain, the loss of which results in diminished DNA binding and reduced efficiency during AmrZ-mediated activation and repression. Demonstration of AmrZ tetramerization also assists in understanding the activation mechanism of the algD promoter. This complex promoter contains a number of transcription factor binding sites with many in the far upstream region. It is unclear how those transcription factors from far upstream contribute to transcription activation. This study identified four AmrZ binding sites within this promoter and showed that each is required for algD transcription activation. We also illustrated phase-dependent activation of this promoter, suggesting interactions between upstream and downstream factors. Furthermore, in vitro fluorescence resonance energy transfer experiments indicate the formation of trans DNA-AmrZ complexes, suggesting that two DNA molecules are held together by AmrZ, likely via AmrZ oligomerization. These results thus provide new support for the DNA looping model of the algD promoter.;Taken together, the work described in this document has significantly enhanced our knowledge of AmrZ-mediated regulation, full understanding of which may provide insights into discovering new means of interfering this regulation and successful control of P. aeruginosa infections.
机译:革兰氏阴性细菌铜绿假单胞菌在自然环境中无处不在,并引起各种人类感染。成功的铜绿假单胞菌感染需要许多毒力因子,例如鞭毛,IV型菌毛和藻酸盐,其表达受到转录因子(例如AmrZ)的严格控制。 AmrZ激活IV型菌毛介导的抽搐运动和藻酸盐产生,同时抑制鞭毛机械。然而,AmrZ介导的抽搐运动激活和藻酸盐生物合成操纵子启动子(algD启动子)的分子机制仍然难以捉摸,并且是这项研究的重点。 ),这是抽搐运动所必需的。 AmrZ regulon包含112个基因,其中许多与毒力有关。但是,这种调节子不包含已知为抽动运动所必需的基因。此外,我们使用了多种生化方法来显示AmrZ通过其C末端结构域四聚,失去它会导致DNA结合减少,并在AmrZ介导的激活和抑制过程中降低效率。 AmrZ四聚体的演示也有助于理解algD启动子的激活机制。该复合启动子包含许多转录因子结合位点,其中许多在远上游区域。尚不清楚那些来自上游的转录因子如何促进转录激活。这项研究确定了该启动子内的四个AmrZ结合位点,并表明每个都是algD转录激活所必需的。我们还说明了该启动子的阶段依赖性激活,表明上游和下游因素之间的相互作用。此外,体外荧光共振能量转移实验表明反式DNA-AmrZ复合物的形成,表明两个DNA分子可能通过AmrZ寡聚被AmrZ结合在一起。因此,这些结果为algD启动子的DNA环化模型提供了新的支持。总而言之,本文档中描述的工作极大地增强了我们对AmrZ介导的调控的认识,对此的充分理解可能为发现新的干扰手段提供见解。这种调节和成功控制铜绿假单胞菌感染。

著录项

  • 作者

    Xu, Binjie.;

  • 作者单位

    The Ohio State University.;

  • 授予单位 The Ohio State University.;
  • 学科 Microbiology.;Biomedical engineering.;Molecular biology.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 210 p.
  • 总页数 210
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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