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枯草芽孢杆菌中受盐胁迫影响的DegS-DegU调控子新成员的特性分析

Characterization of a novel member of the DegS-DegU regulon affected by salt stress in Bacillus subtilis.

作者信息

Dartois V, Débarbouillé M, Kunst F, Rapoport G

机构信息

Unité de Biochimie Microbienne, URA 1300 Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France.

出版信息

J Bacteriol. 1998 Apr;180(7):1855-61. doi: 10.1128/JB.180.7.1855-1861.1998.

DOI:10.1128/JB.180.7.1855-1861.1998
PMID:9537385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC107100/
Abstract

As a soil bacterium also found in estuarine and marine habitats, Bacillus subtilis has evolved various sensing and adaptation systems in order to face salt stress conditions. Among these regulatory mechanisms is the DegS-DegU signal transduction system, which was previously shown to be stimulated by high salt concentrations. A search for promoters regulated in response to salt stress led to the identification of wapA, encoding a wall-associated protein, which is strongly expressed at low salt concentrations and almost completely repressed in the presence of 0.7 M disodium succinate. Repression of wapA transcription by salt stress was shown to require the phosphorylated form of DegU. Moreover, DegU-mediated repression of wapA occurred only in high-salt medium. Alignment between the control region of wapA and other DegU-regulated promoters allowed the identification of a putative DegU target sequence, AGAAN(11)TTCAG. Mutation/deletion analyses of the wapA promoter region confirmed the role of the putative DegU control site in repression of wapA transcription at high salt concentrations and revealed a second site of repression located downstream from the transcription start site. Since residual negative control was observed at this second site in the absence of DegU, it seems likely that an additional repressor acts on the wapA control region to further downregulate wapA transcription under salt stress conditions.

摘要

枯草芽孢杆菌作为一种也存在于河口和海洋栖息地的土壤细菌,已经进化出各种传感和适应系统以应对盐胁迫条件。这些调控机制中包括DegS-DegU信号转导系统,先前已证明该系统会受到高盐浓度的刺激。对响应盐胁迫而被调控的启动子进行搜索,导致鉴定出wapA,其编码一种壁相关蛋白,该蛋白在低盐浓度下强烈表达,而在存在0.7 M琥珀酸钠的情况下几乎完全被抑制。盐胁迫对wapA转录的抑制作用被证明需要磷酸化形式的DegU。此外,DegU介导的对wapA的抑制仅发生在高盐培养基中。对wapA的控制区域与其他DegU调控的启动子进行比对,使得能够鉴定出一个假定的DegU靶序列AGAAN(11)TTCAG。对wapA启动子区域的突变/缺失分析证实了假定的DegU控制位点在高盐浓度下对wapA转录抑制中的作用,并揭示了位于转录起始位点下游的第二个抑制位点。由于在没有DegU的情况下在这个第二个位点观察到残留的负调控,似乎很可能有另一种阻遏物作用于wapA控制区域,以在盐胁迫条件下进一步下调wapA转录。

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