Stolyar Sergey, He Qiang, Joachimiak Marcin P, He Zhili, Yang Zamin Koo, Borglin Sharon E, Joyner Dominique C, Huang Katherine, Alm Eric, Hazen Terry C, Zhou Jizhong, Wall Judy D, Arkin Adam P, Stahl David A
University of Washington, Department of Civil and Environmental Engineering, 616 NE North Lake Place, Box 355014, Seattle, WA 98195-2700, USA.
J Bacteriol. 2007 Dec;189(24):8944-52. doi: 10.1128/JB.00284-07. Epub 2007 Oct 5.
The response of exponentially growing Desulfovibrio vulgaris Hildenborough to pH 10 stress was studied using oligonucleotide microarrays and a study set of mutants with genes suggested by microarray data to be involved in the alkaline stress response deleted. The data showed that the response of D. vulgaris to increased pH is generally similar to that of Escherichia coli but is apparently controlled by unique regulatory circuits since the alternative sigma factors (sigma S and sigma E) contributing to this stress response in E. coli appear to be absent in D. vulgaris. Genes previously reported to be up-regulated in E. coli were up-regulated in D. vulgaris; these genes included three ATPase genes and a tryptophan synthase gene. Transcription of chaperone and protease genes (encoding ATP-dependent Clp and La proteases and DnaK) was also elevated in D. vulgaris. As in E. coli, genes involved in flagellum synthesis were down-regulated. The transcriptional data also identified regulators, distinct from sigma S and sigma E, that are likely part of a D. vulgaris Hildenborough-specific stress response system. Characterization of a study set of mutants with genes implicated in alkaline stress response deleted confirmed that there was protective involvement of the sodium/proton antiporter NhaC-2, tryptophanase A, and two putative regulators/histidine kinases (DVU0331 and DVU2580).
利用寡核苷酸微阵列研究了指数生长的希登伯勒脱硫弧菌对pH 10胁迫的反应,并对一组突变体进行了研究,这些突变体缺失了微阵列数据表明参与碱性胁迫反应的基因。数据显示,普通脱硫弧菌对pH升高的反应总体上与大肠杆菌相似,但显然由独特的调控回路控制,因为在大肠杆菌中有助于这种胁迫反应的替代sigma因子(sigma S和sigma E)在普通脱硫弧菌中似乎不存在。先前报道在大肠杆菌中上调的基因在普通脱硫弧菌中也上调;这些基因包括三个ATP酶基因和一个色氨酸合成酶基因。伴侣蛋白和蛋白酶基因(编码ATP依赖性Clp和La蛋白酶以及DnaK)的转录在普通脱硫弧菌中也升高。与大肠杆菌一样,参与鞭毛合成的基因被下调。转录数据还鉴定出了不同于sigma S和sigma E的调控因子,它们可能是普通脱硫弧菌希登伯勒菌株特异性胁迫反应系统的一部分。对一组缺失了与碱性胁迫反应相关基因的突变体的研究证实,钠/质子反向转运蛋白NhaC-2、色氨酸酶A以及两个假定的调控因子/组氨酸激酶(DVU0331和DVU2580)起到了保护作用。