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枯草芽孢杆菌冷休克反应的全基因组转录分析。

Genomewide transcriptional analysis of the cold shock response in Bacillus subtilis.

作者信息

Beckering Carsten L, Steil Leif, Weber Michael H W, Völker Uwe, Marahiel Mohamed A

机构信息

Philipps-Universität Marburg, FB Chemie, Germany.

出版信息

J Bacteriol. 2002 Nov;184(22):6395-402. doi: 10.1128/JB.184.22.6395-6402.2002.

Abstract

Previous studies with two-dimensional gel electrophoresis techniques revealed that the cold shock response in Bacillus subtilis is characterized by rapid induction and accumulation of two classes of specific proteins, which have been termed cold-induced proteins (CIPs) and cold acclimatization proteins (CAPs), respectively. Only recently, the B. subtilis two-component system encoded by the desKR operon has been demonstrated to be essential for the cold-induced expression of the lipid-modifying desaturase Des, which is required for efficient cold adaptation of the membrane in the absence of isoleucine. At present, one of the most intriguing questions in this research field is whether DesKR plays a global role in cold signal perception and transduction in B. subtilis. In this report, we present the first genomewide transcriptional analysis of a cold-exposed bacterium and demonstrate that the B. subtilis two-component system DesKR exclusively controls the desaturase gene des and is not the cold-triggered regulatory system of global relevance. In addition to this, we identified a set of genes that might participate as novel players in the cold shock adaptation of B. subtilis. Two cold-induced genes, the elongation factor homolog ylaG and the sigma(L)-dependent transcriptional activator homolog yplP, have been examined by construction and analysis of deletion mutants.

摘要

以往利用二维凝胶电泳技术开展的研究表明,枯草芽孢杆菌中的冷休克反应具有两类特定蛋白质快速诱导和积累的特征,这两类蛋白质分别被称为冷诱导蛋白(CIPs)和冷驯化蛋白(CAPs)。直到最近,由desKR操纵子编码的枯草芽孢杆菌双组分系统才被证明对于脂质修饰去饱和酶Des的冷诱导表达至关重要,在缺乏异亮氨酸的情况下,该去饱和酶是细胞膜有效冷适应所必需的。目前,该研究领域最引人关注的问题之一是DesKR在枯草芽孢杆菌的冷信号感知和转导中是否发挥全局作用。在本报告中,我们展示了对冷暴露细菌的首次全基因组转录分析,并证明枯草芽孢杆菌双组分系统DesKR仅控制去饱和酶基因des,并非具有全局相关性的冷触发调节系统。除此之外,我们还鉴定出一组可能作为枯草芽孢杆菌冷休克适应新参与者的基因。通过构建和分析缺失突变体,对两个冷诱导基因,即延伸因子同源物ylaG和σ(L)依赖性转录激活因子同源物yplP进行了研究。

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