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首页> 外文期刊>Journal of bacteriology >Identification of the σB Regulon of Bacillus cereus and Conservation of σB-Regulated Genes in Low-GC-Content Gram-Positive Bacteria
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Identification of the σB Regulon of Bacillus cereus and Conservation of σB-Regulated Genes in Low-GC-Content Gram-Positive Bacteria

机译:蜡样芽孢杆菌σB调节子的鉴定和GC含量低的革兰氏阳性细菌中σB调控的基因的保守性

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摘要

The alternative sigma factor σB has an important role in the acquisition of stress resistance in many gram-positive bacteria, including the food-borne pathogen Bacillus cereus. Here, we describe the identification of the set of σB-regulated genes in B. cereus by DNA microarray analysis of the transcriptome upon a mild heat shock. Twenty-four genes could be identified as being σB dependent as witnessed by (i) significantly lower expression levels of these genes in mutants with a deletion of sigB and rsbY (which encode the alternative sigma factor σB and a crucial positive regulator of σB activity, respectively) than in the parental strain B. cereus ATCC 14579 and (ii) increased expression of these genes upon a heat shock. Newly identified σB-dependent genes in B. cereus include a histidine kinase and two genes that have predicted functions in spore germination. This study shows that the σB regulon of B. cereus is considerably smaller than that of other gram-positive bacteria. This appears to be in line with phylogenetic analyses where σB of the B. cereus group was placed close to the ancestral form of σB in gram-positive bacteria. The data described in this study and previous studies in which the complete σB regulon of the gram-positive bacteria Bacillus subtilis, Listeria monocytogenes, and Staphylococcus aureus were determined enabled a comparison of the sets of σB-regulated genes in the different gram-positive bacteria. This showed that only three genes (rsbV, rsbW, and sigB) are conserved in their σB dependency in all four bacteria, suggesting that the σB regulon of the different gram-positive bacteria has evolved to perform niche-specific functions.
机译:σ替代因子σ B 在许多革兰氏阳性细菌(包括食源性致病菌蜡状芽孢杆菌)的抗逆性获得中具有重要作用。在这里,我们描述了在 B中由σ B 调控的基因集的鉴定。 DNA芯片分析轻度热激后转录组的蜡状通过(i)这些基因在具有 sigB 缺失的突变体中的表达水平显着降低,可以确定二十四个基因是σ B 依赖的。 rsbY (分别编码替代sigma因子σ B 和σ B 活性的关键正调节剂)比亲本菌株 B中的要好。 cereus ATCC 14579和(ii)热休克后这些基因的表达增加。新发现的 B中依赖于σ B 的基因。蜡状细胞包括一个组氨酸激酶和两个在孢子萌发中具有预测功能的基因。研究表明, B的σ B 调节子。蜡状芽孢杆菌比其他革兰氏阳性菌小得多。这似乎与 B的σ B 的系统发育分析一致。蜡状芽孢杆菌组在革兰氏阳性菌中靠近祖先形式的σ B 。本研究和以前的研究中描述的数据,其中革兰氏阳性细菌枯草芽孢杆菌单核细胞增生李斯特菌和确定了金黄色葡萄球菌,以比较不同革兰氏阳性细菌中受σ B 调控的基因组。这表明只有三个基因( rsbV rsbW sigB )在它们的σ B 依赖性中是保守的。所有这四种细菌,表明不同革兰氏阳性细菌的σ B 调节子已经进化为执行特定于生态位的功能。

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