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首页> 外文期刊>Journal of bacteriology >Transcription factor sigma B of Bacillus subtilis controls a large stationary-phase regulon.
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Transcription factor sigma B of Bacillus subtilis controls a large stationary-phase regulon.

机译:枯草芽孢杆菌的转录因子Sigma B控制着一个较大的固定相调节剂。

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Transcription factor sigma B of Bacillus subtilis is active during the stationary growth phase, but its physiological role remains unknown. Understanding the function and regulation of genes controlled by sigma B (csb genes) should provide important clues to sigma B function in stationary-phase cells. To this end, we used a genetic approach to identify six new csb genes. This strategy relies on two elements: (i) random transcriptional fusions between the Escherichia coli lacZ gene and genes on the B. subtilis chromosome, generated in vivo with transposon Tn917lacZ, and (ii) a plate transformation technique to introduce a null sigB mutation into the fusion-bearing recipients directly on indicator plates. This strategy allowed the comparison of fusion expression in strains that were isogenic save for the presence or absence of a functional sigma B protein. Beginning with 1,400 active fusions, we identified 11 that were wholly or partly controlled by sigma B. These fusions mapped to six different loci that exhibit substantial contrasts in their patterns of expression in the logarithmic and stationary growth phases, suggesting that they participate in diverse cellular functions. However, for all six loci, the sigma B-dependent component of their expression was manifest largely in the stationary phase. The high frequency of six independent csb loci detected in a random collection of 1,400 fusions screened, the fact that four of the six new loci were defined by a single fusion, and the absence of the previously identified ctc and csbA genes in the present collection strongly suggest that sigma B controls a large stationary-phase regulon.
机译:枯草芽孢杆菌的转录因子sigma B在静止生长期活跃,但其生理作用仍然未知。理解由sigma B控制的基因(csb基因)的功能和调控应为sigma B在固定相细胞中的功能提供重要线索。为此,我们使用了一种遗传方法来鉴定六个新的csb基因。该策略依赖于两个要素:(i)大肠杆菌lacZ基因与枯草芽孢杆菌染色体上的基因之间的随机转录融合,由转座子Tn917lacZ在体内产生,以及(ii)平板转化技术将无效sigB突变引入将带有融合的接收器直接放在指示板上。该策略允许比较同基因菌株中融合表达的差异,只是存在或不存在功能性Sigma B蛋白。从1,400个主动融合开始,我们确定了11个全部或部分受sigma B控制的融合。这些融合定位到六个不同的基因座,这些基因座在对数生长期和静止生长期的表达方式均表现出明显的差异,表明它们参与了多种细胞职能。但是,对于所有六个基因座,其表达中依赖于sigma B的成分主要表现在静止期。筛选了在1,400个融合体的随机集合中检测到的六个独立csb基因座的高频率,六个新基因座中的四个由一次融合定义的事实,并且当前集合中先前鉴定的ctc和csbA基因不存在提示sigma B控制着较大的固定相调节剂。

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