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在枯草芽孢杆菌W23中,胞质外功能亚家族的两个σ因子σX和σM形成的二元组合,在分批培养条件下对于隔膜和细胞壁合成是必需的。

In Bacillus subtilis W23, the duet sigmaXsigmaM, two sigma factors of the extracytoplasmic function subfamily, are required for septum and wall synthesis under batch culture conditions.

作者信息

Minnig Kathrin, Barblan Jean-Luc, Kehl Sandrine, Möller Siham Beggah, Mauël Catherine

机构信息

Institut de Microbiologie Fondamentale, Université de Lausanne, BB, CH-1015 Lausanne, Switzerland.

出版信息

Mol Microbiol. 2003 Sep;49(5):1435-47. doi: 10.1046/j.1365-2958.2003.03652.x.

DOI:10.1046/j.1365-2958.2003.03652.x
PMID:12940998
Abstract

The synthesis of poly(RboP), the main Bacillus subtilis W23 teichoic acid, is encoded by tarDF-tarABIJKL operons, the latter being controlled by two promoters designated PtarA-int and PtarA-ext. Analysis by lacZ fusions reveals that PtarA-int activity exhibits sharp increases at the beginning and end of the transition between exponential and stationary growth phase. As confirmed by mRNA quantification, these increases are mediated by ECF sigma factors sigmaX and sigmaM respectively. In liquid media, strain W23 sigX sigM double mutants experience serious difficulties in the transition and stationary growth phases. Inactivation of sigmaX- and sigmaM-controlled regulons, which precludes transcription from PtarA-int, leads to (i) delays in chromosome segregation and septation and (ii) a transient loss of up to 30% of the culture OD or lysis. However, specific inactivation of PtarA-int, leading mainly to a shortage of poly(RboP), does not affect growth while, nevertheless, interfering with normal septation, as revealed by electron microscopy. The different sigM transcription in strains W23 and 168 is discussed. In W23, expression of tarA and sigM, which is shown to control divIC, is inversely correlated with growth rate, suggesting that the sigM regulon is involved in the control of cell division.

摘要

枯草芽孢杆菌W23的主要磷壁酸聚(RboP)的合成由tarDF - tarABIJKL操纵子编码,后者受两个启动子PtarA - int和PtarA - ext控制。通过lacZ融合分析表明,PtarA - int活性在指数生长期和稳定生长期过渡的开始和结束时急剧增加。经mRNA定量证实,这些增加分别由ECF σ因子σX和σM介导。在液体培养基中,W23 sigX sigM双突变体菌株在过渡和稳定生长期遇到严重困难。σX和σM控制的调控子失活,这阻止了从PtarA - int的转录,导致(i)染色体分离和隔膜形成延迟,以及(ii)培养物OD值瞬时损失高达30%或细胞裂解。然而,主要导致聚(RboP)短缺的PtarA - int的特异性失活并不影响生长,但如电子显微镜所示,会干扰正常的隔膜形成。讨论了W23和168菌株中不同的sigM转录情况。在W23中,tarA和sigM的表达(已证明其控制divIC)与生长速率呈负相关,这表明sigM调控子参与细胞分裂的控制。

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