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枯草芽孢杆菌spoVB基因的克隆、特性分析及表达

Cloning, characterization, and expression of the spoVB gene of Bacillus subtilis.

作者信息

Popham D L, Stragier P

机构信息

Institut de Biologie Physico-Chimique, Paris, France.

出版信息

J Bacteriol. 1991 Dec;173(24):7942-9. doi: 10.1128/jb.173.24.7942-7949.1991.

Abstract

Mutation of the spoVB gene in Bacillus subtilis causes the production of spores containing a defective cortex and unable to acquire heat resistance. The spoVB locus is highly linked to another spo locus, spoIIIF, characterized by a single mutation (I. L. Lamont and J. Mandelstam, J. Gen. Microbiol. 130:1253-1261, 1984). A 18-kb DNA region overlapping the spoIIIF-spoVB region was cloned in successive steps starting from a Tn917 insertion in the nic locus. The exact location of the spoIIIF and spoVB loci was defined with various integrative plasmids carrying subfragments of that region. DNA sequencing established that spoIIIF and spoVB are a single monocistronic locus encoding a 518-amino-acid polypeptide with features of an integral membrane protein. The precise location of the spoIIIF590 and spoVB91 mutations in that unique open reading frame was determined, and both mutations were sequenced. A null mutation was engineered in the spoIIIF-spoVB locus and led to a typical spoVB phenotype, identical to the phenotype created by either spoIIIF590 or spoVB91, suggesting that the original spoIIIF mutant contained a secondary mutation arresting sporulation at an earlier stage. A transcriptional spoVB-lacZ fusion was constructed, and its expression was found to be directly dependent on RNA polymerase containing sigma E. A null mutation of spoVB had no effect on expression of sspB and cotA, members of the sigma G- and sigma K-controlled regulons respectively, while expression of cotC, a member of the latest known mother cell regulon, was delayed and strongly reduced. These results are consistent with SpoVB being involved in cortex biosynthesis and affecting only indirectly expression of late sporulation genes.

摘要

枯草芽孢杆菌中spoVB基因的突变会导致产生含有缺陷皮层且无法获得耐热性的孢子。spoVB基因座与另一个spo基因座spoIIIF高度连锁,spoIIIF的特征是单个突变(I. L. 拉蒙特和J. 曼德尔斯坦姆,《普通微生物学杂志》130:1253 - 1261,1984年)。从nic基因座中的Tn917插入片段开始,逐步克隆了一个与spoIIIF - spoVB区域重叠的18 kb DNA区域。利用携带该区域亚片段的各种整合质粒确定了spoIIIF和spoVB基因座的确切位置。DNA测序表明,spoIIIF和spoVB是一个单一的单顺反子基因座,编码一种具有整合膜蛋白特征的518个氨基酸的多肽。确定了spoIIIF590和spoVB91突变在该独特开放阅读框中的精确位置,并对这两个突变进行了测序。在spoIIIF - spoVB基因座中构建了一个无效突变,导致了典型的spoVB表型,与spoIIIF590或spoVB91产生的表型相同,这表明原来的spoIIIF突变体包含一个二级突变,在更早阶段阻止孢子形成。构建了转录性spoVB - lacZ融合体,发现其表达直接依赖于含有σE的RNA聚合酶。spoVB的无效突变对分别受σG和σK控制的调节子成员sspB和cotA的表达没有影响,而最新已知母细胞调节子成员cotC的表达则延迟且大幅降低。这些结果与SpoVB参与皮层生物合成且仅间接影响后期孢子形成基因的表达一致。

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