Caramori T, Barilla D, Nessi C, Sacchi L, Galizzi A
Dipartimento di Genetica e Microbiologia "A. Buzzati-Traverso", Universita degli Studi, Pavia, Italy.
J Bacteriol. 1996 Jun;178(11):3113-8. doi: 10.1128/jb.178.11.3113-3118.1996.
The alternative sigma factor sigma D directs transcription of a number of genes involved in chemotaxis, motility, and autolysis in Bacillus subtilis (sigmaD regulon). The activity of SigD is probably in contrast to that of FlgM, which acts as an antisigma factor and is responsible for the coupling of late flagellar gene expression to the assembly of the hook-basal body complex. We have characterized the effects of an in-frame deletion mutation of flgM. By transcriptional fusions to lacZ, we have shown that in FlgM-depleted strains there is a 10-fold increase in transcription from three different sigmaD-dependent promoters, i.e., Phag, PmotAB, and PfliDST. The number of flagellar filaments was only slightly increased by the flgM mutation. Overexpression of FlgM from a multicopy plasmid under control of the isopropyl-beta-D-thiogalactopyranoside-inducible spac promoter drastically reduced the level of transcription from the hag promoter. On the basis of these results, we conclude that, as in Salmonella typhimurium, FlgM inhibits the activity of SigD, but an additional element is involved in determining the number of flagellar filaments.
替代σ因子σD指导枯草芽孢杆菌中一些参与趋化性、运动性和自溶的基因的转录(σD调控子)。SigD的活性可能与FlgM相反,FlgM作为一种抗σ因子,负责将晚期鞭毛基因表达与钩-基体复合体的组装相偶联。我们已经对flgM的框内缺失突变的影响进行了表征。通过与lacZ的转录融合,我们表明在FlgM缺失的菌株中,来自三个不同的σD依赖性启动子,即Phag、PmotAB和PfliDST的转录增加了10倍。flgM突变仅使鞭毛丝的数量略有增加。在异丙基-β-D-硫代半乳糖苷诱导的spac启动子控制下,从多拷贝质粒中过表达FlgM可显著降低hag启动子的转录水平。基于这些结果,我们得出结论,与鼠伤寒沙门氏菌一样,FlgM抑制SigD的活性,但另一个元件参与决定鞭毛丝的数量。