Yano Koichi, Inoue Hiromi, Mori Hirokazu, Yee Lii Mien, Matsuoka Satoshi, Sadaie Yoshito, Asai Kei
Area of Biochemistry and Molecular Biology, Division of Life Science, Graduate School of Science and Engineering, Saitama University, Saitama, Japan.
Biosci Biotechnol Biochem. 2011;75(5):966-75. doi: 10.1271/bbb.110035. Epub 2011 May 20.
Pairs of the ECF sigma factor and its anti-sigma factor, SigW and RsiW, of Bacillus-related species that inhabit extreme environments were heterologously expressed in B. subtilis. All the RsiWs, membrane proteins, failed to fill their function of repressing cognate SigW activity, despite their close structural similarities. Particularly, uncontrolled expression of Oceanobacillus iheyensis OISigW due to abortive OIRsiW was harmful to B. subtilis. Analysis of revertants of this growth defect and site-directed mutagenesis indicated that the insertion of six and a minimum of three hydrophobic amino acid residues occurring in the transmembrane region allowed OIRsiW to function as anti-OISigW. Subcellular localization of OIRsiW was detected by immunoblot analysis, suggesting that both the wild-type and the mutant form of OIRsiW were localized to the membrane. An appropriate length of a transmembrane region required for proper integration into the membrane after translocation might vary among these Bacillus-related species.
栖息于极端环境的芽孢杆菌相关物种的细胞外因子(ECF)σ因子及其抗σ因子SigW和RsiW在枯草芽孢杆菌中进行了异源表达。尽管所有的RsiW(膜蛋白)在结构上非常相似,但它们均未能发挥抑制同源SigW活性的功能。特别是,由于OIRsiW无效导致的嗜盐栖热芽孢杆菌OISigW的失控表达对枯草芽孢杆菌有害。对这种生长缺陷回复突变体的分析和定点诱变表明,跨膜区域中出现的六个以及至少三个疏水氨基酸残基的插入使OIRsiW能够发挥抗OISigW的功能。通过免疫印迹分析检测到OIRsiW的亚细胞定位,表明OIRsiW的野生型和突变型均定位于膜上。这些芽孢杆菌相关物种在转运后正确整合到膜中所需的跨膜区域的适当长度可能有所不同。