Gutowski-Eckel Z, Klein C, Siegers K, Bohm K, Hammelmann M, Entian K D
Institute for Microbiology, Biozentrum der Johann Wolfgang Goethe-Universiät, Frankfurt/Main, Federal Republic of Germany.
Appl Environ Microbiol. 1994 Jan;60(1):1-11. doi: 10.1128/aem.60.1.1-11.1994.
The information responsible for biosynthesis of the lantibiotic subtilin is organized in an operon-like structure that starts with the spaB gene. The spaB gene encodes an open reading frame consisting of 1,030 amino acid residues, and it was calculated that a protein having a theoretical molecular mass of 120.5 kDa could be produced from this gene. This is consistent with the apparent molecular weight for SpaB of 115,000 which was estimated after sodium dodecyl sulfate-gel electrophoresis and identification with SpaB-specific antibodies. The SpaB protein is very similar to proteins EpiB and NisB, which were identified previously as being involved in epidermin and nisin biosynthesis. Upstream from SpaB a characteristic sigma A promoter sequence was identified. An immunoblot analysis revealed that SpaB expression was strongly regulated. No SpaB protein was detected in the early logarithmic growth phase, and maximum SpaB expression was observed in the early stationary growth phase. The expression of SpaB was strongly correlated with subtilin biosynthesis. Deletion mutations in either of two recently identified regulatory genes, spaR and spaK, which act as a "two-component" regulatory system necessary for growth phase-dependent induction of subtilin biosynthesis (C. Klein, C. Kaletta, and K. D. Entian, Appl. Environ. Microbiol. 59:296-303, 1993), also resulted in failure of SpaB expression. To investigate the intracellular localization of SpaB, vesicles of Bacillus subtilis were prepared. The SpaB protein cosedimented with the vesicle fraction and was released only after vigorous resuspension of the vesicles. Our results suggest that SpaB is membrane associated and that subtilin biosynthesis occurs at the cytoplasmic membrane of B. subtilis.
负责羊毛硫抗生素枯草菌素生物合成的信息以一种类似操纵子的结构组织起来,该结构始于spaB基因。spaB基因编码一个由1030个氨基酸残基组成的开放阅读框,经计算,从该基因可产生一种理论分子量为120.5 kDa的蛋白质。这与经十二烷基硫酸钠 - 凝胶电泳并用SpaB特异性抗体鉴定后估计的SpaB表观分子量115,000一致。SpaB蛋白与EpiB和NisB蛋白非常相似,EpiB和NisB蛋白先前已被鉴定参与表皮素和乳链菌肽的生物合成。在SpaB上游鉴定出一个特征性的σA启动子序列。免疫印迹分析表明SpaB的表达受到严格调控。在对数生长早期未检测到SpaB蛋白,而在稳定生长早期观察到SpaB的最大表达。SpaB的表达与枯草菌素的生物合成密切相关。最近鉴定的两个调控基因spaR和spaK中的任何一个发生缺失突变,这两个基因作为枯草菌素生物合成生长阶段依赖性诱导所必需的“双组分”调控系统(C. Klein、C. Kaletta和K. D. Entian,《应用与环境微生物学》59:296 - 303,1993),也导致SpaB表达失败。为了研究SpaB在细胞内的定位,制备了枯草芽孢杆菌的囊泡。SpaB蛋白与囊泡部分共沉降,并且只有在剧烈重悬囊泡后才会释放。我们的结果表明SpaB与膜相关,并且枯草菌素的生物合成发生在枯草芽孢杆菌的细胞质膜上。