van Schaik Willem, Zwietering Marcel H, de Vos Willem M, Abee Tjakko
Wageningen Centre for Food Sciences, Wageningen, The Netherlands.
J Bacteriol. 2004 Jul;186(13):4100-9. doi: 10.1128/JB.186.13.4100-4109.2004.
The alternative sigma factor sigmaB of the food pathogen Bacillus cereus is activated upon stress exposure and plays a role in the adaptive response of vegetative cells. This study describes the identification of sigmaB-dependent genes in B. cereus. Two-dimensional gel electrophoresis was performed with protein extracts from a sigmaB-overproducing B. cereus strain. Nine protein spots, which were absent from the negative control, were identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry or N-terminal sequencing. The sigmaB-dependent expression of the corresponding genes was confirmed by Northern blot analysis with RNA isolated from B. cereus ATCC 14579 and its sigB null mutant. Northern blot analysis also revealed that six other genes were part of sigmaB-dependent operons. The proteins that are predicted to be encoded by the sigmaB-dependent genes include an intracellular protease, a Mg2+ transporter, and a thiamine biosynthesis protein (ThiG). Highly conserved promoter sites were found to precede all sigmaB-dependent genes, with the exception of thiG. By searching the B. cereus genome for this conserved promoter sequence, five more candidate sigmaB-dependent genes were identified. Northern blot analysis and in vitro transcription experiments with a reconstituted B. cereus sigmaB-RNA polymerase holoenzyme confirmed the sigmaB dependency of two of these genes and strongly suggested that two other genes, encoding an oligopeptide-binding OppA-like protein and subunit II of the cytochrome d ubiquinol oxidase, are also sigmaB dependent. In conclusion, sigmaB of B. cereus not only regulates genes directly involved in the stress response but may also control specific metabolic rearrangements.
食品致病菌蜡样芽孢杆菌的替代σ因子σB在应激暴露时被激活,并在营养细胞的适应性反应中发挥作用。本研究描述了蜡样芽孢杆菌中σB依赖性基因的鉴定。用来自过量产生σB的蜡样芽孢杆菌菌株的蛋白质提取物进行二维凝胶电泳。通过基质辅助激光解吸电离飞行时间质谱或N端测序鉴定了阴性对照中不存在的9个蛋白质斑点。用从蜡样芽孢杆菌ATCC 14579及其sigB缺失突变体中分离的RNA进行Northern印迹分析,证实了相应基因的σB依赖性表达。Northern印迹分析还显示,其他6个基因是σB依赖性操纵子的一部分。预计由σB依赖性基因编码的蛋白质包括一种细胞内蛋白酶、一种Mg2+转运蛋白和一种硫胺素生物合成蛋白(ThiG)。除thiG外,在所有σB依赖性基因之前都发现了高度保守的启动子位点。通过在蜡样芽孢杆菌基因组中搜索这种保守的启动子序列,又鉴定出5个候选的σB依赖性基因。用重组的蜡样芽孢杆菌σB-RNA聚合酶全酶进行的Northern印迹分析和体外转录实验证实了其中两个基因的σB依赖性,并强烈表明另外两个编码寡肽结合OppA样蛋白和细胞色素d泛醇氧化酶亚基II的基因也依赖于σB。总之,蜡样芽孢杆菌的σB不仅调节直接参与应激反应的基因,还可能控制特定的代谢重排。