Spink J M, Pullinger G D, Wood M W, Lax A J
Institute for Animal Health, Compton Laboratory, Newbury, Berkshire, UK.
FEMS Microbiol Lett. 1994 Feb 1;116(1):113-21. doi: 10.1111/j.1574-6968.1994.tb06684.x.
The regulation of the spvR promoter from the Salmonella dublin virulence plasmid was monitored using promoter-reporter gene fusion constructs. Activity was dependent upon the presence of the spv region and was affected by the number of copies of the spv region present within the cell. Activity remained constant throughout exponential growth, and increased rapidly with the onset of stationary phase, under both aerobic and anaerobic conditions. Additionally, the level of spvR expression was controlled by the availability of iron, activity being greatest under low iron conditions in stationary phase. The spvA gene product negatively regulated spvR expression in a dose-dependent manner, indicating that SpvA provides a negative feedback mechanism for this operon.
利用启动子-报告基因融合构建体监测了来自都柏林沙门氏菌毒力质粒的spvR启动子的调控。活性取决于spv区域的存在,并且受到细胞内spv区域拷贝数的影响。在需氧和厌氧条件下,活性在整个指数生长期保持恒定,并在稳定期开始时迅速增加。此外,spvR的表达水平受铁可用性的控制,在稳定期低铁条件下活性最高。spvA基因产物以剂量依赖的方式对spvR表达进行负调控,表明SpvA为该操纵子提供了一种负反馈机制。