Marqués S, Manzanera M, González-Pérez M M, Gallegos M T, Ramos J L
Consejo Superior de Investigaciones Científicas, Estación Experimental del Zaidín, Department of Plant Biochemistry, Granada, Spain.
Mol Microbiol. 1999 Feb;31(4):1105-13. doi: 10.1046/j.1365-2958.1999.01249.x.
The Pm promoter of the TOL plasmid of Pseudomonas putida is expressed at high level along the growth curve. This transcription is dependent on the positive regulator XylS activated by 3-methylbenzoate. The sigma factor sigma 38 is required for expression in early stationary phase and thereafter. To test whether sigma 70 was involved in Pm transcription in exponential phase, we have followed mRNA synthesis in a rpoD thermosensitive strain. No difference in Pm transcription was found between the wild type and the thermosensitive strain at the restrictive temperature of 42 degrees C, indicating that transcription was independent of the sigma factor sigma 70. However, basal levels of mRNA expression from Pm in this strain in exponential phase were more than twofold higher at 42 degrees C, suggesting involvement of sigma 32 in Pm transcription. In a rpoH background, no expression of Pm took place in the exponential phase, whereas it increased during stationary phase, and in a rpoH rpoS double mutant no activity from the Pm promoter was detected along the growth curve. We have shown that the increase in the amount of sigma 32 factor necessary for transcription in exponential phase is provided through induction of the heat shock response by the presence of the effector 3-methylbenzoate, which is also required for activation of the positive regulator XylS. We conclude that activation of Pm transcription is achieved through a switch between two stress-responsive factors, sigma 32 in exponential phase and sigma 38 in stationary phase. In both cases, transcription is dependent on the activator XylS and presents the same transcription start point.
恶臭假单胞菌TOL质粒的Pm启动子在整个生长曲线中均高水平表达。这种转录依赖于由3 - 甲基苯甲酸激活的正调控因子XylS。σ因子σ38在稳定期早期及之后的表达中是必需的。为了测试σ70是否参与指数生长期的Pm转录,我们在rpoD温度敏感型菌株中追踪了mRNA合成。在42℃的限制温度下,野生型和温度敏感型菌株之间的Pm转录没有差异,这表明转录不依赖于σ因子σ70。然而,在42℃时,该菌株指数生长期Pm的mRNA基础表达水平高出两倍多,这表明σ32参与了Pm转录。在rpoH背景下,指数生长期不发生Pm表达,而在稳定期表达增加,并且在rpoH rpoS双突变体中,沿生长曲线未检测到Pm启动子的活性。我们已经表明,指数生长期转录所需的σ32因子数量的增加是通过效应物3 - 甲基苯甲酸的存在诱导热休克反应来实现的,3 - 甲基苯甲酸也是激活正调控因子XylS所必需的。我们得出结论,Pm转录的激活是通过两个应激反应因子之间的转换实现的,指数生长期是σ32,稳定期是σ38。在这两种情况下,转录都依赖于激活剂XylS并且具有相同的转录起始点。