Cunliffe H E, Merriman T R, Lamont I L
Department of Biochemistry, University of Otago, Dunedin, New Zealand.
J Bacteriol. 1995 May;177(10):2744-50. doi: 10.1128/jb.177.10.2744-2750.1995.
Cells of Pseudomonas aeruginosa secrete a fluorescent yellow-green siderophore, pyoverdine, when grown under iron-deficient conditions. We describe here the cloning and characterization of a gene, pvdS, which is required for this process. The pvdS gene is required for expression from promoters of at least two pyoverdine synthesis genes and can cause expression from these promoters in Escherichia coli, where they are otherwise inactive. Sequencing of pvdS revealed that it is a member of a subfamily of RNA polymerase sigma factors which direct the synthesis of extracellular products by bacteria. The pvdS gene is expressed only in iron-starved bacteria, and in E. coli cells at least, expression is regulated by the Fur repressor protein. We propose that in iron-rich cells of P. aeruginosa, Fur binds to the pvdS promoter and prevents expression of the gene; under conditions of iron starvation, repression is relieved and PvdS is made, reprogramming the cells for pyoverdine synthesis.
在缺铁条件下生长时,铜绿假单胞菌的细胞会分泌一种荧光黄绿色铁载体——绿脓菌素。我们在此描述了一个基因pvdS的克隆和特性,该基因是这一过程所必需的。pvdS基因是至少两个绿脓菌素合成基因启动子表达所必需的,并且能在大肠杆菌中使这些启动子表达,而在大肠杆菌中这些启动子原本是无活性的。pvdS的测序表明它是RNA聚合酶σ因子亚家族的成员,该亚家族指导细菌合成细胞外产物。pvdS基因仅在缺铁的细菌中表达,并且至少在大肠杆菌细胞中,其表达受Fur阻遏蛋白调控。我们提出,在铜绿假单胞菌富含铁的细胞中,Fur与pvdS启动子结合并阻止该基因的表达;在铁饥饿条件下,阻遏作用解除,PvdS得以产生,从而使细胞重新编程以合成绿脓菌素。