Kidambi Saranga P, Booth Melissa G, Kokjohn Tyler A, Miller Robert V
Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK 74078, USA.
The School of Biological Sciences, University of Nebraska, Lincoln, NE, USA.
Microbiology (Reading). 1996 Apr;142 ( Pt 4):1033-1040. doi: 10.1099/00221287-142-4-1033.
The responses of the autochthonous soil and aquatic organism, Pseudomonas aeruginosa to UV radiation wavelengths (UVA, 320-400 nm, and UVB, 280-320 nm) has been investigated in this study. P. aeruginosa recA mutants were found to be more sensitive to both UVA and UVB radiation than were their isogenic RecA+ parents. Introduction of a low-copy-number plasmid containing the cloned wild-type P. aeruginosa recA gene restored UVA and UVB resistance to recA mutants. The concentration of RecA protein increased twofold 120 min after exposure to either UVA or UVB radiation, suggesting induction of expression of the recA gene by these wavelengths. In this study, we found that a functional RecA protein is required for activation of D3 prophage in lysogenic cells following exposure to UVB radiation. Prophage were not induced by exposure of their hosts to UVA radiation. Induction of damage-inducible (din) genes in response to UVA or UVB irradiation was also shown to be RecA dependent. These data indicate that the recA gene plays a role in the response of P. aeruginosa to exposure to wavelengths of UV radiation found in the solar spectrum.
本研究调查了本地土壤和水生生物铜绿假单胞菌对紫外线辐射波长(UVA,320 - 400纳米,以及UVB,280 - 320纳米)的反应。发现铜绿假单胞菌recA突变体对UVA和UVB辐射都比其同基因的RecA +亲本更敏感。引入含有克隆的野生型铜绿假单胞菌recA基因的低拷贝数质粒可恢复recA突变体对UVA和UVB的抗性。暴露于UVA或UVB辐射120分钟后,RecA蛋白的浓度增加了两倍,表明这些波长可诱导recA基因的表达。在本研究中,我们发现功能性RecA蛋白是溶原性细胞在暴露于UVB辐射后激活D3前噬菌体所必需的。宿主暴露于UVA辐射不会诱导前噬菌体。还表明,响应UVA或UVB照射诱导损伤诱导(din)基因也是RecA依赖性的。这些数据表明recA基因在铜绿假单胞菌对太阳光谱中发现的紫外线辐射波长暴露的反应中起作用。