Donohue T J, McEwan A G, Van Doren S, Crofts A R, Kaplan S
Bacteriology Department, University of Wisconsin, Madison 53706.
Biochemistry. 1988 Mar 22;27(6):1918-25. doi: 10.1021/bi00406a018.
Rhodobacter sphaeroides mutants lacking cytochrome c2 (cyt c2) have been constructed by site-specific recombination between the wild-type genomic cyt c2 structural gene (cycA) and a suicide plasmid containing a defective cyc operon where deletion of cycA sequences was accompanied by insertion of a KnR gene. Southern blot analysis confirmed that the wild-type cyc operon was exchanged for the inactivated cycA gene, presumably by double-reciprocal recombination. Spectroscopic and immunochemical measurements, together with genetic complementation, established that the inability of these mutants to grow under photosynthetic conditions was due to the lack of cyt c2. The cyt c2 deficient strains reduced photooxidized reaction center complexes approximately 4 orders of magnitude more slowly than the parent strain. The phenotype and characteristics of these mutants were restored when a wild-type cyc operon was introduced on a stable low copy number plasmid. These experiments provide the first genetic evidence for the obligatory role of cyt c2 in wild-type cyclic photosynthetic electron transport in R. sphaeroides. We have also observed that the R. sphaeroides cyt c2 deficient strains spontaneously gave rise to photosynthetically competent pseudorevertants at a frequency which suggests that the cyt c2 independent photosynthetic electron transport which suppresses the phenotype of the cyt c2 deficient strains was the result of a single mutation elsewhere in the genome.
通过野生型基因组细胞色素c2(cyt c2)结构基因(cycA)与含有缺陷型cyc操纵子的自杀质粒之间的位点特异性重组,构建了缺乏细胞色素c2(cyt c2)的球形红杆菌突变体,其中cycA序列的缺失伴随着KnR基因的插入。Southern印迹分析证实,野生型cyc操纵子被失活的cycA基因所取代,推测是通过双交换重组实现的。光谱和免疫化学测量以及遗传互补表明,这些突变体在光合条件下无法生长是由于缺乏cyt c2。与亲本菌株相比,cyt c2缺陷菌株还原光氧化反应中心复合物的速度慢约4个数量级。当在稳定的低拷贝数质粒上引入野生型cyc操纵子时,这些突变体的表型和特征得以恢复。这些实验为cyt c2在球形红杆菌野生型循环光合电子传递中的必需作用提供了首个遗传学证据。我们还观察到,球形红杆菌cyt c2缺陷菌株以一定频率自发产生光合能力的假回复体,这表明抑制cyt c2缺陷菌株表型的不依赖cyt c2的光合电子传递是基因组其他位置单个突变的结果。