Koch H G, Hwang O, Daldal F
Department of Biology, Plant Science Institute, University of Pennsylvania, Philadelphia 19104-6018, USA.
J Bacteriol. 1998 Feb;180(4):969-78. doi: 10.1128/JB.180.4.969-978.1998.
The facultative phototrophic bacterium Rhodobacter capsulatus contains only one form of cytochrome (cyt) c oxidase, which has recently been identified as a cbb3-type cyt c oxidase. This is unlike other related species, such as Rhodobacter sphaeroides and Paracoccus denitrificans, which contain an additional mitochondrial-like aa3-type cyt c oxidase. An extensive search for mutants affected in cyt c oxidase activity in R. capsulatus led to the isolation of at least five classes of mutants. Plasmids complementing them to a wild-type phenotype were obtained for all but one of these classes from a chromosomal DNA library. The first class of mutants contained mutations within the structural genes (ccoNOQP) of the cyt cbb3 oxidase. Sequence analysis of these mutants and of the plasmids complementing them revealed that ccoNOQP in R. capsulatus is not flanked by the oxygen response regulator fnr, which is located upstream of these genes in other species. Genetic and biochemical characterizations of mutants belonging to this group indicated that the subunits CcoN, CcoO, and CcoP are required for the presence of an active cyt cbb3 oxidase, and unlike in Bradyrhizobium japonicum, no active CcoN-CcoO subcomplex was found in R. capsulatus. In addition, mutagenesis experiments indicated that the highly conserved open reading frame 277 located adjacent to ccoNOQP is required neither for cyt cbb3 oxidase activity or assembly nor for respiratory or photosynthetic energy transduction in R. capsulatus. The remaining cyt c oxidase-minus mutants mapped outside of ccoNOQP and formed four additional groups. In one of these groups, a fully assembled but inactive cyt cbb3 oxidase was found, while another group had only extremely small amounts of it. The next group was characterized by a pleiotropic effect on all membrane-bound c-type cytochromes, and the remaining mutants not complemented by the plasmids complementing the first four groups formed at least one additional group affecting the biogenesis of the cyt cbb3 oxidase of R. capsulatus.
兼性光合细菌荚膜红杆菌仅含有一种形式的细胞色素(cyt)c氧化酶,最近已被鉴定为cbb3型细胞色素c氧化酶。这与其他相关物种不同,如球形红杆菌和反硝化副球菌,它们还含有一种额外的线粒体样aa3型细胞色素c氧化酶。对荚膜红杆菌中细胞色素c氧化酶活性受影响的突变体进行广泛搜索,导致至少分离出五类突变体。除其中一类外,从染色体DNA文库中获得了将它们互补为野生型表型的质粒。第一类突变体在细胞色素cbb3氧化酶的结构基因(ccoNOQP)内发生了突变。对这些突变体及其互补质粒的序列分析表明,荚膜红杆菌中的ccoNOQP两侧没有氧反应调节因子fnr,而在其他物种中该因子位于这些基因的上游。对属于该组的突变体的遗传和生化特征分析表明,亚基CcoN、CcoO和CcoP是活性细胞色素cbb3氧化酶存在所必需的,并且与日本慢生根瘤菌不同,在荚膜红杆菌中未发现活性CcoN-CcoO亚复合物。此外,诱变实验表明,与ccoNOQP相邻的高度保守的开放阅读框277对于荚膜红杆菌中的细胞色素cbb3氧化酶活性或组装以及呼吸或光合能量转换都不是必需的。其余的细胞色素c氧化酶缺陷型突变体定位在ccoNOQP之外,并形成了另外四组。在其中一组中,发现了一个完全组装但无活性的细胞色素cbb3氧化酶,而另一组只有极少量的该酶。下一组的特征是对所有膜结合的c型细胞色素具有多效性影响,其余未被互补前四组的质粒互补的突变体至少形成了另外一组影响荚膜红杆菌细胞色素cbb3氧化酶生物合成的突变体。