Tzagoloff A, Akai A, Needleman R B
J Biol Chem. 1975 Oct 25;250(20):8228-35.
Mutants of Saccharomyces cereviaiae showing defects in cytochrome oxidase, coenzyme QH2-cytochrome c reductase, and rutamycin-sensitive ATPase are described. The mutations have been established to be nuclear, based on complementation with a cytoplasmic petite tester strain and 2:2 segregation of tetrads. Genetic analysis indicate the coenzyme QH2-cytochrome c reductase and cytochrome oxidase mutants fall into 9 and 10 different complementation groups, respectively. The mutants also form distinct classes based on absorption spectra of the mitochondrial cytochromes. Two of the ATPase mutants lack detectable F1 ATPase, while the third synthesizes F1 but does not integrate it into a membrane complex. The latter mutant is missing one of the mitochondrially synthesized subunits of the rutamycin-sensitive ATPase complex.
本文描述了酿酒酵母中细胞色素氧化酶、辅酶QH2-细胞色素c还原酶以及对鲁塔霉素敏感的ATP酶存在缺陷的突变体。基于与细胞质小菌落测试菌株的互补作用以及四分体的2:2分离,已确定这些突变是核突变。遗传分析表明,辅酶QH2-细胞色素c还原酶和细胞色素氧化酶突变体分别属于9个和10个不同的互补群。根据线粒体细胞色素的吸收光谱,这些突变体也可分为不同类别。其中两个ATP酶突变体检测不到F1 ATP酶,而第三个突变体合成了F1但未将其整合到膜复合物中。后一个突变体缺失了对鲁塔霉素敏感的ATP酶复合物中一个线粒体合成的亚基。