Chevillotte-Brivet P, Salou G, Meunier-Lemesle D
Laboratoire de Chimie Bactérienne du Centre National de la Recherche Scientifique, Marseille, France.
Curr Genet. 1987;12(2):111-7. doi: 10.1007/BF00434665.
The level of core protein I and subunit VI of mitochondrial complex III (which are coded by the nuclear genome) was found to be greatly diminished in a yeast strain carrying a mutation (W7) in the mitochondrial gene coding for cytochrome b. This suggests that intricate interactions occur in complex III biogenesis between proteins of cytoplasmic and mitochondrial origin. This mutant was characterized by a low cytochrome b level and a loss of activity in the b-c1 segment of the respiratory chain. It was compared to another mutant showing similar biochemical characteristics, but which had integrated core protein I, as shown by antibody binding experiments. In mutant devoid of core protein I, cytochrome b was found to be reducible by NADH but not by succinate, suggesting two different electron transfer pathways inside comples III from each substrate to cytochrome b heme(s).
在编码细胞色素b的线粒体基因中携带突变(W7)的酵母菌株中,发现线粒体复合物III的核心蛋白I和亚基VI(由核基因组编码)的水平大幅降低。这表明在复合物III生物合成过程中,细胞质来源和线粒体来源的蛋白质之间发生了复杂的相互作用。该突变体的特征是细胞色素b水平低,呼吸链的b-c1段活性丧失。将其与另一个具有相似生化特征但通过抗体结合实验显示整合了核心蛋白I的突变体进行比较。在缺乏核心蛋白I的突变体中,发现细胞色素b可被NADH还原,但不能被琥珀酸还原,这表明在复合物III内部,从每种底物到细胞色素b血红素存在两条不同的电子传递途径。