Snozzi M, Crofts A R
Biochim Biophys Acta. 1984 Aug 31;766(2):451-63. doi: 10.1016/0005-2728(84)90261-5.
Chromatophores from Rhodopseudomonas sphaeroides GA were fused with liposomes in order to dilute the components of the cyclic photosynthetic electron-transport chain within the membrane. This dilution led to a decrease in the rate of cytochrome b-561 reduction. The original rates could be restored at potentials around 100 mV (where a large part of the quinone pool is chemically reduced), if ubiquinone was incorporated into the liposomes prior to fusion. Similar dilution effects could be observed in synchronized cultures. The membrane obtained after division contained about twice the amount of phospholipids per reaction center when compared to chromatophores prepared from cells harvested just before division. Chromatophores from synchronized cultures are more uniform with respect to the concentration of the different electron-transport components in the membrane than the membranes from normally grown cells. The kinetic behaviour both of fused chromatophores and of membranes from synchronized cultures are in agreement with a modified Q-cycle model for photosynthetic electron transport in Rps. sphaeroides. The results presented in this paper cannot be explained by postulating the presence of a firmly bound quinone, Qz, in the ubiquinol: cytochrome c2 oxidoreductase, as previously proposed.
将球形红假单胞菌GA的载色体与脂质体融合,以稀释膜内循环光合电子传递链的组分。这种稀释导致细胞色素b - 561还原速率降低。如果在融合前将泛醌掺入脂质体中,在约100 mV的电位下(此时大部分醌池被化学还原),可恢复原始速率。在同步培养物中也可观察到类似的稀释效应。与从即将分裂前收获的细胞制备的载色体相比,分裂后获得的膜每个反应中心所含磷脂量约为其两倍。与正常生长细胞的膜相比,同步培养物的载色体在膜中不同电子传递组分的浓度方面更为均匀。融合载色体和同步培养物膜的动力学行为均与球形红假单胞菌光合电子传递的修正Q循环模型一致。本文给出的结果无法通过假定如先前提出的在泛醇:细胞色素c2氧化还原酶中存在紧密结合的醌Qz来解释。