UPR A0 407, CNRS, 91198, Gif sur Yvette, Cedex, France.
Photosynth Res. 1990 Mar;23(3):249-55. doi: 10.1007/BF00034855.
Reaction center-B875 pigment-protein complexes were purified from Rhodocyclus gelatinosus. The proteic components consist of 7-8 polypeptides among which some were identified by their apparent molecular weights: the light harvesting B875 polypeptides α and β of 8 and 6 kDa, reaction center L (23 kDa), M (28 kDa) and H (34 kDa), cytochrome c (43 kDa). Four c-type hemes were found per reaction center. Flash-induced absorbance changes showed the presence of both QA and QB in the complex. Charge recombination times were determined to be: 1.16±0.2 (n=30) for P(+)QAQB (-) and 7-10 ms for P(+)QA (-) in presence of herbicides. From quinone analysis on one hand and kinetics of charge recombination on the other hand, we proposed that in the reaction center of Rhodocyclus gelatinosus QA is menaquinone 8 and QB is ubiquinone 8.
从红杆菌属凝胶状菌中纯化出反应中心-B875 色素-蛋白复合物。蛋白成分由 7-8 种多肽组成,其中一些通过其表观分子量确定:6 和 8 kDa 的光捕获 B875 多肽 α 和 β、反应中心 L(23 kDa)、M(28 kDa)和 H(34 kDa)、细胞色素 c(43 kDa)。每个反应中心发现 4 个 c 型血红素。闪光诱导的吸收变化表明复合物中存在 QA 和 QB。在除草剂存在的情况下,确定电荷复合时间为:1.16±0.2(n=30)为 P(+)QAQB(-),7-10 ms 为 P(+)QA(-)。从醌分析一方面和电荷复合动力学另一方面,我们提出在 Rhodocyclus gelatinosus 的反应中心中,QA 是甲萘醌 8,QB 是泛醌 8。