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膜锚定细胞色素cy介导了红假单胞菌中细胞色素bc1复合物到反应中心的微秒级时间尺度的电子转移。

Membrane-anchored cytochrome cy mediated microsecond time range electron transfer from the cytochrome bc1 complex to the reaction center in Rhodobacter capsulatus.

作者信息

Myllykallio H, Drepper F, Mathis P, Daldal F

机构信息

Department of Biology, Plant Science Institute, University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Biochemistry. 1998 Apr 21;37(16):5501-10. doi: 10.1021/bi973123d.

Abstract

In Rhodobacter capsulatus, the soluble cytochrome (cyt) c2 and membrane-associated cyt cy are the only electron carriers which operate between the photochemical reaction center (RC) and the cyt bc1 complex. In this work, cyt cy mediated microsecond time range electron transfer kinetics were studied by light-activated time-resolved absorption spectroscopy using a mutant strain lacking cyt c2. In intact cells and in isolated chromatophores of this mutant, only approximately 30% of the RCs had their photooxidized primary donor rapidly rereduced by cyt cy. Of these 30%, about half were reduced with a half-time of approximately 5 micros attributed to preformed complexes, and the other half with a half-time of approximately 40 micros attributed to cyt cy having to move from another site. This slower phase was affected by addition of glycerol, indicating its dependence on the viscosity of the medium. Cyt cy, despite its rereduction by ubihydroquinone oxidation in the millisecond time range, remained virtually unable to deliver electrons to other RCs which stayed photooxidized for several seconds. Furthermore, using two flashes separated by a variable time interval, it was shown that the fast electron donating complex was reformed in about 60 micros, a time span probably reflecting electron transfer from cyt c1 to cyt cy. In the absence of the cyt bc1 complex, the steady-state level of cyt cy in the chromatophore membranes obtained using cells grown in minimal medium was decreased to approximately 50%. The remaining cyt cy , however, was able to form the fast electron donating complex with the RC (half-time of approximately 5 micros), whereas the slower phase with a half-time of approximately 40 micros was strongly decelerated. This finding suggests a role for the cyt bc1 complex in stabilizing cyt cy and providing its "other" site, possibly via a close association between these components. Taken together, it is concluded that although cyt cy is present in substoichiometric amount compared to the RCs, it supports efficiently photosynthetic growth of R. capsulatus in the absence of cyt c2 because it can mediate fast electron transfer from the cyt bc1 complex to the RC during multiple turnovers of the cyclic electron flow.

摘要

在荚膜红细菌中,可溶性细胞色素(cyt)c2和与膜相关的细胞色素cy是仅有的在光化学反应中心(RC)和细胞色素bc1复合体之间起作用的电子载体。在这项工作中,通过使用缺乏细胞色素c2的突变菌株,利用光激活时间分辨吸收光谱研究了细胞色素cy介导的微秒时间范围内的电子转移动力学。在该突变体的完整细胞和分离的载色体中,只有大约30%的RCs的光氧化初级供体被细胞色素cy迅速再还原。在这30%中,大约一半在大约5微秒的半衰期被还原,这归因于预先形成的复合体,另一半在大约40微秒的半衰期被还原,这归因于细胞色素cy必须从另一个位点移动过来。这个较慢的阶段受到甘油添加的影响,表明它对介质粘度的依赖性。细胞色素cy尽管在毫秒时间范围内通过泛醌氧化被再还原,但实际上仍然无法将电子传递给其他保持光氧化状态达数秒的RCs。此外,使用两个由可变时间间隔隔开的闪光,结果表明快速供电子复合体在大约60微秒内重新形成,这个时间跨度可能反映了从细胞色素c1到细胞色素cy的电子转移。在没有细胞色素bc1复合体的情况下,使用在基本培养基中生长的细胞获得的载色体膜中细胞色素cy的稳态水平降低到大约50%。然而,剩余的细胞色素cy能够与RC形成快速供电子复合体(半衰期约为5微秒),而半衰期约为40微秒的较慢阶段则大大减速。这一发现表明细胞色素bc1复合体在稳定细胞色素cy并为其提供“另一个”位点方面发挥了作用,可能是通过这些组分之间的紧密结合。综上所述,得出的结论是,尽管与RCs相比,细胞色素cy以亚化学计量存在,但在没有细胞色素c2的情况下,它能有效地支持荚膜红细菌的光合生长,因为它可以在循环电子流的多次周转过程中介导从细胞色素bc1复合体到RC的快速电子转移。

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