Vassiliev I R, Jung Y S, Mamedov M D, Golbeck J H
Department of Biochemistry, G. W. Beadle Center, University of Nebraska, Lincoln 68588-0664, USA.
Biophys J. 1997 Jan;72(1):301-15. doi: 10.1016/S0006-3495(97)78669-7.
The back-reaction kinetics in Photosystem I (PS I) were studied on the microsecond-to-s time scale in cyanobacterial preparations, which differed in the number of iron-sulfur clusters to assess the contributions of particular components to the reduction of P700+. In membrane fragments and in trimeric P700-FA/FB complexes, the major contribution to the absorbance change at 820 nm (delta A820) was the back-reaction of FA- and/or FB- with lifetimes of approximately 10 and 80 ms (approximately 10% and 40% relative amplitude). The decay of photoinduced electric potential (delta psi) across a membrane with directionally incorporated P700-FA/FB complexes had similar kinetics. HgCl2-treated PS I complexes, which contain FA but no FB, retain both of these kinetic components, indicating that neither can be assigned uniquely to a specific acceptor. These results suggest that FA- reduces P700+ directly and argue for a rapid electron equilibration between FA and FB, which would eliminate their kinetic distinction in a back-reaction. In PsaC-depleted P700-Fx cores, as well as in P700-FA/FB complexes with chemically reduced FA and FB, the major contribution to the delta A820 and the delta psi decay is a biphasic back-reaction of F-X (approximately 400 microseconds and 1.5 ms) with some contribution from A-1 (approximately 10 microseconds and 100 microseconds), the latter of which is variable depending on experimental conditions. The delta A820 decay in a P700-A1 core devoid of all iron-sulfur clusters comprises two phases with lifetimes of 10 microseconds and 130 microseconds (2.7:1 ratio). The biexponential back-reaction kinetics found for each of the electron acceptors may be related to existence of different conformational states of the PS I complex. In all preparations studied, excitation at 532 nm with flash energies exceeding 10 mJ gives rise to formation of antenna 3Chl, which also contributes to delta A820 decay on the tens-of-microsecond time scale. A distinction between delta A820 components related to back-reactions and to 3Chl decay can be made by analysis of flash saturation dependencies and by measurements of kinetics with preoxidized P700.
在蓝细菌制剂中,在微秒到秒的时间尺度上研究了光系统I(PS I)中的反向反应动力学,这些制剂中铁硫簇的数量不同,以评估特定组分对P700 +还原的贡献。在膜片段和三聚体P700 - FA/FB复合物中,820 nm处吸光度变化(ΔA820)的主要贡献是FA - 和/或FB - 的反向反应,其寿命约为10和80毫秒(相对幅度约为10%和40%)。具有定向掺入的P700 - FA/FB复合物的膜上光诱导电势(Δψ)的衰减具有相似的动力学。用HgCl2处理的PS I复合物,其中含有FA但不含FB,保留了这两种动力学成分,表明它们都不能唯一地归因于特定的受体。这些结果表明FA - 直接还原P700 +,并支持FA和FB之间的快速电子平衡,这将消除它们在反向反应中的动力学差异。在缺乏PsaC的P700 - Fx核心中,以及在化学还原的FA和FB的P700 - FA/FB复合物中,对ΔA820和Δψ衰减的主要贡献是F - X的双相反向反应(约400微秒和1.5毫秒),A - 1也有一些贡献(约10微秒和100微秒),后者根据实验条件而变化。不含所有铁硫簇的P700 - A1核心中的ΔA820衰减包括两个阶段,寿命分别为10微秒和130微秒(比例为2.7:1)。为每个电子受体发现的双指数反向反应动力学可能与PS I复合物不同构象状态的存在有关。在所有研究的制剂中,用超过10 mJ的闪光能量在532 nm处激发会导致天线3Chl的形成,这也在几十微秒的时间尺度上对ΔA820衰减有贡献。通过分析闪光饱和依赖性和测量预氧化P700的动力学,可以区分与反向反应和3Chl衰减相关的ΔA820成分。