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光系统I内电子转移的体内分析:两个叶醌是否参与其中?

In vivo analysis of the electron transfer within photosystem I: are the two phylloquinones involved?

作者信息

Joliot P, Joliot A

机构信息

Institut de Biologie Physico-Chimique, CNRS UPR 1261, Paris, France.

出版信息

Biochemistry. 1999 Aug 24;38(34):11130-6. doi: 10.1021/bi990857c.

Abstract

Electron transfer within PS I reaction centers has been analyzed in vivo in a mutant of Chlorella sorokiniana which lacks most of the PS II and of the peripheric antennae, using a new spectrophotometric technique with a time resolution of approximately 5 ns. Absorption changes associated with the oxidation of semiphylloquinone (acceptor A(1)(-)) have been characterized in the 371-545 nm spectral range. The oxidation of A(1)(-) and the reduction of an iron-sulfur cluster (F(X), F(A)F(B)) is monitored by an absorption decrease at 377 nm (semiphylloquinone absorption band) and by the decrease of two positive absorption bands around 480 and 515 nm, respectively, very likely associated with a local electrochromic shift induced by A(1)(-) on a carotenoid molecule localized in its vicinity. A(1)(-) undergoes a two-phase oxidation of about equal amplitude with half-times of approximately 18 and approximately 160 ns, respectively. Two hypotheses are proposed to interpret these data: (1) Photosystem I reaction centers are present under two conformational states which differ by the reoxidation rate of A(1)(-). (2) The two phylloquinones corresponding to the two branches of the PS I heterodimer are involved in the electron transfer. The similar amplitude of the two phases implies that the rates of electron transfer from P700 to each of the phylloquinones are about equal. The two different rate constants measured for A(1)(-) oxidation suggests some asymmetry in the relative position of the two phylloquinones with respect to F(X).

摘要

利用一种新的具有约5纳秒时间分辨率的分光光度技术,对缺乏大部分光系统II和外周天线的小球藻突变体的光系统I反应中心内的电子转移进行了体内分析。在371 - 545纳米光谱范围内,已对与半叶醌(受体A(1)(-))氧化相关的吸收变化进行了表征。通过377纳米处的吸收下降(半叶醌吸收带)以及分别在480和515纳米左右的两个正吸收带的下降来监测A(1)(-)的氧化和铁硫簇(F(X)、F(A)F(B))的还原,这很可能与A(1)(-)在其附近定位的类胡萝卜素分子上诱导的局部电致变色位移有关。A(1)(-)经历了一个大约等幅的两相氧化,半衰期分别约为18纳秒和160纳秒。提出了两种假说来解释这些数据:(1)光系统I反应中心以两种构象状态存在,这两种状态在A(1)(-)的再氧化速率上有所不同。(2)与光系统I异二聚体的两个分支相对应的两个叶醌参与了电子转移。两相的相似幅度意味着从P700到每个叶醌的电子转移速率大致相等。为A(1)(-)氧化测量的两个不同速率常数表明,两个叶醌相对于F(X)的相对位置存在一些不对称性。

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