Agalarov Rufat, Brettel Klaus
Service de Bioénergétique, CEA, and URA 2096 CNRS, CEA Saclay, Gif-sur-Yvette, France.
Biochim Biophys Acta. 2003 Apr 18;1604(1):7-12. doi: 10.1016/s0005-2728(03)00024-0.
The temperature dependence of the biphasic electron transfer (ET) from the secondary acceptor A1 (phylloquinone) to iron-sulfur cluster F(X) was investigated by flash absorption spectroscopy in photosystem I (PS I) isolated from Synechocystis sp. PCC 6803. While the slower phase (tau=340 ns at 295 K) slowed upon cooling according to an activation energy of 110 meV, the time constant of the faster phase (tau=11 ns at 295 K) was virtually independent of temperature. Following a suggestion in the literature that the two phases arise from bidirectional ET involving two symmetrically arranged phylloquinones, Q(K)-A and Q(K)-B, it is concluded that energetic parameters (most likely the driving forces) rather than the electronic couplings are different for ET from Q(K)-A to F(X) and from Q(K)-B to F(X). Two alternative schemes of ET in PS I are presented and discussed.
通过闪光吸收光谱法,研究了从集胞藻PCC 6803中分离出的光系统I(PS I)中,二次受体A1(叶绿醌)到铁硫簇F(X)的双相电子转移(ET)的温度依赖性。虽然较慢的相(295 K时τ = 340 ns)根据110 meV的活化能在冷却时变慢,但较快相的时间常数(295 K时τ = 11 ns)实际上与温度无关。根据文献中的建议,这两个相源于涉及两个对称排列的叶绿醌Q(K)-A和Q(K)-B的双向ET,得出的结论是,从Q(K)-A到F(X)以及从Q(K)-B到F(X)的ET,其能量参数(最有可能是驱动力)而非电子耦合是不同的。本文提出并讨论了PS I中ET的两种替代方案。