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Energy transfer and charge separation kinetics in photosystem I

机译:光系统I中的能量转移和电荷分离动力学

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摘要

The energy transfer and charge separation kinetics of a photosystem I (PS I) core particle of an antenna size of 100 chlorophyll/P700 has been studied by combined fluorescence and transient absorption kinetics with picosecond resolution. This is the first combined picosecond study of transient absorption and fluorescence carried out on a PS I particle and the results are consistent with each other. The data were analyzed by both global lifetime and global target analysis procedures. In fluorescence major lifetime components were found to be 12 and 36 ps. The shorter-lived one shows a negative amplitude at long wavelengths and is attributed to an energy transfer process between pigments in the main antenna Chl pool and a small long-wavelength Chl pool emitting around 720 nm whereas the longer-lived component is assigned to the overall charge separation lifetime. The lifetimes resolved in transient absorption are 7-8 ps, 33 ps, and [unk]1 ns. The shortest-lived one is assigned to energy transfer between the same pigment pools as observed also in fluorescence kinetics, the middle component of 33 ps to the overall charge separation, and the long-lived component to the lifetime of the oxidized primary donor P700+. The transient absorption data indicate an even faster, but kinetically unresolved energy transfer component in the main Chl pool with a lifetime <3 ps. Several kinetic models were tested on both the fluorescence and the picosecond absorption data by global target analysis procedures. A model where the long-wave pigments are spatially and kinetically connected with the reaction center P700 is favored over a model where P700 is connected more closely with the main Chl pool. Our data show that the charge separation kinetics in these PS I particles is essentially trap limited. The relevance of our data with respect to other time-resolved studies on PS I core particles is discussed, in particular with respect to the nature and function of the long-wave pigments. From the transient absorption data we do not see any evidence for the occurrence of a reduced Chl primary electron acceptor, but we also can not exclude that possibility, provided that reoxidation of that acceptor should occur within a time <40 ps.
机译:通过结合皮秒分辨率的荧光和瞬态吸收动力学研究了天线尺寸为100叶绿素/ P700的光系统I(PS I)核心粒子的能量转移和电荷分离动力学。这是对PS I粒子进行的瞬态吸收和荧光的首次组合皮秒研究,结果彼此一致。通过全局生命周期和全局目标分析程序对数据进行了分析。在荧光中,发现主要寿命成分为12和36 ps。寿命较短的一个在长波长处显示负振幅,这归因于主天线Chl池中的颜料与一个较小的长波长Chl池之间的能量转移过程,该池发射约720 nm,而寿命更长的成分被分配给了总电荷分离寿命。在瞬态吸收中解析的寿命为7-8 ps,33 ps和[ns] 1 ns。寿命最短的一个被分配给相同的颜料池之间的能量转移,这在荧光动力学中也观察到,中间分量为33 ps,占总电荷分离,寿命长的分量为被氧化的主供体P700 < sup> + 。瞬态吸收数据表明主Chl池中甚至更快,但在动力学上尚未解析的能量传递组件,使用寿命<3 ps。通过整体目标分析程序,在荧光和皮秒吸收数据上测试了几种动力学模型。长波颜料在空间和动力学上与反应中心P700连接的模型比P700与主Chl库更紧密连接的模型更受青睐。我们的数据表明,这些PS I颗粒中的电荷分离动力学本质上受陷阱限制。讨论了我们的数据与PS I核芯颗粒的其他时间分辨研究有关的数据,特别是长波颜料的性质和功能。从瞬态吸收数据中,我们看不到有任何还原的Chl主电子受体发生的证据,但我们也不能排除这种可能性,条件是该受体的再氧化应在<40 ps的时间内发生。

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