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Equilibration kinetics in isolated and membrane-bound photosynthetic reaction centers upon illumination: a method to determine the photoexcitation rate

机译:光照下分离的和与膜结合的光合作用反应中的平衡动力学:确定光激发速率的方法

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摘要

Kinetics of electron transfer, following variation of actinic light intensity, for photosynthetic reaction centers (RCs) of purple bacteria (isolated and membrane-bound) were analyzed by measuring absorbance changes in the primary photoelectron donor absorption band at 865 nm. The bleaching of the primary photoelectron donor absorption band in RCs, following a sudden increase of illumination from the dark to an actinic light intensity of Iexp, obeys a simple exponential law with the rate constant , in which α is a parameter relating the light intensity, measured in mW/cm2, to a corresponding theoretical rate in units of reciprocal seconds, and krec is the effective rate constant of the charge recombination in the photosynthetic RCs. In this work, a method for determining the α parameter value is developed and experimentally verified for isolated and membrane-bound RCs, allowing for rigorous modeling of RC macromolecule dynamics under varied photoexcitation conditions. Such modeling is necessary for RCs due to alterations of the forward photoexcitation rates and relaxation rates caused by illumination history and intramolecular structural dynamics effects. It is demonstrated that the classical Bouguer–Lambert–Beer formalism can be applied for the samples with relatively low scattering, which is not necessarily the case with strongly scattering media or high light intensity excitation.
机译:通过测量865nm初级光电子供体吸收带中的吸光度变化,分析了光化强度变化后紫色细菌(分离的和与膜结合的)的光合作用中心(RC)的电子转移动力学。从黑暗中突然增加到Iexp的光化光强度后,RC中初级光电子供体吸收带的漂白遵循速率常数的简单指数定律,其中α是与光强度有关的参数,以mW / cm 2 为单位,以相应的理论速率(倒数秒)为单位,krec是光合作用RC中电荷重组的有效速率常数。在这项工作中,开发了一种确定α参数值的方法,并通过实验验证了隔离的和膜结合的RC,从而可以在各种光激发条件下对RC大分子动力学进行严格建模。由于正向光激发速率和弛豫速率的变化是由光照历史和分子内结构动力学效应引起的,因此对于RC来说,这种建模是必需的。结果表明,经典的Bouguer–Lambert–Beer形式主义可以应用于具有相对较低散射的样品,而对于具有强散射介质或高光强度激发的情况则不一定如此。

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