如何调整叶绿素的吸收光谱,以便更好地利用可用的太阳光谱

Pedro J. Silva, Maria Osswald-Claro, Rosário Castro Mendonça
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引用次数: 1

摘要

叶绿素和其他发色团在光采集复合体和光系统中捕获的光子是光合作用光反应背后的驱动力。光系统II的激发使其能够接收来自水氧化析氧复合物的电子,并将它们转移到电子传输链上,该电子传输链产生跨膜电化学梯度,并最终还原将其电子提供给光系统I的质体花青素。随后,光系统I的激发导致电子转移到铁氧还蛋白,铁氧还素可以再次还原质体花青素(以所谓的“循环电子流”)并释放能量以维持电化学梯度,或者将NADP+还原为NADPH。尽管太阳光谱中远红色(700–750 nm)部分的光子携带的能量足以使光合电子传递链发挥作用,但大多数现存的光系统通常无法利用它们,因为它们只能吸收波长较短的光。在这项工作中,我们使用计算方法来表征49种叶绿素衍生物的光谱和氧化还原性质,目的是找到合适的候选者,以掺入具有更强使用远红色光子能力的合成生物体中。这些数据为叶绿素a、b、c和d在所有容易合成的单取代叶绿素中的进化选择提供了一个简单而优雅的解释,并鉴定了一种新的候选物(2,12-二甲酰基叶绿素a),其吸收峰向远红色(相对于叶绿素a)移动79nm,其氧化还原特性完全适合其可能并入光系统I(尽管不是光系统II)。我们的数据表明,叶绿素d是最适合结合到利用光系统II的远红光中的候选者,并且发现了几个具有红移的Soret带的候选者,这些带允许通过光捕获复合物捕获大量的蓝光和绿光。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How to tune the absorption spectrum of chlorophylls to enable better use of the available solar spectrum
Photon capture by chlorophylls and other chromophores in light-harvesting complexes and photosystems is the driving force behind the light reactions of photosynthesis. Excitation of photosystem II allows it to receive electrons from the water-oxidizing oxygen-evolution complex and to transfer them to an electron-transport chain that generates a transmembrane electrochemical gradient and ultimately reduces plastocyanin, which donates its electron to photosystem I. Subsequently, excitation of photosystem I leads to electron transfer to a ferredoxin which can either reduce plastocyanin again (in so-called “cyclical electron-flow”) and release energy for the maintenance of the electrochemical gradient, or reduce NADP+ to NADPH. Although photons in the far-red (700–750 nm) portion of the solar spectrum carry enough energy to enable the functioning of the photosynthetic electron-transfer chain, most extant photosystems cannot usually take advantage of them due to only absorbing light with shorter wavelengths. In this work, we used computational methods to characterize the spectral and redox properties of 49 chlorophyll derivatives, with the aim of finding suitable candidates for incorporation into synthetic organisms with increased ability to use far-red photons. The data offer a simple and elegant explanation for the evolutionary selection of chlorophylls a, b, c, and d among all easily-synthesized singly-substituted chlorophylls, and identified one novel candidate (2,12-diformyl chlorophyll a) with an absorption peak shifted 79 nm into the far-red (relative to chlorophyll a) with redox characteristics fully suitable to its possible incorporation into photosystem I (though not photosystem II). chlorophyll d is shown by our data to be the most suitable candidate for incorporation into far-red utilizing photosystem II, and several candidates were found with red-shifted Soret bands that allow the capture of larger amounts of blue and green light by light harvesting complexes.
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