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评估紫色光合细菌捕光复合体2(LH2)中类胡萝卜素瞬态吸收中所谓S*态特征的本质。

Evaluating the Nature of So-Called S*-State Feature in Transient Absorption of Carotenoids in Light-Harvesting Complex 2 (LH2) from Purple Photosynthetic Bacteria.

作者信息

Niedzwiedzki Dariusz M, Hunter C Neil, Blankenship Robert E

机构信息

Department of Molecular Biology and Biotechnology, University of Sheffield , Sheffield S10 2TN, United Kingdom.

出版信息

J Phys Chem B. 2016 Nov 3;120(43):11123-11131. doi: 10.1021/acs.jpcb.6b08639. Epub 2016 Oct 20.

DOI:10.1021/acs.jpcb.6b08639
PMID:27726397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5098231/
Abstract

Carotenoids are a class of natural pigments present in all phototrophic organisms, mainly in their light-harvesting proteins in which they play roles of accessory light absorbers and photoprotectors. Extensive time-resolved spectroscopic studies of these pigments have revealed unexpectedly complex photophysical properties, particularly for carotenoids in light-harvesting LH2 complexes from purple bacteria. An ambiguous, optically forbidden electronic excited state designated as S* has been postulated to be involved in carotenoid excitation relaxation and in an alternative carotenoid-to-bacteriochlorophyll energy transfer pathway, as well as being a precursor of the carotenoid triplet state. However, no definitive and satisfactory origin of the carotenoid S* state in these complexes has been established, despite a wide-ranging series of studies. Here, we resolve the ambiguous origin of the carotenoid S* state in LH2 complex from Rba. sphaeroides by showing that the S* feature can be seen as a combination of ground state absorption bleaching of the carotenoid pool converted to cations and the Stark spectrum of neighbor neutral carotenoids, induced by temporal electric field brought by the carotenoid cation-bacteriochlorophyll anion pair. These findings remove the need to assign an S* state, and thereby significantly simplify the photochemistry of carotenoids in these photosynthetic antenna complexes.

摘要

类胡萝卜素是一类存在于所有光合生物中的天然色素,主要存在于它们的捕光蛋白中,在其中它们起着辅助光吸收剂和光保护剂的作用。对这些色素进行的广泛的时间分辨光谱研究揭示了出乎意料的复杂光物理性质,特别是对于来自紫色细菌的捕光LH2复合物中的类胡萝卜素。一种被指定为S的模糊的、光学禁阻的电子激发态被假定参与类胡萝卜素的激发弛豫以及另一种类胡萝卜素到细菌叶绿素的能量转移途径,并且还是类胡萝卜素三重态的前体。然而,尽管进行了一系列广泛的研究,但这些复合物中类胡萝卜素S态的确切且令人满意的起源尚未确定。在这里,我们通过表明S特征可以被视为由类胡萝卜素阳离子-细菌叶绿素阴离子对产生的瞬态电场诱导的、转化为阳离子的类胡萝卜素池的基态吸收漂白和相邻中性类胡萝卜素的斯塔克光谱的组合,解决了球形红杆菌LH2复合物中类胡萝卜素S态的模糊起源问题。这些发现消除了指定S*态的必要性,从而显著简化了这些光合天线复合物中类胡萝卜素的光化学过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ebb/5098231/4ec279c8273e/jp-2016-08639y_0008.jpg
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