叶绿素 a 在采光复合物中的红移吸收的寄生叶绿体模型

IF 5.2 1区 生物学 Q1 BIOLOGY Communications Biology Pub Date : 2024-10-29 DOI:10.1038/s42003-024-07101-9
Alessandro Agostini, David Bína, Dovilė Barcytė, Marco Bortolus, Marek Eliáš, Donatella Carbonera, Radek Litvín
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引用次数: 0

摘要

光合生物利用光获取能量。一些真核藻类专门通过调整叶绿素 a 的吸收来获取远红光,其机制仍有待阐明。在这里,我们结合光学检测磁共振和脉冲电子顺磁共振测量,对从淡水尾柱藻中分离出来的红色适应光收集复合物(rVCP)进行了研究,以确定负责这种显著适应的色素的位置。研究发现,这些色素属于叶绿素 a 的激发簇,位于复合体的核心,靠近 L1/L2 位点的类胡萝卜素中心。Chl a403/a603 结合位点的一对结构特征,即镁连接残基中组氨酸对天冬酰胺的取代和 i-4 位氨基酸的小尺寸,导致了[A/G]xxxN 主题,被认为是这一特征的起源。对各种真核生物红触角的系统发育分析发现,有几种潜在的 LHC 可能共享这种调谐机制。对藻类红光适应机制的了解有助于合理设计藻类品系,从而提高大规模生物技术应用中的光捕获能力和效率。组氨酸到天冬酰胺的交换以及叶绿素 a403/a603 结合位点 i-4 位上的小侧链残基是小栉水母和其他真核藻类采光复合物红移光适应性的原因。
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Eustigmatophyte model of red-shifted chlorophyll a absorption in light-harvesting complexes
Photosynthetic organisms harvest light for energy. Some eukaryotic algae have specialized in harvesting far-red light by tuning chlorophyll a absorption through a mechanism still to be elucidated. Here, we combined optically detected magnetic resonance and pulsed electron paramagnetic resonance measurements on red-adapted light-harvesting complexes, rVCP, isolated from the freshwater eustigmatophyte alga Trachydiscus minutus to identify the location of the pigments responsible for this remarkable adaptation. The pigments have been found to belong to an excitonic cluster of chlorophylls a at the core of the complex, close to the central carotenoids in L1/L2 sites. A pair of structural features of the Chl a403/a603 binding site, namely the histidine-to-asparagine substitution in the magnesium-ligation residue and the small size of the amino acid at the i-4 position, resulting in a [A/G]xxxN motif, are proposed to be the origin of this trait. Phylogenetic analysis of various eukaryotic red antennae identified several potential LHCs that could share this tuning mechanism. This knowledge of the red light acclimation mechanism in algae is a step towards rational design of algal strains in order to enhance light capture and efficiency in large-scale biotechnology applications. A histidine-to-asparagine exchange and a small-sidechain residue at the i-4 position of the chlorophyll a403/a603 binding sites are responsible for the red-shifted light adaption of the light harvesting complexes from Trachydiscus minutus and other eukaryotic algae.
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来源期刊
Communications Biology
Communications Biology Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
1.70%
发文量
1233
审稿时长
13 weeks
期刊介绍: Communications Biology is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the biological sciences. Research papers published by the journal represent significant advances bringing new biological insight to a specialized area of research.
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