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Energy transfer dynamics in a red-shifted violaxanthin-chlorophyll a light-harvesting complex
Authors:David Bína  Milan Durchan  Valentyna Kuznetsova  Franti?ek Vácha  Radek Litvín  Tomá? Polívka
Institution:1. Institute of Chemistry, Faculty of Science, University of South Bohemia, Brani?ovská 1760, 37005 ?eské Budějovice, Czech Republic;2. Institute of Physics, Faculty of Science, University of South Bohemia, Brani?ovská 1760, 37005 ?eské Budějovice, Czech Republic;3. Institute of Plant Molecular Biology, Biological Centre, Czech Academy of Sciences, Brani?ovská 31, ?eské Budějovice, Czech Republic
Abstract:Photosynthetic eukaryotes whose cells harbor plastids originating from secondary endosymbiosis of a red alga include species of major ecological and economic importance. Since utilization of solar energy relies on the efficient light-harvesting, one of the critical factors for the success of the red lineage in a range of environments is to be found in the adaptability of the light-harvesting machinery, formed by the proteins of the light-harvesting complex (LHC) family. A number of species are known to employ mainly a unique class of LHC containing red-shifted chlorophyll a (Chl a) forms absorbing above 690?nm. This appears to be an adaptation to shaded habitats. Here we present a detailed investigation of excitation energy flow in the red-shifted light-harvesting antenna of eustigmatophyte Trachydiscus minutus using time-resolved fluorescence and ultrafast transient absorption measurements. The main carotenoid in the complex is violaxanthin, hence this LHC is labeled the red-violaxanthin-Chl a protein, rVCP. Both the carotenoid-to-Chl a energy transfer and excitation dynamics within the Chl a manifold were studied and compared to the related antenna complex, VCP, that lacks the red-Chl a. Two spectrally defined carotenoid pools were identified in the red antenna, contributing to energy transfer to Chl a, mostly via S2 and hot S1 states. Also, Chl a triplet quenching by carotenoids is documented. Two separate pools of red-shifted Chl a were resolved, one is likely formed by excitonically coupled Chl a molecules. The structural implications of these observations are discussed.
Keywords:Corresponding author: Institute of Physics and Biophysics  Faculty of Science  University of South Bohemia  Brani?ovská 1760  370 05 ?eské Budějovice  Czech Republic  
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