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Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis

Absorption, fluorescence spectra of chlorophyll a (Chl-a) and all-trans-β-carotene (β-Car) mixing solution are investigated in different polarity and polarizability solvents. The carotenoids regulate the energy flow in photosynthesis by interaction with chlorophyll, leading to an observable reductio...

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Autores principales: Chen, Chen, Gong, Nan, Li, Zuowei, Sun, Chenglin, Men, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151392/
https://www.ncbi.nlm.nih.gov/pubmed/28934156
http://dx.doi.org/10.3390/molecules22101585
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author Chen, Chen
Gong, Nan
Li, Zuowei
Sun, Chenglin
Men, Zhiwei
author_facet Chen, Chen
Gong, Nan
Li, Zuowei
Sun, Chenglin
Men, Zhiwei
author_sort Chen, Chen
collection PubMed
description Absorption, fluorescence spectra of chlorophyll a (Chl-a) and all-trans-β-carotene (β-Car) mixing solution are investigated in different polarity and polarizability solvents. The carotenoids regulate the energy flow in photosynthesis by interaction with chlorophyll, leading to an observable reduction of Chl-a fluorescence. The fluorescence red shifts with the increasing solvent polarizability. The energy transfer in the Chl-a and β-Car system is proposed. The electron transfer should be dominant in quenching Chl-a fluorescence rather than the energy transfer in this system. Polar solvent with large polarizability shows high quenching efficiency. When dissolved in carbon tetrachloride, Chl-a presents red shift of absorption and blue shift of fluorescence spectra with increasing β-Car concentration, which implies a Chl-a conformational change.
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spelling pubmed-61513922018-11-13 Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis Chen, Chen Gong, Nan Li, Zuowei Sun, Chenglin Men, Zhiwei Molecules Letter Absorption, fluorescence spectra of chlorophyll a (Chl-a) and all-trans-β-carotene (β-Car) mixing solution are investigated in different polarity and polarizability solvents. The carotenoids regulate the energy flow in photosynthesis by interaction with chlorophyll, leading to an observable reduction of Chl-a fluorescence. The fluorescence red shifts with the increasing solvent polarizability. The energy transfer in the Chl-a and β-Car system is proposed. The electron transfer should be dominant in quenching Chl-a fluorescence rather than the energy transfer in this system. Polar solvent with large polarizability shows high quenching efficiency. When dissolved in carbon tetrachloride, Chl-a presents red shift of absorption and blue shift of fluorescence spectra with increasing β-Car concentration, which implies a Chl-a conformational change. MDPI 2017-09-21 /pmc/articles/PMC6151392/ /pubmed/28934156 http://dx.doi.org/10.3390/molecules22101585 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Letter
Chen, Chen
Gong, Nan
Li, Zuowei
Sun, Chenglin
Men, Zhiwei
Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title_full Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title_fullStr Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title_full_unstemmed Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title_short Concentration Effect on Quenching of Chlorophyll a Fluorescence by All-Trans-β-Carotene in Photosynthesis
title_sort concentration effect on quenching of chlorophyll a fluorescence by all-trans-β-carotene in photosynthesis
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151392/
https://www.ncbi.nlm.nih.gov/pubmed/28934156
http://dx.doi.org/10.3390/molecules22101585
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