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pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas

Sunlight drives photosynthesis but can also cause photodamage. To protect themselves, photosynthetic organisms dissipate the excess absorbed energy as heat, in a process known as nonphotochemical quenching (NPQ). In green algae, diatoms, and mosses, NPQ depends on the light-harvesting complex stress...

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Autores principales: Tian, Lijin, Nawrocki, Wojciech J., Liu, Xin, Polukhina, Iryna, van Stokkum, Ivo H. M., Croce, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486713/
https://www.ncbi.nlm.nih.gov/pubmed/30962362
http://dx.doi.org/10.1073/pnas.1817796116
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author Tian, Lijin
Nawrocki, Wojciech J.
Liu, Xin
Polukhina, Iryna
van Stokkum, Ivo H. M.
Croce, Roberta
author_facet Tian, Lijin
Nawrocki, Wojciech J.
Liu, Xin
Polukhina, Iryna
van Stokkum, Ivo H. M.
Croce, Roberta
author_sort Tian, Lijin
collection PubMed
description Sunlight drives photosynthesis but can also cause photodamage. To protect themselves, photosynthetic organisms dissipate the excess absorbed energy as heat, in a process known as nonphotochemical quenching (NPQ). In green algae, diatoms, and mosses, NPQ depends on the light-harvesting complex stress-related (LHCSR) proteins. Here we investigated NPQ in Chlamydomonas reinhardtii using an approach that maintains the cells in a stable quenched state. We show that in the presence of LHCSR3, all of the photosystem (PS) II complexes are quenched and the LHCs are the site of quenching, which occurs at a rate of ∼150 ps(−1) and is not induced by LHCII aggregation. The effective light-harvesting capacity of PSII decreases upon NPQ, and the NPQ rate is independent of the redox state of the reaction center. Finally, we could measure the pH dependence of NPQ, showing that the luminal pH is always above 5.5 in vivo and highlighting the role of LHCSR3 as an ultrasensitive pH sensor.
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spelling pubmed-64867132019-05-07 pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas Tian, Lijin Nawrocki, Wojciech J. Liu, Xin Polukhina, Iryna van Stokkum, Ivo H. M. Croce, Roberta Proc Natl Acad Sci U S A Biological Sciences Sunlight drives photosynthesis but can also cause photodamage. To protect themselves, photosynthetic organisms dissipate the excess absorbed energy as heat, in a process known as nonphotochemical quenching (NPQ). In green algae, diatoms, and mosses, NPQ depends on the light-harvesting complex stress-related (LHCSR) proteins. Here we investigated NPQ in Chlamydomonas reinhardtii using an approach that maintains the cells in a stable quenched state. We show that in the presence of LHCSR3, all of the photosystem (PS) II complexes are quenched and the LHCs are the site of quenching, which occurs at a rate of ∼150 ps(−1) and is not induced by LHCII aggregation. The effective light-harvesting capacity of PSII decreases upon NPQ, and the NPQ rate is independent of the redox state of the reaction center. Finally, we could measure the pH dependence of NPQ, showing that the luminal pH is always above 5.5 in vivo and highlighting the role of LHCSR3 as an ultrasensitive pH sensor. National Academy of Sciences 2019-04-23 2019-04-08 /pmc/articles/PMC6486713/ /pubmed/30962362 http://dx.doi.org/10.1073/pnas.1817796116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Tian, Lijin
Nawrocki, Wojciech J.
Liu, Xin
Polukhina, Iryna
van Stokkum, Ivo H. M.
Croce, Roberta
pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title_full pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title_fullStr pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title_full_unstemmed pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title_short pH dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in Chlamydomonas
title_sort ph dependence, kinetics and light-harvesting regulation of nonphotochemical quenching in chlamydomonas
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486713/
https://www.ncbi.nlm.nih.gov/pubmed/30962362
http://dx.doi.org/10.1073/pnas.1817796116
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