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Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)

Photosynthesis fuels life on Earth using sunlight as energy source. However, light has a simultaneous detrimental effect on the enzyme triggering photosynthesis and producing oxygen, photosystem II (PSII). Photoinhibition, the light-dependent decrease of PSII activity, results in a major limitation...

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Detalles Bibliográficos
Autores principales: Nawrocki, Wojciech J., Liu, Xin, Raber, Bailey, Hu, Chen, de Vitry, Catherine, Bennett, Doran I. G., Croce, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694598/
https://www.ncbi.nlm.nih.gov/pubmed/34936440
http://dx.doi.org/10.1126/sciadv.abj0055
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author Nawrocki, Wojciech J.
Liu, Xin
Raber, Bailey
Hu, Chen
de Vitry, Catherine
Bennett, Doran I. G.
Croce, Roberta
author_facet Nawrocki, Wojciech J.
Liu, Xin
Raber, Bailey
Hu, Chen
de Vitry, Catherine
Bennett, Doran I. G.
Croce, Roberta
author_sort Nawrocki, Wojciech J.
collection PubMed
description Photosynthesis fuels life on Earth using sunlight as energy source. However, light has a simultaneous detrimental effect on the enzyme triggering photosynthesis and producing oxygen, photosystem II (PSII). Photoinhibition, the light-dependent decrease of PSII activity, results in a major limitation to aquatic and land photosynthesis and occurs upon all environmental stress conditions. In this work, we investigated the molecular origins of photoinhibition focusing on the paradoxical energy dissipation process of unknown nature coinciding with PSII damage. Integrating spectroscopic, biochemical, and computational approaches, we demonstrate that the site of this quenching process is the PSII reaction center. We propose that the formation of quenching and the closure of PSII stem from the same event. We lastly reveal the heterogeneity of PSII upon photoinhibition using structure-function modeling of excitation energy transfer. This work unravels the functional details of the damage-induced energy dissipation at the heart of photosynthesis.
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spelling pubmed-86945982022-01-03 Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I) Nawrocki, Wojciech J. Liu, Xin Raber, Bailey Hu, Chen de Vitry, Catherine Bennett, Doran I. G. Croce, Roberta Sci Adv Biomedicine and Life Sciences Photosynthesis fuels life on Earth using sunlight as energy source. However, light has a simultaneous detrimental effect on the enzyme triggering photosynthesis and producing oxygen, photosystem II (PSII). Photoinhibition, the light-dependent decrease of PSII activity, results in a major limitation to aquatic and land photosynthesis and occurs upon all environmental stress conditions. In this work, we investigated the molecular origins of photoinhibition focusing on the paradoxical energy dissipation process of unknown nature coinciding with PSII damage. Integrating spectroscopic, biochemical, and computational approaches, we demonstrate that the site of this quenching process is the PSII reaction center. We propose that the formation of quenching and the closure of PSII stem from the same event. We lastly reveal the heterogeneity of PSII upon photoinhibition using structure-function modeling of excitation energy transfer. This work unravels the functional details of the damage-induced energy dissipation at the heart of photosynthesis. American Association for the Advancement of Science 2021-12-22 /pmc/articles/PMC8694598/ /pubmed/34936440 http://dx.doi.org/10.1126/sciadv.abj0055 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Nawrocki, Wojciech J.
Liu, Xin
Raber, Bailey
Hu, Chen
de Vitry, Catherine
Bennett, Doran I. G.
Croce, Roberta
Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title_full Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title_fullStr Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title_full_unstemmed Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title_short Molecular origins of induction and loss of photoinhibition-related energy dissipation q(I)
title_sort molecular origins of induction and loss of photoinhibition-related energy dissipation q(i)
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694598/
https://www.ncbi.nlm.nih.gov/pubmed/34936440
http://dx.doi.org/10.1126/sciadv.abj0055
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