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Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations

Photosynthetic organisms use sunlight as the primary energy source to fix CO(2). However, in nature, light energy is highly variable, reaching levels of saturation for periods ranging from milliseconds to hours. In the green microalga Chlamydomonas reinhardtii, safe dissipation of excess light energ...

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Autores principales: Steen, Collin J., Burlacot, Adrien, Short, Audrey H., Niyogi, Krishna K., Fleming, Graham R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540987/
https://www.ncbi.nlm.nih.gov/pubmed/35678230
http://dx.doi.org/10.1111/pce.14372
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author Steen, Collin J.
Burlacot, Adrien
Short, Audrey H.
Niyogi, Krishna K.
Fleming, Graham R.
author_facet Steen, Collin J.
Burlacot, Adrien
Short, Audrey H.
Niyogi, Krishna K.
Fleming, Graham R.
author_sort Steen, Collin J.
collection PubMed
description Photosynthetic organisms use sunlight as the primary energy source to fix CO(2). However, in nature, light energy is highly variable, reaching levels of saturation for periods ranging from milliseconds to hours. In the green microalga Chlamydomonas reinhardtii, safe dissipation of excess light energy by nonphotochemical quenching (NPQ) is mediated by light‐harvesting complex stress‐related (LHCSR) proteins and redistribution of light‐harvesting antennae between the photosystems (state transition). Although each component underlying NPQ has been documented, their relative contributions to NPQ under fluctuating light conditions remain unknown. Here, by monitoring NPQ in intact cells throughout high light/dark cycles of various illumination periods, we find that the dynamics of NPQ depend on the timescales of light fluctuations. We show that LHCSRs play a major role during the light phases of light fluctuations and describe their role in growth under rapid light fluctuations. We further reveal an activation of NPQ during the dark phases of all high light/dark cycles and show that this phenomenon arises from state transition. Finally, we show that LHCSRs and state transition synergistically cooperate to enable NPQ response during light fluctuations. These results highlight the dynamic functioning of photoprotection under light fluctuations and open a new way to systematically characterize the photosynthetic response to an ever‐changing light environment.
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spelling pubmed-95409872022-10-14 Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations Steen, Collin J. Burlacot, Adrien Short, Audrey H. Niyogi, Krishna K. Fleming, Graham R. Plant Cell Environ Original Articles Photosynthetic organisms use sunlight as the primary energy source to fix CO(2). However, in nature, light energy is highly variable, reaching levels of saturation for periods ranging from milliseconds to hours. In the green microalga Chlamydomonas reinhardtii, safe dissipation of excess light energy by nonphotochemical quenching (NPQ) is mediated by light‐harvesting complex stress‐related (LHCSR) proteins and redistribution of light‐harvesting antennae between the photosystems (state transition). Although each component underlying NPQ has been documented, their relative contributions to NPQ under fluctuating light conditions remain unknown. Here, by monitoring NPQ in intact cells throughout high light/dark cycles of various illumination periods, we find that the dynamics of NPQ depend on the timescales of light fluctuations. We show that LHCSRs play a major role during the light phases of light fluctuations and describe their role in growth under rapid light fluctuations. We further reveal an activation of NPQ during the dark phases of all high light/dark cycles and show that this phenomenon arises from state transition. Finally, we show that LHCSRs and state transition synergistically cooperate to enable NPQ response during light fluctuations. These results highlight the dynamic functioning of photoprotection under light fluctuations and open a new way to systematically characterize the photosynthetic response to an ever‐changing light environment. John Wiley and Sons Inc. 2022-06-21 2022-08 /pmc/articles/PMC9540987/ /pubmed/35678230 http://dx.doi.org/10.1111/pce.14372 Text en © 2022 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Steen, Collin J.
Burlacot, Adrien
Short, Audrey H.
Niyogi, Krishna K.
Fleming, Graham R.
Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title_full Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title_fullStr Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title_full_unstemmed Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title_short Interplay between LHCSR proteins and state transitions governs the NPQ response in Chlamydomonas during light fluctuations
title_sort interplay between lhcsr proteins and state transitions governs the npq response in chlamydomonas during light fluctuations
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540987/
https://www.ncbi.nlm.nih.gov/pubmed/35678230
http://dx.doi.org/10.1111/pce.14372
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