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The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas

PSBO is essential for the assembly of the oxygen‐evolving complex in plants and green algae. Despite its importance, we lack essential information on its lifetime and how it depends on the environmental conditions. We have generated nitrate‐inducible PSBO amiRNA lines in the green alga Chlamydomonas...

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Autores principales: Vidal‐Meireles, André, Kuntam, Soujanya, Széles, Eszter, Tóth, Dávid, Neupert, Juliane, Bock, Ralph, Tóth, Szilvia Z.
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/PMC10100022/
https://www.ncbi.nlm.nih.gov/pubmed/36320098
http://dx.doi.org/10.1111/pce.14481
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author Vidal‐Meireles, André
Kuntam, Soujanya
Széles, Eszter
Tóth, Dávid
Neupert, Juliane
Bock, Ralph
Tóth, Szilvia Z.
author_facet Vidal‐Meireles, André
Kuntam, Soujanya
Széles, Eszter
Tóth, Dávid
Neupert, Juliane
Bock, Ralph
Tóth, Szilvia Z.
author_sort Vidal‐Meireles, André
collection PubMed
description PSBO is essential for the assembly of the oxygen‐evolving complex in plants and green algae. Despite its importance, we lack essential information on its lifetime and how it depends on the environmental conditions. We have generated nitrate‐inducible PSBO amiRNA lines in the green alga Chlamydomonas reinhardtii. Transgenic strains grew normally under non‐inducing conditions, and their photosynthetic performance was comparable to the control strain. Upon induction of the PSBO amiRNA constructs, cell division halted. In acetate‐containing medium, cellular PSBO protein levels decreased by 60% within 24 h in the dark, by 75% in moderate light, and in high light, the protein completely degraded. Consequently, the photosynthetic apparatus became strongly damaged, probably due to ‘donor‐side‐induced photoinhibition’, and cellular ultrastructure was also severely affected. However, in the absence of acetate during induction, PSBO was remarkably stable at all light intensities and less substantial changes occurred in photosynthesis. Our results demonstrate that the lifetime of PSBO strongly depends on the light intensity and carbon availability, and thus, on the metabolic status of the cells. We also confirm that PSBO is required for photosystem II stability in C. reinhardtii and demonstrate that its specific loss also entails substantial changes in cell morphology and cell cycle.
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spelling pubmed-101000222023-04-14 The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas Vidal‐Meireles, André Kuntam, Soujanya Széles, Eszter Tóth, Dávid Neupert, Juliane Bock, Ralph Tóth, Szilvia Z. Plant Cell Environ Original Articles PSBO is essential for the assembly of the oxygen‐evolving complex in plants and green algae. Despite its importance, we lack essential information on its lifetime and how it depends on the environmental conditions. We have generated nitrate‐inducible PSBO amiRNA lines in the green alga Chlamydomonas reinhardtii. Transgenic strains grew normally under non‐inducing conditions, and their photosynthetic performance was comparable to the control strain. Upon induction of the PSBO amiRNA constructs, cell division halted. In acetate‐containing medium, cellular PSBO protein levels decreased by 60% within 24 h in the dark, by 75% in moderate light, and in high light, the protein completely degraded. Consequently, the photosynthetic apparatus became strongly damaged, probably due to ‘donor‐side‐induced photoinhibition’, and cellular ultrastructure was also severely affected. However, in the absence of acetate during induction, PSBO was remarkably stable at all light intensities and less substantial changes occurred in photosynthesis. Our results demonstrate that the lifetime of PSBO strongly depends on the light intensity and carbon availability, and thus, on the metabolic status of the cells. We also confirm that PSBO is required for photosystem II stability in C. reinhardtii and demonstrate that its specific loss also entails substantial changes in cell morphology and cell cycle. John Wiley and Sons Inc. 2022-11-17 2023-02 /pmc/articles/PMC10100022/ /pubmed/36320098 http://dx.doi.org/10.1111/pce.14481 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
Vidal‐Meireles, André
Kuntam, Soujanya
Széles, Eszter
Tóth, Dávid
Neupert, Juliane
Bock, Ralph
Tóth, Szilvia Z.
The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title_full The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title_fullStr The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title_full_unstemmed The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title_short The lifetime of the oxygen‐evolving complex subunit PSBO depends on light intensity and carbon availability in Chlamydomonas
title_sort lifetime of the oxygen‐evolving complex subunit psbo depends on light intensity and carbon availability in chlamydomonas
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100022/
https://www.ncbi.nlm.nih.gov/pubmed/36320098
http://dx.doi.org/10.1111/pce.14481
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