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Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation

Understanding the mechanistic basis of balanced excitation energy distribution between photosystem II and photosystem I (PSII and PSI) requires detailed investigation of the thylakoid light‐harvesting system composed of energetically connected LHCII trimers. The exact mechanisms controlling the exci...

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Autores principales: Rantala, Sanna, Tikkanen, Mikko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508491/
https://www.ncbi.nlm.nih.gov/pubmed/31245706
http://dx.doi.org/10.1002/pld3.39
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author Rantala, Sanna
Tikkanen, Mikko
author_facet Rantala, Sanna
Tikkanen, Mikko
author_sort Rantala, Sanna
collection PubMed
description Understanding the mechanistic basis of balanced excitation energy distribution between photosystem II and photosystem I (PSII and PSI) requires detailed investigation of the thylakoid light‐harvesting system composed of energetically connected LHCII trimers. The exact mechanisms controlling the excitation energy distribution remain elusive, but reversible phosphorylation is known to be one important component. Here, we addressed the role of grana margins in regulation of excitation energy distribution, as these thylakoid domains host all the complexes of photosynthetic light reactions with dynamic response to environmental cues. First, the effect of detergents for the thylakoid membrane connectivity is explained. We show that a specific interaction between the separate LHCII trimers as well as between the LHCII trimers and the PSII and PSI–LHCI complexes is a prerequisite for energetically connected and functional thylakoid membrane. Second, we demonstrate that the optimization of light reactions under changing light conditions takes place in energetically connected LHCII lake and is attained by lateral rearrangements of the PSII–LHCII and PSI–LHCI–LHCII complexes depending especially on the phosphorylation status of the LHCII protein isoform LHCB2.
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spelling pubmed-65084912019-06-26 Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation Rantala, Sanna Tikkanen, Mikko Plant Direct Original Research Understanding the mechanistic basis of balanced excitation energy distribution between photosystem II and photosystem I (PSII and PSI) requires detailed investigation of the thylakoid light‐harvesting system composed of energetically connected LHCII trimers. The exact mechanisms controlling the excitation energy distribution remain elusive, but reversible phosphorylation is known to be one important component. Here, we addressed the role of grana margins in regulation of excitation energy distribution, as these thylakoid domains host all the complexes of photosynthetic light reactions with dynamic response to environmental cues. First, the effect of detergents for the thylakoid membrane connectivity is explained. We show that a specific interaction between the separate LHCII trimers as well as between the LHCII trimers and the PSII and PSI–LHCI complexes is a prerequisite for energetically connected and functional thylakoid membrane. Second, we demonstrate that the optimization of light reactions under changing light conditions takes place in energetically connected LHCII lake and is attained by lateral rearrangements of the PSII–LHCII and PSI–LHCI–LHCII complexes depending especially on the phosphorylation status of the LHCII protein isoform LHCB2. John Wiley and Sons Inc. 2018-02-14 /pmc/articles/PMC6508491/ /pubmed/31245706 http://dx.doi.org/10.1002/pld3.39 Text en © 2018 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://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 Research
Rantala, Sanna
Tikkanen, Mikko
Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title_full Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title_fullStr Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title_full_unstemmed Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title_short Phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
title_sort phosphorylation‐induced lateral rearrangements of thylakoid protein complexes upon light acclimation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508491/
https://www.ncbi.nlm.nih.gov/pubmed/31245706
http://dx.doi.org/10.1002/pld3.39
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