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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6508491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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