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Ion antiport accelerates photosynthetic acclimation in fluctuating light environments
Many photosynthetic organisms globally, including crops, forests and algae, must grow in environments where the availability of light energy fluctuates dramatically. How photosynthesis maintains high efficiency despite such fluctuations in its energy source remains poorly understood. Here we show th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243252/ https://www.ncbi.nlm.nih.gov/pubmed/25451040 http://dx.doi.org/10.1038/ncomms6439 |
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author | Armbruster, Ute Carrillo, L. Ruby Venema, Kees Pavlovic, Lazar Schmidtmann, Elisabeth Kornfeld, Ari Jahns, Peter Berry, Joseph A. Kramer, David M. Jonikas, Martin C. |
author_facet | Armbruster, Ute Carrillo, L. Ruby Venema, Kees Pavlovic, Lazar Schmidtmann, Elisabeth Kornfeld, Ari Jahns, Peter Berry, Joseph A. Kramer, David M. Jonikas, Martin C. |
author_sort | Armbruster, Ute |
collection | PubMed |
description | Many photosynthetic organisms globally, including crops, forests and algae, must grow in environments where the availability of light energy fluctuates dramatically. How photosynthesis maintains high efficiency despite such fluctuations in its energy source remains poorly understood. Here we show that Arabidopsis thaliana K(+) efflux antiporter (KEA3) is critical for high photosynthetic efficiency under fluctuating light. On a shift from dark to low light, or high to low light, kea3 mutants show prolonged dissipation of absorbed light energy as heat. KEA3 localizes to the thylakoid membrane, and allows proton efflux from the thylakoid lumen by proton/potassium antiport. KEA3’s activity accelerates the downregulation of pH-dependent energy dissipation after transitions to low light, leading to faster recovery of high photosystem II quantum efficiency and increased CO(2) assimilation. Our results reveal a mechanism that increases the efficiency of photosynthesis under fluctuating light. |
format | Online Article Text |
id | pubmed-4243252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42432522014-12-05 Ion antiport accelerates photosynthetic acclimation in fluctuating light environments Armbruster, Ute Carrillo, L. Ruby Venema, Kees Pavlovic, Lazar Schmidtmann, Elisabeth Kornfeld, Ari Jahns, Peter Berry, Joseph A. Kramer, David M. Jonikas, Martin C. Nat Commun Article Many photosynthetic organisms globally, including crops, forests and algae, must grow in environments where the availability of light energy fluctuates dramatically. How photosynthesis maintains high efficiency despite such fluctuations in its energy source remains poorly understood. Here we show that Arabidopsis thaliana K(+) efflux antiporter (KEA3) is critical for high photosynthetic efficiency under fluctuating light. On a shift from dark to low light, or high to low light, kea3 mutants show prolonged dissipation of absorbed light energy as heat. KEA3 localizes to the thylakoid membrane, and allows proton efflux from the thylakoid lumen by proton/potassium antiport. KEA3’s activity accelerates the downregulation of pH-dependent energy dissipation after transitions to low light, leading to faster recovery of high photosystem II quantum efficiency and increased CO(2) assimilation. Our results reveal a mechanism that increases the efficiency of photosynthesis under fluctuating light. Nature Pub. Group 2014-11-13 /pmc/articles/PMC4243252/ /pubmed/25451040 http://dx.doi.org/10.1038/ncomms6439 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Armbruster, Ute Carrillo, L. Ruby Venema, Kees Pavlovic, Lazar Schmidtmann, Elisabeth Kornfeld, Ari Jahns, Peter Berry, Joseph A. Kramer, David M. Jonikas, Martin C. Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title | Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title_full | Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title_fullStr | Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title_full_unstemmed | Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title_short | Ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
title_sort | ion antiport accelerates photosynthetic acclimation in fluctuating light environments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243252/ https://www.ncbi.nlm.nih.gov/pubmed/25451040 http://dx.doi.org/10.1038/ncomms6439 |
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