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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...

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Autores principales: Armbruster, Ute, Carrillo, L. Ruby, Venema, Kees, Pavlovic, Lazar, Schmidtmann, Elisabeth, Kornfeld, Ari, Jahns, Peter, Berry, Joseph A., Kramer, David M., Jonikas, Martin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
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.
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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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