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Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942

Iron is an essential component in many protein complexes involved in photosynthesis, but environmental iron availability is often low as oxidized forms of iron are insoluble in water. To adjust to low environmental iron levels, cyanobacteria undergo numerous changes to balance their iron budget and...

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Autores principales: Fraser, Jared M., Tulk, Sarah E., Jeans, Jennifer A., Campbell, Douglas A., Bibby, Thomas S., Cockshutt, Amanda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602374/
https://www.ncbi.nlm.nih.gov/pubmed/23527279
http://dx.doi.org/10.1371/journal.pone.0059861
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author Fraser, Jared M.
Tulk, Sarah E.
Jeans, Jennifer A.
Campbell, Douglas A.
Bibby, Thomas S.
Cockshutt, Amanda M.
author_facet Fraser, Jared M.
Tulk, Sarah E.
Jeans, Jennifer A.
Campbell, Douglas A.
Bibby, Thomas S.
Cockshutt, Amanda M.
author_sort Fraser, Jared M.
collection PubMed
description Iron is an essential component in many protein complexes involved in photosynthesis, but environmental iron availability is often low as oxidized forms of iron are insoluble in water. To adjust to low environmental iron levels, cyanobacteria undergo numerous changes to balance their iron budget and mitigate the physiological effects of iron depletion. We investigated changes in key protein abundances and photophysiological parameters in the model cyanobacteria Synechococcus PCC 7942 and Synechocystis PCC 6803 over a 120 hour time course of iron deprivation. The iron stress induced protein (IsiA) accumulated to high levels within 48 h of the onset of iron deprivation, reaching a molar ratio of ∼42 IsiA : Photosystem I in Synechococcus PCC 7942 and ∼12 IsiA : Photosystem I in Synechocystis PCC 6803. Concomitantly the iron-rich complexes Cytochrome b(6)f and Photosystem I declined in abundance, leading to a decrease in the Photosystem I : Photosystem II ratio. Chlorophyll fluorescence analyses showed a drop in electron transport per Photosystem II in Synechococcus, but not in Synechocystis after iron depletion. We found no evidence that the accumulated IsiA contributes to light capture by Photosystem II complexes.
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spelling pubmed-36023742013-03-22 Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942 Fraser, Jared M. Tulk, Sarah E. Jeans, Jennifer A. Campbell, Douglas A. Bibby, Thomas S. Cockshutt, Amanda M. PLoS One Research Article Iron is an essential component in many protein complexes involved in photosynthesis, but environmental iron availability is often low as oxidized forms of iron are insoluble in water. To adjust to low environmental iron levels, cyanobacteria undergo numerous changes to balance their iron budget and mitigate the physiological effects of iron depletion. We investigated changes in key protein abundances and photophysiological parameters in the model cyanobacteria Synechococcus PCC 7942 and Synechocystis PCC 6803 over a 120 hour time course of iron deprivation. The iron stress induced protein (IsiA) accumulated to high levels within 48 h of the onset of iron deprivation, reaching a molar ratio of ∼42 IsiA : Photosystem I in Synechococcus PCC 7942 and ∼12 IsiA : Photosystem I in Synechocystis PCC 6803. Concomitantly the iron-rich complexes Cytochrome b(6)f and Photosystem I declined in abundance, leading to a decrease in the Photosystem I : Photosystem II ratio. Chlorophyll fluorescence analyses showed a drop in electron transport per Photosystem II in Synechococcus, but not in Synechocystis after iron depletion. We found no evidence that the accumulated IsiA contributes to light capture by Photosystem II complexes. Public Library of Science 2013-03-19 /pmc/articles/PMC3602374/ /pubmed/23527279 http://dx.doi.org/10.1371/journal.pone.0059861 Text en © 2013 Fraser et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fraser, Jared M.
Tulk, Sarah E.
Jeans, Jennifer A.
Campbell, Douglas A.
Bibby, Thomas S.
Cockshutt, Amanda M.
Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title_full Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title_fullStr Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title_full_unstemmed Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title_short Photophysiological and Photosynthetic Complex Changes during Iron Starvation in Synechocystis sp. PCC 6803 and Synechococcus elongatus PCC 7942
title_sort photophysiological and photosynthetic complex changes during iron starvation in synechocystis sp. pcc 6803 and synechococcus elongatus pcc 7942
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602374/
https://www.ncbi.nlm.nih.gov/pubmed/23527279
http://dx.doi.org/10.1371/journal.pone.0059861
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