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Reduction-dependent siderophore assimilation in a model pennate diatom

Iron uptake by diatoms is a biochemical process with global biogeochemical implications. In large regions of the surface ocean diatoms are both responsible for the majority of primary production and frequently experiencing iron limitation of growth. The strategies used by these phytoplankton to extr...

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Autores principales: Coale, Tyler H., Moosburner, Mark, Horák, Aleš, Oborník, Miroslav, Barbeau, Katherine A., Allen, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876252/
https://www.ncbi.nlm.nih.gov/pubmed/31685631
http://dx.doi.org/10.1073/pnas.1907234116
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author Coale, Tyler H.
Moosburner, Mark
Horák, Aleš
Oborník, Miroslav
Barbeau, Katherine A.
Allen, Andrew E.
author_facet Coale, Tyler H.
Moosburner, Mark
Horák, Aleš
Oborník, Miroslav
Barbeau, Katherine A.
Allen, Andrew E.
author_sort Coale, Tyler H.
collection PubMed
description Iron uptake by diatoms is a biochemical process with global biogeochemical implications. In large regions of the surface ocean diatoms are both responsible for the majority of primary production and frequently experiencing iron limitation of growth. The strategies used by these phytoplankton to extract iron from seawater constrain carbon flux into higher trophic levels and sequestration into sediments. In this study we use reverse genetic techniques to target putative iron-acquisition genes in the model pennate diatom Phaeodactylum tricornutum. We describe components of a reduction-dependent siderophore acquisition pathway that relies on a bacterial-derived receptor protein and provides a viable alternative to inorganic iron uptake under certain conditions. This form of iron uptake entails a close association between diatoms and siderophore-producing organisms during low-iron conditions. Homologs of these proteins are found distributed across diatom lineages, suggesting the significance of siderophore utilization by diatoms in the marine environment. Evaluation of specific proteins enables us to confirm independent iron-acquisition pathways in diatoms and characterize their preferred substrates. These findings refine our mechanistic understanding of the multiple iron-uptake systems used by diatoms and help us better predict the influence of iron speciation on taxa-specific iron bioavailability.
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spelling pubmed-68762522019-11-29 Reduction-dependent siderophore assimilation in a model pennate diatom Coale, Tyler H. Moosburner, Mark Horák, Aleš Oborník, Miroslav Barbeau, Katherine A. Allen, Andrew E. Proc Natl Acad Sci U S A PNAS Plus Iron uptake by diatoms is a biochemical process with global biogeochemical implications. In large regions of the surface ocean diatoms are both responsible for the majority of primary production and frequently experiencing iron limitation of growth. The strategies used by these phytoplankton to extract iron from seawater constrain carbon flux into higher trophic levels and sequestration into sediments. In this study we use reverse genetic techniques to target putative iron-acquisition genes in the model pennate diatom Phaeodactylum tricornutum. We describe components of a reduction-dependent siderophore acquisition pathway that relies on a bacterial-derived receptor protein and provides a viable alternative to inorganic iron uptake under certain conditions. This form of iron uptake entails a close association between diatoms and siderophore-producing organisms during low-iron conditions. Homologs of these proteins are found distributed across diatom lineages, suggesting the significance of siderophore utilization by diatoms in the marine environment. Evaluation of specific proteins enables us to confirm independent iron-acquisition pathways in diatoms and characterize their preferred substrates. These findings refine our mechanistic understanding of the multiple iron-uptake systems used by diatoms and help us better predict the influence of iron speciation on taxa-specific iron bioavailability. National Academy of Sciences 2019-11-19 2019-11-04 /pmc/articles/PMC6876252/ /pubmed/31685631 http://dx.doi.org/10.1073/pnas.1907234116 Text en Copyright © 2019 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle PNAS Plus
Coale, Tyler H.
Moosburner, Mark
Horák, Aleš
Oborník, Miroslav
Barbeau, Katherine A.
Allen, Andrew E.
Reduction-dependent siderophore assimilation in a model pennate diatom
title Reduction-dependent siderophore assimilation in a model pennate diatom
title_full Reduction-dependent siderophore assimilation in a model pennate diatom
title_fullStr Reduction-dependent siderophore assimilation in a model pennate diatom
title_full_unstemmed Reduction-dependent siderophore assimilation in a model pennate diatom
title_short Reduction-dependent siderophore assimilation in a model pennate diatom
title_sort reduction-dependent siderophore assimilation in a model pennate diatom
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876252/
https://www.ncbi.nlm.nih.gov/pubmed/31685631
http://dx.doi.org/10.1073/pnas.1907234116
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