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Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide
Nitrogen fixation rates of the globally distributed, biogeochemically important marine cyanobacterium Trichodesmium increase under high carbon dioxide (CO(2)) levels in short-term studies due to physiological plasticity. However, its long-term adaptive responses to ongoing anthropogenic CO(2) increa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569722/ https://www.ncbi.nlm.nih.gov/pubmed/26327191 http://dx.doi.org/10.1038/ncomms9155 |
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author | Hutchins, David A. Walworth, Nathan G. Webb, Eric A. Saito, Mak A. Moran, Dawn McIlvin, Matthew R. Gale, Jasmine Fu, Fei-Xue |
author_facet | Hutchins, David A. Walworth, Nathan G. Webb, Eric A. Saito, Mak A. Moran, Dawn McIlvin, Matthew R. Gale, Jasmine Fu, Fei-Xue |
author_sort | Hutchins, David A. |
collection | PubMed |
description | Nitrogen fixation rates of the globally distributed, biogeochemically important marine cyanobacterium Trichodesmium increase under high carbon dioxide (CO(2)) levels in short-term studies due to physiological plasticity. However, its long-term adaptive responses to ongoing anthropogenic CO(2) increases are unknown. Here we show that experimental evolution under extended selection at projected future elevated CO(2) levels results in irreversible, large increases in nitrogen fixation and growth rates, even after being moved back to lower present day CO(2) levels for hundreds of generations. This represents an unprecedented microbial evolutionary response, as reproductive fitness increases acquired in the selection environment are maintained after returning to the ancestral environment. Constitutive rate increases are accompanied by irreversible shifts in diel nitrogen fixation patterns, and increased activity of a potentially regulatory DNA methyltransferase enzyme. High CO(2)-selected cell lines also exhibit increased phosphorus-limited growth rates, suggesting a potential advantage for this keystone organism in a more nutrient-limited, acidified future ocean. |
format | Online Article Text |
id | pubmed-4569722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45697222015-09-28 Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide Hutchins, David A. Walworth, Nathan G. Webb, Eric A. Saito, Mak A. Moran, Dawn McIlvin, Matthew R. Gale, Jasmine Fu, Fei-Xue Nat Commun Article Nitrogen fixation rates of the globally distributed, biogeochemically important marine cyanobacterium Trichodesmium increase under high carbon dioxide (CO(2)) levels in short-term studies due to physiological plasticity. However, its long-term adaptive responses to ongoing anthropogenic CO(2) increases are unknown. Here we show that experimental evolution under extended selection at projected future elevated CO(2) levels results in irreversible, large increases in nitrogen fixation and growth rates, even after being moved back to lower present day CO(2) levels for hundreds of generations. This represents an unprecedented microbial evolutionary response, as reproductive fitness increases acquired in the selection environment are maintained after returning to the ancestral environment. Constitutive rate increases are accompanied by irreversible shifts in diel nitrogen fixation patterns, and increased activity of a potentially regulatory DNA methyltransferase enzyme. High CO(2)-selected cell lines also exhibit increased phosphorus-limited growth rates, suggesting a potential advantage for this keystone organism in a more nutrient-limited, acidified future ocean. Nature Pub. Group 2015-09-01 /pmc/articles/PMC4569722/ /pubmed/26327191 http://dx.doi.org/10.1038/ncomms9155 Text en Copyright © 2015, 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 Hutchins, David A. Walworth, Nathan G. Webb, Eric A. Saito, Mak A. Moran, Dawn McIlvin, Matthew R. Gale, Jasmine Fu, Fei-Xue Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title | Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title_full | Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title_fullStr | Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title_full_unstemmed | Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title_short | Irreversibly increased nitrogen fixation in Trichodesmium experimentally adapted to elevated carbon dioxide |
title_sort | irreversibly increased nitrogen fixation in trichodesmium experimentally adapted to elevated carbon dioxide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569722/ https://www.ncbi.nlm.nih.gov/pubmed/26327191 http://dx.doi.org/10.1038/ncomms9155 |
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