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Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability
The filamentous diazotrophic cyanobacterium Trichodesmium is responsible for a significant fraction of marine di-nitrogen (N(2)) fixation. Growth and distribution of Trichodesmium and other diazotrophs in the vast oligotrophic subtropical gyres is influenced by iron (Fe) and phosphorus (P) availabil...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941076/ https://www.ncbi.nlm.nih.gov/pubmed/34819612 http://dx.doi.org/10.1038/s41396-021-01151-1 |
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author | Cerdan-Garcia, E. Baylay, A. Polyviou, D. Woodward, E. M. S. Wrightson, L. Mahaffey, C. Lohan, M. C. Moore, C. M. Bibby, T. S. Robidart, J. C. |
author_facet | Cerdan-Garcia, E. Baylay, A. Polyviou, D. Woodward, E. M. S. Wrightson, L. Mahaffey, C. Lohan, M. C. Moore, C. M. Bibby, T. S. Robidart, J. C. |
author_sort | Cerdan-Garcia, E. |
collection | PubMed |
description | The filamentous diazotrophic cyanobacterium Trichodesmium is responsible for a significant fraction of marine di-nitrogen (N(2)) fixation. Growth and distribution of Trichodesmium and other diazotrophs in the vast oligotrophic subtropical gyres is influenced by iron (Fe) and phosphorus (P) availability, while reciprocally influencing the biogeochemistry of these nutrients. Here we use observations across natural inverse gradients in Fe and P in the North Atlantic subtropical gyre (NASG) to demonstrate how Trichodesmium acclimates in situ to resource availability. Transcriptomic analysis identified progressive upregulation of known iron-stress biomarker genes with decreasing Fe availability, and progressive upregulation of genes involved in the acquisition of diverse P sources with decreasing P availability, while genes involved in N(2) fixation were upregulated at the intersection under moderate Fe and P availability. Enhanced N(2) fixation within the Fe and P co-stressed transition region was also associated with a distinct, consistent metabolic profile, including the expression of alternative photosynthetic pathways that potentially facilitate ATP generation required for N(2) fixation with reduced net oxygen production. The observed response of Trichodesmium to availability of both Fe and P supports suggestions that these biogeochemically significant organisms employ unique molecular, and thus physiological responses as adaptations to specifically exploit the Fe and P co-limited niche they construct. |
format | Online Article Text |
id | pubmed-8941076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89410762022-04-08 Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability Cerdan-Garcia, E. Baylay, A. Polyviou, D. Woodward, E. M. S. Wrightson, L. Mahaffey, C. Lohan, M. C. Moore, C. M. Bibby, T. S. Robidart, J. C. ISME J Article The filamentous diazotrophic cyanobacterium Trichodesmium is responsible for a significant fraction of marine di-nitrogen (N(2)) fixation. Growth and distribution of Trichodesmium and other diazotrophs in the vast oligotrophic subtropical gyres is influenced by iron (Fe) and phosphorus (P) availability, while reciprocally influencing the biogeochemistry of these nutrients. Here we use observations across natural inverse gradients in Fe and P in the North Atlantic subtropical gyre (NASG) to demonstrate how Trichodesmium acclimates in situ to resource availability. Transcriptomic analysis identified progressive upregulation of known iron-stress biomarker genes with decreasing Fe availability, and progressive upregulation of genes involved in the acquisition of diverse P sources with decreasing P availability, while genes involved in N(2) fixation were upregulated at the intersection under moderate Fe and P availability. Enhanced N(2) fixation within the Fe and P co-stressed transition region was also associated with a distinct, consistent metabolic profile, including the expression of alternative photosynthetic pathways that potentially facilitate ATP generation required for N(2) fixation with reduced net oxygen production. The observed response of Trichodesmium to availability of both Fe and P supports suggestions that these biogeochemically significant organisms employ unique molecular, and thus physiological responses as adaptations to specifically exploit the Fe and P co-limited niche they construct. Nature Publishing Group UK 2021-11-24 2022-04 /pmc/articles/PMC8941076/ /pubmed/34819612 http://dx.doi.org/10.1038/s41396-021-01151-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cerdan-Garcia, E. Baylay, A. Polyviou, D. Woodward, E. M. S. Wrightson, L. Mahaffey, C. Lohan, M. C. Moore, C. M. Bibby, T. S. Robidart, J. C. Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title | Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title_full | Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title_fullStr | Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title_full_unstemmed | Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title_short | Transcriptional responses of Trichodesmium to natural inverse gradients of Fe and P availability |
title_sort | transcriptional responses of trichodesmium to natural inverse gradients of fe and p availability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941076/ https://www.ncbi.nlm.nih.gov/pubmed/34819612 http://dx.doi.org/10.1038/s41396-021-01151-1 |
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