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Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism

In nitrogen-limited boreal forests, associations between feathermoss and diazotrophic cyanobacteria control nitrogen inputs and thus carbon cycling, but little is known about the molecular regulators required for initiation and maintenance of these associations. Specifically, a benefit to the cyanob...

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Autores principales: Stuart, Rhona K., Pederson, Eric R. A., Weyman, Philip D., Weber, Peter K., Rassmussen, Ulla, Dupont, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784912/
https://www.ncbi.nlm.nih.gov/pubmed/32814866
http://dx.doi.org/10.1038/s41396-020-00738-4
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author Stuart, Rhona K.
Pederson, Eric R. A.
Weyman, Philip D.
Weber, Peter K.
Rassmussen, Ulla
Dupont, Christopher L.
author_facet Stuart, Rhona K.
Pederson, Eric R. A.
Weyman, Philip D.
Weber, Peter K.
Rassmussen, Ulla
Dupont, Christopher L.
author_sort Stuart, Rhona K.
collection PubMed
description In nitrogen-limited boreal forests, associations between feathermoss and diazotrophic cyanobacteria control nitrogen inputs and thus carbon cycling, but little is known about the molecular regulators required for initiation and maintenance of these associations. Specifically, a benefit to the cyanobacteria is not known, challenging whether the association is a nutritional mutualism. Targeted mutagenesis of the cyanobacterial alkane sulfonate monooxygenase results in an inability to colonize feathermosses by the cyanobacterium Nostoc punctiforme, suggesting a role for organic sulfur in communication or nutrition. Isotope probing paired with high-resolution imaging mass spectrometry (NanoSIMS) demonstrated bidirectional elemental transfer between partners, with carbon and sulfur both being transferred to the cyanobacteria, and nitrogen transferred to the moss. These results support the hypothesis that moss and cyanobacteria enter a mutualistic exosymbiosis with substantial bidirectional material exchange of carbon and nitrogen and potential signaling through sulfur compounds.
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spelling pubmed-77849122021-01-14 Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism Stuart, Rhona K. Pederson, Eric R. A. Weyman, Philip D. Weber, Peter K. Rassmussen, Ulla Dupont, Christopher L. ISME J Article In nitrogen-limited boreal forests, associations between feathermoss and diazotrophic cyanobacteria control nitrogen inputs and thus carbon cycling, but little is known about the molecular regulators required for initiation and maintenance of these associations. Specifically, a benefit to the cyanobacteria is not known, challenging whether the association is a nutritional mutualism. Targeted mutagenesis of the cyanobacterial alkane sulfonate monooxygenase results in an inability to colonize feathermosses by the cyanobacterium Nostoc punctiforme, suggesting a role for organic sulfur in communication or nutrition. Isotope probing paired with high-resolution imaging mass spectrometry (NanoSIMS) demonstrated bidirectional elemental transfer between partners, with carbon and sulfur both being transferred to the cyanobacteria, and nitrogen transferred to the moss. These results support the hypothesis that moss and cyanobacteria enter a mutualistic exosymbiosis with substantial bidirectional material exchange of carbon and nitrogen and potential signaling through sulfur compounds. Nature Publishing Group UK 2020-08-19 2020-12 /pmc/articles/PMC7784912/ /pubmed/32814866 http://dx.doi.org/10.1038/s41396-020-00738-4 Text en © The Author(s) 2020 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/.
spellingShingle Article
Stuart, Rhona K.
Pederson, Eric R. A.
Weyman, Philip D.
Weber, Peter K.
Rassmussen, Ulla
Dupont, Christopher L.
Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title_full Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title_fullStr Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title_full_unstemmed Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title_short Bidirectional C and N transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
title_sort bidirectional c and n transfer and a potential role for sulfur in an epiphytic diazotrophic mutualism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784912/
https://www.ncbi.nlm.nih.gov/pubmed/32814866
http://dx.doi.org/10.1038/s41396-020-00738-4
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