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Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm

Increasing anthropogenic inputs of fixed nitrogen are leading to greater eutrophication of aquatic environments, but it is unclear how this impacts the flux and fate of carbon in lacustrine and riverine systems. Here, we present evidence that the form of nitrogen governs the partitioning of carbon a...

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Autores principales: Anderton, Christopher R., Mobberley, Jennifer M., Cole, Jessica K., Nunez, Jamie R., Starke, Robert, Boaro, Amy A., Yesiltepe, Yasemin, Morton, Beau R., Cory, Alexandra B., Cardamone, Hayley C., Hofmockel, Kirsten S., Lipton, Mary S., Moran, James J., Renslow, Ryan S., Fredrickson, James K., Lindemann, Stephen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289588/
https://www.ncbi.nlm.nih.gov/pubmed/32518194
http://dx.doi.org/10.1128/mSystems.00260-20
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author Anderton, Christopher R.
Mobberley, Jennifer M.
Cole, Jessica K.
Nunez, Jamie R.
Starke, Robert
Boaro, Amy A.
Yesiltepe, Yasemin
Morton, Beau R.
Cory, Alexandra B.
Cardamone, Hayley C.
Hofmockel, Kirsten S.
Lipton, Mary S.
Moran, James J.
Renslow, Ryan S.
Fredrickson, James K.
Lindemann, Stephen R.
author_facet Anderton, Christopher R.
Mobberley, Jennifer M.
Cole, Jessica K.
Nunez, Jamie R.
Starke, Robert
Boaro, Amy A.
Yesiltepe, Yasemin
Morton, Beau R.
Cory, Alexandra B.
Cardamone, Hayley C.
Hofmockel, Kirsten S.
Lipton, Mary S.
Moran, James J.
Renslow, Ryan S.
Fredrickson, James K.
Lindemann, Stephen R.
author_sort Anderton, Christopher R.
collection PubMed
description Increasing anthropogenic inputs of fixed nitrogen are leading to greater eutrophication of aquatic environments, but it is unclear how this impacts the flux and fate of carbon in lacustrine and riverine systems. Here, we present evidence that the form of nitrogen governs the partitioning of carbon among members in a genome-sequenced, model phototrophic biofilm of 20 members. Consumption of NO(3)(−) as the sole nitrogen source unexpectedly resulted in more rapid transfer of carbon to heterotrophs than when NH(4)(+) was also provided, suggesting alterations in the form of carbon exchanged. The form of nitrogen dramatically impacted net community nitrogen, but not carbon, uptake rates. Furthermore, this alteration in nitrogen form caused very large but focused alterations to community structure, strongly impacting the abundance of only two species within the biofilm and modestly impacting a third member species. Our data suggest that nitrogen metabolism may coordinate coupled carbon-nitrogen biogeochemical cycling in benthic biofilms and, potentially, in phototroph-heterotroph consortia more broadly. It further indicates that the form of nitrogen inputs may significantly impact the contribution of these communities to carbon partitioning across the terrestrial-aquatic interface. IMPORTANCE Anthropogenic inputs of nitrogen into aquatic ecosystems, and especially those of agricultural origin, involve a mix of chemical species. Although it is well-known in general that nitrogen eutrophication markedly influences the metabolism of aquatic phototrophic communities, relatively little is known regarding whether the specific chemical form of nitrogen inputs matter. Our data suggest that the nitrogen form alters the rate of nitrogen uptake significantly, whereas corresponding alterations in carbon uptake were minor. However, differences imposed by uptake of divergent nitrogen forms may result in alterations among phototroph-heterotroph interactions that rewire community metabolism. Furthermore, our data hint that availability of other nutrients (i.e., iron) might mediate the linkage between carbon and nitrogen cycling in these communities. Taken together, our data suggest that different nitrogen forms should be examined for divergent impacts on phototrophic communities in fluvial systems and that these anthropogenic nitrogen inputs may significantly differ in their ultimate biogeochemical impacts.
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spelling pubmed-72895882020-06-25 Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm Anderton, Christopher R. Mobberley, Jennifer M. Cole, Jessica K. Nunez, Jamie R. Starke, Robert Boaro, Amy A. Yesiltepe, Yasemin Morton, Beau R. Cory, Alexandra B. Cardamone, Hayley C. Hofmockel, Kirsten S. Lipton, Mary S. Moran, James J. Renslow, Ryan S. Fredrickson, James K. Lindemann, Stephen R. mSystems Research Article Increasing anthropogenic inputs of fixed nitrogen are leading to greater eutrophication of aquatic environments, but it is unclear how this impacts the flux and fate of carbon in lacustrine and riverine systems. Here, we present evidence that the form of nitrogen governs the partitioning of carbon among members in a genome-sequenced, model phototrophic biofilm of 20 members. Consumption of NO(3)(−) as the sole nitrogen source unexpectedly resulted in more rapid transfer of carbon to heterotrophs than when NH(4)(+) was also provided, suggesting alterations in the form of carbon exchanged. The form of nitrogen dramatically impacted net community nitrogen, but not carbon, uptake rates. Furthermore, this alteration in nitrogen form caused very large but focused alterations to community structure, strongly impacting the abundance of only two species within the biofilm and modestly impacting a third member species. Our data suggest that nitrogen metabolism may coordinate coupled carbon-nitrogen biogeochemical cycling in benthic biofilms and, potentially, in phototroph-heterotroph consortia more broadly. It further indicates that the form of nitrogen inputs may significantly impact the contribution of these communities to carbon partitioning across the terrestrial-aquatic interface. IMPORTANCE Anthropogenic inputs of nitrogen into aquatic ecosystems, and especially those of agricultural origin, involve a mix of chemical species. Although it is well-known in general that nitrogen eutrophication markedly influences the metabolism of aquatic phototrophic communities, relatively little is known regarding whether the specific chemical form of nitrogen inputs matter. Our data suggest that the nitrogen form alters the rate of nitrogen uptake significantly, whereas corresponding alterations in carbon uptake were minor. However, differences imposed by uptake of divergent nitrogen forms may result in alterations among phototroph-heterotroph interactions that rewire community metabolism. Furthermore, our data hint that availability of other nutrients (i.e., iron) might mediate the linkage between carbon and nitrogen cycling in these communities. Taken together, our data suggest that different nitrogen forms should be examined for divergent impacts on phototrophic communities in fluvial systems and that these anthropogenic nitrogen inputs may significantly differ in their ultimate biogeochemical impacts. American Society for Microbiology 2020-06-09 /pmc/articles/PMC7289588/ /pubmed/32518194 http://dx.doi.org/10.1128/mSystems.00260-20 Text en Copyright © 2020 Anderton et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Anderton, Christopher R.
Mobberley, Jennifer M.
Cole, Jessica K.
Nunez, Jamie R.
Starke, Robert
Boaro, Amy A.
Yesiltepe, Yasemin
Morton, Beau R.
Cory, Alexandra B.
Cardamone, Hayley C.
Hofmockel, Kirsten S.
Lipton, Mary S.
Moran, James J.
Renslow, Ryan S.
Fredrickson, James K.
Lindemann, Stephen R.
Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title_full Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title_fullStr Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title_full_unstemmed Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title_short Nitrogen Source Governs Community Carbon Metabolism in a Model Hypersaline Benthic Phototrophic Biofilm
title_sort nitrogen source governs community carbon metabolism in a model hypersaline benthic phototrophic biofilm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289588/
https://www.ncbi.nlm.nih.gov/pubmed/32518194
http://dx.doi.org/10.1128/mSystems.00260-20
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