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Metabolic network analysis reveals microbial community interactions in anammox granules

Microbial communities mediating anaerobic ammonium oxidation (anammox) represent one of the most energy-efficient environmental biotechnologies for nitrogen removal from wastewater. However, little is known about the functional role heterotrophic bacteria play in anammox granules. Here, we use genom...

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Autores principales: Lawson, Christopher E., Wu, Sha, Bhattacharjee, Ananda S., Hamilton, Joshua J., McMahon, Katherine D., Goel, Ramesh, Noguera, Daniel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460018/
https://www.ncbi.nlm.nih.gov/pubmed/28561030
http://dx.doi.org/10.1038/ncomms15416
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author Lawson, Christopher E.
Wu, Sha
Bhattacharjee, Ananda S.
Hamilton, Joshua J.
McMahon, Katherine D.
Goel, Ramesh
Noguera, Daniel R.
author_facet Lawson, Christopher E.
Wu, Sha
Bhattacharjee, Ananda S.
Hamilton, Joshua J.
McMahon, Katherine D.
Goel, Ramesh
Noguera, Daniel R.
author_sort Lawson, Christopher E.
collection PubMed
description Microbial communities mediating anaerobic ammonium oxidation (anammox) represent one of the most energy-efficient environmental biotechnologies for nitrogen removal from wastewater. However, little is known about the functional role heterotrophic bacteria play in anammox granules. Here, we use genome-centric metagenomics to recover 17 draft genomes of anammox and heterotrophic bacteria from a laboratory-scale anammox bioreactor. We combine metabolic network reconstruction with metatranscriptomics to examine the gene expression of anammox and heterotrophic bacteria and to identify their potential interactions. We find that Chlorobi-affiliated bacteria may be highly active protein degraders, catabolizing extracellular peptides while recycling nitrate to nitrite. Other heterotrophs may also contribute to scavenging of detritus and peptides produced by anammox bacteria, and potentially use alternative electron donors, such as H(2), acetate and formate. Our findings improve the understanding of metabolic activities and interactions between anammox and heterotrophic bacteria and offer the first transcriptional insights on ecosystem function in anammox granules.
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spelling pubmed-54600182017-06-12 Metabolic network analysis reveals microbial community interactions in anammox granules Lawson, Christopher E. Wu, Sha Bhattacharjee, Ananda S. Hamilton, Joshua J. McMahon, Katherine D. Goel, Ramesh Noguera, Daniel R. Nat Commun Article Microbial communities mediating anaerobic ammonium oxidation (anammox) represent one of the most energy-efficient environmental biotechnologies for nitrogen removal from wastewater. However, little is known about the functional role heterotrophic bacteria play in anammox granules. Here, we use genome-centric metagenomics to recover 17 draft genomes of anammox and heterotrophic bacteria from a laboratory-scale anammox bioreactor. We combine metabolic network reconstruction with metatranscriptomics to examine the gene expression of anammox and heterotrophic bacteria and to identify their potential interactions. We find that Chlorobi-affiliated bacteria may be highly active protein degraders, catabolizing extracellular peptides while recycling nitrate to nitrite. Other heterotrophs may also contribute to scavenging of detritus and peptides produced by anammox bacteria, and potentially use alternative electron donors, such as H(2), acetate and formate. Our findings improve the understanding of metabolic activities and interactions between anammox and heterotrophic bacteria and offer the first transcriptional insights on ecosystem function in anammox granules. Nature Publishing Group 2017-05-31 /pmc/articles/PMC5460018/ /pubmed/28561030 http://dx.doi.org/10.1038/ncomms15416 Text en Copyright © 2017, The Author(s) 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
Lawson, Christopher E.
Wu, Sha
Bhattacharjee, Ananda S.
Hamilton, Joshua J.
McMahon, Katherine D.
Goel, Ramesh
Noguera, Daniel R.
Metabolic network analysis reveals microbial community interactions in anammox granules
title Metabolic network analysis reveals microbial community interactions in anammox granules
title_full Metabolic network analysis reveals microbial community interactions in anammox granules
title_fullStr Metabolic network analysis reveals microbial community interactions in anammox granules
title_full_unstemmed Metabolic network analysis reveals microbial community interactions in anammox granules
title_short Metabolic network analysis reveals microbial community interactions in anammox granules
title_sort metabolic network analysis reveals microbial community interactions in anammox granules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460018/
https://www.ncbi.nlm.nih.gov/pubmed/28561030
http://dx.doi.org/10.1038/ncomms15416
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