Cargando…

Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture

Reduction of the greenhouse gas N(2)O to N(2) is a trait among denitrifying and non-denitrifying microorganisms having an N(2)O reductase, encoded by nosZ. The nosZ phylogeny has two major clades, I and II, and physiological differences among organisms within the clades may affect N(2)O emissions fr...

Descripción completa

Detalles Bibliográficos
Autores principales: Conthe, Monica, Wittorf, Lea, Kuenen, J. Gijs, Kleerebezem, Robbert, van Loosdrecht, Mark C. M., Hallin, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864245/
https://www.ncbi.nlm.nih.gov/pubmed/29416125
http://dx.doi.org/10.1038/s41396-018-0063-7
_version_ 1783308506243268608
author Conthe, Monica
Wittorf, Lea
Kuenen, J. Gijs
Kleerebezem, Robbert
van Loosdrecht, Mark C. M.
Hallin, Sara
author_facet Conthe, Monica
Wittorf, Lea
Kuenen, J. Gijs
Kleerebezem, Robbert
van Loosdrecht, Mark C. M.
Hallin, Sara
author_sort Conthe, Monica
collection PubMed
description Reduction of the greenhouse gas N(2)O to N(2) is a trait among denitrifying and non-denitrifying microorganisms having an N(2)O reductase, encoded by nosZ. The nosZ phylogeny has two major clades, I and II, and physiological differences among organisms within the clades may affect N(2)O emissions from ecosystems. To increase our understanding of the ecophysiology of N(2)O reducers, we determined the thermodynamic growth efficiency of N(2)O reduction and the selection of N(2)O reducers under N(2)O- or acetate-limiting conditions in a continuous culture enriched from a natural community with N(2)O as electron acceptor and acetate as electron donor. The biomass yields were higher during N(2)O limitation, irrespective of dilution rate and community composition. The former was corroborated in a continuous culture of Pseudomonas stutzeri and was potentially due to cytotoxic effects of surplus N(2)O. Denitrifiers were favored over non-denitrifying N(2)O reducers under all conditions and Proteobacteria harboring clade I nosZ dominated. The abundance of nosZ clade II increased when allowing for lower growth rates, but bacteria with nosZ clade I had a higher affinity for N(2)O, as defined by μ(max)/K(s). Thus, the specific growth rate is likely a key factor determining the composition of communities living on N(2)O respiration under growth-limited conditions.
format Online
Article
Text
id pubmed-5864245
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58642452018-06-20 Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture Conthe, Monica Wittorf, Lea Kuenen, J. Gijs Kleerebezem, Robbert van Loosdrecht, Mark C. M. Hallin, Sara ISME J Article Reduction of the greenhouse gas N(2)O to N(2) is a trait among denitrifying and non-denitrifying microorganisms having an N(2)O reductase, encoded by nosZ. The nosZ phylogeny has two major clades, I and II, and physiological differences among organisms within the clades may affect N(2)O emissions from ecosystems. To increase our understanding of the ecophysiology of N(2)O reducers, we determined the thermodynamic growth efficiency of N(2)O reduction and the selection of N(2)O reducers under N(2)O- or acetate-limiting conditions in a continuous culture enriched from a natural community with N(2)O as electron acceptor and acetate as electron donor. The biomass yields were higher during N(2)O limitation, irrespective of dilution rate and community composition. The former was corroborated in a continuous culture of Pseudomonas stutzeri and was potentially due to cytotoxic effects of surplus N(2)O. Denitrifiers were favored over non-denitrifying N(2)O reducers under all conditions and Proteobacteria harboring clade I nosZ dominated. The abundance of nosZ clade II increased when allowing for lower growth rates, but bacteria with nosZ clade I had a higher affinity for N(2)O, as defined by μ(max)/K(s). Thus, the specific growth rate is likely a key factor determining the composition of communities living on N(2)O respiration under growth-limited conditions. Nature Publishing Group UK 2018-02-07 2018-04 /pmc/articles/PMC5864245/ /pubmed/29416125 http://dx.doi.org/10.1038/s41396-018-0063-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.
spellingShingle Article
Conthe, Monica
Wittorf, Lea
Kuenen, J. Gijs
Kleerebezem, Robbert
van Loosdrecht, Mark C. M.
Hallin, Sara
Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title_full Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title_fullStr Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title_full_unstemmed Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title_short Life on N(2)O: deciphering the ecophysiology of N(2)O respiring bacterial communities in a continuous culture
title_sort life on n(2)o: deciphering the ecophysiology of n(2)o respiring bacterial communities in a continuous culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864245/
https://www.ncbi.nlm.nih.gov/pubmed/29416125
http://dx.doi.org/10.1038/s41396-018-0063-7
work_keys_str_mv AT conthemonica lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture
AT wittorflea lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture
AT kuenenjgijs lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture
AT kleerebezemrobbert lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture
AT vanloosdrechtmarkcm lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture
AT hallinsara lifeonn2odecipheringtheecophysiologyofn2orespiringbacterialcommunitiesinacontinuousculture