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Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata

Nitrous oxide (N(2)O) and nitric oxide (NO) are atmospheric trace gases that contribute to climate change and affect stratospheric and ground-level ozone concentrations. Ammonia oxidizing bacteria (AOB) and archaea (AOA) are key players in the nitrogen cycle and major producers of N(2)O and NO globa...

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Autores principales: Kits, K. Dimitri, Jung, Man-Young, Vierheilig, Julia, Pjevac, Petra, Sedlacek, Christopher J., Liu, Shurong, Herbold, Craig, Stein, Lisa Y., Richter, Andreas, Wissel, Holger, Brüggemann, Nicolas, Wagner, Michael, Daims, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478695/
https://www.ncbi.nlm.nih.gov/pubmed/31015413
http://dx.doi.org/10.1038/s41467-019-09790-x
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author Kits, K. Dimitri
Jung, Man-Young
Vierheilig, Julia
Pjevac, Petra
Sedlacek, Christopher J.
Liu, Shurong
Herbold, Craig
Stein, Lisa Y.
Richter, Andreas
Wissel, Holger
Brüggemann, Nicolas
Wagner, Michael
Daims, Holger
author_facet Kits, K. Dimitri
Jung, Man-Young
Vierheilig, Julia
Pjevac, Petra
Sedlacek, Christopher J.
Liu, Shurong
Herbold, Craig
Stein, Lisa Y.
Richter, Andreas
Wissel, Holger
Brüggemann, Nicolas
Wagner, Michael
Daims, Holger
author_sort Kits, K. Dimitri
collection PubMed
description Nitrous oxide (N(2)O) and nitric oxide (NO) are atmospheric trace gases that contribute to climate change and affect stratospheric and ground-level ozone concentrations. Ammonia oxidizing bacteria (AOB) and archaea (AOA) are key players in the nitrogen cycle and major producers of N(2)O and NO globally. However, nothing is known about N(2)O and NO production by the recently discovered and widely distributed complete ammonia oxidizers (comammox). Here, we show that the comammox bacterium Nitrospira inopinata is sensitive to inhibition by an NO scavenger, cannot denitrify to N(2)O, and emits N(2)O at levels that are comparable to AOA but much lower than AOB. Furthermore, we demonstrate that N(2)O formed by N. inopinata formed under varying oxygen regimes originates from abiotic conversion of hydroxylamine. Our findings indicate that comammox microbes may produce less N(2)O during nitrification than AOB.
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spelling pubmed-64786952019-04-25 Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata Kits, K. Dimitri Jung, Man-Young Vierheilig, Julia Pjevac, Petra Sedlacek, Christopher J. Liu, Shurong Herbold, Craig Stein, Lisa Y. Richter, Andreas Wissel, Holger Brüggemann, Nicolas Wagner, Michael Daims, Holger Nat Commun Article Nitrous oxide (N(2)O) and nitric oxide (NO) are atmospheric trace gases that contribute to climate change and affect stratospheric and ground-level ozone concentrations. Ammonia oxidizing bacteria (AOB) and archaea (AOA) are key players in the nitrogen cycle and major producers of N(2)O and NO globally. However, nothing is known about N(2)O and NO production by the recently discovered and widely distributed complete ammonia oxidizers (comammox). Here, we show that the comammox bacterium Nitrospira inopinata is sensitive to inhibition by an NO scavenger, cannot denitrify to N(2)O, and emits N(2)O at levels that are comparable to AOA but much lower than AOB. Furthermore, we demonstrate that N(2)O formed by N. inopinata formed under varying oxygen regimes originates from abiotic conversion of hydroxylamine. Our findings indicate that comammox microbes may produce less N(2)O during nitrification than AOB. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478695/ /pubmed/31015413 http://dx.doi.org/10.1038/s41467-019-09790-x Text en © The Author(s) 2019 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
Kits, K. Dimitri
Jung, Man-Young
Vierheilig, Julia
Pjevac, Petra
Sedlacek, Christopher J.
Liu, Shurong
Herbold, Craig
Stein, Lisa Y.
Richter, Andreas
Wissel, Holger
Brüggemann, Nicolas
Wagner, Michael
Daims, Holger
Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title_full Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title_fullStr Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title_full_unstemmed Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title_short Low yield and abiotic origin of N(2)O formed by the complete nitrifier Nitrospira inopinata
title_sort low yield and abiotic origin of n(2)o formed by the complete nitrifier nitrospira inopinata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478695/
https://www.ncbi.nlm.nih.gov/pubmed/31015413
http://dx.doi.org/10.1038/s41467-019-09790-x
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