Cargando…
Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia
Nitrous oxide (N(2)O), a potent greenhouse gas, can be generated by compositionally complex microbial populations in diverse contexts. Accurately tracking the dominant biological sources of N(2)O has the potential to improve our understanding of N(2)O fluxes from soils as well as inform the diagnosi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592819/ https://www.ncbi.nlm.nih.gov/pubmed/37873075 http://dx.doi.org/10.1101/2023.10.13.562248 |
_version_ | 1785124349462708224 |
---|---|
author | Wang, Renée Z. Lonergan, Zachery R. Wilbert, Steven A. Eiler, John M. Newman, Dianne K. |
author_facet | Wang, Renée Z. Lonergan, Zachery R. Wilbert, Steven A. Eiler, John M. Newman, Dianne K. |
author_sort | Wang, Renée Z. |
collection | PubMed |
description | Nitrous oxide (N(2)O), a potent greenhouse gas, can be generated by compositionally complex microbial populations in diverse contexts. Accurately tracking the dominant biological sources of N(2)O has the potential to improve our understanding of N(2)O fluxes from soils as well as inform the diagnosis of human infections. Isotopic “Site Preference” (SP) values have been used towards this end, as bacterial and fungal nitric oxide reductases produce N(2)O with different isotopic fingerprints. Here we show that flavohemoglobin, a hitherto biogeochemically neglected yet widely distributed detoxifying bacterial NO reductase, imparts a distinct SP value onto N(2)O under anoxic conditions that correlates with typical environmental N(2)O SP measurements. We suggest a new framework to guide the attribution of N(2)O biological sources in nature and disease. |
format | Online Article Text |
id | pubmed-10592819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105928192023-10-24 Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia Wang, Renée Z. Lonergan, Zachery R. Wilbert, Steven A. Eiler, John M. Newman, Dianne K. bioRxiv Article Nitrous oxide (N(2)O), a potent greenhouse gas, can be generated by compositionally complex microbial populations in diverse contexts. Accurately tracking the dominant biological sources of N(2)O has the potential to improve our understanding of N(2)O fluxes from soils as well as inform the diagnosis of human infections. Isotopic “Site Preference” (SP) values have been used towards this end, as bacterial and fungal nitric oxide reductases produce N(2)O with different isotopic fingerprints. Here we show that flavohemoglobin, a hitherto biogeochemically neglected yet widely distributed detoxifying bacterial NO reductase, imparts a distinct SP value onto N(2)O under anoxic conditions that correlates with typical environmental N(2)O SP measurements. We suggest a new framework to guide the attribution of N(2)O biological sources in nature and disease. Cold Spring Harbor Laboratory 2023-10-14 /pmc/articles/PMC10592819/ /pubmed/37873075 http://dx.doi.org/10.1101/2023.10.13.562248 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Wang, Renée Z. Lonergan, Zachery R. Wilbert, Steven A. Eiler, John M. Newman, Dianne K. Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title | Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title_full | Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title_fullStr | Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title_full_unstemmed | Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title_short | Widespread detoxifying NO reductases impart a distinct isotopic fingerprint on N(2)O under anoxia |
title_sort | widespread detoxifying no reductases impart a distinct isotopic fingerprint on n(2)o under anoxia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592819/ https://www.ncbi.nlm.nih.gov/pubmed/37873075 http://dx.doi.org/10.1101/2023.10.13.562248 |
work_keys_str_mv | AT wangreneez widespreaddetoxifyingnoreductasesimpartadistinctisotopicfingerprintonn2ounderanoxia AT lonerganzacheryr widespreaddetoxifyingnoreductasesimpartadistinctisotopicfingerprintonn2ounderanoxia AT wilbertstevena widespreaddetoxifyingnoreductasesimpartadistinctisotopicfingerprintonn2ounderanoxia AT eilerjohnm widespreaddetoxifyingnoreductasesimpartadistinctisotopicfingerprintonn2ounderanoxia AT newmandiannek widespreaddetoxifyingnoreductasesimpartadistinctisotopicfingerprintonn2ounderanoxia |