Cargando…
Phanerozoic radiation of ammonia oxidizing bacteria
The modern nitrogen cycle consists of a web of microbially mediated redox transformations. Among the most crucial reactions in this cycle is the oxidation of ammonia to nitrite, an obligately aerobic process performed by a limited number of lineages of bacteria (AOB) and archaea (AOA). As this proce...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822890/ https://www.ncbi.nlm.nih.gov/pubmed/33483596 http://dx.doi.org/10.1038/s41598-021-81718-2 |
_version_ | 1783639729357455360 |
---|---|
author | Ward, L. M. Johnston, D. T. Shih, P. M. |
author_facet | Ward, L. M. Johnston, D. T. Shih, P. M. |
author_sort | Ward, L. M. |
collection | PubMed |
description | The modern nitrogen cycle consists of a web of microbially mediated redox transformations. Among the most crucial reactions in this cycle is the oxidation of ammonia to nitrite, an obligately aerobic process performed by a limited number of lineages of bacteria (AOB) and archaea (AOA). As this process has an absolute requirement for O(2), the timing of its evolution—especially as it relates to the Great Oxygenation Event ~ 2.3 billion years ago—remains contested and is pivotal to our understanding of nutrient cycles. To estimate the antiquity of bacterial ammonia oxidation, we performed phylogenetic and molecular clock analyses of AOB. Surprisingly, bacterial ammonia oxidation appears quite young, with crown group clades having originated during Neoproterozoic time (or later) with major radiations occurring during Paleozoic time. These results place the evolution of AOB broadly coincident with the pervasive oxygenation of the deep ocean. The late evolution AOB challenges earlier interpretations of the ancient nitrogen isotope record, predicts a more substantial role for AOA during Precambrian time, and may have implications for understanding of the size and structure of the biogeochemical nitrogen cycle through geologic time. |
format | Online Article Text |
id | pubmed-7822890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78228902021-01-26 Phanerozoic radiation of ammonia oxidizing bacteria Ward, L. M. Johnston, D. T. Shih, P. M. Sci Rep Article The modern nitrogen cycle consists of a web of microbially mediated redox transformations. Among the most crucial reactions in this cycle is the oxidation of ammonia to nitrite, an obligately aerobic process performed by a limited number of lineages of bacteria (AOB) and archaea (AOA). As this process has an absolute requirement for O(2), the timing of its evolution—especially as it relates to the Great Oxygenation Event ~ 2.3 billion years ago—remains contested and is pivotal to our understanding of nutrient cycles. To estimate the antiquity of bacterial ammonia oxidation, we performed phylogenetic and molecular clock analyses of AOB. Surprisingly, bacterial ammonia oxidation appears quite young, with crown group clades having originated during Neoproterozoic time (or later) with major radiations occurring during Paleozoic time. These results place the evolution of AOB broadly coincident with the pervasive oxygenation of the deep ocean. The late evolution AOB challenges earlier interpretations of the ancient nitrogen isotope record, predicts a more substantial role for AOA during Precambrian time, and may have implications for understanding of the size and structure of the biogeochemical nitrogen cycle through geologic time. Nature Publishing Group UK 2021-01-22 /pmc/articles/PMC7822890/ /pubmed/33483596 http://dx.doi.org/10.1038/s41598-021-81718-2 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ward, L. M. Johnston, D. T. Shih, P. M. Phanerozoic radiation of ammonia oxidizing bacteria |
title | Phanerozoic radiation of ammonia oxidizing bacteria |
title_full | Phanerozoic radiation of ammonia oxidizing bacteria |
title_fullStr | Phanerozoic radiation of ammonia oxidizing bacteria |
title_full_unstemmed | Phanerozoic radiation of ammonia oxidizing bacteria |
title_short | Phanerozoic radiation of ammonia oxidizing bacteria |
title_sort | phanerozoic radiation of ammonia oxidizing bacteria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822890/ https://www.ncbi.nlm.nih.gov/pubmed/33483596 http://dx.doi.org/10.1038/s41598-021-81718-2 |
work_keys_str_mv | AT wardlm phanerozoicradiationofammoniaoxidizingbacteria AT johnstondt phanerozoicradiationofammoniaoxidizingbacteria AT shihpm phanerozoicradiationofammoniaoxidizingbacteria |