Phanerozoic radiation of ammonia oxidizing bacteria
Abstract 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 t...
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2021
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oai:doaj.org-article:152eeb90747b41c2a9c7673414de9dbb2021-12-02T13:56:55ZPhanerozoic radiation of ammonia oxidizing bacteria10.1038/s41598-021-81718-22045-2322https://doaj.org/article/152eeb90747b41c2a9c7673414de9dbb2021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81718-2https://doaj.org/toc/2045-2322Abstract 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 O2, 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.L. M. WardD. T. JohnstonP. M. ShihNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021) |
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Medicine R Science Q L. M. Ward D. T. Johnston P. M. Shih Phanerozoic radiation of ammonia oxidizing bacteria |
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Abstract 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 O2, 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 |
article |
author |
L. M. Ward D. T. Johnston P. M. Shih |
author_facet |
L. M. Ward D. T. Johnston P. M. Shih |
author_sort |
L. M. Ward |
title |
Phanerozoic radiation of ammonia oxidizing bacteria |
title_short |
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_sort |
phanerozoic radiation of ammonia oxidizing bacteria |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/152eeb90747b41c2a9c7673414de9dbb |
work_keys_str_mv |
AT lmward phanerozoicradiationofammoniaoxidizingbacteria AT dtjohnston phanerozoicradiationofammoniaoxidizingbacteria AT pmshih phanerozoicradiationofammoniaoxidizingbacteria |
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