Cargando…
Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event
The anaerobic ammonium oxidation (anammox) bacteria can transform ammonium and nitrite to dinitrogen gas, and this obligate anaerobic process accounts for up to half of the global nitrogen loss in surface environments. Yet its origin and evolution, which may give important insights into the biogeoch...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387917/ https://www.ncbi.nlm.nih.gov/pubmed/35920138 http://dx.doi.org/10.1093/molbev/msac170 |
_version_ | 1784770107943157760 |
---|---|
author | Liao, Tianhua Wang, Sishuo Stüeken, Eva E Luo, Haiwei |
author_facet | Liao, Tianhua Wang, Sishuo Stüeken, Eva E Luo, Haiwei |
author_sort | Liao, Tianhua |
collection | PubMed |
description | The anaerobic ammonium oxidation (anammox) bacteria can transform ammonium and nitrite to dinitrogen gas, and this obligate anaerobic process accounts for up to half of the global nitrogen loss in surface environments. Yet its origin and evolution, which may give important insights into the biogeochemistry of early Earth, remain enigmatic. Here, we performed a comprehensive phylogenomic and molecular clock analysis of anammox bacteria within the phylum Planctomycetes. After accommodating the uncertainties and factors influencing time estimates, which include implementing both a traditional cyanobacteria-based and a recently developed mitochondria-based molecular dating approach, we estimated a consistent origin of anammox bacteria at early Proterozoic and most likely around the so-called Great Oxidation Event (GOE; 2.32–2.5 Ga) which fundamentally changed global biogeochemical cycles. We further showed that during the origin of anammox bacteria, genes involved in oxidative stress adaptation, bioenergetics, and anammox granules formation were recruited, which might have contributed to their survival on an increasingly oxic Earth. Our findings suggest the rising levels of atmospheric oxygen, which made nitrite increasingly available, was a potential driving force for the emergence of anammox bacteria. This is one of the first studies that link the GOE to the evolution of obligate anaerobic bacteria. |
format | Online Article Text |
id | pubmed-9387917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93879172022-08-19 Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event Liao, Tianhua Wang, Sishuo Stüeken, Eva E Luo, Haiwei Mol Biol Evol Discoveries The anaerobic ammonium oxidation (anammox) bacteria can transform ammonium and nitrite to dinitrogen gas, and this obligate anaerobic process accounts for up to half of the global nitrogen loss in surface environments. Yet its origin and evolution, which may give important insights into the biogeochemistry of early Earth, remain enigmatic. Here, we performed a comprehensive phylogenomic and molecular clock analysis of anammox bacteria within the phylum Planctomycetes. After accommodating the uncertainties and factors influencing time estimates, which include implementing both a traditional cyanobacteria-based and a recently developed mitochondria-based molecular dating approach, we estimated a consistent origin of anammox bacteria at early Proterozoic and most likely around the so-called Great Oxidation Event (GOE; 2.32–2.5 Ga) which fundamentally changed global biogeochemical cycles. We further showed that during the origin of anammox bacteria, genes involved in oxidative stress adaptation, bioenergetics, and anammox granules formation were recruited, which might have contributed to their survival on an increasingly oxic Earth. Our findings suggest the rising levels of atmospheric oxygen, which made nitrite increasingly available, was a potential driving force for the emergence of anammox bacteria. This is one of the first studies that link the GOE to the evolution of obligate anaerobic bacteria. Oxford University Press 2022-08-03 /pmc/articles/PMC9387917/ /pubmed/35920138 http://dx.doi.org/10.1093/molbev/msac170 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Liao, Tianhua Wang, Sishuo Stüeken, Eva E Luo, Haiwei Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title | Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title_full | Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title_fullStr | Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title_full_unstemmed | Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title_short | Phylogenomic Evidence for the Origin of Obligate Anaerobic Anammox Bacteria Around the Great Oxidation Event |
title_sort | phylogenomic evidence for the origin of obligate anaerobic anammox bacteria around the great oxidation event |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387917/ https://www.ncbi.nlm.nih.gov/pubmed/35920138 http://dx.doi.org/10.1093/molbev/msac170 |
work_keys_str_mv | AT liaotianhua phylogenomicevidencefortheoriginofobligateanaerobicanammoxbacteriaaroundthegreatoxidationevent AT wangsishuo phylogenomicevidencefortheoriginofobligateanaerobicanammoxbacteriaaroundthegreatoxidationevent AT stuekenevae phylogenomicevidencefortheoriginofobligateanaerobicanammoxbacteriaaroundthegreatoxidationevent AT luohaiwei phylogenomicevidencefortheoriginofobligateanaerobicanammoxbacteriaaroundthegreatoxidationevent |