Cargando…
Anaerobic endosymbiont generates energy for ciliate host by denitrification
Mitochondria are specialized eukaryotic organelles that have a dedicated function in oxygen respiration and energy production. They evolved about 2 billion years ago from a free-living bacterial ancestor (probably an alphaproteobacterium), in a process known as endosymbiosis(1,2). Many unicellular e...
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/PMC7969357/ https://www.ncbi.nlm.nih.gov/pubmed/33658719 http://dx.doi.org/10.1038/s41586-021-03297-6 |
_version_ | 1783666228694351872 |
---|---|
author | Graf, Jon S. Schorn, Sina Kitzinger, Katharina Ahmerkamp, Soeren Woehle, Christian Huettel, Bruno Schubert, Carsten J. Kuypers, Marcel M. M. Milucka, Jana |
author_facet | Graf, Jon S. Schorn, Sina Kitzinger, Katharina Ahmerkamp, Soeren Woehle, Christian Huettel, Bruno Schubert, Carsten J. Kuypers, Marcel M. M. Milucka, Jana |
author_sort | Graf, Jon S. |
collection | PubMed |
description | Mitochondria are specialized eukaryotic organelles that have a dedicated function in oxygen respiration and energy production. They evolved about 2 billion years ago from a free-living bacterial ancestor (probably an alphaproteobacterium), in a process known as endosymbiosis(1,2). Many unicellular eukaryotes have since adapted to life in anoxic habitats and their mitochondria have undergone further reductive evolution(3). As a result, obligate anaerobic eukaryotes with mitochondrial remnants derive their energy mostly from fermentation(4). Here we describe ‘Candidatus Azoamicus ciliaticola’, which is an obligate endosymbiont of an anaerobic ciliate and has a dedicated role in respiration and providing energy for its eukaryotic host. ‘Candidatus A. ciliaticola’ contains a highly reduced 0.29-Mb genome that encodes core genes for central information processing, the electron transport chain, a truncated tricarboxylic acid cycle, ATP generation and iron–sulfur cluster biosynthesis. The genome encodes a respiratory denitrification pathway instead of aerobic terminal oxidases, which enables its host to breathe nitrate instead of oxygen. ‘Candidatus A. ciliaticola’ and its ciliate host represent an example of a symbiosis that is based on the transfer of energy in the form of ATP, rather than nutrition. This discovery raises the possibility that eukaryotes with mitochondrial remnants may secondarily acquire energy-providing endosymbionts to complement or replace functions of their mitochondria. |
format | Online Article Text |
id | pubmed-7969357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79693572021-03-28 Anaerobic endosymbiont generates energy for ciliate host by denitrification Graf, Jon S. Schorn, Sina Kitzinger, Katharina Ahmerkamp, Soeren Woehle, Christian Huettel, Bruno Schubert, Carsten J. Kuypers, Marcel M. M. Milucka, Jana Nature Article Mitochondria are specialized eukaryotic organelles that have a dedicated function in oxygen respiration and energy production. They evolved about 2 billion years ago from a free-living bacterial ancestor (probably an alphaproteobacterium), in a process known as endosymbiosis(1,2). Many unicellular eukaryotes have since adapted to life in anoxic habitats and their mitochondria have undergone further reductive evolution(3). As a result, obligate anaerobic eukaryotes with mitochondrial remnants derive their energy mostly from fermentation(4). Here we describe ‘Candidatus Azoamicus ciliaticola’, which is an obligate endosymbiont of an anaerobic ciliate and has a dedicated role in respiration and providing energy for its eukaryotic host. ‘Candidatus A. ciliaticola’ contains a highly reduced 0.29-Mb genome that encodes core genes for central information processing, the electron transport chain, a truncated tricarboxylic acid cycle, ATP generation and iron–sulfur cluster biosynthesis. The genome encodes a respiratory denitrification pathway instead of aerobic terminal oxidases, which enables its host to breathe nitrate instead of oxygen. ‘Candidatus A. ciliaticola’ and its ciliate host represent an example of a symbiosis that is based on the transfer of energy in the form of ATP, rather than nutrition. This discovery raises the possibility that eukaryotes with mitochondrial remnants may secondarily acquire energy-providing endosymbionts to complement or replace functions of their mitochondria. Nature Publishing Group UK 2021-03-03 2021 /pmc/articles/PMC7969357/ /pubmed/33658719 http://dx.doi.org/10.1038/s41586-021-03297-6 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 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 Graf, Jon S. Schorn, Sina Kitzinger, Katharina Ahmerkamp, Soeren Woehle, Christian Huettel, Bruno Schubert, Carsten J. Kuypers, Marcel M. M. Milucka, Jana Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title | Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title_full | Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title_fullStr | Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title_full_unstemmed | Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title_short | Anaerobic endosymbiont generates energy for ciliate host by denitrification |
title_sort | anaerobic endosymbiont generates energy for ciliate host by denitrification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969357/ https://www.ncbi.nlm.nih.gov/pubmed/33658719 http://dx.doi.org/10.1038/s41586-021-03297-6 |
work_keys_str_mv | AT grafjons anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT schornsina anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT kitzingerkatharina anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT ahmerkampsoeren anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT woehlechristian anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT huettelbruno anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT schubertcarstenj anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT kuypersmarcelmm anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification AT miluckajana anaerobicendosymbiontgeneratesenergyforciliatehostbydenitrification |