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Anaerobic endosymbiont generates energy for ciliate host by denitrification
Graf, J.S.; Schorn, S.; Kitzinger, K.; Ahmerkamp, S.; Woehle, C.; Huettel, B.; Schubert, C.J.; Kuypers, M.M.; Milucka, J. (2021). Anaerobic endosymbiont generates energy for ciliate host by denitrification. Nature (Lond.) 591(7850): 445-450. https://dx.doi.org/10.1038/s41586-021-03297-6
In: Nature: International Weekly Journal of Science. Nature Publishing Group: London. ISSN 0028-0836; e-ISSN 1476-4687, meer
|   |
| Auteurs | | Top |
- Graf, J.S.
- Schorn, S.
- Kitzinger, K.
|
- Ahmerkamp, S.
- Woehle, C.
- Huettel, B.
|
- Schubert, C.J.
- Kuypers, M.M.
- Milucka, J.
|
| Abstract |
Mitochondria are specialized eukaryotic organelles that have a dedicated function in oxygen respiration and energy production. They evolved about billion years ago from a free-living bacterial ancestor (probably an alphaproteobacterium), in a process known as endosymbiosis. Many unicellular eukaryotes have since adapted to life in anoxic habitats and their mitochondria have undergone further reductive evolution. As a result, obligate anaerobic eukaryotes with mitochondrial remnants derive their energy mostly from fermentation. 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. |
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