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Chemolithoautotroph

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Achemolithoautotroph is an organism that that uses inorganic chemical compounds to source its energy and electrons, and use carbon dioxide as a carbon source.[1] They do not require organic compounds or light.

Hydrothermal vent in the Atlantic Ocean. These communities are inhabited by abundant chemolithoautotrophs.

Overview

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Depiction of the proton gradient force generated by the electron transport chain.

Mostchemoautotrophs arelithotrophs, using inorganic electron donors such as hydrogen sulfide,hydrogen gas, elementalsulfur,ammonium andferrous oxide as reducing agents and hydrogen sources forbiosynthesis and chemical energy release. Chemolithoautotrophs aremicroorganisms that synthesize energy through the oxidation of inorganic compounds.[2] They can sustain themselves entirely on atmospheric CO₂ and inorganic chemicals without the need for light or organic compounds. They enzymatically catalyze redox reactions using mineral substrates to generate ATP energy. Autotrophs use a portion of theATP produced during photosynthesis or the oxidation of chemical compounds to reduceNADP+ to NADPH to form organic compounds.[3] These substrates primarily include hydrogen, iron, nitrogen, and sulfur. Its ecological niche is specialized to deep marine hydrothermal vents, stratified sediment, and subsurface rock. Their metabolic processes play a key role in supporting microbial food webs as primary producers, and biogeochemical fluxes.

Metabolism and ecological role

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Generation of ATP using the proton gradient force.

Chemolithoautotrophs are microbes that derive energy from the oxidation of inorganic compounds. They fix atmospheric CO₂ as their sole carbon source. Unlikephotoautotrophs, they do not use light (but rather chemical energy). Throughoxidative phosphorylation, they use a proton gradient force to generate the production ofadenosine triphosphate (ATP), which is the primary energy source of living organisms. In order to fix CO₂, they reverse theelectron transport chain using electron donors with high redox potentials.[4][3][5]

Chemolithoautotrophs add nutrients throughnitrification (ammonia to nitrate), sulfur oxidation (hydrogen sulfide to sulfate), and iron oxidation. This metabolic activity fertilizes soil, affects water quality, and atmospheric composition.[6][7] They inhabit extreme environments such as deep-seathermal vents, acidic hot springs, and underground.[6] In hydrothermal vents, they are the base of the food web.[8][9][10] Taxa such as aquificae, sulfurimonas, and nitratifactor dominate microbial communities within water samples, fauna, and rocks, respectively.[11]

References

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  1. ^Bruslind, Linda. "11: Microbial Nutrition".Microbiology. Open Oregon.
  2. ^"5.10A: The Energetics of Chemolithotrophy".Biology LibreTexts. 2017-05-09.
  3. ^abBruslind, Linda (2019-08-01)."Chemolithotrophy & Nitrogen Metabolism".General Microbiology.
  4. ^Keenleyside, Wendy (2019-07-23)."8.6 Lithotrophy".Microbiology: Canadian Edition.
  5. ^"14: Chemolithotrophy & Nitrogen Metabolism".Biology LibreTexts. 2018-02-06.
  6. ^abSeto, Mayumi; Iwasa, Yoh (2019-10-14)."The fitness of chemotrophs increases when their catabolic by-products are consumed by other species".Ecology Letters.22 (12):1994–2005.Bibcode:2019EcolL..22.1994S.doi:10.1111/ele.13397.PMC 6899997.PMID 31612608.
  7. ^Hooper, Alan B. (2004). "Chemolithotrophy".Encyclopedia of Biological Chemistry. pp. 419–424.doi:10.1016/B0-12-443710-9/00104-6.ISBN 978-0-12-443710-4.
  8. ^Frumkin, Amos; Chipman, Ariel D.; Naaman, Israel (2023-01-26)."An isolated chemolithoautotrophic ecosystem deduced from environmental isotopes: Ayyalon cave (Israel)".Frontiers in Ecology and Evolution.10.Bibcode:2023FrEEv..1040385F.doi:10.3389/fevo.2022.1040385.
  9. ^Sievert, Stefan; Vetriani, Costantino (March 2012). "Chemoautotrophy at Deep-Sea Vents: Past, Present, and Future".Oceanography.25 (1):218–233.Bibcode:2012Ocgpy..25a.218S.doi:10.5670/oceanog.2012.21.hdl:1912/5172.
  10. ^Deng, Wenchao; Zhao, Zihao; Li, Yufang; Cao, Rongguang; Chen, Mingming; Tang, Kai; Wang, Deli; Fan, Wei; Hu, Anyi; Chen, Guangcheng; Chen, Chen-Tung Arthur; Zhang, Yao (2023-12-05)."Strategies of chemolithoautotrophs adapting to high temperature and extremely acidic conditions in a shallow hydrothermal ecosystem".Microbiome.11 (1): 270.doi:10.1186/s40168-023-01712-w.PMC 10696704.PMID 38049915.
  11. ^Gallucci, Luigi."Hydrothermal Vent Ecology".Max Planck Institute for Marine Microbiology.
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