Chemolithoautotroph

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

Overview

Depiction of the proton gradient force generated by the electron transport chain. Electron transport chain with NADH.gif
Depiction of the proton gradient force generated by the electron transport chain.

Most chemoautotrophs are lithotrophs, using inorganic electron donors such as hydrogen sulfide, hydrogen gas, elemental sulfur, ammonium and ferrous oxide as reducing agents and hydrogen sources for biosynthesis and chemical energy release. Chemolithoautotrophs are microorganisms that synthesize energy through the oxidation of inorganic compounds. [1] 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 the ATP produced during photosynthesis or the oxidation of chemical compounds to reduce NADP+ to NADPH to form organic compounds. [2] 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.

Contents

Metabolism and ecological role

Generation of ATP using the proton gradient force. ATP synthase chemiosmosis and oxidative phosphorylation.gif
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. Unlike photoautotrophs, they do not use light (but rather chemical energy). Through oxidative phosphorylation, they use a proton gradient force to generate the production of adenosine triphosphate (ATP), which is the primary energy source of living organisms. In order to fix CO₂, they reverse the electron transport chain using electron donors with high redox potentials. [3] [2] [4]

Chemolithoautotrophs add nutrients through nitrification (ammonia to nitrate), sulfur oxidation (hydrogen sulfide to sulfate), and iron oxidation. This metabolic activity fertilizes soil, affects water quality, and atmospheric composition. [5] [6] They inhabit extreme environments such as deep-sea thermal vents, acidic hot springs, and underground. [5] In hydrothermal vents, they are the base of the food web. [7] [8] [9] Taxa such as aquificae, sulfurimonas, and nitratifactor dominate microbial communities within water samples, fauna, and rocks, respectively. [10]

References

  1. "5.10A: The Energetics of Chemolithotrophy". Biology LibreTexts. 2017-05-09.
  2. 1 2 Bruslind, Linda (2019-08-01). "Chemolithotrophy & Nitrogen Metabolism". General Microbiology.
  3. Keenleyside, Wendy (2019-07-23). "8.6 Lithotrophy". Microbiology: Canadian Edition.
  4. "14: Chemolithotrophy & Nitrogen Metabolism". Biology LibreTexts. 2018-02-06.
  5. 1 2 Seto, 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.
  6. 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.
  7. 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 .
  8. 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 .
  9. 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.
  10. Gallucci, Luigi. "Hydrothermal Vent Ecology". Max Planck Institute for Marine Microbiology.