Detailed Information on Publication Record
2020
A Model of Aerobic and Anaerobic Metabolism of Hydrogen in the Extremophile Acidithiobacillus ferrooxidans
KUČERA, Jiří, Jan LOCHMAN, Pavel BOUCHAL, Eva PAKOSTOVA, Kamil MIKULÁŠEK et. al.Basic information
Original name
A Model of Aerobic and Anaerobic Metabolism of Hydrogen in the Extremophile Acidithiobacillus ferrooxidans
Authors
KUČERA, Jiří (203 Czech Republic, guarantor, belonging to the institution), Jan LOCHMAN (203 Czech Republic, belonging to the institution), Pavel BOUCHAL (203 Czech Republic, belonging to the institution), Eva PAKOSTOVA, Kamil MIKULÁŠEK (203 Czech Republic, belonging to the institution), Sabrina HEDRICH, Oldřich JANICZEK (203 Czech Republic, belonging to the institution), Martin MANDL (203 Czech Republic, belonging to the institution) and D. Barrie JOHNSON
Edition
Frontiers in Microbiology, Lausanne, Frontiers Media SA, 2020, 1664-302X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.640
RIV identification code
RIV/00216224:14310/20:00117533
Organization unit
Faculty of Science
UT WoS
000598487900001
Keywords in English
Acidithiobacillus; extremophiles; ferric iron reduction; hydrogen metabolism; multi-omics; oxygen reduction
Tags
International impact, Reviewed
Změněno: 17/2/2023 22:19, Mgr. Jiří Kučera, Ph.D.
Abstract
V originále
Hydrogen can serve as an electron donor for chemolithotrophic acidophiles, especially in the deep terrestrial subsurface and geothermal ecosystems. Nevertheless, the current knowledge of hydrogen utilization by mesophilic acidophiles is minimal. A multi-omics analysis was applied on Acidithiobacillus ferrooxidans growing on hydrogen, and a respiratory model was proposed. In the model, [NiFe] hydrogenases oxidize hydrogen to two protons and two electrons. The electrons are used to reduce membrane-soluble ubiquinone to ubiquinol. Genetically associated iron-sulfur proteins mediate electron relay from the hydrogenases to the ubiquinone pool. Under aerobic conditions, reduced ubiquinol transfers electrons to either cytochrome aa(3) oxidase via cytochrome bc(1) complex and cytochrome c(4) or the alternate directly to cytochrome bd oxidase, resulting in proton efflux and reduction of oxygen. Under anaerobic conditions, reduced ubiquinol transfers electrons to outer membrane cytochrome c (ferrireductase) via cytochrome bc(1) complex and a cascade of electron transporters (cytochrome c(4), cytochrome c(552), rusticyanin, and high potential iron-sulfur protein), resulting in proton efflux and reduction of ferric iron. The proton gradient generated by hydrogen oxidation maintains the membrane potential and allows the generation of ATP and NADH. These results further clarify the role of extremophiles in biogeochemical processes and their impact on the composition of the deep terrestrial subsurface.
Links
LM2018127, research and development project |
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