scholarly journals A Model of Aerobic and Anaerobic Metabolism of Hydrogen in the Extremophile Acidithiobacillus ferrooxidans

2020 ◽  
Vol 11 ◽  
Author(s):  
Jiri Kucera ◽  
Jan Lochman ◽  
Pavel Bouchal ◽  
Eva Pakostova ◽  
Kamil Mikulasek ◽  
...  

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 aa3 oxidase via cytochrome bc1 complex and cytochrome c4 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 bc1 complex and a cascade of electron transporters (cytochrome c4, cytochrome c552, 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.

Biochemistry ◽  
1999 ◽  
Vol 38 (48) ◽  
pp. 15791-15806 ◽  
Author(s):  
Antony R. Crofts ◽  
Mariana Guergova-Kuras ◽  
LiShar Huang ◽  
Richard Kuras ◽  
Zhaolei Zhang ◽  
...  

1995 ◽  
Vol 50 (1) ◽  
pp. 75-80 ◽  
Author(s):  
Moshe Belinskii ◽  
Ivano Bertini ◽  
Oleg Galas ◽  
Claudio Luchinat

The recently obtained Mössbauer and EPR parameters of the Fe4S43+ polymetallic center in the High Potential Iron-Sulfur Protein (HiPIP) II from E. halophila have been reproduced with models based on pure Heisenberg exchange. The role of double exchange versus ./-inequivalence is discussed. An evaluation of the upper limit of the double exchange parameter in the Fe4S43+ bimetallic center is also presented. The present calculations shed further light on the electronic structure of the Fe4S43+ center.


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