Journal
FEMS MICROBIOLOGY REVIEWS
Volume 37, Issue 2, Pages 182-203Publisher
OXFORD UNIV PRESS
DOI: 10.1111/j.1574-6976.2012.00346.x
Keywords
hydrogenase; evolution; respiratory complexes; archaea
Categories
Funding
- Chemical Sciences, Geosciences and Biosciences Division of the Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [FG05-95ER20175]
- Office of Biological and Environmental Research of the Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy [FG02-08ER64690]
- Low Temperature Geobiology and Geochemsitry program of the National Science Foundation [EAR-1123689]
- NASA Astrobiology Institute [NNA08C-N85A]
- Division Of Earth Sciences
- Directorate For Geosciences [1123689] Funding Source: National Science Foundation
- Div Of Biological Infrastructure
- Direct For Biological Sciences [963175] Funding Source: National Science Foundation
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Hydrogen production is a vital metabolic process for many anaerobic organisms, and the enzyme responsible, hydrogenase, has been studied since the 1930s. A novel subfamily with unique properties was recently recognized, represented by the 14-subunit membrane-bound [NiFe] hydrogenase from the archaeon Pyrococcus furiosus. This so-called energy-converting hydrogenase links the thermodynamically favorable oxidation of ferredoxin with the formation of hydrogen and conserves energy in the form of an ion gradient. It is therefore a simple respiratory system within a single complex. This hydrogenase shows a modular composition represented by a Na+/H+ antiporter domain (Mrp) and a [NiFe] hydrogenase domain (Mbh). An analysis of the large number of microbial genome sequences available shows that homologs of Mbh and Mrp tend to be clustered within the genomes of a limited number of archaeal and bacterial species. In several instances, additional genes are associated with the Mbh and Mrp gene clusters that encode proteins that catalyze the oxidation of formate, CO or NAD(P)H. The Mbh complex also shows extensive homology to a number of subunits within the NADH quinone oxidoreductase or complex I family. The respiratory-type membrane-bound hydrogenase complex appears to be closely related to the common ancestor of complex I and [NiFe] hydrogenases in general.
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