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      Genomic and metagenomic surveys of hydrogenase distribution indicate H 2 is a widely utilised energy source for microbial growth and survival

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          Abstract

          Recent physiological and ecological studies have challenged the long-held belief that microbial metabolism of molecular hydrogen (H 2) is a niche process. To gain a broader insight into the importance of microbial H 2 metabolism, we comprehensively surveyed the genomic and metagenomic distribution of hydrogenases, the reversible enzymes that catalyse the oxidation and evolution of H 2. The protein sequences of 3286 non-redundant putative hydrogenases were curated from publicly available databases. These metalloenzymes were classified into multiple groups based on (1) amino acid sequence phylogeny, (2) metal-binding motifs, (3) predicted genetic organisation and (4) reported biochemical characteristics. Four groups (22 subgroups) of [NiFe]-hydrogenase, three groups (6 subtypes) of [FeFe]-hydrogenases and a small group of [Fe]-hydrogenases were identified. We predict that this hydrogenase diversity supports H 2-based respiration, fermentation and carbon fixation processes in both oxic and anoxic environments, in addition to various H 2-sensing, electron-bifurcation and energy-conversion mechanisms. Hydrogenase-encoding genes were identified in 51 bacterial and archaeal phyla, suggesting strong pressure for both vertical and lateral acquisition. Furthermore, hydrogenase genes could be recovered from diverse terrestrial, aquatic and host-associated metagenomes in varying proportions, indicating a broad ecological distribution and utilisation. Oxygen content ( pO 2) appears to be a central factor driving the phylum- and ecosystem-level distribution of these genes. In addition to compounding evidence that H 2 was the first electron donor for life, our analysis suggests that the great diversification of hydrogenases has enabled H 2 metabolism to sustain the growth or survival of microorganisms in a wide range of ecosystems to the present day. This work also provides a comprehensive expanded system for classifying hydrogenases and identifies new prospects for investigating H 2 metabolism.

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          Author and article information

          Journal
          ISME J
          ISME J
          The ISME Journal
          Nature Publishing Group
          1751-7362
          1751-7370
          March 2016
          25 September 2015
          : 10
          : 3
          : 761-777
          Affiliations
          [1 ] Department of Microbiology and Immunology, University of Otago , Dunedin, New Zealand
          [2 ] The Commonwealth Scientific and Industrial Research Organisation, Land and Water Flagship , Acton, Australian Capital Territory, Australia
          [3 ] GNS Science, Wairakei Research Centre , Taupō, New Zealand
          [4 ] Scion, Te Papa Tipu Innovation Park , Rotorua, New Zealand
          [5 ] Australian National University, Research School of Chemistry , Acton, Australian Capital Territory, Australia
          [6 ] University of Auckland, Maurice Wilkins Centre for Molecular Biodiscovery , Auckland, New Zealand
          Author notes
          [* ] The Commonwealth Scientific and Industrial Organisation, Land and Water Flagship , Clunies Ross Street, Acton, Australian Capital Territory 2060, Australia. E-mail: chris.greening@ 123456csiro.au
          [* ] Department of Microbiology and Immunology, University of Otago , 720 Cumberland Street, North Dunedin, Dunedin 9054, New Zealand. E-mail: sergio.morales@ 123456otago.ac.nz
          Article
          PMC4817680 PMC4817680 4817680 ismej2015153
          10.1038/ismej.2015.153
          4817680
          26405831
          979fa58e-04ad-45b2-bcab-e826e4cec02e
          Copyright © 2016 International Society for Microbial Ecology
          History
          : 03 May 2015
          : 20 June 2015
          : 20 July 2015
          Categories
          Original Article

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