Chris Greening
Eric Boyd- 1School of Biological Sciences, Monash University, Clayton, VIC, Australia
- 2Department of Microbiology and Immunology, Montana State University, Bozeman, MT, United States
Editorial on the Research Topic
Microbial Hydrogen Metabolism
Among the most ancient and widespread metabolic traits of microbial life is the ability to interconvert molecular hydrogen (H2; Lane et al., 2010; Schwartz et al., 2013; Peters et al., 2015). Two classes of metalloenzymes, [FeFe]-hydrogenase and [NiFe]-hydrogenase, catalyze the reversible oxidation of H2 to electrons and protons (Volbeda et al., 1995; Peters et al., 1998); a third class of hydrogenase, termed [Fe]-hydrogenase or Hmd, catalyzes the reduction of the substrate methenyltetrahydromethanopterin with H2 (Shima et al., 2008). The three classes of enzyme differ structurally and are phylogenetically unrelated. As such, they represent profound examples of convergent evolution (Wu and Mandrand, 1993; Vignais and Billoud, 2007; Greening et al., 2016).
Approximately a third of sequenced microorganisms, spanning at least 70 microbial phyla, encode hydrogenases and are thus predicted to be capable of interconverting H2 (Peters et al., 2015; Greening et al., 2016). The earliest evolving hydrogenase enzymes harbor a [NiFe] co-factor and these are thought to have functioned oxidatively (Boyd et al., 2014; Weiss et al., 2016), with [FeFe]-hydrogenases thought to have emerged more recently (Mulder et al., 2010). Both [NiFe] and [FeFe]-hydrogenases have since diversified to function in aerobic and anaerobic, heterotrophic, and autotrophic, and chemotrophic and phototrophic metabolic backgrounds (Kovács et al., 2005; Tamagnini et al., 2007; Thauer et al., 2010; Schwartz et al., 2013; Koch et al., 2014; Schuchmann and Muller, 2014; Pinske and Sawers, 2016). Many bacteria and archaea oxidize H2 as a low potential electron donor, an activity typically (albeit not exclusively) attributed to various lineages of [NiFe]-hydrogenase enzymes. Various bacteria, archaea, and microbial eukaryotes also evolve H2 as a diffusible end product during fermentative metabolism through the activity of [FeFe]- or [NiFe]-hydrogenases (Horner et al., 2000; Kim and Kim, 2011; Marreiros et al., 2013; Schwartz et al., 2013; Pinske and Sawers, 2016). In many organisms, the ability to metabolize H2 is a facultative trait that is regulated through the expression and maturation of hydrogenases (Schwartz et al., 2013; Greening and Cook, 2014). In such taxa, H2 represents a substrate that organisms utilize to supplement their energy metabolism, thereby allowing for an expansion of their niche space in ecosystems where other sources of reductant are low or variable in supply (e.g., Amenabar et al., 2018).
The implications of H2 in ecosystem level processes is increasingly being realized in both environmental and biomedical settings. A wide range of ecosystems have now been described where H2 cycling supports the bulk of primary production and where it forms the basis by which species interact, leading to ecologically structured communities. Much of the research on H2 metabolism to date has focused on ecosystems where H2 is present at elevated concentrations due to biological activity (e.g., anoxic sediments, gastrointestinal tracts; Sørensen et al., 1981; Wolf et al., 2016; Greening et al., 2019; Kessler et al., 2019) or geological activity (e.g., hydrothermal vents, subsurface systems; Petersen et al., 2011; Brazelton et al., 2012; Telling et al., 2015; Dong et al., 2019; Lindsay et al., 2019). More recently, it has been recognized that atmospheric H2 can serve as source of reductant for aerobic soil microorganisms and that this can influence the composition of the atmosphere (Conrad, 1996; Constant et al., 2010; Ji et al., 2017; Cordero et al., 2019). In parallel, medical microbiologists have shown that H2 metabolism is critical for the virulence of numerous pathogens, including Helicobacter, Clostridia, and Enterobacteriaceae (Kaji et al., 1999; Olson and Maier, 2002; Maier et al., 2004, 2013).
This special issue, featuring 10 articles from 46 different authors, explores microbial H2 metabolism from the molecular to the ecosystem scale. In the area of anaerobic metabolism, there are articles exploring the metabolism of H2-metabolizing bacteria capable of sulfate reduction, acetogenesis, halorespiration, and fermentation. Two articles investigate H2 oxidation in sulfate-reducing bacteria using the model system Desulfovibrio vulgaris (Fauque et al., 1988; Caffrey et al., 2007). Smith et al. present a mathematical model of the growth and metabolism of this bacterium, whereas Löffler et al. investigate the kinetic isotope fractionation associated with its H2 oxidation activity. A comprehensive review led by Schuchmann et al. covers recent advances in understanding clostridial H2 metabolism; it details the discovery and characterization of multimeric electron-bifurcating [FeFe]-hydrogenases, including those associated with formate dehydrogenases (Schut and Adams, 2009; Schuchmann and Müller, 2012, 2013; Buckel and Thauer, 2018). Another article led by Dragomirova et al. focuses on heterologous expression of a [NiFe]-hydrogenase from dehalogenating Chloroflexi (Kublik et al., 2016; Hartwig et al., 2017), reporting another unexpected association with formate dehydrogenase activity. Pinske explores a third type of formate dehydrogenase-linked hydrogenase, namely the classical formate hydrogenlyase complex of Enterobacteriaceae (McDowall et al., 2014), and its association with two novel iron-sulfur proteins.
Several articles also investigate aerobic H2 metabolism. Islam et al. report two other novel iron-sulfur proteins in mycobacteria, demonstrating that they are essential for the activity of the two high-affinity hydrogenases described in this lineage (Greening et al., 2014). Carere et al. meanwhile, build on the recent discovery that verrucomicrobial methanotrophs are facultative mixotrophs (Carere et al., 2017; Mohammadi et al., 2017) by showing resource allocation of Methylacidiphilum varies depending on H2 availability. Three articles also explore H2 metabolism at the ecosystem level. Adam and Perner explore the diversity of aerobic and anaerobic H2 metabolism in deep-sea hydrothermal vent systems, whereas Meyer-Dombard et al. investigate the influence of H2 on biogeochemical cycling in serpentinizing springs in the Philippines. Teng et al. review the previously underexplored area of H2 metabolism in bioremediation, including in the reduction of organohalides, nitroaromatic compounds, and heavy metals (Chardin et al., 2003; Hong et al., 2008; Schubert et al., 2018).
In summary, this special Research Topic sheds light on the diverse role of H2 in microbial metabolism and uncovers novel enzymes and pathways that mediate this process. This body of work highlights the intricate linkages between H2 cycling and the cycling of various other compounds, including methane, formate, carbon dioxide, sulfate, and organohalides, among others. In turn, these findings pave way for future studies on the biochemistry, physiology, ecology, and industrial applications of microbial H2 metabolism.
Author Contributions
CG and EB drafted this editorial together and approve its submission.
Funding
This work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award DE-SC0020246 (EB).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to acknowledge all authors, peer reviewers, guest editors, and the Frontiers team for their support in developing this Research Topic. The salary of CG is covered by an Australian Research Council DECRA Fellowship (DE170100310) and a National Health & Medical Research Council EL2 Fellowship (APP1178715).
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Keywords: hydrogen, hydrogen metabolism, hydrogenase, fermentation, respiration
Citation: Greening C and Boyd E (2020) Editorial: Microbial Hydrogen Metabolism. Front. Microbiol. 11:56. doi: 10.3389/fmicb.2020.00056
Received: 20 November 2019; Accepted: 13 January 2020;
Published: 30 January 2020.
Edited by:
Patricia Coutinho Dos Santos, Wake Forest University, United StatesReviewed by:
Shawn E. McGlynn, Tokyo Institute of Technology, JapanCopyright © 2020 Greening and Boyd. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chris Greening, Y2hyaXMuZ3JlZW5pbmcmI3gwMDA0MDttb25hc2guZWR1; Eric Boyd, ZWJveWQmI3gwMDA0MDttb250YW5hLmVkdQ==