Microbial paths to renewable hydrogen production

• Tollefson J. Hydrogen vehicles: fuel of the future?Nature464,1262–1264 (2010).
   PubMed Web of Science ®Google Scholar
• Kohse-Höinghaus K, Osswald P, Cool TAet al. Biofuel combustion chemistry: from ethanol to biodiesel.Angew. Chem.49(21),3572–3597 (2010).
   Google Scholar
• Jacoby M. Filling up with hydrogen.Chem. Eng. News83,42–47 (2005).
   Google Scholar
• Tanksale A, Beltramini JN, Lu GM. A review of catalytic hydrogen production processes from biomass.Renew. Sust. Ener. Rev.14(1),166–182 (2010).
   Web of Science ®Google Scholar
• Magnuson A, Anderlund M, Johansson Oet al. Biomimetic and microbial approaches to solar fuel generation.Acc. Chem. Res.42(12),1899–1909 (2009).
   PubMed Web of Science ®Google Scholar
• Fukuzumi S. Bioinspired energy conversion systems for hydrogen production and storage.Eur. J. Inorgan. Chem.2008(9),1351–1362 (2008).
   Google Scholar
• Vignais PM, Billoud B. Occurrence, classification, and biological function of hydrogenases: an overview.Chem. Rev.107(10),4206–4272 (2007).
   PubMed Web of Science ®Google Scholar
• Hallenbeck PC. Fermentative hydrogen production: principles, progress, and prognosis.Int. J. Hydrogen Energy34(17),7379–7389 (2009).
   Web of Science ®Google Scholar
• Vignais PM. Hydrogenases and H(+)-reduction in primary energy conservation.Results Probl. Cell Differ.45,223–252 (2008).
   PubMedGoogle Scholar
• Hedderich R, Forzi L. Energy-converting NiFe hydrogenases: more than just H-2 activation.J. Mol. Microbiol. Biotechnol.10(2–4),92–104 (2005).
   PubMed Web of Science ®Google Scholar
• Heinekey DM. Hydrogenase enzymes: recent structural studies and active site models.J. Organometallic Chem.694(17),2671–2680 (2009).
   Web of Science ®Google Scholar
• Böck A, King PW, Blokesch M, Posewitz MC. Maturation of hydrogenases.Adv. Microb. Physiol.51,1–71 (2006).
   PubMed Web of Science ®Google Scholar
• Hu YL, Fay AW, Lee CC, Yoshizawa J, Ribbe MW. Assembly of nitrogenase MoFe protein.Biochem.47(13),3973–3981 (2008).
   PubMed Web of Science ®Google Scholar
• Hallenbeck PC, Ghosh D. Advances in fermentative biohydrogen production: the way forward?Trends Biotechnol.27(5),287–297 (2009).
   PubMed Web of Science ®Google Scholar
• Meyer J. FeFe hydrogenases and their evolution: a genomic perspective.Cell. Mol. Life Sci.64(9),1063–1084 (2007).
   PubMed Web of Science ®Google Scholar
• Calusinska M, Happe T, Joris B, Wilmotte A. The surprising diversity of clostridial hydrogenases: a comparative genomic perspective.Microbiology156(Pt 6),1575–1588 (2010).
   PubMed Web of Science ®Google Scholar
• Kapdan IK, Kargi F. Bio-hydrogen production from waste materials.Enz. Micro. Tech.38(5),569–582 (2006).
   Web of Science ®Google Scholar
• Li CL, Fang HHP. Fermentative hydrogen production from wastewater and solid wastes by mixed cultures.Crit. Rev. Environ. Sci. Technol.37(1),1–39 (2007).
   Web of Science ®Google Scholar
• Ghosh D, Hallenbeck PC. Fermentative hydrogen yields from different sugars by batch cultures of metabolically engineeredEscherichia coli DJT135.Int. J. Hydrogen Energy34(19),7979–7982 (2009).
   Web of Science ®Google Scholar
• Hallenbeck PC. Fundamentals of the fermentative production of hydrogen.Water Sci. Technol.52(1–2),21–29 (2005).
   PubMed Web of Science ®Google Scholar
• Schut GJ, Adams MWW. The iron-hydrogenase ofThermotoga maritima utilizes ferredoxin and NADH synergistically: a new perspective on anaerobic hydrogen production.J. Bacteriol.191(13),4451–4457 (2009).
   PubMed Web of Science ®Google Scholar
• Herrmann G, Jayamani E, Mai G, Buckel W. Energy conservation via electron-transferring flavoprotein in anaerobic bacteria.J. Bacteriol.190(3),784–791 (2008).
   PubMed Web of Science ®Google Scholar
• Hallenbeck PC, Ghosh D, Abo-Hashesh M, Wang R. Metabolic engineering for enhanced biofuels production with emphasis on the biological production of hydrogen. In:Advances in Chemistry Research Volume 6. Nova Science Publishers, Hauppauge, NY, USA125–154 (2011).
   Google Scholar
• Logan BE, Call D, Cheng Set al. Microbial electrolysis cells for high yield hydrogen gas production from organic matter.Environ. Sci. Technol.42(23),8630–8640 (2008).
   PubMed Web of Science ®Google Scholar
• Hong Liu H, Hu H, Chignell J, Fan Y. Microbial electrolysis: novel technology for hydrogen production from biomass.Biofuels1(1),129–142 (2010).
   Google Scholar
• Geelhoed JS, Hamelers HVM, Stams AJM. Electricity-mediated biological hydrogen production.Curr. Opin. Microbiol.13(3),307–315 (2010).
   PubMed Web of Science ®Google Scholar
• Logan BE. Scaling up microbial fuel cells and other bioelectrochemical systems.Appl. Microbiol. Biotechnol.85(6),1665–1671 (2010).
   PubMed Web of Science ®Google Scholar
• Logan BE. Exoelectrogenic bacteria that power microbial fuel cells.Nat. Rev. Microbiol.7(5),375–381 (2009).
   PubMed Web of Science ®Google Scholar
• Wang AJ, Sun D, Ren NQet al. A rapid selection strategy for an anodophilic consortium for microbial fuel cells.Bioresour. Technol.101(14),5733–5735 (2010).
   PubMed Web of Science ®Google Scholar
• Lu L, Xing DF, Xie TH, Ren NQ, Logan BE. Hydrogen production from proteins via electrohydrogenesis in microbial electrolysis cells.Biosens. Bioelectron.25(12),2690–2695 (2010).
   PubMed Web of Science ®Google Scholar
• Cheng SA, Xing DF, Call DF, Logan BE. Direct biological conversion of electrical current into methane by electromethanogenesis.Environ. Sci. Technol.43(10),3953–3958 (2009).
   PubMed Web of Science ®Google Scholar
• Cao XX, Huang X, Liang Pet al. A new method for water desalination using microbial desalination cells.Environ. Sci. Technol.43(18),7148–7152 (2009).
   PubMed Web of Science ®Google Scholar
• Call D, Logan BE. Hydrogen production in a single chamber microbial electrolysis cell (MEC) lacking a membrane.Environ. Sci. Technol.42(9),3401–3406 (2008).
   PubMed Web of Science ®Google Scholar
• Hu H, Fan Y, Liu H. Hydrogen production using single-chamber membrane-free microbial electrolysis cells.Water Res.42(15),4172–4178 (2008).
   PubMed Web of Science ®Google Scholar
• Lee HS, Rittmann BE. Significance of biological hydrogen oxidation in a continuous single-chamber microbial electrolysis cell.Environ. Sci. Technol.44(3),948–954 (2010).
   PubMed Web of Science ®Google Scholar
• Selembo PA, Merrill MD, Logan BE. The use of stainless steel and nickel alloys as low-cost cathodes in microbial electrolysis cells.J. Power Sources190(2),271–278 (2009).
   Web of Science ®Google Scholar
• Jeremiasse AW, Hamelers HVM, Buisman CJN. Microbial electrolysis cell with a microbial biocathode.Bioelectrochemistry78(1),39–43 (2010).
   PubMed Web of Science ®Google Scholar
• Jeremiasse AW, Hamelers HVM, Kleijn JM, Buisman CJN. Use of biocompatible buffers to reduce the concentration overpotential for hydrogen evolution.Environ. Sci. Technol.43(17),6882–6887 (2009).
   PubMed Web of Science ®Google Scholar
• Ghirardi ML, Dubini A, Yu JP, Maness PC. Photobiological hydrogen-producing systems.Chem. Soc. Rev.38(1),52–61 (2009); Erratum in:38(12),3505 (2009).
   PubMed Web of Science ®Google Scholar
• Ghirardi ML, Mohanty P. Oxygenic hydrogen photoproduction – current status of the technology.Curr. Sci.98(4),499–507 (2010).
   Web of Science ®Google Scholar
• McKinlay JB, Harwood CS. Photobiological production of hydrogen gas as a biofuel.Curr. Opin. Biotechnol.21(3),244–251 (2010).
   PubMed Web of Science ®Google Scholar
• Beer LL, Boyd ES, Peters JW, Posewitz MC. Engineering algae for biohydrogen and biofuel production.Curr. Opin. Biotechnol.20(3),264–271 (2009).
   PubMed Web of Science ®Google Scholar
• Radakovits R, Jinkerson RE, Darzins A, Posewitz MC. Genetic engineering of algae for enhanced biofuel production.Eukaryotic Cell9(4),486–501 (2010).
   PubMed Web of Science ®Google Scholar
• Wijffels RH, Barbosa MJ, Eppink MHM. Microalgae for the production of bulk chemicals and biofuels.Biofuels Bioprod. Bior.4(3),287–295 (2010).
   Web of Science ®Google Scholar
• Angermayr SA, Hellingwerf KJ, Lindblad P, de Mattos MJT. Energy biotechnology with cyanobacteria.Curr. Opin. Biotechnol.20(3),257–263 (2009).
   PubMed Web of Science ®Google Scholar
• Atsumi S, Higashide W, Liao JC. Direct photosynthetic recycling of carbon dioxide to isobutyraldehyde.Nat. Biotechnol.27(12),1177–1180 (2009).
   PubMed Web of Science ®Google Scholar
• Mariscal V, Flores F. Multicellularity in a heterocyst-forming cyanobacterium: pathways for intercellular communication. In:Recent Advances in Phototrophic Prokaryotes. Hallenbeck PC (Ed.). Springer, Berlin, Germany (2010).
   Google Scholar
• Kumar K, Mella-Herrera RA, Golden JW. Cyanobacterial heterocysts.Cold Spring Harb. Perspect. Biol.2(4),a000315 (2010).
   PubMed Web of Science ®Google Scholar
• Lopez-Igual R, Flores E, Herrero A. Inactivation of a heterocyst-specific invertase indicates a principal role of sucrose catabolism in heterocysts ofAnabaena sp.J. Bacteriol.192(20),5526–5533 (2010).
   PubMed Web of Science ®Google Scholar
• Summers ML, Wallis JG, Campbell EL, Meeks JC. Genetic evidence of a major role for glucose-6-phosphate-dehydrogenase in nitrogen-fixation and dark growth of the cyanobacteriumNostoc sp. strain ATCC-29133.J. Bacteriol.177(21),6184–6194 (1995).
   PubMed Web of Science ®Google Scholar
• Ludwig M, Schulz-Friedrich R, Appel J. Occurrence of hydrogenases in cyanobacteria and anoxygenic photosynthetic bacteria: implications for the phylogenetic origin of cyanobacterial and algal hydrogenases.J. Mol. Evol.63(6),758–768 (2006).
   PubMed Web of Science ®Google Scholar
• Benemann JR, Weare NM. Hydrogen evolution by nitrogen-fixingAnabaena cylindrica cultures.Science184,174–175 (1974).
   PubMed Web of Science ®Google Scholar
• Weissman JC, Benemann JR. Hydrogen production by nitrogen-starved cultures ofAnabaena cylindrica.Appl. Environ. Microbiol.33(1),123–131 (1977).
   PubMed Web of Science ®Google Scholar
• Miyamoto K, Hallenbeck PC, Benemann JR. Solar-energy conversion by nitrogen-limited cultures ofAnabaena cylindrica.J. Ferm. Technol.57(4),287–293 (1979).
   Google Scholar
• Yoon JH, Hae Shin J, Kim MS, Jun Sim S, Park TH. Evaluation of conversion efficiency of light to hydrogen energy byAnabaena variabilis.Int. J. Hydrogen Energy31(6),721–727 (2006).
   Web of Science ®Google Scholar
• Berberoglu H, Jay J, Pilon L. Effect of nutrient media on photobiological hydrogen production byAnabaena variabilis ATCC 29413.Int. J. Hydrogen Energy33(4),1172–1184 (2008).
   Web of Science ®Google Scholar
• Sakurai H, Masukawa H. Promoting R & D in photobiological hydrogen production utilizing mariculture-raised cyanobacteria.Mar. Biotechnol.9(2),128–145 (2007).
   PubMed Web of Science ®Google Scholar
• Tsygankov AA, Fedorov AS, Kosourov SN, Rao KK. Hydrogen production by cyanobacteria in an automated outdoor photobioreactor under aerobic conditions.Biotechnol. Bioeng.80(7),777–783 (2002)
   PubMed Web of Science ®Google Scholar
• Min HT, Sherman LA. Hydrogen production by the unicellular, diazotrophic cyanobacteriumCyanothece sp. strain ATCC 51142 under conditions of continuous light.Appl. Environ. Microbiol.76(13),4293–4301 (2010).
   PubMed Web of Science ®Google Scholar
• Schwarz S, Poss Z, Hoffmann D, Appel J. Hydrogenases and hydrogen metabolism in photosynthetic prokaryotes. In:Recent Advances in Phototrophic Prokaryotes. Hallenbeck PC (Ed.). Springer, Berlin, Germany (2010).
   Google Scholar
• Huesemann MH, Hausmann TS, Carter BM, Gerschler JJ, Benemann JR. Hydrogen generation through indirect biophotolysis in batch cultures of the nonheterocystous nitrogen-fixing cyanobacteriumPlectonema boryanum.Appl. Biochem. Biotechnol.162(1),208–220 (2010).
   PubMed Web of Science ®Google Scholar
• McNeely K, Xu Y, Bennette N, Bryant DA, Dismukes GC. Redirecting reductant flux into hydrogen production via metabolic engineering of fermentative carbon metabolism in a cyanobacterium.Appl. Environ. Microbiol.76(15),5032–5038 (2010).
   PubMed Web of Science ®Google Scholar
• Melis A, Zhang LP, Forestier M, Ghirardi ML, Seibert M. Sustained photobiological hydrogen gas production upon reversible inactivation of oxygen evolution in the green algaChlamydomonas reinhardtii.Plant Physiol.122(1),127–135 (2000).
   PubMed Web of Science ®Google Scholar
• Melis A. Photosynthetic H-2 metabolism inChlamydomonas reinhardtii (unicellular green algae).Planta226(5),1075–1086 (2007).
   PubMed Web of Science ®Google Scholar
• Kruse O, Hankamer B. Microalgal hydrogen production.Curr. Opin. Biotechnol.21(3),238–243 (2010).
   PubMed Web of Science ®Google Scholar
• Chochois V, Dauvillee D, Beyly Aet al. Hydrogen production inChlamydomonas: photosystem II-dependent and -independent pathways differ in their requirement for starch metabolism.Plant Physiol.151(2),63, 1–640 (2009).
   Google Scholar
• Jans F, Mignolet E, Houyoux PAet al. A type II NAD(P) H dehydrogenase mediates light-independent plastoquinone reduction in the chloroplast ofChlamydomonas.Proc. Natl Acad. Sci. USA105(51),20546–20551 (2008).
   PubMed Web of Science ®Google Scholar
• Peltier G, Tolleter D, Billon E, Cournac L. Auxiliary electron transport pathways in chloroplasts of microalgae.Photosynth. Res.106(1–2),19–31 (2010).
   PubMed Web of Science ®Google Scholar
• Nagy LE, Meuser JE, Plummer Set al. Application of gene-shuffling for the rapid generation of novel [FeFe]-hydrogenase libraries.Biotechnol. Lett.29(3),421–430 (2007).
   PubMed Web of Science ®Google Scholar
• Boyd ES, Spear JR, Peters JW. FeFe hydrogenase genetic diversity provides insight into molecular adaptation in a saline microbial mat community.Appl. Environ. Microbiol.75(13),4620–4623 (2009).
   PubMed Web of Science ®Google Scholar
• Constant P, Chowdhury SP, Pratscher J, Conrad R.Streptomycetes contributing to atmospheric molecular hydrogen soil uptake are widespread and encode a putative high-affinity NiFe-hydrogenase.Environ. Microbiol.12(3),821–829 (2010).
   PubMed Web of Science ®Google Scholar
• Li RY, Fang HHP. Heterotrophic photo fermentative hydrogen production.Crit. Rev. Environ. Sci. Technol.39(12),1081–1108 (2009).
   Web of Science ®Google Scholar
• Laguna R, Joshi GS, Dangel AW, Amanda K. Luther AK, Tabita FR. Integrative control of carbon, nitrogen, hydrogen, and sulfur metabolism: the central role of the Calvin–Benson–Bassham cycle. In:Recent Advances in Phototrophic Prokaryotes. Hallenbeck PC (Ed.). Springer, Berlin, Germany (2010).
   Google Scholar
• McKinlay JB, Harwood CS. Carbon dioxide fixation as a central redox cofactor recycling mechanism in bacteria.Proc. Natl Acad. Sci. USA107(26),11669–11675 (2010).
   PubMed Web of Science ®Google Scholar
• Sabourin-Provost G, Hallenbeck PC. High yield conversion of a crude glycerol fraction from biodiesel production to hydrogen by photofermentation.Bioresour. Technol.100(14),3513–3517 (2009).
   PubMed Web of Science ®Google Scholar
• Levin DB, Pitt L, Love M. Biohydrogen production: prospects and limitations to practical application.Int. J. Hydrogen Energy29(2),173–185 (2004); Erratum in:Int. J. Hydrogen Energy29(13),1425–1426 (2004).
   Web of Science ®Google Scholar

▪ Websites

• US Department of Energy, Hydrogen, Fuel Cells and Infrastructure Technologies Program. Hydrogen Posture Plan.www.hydrogen.energy.gov
   Google Scholar
• US Department of Energy. Hydrogen properties, hydrogen fuel cell engines and related technologies.http://hydrogen.pnl.gov/cocoon/morf/hydrogen/article/401
   Google Scholar
• US Department of Energy Hydrogen Program. Record 8020: reduction in fuel consumption with fuel cell vehicles.www.hydrogen.energy.gov/program_records.html
   Google Scholar