Carbon dioxide reduction to methane and coupling with acetylene to form propylene catalyzed by remodeled nitrogenase

A doubly substituted form of the nitrogenase MoFe protein (α-70Val→Ala, α-195His→Gln) has the capacity to catalyze the reduction of carbon dioxide (CO2) to yield methane (CH4). Under optimized conditions, 1 nmol of the substituted MoFe protein catalyzes the formation of 21 nmol of CH4 within 20 min. The catalytic rate depends on the partial pressure of CO2 (or concentration of HCO3−) and the electron flux through nitrogenase. The doubly substituted MoFe protein also has the capacity to catalyze the unprecedented formation of propylene (H2C = CH-CH3) through the reductive coupling of CO2 and acetylene (HC≡CH). In light of these observations, we suggest that an emerging understanding of the mechanistic features of nitrogenase could be relevant to the design of synthetic catalysts for CO2 sequestration and formation of olefins.

[1]  M. Khandelwal,et al.  Deoxygenative reduction of carbon dioxide to methane, toluene, and diphenylmethane with [Et2Al]+ as catalyst. , 2012, Angewandte Chemie.

[2]  I. Omae Recent developments in carbon dioxide utilization for the production of organic chemicals , 2012 .

[3]  N. Oreskes The Hockey Stick and the Climate Wars: Dispatches from the Front Lines , 2012 .

[4]  L. Seefeldt,et al.  Electron transfer in nitrogenase catalysis. , 2012, Current opinion in chemical biology.

[5]  L. Seefeldt,et al.  Unification of reaction pathway and kinetic scheme for N2 reduction catalyzed by nitrogenase , 2012, Proceedings of the National Academy of Sciences.

[6]  H. Herzog,et al.  Lifetime of carbon capture and storage as a climate-change mitigation technology , 2012, Proceedings of the National Academy of Sciences.

[7]  M. Mann The Hockey Stick and the Climate Wars: Dispatches from the Front Lines , 2012 .

[8]  D. Rees,et al.  Evidence for Interstitial Carbon in Nitrogenase FeMo Cofactor , 2011, Science.

[9]  Frank Neese,et al.  X-ray Emission Spectroscopy Evidences a Central Carbon in the Nitrogenase Iron-Molybdenum Cofactor , 2011, Science.

[10]  B. Rieger,et al.  Transformation of carbon dioxide with homogeneous transition-metal catalysts: a molecular solution to a global challenge? , 2011, Angewandte Chemie.

[11]  Yilin Hu,et al.  Extending the Carbon Chain: Hydrocarbon Formation Catalyzed by Vanadium/Molybdenum Nitrogenases , 2011, Science.

[12]  Thomas Schaub,et al.  A process for the synthesis of formic acid by CO2 hydrogenation: thermodynamic aspects and the role of CO. , 2011, Angewandte Chemie.

[13]  G. Olah,et al.  Anthropogenic chemical carbon cycle for a sustainable future. , 2011, Journal of the American Chemical Society.

[14]  Yugen Zhang,et al.  Catalytic hydrocarboxylation of alkenes and alkynes with CO2. , 2011, Angewandte Chemie.

[15]  Wei Wang,et al.  Recent advances in catalytic hydrogenation of carbon dioxide. , 2011, Chemical Society reviews.

[16]  L. Seefeldt,et al.  Molybdenum Nitrogenase Catalyzes the Reduction and Coupling of CO to Form Hydrocarbons*♦ , 2011, The Journal of Biological Chemistry.

[17]  Timothy R. Cook,et al.  Solar energy supply and storage for the legacy and nonlegacy worlds. , 2010, Chemical reviews.

[18]  D. Darensbourg,et al.  Chemistry of carbon dioxide relevant to its utilization: a personal perspective. , 2010, Inorganic chemistry.

[19]  Yilin Hu,et al.  Vanadium Nitrogenase Reduces CO , 2010, Science.

[20]  E. Fujita,et al.  Molecular Approaches to the Photocatalytic Reduction of Carbon Dioxide for Solar Fuels , 2010 .

[21]  L. Seefeldt,et al.  Is Mo involved in hydride binding by the four-electron reduced (E4) intermediate of the nitrogenase MoFe protein? , 2010, Journal of the American Chemical Society.

[22]  Daniel L DuBois,et al.  Development of molecular electrocatalysts for CO2 reduction and H2 production/oxidation. , 2009, Accounts of chemical research.

[23]  L. Seefeldt,et al.  Mechanism of Mo-dependent nitrogenase. , 2009, Annual review of biochemistry.

[24]  L. Seefeldt,et al.  Climbing nitrogenase: toward a mechanism of enzymatic nitrogen fixation. , 2009, Accounts of chemical research.

[25]  Aaron J. Sathrum,et al.  Electrocatalytic and homogeneous approaches to conversion of CO2 to liquid fuels. , 2009, Chemical Society reviews.

[26]  S. Ragsdale,et al.  Acetogenesis and the Wood-Ljungdahl pathway of CO(2) fixation. , 2008, Biochimica et biophysica acta.

[27]  T. Reda,et al.  Reversible interconversion of carbon dioxide and formate by an electroactive enzyme , 2008, Proceedings of the National Academy of Sciences.

[28]  Anne-Kristin Kaster,et al.  Methanogenic archaea: ecologically relevant differences in energy conservation , 2008, Nature Reviews Microbiology.

[29]  S. Ragsdale Enzymology of the Wood–Ljungdahl Pathway of Acetogenesis , 2008, Annals of the New York Academy of Sciences.

[30]  Hiroyuki Yasuda,et al.  Transformation of carbon dioxide. , 2007, Chemical reviews.

[31]  L. Seefeldt,et al.  Diazene (HN=NH) is a substrate for nitrogenase: insights into the pathway of N2 reduction. , 2007, Biochemistry.

[32]  Tsukasa Matsuo,et al.  From carbon dioxide to methane: homogeneous reduction of carbon dioxide with hydrosilanes catalyzed by zirconium-borane complexes. , 2006, Journal of the American Chemical Society.

[33]  G. Olah Beyond oil and gas: the methanol economy. , 2006, Angewandte Chemie.

[34]  K. Fisher,et al.  Variant MoFe proteins of Azotobacter vinelandii: effects of carbon monoxide on electron paramagnetic resonance spectra generated during enzyme turnover , 2005, JBIC Journal of Biological Inorganic Chemistry.

[35]  L. Seefeldt,et al.  Trapping H- bound to the nitrogenase FeMo-cofactor active site during H2 evolution: characterization by ENDOR spectroscopy. , 2005, Journal of the American Chemical Society.

[36]  L. Seefeldt,et al.  Substrate interactions with the nitrogenase active site. , 2005, Accounts of chemical research.

[37]  Klaus S. Lackner,et al.  A Guide to CO2 Sequestration , 2003, Science.

[38]  K. Lackner,et al.  Climate change. A guide to CO2 sequestration. , 2003, Science.

[39]  P. Ludden,et al.  Carbon monoxide dehydrogenase from Rhodospirillumrubrum produces formate , 2002, JBIC Journal of Biological Inorganic Chemistry.

[40]  B. Dave,et al.  Enzymatic Conversion of Carbon Dioxide to Methanol: Enhanced Methanol Production in Silica Sol−Gel Matrices , 1999 .

[41]  W. Lanzilotta,et al.  Catalytic and biophysical properties of a nitrogenase Apo-MoFe protein produced by a nifB-deletion mutant of Azotobacter vinelandii. , 1998, Biochemistry.

[42]  B. Hoffman,et al.  CO Binding to the FeMo Cofactor of CO-Inhibited Nitrogenase: 13CO and 1H Q-Band ENDOR Investigation , 1997 .

[43]  W. Newton,et al.  Evidence for multiple substrate-reduction sites and distinct inhibitor-binding sites from an altered Azotobacter vinelandii nitrogenase MoFe protein. , 1997, Biochemistry.

[44]  B. Burgess,et al.  Mechanism of Molybdenum Nitrogenase. , 1996, Chemical reviews.

[45]  B. Hoffman,et al.  IDENTIFICATION OF THE CO-BINDING CLUSTER IN NITROGENASE MOFE PROTEIN BY ENDOR OF 57FE ISOTOPOMERS , 1996 .

[46]  V. DeRose,et al.  INVESTIGATION OF CO BOUND TO INHIBITED FORMS OF NITROGENASE MOFE PROTEIN BY 13C ENDOR , 1995 .

[47]  M. Rasche,et al.  Carbonyl sulfide and carbon dioxide as new substrates, and carbon disulfide as a new inhibitor, of nitrogenase. , 1995, Biochemistry.

[48]  W. Song,et al.  A method for preparing analytically pure sodium dithionite. Dithionite quality and observed nitrogenase-specific activities. , 1991, Biochimica et biophysica acta.

[49]  L. Davis,et al.  Iron-sulfur clusters in the molybdenum-iron protein component of nitrogenase. Electron paramagnetic resonance of the carbon monoxide inhibited state. , 1979, Biochemistry.

[50]  R. Burris,et al.  Interactions among substrates and inhibitors of nitrogenase , 1975, Journal of bacteriology.

[51]  R. Burris,et al.  Inhibition of nitrogenase-catalyzed reductions. , 1973, Biochimica et biophysica acta.