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SUMMARY:From Nitrogen Fixation to Carbon Valorization: Engineering Nitroge
 nases for New Chemistry - CH-636
DTSTART:20261208T161500
DTEND:20261208T171500
DTSTAMP:20261109T180215Z
UID:9d191fca8fc3355e5744cd66ee6e27e0d95b59aa277ff58872684b63
CATEGORIES:Conferences - Seminars
DESCRIPTION:Prof. Johannes Rebelein (University Düsseldorf & Forschungsze
 ntrum Jülich)\nSpeaker: Prof. Dr. Johannes Rebelein (University Düsseld
 orf & Forschungszentrum Jülich)\n\nAbstract: Nitrogenases are the only k
 nown enzymes that catalyze the reduction of molecular nitrogen (N2) to amm
 onia (NH3)\, and with this driving the global nitrogen cycle. Besides the 
 conversion of N2\, we showed that nitrogenases convert carbon dioxide (CO2
 ) to carbon monoxide\, formate and hydrocarbons (1-3)\, suggesting new pat
 hways for CO2 activation and the formation of value-added products.\nThe m
 echanistic basis and structural determinants for these activities\, substr
 ate specificity and product profiles remain poorly understood. We demonstr
 ated that the iron (Fe)-nitrogenase reduces CO₂ nearly threefold more ef
 ficiently than the canonical molybdenum (Mo) nitrogenase (2). This catalyt
 ic preference is conserved in vivo\, where Rhodobacter capsulatus strains 
 expressing the Fe-nitrogenase physiologically convert CO₂ to formate and
  methane. Leveraging high-resolution cryo-EM (3-5)\, we map structural fea
 tures governing substrate channeling and catalysis of nitrogenase(-like) e
 nzymes\, to obtain a better understanding of the structure-function relati
 onship (Figure 1\, 3-6). Why do the different nitrogenase isoforms\, the m
 olybdenum (Mo)\, the vanadium (V) and the iron (Fe) nitrogenase have diffe
 rent activities and specificities for the reduction of N2\, CO and CO2? Ev
 en more surprising is that the nitrogenase-like methylthio-alkane reductas
 e cleaves carbon-sulfur bonds in vivo and is unable to activate N2 althoug
 h it harbors a nitrogenase P- and L-cluster (5). \nGuided by these insigh
 ts\, we engineered nitrogenase variants that shift the product profile tow
 ard hydrocarbons and significantly enhance CO₂ reduction selectivity in 
 the presence of N₂ (3). These findings redefine nitrogenase substrate pr
 omiscuity\, provide a mechanistic blueprint for engineering CO₂-reducing
  biocatalysts\, and establish Fe-nitrogenase as a promising platform for s
 ustainable carbon valorization.\n \n\n© 2026 EPFL\n\n\nFigure 1. A schem
 atic overview of FeMoco maturase\, Mo-nitrogenase and methylthio-alkane re
 ductase with their contained metalloclusters responsible for electron tran
 sfer and catalysis. The catalyzed main reactions are shown below.\n\nRefer
 ences :\n\n\n	N. N. Oehlmann\, J. G. Rebelein\, ChemBioChem 23\, e20210045
 3 (2022).\n	N. N. Oehlmann et al.\, Sci. Adv. 10\, eado7729 (2024).\n	N. N
 . Oehlmann et al.\, bioRxiv. doi:10.64898/2026.07.08.737278 (2026).\n	F. V
 . Schmidt et al.\, Nat. Struct. Mol. Biol. 31\, 150-158 (2024).\n	Lago-Mac
 iel et al.\, Nat. Catal. 8\, 1086-1099 (2025).\n	Lago-Maciel et al.\, Tren
 ds Biochem. Sci. 51\, 187-202 (2026).\n\n\nBiography: Prof. Dr. Johannes 
 Rebelein is Professor of Sustainable Biotechnology at Heinrich Heine Unive
 rsity Düsseldorf and Director of the Institute for Molecular Enzyme Techn
 ology (IMET) at Forschungszentrum Jülich. His research focuses on metallo
 enzyme biochemistry and catalysis\, particularly nitrogenase and nitrogena
 se-like enzymes. Combining biochemical\, structural\, synthetic microbiolo
 gy and enzyme-engineering approaches\, his group investigates how complex 
 metallocofactors convert small molecules\, including nitrogen and carbon d
 ioxide\, and how these principles can be harnessed to develop sustainable 
 biotechnological solutions for greenhouse-gas valorization and artificial 
 metalloenzyme design.\nBefore his appointment in Düsseldorf/Jülich\, Reb
 elein led an Emmy Noether Research Group at the Max Planck Institute for T
 errestrial Microbiology in Marburg and was a Junior Group Leader at the LO
 EWE Center for Synthetic Microbiology at Philipps-University Marburg. He c
 ompleted postdoctoral training with Prof. Thomas Ward at the University of
  Basel and earned his Ph.D. in Biological Sciences at the University of Ca
 lifornia\, Irvine\, under Prof. Markus W. Ribbe. He holds B.Sc. and M.Sc. 
 degrees in Biotechnology\, with honors\, from TU Braunschweig. Prof. Rebel
 ein’s contributions to the field have been recognized with several prest
 igious honors\, including the European Molecular Biology Organization (EMB
 O) Young Investigator Award and the VAAM (Association for General and Appl
 ied Microbiology) Research Award.\n 
LOCATION:CE 1 105 https://plan.epfl.ch/?room==CE%201%20105
STATUS:CONFIRMED
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