Publication | Open Access
Functional Synthetic Model for the Lanthanide-Dependent Quinoid Alcohol Dehydrogenase Active Site
61
Citations
36
References
2017
Year
Bioorganic ChemistryEngineeringAldo-keto ReductaseMethanolMolecular BiologyFunctional Synthetic ModelOrganic ChemistryChemistryChemical BiologyRedox BiologyXoxf DehydrogenaseStructure-function Enzyme KineticsAlcohol DehydrogenasesAldehyde DehydrogenaseBiochemistryActive SiteCatalysisHydrogenDehydrogenase EnzymesNatural SciencesEnzyme CatalysisDeoxygenationCarbonyl Metabolism
The oxidation of methanol by dehydrogenase enzymes is an essential part of the bacterial methane metabolism cycle. The recent discovery of a lanthanide (Ln) cation in the active site of the XoxF dehydrogenase represents the only example of a rare-earth element in a physiological role. Herein, we report the first synthetic, functional model of Ln-dependent dehydrogenase and its stoichiometric and catalytic dehydrogenation of a benzyl alcohol. Density functional theory calculations implicate a hydride transfer mechanism for these reactions.
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