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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Terminal hydride formation in [FeFe] hydrogenase: understanding the role of the dithiolate bridgehead
Anjali Depala1, Manon T Lachmann2, Simone Morra3
1Department of Chemistry, University of Oxford, Inorganic Chemistry laboratory, South Parks Road, Oxford, OX1 3QR, UK.
Abstract:
[FeFe]-hydrogenases are highly-active hydrogen-conversion biocatalysts using Earth-abundant metals in their active-site. Understanding their mechanism may enable design of catalysts for renewable energy storage. Here, observation of the crucial Fe-hydride-containing (Hhyd) intermediate in a PDT-variant of [FeFe]-hydrogenase reveals deeper insight into the role of the dithiolate bridgehead in the catalytic mechanism.
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