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    <title>Catalytic Electron Transport in Chromatium Vinosum [NiFe]-Hydrogenase: Application of Voltammetry in Detecting Redox-Active Centers and Establishing That Hydrogen Oxidation Is Very Fast Even at Potentials Close to the Reversible H+/H2 Value</title>
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  <name type="personal">
    <namePart>Pershad, H.R.</namePart>
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  <name type="personal">
    <namePart>Duff, J.L.C.</namePart>
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  <name type="personal">
    <namePart>Heering, H.A.</namePart>
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  <name type="personal">
    <namePart>Duin, E.C.</namePart>
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  <name type="personal">
    <namePart>Albracht, S.P.J.</namePart>
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  <name type="personal">
    <namePart>Armstrong, F.A.</namePart>
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  <abstract>The nickel-iron hydrogenase from Chromatium Vinosum adsorbs at a pyrolytic graphite edgeplane (PGE)electrode and catalyzes rapid interconversion of H+ (aq)and H2 at potentials expected for the half-cell reaction 2H+ a H2, i.e., without the need for overpotentials. The voltammetry mirrors characteristics determined by conventional methods, while affording the capabilities for exquisite control and measurement of potential-dependent activities and substrate-product mass transport. Oxidation of H2 is extremely rapid; at 10</abstract>
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      <title>BioChemistry, 38, p.8992-8999, 1999</title>
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