On the relationship between affinity for molecular hydrogen and the physiological directionality of hydrogenases
Daan J. van Haaster, Peter‐Leon Hagedoorn, J. A. Jongejan, Wilfred R. Hagen
Abstract
Daan J. van Haaster, Peter‐Leon Hagedoorn, J. A. Jongejan, Wilfred R. Hagen
Abstract
The physiological significance of the generic reaction H(2)<-->2[H] is not always clear because hydrogenases may function in the breakdown of molecular hydrogen or in its synthesis or in both directions. Fe-hydrogenases have nevertheless been most often associated with proton reduction and NiFe-hydrogenases with hydrogen oxidation. A re-determination of the K(M) of H(2) oxidation by Pyrococcus furiosus NiFe-hydrogenase-I and by Desulfovibrio vulgaris Fe-hydrogenase suggests that affinity for hydrogen has been seriously underestimated and that the kinetics of hydrogen activation in relation to the directionality of hydrogenases should be re-evaluated.
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The physiological significance of the generic reaction H(2)<-->2[H] is not always clear because hydrogenases may function in the breakdown of molecular hydrogen or in its synthesis or in both directions. Fe-hydrogenases have nevertheless been most often associated with proton reduction and NiFe-hydrogenases with hydrogen oxidation. A re-determination of the K(M) of H(2) oxidation by Pyrococcus furiosus NiFe-hydrogenase-I and by Desulfovibrio vulgaris Fe-hydrogenase suggests that affinity for hydrogen has been seriously underestimated and that the kinetics of hydrogen activation in relation to the directionality of hydrogenases should be re-evaluated.
Key concepts: Hydrogenase, Pyrococcus furiosus, Desulfovibrio vulgaris, Hydrogen, Chemistry, Kinetics, Hydrogen molecule, Desulfovibrio