FEBS Letters · 2001 · 44 citations · 18 references
Life SciencesBiochemistryBioengineeringBiocatalysisRedox BiochemistryStructural BiologyReactive Oxygen SpeciesRedox ChemistryRedox CofactorsRedox EnzymesBinding Pocket EngineeringHydrogen Peroxide TreatmentManganese EnzymesManganese-binding ProteinsPeroxidase CatalysisPeroxidase EnzymesPeroxidase InactivationProtein Conformational Changes
The manganese peroxidase produced by Phanerochaete chrysosporium, which catalyzes the oxidation of Mn(2+) to Mn(3+), is easily inactivated by the hydrogen peroxide (H2O2) presented in the reaction. We attempted to increase H2O2 resistance by the conformational stabilization around the H2O2-binding pocket. Based on its structural model, engineering of oxidizable Met273 located near the pocket to a non-oxidizable Leu showed a great improvement. Furthermore, after treatment at 1 mM H2O2 where the wild-type is completely inactivated, full activity can be retained by engineering the Asn81, which might have conformational changes due to the environment of the pocket, to a non-bulky and non-oxidizable Ser.
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Terrence L. Geiger, Steven Clarke · Journal of Biological Chemistry · 1987 · 1.3K citations · Full text