Journal of Agricultural and Food Chemistry · 2006 · 11 citations · 31 references
AgricultureBiochemistryEgg ScienceEnzymology Of FoodsFood ChemistryEnzyme KineticsOxidative Enzymes In FoodsAmmonium Sulfate FractionationAmmonium Sulfate PrecipitationCysteine-targeted InhibitorsDesign MethodologyExperimental MethodologyMulti-level Experimental UnitsNoncompetitive InhibitionPolyphenol Oxidase Activity
Polyphenol oxidase (PPO) from eggplant was extracted and partially purified by a two-step fractionation-precipitation using ammonium sulfate and phenylsepharose hydrophobic interaction chromatography. The eggplant PPO extract was characterized concerning its kinetic properties. Optimal conditions to obtain Maillard reaction products (MRPs) with a maximal inhibitory potency (IP) toward PPO activity were determined using the surface response methodology and a four-factor and five-level experimental design. The MRPs were prepared from cysteine (0.25 M) and glucose (0-1 M), at several initial pH values (2-6) and at differing heating times (3-19 h) and temperatures (95-115 degrees C). The maximal IP was obtained after heating a model system of glucose/cysteine (1/0.25 M) at pH 2 for 3 h 20 min at 115 degrees C. The soluble part of this MRP, called MRP(IPmax), was a noncompetitive inhibitor toward eggplant PPO. The IP of MRP(IPmax) on PPO activity was very potent as compared to that displayed by benzoic, p-coumaric, and t-cinnamic acids, as well as sorbic acid and 4-hexylresorcinol. The activity of preincubated PPO at 0 degrees C with MRP(IPmax) was only slightly restored after dialysis or gel filtration.
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George L. Ellman · Archives of Biochemistry and Biophysics · 1959 · 26.2K citations
Plant phenolic compounds and the isolation of plant enzymes
W.David Loomis, J. Battaile · Phytochemistry · 1966 · 841 citations