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Isolation and characterization of a 'quinone-trapping' substance from a crude Carica papaya protein preparation
Authors:Florence Richard-Forget  Muriel Cerny  Nina Fayad  Thierry Saunier  & Patrick Varoquaux
Affiliation:1 INRA, Station de Technologie, Domaine St Paul, Site Agroparc, F-84914 AVIGNON cedex, France; CNAM, Chaire de Biochimie Industrielle et Agro-Alimentaire, 292 Rue Saint Martin, 75141 Paris Cedex 03, France
Abstract:The oxidation of different phenols 4-methylcatechol, chlorogenic acid, (?)-epicatechin and (+)-catechin] by endive polyphenoloxidase (PPO) was investigated in the presence of an extract from Carica papaya . The occurrence of cysteine and another 'quinone-trapping' substance in the extract was demonstrated. The unknown substance was purified, as a 4-methylcatechol conjugate form, by a combination of Bio-gel Pz chromatography and semipreparative high-performance liquid chromatography (HPLC). Use of liquid chromatography/tandem mass spectroscopy (LC–MS/MS) equipment and an amino acid analyser allowed us to identify this agent as a dipeptide cysteine-glutamic acid, commercially available as γ-Glu-Cys. γ-Glu-Cys formed one adduct compound with 4-methylcatechol and chlorogenic acid, and two with the flavan-3-ols. The thiol adducts were not substrates for endive PPO but, in the case of the 4-methylcatechol conjugate, they acted as competitive PPO inhibitors.
Keywords:Enzymatic browning  inhibition  papain  polyphenoloxidase  thiol compounds
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