OXIDATION OF FLAVONOLS AND FLAVONOL GLYCOSIDES BY A HYPODERMAL PEROXIDASE ISOENZYME FROM GAMAY ROUGE GRAPE (VITIS-VINIFERA) BERRIES

The ability of the grapevine hypodermal peroxidase isoenzyme B-5 to ox idise the flavonols, quercetin and myricetin, and the flavonol glycosi des quercetin-3-arabinoside, quercetin-3-rhamnoside (quercitrin) and m yricetin-3-rhamnoside (myricitrin), has been studied. The results show ed that, whilst the aglycones were good substrates of this peroxidase isoenzyme, their corresponding glycosides were poorly oxidised under t he assay conditions. The oxidation of quercetin and myricetin catalyse d by the hypodermal peroxidase isoenzyme B-5 was strictly dependent on hydrogen peroxide (H2O2). The kinetic characteristics of the flavonol oxidation were also studied. Whilst the apparent K(m) values for quer cetin and myricetin were roughly equal (38 and 54 mum, respectively), the apparent K(m) values for H2O2 in each reaction were appreciably di fferent (168 and 8 mum, respectively). Besides, the optimal pH for que rcetin oxidation was 4.0 whereas for myricetin it was 6.0-7.0. The res ults are discussed in view of the possible involvement of the vacuolar hypodermal B-5 isoperoxidase in the turnover of flavonol and flavonol glycosides in grapes.