Polyphenol oxidase from dominga table grape

Dominga grape polyphenol oxidase (PPO) was extracted using phase partitioning with Triton X-114. The enzyme was obtained in latent state and could be optimally activated by the presence of 0.2% sodium dodecyl sulfate (SIDS) at pH 6.0. In the absence of SIDS, the enzyme showed maximum activity at acid pH. The kinetic parameters of the enzyme at pH 3.0 and 6.0 in the presence of SDS were calculated. The effect of several inhibitors was studied, tropolone being the most effective with a Ki value of 18 mu M. The effect of cyclodextrins was also studied, and the complexation constant K-c between G(2)-beta-cyclodextrins and 4-tert-butylcatechol was calculated using the enzymatic method (Kc = 13960 M-1). The evolution of the color parameters (L*, a*, b*) of liquefied grape berries was inhibited by inhibitors of PPO activity, such as diethyldithiocarbamate, metabisulfite, and G(2)-beta-cyclodextrins, indicating that enzymatic browning by PPO is the main process involved in the browning of Dominga grape juice at room temperature.