الخلاصة:
I 
 
 
 
 
 
 
Mots clés: dattes de Phoenix dactylifera L., brunissement enzymatique, polyphénol oxydase, peroxydase, inhibition, pyrocatéchol, gaïacol. 
 
Enzymatic browning control was essential to maintaining the commercial quality of food products and meeting consumer needs. Therefore, the 
production of dates must take into account their post-harvest conservation to maintain their freshness and prevent their degradation and alteration. 
This study is consecrated to the research for inhibitors of natural origin of the two enzymes: peroxidase and polyphenol oxidase extracted from 
the dates of Phoenix dactylifera L., of three varieties (Deglet Nour, Ghars and Adala) harvested from the Metlili – Ghardaïa region; as an assay to help 
alleviate some of the problems of dates enzymatic browning. 
First, enzymatic extraction was carried out using two methods, distilled water and theTamopn -PVP. Thus, the raw extracts were tested directly 
for  their  enzymatic  activity,  using  gaïacol  and  pyrocatechol  as  substrates  for  both  POD  and  PPO  enzymes  respectively.  The  results  obtained  showed 
positive activity and the Tampon PVP extracts showed better rates of enzymatic activity compared to the Water extracts. Also, the influence of substrate 
concentration on the enzymatic activity of the POD and PPO shows a classic Michaelian response with variable values of Vmax and Km. 
The evaluation of the anti-peroxidase activity indicates that the different extracts studied are able to inhibit the POD, while no effect is noted 
with  the  variety  Deglet  Nour.  However,  the  same  extracts  showed  no  inhibitory  efficacy  against  PPO.  Also,  the  inhibition  of PPO  was  tested  with the 
ascorbic acid, the results show that ascorbic acid caused a significant decrease in the activity of PPO with percentages of inhibition of up to 53.09% for 
TPS-PVP  enzymatic  extract  of  the  Adala  variety. A mixed  non-competitive  and an  uncompetitive  inhibition  type  was  obtained  with  the  extracts  at  the 
more potent inhibition rate.