Enzymatic reaction of pentachlorophenol (PCP) catalyzed by horseradish
peroxidase (HRP) was investigated under the influence of humic precur
sors. Six phenolic acids were used as the humic precursors. Three of t
hem were substituted p-hydroxy cinnamic acids and others were substitu
ted p-hydroxy benzoic acids. When PCP was incubated alone, about 40% o
f PCP was enzymatically transformed by HRP and 4% of that was converte
d to octachlorodibenzo-p-dioxin (OCDD). The presence of phenolic acids
containing no methoxyl groups, ie., p-coumaric acid and p-hydroxybenz
oic acid, accelerated the PCP transformation significantly and lessene
d production of OCDD. In the presence of p-coumaric acid, more than 90
% of PCP was removed in the first 15 min and no OCDD was detected in a
ddition to almost no other products. The color of the solution mixture
turned slightly yellow and no precipitates were observed. The solutio
n with p-hydroxy benzoic acid showed similar results. Ferulic acid kep
t PCP decreasing more than 20 minutes that caused the final degradatio
n rate to be larger and also lessened the amount of products. Vanillic
acid however did not seem to affect the transformation of PCP to any
great extent. Phenolic acids with two methoxyl groups interfered with
PCP degradation for the first 15 min of incubation. Thus the number of
methoxyl groups adjacent to the hydroxyl group is very important in e
valuating the effects of phenolic acids to the enzymatic reaction of P
CP. (C) 1997 Elsevier Science Ltd.