A phenol oxidase (E.C. 1.10.3.1) preparation from adult female Trichur
is suis was assayed by both polarographic and spectrophotometric techn
iques. The T. suis enzyme oxidized most diphenols including 4-methylca
techol (4MC) and dihydroxyphenylalanine but did not oxidize tyrosine.
The pH and temperature optima were 6.8 and 36 C, respectively. The K-m
measured using 4MC as a substrate ranged from 0.12 to 0.4 mM. The hig
hest phenol oxidase activity was isolated in fractions from the adult
females that were enriched in eggs relative to the activity in somatic
tissue from females and all male tissues that were assayed. Phenol ox
idase activity was localized on sodium dodecyl sulfate-polyacrylamide
gel electrophoresis substrate gels into 2 bands with M(r)'s of 44,000
and 53,000. An antibody to the 44,000 band recognized 2 bands of 40,00
0 and 45,000 M(r) on western blot analysis of the enzyme preparation.
Immunocytochemical localization of anti-phenol oxidase antibody in ser
ial cross sections of adult female worms indicates that the enzyme is
found exclusively in the anterior part of the parasite in the proximal
part of the uterus that is posterior to the junction with the stichos
ome. Eggs located in more distal parts of the reproductive system did
not react with the antibody. The results indicate that a phenol oxidas
e is located in the fertilized eggs of adult female T. suis. It is lik
ely that phenol oxidase contributes significantly to the chemical hard
ening process in the eggs when they pass out into the external environ
ment. Inhibition of phenol oxidase may reduce the survivability of the
eggs and thus minimize contamination of livestock facilities.