Biomass of the fungus Fusarium proliferatum was produced and used to o
btain a crude extract (FI) of lipoxygenase. The enzyme was further pur
ified by ammonium sulfate precipitation at 40% of saturation (FII). Th
e enzymatic extract (FII) showed its optimum activity at pH 6.0. The a
pparent K-m and V-max values for the lipoxygenase (FII) were calculate
d to be 5.15 x 10(-5) M and 1.61 mu mol hydroperoxide/mg protein/min,
respectively. Enzyme activity remained relatively stable at potassium
cyanide concentrations as high as 60 mM. The presence of 5 mM ethylene
diaminetetraacetate activated the enzyme by 50%, whereas the use of 1.
2 mM hydroquinone resulted in a 2-fold increase in lipoxygenase activi
ty. The partially purified enzyme (FII) showed a three-fold enhancemen
t of activity towards linoleic acid compared to linolenic acid as well
as mono-, di- and trilinolein.