The inactivation of rice bran lipase was studied in vitro and in vivo
using metal ions in methanol or HCl. Lipase was extracted from rice br
an in 0.1 m potassium phosphate buffer, pH 7.0 and purified by ammoniu
m sulphate fractionation. The 25-55 % ammonium sulphate fraction was s
ubjected to DEAE-cellulose ion exchange chromatography and the fractio
n (F6) eluted at V(e)/V(o) of 14.37 was purified about 333-fold. In-vi
tro studies on F6 lipase showed that Fe3+ and Ni2+ completely inhibite
d the lipase activity at 5 x 10(-5) m concentration, while Zn2+ and Cu
2+ did so at 2.5 x 10(-4) m. The results on in-vivo inactivation of ri
ce bran lipase showed that Fe3+ and Ni2+ at 200 mug g-1 significantly
checked the release of free fatty acids (FFA) from rice bran for 6 day
s of storage when compared with using concentrated HCl (2 %, v/w) only
. The triglyceride content of oil was also maximum with Fe3+ and Ni2treatment at 200 mug g-1. The present results suggest that Fe3+ and Ni
2+ could be effectively used to arrest the release of FFA in rice bran
and thus contribute to improving the edible quality of rice bran oil.