Abstract

Lipoxygenase from Khao Dawk Mali 105 aromatic brown rice was isolated by extracting brown rice liquid nitrogen powder using 0.2 M phosphate buffer pH 7, fractionating with 30–60% (NH4)2SO4, dialyzing and gel filtration on Sephadex G-200. The optimum pHs for dialyzed lipoxygenase activity were around 7.5 and 9.5. The enzyme appeared to be completely inactivated after heating 30 min at 70°C, 20 min at 80°C and 10 min at 90°C. The enzyme could be inhibited by MgCl2, ZnCl2, KCl, BHA, vitamin E, vitamin C, and BHT; however, CaCl2 acted as the enzyme activator.

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