J. Nishiyama et al., INHIBITION OF SOYBEAN LIPOXYGENASE-1 BY SUCROSE ESTERS OF FATTY-ACIDS, Bioscience, biotechnology, and biochemistry, 57(4), 1993, pp. 557-560
The effect of sucrose esters of fatty acids with carbon numbers from 8
to 16 on soybean lipoxygenase-1 (L-1) was investigated. The sucrose e
sters inhibited L-1 and the inhibitory effect increased with an increa
se in the carbon number of the fatty acid up to 12, being constant abo
ve 12. Kinetic studies showed that two molecules of the sucrose ester
hound to L-1 and inhibited it competitively. Based on the behavior of
pK(i) dependence on the carbon chain length of the sucrose esters, the
dodecyl group appeared to be optimum to bind L-1. The results suggest
that sucrose esters bind to the catalytic site of L-1 by hydrophobic
interaction of the fatty acid and lead to the loss of activity. Sucros
e esters, which are widely used as an emulsifier, can be an effective
inhibitor of enzymatic lipid peroxidation in food processing.