Although there are many studies about the inhibition of organophosphours pesticides(OPs) against plant-esterase,most of which emphase on the effect of reaction time,temperature and PH,the toxicity of pesticides against plant-esterase with respect to enantioselectivity has so far received limited attention. In this study,the kinetic constants of plant-esterase inhibited by the racemate and enantiomers of malaoxon,isomalathion,and methamidophos were investigated. The inhibition on plant-esterase tested with optically pure stereoisomers of malaoxon,isomalathion and methamidophos showed its stereoselectivity. As for malaoxon,and isomalathion,R-configure were more toxic than the S-configure enantiomers to test esterase. In contrast,the S-methamidophos was a stronger inhibitor to test esterase. These results suggest that the biotoxicity of chiral OPs to nontargeted organisms is enantioselective and therefore should be reevaluated with their pure enantiomers.
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