Kinetic efficiency of mutant carboxylesterases implicated in organophosphate insecticide resistance

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• 作者：Devonshire ; A.L. ; Heidari ; R. ; Bell ; K.L. ; Campbell ; P.M. ; Campbell ; B.E. ; Odgers ; W.A. ; Oakeshott ; J.G. ; et. al.
• 关键词：Kinetics ; Malathion carboxylesterase ; Organophosphorus hydrolase ; Insecticide resistance
• 刊名：Pesticide Biochemistry and Physiology
• 出版年：2003
• 出版时间：May, 2003
• 年：2003
• 卷：76
• 期：1
• 页码：1-13
• 全文大小：203 K

文摘

Resistance to organophosphorus (OP) insecticides in Lucilia cuprina arises from two mutations in carboxylesterase E3 that enable it to hydrolyse the phosphate ester of various organophosphates, plus the carboxlyester in the leaving group in the case of malathion. These mutations are not found naturally in the orthologous EST23 enzyme in Drosophila melanogaster. We have introduced the two mutations (G137D and W251L) into cloned genes encoding E3 and EST23 from susceptible L. cuprina and D. melanogaster and expressed them in vitro with the baculovirus system. The ability of the resultant enzymes to hydrolyse the phosphate ester of diethyl and dimethyl organophosphates was studied by a novel fluorometric assay, which also provided a sensitive titration technique for the molar amount of esterase regardless of its ability to hydrolyse the fluorogenic substrate used. Malathion carboxylesterase activity was also measured. The G137D mutation markedly enhanced (>30-fold) hydrolysis of both classes of phosphate ester by E3 but only had a similar effect on the hydrolysis of dimethyl organophosphate in EST23. Introduction of the W251L mutation into either gene enhanced dimethyl (23–30-fold) more than diethyl (6–10-fold) organophosphate hydrolysis and slightly improved (2–4-fold) malathion carboxylesterase activity, but only at high substrate concentration.