1990
DOI: 10.1584/jpestics.15.593
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Enzymological Properties of Three Soil Hydrolases and Effects of Several Pesticides on Their Activities

Abstract: Effects of pesticides on the activities of acid phosphatase, arylesterase and aryl acylamidase in soil were examined under upland field and/or laboratory conditions. We established methods to assay the activities of arylesterase and aryl acylamidase, while a known method was applied for acid phosphatase. Fenitrothion EC, chlorothalonil WP and paraquat SL were the main pesticides used and trichlorfon was additional for laboratory tests. Effects of the pesticides on the activities of acid phosphatase and arylest… Show more

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Cited by 13 publications
(5 citation statements)
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“…The H 2 O‐soluble and NH 4 NO 3 ‐exchangeable fractions are among the more soluble TE fractions in soils and, therefore, simulate those more likely to interact with microrganisms and enzyme molecules in soil. However, while inhibitory effects of organic pollutants on soil arylesterase activity have been characterized (Nakamura et al , 1990; Moon & Smith, 2005), information on inhibitory effects of TE on soil arylesterase activity is scarce. Arylesterase activity cleaves carboxyl groups adjacent to ester bonds and, differently from other hydrolase activities for which metal ions can be important functional cofactors (Coleman, 1992; Bouma et al , 1997; Holm & Sander, 1997), to our knowledge hydrolysis of p‐nitrophenyl acetate by this enzyme activity does not require metal ions (Kaiser et al , 2006; Torres et al , 2009), and variable effects of various TE on arylesterase from in vitro studies have been reported (Kaiser et al , 2006; Fahmy et al , 2008; Torres et al , 2009).…”
Section: Discussionmentioning
confidence: 99%
“…The H 2 O‐soluble and NH 4 NO 3 ‐exchangeable fractions are among the more soluble TE fractions in soils and, therefore, simulate those more likely to interact with microrganisms and enzyme molecules in soil. However, while inhibitory effects of organic pollutants on soil arylesterase activity have been characterized (Nakamura et al , 1990; Moon & Smith, 2005), information on inhibitory effects of TE on soil arylesterase activity is scarce. Arylesterase activity cleaves carboxyl groups adjacent to ester bonds and, differently from other hydrolase activities for which metal ions can be important functional cofactors (Coleman, 1992; Bouma et al , 1997; Holm & Sander, 1997), to our knowledge hydrolysis of p‐nitrophenyl acetate by this enzyme activity does not require metal ions (Kaiser et al , 2006; Torres et al , 2009), and variable effects of various TE on arylesterase from in vitro studies have been reported (Kaiser et al , 2006; Fahmy et al , 2008; Torres et al , 2009).…”
Section: Discussionmentioning
confidence: 99%
“…Aqueous layer (0.5ml) was taken to which 0.5ml (1M) sodium hydroxide and 4 ml double distilled water were added. Reading was taken at 400nm and enzyme activity was expressed as μg pNP released g -1 dry soil h -1 [ 33 ] .…”
Section: Methodsmentioning
confidence: 99%
“…0.5 ml of aqueous layer was taken; 0.5 ml NaOH and ddw (4 ml) were added. Absorbance was taken at 400 nm [ 34 ].…”
Section: Methodsmentioning
confidence: 99%