No abstract

An efficient and modified Quick Easy Cheap Effective Rugged and Safe (QuEChERS) method combined with liquid chromatography-electrospray ionization with tandem mass spectrometric detection were evaluated for the analysis of residues of 72 pesticides in brown rice including acidic sulfonylurea herbicides. For extraction of pesticides and clean-up of the extract, 1% formic acid in acetonitrile and dispersive solid phase extraction were used, respectively. Two fortified spikes at 50 and 200 µg L -1 levels were performed for recovery test. Mean recoveries of majority of pesticides at two spike levels ranged from 90 to 110% with standard error (Coefficient of Variation) less than 10%. The limits of detection and quantification ranged from 0.24 to 19.92 µg L -1 and 0.79 to 65.74 µg L -1 , respectively. Good linearity of calibration curves were achieved with R 2 > 0.9943 within the observed concentration range (from 20 to 400 µg L -1 ). The modified method also provided satisfactory results for sulfonylurea herbicides, which could not be determined properly with previously reported methods. This method was applied to determine residues of target pesticides in real samples. A total of 22 pesticides in 31 out of 40 tested samples were observed. The highest concentration was observed for tricyclazole at 1.17 mg L -1 . This pesticide found in two brown rice samples exceeded its MRL regulated for rice in Republic of Korea. Except this pesticide, concentrations of all observed pesticides were lower than their MRLs. The results reveal that the method is applicable for routine analysis of residues of target pesticides in brown rice.

For bioremediation of toxic endosulfan, endosulfan degradation bacteria, which do not form toxic endosulfan sulfate, were isolated from various soil samples using endosulfan as sole carbon and energy source. Among the 40 isolated bacteria, strain KE-1, which was identified as Klebsiella pneumoniae by physiological and 16S rDNA sequence analysis, showed superior endosulfan degradation activity. Analysis of culture pH, growth, free sulfate and endosulfan and its metabolites demonstrated that KE-1 biologically degrades 8.72 microg endosulfan ml(-1) day(-1) when incubated with 93.9 microg ml(-1) endosulfan for 10 days without formation of toxic endosulfan sulfate. Our results suggest that K. pneumoniae KE-1 degraded endosulfan by a non-oxidative pathway and that strain KE-1 has potential as a biocatalyst for endosulfan bioremediation.