Complete biodegradation of fungicide carboxin and its metabolite aniline by Delftia sp. HFL-1.

Fungicide carboxin was commonly used in the form of seed coating for the prevention of smut, wheat rust and cotton damping-off, leading carboxin and its probable carcinogenic metabolite aniline to directly enter the soil with the seeds, causing residual pollution. In this study, a novel carboxin degrading strain, Delftia sp. HFL-1, was isolated. Strain HFL-1 could use carboxin as the carbon source for growth and completely degrade 50 mg/L carboxin and its metabolite aniline within 24 h. The optimal temperatures and pH for carboxin degrading by strain HFL-1 were 30 to 42 °C and 5 to 9, respectively. Furthermore, the complete mineralization pathway of carboxin by strain HFL-1 was revealed by High Resolution Mass Spectrometer (HRMS). Carboxin was firstly hydrolyzed into aniline and further metabolized into catechol through multiple oxidation processes, and finally converted into 4-hydroxy-2-oxopentanoate, a precursor of the tricarboxylic acid cycle. Genome sequencing revealed the corresponding degradation genes and cluster of carboxin. Among them, amidohydrolase and dioxygenase were key enzymes involved in the degradation of carboxin and aniline. The discovery of transposons indicated that the aniline degradation gene cluster in strain HFL-1 was obtained via horizontal transfer. Furthermore, the degradation genes were cloned and overexpressed. The in vitro test showed that the expressed degrading enzyme could efficiently degrade aniline. This study provides an efficient strain resource for the bioremediation of carboxin and aniline in contaminated soil, and further revealing the molecular mechanism of biodegradation of carboxin and aniline.

In situ monitoring of chlorothalonil and lambda-cyhalothrin by polyethylene passive samplers under fields and greenhouse conditions.

Sampling is a critical step in pesticide atmospheric analysis. Passive sampling offers advantages of inexpensive and convenient air monitoring. Polyethylene films (PE) were used as a passive sampler at multiple heights in greenhouse and agricultural field for 15 days to trap atmospheric chlorothalonil and lambda-cyhalothrin in the months of May and July. Among the two PE film thicknesses (20 and 80 µm), 20 µm PE was the most effective at absorbing target pesticides from air and attains equilibrium stage earlier than 80 µm PE film. After approximately 240 h of PE exposure in greenhouse and fields, chlorothalonil and lambda-cyhalothrin reached an equilibrium stage of partitioning between air and PE. Atmospheric concentrations of chlorothalonil (p < 0.01) and lambda-cyhalothrin (p < 0.001) at 1.5 m height were higher with the concentrations of 1855.59 ± 243.85 ng/m3 and 3682.11 ± 316.71 ng/m3, respectively, in the month of May as compared to the other three respective heights. The concentrations of chlorothalonil in air at 2 m height (1587.27 ± 284.19 ng/m3) were slightly higher than 0.5 m (1392.28 ± 205.09 ng/m3). Atmospheric concentrations of lambda-cyhalothrin at 2 m (3178.26 ± 299.29 ng/m3) were significantly lower than the other heights (p < 0.05). The greenhouse air concentrations of chlorothalonil and lambda-cyhalothrin in the months of May (1855.59 ± 243.85 and 3682.11 ± 316.71 ng/m3, respectively) and July (1749.33 ± 378.61 and 3445.08 ± 390.32 ng/m3, respectively) were higher than fields. The results indicate the usability of PE films to monitor chlorothalonil and lambda-cyhalothrin and potential other semi-volatile pesticides in agricultural fields.