AI Article Synopsis

  • Microbial degradation is the primary method through which the nematicide oxamyl is broken down in the environment, but knowledge about the specific microorganisms that carry out this process is limited.
  • Researchers isolated four bacterial strains from agricultural soil that effectively degrade oxamyl and identified them as part of the Pseudomonas genus through multilocus sequence analysis (MLSA).
  • These bacteria convert oxamyl into oxamyl oxime, utilize methylamine as a nutrient source, and contain a gene similar to a previously known carbamate-hydrolase gene, indicating their role in oxamyl hydrolysis and the ability to degrade other similar carbamate compounds.

Article Abstract

Microbial degradation is the main process controlling the environmental dissipation of the nematicide oxamyl. Despite that, little is known regarding the microorganisms involved in its biotransformation. We report the isolation of four oxamyl-degrading bacterial strains from an agricultural soil exhibiting enhanced biodegradation of oxamyl. Multilocus sequence analysis (MLSA) assigned the isolated bacteria to different subgroups of the genus Pseudomonas. The isolated bacteria hydrolyzed oxamyl to oxamyl oxime, which was not further transformed, and utilized methylamine as a C and N source. This was further supported by the detection of methylamine dehydrogenase in three of the four isolates. All oxamyl-degrading strains carried a gene highly homologous to a carbamate-hydrolase gene cehA previously identified in carbaryl- and carbofuran-degrading strains. Transcription analysis verified its direct involvement in the hydrolysis of oxamyl. Selected isolates exhibited relaxed degrading specificity and transformed all carbamates tested including the oximino carbamates aldicarb and methomyl (structurally related to oxamyl) and the aryl-methyl carbamates carbofuran and carbaryl which share with oxamyl only the carbamate moiety.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850150PMC
http://dx.doi.org/10.3389/fmicb.2016.00616DOI Listing

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