4.7 Article

Identification of sulfonylurea biodegradation pathways enabled by a novel nicosulfuron-transforming strain Pseudomonas fluorescens SG-1: Toxicity assessment and effect of formulation

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 324, Issue -, Pages 184-193

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2016.10.048

Keywords

Nicosulfuron; Metsulfuron-methyl; Tribenuron-methyl; Metabolite; Microtox (R)

Funding

  1. Region Auvergne
  2. French Ministry for Higher Education and Research
  3. European Regional Development Fund

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Nicosulfuron is a selective herbicide belonging to the sulfonylurea family, commonly used on maize culture. A bacterial strain SG-1 was isolated from an agricultural soil previously treated with nicosulfuron. This strain was identified as Pseudomonas fluorescens and is able to quantitatively dissipate 77.5% of nicosulfuron (1 mM) at 28 degrees C in the presence of glucose within the first day of incubation. Four metabolites were identified among which ASDM (2-(aminosulfony1)-N,N-dirnethyl-3-pyridinecarboxamide) and ADMP (2-amino-4,6-dimethoxypyrimidine) in substantial proportions, corresponding to the hydrolytic sulfonylurea cleavage. Two-phase dissipation kinetics of nicosulfuron by SG-1 were observed at the highest concentrations tested (0.5 and 1 mM) due to biosorption. The extend and rate of formulated nicosulfuron transformation were considerably reduced compared to those with the pure active ingredient (appearance of a lag phase, 30% dissipation after 10 days of incubation instead of 100% with the pure herbicide) but the same metabolites were observed. The toxicity of metabolites (standardized Microtox test) showed a 20-fold higher toxicity of ADMP than nicosulfuron. P. fluorescens strain SG-1' was also able to biotransform two other sulfonylureas (metsulfuron-methyl and tribenuron-methyl) with various novel pathways. These results provide new tools for a comprehensive picture of the sulfonylurea environmental fate and toxicity of nicosulfuron in the environment. (C) 2016 Elsevier B.V. All rights reserved.

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