4.7 Article

Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep

Journal

MICROBIAL CELL FACTORIES
Volume 19, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12934-020-1276-9

Keywords

Comamonas sp; SWP-3; Alicycliphilus sp; PH-34; Consortium; Swep; 3; 4-Dichloroaniline; Degradation

Funding

  1. National Natural Science Foundation of China [31670111, 31870087, 31900077]
  2. National Key R&D Program of China [2018YFA0901200]
  3. China Postdoctoral Science Foundation [2018M630566]

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Background Swep is an excellent carbamate herbicide that kills weeds by interfering with metabolic processes and inhibiting cell division at the growth point. Due to the large amount of use, swep residues in soil and water not only cause environmental pollution but also accumulate through the food chain, ultimately pose a threat to human health. This herbicide is degraded in soil mainly by microbial activity, but no studies on the biotransformation of swep have been reported. Results In this study, a consortium consisting of two bacterial strains, Comamonas sp. SWP-3 and Alicycliphilus sp. PH-34, was enriched from a contaminated soil sample and shown to be capable of mineralizing swep. Swep was first transformed by Comamonas sp. SWP-3 to the intermediate 3,4-dichloroaniline (3,4-DCA), after which 3,4-DCA was mineralized by Alicycliphilus sp. PH-34. An amidase gene, designated as ppa, responsible for the transformation of swep into 3,4-DCA was cloned from strain SWP-3. The expressed Ppa protein efficiently hydrolyzed swep and a number of other structural analogues, such as propanil, chlorpropham and propham. Ppa shared less than 50% identity with previously reported arylamidases and displayed maximal activity at 30 degrees C and pH 8.6. Gly449 and Val266 were confirmed by sequential error prone PCR to be the key catalytic sites for Ppa in the conversion of swep. Conclusions These results provide additional microbial resources for the potential remediation of swep-contaminated sites and add new insights into the catalytic mechanism of amidase in the hydrolysis of swep.

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