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Plasmid‐mediated dimethoate degradation in Pseudomonas aeruginosa MCMB‐427
Author(s) -
Deshpande N.M.,
Dhakephalkar P.K.,
Kanekar P.P.
Publication year - 2001
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1046/j.1472-765x.2001.00995.x
Subject(s) - dimethoate , plasmid , pseudomonas aeruginosa , biology , microbiology and biotechnology , ethidium bromide , escherichia coli , dna , bacteria , genetics , gene , pesticide , agronomy
Aims: To investigate the genetics of dimethoate degradation in Pseudomonas aeruginosa MCMB‐427. Methods and Results: Pseudomonas aeruginosa MCMB‐427 demonstrated the ability to degrade dimethoate, a synthetic organophosphate insecticide. Total DNA preparation of MCMB‐427 revealed the presence of a 6·6 kbp plasmid (designated as pDMD427). Escherichia coli NovaBlue transformed with plasmid pDMD427 subsequently acquired the ability to degrade dimethoate. Curing of the plasmid by plumbagin or ethidium bromide resulted in the loss of ability of MCMB‐427 to degrade dimethoate. Plasmid pDMD427 was stable in MCMB‐427 over 20 passages without selection. Genes encoding resistance to norfloxacin and cobalt were also located on plasmid pDMD427. Conclusions: The ability of Ps. aeruginosa MCMB‐427 to degrade dimethoate is plasmid‐mediated and transferable to other strains. Significance and Impact of the Study: As far as is known, this is the first report of plasmid‐mediated dimethoate biodegradation. This study contributes significantly towards an understanding of the genetics of bacterial dimethoate degradation.