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Published on: May 4, 2018
Plasmid-mediated dimethoate degradation in Pseudomonas aeruginosa MCMB-427
N M Deshpande1, P K Dhakephalkar, P P Kanekar
1Microbial Sciences Division, Agharkar Research Institute, G.G. Agharkar Road, Pune 411004, India.
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.
Conclusion:
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.
Insights
The bacterium Pseudomonas aeruginosa MCMB-427 degrades the organophosphate insecticide dimethoate via a transferable plasmid. This plasmid-mediated biodegradation is a significant finding for bacterial genetics and pesticide management.
Area of Science:
- Microbiology
- Environmental Science
- Genetics
Background:
- Dimethoate is a widely used synthetic organophosphate insecticide.
- Understanding the microbial degradation pathways of pesticides is crucial for environmental remediation.
- Pseudomonas aeruginosa is known for its metabolic versatility.
Purpose of the Study:
- To investigate the genetic basis of dimethoate degradation in Pseudomonas aeruginosa MCMB-427.
- To identify the role of plasmids in this degradation process.
Main Methods:
- Isolation and characterization of a plasmid from Pseudomonas aeruginosa MCMB-427.
- Transformation of Escherichia coli with the isolated plasmid.
- Plasmid curing experiments using plumbagin and ethidium bromide.
- Assessment of dimethoate degradation ability in native and transformed strains.
Main Results:
- Pseudomonas aeruginosa MCMB-427 possesses a 6.6 kbp plasmid (pDMD427) essential for dimethoate degradation.
- Transfer of pDMD427 to Escherichia coli conferred dimethoate degradation ability.
- Loss of the plasmid resulted in the loss of dimethoate degradation capacity.
- The plasmid also carried genes for resistance to norfloxacin and cobalt.
Conclusions:
- Dimethoate degradation in Pseudomonas aeruginosa MCMB-427 is mediated by a transferable plasmid.
- This is the first report of plasmid-mediated dimethoate biodegradation.
- The findings advance the understanding of bacterial pesticide degradation genetics.
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