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Isolation of Methyl Parathion-Degrading Strain M6 and Cloning of the Methyl Parathion Hydrolase Gene
Open accessAbstract
A degradative bacterium, M6, was isolated and presumptively identified as Plesiomonas sp. strain M6 was able to hydrolyze methyl parathion to p -nitrophenol. A novel organophosphate hydrolase gene designated mpd was selected from its genomic library prepared by shotgun cloning. The nucleotide sequence of the mpd gene was determined. The gene could be effectively expressed in Esherichia coli .
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Citations
Cited by
Microbial degradation of organophosphorus compounds
Singh, B. K., & Walker, A. (2006) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2006.00018.x · Cited by 1,013
Singh, B. K., Walker, A., Morgan, J. A. W., & Wright, D. J. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.8.4855-4863.2004 · Cited by 434
Wei, X., Xie, B., Wan, C., Song, R., Zhong, W., Xin, S., & Song, K. (2024) · Agronomy · doi:10.3390/agronomy14030609 · Cited by 280
Russell, R. J., Scott, C., Jackson, C. J., Pandey, R., Pandey, G., Taylor, M. C., Coppin, C. W., Liu, J., & Oakeshott, J. G. (2011) · Evolutionary Applications · doi:10.1111/j.1752-4571.2010.00175.x · Cited by 130
Metadata
- Authors
- Zhongli, C., Shunpeng, L., & Guoping, F.
- Venue
- Applied and Environmental Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2001-10
- Volume
- 67
- Issue
- 10
- Pages
- 4922-4925
- ISSN
- 0099-2240 (ISSN-L)
- 1098-5336
- OpenAlex
- W2121880975
- Cited by
- 268
- References
- 0
- FWCI
- 5.33
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Isolation of Methyl Parathion-Degrading Strain M6 and Cloning of the Methyl Parathion Hydrolase Gene. https://app.cochat.ai/papers/10.1128/aem.67.10.4922-4925.2001
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- Zhongli, C., Shunpeng, L., & Guoping, F. (2001). Isolation of Methyl Parathion-Degrading Strain M6 and Cloning of the Methyl Parathion Hydrolase Gene. Applied and Environmental Microbiology. https://doi.org/10.1128/aem.67.10.4922-4925.2001
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