Original Article

Aerobic dichlorvos degradation by Pseudomonas stutzeri smk: complete pathway and implications for toxicity in Mus musculus

Abstract

Background and Objectives: Excess use of pesticides in agricultural field not only compromised soil fertility but also posed serious threat to water bodies and life in the surrounding environment. The leftover pesticide residue needs to be remediated effectively. Compared to physical, chemical and enzymatic remediation options the microbial remediation is more practical and sustainable.
Materials and Methods: The Pseudomonas stutzeri smk strain was found to use dichlorvos as the solitary carbon source. Minimal medium supplemented with dichlorvos was used to test ability of bacterium to degrade pesticide aerobically. The metabolites produced by the bacterium were studied with UV-Vis spectrophotometry, HPLC, FTIR and GC-MS techniques. The toxicity studies of neat dichlorvos and P. stutzeri smk degraded metabolites were studied by subcutaneous injection in Mus musculus.
Results: The P. stutzeri smk strain was found to degrade as high as 80% of dichlorvos on 7th day of incubation, at 30 °C temperature and at pH 7. In five steps complete aerobic degradation of 2,2dicholorvinyl dimethyl phosphate (dichlorvos) resulted in production of free methyl and phosphate. The degradation intermediates produced are 2-Chlorovinyl dimethyl phosphate, vinyl dimethyl phosphate, dimethyl phosphate, methylphosphate and finally free phosphate. The histopathological analysis of liver, spleen and thymus of M. musculus were performed to study toxicity of dichlorvos and degraded metabolites.
Conclusion: P. stutzeri smk could result highest aerobic degradation of dichlorvos to produce free methyl and phosphate. Degradation metabolites could reverse largely toxic effects of dichlorvos when studied in M. musculus.

1. Kang DG, Choi SS, Cha HJ. Enhanced biodegradation of toxic organophosphate compounds using recombinant Escherichia coli with sec pathway-driven periplasmic secretion of organophosphorus hydrolase. Biotechnol Prog 2006; 22: 406-410.
2. Bakry NM, el-Rashidy AH, Eldefrawi AT, Eldefrawi ME. Direct actions of organophosphate anticholinesterases on nicotinic and muscarinic acetylcholinic receptors. J Biochem Toxicol 1988; 3: 235-259.
3. Grimsley J, Rastogi V, Wild J. Biological detoxification of organophosphorus neurotoxins. In: Bioremediation Principles and Practice-Biodegradation Technology Developments (S. Sikdar and R. Irvine, Eds). Technomic Publishers, New York. 1998; pp 557-613
4. Miller WR, Sharpe RM. Environmental estrogens and human reproductive cancers. Endocr-Relat Cancer 1998; 5: 69-96.
5. Dua M, Singh A, Sethunathan N, Johri AK. Biotechnology and bioremediation successes and limitations. Appl Microbiol Biotechnol 2002; 59: 143-152.
6. Richins RD, Kanera I, Mulchandani A, Chen W. Biodegradation of organophosphorus pesticides by surface-expressed organophosphorus hydrolase. Nat Biotechnol 1997; 15: 984-987.
7. Singh BK, Walker A, Wright DJ. Degradation of chlorpyrifos, fenamiphos, and chlorothalonil alone and in combination and their effects on soil microbial activity. Environ Toxicol Chem 2002; 21: 2600-2605.
8. Yang L, Zhao Y, Zhang B, Yang C, Zhang X. Isolation and characterization of a chlorpyrifos and 3,5,6-trichloro-2-pyridinol degrading bacterium. FEMS Microbiol Lett 2005; 251: 67-73.
9. Lakshmi CV, Kumar M, Khanna S. Biodegradation of chlorpyrifos in soil by enriched cultures. Curr Microbiol 2009; 58: 35-38.
10. Zhongli C, Shunpeng L, Guoping F. Isolation of methyl parathion-degrading strain M6 and cloning of the methyl parathion hydrolase gene. Appl Environ Microbiol 2001; 67: 4922-4925.
11. Chang TC, Chang HC, Yu FW, Lenie D, Mario V, Chung TT. Species-level identification of isolates of the Acinetobacter calcoaceticus-Acinetobacter baumannii complex by sequence analysis of the 16S-23S rRNA gene spacer region. J Clin Microbiol 2005; 43:1632-1639.
12. Horne I, Harcourt RL, Sutherland TD, Russel RJ, Oakeshott JG. Isolation of a Pseudomonas monteili strain with a novel phosphotriesterase. FEMS Microbiol Lett 2002; 206: 51-55.
13. Huang J, Qiyo CL, Li X, Xing JM. Cloning and fusion expression of detoxifying gene in Escherichia coli. Acta Genetica Sinica 2001; 28:583-588.
14. Parte SG, Kharat AS. Aerobic degradation of clothianidin to 2-chloro-methyl thiazole and methyl 3-(thiazole-yl) methyl guanidine produced by Pseudomonas stutzeri smk. J Environ Public Health 2019; 2019:4807913.
15. Parte SG, Kharat AS, Mohekar AD. Isolation and characterization of dichlorvos degrading bacterial strain Pseudomonas stutzeri smk. RJLBPCS 2017; 2: 282-288.
16. Jiang Y, Deng Y, Liu X, Xie B, Hu F. Isolation and identification of a bacterial strain JS018 capable of degrading several kinds of organophosphate pesticides. Wei Sheng Wu Xue Bao 2006; 46: 463-466.
17. Agarry SE, Olu-Arotiowa OA, Aremu MO, Jimoda LA. Biodegradation of Dichlorovos (Organophosphate pesticide) in soil by bacterial isolates. J Nat Sci Res 2013; 3:12-17.
18. Ning J, Gang G, Bai Z, Hu Q, Qi H, Ma A, et al. In situ enhanced bioremediation dichlorvos by a phyllosphere Flavobacterium strain. Front Env Sci Eng 2012; 6:231-237.
19. Oncescu T, Oancea P, Enache M, Popescu G, Dumitru L, Kamekura M. Halophilic bacteria are able to decontaminate dichlorvos, a pesticide, from saline environments. Cent Eur J Biol 2007; 2:563-573.
20. Sukirtha TH, Usharani MV. Production and qualitative analysis of biosurfactant and biodegradation of the organophosphate by Nocardia mediterranie. J Bioremed Biodeg 2013; 4: 198.
21. Deshpande NM, Sarnaik SS, Paranjpe SA, Kanekar PP. Optimization of dimethoate degradation by Brevundimonas sp. MCM B-427 using factorial design: studies on interactive effects of environmental factors. World J Microb Biotechnol 2004; 20: 455-462.
22. Deshpande NM, Dhakephalkar PK, Kanekar PP. Plasmid-mediated dimethoate degradation in Pseudomonas aeruginosa strain MCMB-427. Lett Appl Microbiol 2001; 33:275-279.
23. Phugare SS, Gaikwad YB, Jadhav JP. Biodegradation of acephate using a developed bacterial consortium and toxicological analysis using earthworms (Lumbricusterrestris) as a model animal. Int Biodeter Biodegr 2012; 69: 1-9.
24. Sharma P, Singh R. Dichlorvos and Lindane induced oxidative stress in rat brain: Protective effects of ginger. Pharmacognosy Res 2012; 4: 27-32.
25. Owoeye O, Edem FV, Akinyoola BS, Rahaman S, Akang EE, Arinola GO. Histological changes in liver and lungs of rats exposed to dichlorvos before and after vitamin supplementation. Eur J Anat 2012; 16: 190-198.
26. El-bendary HM, Shaker MH, Saleh AA, Negm SE, Khadey ME, Hosam Eldeen FA. Histopathological changes associated with exposure of male mice to profenofos and chlorpyrifos. Annu Res Rev Biol 2014; 4: 766-777.
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IssueVol 12 No 2 (2020) QRcode
SectionOriginal Article(s)
DOI https://doi.org/10.18502/ijm.v12i2.2619
Keywords
Biodegradation; Pseudomonas stutzeri; Fourier-transformed infrared spctroscopy; High performance liquid chromatography; Dichlorvos

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How to Cite
1.
Parte S, Mohekar A, Kharat A. Aerobic dichlorvos degradation by Pseudomonas stutzeri smk: complete pathway and implications for toxicity in Mus musculus. Iran J Microbiol. 2020;12(2):138-147.