Biodegradation of chlorpyrifos by Enterobacter strain B-14 and its use in bioremediation of contaminated soils

Six chlorpyrifos-degrading bacteria were isolated from an Australian soil and compared by biochemical and molecular methods. The isolates were indistinguishable, and one (strain B-14) was selected for further analysis. This strain showed greatest similarity to members of the order Enterobacteriales...

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Veröffentlicht in:Applied and Environmental Microbiology 2004-08, Vol.70 (8), p.4855-4863
Hauptverfasser: Singh, B.K, Walker, A, Morgan, J.A.W, Wright, D.J
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description Six chlorpyrifos-degrading bacteria were isolated from an Australian soil and compared by biochemical and molecular methods. The isolates were indistinguishable, and one (strain B-14) was selected for further analysis. This strain showed greatest similarity to members of the order Enterobacteriales and was closest to members of the Enterobacter asburiae group. The ability of the strain to mineralize chlorpyrifos was investigated under different culture conditions, and the strain utilized chlorpyrifos as the sole source of carbon and phosphorus. Studies with ring or uniformly labeled [14C]chlorpyrifos in liquid culture demonstrated that the isolate hydrolyzed chlorpyrifos to diethylthiophospshate (DETP) and 3, 5, 6-trichloro-2-pyridinol, and utilized DETP for growth and energy. The isolate was found to possess mono- and diphosphatase activities along with a phosphotriesterase activity. Addition of other sources of carbon (glucose and succinate) resulted in slowing down of the initial rate of degradation of chlorpyrifos. The isolate degraded the DETP-containing organophosphates parathion, diazinon, coumaphos, and isazofos when provided as the sole source of carbon and phosphorus, but not fenamiphos, fonofos, ethoprop, and cadusafos, which have different side chains. Studies of the molecular basis of degradation suggested that the degrading ability could be polygenic and chromosome based. Further studies revealed that the strain possessed a novel phosphotriesterase enzyme system, as the gene coding for this enzyme had a different sequence from the widely studied organophosphate-degrading gene (opd). The addition of strain B-14 (10(6) cells g-1) to soil with a low indigenous population of chlorpyrifos-degrading bacteria treated with 35 mg of chlorpyrifos kg-1 resulted in a higher degradation rate than was observed in noninoculated soils. These results highlight the potential of this bacterium to be used in the cleanup of contaminated pesticide waste in the environment.
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The isolate degraded the DETP-containing organophosphates parathion, diazinon, coumaphos, and isazofos when provided as the sole source of carbon and phosphorus, but not fenamiphos, fonofos, ethoprop, and cadusafos, which have different side chains. Studies of the molecular basis of degradation suggested that the degrading ability could be polygenic and chromosome based. Further studies revealed that the strain possessed a novel phosphotriesterase enzyme system, as the gene coding for this enzyme had a different sequence from the widely studied organophosphate-degrading gene (opd). The addition of strain B-14 (10(6) cells g-1) to soil with a low indigenous population of chlorpyrifos-degrading bacteria treated with 35 mg of chlorpyrifos kg-1 resulted in a higher degradation rate than was observed in noninoculated soils. 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Economical aspects ; insecticide residues ; Insecticides - metabolism ; Microbiology ; mineralization ; Molecular Sequence Data ; nucleotide sequences ; polluted soils ; ribosomal RNA ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, DNA ; soil bacteria ; Soil Microbiology ; Soil Pollutants - metabolism ; soil pollution</subject><ispartof>Applied and Environmental Microbiology, 2004-08, Vol.70 (8), p.4855-4863</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright © 2004, American Society for Microbiology 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-fc523814eea74e22d6d0c6c720c96d1208b200dc9729255d044dc976683308403</citedby><cites>FETCH-LOGICAL-c591t-fc523814eea74e22d6d0c6c720c96d1208b200dc9729255d044dc976683308403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC492451/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC492451/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,3175,3176,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16006524$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15294824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, B.K</creatorcontrib><creatorcontrib>Walker, A</creatorcontrib><creatorcontrib>Morgan, J.A.W</creatorcontrib><creatorcontrib>Wright, D.J</creatorcontrib><title>Biodegradation of chlorpyrifos by Enterobacter strain B-14 and its use in bioremediation of contaminated soils</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Six chlorpyrifos-degrading bacteria were isolated from an Australian soil and compared by biochemical and molecular methods. 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The isolate degraded the DETP-containing organophosphates parathion, diazinon, coumaphos, and isazofos when provided as the sole source of carbon and phosphorus, but not fenamiphos, fonofos, ethoprop, and cadusafos, which have different side chains. Studies of the molecular basis of degradation suggested that the degrading ability could be polygenic and chromosome based. Further studies revealed that the strain possessed a novel phosphotriesterase enzyme system, as the gene coding for this enzyme had a different sequence from the widely studied organophosphate-degrading gene (opd). The addition of strain B-14 (10(6) cells g-1) to soil with a low indigenous population of chlorpyrifos-degrading bacteria treated with 35 mg of chlorpyrifos kg-1 resulted in a higher degradation rate than was observed in noninoculated soils. 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The isolates were indistinguishable, and one (strain B-14) was selected for further analysis. This strain showed greatest similarity to members of the order Enterobacteriales and was closest to members of the Enterobacter asburiae group. The ability of the strain to mineralize chlorpyrifos was investigated under different culture conditions, and the strain utilized chlorpyrifos as the sole source of carbon and phosphorus. Studies with ring or uniformly labeled [14C]chlorpyrifos in liquid culture demonstrated that the isolate hydrolyzed chlorpyrifos to diethylthiophospshate (DETP) and 3, 5, 6-trichloro-2-pyridinol, and utilized DETP for growth and energy. The isolate was found to possess mono- and diphosphatase activities along with a phosphotriesterase activity. Addition of other sources of carbon (glucose and succinate) resulted in slowing down of the initial rate of degradation of chlorpyrifos. The isolate degraded the DETP-containing organophosphates parathion, diazinon, coumaphos, and isazofos when provided as the sole source of carbon and phosphorus, but not fenamiphos, fonofos, ethoprop, and cadusafos, which have different side chains. Studies of the molecular basis of degradation suggested that the degrading ability could be polygenic and chromosome based. Further studies revealed that the strain possessed a novel phosphotriesterase enzyme system, as the gene coding for this enzyme had a different sequence from the widely studied organophosphate-degrading gene (opd). The addition of strain B-14 (10(6) cells g-1) to soil with a low indigenous population of chlorpyrifos-degrading bacteria treated with 35 mg of chlorpyrifos kg-1 resulted in a higher degradation rate than was observed in noninoculated soils. 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source American Society for Microbiology; MEDLINE; PubMed Central; Alma/SFX Local Collection
subjects Biodegradation
Biodegradation of pollutants
Biodegradation, Environmental
Biological and medical sciences
bioremediation
Biotechnology
chlorpyrifos
Chlorpyrifos - metabolism
Culture Media
DNA, Ribosomal - analysis
Enterobacter
Enterobacter - genetics
Enterobacter - growth & development
Enterobacter - isolation & purification
Enterobacter - metabolism
Enterobacter asburiae
Environment and pollution
Freshwater
Fundamental and applied biological sciences. Psychology
genes
Industrial applications and implications. Economical aspects
insecticide residues
Insecticides - metabolism
Microbiology
mineralization
Molecular Sequence Data
nucleotide sequences
polluted soils
ribosomal RNA
RNA, Ribosomal, 16S - genetics
Sequence Analysis, DNA
soil bacteria
Soil Microbiology
Soil Pollutants - metabolism
soil pollution
title Biodegradation of chlorpyrifos by Enterobacter strain B-14 and its use in bioremediation of contaminated soils
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