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Biodegradation of Chlorpyrifos by Enterobacter Strain B-14 and Its Use in Bioremediation of Contaminated Soils

机译:肠杆菌B-14对毒死rif的生物降解及其在污染土壤的生物修复中的应用

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摘要

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 (106 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.
机译:从澳大利亚的土壤中分离出六种毒死rif降解细菌,并通过生化和分子方法进行比较。分离物没有区别,并选择了一种(菌株B-14)进行进一步分析。该菌株显示出与肠杆菌科成员最大的相似性,并且最接近于白色肠杆菌科成员。在不同的培养条件下,研究了毒死mineral的毒化能力,并以毒死as为唯一的碳,磷源。用环或均匀标记的[ 14 C]毒死rif进行液体培养的研究表明,该分离物将毒死rif水解为二乙基硫代磷酸酯(DETP)和3,5,6-三氯-2-吡啶醇,并利用DETP进行生长。和能量。发现该分离物具有单磷酸酶和二磷酸酶活性以及磷酸三酯酶活性。添加其他碳源(葡萄糖和琥珀酸盐)会导致毒死rif的初始降解速度减慢。当作为唯一的碳和磷的来源提供时,该分离物降解了含DETP的有机磷对硫磷,二嗪农,库马磷和异唑磷,但对具有不同侧链的非灭草磷,fonofos,ethoprop和cadusafos无效。对降解的分子基础的研究表明,降解能力可能是多基因的且基于染色体。进一步的研究表明,该菌株具有新型的磷酸三酯酶系统,因为编码该酶的基因与广泛研究的有机磷酸降解基因(opd)具有不同的序列。将B-14菌株(10 6 细胞g −1 )添加到土壤中含有低毒死rif降解细菌的土壤中,用35 mg毒死kg kg -1 导致的降解率高于未接种土壤。这些结果突出了该细菌在清洁环境中受污染的农药废物中的潜力。

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