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Isolation, characterization and fingerprinting of some chlorpyrifos- degrading bacterial strains isolated from Egyptian pesticides-polluted soils

机译:从埃及农药污染的土壤中分离出的一些降解毒死rif的细菌菌株的分离,表征和指纹图谱

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Five bacterial isolates (B-CP5- B-CP6 - B-CP7- B-CP8- B-CP9) were isolated from pesticides- contaminated soil in Egypt. The capability of these isolates to degrade chlorpyrifos was investigated using enrichment mineral salt (MS) medium containing chlorpyrifos. Two different PCR-based techniques, RAPD-PCR and PCR-RFLP for amplified16S rRNA fragment were used to conduct genetic fingerprinting and obtain specific molecular markers for the studied isolates. The isolates exhibited substantial growth in mineral salt medium supplemented with 100-300 mg/L chlorpyrifos as a sole source of carbon and energy. Based on their morphological, cultural and biochemical characters, the isolates have been identified as?Pseudomonas stuzeri, Enterobacter aerogenes, Pseudomonas pseudoalcaligenes, Pseudomonas maltophila?andPseudomonas vesicularis?respectively.?Pseudomonas?stuzeri?was the most potent degrader strain. Five specific markers for this strain were determined. The highest genetic similarity was observed between CP8 and CP7 (66%), while the lowest genetic similarity was detected between CP8 and CP6 (37%). All isolates had the same pattern after digestion of 16S rRNA amplified fragment with two restriction enzymes (EcoRI and AluI) except?Enterobacter aerogenes,?which generate two monomorphic bands at 420 and 130 bp, respectively. In conclusion, the strain?Pseudomonas stuzeri?could be used to clean up the areas contaminated with Chlorpyrifos. Obtained molecular markers might be used for identifying and tracking the most potent bacterial isolate. The used PCR techniques represent a powerful tool and could be used for rapid typing of this strain.
机译:从埃及受农药污染的土壤中分离出五种细菌分离株(B-CP5- B-CP6- B-CP7- B-CP8- B-CP9)。使用含有毒死rif的富集无机盐(MS)培养基研究了这些分离物降解毒死rif的能力。两种不同的基于PCR的技术,用于扩增的16S rRNA片段的RAPD-PCR和PCR-RFLP用于进行基因指纹分析并获得所研究菌株的特异性分子标记。分离物在补充有100-300 mg / L毒死rif作为唯一碳和能量来源的矿物盐培养基中显示出大量生长。根据它们的形态,文化和生化特性,分离株分别被鉴定为:产假单胞菌,产气肠杆菌,假产假单胞菌,麦芽假单胞菌和水疱假单胞菌。最强的降解菌株是假单胞菌。确定了该菌株的五个特异性标记。 CP8和CP7之间的遗传相似性最高(66%),而CP8和CP6之间的遗传相似性最低(37%)。用两个限制性内切酶(EcoRI和AluI)消化16S rRNA扩增片段后,所有分离株的模式都相同。总之,菌株“ Pseudomonas stuzeri”可用于清理受毒死rif污染的区域。获得的分子标记可用于鉴定和追踪最有效的细菌分离株。所用的PCR技术代表了强大的工具,可用于对该菌株进行快速分型。

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