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Influence of petroleum contamination and biostimulation treatment on the diversity of Pseudomonas spp. in soil microcosms as evaluated by 16S rRNA based-PCR and DGGE

机译:石油污染和生物刺激处理对假单胞菌多样性的影响。通过基于16S rRNA的PCR和DGGE评估土壤微观

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Aims: The aim of this study was to apply a group specific PCR system followed by denaturing gradient gel electrophoresis (DGGE) analysis to evaluate the effect of oil contamination and the biostimulation process on the diversity of Pseudomonas populations in soil ecosystems. Methods and Results: Direct DNA extraction from biostimulated- and oil-contaminated soil samples was performed. Primers specific for the genus Pseudomonas spp. were used to amplify 16S rRNA genes and then a semi-nested PCR reaction was applied to obtain smaller fragments for comparing the PCR products by DGGE. Whether in bulk, oil-contaminated or biostimulated soils, the DGGE profiles revealed little change in Pseudomonas community throughout the 270 days of experiment. The presence of a few additional bands observed only in treated samples indicated that a bacterial shift occurred with the addition of nutrients and with oil contamination. Conclusions, Significance and Impact of the Study: The combination of semi-nested PCR andDGGE was found to be a rapid and sensitive technique to study the diversity within the genus Pseudomonas and may be suitable for further studies concerning the role of this bacterial group in large-scale oil-contaminated areas.
机译:目的:本研究的目的是应用特定组的PCR系统,然后进行变性梯度凝胶电泳(DGGE)分析,以评估油污和生物刺激过程对土壤生态系统中假单胞菌种群多样性的影响。方法和结果:从受生物刺激和油污染的土壤样品中直接进行DNA提取。特定于假单胞菌属的引物。将其用于扩增16S rRNA基因,然后应用半巢式PCR反应获得较小的片段,以比较DGGE的PCR产物。无论是散装,受油污染的土壤还是经过生物刺激的土壤,DGGE分布图在整个270天的实验中都显示出假单胞菌群落几乎没有变化。仅在处理过的样品中观察到一些其他条带的存在表明,随着营养的添加和油的污染,细菌发生了移位。研究的结论,意义和影响:发现半巢式PCR和DGGE结合是研究假单胞菌属内多样性的一种快速而灵敏的技术,可能适合于进一步研究该细菌群在大型细菌中的作用。大规模的石油污染地区。

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