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Molecular monitoring of microbial populations during bioremediation of contaminated soils.

机译:污染土壤生物修复过程中微生物种群的分子监测。

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Microbes are being used to help clean up polluted sites around the world. Yet, the current knowledge of the complex assemblages of microbes in natural or polluted environments is limited due to inability to culture so many of the organisms by conventional microbiological methods. Many questions about what impact a pollutant or a treatment regime may have on the microbial community still remain to be answered. Molecular techniques have rapidly become valid methods for examining microbial communities in situ and are helping to answer many of these questions. Digesting nucleic acids with restriction endonucleases cuts DNA into different length fragments. Subsequent electrophoretic separation of the fragments will produce banding profiles (DNA fingerprints) that can be used to discriminate between populations. Variations of this restriction fragment length polymorphism (RFLP) method have successfully been used to monitor microbial community dynamics during bioremediation. The restriction fragment-based techniques (e.g., RFLP, T-RFLP) give some indication of the complexities of the communities but still underestimate the true diversity or dynamics of the microbial community. Amplicon length heterogeneity-PCR (LH-PCR) is a molecular technique that discriminates between different bacteria based on the natural sequence variations in the lengths of the 16S ribosomal DNA (rDNA) genes not on restriction enzyme recognition sites. Soils contaminated with petroleum hydrocarbons were treated in bench-scale bioreactors. Whole community DNA extracted from the bioreactor samples and the polymerase chain reaction (PCR) was used to amplify the 16S rDNA genes. The three DNA fingerprinting methods were compared to each other and to non-molecular techniques to ascertain which of the techniques could be used to monitor whole community dynamics. The LH-PCR method proved to be the most robust, reproducible and diagnostic of all the techniques tested. The LH-PCR technique was able to detect greater genetic diversity within the microbial communities. It also profiled significant differences in community structure between the bioreactor microbial communities undergoing different bioremediation treatment regimes. The LH-PCR technique has great potential as a monitoring tool that can significantly contribute to the basic understanding of the bioremediation processes.
机译:微生物被用来帮助清理世界各地的污染场地。然而,由于无法通过常规微生物方法培养如此众多的生物,因此目前对自然或污染环境中微生物复杂组合的了解有限。关于污染物或处理方案可能对微生物群落产生何种影响的许多问题仍有待回答。分子技术已迅速成为检查微生物群落的有效方法,并正在帮助回答其中的许多问题。用限制性核酸内切酶消化核酸可将DNA切割成不同长度的片段。片段的后续电泳分离将产生带状谱(DNA指纹),可用于区分种群。这种限制性片段长度多态性(RFLP)方法的变异已成功地用于监测生物修复过程中的微生物群落动态。基于限制性片段的技术(例如RFLP,T-RFLP)在某种程度上表明了群落的复杂性,但仍然低估了微生物群落的真正多样性或动态。扩增子长度异质性PCR(LH-PCR)是一种分子技术,可根据不在限制酶识别位点上的16S核糖体DNA(rDNA)基因长度的自然序列差异来区分不同细菌。在台式规模的生物反应器中处理了被石油烃污染的土壤。从生物反应器样品中提取的整个群落DNA和聚合酶链反应(PCR)用于扩增16S rDNA基因。将这三种DNA指纹图谱方法相互比较,并与非分子技术进行比较,以确定哪种技术可以用来监测整个社区的动态。 LH-PCR方法被证明是所有测试技术中最可靠,可重现和诊断的方法。 LH-PCR技术能够检测到微生物群落内更大的遗传多样性。它还分析了经历不同生物修复治疗方案的生物反应器微生物群落之间群落结构的显着差异。 LH-PCR技术作为监测工具具有巨大潜力,可以极大地促进对生物修复过程的基本了解。

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