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Coupling of Denaturing High-Performance Liquid Chromatography and Terminal Restriction Fragment Length Polymorphism with Precise Fragment Sizing for Microbial Community Profiling and Characterization

机译:变性高效液相色谱和末端限制片段长度多态性与精确片段大小的耦合用于微生物群落分析和表征

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摘要

Terminal restriction fragment length polymorphism (T-RFLP) is used to monitor the structural diversity of complex microbial communities in terms of richness, relative abundance, and distribution of the major subpopulations and individual members. However, discrepancies of several nucleotides between expected and experimentally observed lengths of terminal restriction fragments (T-RFs), together with the difficulty of obtaining DNA sequence information from T-RFLP profiling, often prevent accurate phylogenetic characterization of the microbial community of interest. In this study, T-RFLP analysis of DNA from an artificial assembly of five bacterial strains was carried out with a combination of two size markers with different fluorescent tags. Precise sizing of T-RFs in the 50- to 500-nucleotide range was achieved by using the same dye for both samples and size markers. Phylogenetic assignment of the component microbial strains was facilitated by coupling T-RFLP to denaturing high-performance liquid chromatography (D-HPLC) of 16S RNA gene fragments followed by direct sequencing. The proposed coupling of D-HPLC and T-RFLP provides unambiguous characterization of microbial communities containing less than 15 microbial strains.
机译:末端限制性片段长度多态性(T-RFLP)用于监测复杂微生物群落的结构多样性,包括主要亚种群和单个成员的丰富度,相对丰度和分布。但是,预期和实验观察到的末端限制性片段(T-RFs)长度之间的几个核苷酸差异,加上难以从T-RFLP分析中获得DNA序列信息,经常会妨碍目标微生物群落的准确系统发育特征。在这项研究中,T-RFLP分析了五个细菌菌株的人工装配中的DNA,并结合了两个大小不同的荧光标记的大小标记。通过对样品和大小标记使用相同的染料,可以精确确定T-RF在50至500个核苷酸范围内的大小。通过将T-RFLP偶联至变性的16S RNA基因片段的高效液相色谱(D-HPLC),然后进行直接测序,可促进组分微生物菌株的系统发生分配。拟议的D-HPLC和T-RFLP偶联提供了包含少于15种微生物菌株的微生物群落的明确表征。

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