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Application of Denaturing High-Performance Liquid Chromatography in Microbial Ecology: Fermentor Sludge Compost and Soil Community Profiling

机译:变性高效液相色谱法在微生物生态学中的应用:发酵罐污泥堆肥和土壤群落概况

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摘要

Genetic fingerprinting methods, such as denaturing gradient gel electrophoresis (DGGE), are used in microbial ecology for the analysis of mixed microbial communities but are associated with various problems. In the present study we used a new alternative method: denaturing high-performance liquid chromatography (dHPLC). This method was previously shown to work with samples from water and gut flora but had not yet been applied to complex environmental samples. In contrast to other publications dealing with dHPLC, we used a commonly available HPLC system. Samples from different origins (fermentor sludge, compost, and soil), all ecologically significant, were tested, and the 16S rRNA gene was amplified via PCR. After optimization of the HPLC elution conditions, amplicons of pure cultures and mixed microbial populations could be separated successfully. Systematic differentiation was carried out by a cloning approach, since fraction collection of the peaks did not result in satisfactory fragment separation. dHPLC was evaluated as a tool for microbial community analysis on a genetic level and demonstrated major improvements compared to gel-based fingerprinting methods, such as DGGE, that are commonly used in microbial ecology.
机译:遗传指纹图谱方法,例如变性梯度凝胶电泳(DGGE),已在微生物生态学中用于分析混合微生物群落,但存在各种问题。在本研究中,我们使用了一种新的替代方法:变性高效液相色谱(dHPLC)。先前已证明此方法可用于水和肠道菌群的样品,但尚未应用于复杂的环境样品。与其他有关dHPLC的出版物相比,我们使用了一种通用的HPLC系统。测试了具有不同生态意义的不同来源的样品(发酵罐污泥,堆肥和土壤),并通过PCR扩增了16S rRNA基因。优化HPLC洗脱条件后,可以成功分离纯培养物和混合微生物种群的扩增子。通过克隆方法进行系统分化,因为峰的馏分收集未导致令人满意的片段分离。 dHPLC被评估为在遗传水平上进行微生物群落分析的工具,并且与微生物生态学中常用的基于凝胶的指纹图谱方法(例如DGGE)相比,显示出重大改进。

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