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首页> 外文期刊>Environmental Science & Technology >Development of a DNA Microarray Chip for the Identification of Sludge Bacteria Using an Unsequenced Random Genomic DNA Hybridization Method
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Development of a DNA Microarray Chip for the Identification of Sludge Bacteria Using an Unsequenced Random Genomic DNA Hybridization Method

机译:使用无序随机基因组DNA杂交方法鉴定污泥细菌的DNA微阵列芯片的开发。

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摘要

A tool, based upon the DNA microarray chip, for the identification of specific bacteria from activated sludge, using the hybridization of genomic DNA with random probes, is described. This chip was developed using the genomic DNAs from Gordonia amarae, the natural filamentous actinomycete that causes sludge foaming and bulking, as well as a nonfilamentous floe forming bacterium (Zoogloea ramigera) and the skin pathogen Mycobacteriumperegrinum without any sequence information. The sets of target probes on amine-coated glass were made from a genomic library, constructed with PCR products derived from randomly fragmented genomic DNAs extracted from pure cultures of the three strains. Initial hybridization results, when pure cultures were employed, showed the specificity of the probes as well as the resolution of the system, demonstrating the capabilities of this system to identify specific bacterial strains. The microarray was also tested for its ability to distinguish specific bacteria from among mixed bacterial communities, such as in sludge, soil, or spiked genomic DNA samples. The results showed that the probes are specific, with only mild cross-hybridization occurring in a small number of cases. Furthermore, the chip clearly discriminated the presence of all three strains when they were present alone or together within mixed samples. Moreover, using the spot intensity and DNA hybridization kinetics, the starting genomic DNA concentrations could be estimated relatively well, which would make it possible to predict the number of specific bacteria present within the test samples. Therefore, the random genomic hybridization approach, i.e., without any sequence information available for the probes, is a practical protocol for the identification of and screening for specific bacteria within any complex bacterial community from the environmental samples, such as in activated sludge, although the possibility of cross-hybridization may still exist.
机译:描述了一种基于DNA微阵列芯片的工具,该工具使用基因组DNA与随机探针的杂交来从活性污泥中鉴定特定细菌。该芯片是使用来自G紫菜(Gordonia amarae)的基因组DNA(天然的丝状放线菌,导致污泥起泡和膨胀),以及无丝状的絮凝形成细菌(Zoogloea ramigera)和皮肤病原体分枝杆菌(Mycobacteriumperegrinumum)开发的,没有任何序列信息。涂有胺的玻璃上的目标探针组是由一个基因组文库制成的,该文库由PCR产物构建而成,该PCR产物得自从三株纯培养物中提取的随机片段化的基因组DNA。当使用纯培养物时,最初的杂交结果显示了探针的特异性以及系统的分辨率,证明了该系统鉴定特定细菌菌株的能力。还测试了微阵列从混合细菌群落(如污泥,土壤或加标基因组DNA样品)中区分特定细菌的能力。结果表明,这些探针是特异性的,在少数情况下仅发生轻度交叉杂交。此外,当它们在混合样品中单独存在或一起存在时,芯片清楚地区分了所有三种菌株的存在。而且,利用斑点强度和DNA杂交动力学,可以相对好地估计起始基因组DNA的浓度,这将有可能预测测试样品中存在的特定细菌的数量。因此,随机基因组杂交方法(即没有任何可用于探针的序列信息)是一种用于从环境样品(例如活性污泥)中识别和筛选任何复杂细菌群落中特定细菌的实用方案,尽管交叉杂交的可能性仍然存在。

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