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PCR-based 16S rDNA Technique for Bacterial Detection in the Zhenjiang Municipal Sewage

机译:基于PCR的16S RDNA技术在镇江市污水中的细菌检测技术

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A 16S ribosomal DNA clone library from Zhenjiang municipal sewage was established by PCR using suitable primers. The total of 100 clones were selected by plasmid extraction and PCR identification. 28 clones were obtained and sequenced. From the DNA databases all sequences had > 94 % similarity to reference sequences of the closest related organisms. The sequences analysis indicated that these were identified as Arcobacter sp., Fusobacterium necrophorum, anaerobic bacterium and Clostridium sp. In the municipal sewage. And Arcobacter sp. Predominates in the study, constituting 89.2% of the 28 clones. The results also showed that these bacteria were almost pathogenic organisms. Use of this molecular method establishes the rapid detection of bacterial different from those isolated and identified by traditional cultures. The bacteria detection in Zhenjiang municipal sewage provides reference for the deep study of pathogenic organisms and the assessment of sewage discharge security.
机译:来自镇江市污水的16S核糖体DNA克隆图书馆使用合适的引物建立了PCR。 通过质粒提取和PCR鉴定选择100种克隆。 获得28个克隆并测序。 从DNA数据库中,所有序列都具有与最接近的相关生物的参考序列相似的> 94%。 序列分析表明,这些被鉴定为Arcobacter sp。,肮脏的核菌,厌氧细菌和梭菌sp。 在市政污水中。 和arcobacter sp。 在研究中占主导地位,构成了28个克隆的89.2%。 结果还表明,这些细菌几乎是致病生物。 使用这种分子法确定了与传统培养物分离的细菌不同的细菌。 镇江市污水的细菌检测为致病生物的深入研究提供了参考,以及污水排放安全的评估。

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