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活性污泥中氨氧化菌实时荧光定量PCR标准品制备方法的比较 被引量:2

A Comparative Study of the Standard Preparation Methods of Real-time Fluorescence Quantitative PCR of Ammonia Oxidizing Bacteria in Activated Sludge
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摘要 为了快速准确地检测活性污泥中氨氧化菌(AOB)的拷贝数,探求一种新的快速简便的绝对定量标准品的制备方法。利用纯化的PCR产物和重组质粒标准品分别进行绝对定量,比较两者熔解曲线、扩增曲线、标准曲线和绝对拷贝数等方面的差异,分析两种标准品制备方法应用方面的优势。结果显示,两种标准品制备的熔解曲线都呈单一尖峰、扩增曲线指数期平行、标准曲线R2>99%,PCR产物作为标准品得到的AOB绝对拷贝数小于质粒标准品的结果(P<0.05),表明纯化的PCR产物作为标准品较制备重组质粒标准品而言,操作过程更加简便、经济、对人员专业要求更低,在其纯度较高的情况下,具有和重组质粒标准品一样的应用效果。 To detect the copy number of ammonia oxidizing and to explore an easy preparation method of absolute quan bacteria (AOB) of activated sludge rapidly and accurately, titative PCR standard, this study used purified PCR product and preparative recombinant plasmid, respectively, to conduct absolute quantification PCR (AQ-PCR). The melting curve, amplification curve, standard curve and differences of absolute copy number were compared, the advantages of the two standard preparation method were analyzed. The results showed that the two melting curves of preparation standard were a single peak, the index phases of the amplification curves were parallel, R2 values of standard curves were more than 99%, the AOB absolute copy number of PCR product as a standard was less than the results of recombinant plasmid standard (P 〈 0. 05 ). It indicates the purification of PCR products as a standard is more convenient, more economic, and lower personnel professional requirements than the recombinant plasmid standard. In the case of the high purity, PCR product has the same application effect with recombinant plasmid standard.
出处 《实验室研究与探索》 CAS 北大核心 2017年第10期17-20,共4页 Research and Exploration In Laboratory
基金 国家研发计划项目(2016YFC0401103) 国家自然科学基金项目(51478284 51408387) 苏州市分离净化材料与技术重点实验室项目(SZS201512) 江苏省高等教育教改研究项目(2015JSJG248)
关键词 氨氧化菌 绝对定量 PCR产物 重组质粒 腐殖酸 ammonia oxidizing bacteria (AOB) absolute quantification PCR product recombinant plasmid humic acid
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