首页> 外文会议>Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009 >A Rapid Quantitative Detection Method for Anaerobic Denitrifying Bacteria (ADNB)
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A Rapid Quantitative Detection Method for Anaerobic Denitrifying Bacteria (ADNB)

机译:厌氧反硝化细菌(ADNB)的快速定量检测方法

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There was a long detection circle and higher cost in the quantitative detection of anaerobic deitrifying bacteria (ADNB) in the wastewater of bioreactor and oil field. To solve these issues, the ADNB-MPN-PCR method, combining polymerase chain reaction(PCR) technology with most probable number, was studied as a rapid quantitative detection method for ADNB. The bacterium solution directly used for PCR amplification was prepared from wastewater, which ensured the accuracy of quantification; the universal primers, ADNB341 and ADNB870, located at 16 S rDNA genes of ADNB were designed, and the amplified fragment was 548 bp; the reaction system and amplification conditions of PCR were also optimized. The results indicate that the order of magnitude of this method is two magnitudes higher than that of MPN-Gries, which truly represents the actual quantity of ADNB in wastewater. The whole procedure takes only 3~4 hours and the results of the detection are extremely stable, so the cost is reduced and ADNB-MPN-PCR can be applied in practical processes.
机译:生物反应器和油田废水中厌氧反硝化细菌(ADNB)的定量检测存在一个较长的检测周期和较高的成本。为了解决这些问题,研究了ADNB-MPN-PCR方法,该方法结合了聚合酶链反应(PCR)技术和最有可能的数目,作为ADNB的快速定量检测方法。用废水制备直接用于PCR扩增的细菌溶液,保证了定量的准确性。设计了位于ADNB 16 S rDNA基因的通用引物ADNB341和ADNB870,扩增片段为548 bp。优化了反应体系和PCR扩增条件。结果表明,该方法的数量级比MPN-Gries的数量级高两个数量级,这确实代表了废水中ADNB的实际含量。整个过程仅需3到4个小时,检测结果非常稳定,因此降低了成本,ADNB-MPN-PCR可以在实际过程中应用。

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