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生物硝化池污水中硝化细菌的快速定量研究
引用本文:明镇寰,岳春梅.生物硝化池污水中硝化细菌的快速定量研究[J].环境科学学报,2002,22(6):796-798.
作者姓名:明镇寰  岳春梅
作者单位:浙江大学生命科学学院,杭州,310012
基金项目:浙江省科技厅重点项目 (0 0 110 3172 ),浙江省环保局项目资助
摘    要:实验采用聚合酶链式反应(PCR)技术与最大几率数法(MPN)相结合的MPN-PCR法对生物硝化池污水中的硝化细菌进行快速定量。所用的一对PCR引物是在对硝化细菌的16SrRNA基因进行系统比较的基础上设计合成的,可以扩增出大小为388bp的DNA片段。以从生物硝化池污水中抽提的含硝化细菌DNA的混合DNA为模板,进行PCR扩增并确定合适的扩增条件。运用MPN-PCR法进行定量检测的整个过程可在几小时之内完成。

关 键 词:生物硝化池  硝化细菌  MPN-PCR法  定量检测  污水处理  聚合酶链反应
文章编号:0253-2468(2002)-06-0796-03
收稿时间:2002/2/11 0:00:00
修稿时间:2002年2月11日

Study on fast quantitative detection for Nitrobacteria in wastewater of biological nitrification stage
MING Zhenhuan and YUE Chunmei.Study on fast quantitative detection for Nitrobacteria in wastewater of biological nitrification stage[J].Acta Scientiae Circumstantiae,2002,22(6):796-798.
Authors:MING Zhenhuan and YUE Chunmei
Institution:College of Life Science, Zhejiang University Hangzhou, 310012 and College of Life Science, Zhejiang University Hangzhou, 310012
Abstract:The MPN\|PCR method,based on the combination of polymerase chain reaction with most probable number,was applied for quantitative detection of Nitrobacteria in wastewater of biological nitrification stage.The oligonucleotide primers,designed by comparing the total 16SrRNA gene sequences of Nitrobacteria , were used to generate a 388 bp DNA fragment.The mixed DNA (with the Nitrobacteria DNA from the wastewater in the biological nitrification stage) Served as template for PCR and the best amplification condition was determined.It took only several hours to count Nitrobacteria by MPN\|PCR procedure.By comparing the results of MPN\|PCR with that of MPN\|Griess,it was found that MPN\|PCR can sensitively,consistently,efficiently and rapidly assay,which is effective to detect and count the Nitrobacteria in the wastewater of the biological nitrification stage.
Keywords:Nitrobacteria  wastewater  MPN\|PCR assay  quantitative detection  
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