摘要
建立了从活性污泥中快速提取基因组DNA的新方法,过程包括粗提与精制两个步骤,简化了繁琐的提取程序,提高了提取效率.用该方法提取的基因组DNA做模板,进行扩增核糖体限制性酶切片断分析(ARDRA)及核糖体基因间区序列分析(R ISA),均获得了理想的多态性指纹图谱;采用两对特异性引物(鞘氨醇单胞菌属和氨加氧酶基因)对所提污泥基因组DNA进行扩增,均获得了正确的PCR产物.该方法提取的污泥基因组DNA不但适用于研究污泥系统中菌群多样性分析,而且还可以对特定基因进行跟踪监测.
A novel approach for rapid extraction of genomic DNA from activated sludge was developed. The extraction protocol comprised two steps： crude extraction and further purification, which simplified the complicated extraction process. The satisfied multiple fingerprints were obtained by this template DNA for both ARDRA （amplified ribosomal DNA restriction analysis） and RISA （ribosomal intergenic space analysis）. Simultaneously, two pairs of specific primers （Sphingomonas sp. and amo gene） were used to perform PCR, and the correct PCR products were obtained. The proposed protocol was rapid and efficient not only for analysis of microbial community diversity, but also for monitoring specific gene in activated sludge.
出处
《大连理工大学学报》
EI
CAS
CSCD
北大核心
2006年第3期335-339,共5页
Journal of Dalian University of Technology
