首页> 外文期刊>Journal of Environmental Science and Health. A >IDENTIFYING THE SOURCES BIOSOLID DERIVED PATHOGEN INDICATOR ORGANISMS IN AEROSOLS BY RIBOSOMAL DAN
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IDENTIFYING THE SOURCES BIOSOLID DERIVED PATHOGEN INDICATOR ORGANISMS IN AEROSOLS BY RIBOSOMAL DAN

机译:通过核糖体DAN鉴定气溶胶中源于类固醇的病原菌指示剂

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The application of the ribosomal DNA (rDNA) fingerprinting method to identify the sources of aerosolized clostridia isolates at a commercial biosolid land application site is being reported. Clostridia isolates were initially isolated from aerosol samples as well as from biosolid piles on the ground. Oligonucleotide primers, specific to the bacterial 16S-23S interspacer region were employed in gene amplification reactions to amplify the region. For those isolates the generated similar sized amplification products, the products were digested with the HindIII restriction endonuclease to determine genetic differences. Using this approach, it was possible to genetically link some of the aerosol isolates to the biosolid piles. The results suggest that for tracking the sources of aerosolized clostridia, it would be necessary to amplify the 16S-23S region, and if necessary, followed by restriction enzyme anlayses of product. The region, and if necessary, followed by restriction enzyme analyses of product. The need for restriction enzyme analyses would necessary only if the isolates in question had amplification products of similar sizes.
机译:据报道,核糖体DNA(rDNA)指纹法在商业生物固体土地应用场所鉴定气溶胶化梭状芽胞杆菌分离物的来源。梭状芽胞杆菌分离物最初是从气溶胶样品以及地面上的生物固体堆中分离出来的。对细菌16S-23S间隔区特异的寡核苷酸引物被用于基因扩增反应中,以扩增该区域。对于那些分离物,产生的相似大小的扩增产物,将产物用HindIII限制性核酸内切酶消化,以确定遗传差异。使用这种方法,可以将某些气溶胶分离物遗传连接到生物固体堆上。结果表明,为了追踪气溶胶化梭状芽胞杆菌的来源,有必要扩增16S-23S区域,必要时再进行产物限制性酶切。对该区域进行分析,必要时再进行产物的限制酶分析。仅当所讨论的分离物具有相似大小的扩增产物时,才需要进行限制酶分析。

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