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首页> 外文期刊>日本水産学会誌 >Development of 16S rRNA targeted PCR for the identification of Vibrio spp., the causative bacteria of the disease in cultured sea urchin Strongylocentrotus intermedius occurring at low water temperatures [Japanese]
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Development of 16S rRNA targeted PCR for the identification of Vibrio spp., the causative bacteria of the disease in cultured sea urchin Strongylocentrotus intermedius occurring at low water temperatures [Japanese]

机译:16S RRNA靶向PCR的研发,用于鉴定vibrio spp。,在低水压下发生培养的海胆中血管株疾病的致病细菌[日文]

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摘要

The causative bacteria, Vibrio spp., have been isolated from the diseased sea urchin Strongylocentrotus intermedius at low water temperatures. To develop a specific identification method for the pathogens, species-specific nucleotide sequences in the 16S rRNA of Vibrio spp., were determined. We designed two PCR primers, DA2F and SK1F, based on the nucleotide sequences: DA2F forward primer (nucleotide numbers 456 to 476 in Escherichia coli 16S rRNA) for Date isolates and Sk1F for-ward primer (nucleotide numbers 455 to 478 in E. coli 16S rRNA) for Shiriuchi and Shikabe isolates.
机译:致病菌,vibrio spp。,在低水温下从患病的海胆激素中间体中分离出来。 为vibriOSPP的16S rRNA中的病原体,物种特异性核苷酸序列进行特异性鉴定方法。 我们基于核苷酸序列设计了两个PCR引物,DA2F和SK1F:DA2F前底漆(在大肠杆菌中的大肠杆菌16S rRNA中的核苷酸编号456至476),用于日期分离物和SK1F用于病房引物(大肠杆菌中的核苷酸编号455至478 16S rRNA)用于shiriuchi和shikabe分离物。

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