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用于快速鉴定属酵母属的酵母的种特异性 PCR 引物。

Species-specific PCR primers for the rapid identification of yeasts of the genus Zygosaccharomyces.

机构信息

Department of Biology and Biochemistry, University of Bath, Bath, UK.

出版信息

FEMS Yeast Res. 2011 Jun;11(4):356-65. doi: 10.1111/j.1567-1364.2011.00724.x. Epub 2011 Mar 16.

Abstract

Species-specific primer pairs that produce a single band of known product size have been developed for members of the Zygosaccharomyces clade including Zygosaccharomyces bailii, Zygosaccharomyces bisporus, Zygosaccharomyces kombuchaensis, Zygosaccharomyces lentus, Zygosaccharomyces machadoi, Zygosaccharomyces mellis and Zygosaccharomyces rouxii. An existing primer pair for the provisional new species Zygosaccharomyces pseudorouxii has been confirmed as specific. The HIS3 gene, encoding imidazole-glycerolphosphate dehydratase, was used as the target gene. This housekeeping gene evolves slowly and is thus well conserved among different isolates, but shows a significant number of base pair changes between even closely related species, sufficient for species-specific primer design. The primers were tested on type and wild strains of the genus Zygosaccharomyces and on members of the Saccharomycetaceae. Sequencing of the D1/D2 region of rDNA was used to confirm the identification of all nonculture collection isolates. This approach used extracted genomic DNA, but in practice, it can be used efficiently with a rapid colony PCR protocol. The method also successfully detected known and new hybrid strains of Z. rouxii and Z. pseudorouxii. The method is rapid, robust and inexpensive. It requires little expertise by the user and is thus useful for preliminary, large-scale screens.

摘要

已为毕赤酵母属的成员(包括巴氏毕赤酵母、两型接合酵母、康氏酵母、迟缓毕赤酵母、马克斯克鲁维酵母、蜂蜜酵母和鲁氏酵母)开发出了产生已知产物大小单带的种特异性引物对。一个现有的暂定新种拟鲁氏酵母的引物对已被证实是特异性的。所选的靶基因是编码组氨酸基因(HIS3),该基因编码咪唑甘油磷酸脱水酶。这种管家基因进化缓慢,因此在不同的分离株中得到很好的保守,但即使在密切相关的物种之间也显示出大量的碱基对变化,足以进行种特异性引物设计。这些引物已在毕赤酵母属的模式和野生菌株以及酿酒酵母科的成员上进行了测试。使用 rDNA 的 D1/D2 区域的测序来确认所有非培养分离物的鉴定。该方法使用提取的基因组 DNA,但实际上,它可以与快速的菌落 PCR 方案一起高效使用。该方法还成功检测到已知和新的鲁氏酵母和拟鲁氏酵母的杂交菌株。该方法快速、稳健且廉价。它需要用户的专业知识很少,因此对于初步的大规模筛选很有用。

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