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Development of an affordable typing method for Meyerozyma guilliermondii using microsatellite markers

机译:利用微卫星标记物开发一种经济的瓜叶霉菌打字方法

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摘要

Despite previously published methods, there is still a lack of rapid and affordable methods for genotyping the Meyerozyma guilliermondii yeast species. The development of microsatellite markers is a useful genotyping method in several yeast species. Using the Tandem Repeat Finder Software, a total of 19 microsatellite motifs (di-, tri-, and tetra- repetition) were found in silico in seven of the nine scaffolds published so far. Primer pairs were designed for all of them, although only four were used in this work. All microsatellite amplifications showed size polymorphism, and the results were identical when repeated. The combination of three microsatellite markers (sc15F/R, sc32 F/R and sc72 F/R) produced a different pattern for each of the Type Culture Collection strains of M. guilliermondii used to optimize the method. The three primer pairs can be used in the same PCR reaction, which reduces costs, in tandem with the fluorescent labeling of only the forward primer in each primer pair. Microsatellite typing was applied on 40 more M guilliermondii strains. The results showed that no pattern is repeated between the different environmental niches. Four M. guilliermondii strains were only amplified with primer pair sc32 F/R, and subsequently identified as Meyerozyma caribbica by Taq I-RFLP of the 5.8S ITS rDNA. Most out-group species gave negative results even for physiologically similarly species such as Debaryomyces hansenii. The microsatellite markers used in this work were stable over time, which enables their use as a traceability tool. (C) 2015 Elsevier B.V. All rights reserved.
机译:尽管先前已经发表了方法,但是仍然缺乏用于对麦芽气单胞菌酵母菌种进行基因分型的快速且负担得起的方法。微卫星标记的发展是几种酵母菌种的有用的基因分型方法。使用Tandem Repeat Finder软件,在迄今出版的九种支架中的七种中,在计算机中共发现了19种微卫星基序(二重复,三重复和四重复)。引物对是为所有引物设计的,尽管在这项工作中仅使用了四个。所有微卫星扩增均显示出大小多态性,重复时结果相同。三种微卫星标记(sc15F / R,sc32 F / R和sc72 F / R)的组合为用于优化方法的瓜地分枝杆菌的每个Type Culture Collection菌株产生了不同的模式。可以将三个引物对用于同一PCR反应,这与每个引物对中仅正向引物的荧光标记串联在一起,从而降低了成本。将微卫星分型应用到另外40个M guilliermondii菌株上。结果表明,不同的环境生态位之间没有重复的模式。仅用引物对sc32 F / R扩增了4个guilliermondii菌株,并随后通过5.8S ITS rDNA的Taq I-RFLP鉴定为加勒比Meyerozyma caribbica。多数外群物种甚至对生理上相似的物种(例如汉逊德巴利酵母)也给出了负面结果。这项工作中使用的微卫星标记物随时间推移是稳定的,因此可以用作可追溯性工具。 (C)2015 Elsevier B.V.保留所有权利。

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