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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Method to purify mitochondrial DNA directly from yeast total DNA.
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Method to purify mitochondrial DNA directly from yeast total DNA.

机译:直接从酵母总DNA中纯化线粒体DNA的方法。

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During the purification of total DNA from yeast, both nuclear and mitochondrial DNA (mtDNA) molecules are obtained. Here, we describe a simple enzymatic method using a combination of lambda exonuclease and RecJ(f) to obtain pure and intact mtDNA by removing linear DNA from total DNA isolated from yeast cells. The combination of the two enzymes efficiently removed linear DNA from the total DNA of Candida (Torulopsis) glabrata, leaving the mtDNA intact. The purity and integrity of mtDNA was assayed by PCR amplification of ARG1/2/5/8, URA3 and COX1, and by RFLP analysis, respectively. This method can be used to prepare mtDNA for PCR amplification or RFLP analysis without the need for purification of mitochondria by gradient ultracentrifugation or fractional precipitation. The method was also successfully applied to the yeast species Saccharomyces cerevisiae, Candida utilis, Pichia pastoris and Yarrowia lypolytica.
机译:在从酵母中纯化总DNA的过程中,同时获得了核和线粒体DNA(mtDNA)分子。在这里,我们描述了一种简单的酶促方法,该方法结合使用了λ核酸外切酶和RecJ(f),通过从酵母细胞分离的总DNA中去除线性DNA来获得纯净和完整的mtDNA。两种酶的结合有效地从光滑念珠菌的总DNA中去除了线性DNA,而保持了完整的mtDNA。分别通过ARG1 / 2/5/8,URA3和COX1的PCR扩增以及RFLP分析来测定mtDNA的纯度和完整性。该方法可用于制备用于PCR扩增或RFLP分析的mtDNA,而无需通过梯度超速离心或分级沉淀纯化线粒体。该方法也成功地应用于酿酒酵母,假丝酵母​​,巴斯德毕赤酵母和耶氏酵母。

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