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Comparative Different DNA Isolation Protocols from Ziziphus spina-christi (L.) Leaves through RAPD and ISSR Markers

机译:通过RAPD和ISSR标记从刺枣(L.)的叶子中比较不同的DNA分离方案

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Genomic analysis of plants relies on high quantity and quality of pure DNA. Extraction and purification of DNA from woody and medicinal plants, such as fruit trees present a great challenge due to accumulation of a large amount of co-purify with DNA, including polysaccharides, polyphenols and proteins. Therefore, it is necessary to optimize the extraction protocols to reduce these compounds to the lowest level. A study was conducted to compare six DNA extraction and precipitation methods for genomic analysis in Ziziphus spina-christi (L.) plant tissues. The results showed significant differences in DNA contents among the six methods. Quantity and quality of extracted genomic DNAs were compared by employing the spectrophotometer, Nano-Drop, agarose gel electrophoresis, digestion by restriction enzymes and polymerase chain reaction (PCR) methods and molecular marker such as RAPD and ISSR. The method of Vroh Bi et al., provided the best results (208.89 ng/μL) in terms of quantity and quality of DNA, and Doyle and Doyle method as second method for leaves sample were chosen. According to the results, the method of Bi et al. is recommended for DNA extraction from plant tissues having high level of polysaccharides and phenol compounds.
机译:植物的基因组分析取决于大量和高质量的纯DNA。从木本和药用植物(例如果树)中提取和纯化DNA提出了巨大的挑战,这是因为积累了大量与DNA共同纯化的产物,包括多糖,多酚和蛋白质。因此,有必要优化提取方案以将这些化合物减少到最低水平。进行了一项研究,以比较六种DNA提取和沉淀方法,用于在Ziziphus spina-christi(L.)植物组织中进行基因组分析。结果表明,这六种方法的DNA含量存在显着差异。通过分光光度计,Nano-Drop,琼脂糖凝胶电泳,限制性内切酶和聚合酶链反应(PCR)方法以及RAPD和ISSR等分子标记对提取的基因组DNA的数量和质量进行比较。 Vroh Bi等人的方法在DNA的数量和质量方面提供了最好的结果(208.89 ng /μL),并且选择了Doyle和Doyle方法作为叶片样品的第二种方法。根据结果​​,Bi等人的方法。推荐从多糖和酚类化合物含量高的植物组织中提取DNA。

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