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Comparative Evaluation of Three Different Extraction Methods for Rice(Oryza sativa L.)Genomic DNA

机译:三种水稻提取基因组DNA提取方法的比较评价

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Recently,more immediate and precise cultivar-identifying methods targeting the specific and/or introduced gene(s)have been put into practical use for various rice cultivars.However trustworthy and innovative the biotechnological analyses may be,DNA purity and quality do have unpredictable influences upon the identification.Extraction methods of rice DNA have hardly ever been compared in a comprehensive manner.In this study,we investigated extraction characteristics of three methods by using 10 rice cultivars and then examined template availability of rice DNAs thereby extracted.An UV spectrophotometric study with a view toward methods revealed three different facts:The Isoplant II kit method with inhibitor absorption yielded the most DNAs,the Takara kit method with magnetic trapping produced the best DNAs free from contaminative proteins,and the enzymatic digestion method exclusively with enzymatic digestions prepared the best DNAs free from contaminative polysaccharides.Moreover,with a view toward cultivars,an insignificant difference in yield was not entirely bore out,and some difference in cultivar might cause significant difference in yield;however,no significant difference in purity was found among the cultivars used.On the other hand,electrophoretic images of the DNAs from the same cultivars showed considerable differences in quality among the methods.Furthermore,the DNA extracts from certain brands of rice proved really available for cultivar identification by using polymerase chain reaction(PCR)related to sequence-tagged sites.Therefore,this study suggested that these extraction methods may be used as the situation demands and that the DNAs thereby extracted might work successfully even in cultivar-identifying PCRs.
机译:最近,针对特定和/或导入基因的更直接,更精确的品种鉴定方法已在各种水稻品种中得到实际应用。尽管生物技术分析值得信赖和创新,但DNA纯度和质量确实具有不可预测的影响几乎没有全面比较过稻米DNA的提取方法。在本研究中,我们研究了使用10个水稻品种的三种方法的提取特性,然后检查了由此提取的稻米DNA的模板可用性。从方法角度出发,揭示了三个不同的事实:具有抑制剂吸收作用的Isoplant II试剂盒产生了最多的DNA,采用磁阱的Takara试剂盒方法产生了无污染蛋白质的最佳DNA,仅通过酶消化的酶消化方法制备了DNA。不含污染多糖的最佳DNA。此外,从品种的角度来看,产量的微小差异并没有完全消除,品种上的一些差异可能会导致产量的显着差异;然而,所使用的品种之间在纯度上却没有显着差异。相同品种的DNA在方法上质量上有很大差异。此外,通过使用与序列标记位点相关的聚合酶链反应(PCR),证明某些品牌大米的DNA提取物确实可用于品种鉴定。因此,本研究因此,建议根据情况需要使用这些提取方法,并且由此提取的DNA即使在鉴定品种的PCR中也可能成功工作。

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