An efficient and simple CTAB based method for total genomic DNA isolation from low amounts of aquatic plants leaves with a high level of secondary metabolites

S. Afsharzadeh, Shabnam Abbasi
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引用次数: 6

Abstract

An efficient DNA isolation protocol specifically modified to get pure quality DNA required for molecular studieshas been reported in this paper. Some aquatic plants (Potamogeton spp., Ceratophyllum demersum and Myriophyllum spicatum) were used for the study. The protocol developed will be useful in getting high and pure DNA. Instead of using the available DNA extraction kits, this protocol can be used to get pure quality DNA, freefrom proteins and polysaccharide compounds. The absorbance rate A260/A280 was 1.92 ± 0.069 and A260/A230 was 1.73 by spectrophotometer and NanoDrop machines which showed the sample genomic DNA is pure, free from contaminant proteins and polyphenolics/polysaccharides compound. The highest concentration of DNA was 640 ± 340.58 ng/μl when measured at 260 nm. When we run on agarose gel also, the isolated DNA gave a clear and sharp band. Thus, the DNA does not need any additional purification before proceeding for molecular analysis of the isolated DNA samples. This protocol is very simple and economical which will find wide applications in genomic studies of aquatic plants.
一种高效、简单的基于CTAB的方法,用于从少量具有高水平次生代谢产物的水生植物叶片中分离总基因组DNA
本文报道了一种有效的DNA分离方案,专门用于获得分子研究所需的纯质量DNA。以几种水生植物为研究对象,分别为马铃薯属植物、长尾角藻属植物和细刺狐尾藻属植物。该方案将有助于获得高纯度的DNA。代替使用现有的DNA提取试剂盒,该方案可用于获得纯质量的DNA,不含蛋白质和多糖化合物。通过分光光度计和NanoDrop仪检测到A260/A280的吸光度为1.92±0.069,A260/A230的吸光度为1.73,表明样品基因组DNA纯度高,不含蛋白质和多酚类/多糖化合物。260 nm处DNA浓度最高,为640±340.58 ng/μl。当我们在琼脂糖凝胶上运行时,分离的DNA呈现出清晰而锐利的条带。因此,在分离的DNA样品进行分子分析之前,DNA不需要任何额外的纯化。该方法简便、经济,在水生植物基因组学研究中具有广泛的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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