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A Reliable and Efficient Method for Total RNA Isolation from Various Members of Spurge Family (Euphorbiaceae)

机译:一种可靠有效的方法,可从大戟科(大戟科)的各个成员中提取总RNA

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Introduction - It is prerequisite and crucial to extract RNA with high quality and integrity in order to carry out molecular biology studies in any plant species of a family. Euphorbiaceae members are known for high levels of their waxes, oils with polysaccharides, polyphenolics and secondary metabolites. These conditions are recognised to interfere unfavourably with various methodologies of RNA isolation.Objective - To develop a simple, rapid and reproducible cetyltrimethylamonium bromide (CTAB)-based protocol, to reduce the time and cost of extraction without reducing quality and yield of RNA extracted from various recalcitrant Euphorbiaceae member plant tissues such as from tree leaves (Hevea brasilensis), woody shrubs leaves (Ricinus communis, Jatropha curcas, Manihot esculenta) and storage root tissue (M. esculenta).Methodology - Simple modifications and fast steps were introduced to the original CTAB protocol. All centrifugation steps were carried out at 4 degrees C at 12000 rpm for 10 min, the sample weight was decreased and usage of spermidine and LiCl was omitted, reducing incubation time prior to RNA precipitation. This rapid CTAB protocol was compared with various RNA isolation methods intended for use with plants rich in polysaccharides and secondary metabolites.Results - The procedure can be completed within 2 h and many samples can be processed at the same time. RNA of high quality could be isolated from all the tissues of species that we tried. The isolated RNA from different species served as a robust template for RT-PCR analysis.Conclusion - The study has shown that the improvement of a CTAB-based protocol allows the rapid isolation of high-quality RNA from various recalcitrant Euphorbiaceae members. Copyright
机译:简介-提取高质量和完整性的RNA以便在任何家族植物中进行分子生物学研究是前提和关键。大戟科成员以其高含量的蜡,含多糖的油,多酚和次生代谢产物而闻名。认识到这些条件会不利地干扰各种RNA分离方法。目的-开发简单,快速且可重现的十六烷基三甲基溴化铵(CTAB)方案,以减少提取时间和成本,而不会降低从中提取RNA的质量和产量各种顽强的大戟科成员植物组织,例如来自树叶(巴西橡胶树),木质灌木叶(Ricinus communis,Jatropha curcas,Manihot esculenta)和储藏根组织(M. esculenta)。原始CTAB协议。所有离心步骤均在4摄氏度,12000 rpm下进行10分钟,减少了样品重量,并省略了亚精胺和LiCl的使用,从而减少了RNA沉淀前的孵育时间。将该快速CTAB方案与旨在用于富含多糖和次生代谢产物的植物的各种RNA分离方法进行了比较。结果-该过程可在2 h内完成,并且可以同时处理许多样品。可以从我们尝试过的物种的所有组织中分离出高质量的RNA。来自不同物种的分离出的RNA为RT-PCR分析提供了强大的模板。结论-研究表明,基于CTAB的实验方案的改进可以从顽固的大戟科成员中快速分离出高质量的RNA。版权

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