木薯块根总RNA提取方法的比较和改进  被引量:4

Comparison and Improvement of the Method of Extraction Total RNA form Tubers of Manihot esculenta Crantz

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作  者:余洁[1] 郭运玲[1] 郭安平[1] 贺立卡[1] 

机构地区:[1]中国热带农业科学院热带生物技术研究所,海南海口571101

出  处:《安徽农业科学》2008年第12期4872-4873,4887,共3页Journal of Anhui Agricultural Sciences

基  金:中央级公益性科研院所基本科研业务费项目"热带能源植物遗传改良与分子育种"中国热带农业科学院科技基金项目(RKY0724)

摘  要:[目的]为更好地利用基因操作手段改良木薯品质和提取高质量的木薯总RNA提供科学依据。[方法]采用4种方法提取木薯块根RNA,筛选一种最简单、有效的方法,并利用RT-PCR技术克隆木薯淀粉分支酶,分析所提取RNA的质量。[结果]结果表明,用改进的CTAB法和plant RNAReagent kit均能提取高质量的RNA,用plant RNAReagent更能节省时间,而且纯度比较高。对plant RNAReagent提取的RNA进行RT-PCR克隆,克隆出了与木薯淀粉合成有关的SBEII基因。[结论]plant RNAReagent kit提取的RNA,其质量可以满足基本的试验要求。[Objective] The purpose was to provide the scientific basis for improving the quality of Manihot esculenta Crantz and extracting the high-quality total RNA form tubers of Manihot esculenta Crantz by genic method.[Method]The best simple and effective method from four measures which can extract RNA form tubers of Manihot esculenta Crantz was applied.Branching enzyme of cassava was cloned with RT-PCR technology and the quality of RNA extracted was analyzed.[Result] The results showed that the developed CTAB and plant RNA Reagent kit could get the high-quality RNA,and the latter was with the less time and higher purity.By RT-PCR cloning RNA extracted with plant RNA Reagent kit,SBELL gene which was related to synthesis of the cassava was got.[Conclusion]The quality of RNA extracted with plant RNA Reagent kit can meet the demands for experiment.

关 键 词:木薯 块根 总RNA提取 SBEII基因 基因克隆 

分 类 号:S533[农业科学—作物学]

 

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