首页 | 本学科首页   官方微博 | 高级检索  
     

不同处理对柿属植物DNA提取产率和品质的影响
引用本文:易庆平,罗正荣. 不同处理对柿属植物DNA提取产率和品质的影响[J]. 西北农业学报, 2012, 21(8): 158-163
作者姓名:易庆平  罗正荣
作者单位:1. 湖北省荆楚理工学院生物工程学院,湖北荆门,448200
2. 华中农业大学,园艺植物生物学教育部重点实验室,武汉430070
基金项目:国家自然科学基金(30900975);高等学校博士学科点专项科研基金(20110146110018)
摘    要:
基于CTAB法对鄂柿一号、前川次郎、君迁子3份材料进行DNA提取纯化,探讨不同采样时期、不同的纯化及沉淀方法对柿属植物DNA产率和品质的影响.结果表明,不同时期采样对DNA产率影响很大,随叶片生长,DNA产率不断下降,成熟叶片DNA产率仅为幼嫩叶片的16.7%~19.4%;在苯酚氯仿法、高盐乙醚法、CTAB沉淀法中以高盐乙醚法效果最好,可酶切,能有效去除多糖污染,产率较高;4种沉淀方法中,高浓度的盐溶液有助于去除多糖、多酚等杂质,相比单纯的乙醇或异丙醇沉淀可获得更高品质的DNA.另外,不同材料间提取DNA难度存在较大差异.

关 键 词:柿属植物  DNA提取纯化  优化

Effect of Different Treatments on Genomic DNA Extraction in Diospyros spp
YI Qingpingand LUO Zhengrong. Effect of Different Treatments on Genomic DNA Extraction in Diospyros spp[J]. Acta Agriculturae Boreali-occidentalis Sinica, 2012, 21(8): 158-163
Authors:YI Qingpingand LUO Zhengrong
Affiliation:1.Department of Bio-Engineering,Jingchu College of Technology,Jingmen Hubei 448200,China;2.Key Laboratory of Horticultural Plant Biology,Ministry of Education,Huazhong Agricultural University,Wuhan 430070,China)
Abstract:
The efficiency of many nucleic acid isolation techniques is affected by the presence of plant metabolites such as polysaccharides,polyphones,etc.Based on CTAB DNA extraction method,some treatments with different sampling,purifying and precipitating were studied to preserve the effect on genomic DNA extraction in three materials of Diospyros spp.The results indicated that as the tissue developed,the yield of DNA decreased.Compared with tender shoots,the amount of DNA from mature leaves was 16.7%-18.4%.Among three purification methods,the high salt/water-saturated ether obtained high-quality easily digested DNA with higher yield.In addition,add high concentration salt before organic precipitation is helpful to remove the impurity,could gain higher-quality DNA.The efficiency of DNA extraction form cultivars differs much.
Keywords:Diospyros spp  DNA extraction and purification  Optimize
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《西北农业学报》浏览原始摘要信息
点击此处可从《西北农业学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号