适合于胞质基因组扩增的红麻成熟叶片DNA提取改良方法
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

福建省科技厅南方黄/红麻种质资源创新平台


A New Extraction Method of Mature Kenaf Leaf ’s DNA for Cytoplasmic Genome Amplifying
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    为了从成熟红麻叶片中提取高质量、高产量的基因组DNA,针对红麻成熟叶片含多糖、多酚的特性,利用改良CTAB法及改良的SDS法分别提取红麻品种福红952成熟叶基因组DNA,并通过琼脂糖凝胶电泳和紫外分光光度计测定进行DNA质量检测。结果表明:改良CTAB法提取的基因组DNA电泳时点样孔干净,条带整齐无拖带,OD260/OD280 为1.9左右,产率可达1.84μg/g,其质量、产量都高于改良SDS法,所提取的DNA可用于红麻RAPD分子标记、线粒体DNA、叶绿体DNA通用引物PCR扩增。改良CTAB法是提取成熟红麻叶片中高质量、高产量基因组DNA的有效方法,并且可用于红麻分子标记及胞质基因组学研究。

    Abstract:

    The research aimed to extract the high quality and yield genomic DNA from mature kenaf(Hibiscus cannabinus L.) leaves.According to the character of containing amylase and polyphenol,the kenaf varieties Fuhong 952 mature leaves were extracted by improved CTAB and SDS method, and they were identified by agarose gel electrophoresis,ultraviolet spectrophotometer method.The results showed that the sample hole was clean and no pulling,OD260/OD280 was about 1.9,the yield was up to 1.84μg/g . when the genomic DNA extracted by improved CTAB method was electrophoresis.and its quality and yield was higher than that extracted by improved SDS method. Genomic DNA extracted by improved CTAB also can be used in kenaf RAPD ( Random Amplified Polymorphic DNA) Molecular markers, mitochondrial DNA, chloroplast DNA universal primer PCR amplification .therefor, the improved CTAB method was the effective methed of extracting the high quality and yield genomic DNA from mature kenaf leaves,and can be used for the kenaf molecular markers and cytoplasmic genomics research.

    参考文献
    相似文献
    引证文献
引用本文

徐建堂,祁建民,陈涛,等.适合于胞质基因组扩增的红麻成熟叶片DNA提取改良方法[J].植物遗传资源学报,2013,14(2):347-351.

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2012-04-19
  • 最后修改日期:2012-07-10
  • 录用日期:2013-01-15
  • 在线发布日期: 2013-01-29
  • 出版日期:
您是第位访问者
ICP:京ICP备09069690号-23
京ICP备09069690号-23
植物遗传资源学报 ® 2024 版权所有
技术支持:北京勤云科技发展有限公司