首页 | 本学科首页   官方微博 | 高级检索  
     检索      

纤毛虫单细胞基因组DNA微量提取方法的比较及优化
引用本文:伊珍珍,黄丽娟,李继秋,林晓凤.纤毛虫单细胞基因组DNA微量提取方法的比较及优化[J].中国海洋大学学报(自然科学版),2012(Z2):60-63.
作者姓名:伊珍珍  黄丽娟  李继秋  林晓凤
作者单位:华南师范大学生命科学学院,广东省高等学校生态与环境科学重点实验室
基金项目:国家自然科学基金项目(41006098;31071893);广东高校优秀青年创新人才培养计划(LYM10060)资助
摘    要:在纤毛虫的分子生物学研究中,单细胞基因组DNA的微量提取是后续基因分析的关键。本研究以海洋纤毛虫红色伪角毛虫为材料,采用直接取完整虫体、裂解法以及3种改良后的试剂盒微量提取DNA方法,分别提取了新鲜样品与4种不同方法保存样品的基因组DNA,比较了9种组合在PCR产物质量、提取所需时间、成本及便捷性方面的优劣,并进一步比较、讨论和探索了4种样品保存方法和5种DNA微量提取方法在纤毛虫单细胞基因组PCR扩增中的可行性。本工作旨在为后续的纤毛虫分子生物学研究提供可资借鉴的技术路线和方法。

关 键 词:纤毛虫  红色伪角毛虫  单细胞DNA微量提取  样品保存  基因扩增

Comparison and Improvement of DNA Micro-Extraction Methods Using Single Cell of Ciliates
YI Zhen-Zhen,HUANG Li-Juan,LI Ji-Qiu,LIN Xiao-Feng.Comparison and Improvement of DNA Micro-Extraction Methods Using Single Cell of Ciliates[J].Periodical of Ocean University of China,2012(Z2):60-63.
Authors:YI Zhen-Zhen  HUANG Li-Juan  LI Ji-Qiu  LIN Xiao-Feng
Institution:(The Key Laboratory of Ecology and Environment Science in Guangdong Higher Education,South China Normal University,Guangzhou 510631,China)
Abstract:DNA micro-extraction is one of the bottlenecks for molecular investigations on ciliated protozoa since most ciliates are difficult to be cultured.Using Pseudokeronopsis rubra,a marine hypotrichous ciliate,as sample,five DNA micro-extraction methods(viz.three improved DNA micro-extraction kit methods,lysis method and using single cell directly) for living single cell and four sample preservation methods(viz.95% alcohol with 100μM EDTA,two kits) are performed.By comparing these nine combination methods for DNA micro-extraction and sample preservation,following conclusions could be drawn: REDExtract-N-AmpTM Tissue PCR Kit and lysis method are the best ones for living samples,and DNeasy Blood & Tissue Kit and Indicating Whatman FTA Elute Cards are suggested for DNA micro-extraction of environmental samples,which could not be treated in time.
Keywords:ciliates  Pseudokeronopsis rubra  DNA micro-extraction of single cell  sample preservation  gene amplification
本文献已被 CNKI 等数据库收录!
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