首页 | 本学科首页   官方微博 | 高级检索  
     

基于简单加权分析的花椒果皮DNA快速提取方法比较研究
引用本文:易秋菊,邢冉冉,王琳,葛毅强,陈 颖.基于简单加权分析的花椒果皮DNA快速提取方法比较研究[J].食品安全质量检测技术,2024,15(6):101-108.
作者姓名:易秋菊  邢冉冉  王琳  葛毅强  陈 颖
作者单位:中国检验检疫科学研究院,中国检验检疫科学研究院,中国检验检疫科学研究院,中国农业大学食品科学与营养工程学院;中国农村技术开发中心,中国检验检疫科学研究院
基金项目:国家市场监督管理总局科技计划项目(2022MK193)、国家重点研发计划项目(2023YFF1104700)
摘    要:目的 开发和探究适用于花椒基因组DNA的快速提取方法。方法 选取8种不同品种的花椒,分别利用3种不同的DNA提取方法,包括一管式植物DNA抽提试剂盒、基于载体的纤维素滤纸提取法和无菌拭子浸入法,进行花椒果皮基因组DNA快速提取,比较不同DNA提取方法在花椒果皮基因组提取中的效果。其中纤维素滤纸提取法和无菌拭子浸入法均通过载体转移进行DNA的快速提取,基于十六烷基三甲基溴化铵(hexadecyl trimethyl ammonium bromide, CTAB)和十二烷基硫酸钠(sodium dodecyl sulfate, SDS)两种不同的裂解液,在3 min以内即可提取DNA并得到聚合酶链式反应(polymerase chain reaction, PCR)扩增体系。通过简单加权(simple additive weighting, SAW)分析,基于PCR扩增能力、提取时间、提取成本、试剂安全性、程序简单性等方面进行综合评分。结果 所选的快速提取试剂盒不适用于花椒果皮这类含次生代谢物较多的实验材料,而无菌拭子、纤维素滤纸两种载体提取得到的花椒果皮DNA均可以进行后续的PCR操作,...

关 键 词:花椒果皮  DNA提取  简单加权  快速提取
收稿时间:2023/12/26 0:00:00
修稿时间:2024/3/15 0:00:00

A comparative study on the rapid extraction methods of Zanthoxylum pericarp dna based on simple weighted analysis
YI Qiuju,XING Ranran,WANG Lin,GE Yiqiang and CHEN Ying.A comparative study on the rapid extraction methods of Zanthoxylum pericarp dna based on simple weighted analysis[J].Food Safety and Quality Detection Technology,2024,15(6):101-108.
Authors:YI Qiuju  XING Ranran  WANG Lin  GE Yiqiang and CHEN Ying
Abstract:Objective To develop and explore a rapid extraction method for genomic DNA of Zanthoxylum. Methods Eight different varieties of Zanthoxylum were selected, and 3 kinds of different DNA extraction methods, including one-tube plant DNA extraction kit, carrier-based cellulose filter paper extraction method and sterile swab immersion method, were used to quickly extract genomic DNA from the peel of Zanthoxylum, and the effects of different DNA extraction methods on the extraction of genomic DNA from the peel of Zanthoxylum were compared. Among them, the cellulose filter paper extraction method and the sterile swab immersion method were used to quickly extract DNA by vector transfer. Based on two different lysis buffers of hexadecyl trimethyl ammonium bromide (CTAB) and sodium dodecyl sulfate (SDS), DNA could be extracted in less than 3 minutes and a polymerase chain reaction (PCR) amplification system was obtained. Through simple additive weighting (SAW) analysis, comprehensive scoring was performed based on PCR amplification ability, extraction time, extraction cost, reagent safety, and program simplicity. Results The selected rapid extraction kit was not suitable for experimental materials containing more secondary metabolites such as Zanthoxylum pericarp, while the DNA extracted from the pericarp of Zanthoxylum by sterile swab and cellulose filter paper could be used for subsequent PCR operations, and finally, the CTAB cellulose filter paper method ranked first with its advantages of low cost, short time and high amplification efficiency. Conclusion In this study, a rapid extraction method suitable for the genomic DNA of Zanthoxylum pericarp is explored, and the CTAB cellulose filter paper method is the best choice through SAW analysis, indicating that the vector transfer method can be used as one of the rapid extraction methods for the genomic DNA of Zanthoxylum, which provide areference scheme for the rapid extraction of Zanthoxylum genomic DNA, and provide a reference for the rapid extraction of similar animal and plant genomic DNA.
Keywords:Zanthoxylum pericarp  DNA extraction  simple additive weighting  fast extraction
点击此处可从《食品安全质量检测技术》浏览原始摘要信息
点击此处可从《食品安全质量检测技术》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