王萍亚,金雨婷,黄朱梁,汤海凤,孙 瑛,赵 进,管 峰.乌贼DNA条形码的筛选与验证[J].食品安全质量检测学报,2019,10(17):5809-5815
乌贼DNA条形码的筛选与验证
Selection and verification of DNA barcoding for cuttlefish
投稿时间:2019-06-25  修订日期:2019-09-02
DOI:
中文关键词:  DNA条形码  引物组  优化  乌贼鉴定
英文关键词:DNA barcoding  primer sets  optimization  cuttlefish identification
基金项目:浙江省科技计划项目(2017C32081)
作者单位
王萍亚 舟山市食品药品检验检测研究院 
金雨婷 中国计量大学生命科学学院 
黄朱梁 舟山市食品药品检验检测研究院 
汤海凤 舟山市食品药品检验检测研究院 
孙 瑛 舟山市食品药品检验检测研究院 
赵 进 中国计量大学生命科学学院 
管 峰 中国计量大学生命科学学院 
AuthorInstitution
WANG Ping-Ya Zhoushan Institute for Food and Drug Inspection and Testing 
JIN Yu-Ting College of Life Sciences, China Jiliang University 
HUANG Zhu-Liang Zhoushan Institute for Food and Drug Inspection and Testing 
TANG Hai-Feng Zhoushan Institute for Food and Drug Inspection and Testing 
SUN Ying Zhoushan Institute for Food and Drug Inspection and Testing 
ZHAO Jin College of Life Sciences, China Jiliang University 
GUAN Feng College of Life Sciences, China Jiliang University 
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中文摘要:
      目的 筛选适于鉴定乌贼的DNA条形码, 建立鉴定舟山常见乌贼种类的DNA条形码技术体系。方法 用聚合酶链反应(polymerase chain reaction, PCR)对现有5组DNA条形码引物组合进行了筛选, 设计一对新的DNA条形码引物以供筛选备用。结果 现有引物与部分乌贼的DNA模板存在错配而缺乏通用性, 在部分乌贼DNA的扩增受阻。本实验设计的12S rRNA基因引物可以特异性扩增乌贼的DNA, 提高了乌贼鉴定的准确度。结论 本研究设计的12S rRNA基因引物可以作为现有乌贼DNA条形码鉴定的补充。
英文摘要:
      Objective To find the most suitable DNA barcoding primers and develop the DNA barcoding technology system for identification of Zhoushan cuttlefish species. Methods Five existing DNA barcoding primer sets were chosen and optimized by polymerase chain reaction (PCR), and another new primer pair was designed for further selection in this study. Results The existed 5 DNA barcoding primer sets had mismatched base with part of cuttlefish DNA samples, which resulted in PCR amplification was blocked in some cuttlefish species. The new designed pair of primer pair could amplify cuttlefish 12S rRNA region specifically, which improved the efficiency and accuracy of species identification. Conclusion The 12S rRNA gene primer designed in this experiment can be used as a supplement to the identification of existing squid DNA barcodes.
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