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Sensitive and Rapid Detection of Genetic Modified Soybean (Roundup Ready) by Loop-Mediated Isothermal Amplification
Liu, Mei1; Luo, Yan2; Tao, Ran1,3; He, Ru4; Jiang, Keyong1; Wang, Baojie1; Wang, Lei1; Wang, L, Chinese Acad Sci, R&D Ctr Marine Biotechnol, Inst Oceanol, Qingdao 266071, Peoples R China
2009-11-01
发表期刊BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
ISSN0916-8451
卷号73期号:11页码:2365-2369
文章类型Article
摘要Using the LAMP method, a highly specific and sensitive detection system for genetically modified soybean (Roundup Ready) was designed. In this detection system, a set of four primers was designed by targeting the exogenous 35S epsps gene. Target DNA was amplified and visualized on agarose gel within 45 min under isothermal conditions at 65 degrees C. Without gel electrophoresis, the LAMP amplicon was visualized directly in the reaction tube by the addition of SYBR Green I for naked-eye inspection. The detection sensitivity of LAMP was 10-fold higher than the nested PCR established in our laboratory. Moreover, the LAMP method was much quicker, taking only 70 min, as compared with 300 min for nested PCR to complete the analysis of the GM soybean. Compared with traditional PCR approaches, the LAMP procedure is faster and more sensitive, and there is no need for a special PCR machine or electrophoresis equipment. Hence, this method can be a very useful tool for GMO detection and is particularly convenient for fast screening.; Using the LAMP method, a highly specific and sensitive detection system for genetically modified soybean (Roundup Ready) was designed. In this detection system, a set of four primers was designed by targeting the exogenous 35S epsps gene. Target DNA was amplified and visualized on agarose gel within 45 min under isothermal conditions at 65 degrees C. Without gel electrophoresis, the LAMP amplicon was visualized directly in the reaction tube by the addition of SYBR Green I for naked-eye inspection. The detection sensitivity of LAMP was 10-fold higher than the nested PCR established in our laboratory. Moreover, the LAMP method was much quicker, taking only 70 min, as compared with 300 min for nested PCR to complete the analysis of the GM soybean. Compared with traditional PCR approaches, the LAMP procedure is faster and more sensitive, and there is no need for a special PCR machine or electrophoresis equipment. Hence, this method can be a very useful tool for GMO detection and is particularly convenient for fast screening.
关键词Loop-mediated Isothermal Amplification Roundup Ready (Rr) Soybean Genetically Modified Organism (Gmo) Detection
学科领域Biochemistry & Molecular Biology ; Biotechnology & Applied Microbiology ; Chemistry, Applied ; Food Science & Technology
DOI10.1271/bbb.80723
URL查看原文
收录类别SCI
语种英语
WOS记录号WOS:000272319900001
引用统计
被引频次:31[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/1854
专题海洋生物技术研发中心
通讯作者Wang, L, Chinese Acad Sci, R&D Ctr Marine Biotechnol, Inst Oceanol, Qingdao 266071, Peoples R China
作者单位1.Chinese Acad Sci, R&D Ctr Marine Biotechnol, Inst Oceanol, Qingdao 266071, Peoples R China
2.Ocean Univ China, Sch Life Sci, Qingdao 266003, Peoples R China
3.Rongcheng Entry Exit Inspect & Quarantine Bur, Rongcheng 264300, Peoples R China
4.Haerbin Univ Ind, Weihai Branch, Weihai 264209, Peoples R China
第一作者单位中国科学院海洋研究所
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Liu, Mei,Luo, Yan,Tao, Ran,et al. Sensitive and Rapid Detection of Genetic Modified Soybean (Roundup Ready) by Loop-Mediated Isothermal Amplification[J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY,2009,73(11):2365-2369.
APA Liu, Mei.,Luo, Yan.,Tao, Ran.,He, Ru.,Jiang, Keyong.,...&Wang, L, Chinese Acad Sci, R&D Ctr Marine Biotechnol, Inst Oceanol, Qingdao 266071, Peoples R China.(2009).Sensitive and Rapid Detection of Genetic Modified Soybean (Roundup Ready) by Loop-Mediated Isothermal Amplification.BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY,73(11),2365-2369.
MLA Liu, Mei,et al."Sensitive and Rapid Detection of Genetic Modified Soybean (Roundup Ready) by Loop-Mediated Isothermal Amplification".BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY 73.11(2009):2365-2369.
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