Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers  被引量:1

Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers

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作  者:CHAO Wen-zheng TANG Chuan-hong ZHANG Jing-song YU Ling Honda Yoichi 

机构地区:[1]School of Perfume and Aroma Technology,Shanghai Institute of Technology [2]Key Laboratory of Edible Fungus Resources and Utilization (South),Ministry of Agriculture/National Engineering Research Center of Edible Fungi/National R&D Center for Edible Fungi Processing/Key Laboratory of Agriculture Genetics and Breeding of Shanghai,Institute of Edible Fungi,Shanghai Academy of Agricultural Sciences [3]Laboratory of Forest Biochemistry,Graduate School of Agriculture,Kyoto University

出  处:《Journal of Integrative Agriculture》2018年第1期130-138,共9页农业科学学报(英文版)

基  金:financially supported by the National Natural Science Foundation of China (31401933);the Shanghai Municipal Committee of Agriculture,China (G2014070107)

摘  要:The cultivar Ganoderma lucidum Hunong 5 was obtained using cross-breeding. Hunong 5 has high commercial value due to its high polysaccharide and triterpene content, This is the first report of using a DNA pooling method to develop a stable sequence characterized amplified region (SCAR) marker for rapid identification of the G. lucidum Hunong 5 cultivar. The SCAR marker was developed by first generating and sequencing a distinctive inter simple sequence repeat (ISSR) fragment (882 bp) from G. lucidum Hunong 5 cultivar. A stable SCAR primer pair GLH5F/GLH5R were obtained to identify the cultivar and the SCAR marker is a DNA fragment of 773 bp.The cultivar Ganoderma lucidum Hunong 5 was obtained using cross-breeding. Hunong 5 has high commercial value due to its high polysaccharide and triterpene content, This is the first report of using a DNA pooling method to develop a stable sequence characterized amplified region (SCAR) marker for rapid identification of the G. lucidum Hunong 5 cultivar. The SCAR marker was developed by first generating and sequencing a distinctive inter simple sequence repeat (ISSR) fragment (882 bp) from G. lucidum Hunong 5 cultivar. A stable SCAR primer pair GLH5F/GLH5R were obtained to identify the cultivar and the SCAR marker is a DNA fragment of 773 bp.

关 键 词:DNA pooling Ganoderma lucidum Hunong 5 cultivar ISSR marker SCAR marker 

分 类 号:S0[农业科学]

 

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