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作 者:宋驰[1,2] 陈强[2] 徐璟煜[2] 张金霞[2] 边银丙[1] 黄晨阳[2]
机构地区:[1]华中农业大学应用真菌研究所,武汉430070 [2]中国农业科学院农业资源与农业区划研究所,北京100081
出 处:《菌物学报》2011年第4期663-668,共6页Mycosystema
基 金:中央级公益性科研院所基本科研业务费专项(No.2009-13)
摘 要:以侧耳属Pleurotus15个种的15个菌株为材料,根据GenBank上侧耳属细胞色素c氧化酶亚基Ⅰ基因(cytochrome c oxidase subunit1gene,CO1)序列信息,设计引物CO332F、CO332R,进行第一轮PCR扩增,结果显示所有菌株都能得到单一条带,根据条带大小,15个菌株可分为4组。随后针对每个种设计特异性引物,进行第二轮PCR扩增,结果显示每个菌株只有在自己特异的引物中出现目的条带。通过两轮扩增,根据扩增条带的大小和有无,即可对15个种进行快速鉴定。15 strains belonging to 15 species of Pleurotus were used.Primer CO332F and CO332R were designed by the cytochrome c oxidase subunit 1 gene (CO1) sequence of Pleurotus downloaded from GenBank.Results of the first-step PCR amplification showed that all the strains can get one band.The 15 strains were divided into four groups by the band size.Species-specific primers were designed accordingly.Results of the second-step PCR amplification showed that each species can get one band by the species-specific primers.In conclusion,the 15 species of Pleurotus can be identified by two-step PCR in accordance with the band size and the presence or absence of the band.
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