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作 者:张小平[1] 李登煜[1] NICK Giselle LINDSTR M Kristina
机构地区:[1]四川农业大学农学院应用微生物系
出 处:《应用与环境生物学报》1998年第1期70-73,共4页Chinese Journal of Applied and Environmental Biology
基 金:国家自然科学基金;联合国科教文组织生物工程基金
摘 要:用REP1R1和REP21DNA为引物,对22株四川土著慢生花生根瘤菌染色体DNA的基因外回文重复序列(RepetitiveExtrogenicpalindromicsequenceREP)进行了PCR扩增和凝胶电泳,并对电泳结果的指纹图型进行了相似性聚类分析.结果表明了四川土著慢生花生根瘤菌的遗传多样性.The distribution of repetitive DNA(repetitive extragenic palindromic )sequences in the genomes of 22 peanut bradyrhizobial strains isolated from the different cultivars and locations in Sichuan was examined by using conserved primers corresponding to repetitive extragenic palindromic sequences and polymerase chain reaction(PCR).The fingerprint patterns of the resulting REP PCR products were visualized on 1.5% agarose gel and found to be strain specific. The dendrogram generated on the basis of the similarities of the REP PCR fingerprint patterns grouped the strains in correspondence with the isolation sites and cultivars.This result indicated that Sichuan peanut bradyrhizobia were genetically very diverse since 7 clusters were formed among the 22 strains tested.REP PCR technique is a useful tool for the studies on the diversity of those closely related rhizobial and bradyrhizobial strains.
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