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A PCR technique based on the Hip1 interspersed repetitive sequence distinguishes cyanobacterial species and strains

机译:基于Hip1散布的重复序列的PCR技术可以区分蓝细菌的种类和菌株

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摘要

The use of primers based on the Hip1 sequence as a typing technique for cyanobacteria has been investigated. The discovery of short repetitive sequence structures in bacterial DNA during the last decade has led to the development of PCR-based methods for typing, i.e. distinguishing and identifying, bacterial species and strains. An octameric palindromic sequence known as Hip1 has been shown to be present in the chromosomal DNA of many species of cyanobacteria as a highly repetitious interspersed sequence. PCR primers were constructed that extended the Hip1 sequence at the 3' end by two bases. Five of the 16 possible extended primers were tested. Each of the five primers produced a different set of products when used to prime PCR from cyanobacterial genomic DNA, Each primer produced a distinct set of products for each of the 15 cyanobacterial species tested. The ability of Hip1-based PCR to resolve taxonomic differences was assessed by analysis of independent isolates of Anabaena flos-aquae and Nostoc ellipsosporum obtained from the CCAP (Culture Collection of Algae and Protozoa, IFE, Cumbria, UK), A PCR-based RFLP analysis of products amplified from the 23S-16S rDNA intergenic region was used to characterize the isolates and to compare with the Hip1 typing data. The RFLP and Hip1 typing yielded similar results and both techniques were able to distinguish different strains. On the basis of these results it is suggested that the Hip1 PCR technique may assist in distinguishing cyanobacterial species and strains.
机译:已经研究了使用基于Hip1序列的引物作为蓝细菌的分型技术。在过去的十年中,细菌DNA中短重复序列结构的发现导致了基于PCR的方法的发展,该方法用于分类,即区分和鉴定细菌种类和菌株。已经显示出称为Hip1的八聚体回文序列以高度重复的散布序列存在于许多蓝细菌物种的染色体DNA中。构建了PCR引物,该引物将Hip1序列在3'端延伸了两个碱基。测试了16种可能的引物中的5种。当用于从蓝细菌基因组DNA进行PCR引物时,五种引物中的每一种都产生不同的一组产物。对于所测试的15种蓝细菌物种中的每一种,每种引物产生一套不同的产物。基于Hip1的PCR解决分类学差异的能力是通过分析从CCAP(藻类和原生动物的培养物保藏中心,IFE,坎布里亚郡,英国)获得的鱼腥藻和Nostoc ellipsosporum的独立分离物的分析来评估的从23S-16S rDNA基因间区域扩增的产物的分析用于表征分离物并与Hip1分型数据进行比较。 RFLP和Hip1分型产生相似的结果,并且两种技术都能够区分不同的菌株。根据这些结果,建议Hip1 PCR技术可能有助于区分蓝细菌的种类和菌株。

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