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Molecular differentiation of Lactococcus lactis subspecies lactis andcremoris strains by ribotyping and site specific-PCR

机译:核糖分型和位点特异性PCR技术鉴定乳酸乳球菌乳酸亚种和cremoris菌株

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摘要

Twenty-five strains of Lactococcus lactis subspecies lactis and subspecies cremoris obtained from dairy industry and environmental collections were examined by 16S RNA automated ribotyping profiles and site-specific PCR (S-PCR). By automated ribotyping, the majority of strains were classified in accordance with phenotypic characterization, with the exception of one lactis (220) and two cremoris (BO32 and 140) strains. A complete differentiation of subspecies lactis and cremoris in agreement with conventional phenotypic methods was achieved by S-PCR with a set of site-specific primer pairs (PR1, RM4, and F3) designed particularly from a deletion region found in subspecies cremoris, but not in lactis, Therefore, S-PCR with primers (PR1, RM4, and F3) is a rapid and very sensitive method for the distinction of lactis and cremoris subspecies in dairy production.
机译:通过16S RNA自动核型分析和位点特异性PCR(S-PCR)检查了从乳品工业和环境收集物中获得的25个乳酸乳球菌乳酸亚种和cremoris亚种。通过自动核糖分型,除了一株乳酸菌(220)和两株creemoris(BO32和140)菌株外,大多数菌株根据表型特征分类。通过S-PCR,使用一组专门针对从creemoris亚种中发现的缺失区域设计的位点特异性引物对(PR1,RM4和F3)进行S-PCR,从而与常规表型方法完全分离出乳酸亚种和cremoris亚种。因此,用引物(PR1,RM4和F3)进行S-PCR是在乳制品生产中区分乳酸亚种和cremoris亚种的快速且非常灵敏的方法。

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