DNA probe and PCR-specific reaction for Lactobacillus plantarum

被引:103
作者
Quere, F
Deschamps, A
Urdaci, MC
机构
[1] UNIV BORDEAUX 1,ISTAB,LAB MICROBIOL & BIOTECHNOL,ENITA,F-33405 TALENCE,FRANCE
[2] UNICOPA NUTR ANIM,LANGUIDIC,FRANCE
关键词
D O I
10.1046/j.1365-2672.1997.00157.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A 300 bp DNA fragment of Lactobacillus plantarum isolated by randomly amplified polymorphic DNA (RAPD) analysis was cloned and sequenced. This fragment was tested using a dot-blot DNA hybridization technique for its ability to identify Lact. plantarum strains. This probe hybridized with all Lact. plantarum strains tested and with some strains of Lact. pentosus, albeit more weakly. Two internal primers of this probe were selected (LbP11 and LbP12) and polymerase chain reaction (PCR) was carried out, All Lact. plantarum strains tested amplified a 250 bp fragment contrary to the other LAB species tested, This specific PCR for Lact. plantarum was also performed from colonies grown on MRS medium with similar results. These methods enabled the rapid and specific detection and identification of Lact. plantarum.
引用
收藏
页码:783 / 790
页数:8
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