Multiplex PCR for the detection of Lactobacillus pontis and two related species in a sourdough fermentation

被引:26
作者
Müller, MRA [1 ]
Ehrmann, MA [1 ]
Vogel, RF [1 ]
机构
[1] Tech Univ Munich, Lehrstuhl Tech Mikrobiol, D-85350 Freising, Germany
关键词
D O I
10.1128/AEM.66.5.2113-2116.2000
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 specific multiplex PCR assay based on the amplification of parts of the 16S rRNA molecule was designed. Primers derived from variable regions of the 16S rRNA provided a means of easily differentiating the species Lactobacillus pontis and Lactobacillus panis, They could be clearly discriminated from the phylogenetically related species Lactobacillus vaginalis, Lactobacillus oris, and Lactobacillus reuteri and from other lactobacilli commonly known to be present in sourdough, Other strains isolated together with L, pontis from an industrial sourdough fermentation could be clearly separated from these species by comparative sequence analysis and construction of a specific PCR primer. For a fast identification a DNA isolation protocol based on the ultrasonic lysis of cells from single colonies was developed. To demonstrate the potential of such techniques for tracking these organisms in a laboratory-scale fermentation, we combined the specific PCR assay with direct DNA extraction from the organisms in the sourdough without previous cultivation.
引用
收藏
页码:2113 / 2116
页数:4
相关论文
共 17 条
[1]   Culture-independent quantification of physiologically-active microbial groups in fermented foods using rRNA-targeted oligonucleotide probes: application to pozol, a Mexican lactic acid fermented maize dough [J].
Ampe, F ;
ben Omar, N ;
Guyot, JP .
JOURNAL OF APPLIED MICROBIOLOGY, 1999, 87 (01) :131-140
[2]   IDENTIFICATION OF LACTOCOCCI AND ENTEROCOCCI BY COLONY HYBRIDIZATION WITH 23S RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDE PROBES [J].
BETZL, D ;
LUDWIG, W ;
SCHLEIFER, KH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (09) :2927-2929
[3]  
Bocker G., 1995, GETREIDE MEHL BROT, V49, P370
[4]  
EHRMANN M, 1994, FEMS MICROBIOL LETT, V117, P143, DOI [10.1016/0378-1097(94)90186-4, 10.1111/j.1574-6968.1994.tb06756.x]
[5]  
Gänzle MG, 1998, APPL ENVIRON MICROB, V64, P2616
[6]   Characterization of the bacterial flora of Sudanese sorghum flour and sorghum sourdough [J].
Hamad, SH ;
Dieng, MC ;
Ehrmann, MA ;
Vogel, RF .
JOURNAL OF APPLIED MICROBIOLOGY, 1997, 83 (06) :764-770
[7]   IDENTIFICATION OF MESOPHILIC LACTIC-ACID BACTERIA BY USING POLYMERASE CHAIN REACTION-AMPLIFIED VARIABLE REGIONS OF 16S RIBOSOMAL-RNA AND SPECIFIC DNA PROBES [J].
KLIJN, N ;
WEERKAMP, AH ;
DEVOS, WM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (11) :3390-3393
[8]   RAPID SMALL-SCALE PREPARATION OF BACTERIAL GENOMIC DNA, SUITABLE FOR CLONING AND HYBRIDIZATION ANALYSIS [J].
LEWINGTON, J ;
GREENAWAY, SD ;
SPILLANE, BJ .
LETTERS IN APPLIED MICROBIOLOGY, 1987, 5 (03) :51-53
[9]   Biotechnology of bread baking [J].
Linko, YY ;
Javanainen, P ;
Linko, S .
TRENDS IN FOOD SCIENCE & TECHNOLOGY, 1997, 8 (10) :339-344
[10]   A new version of the RDP (Ribosomal Database Project) [J].
Maidak, BL ;
Cole, JR ;
Parker, CT ;
Garrity, GM ;
Larsen, N ;
Li, B ;
Lilburn, TG ;
McCaughey, MJ ;
Olsen, GJ ;
Overbeek, R ;
Pramanik, S ;
Schmidt, TM ;
Tiedje, JM ;
Woese, CR .
NUCLEIC ACIDS RESEARCH, 1999, 27 (01) :171-173