Gevers D, Huys G, Swings J
Laboratory of Microbiology, Department of Biochemistry, Ghent University, K.L. Ledeganckstraat 35, 9000 Gent, Belgium.
FEMS Microbiol Lett. 2001 Nov 27;205(1):31-6. doi: 10.1111/j.1574-6968.2001.tb10921.x.
PCR amplification of repetitive bacterial DNA elements fingerprinting using the (GTG)(5) primer ((GTG)(5)-PCR) was proven to be useful for differentiation of a wide range of lactobacilli (i.e. 26 different (sub)species) at the species, subspecies and potentially up to the strain level. Using this rapid and reproducible genotypic technique, new Lactobacillus isolates recovered from different types of fermented dry sausage could be reliable identified at the (sub)species level. In conclusion, (GTG)(5)-PCR was found to be a promising genotypic tool for rapid and reliable speciation and typing of lactobacilli and other lactic acid bacteria important in food-fermentation industries.
使用(GTG)₅引物进行重复性细菌DNA元件指纹图谱的PCR扩增((GTG)₅-PCR)已被证明可用于在种、亚种以及潜在的菌株水平上区分多种乳酸杆菌(即26个不同的(亚)种)。利用这种快速且可重复的基因型技术,从不同类型发酵干香肠中分离出的新型乳酸杆菌菌株能够在(亚)种水平上得到可靠鉴定。总之,(GTG)₅-PCR被发现是一种有前景的基因型工具,可用于乳酸杆菌及食品发酵工业中其他重要乳酸菌的快速可靠的物种鉴定和分型。