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PCR结合变性高效液相色谱快速检测发酵乳酸杆菌

Rapid detection of Lactobacillus fermentum by PCR-DHPLC
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摘要 采用多聚酶链式反应结合变性高效液相色谱技术建立了发酵乳酸杆菌的快速检测方法。以编码发酵乳酸杆菌Lactobacillus fermentum延伸因子(EF-Tu)基因为靶基因设计引物,优化PCR体系,以加氏乳酸杆菌等26株试验菌株做特异性检测;并将标准菌株稀释成不同梯度,做灵敏度检测。试验结果表明,该方法有很好的特异性,且灵敏度高,检测限可达到100CFU/ml。 Rapid detection of Lactobacillus fermentum was established by using polymerase chain reaction(PCR) and denaturing high-performance liquid chromatography(DHPLC).The primers were designed and the PCR system was optimized with the elongation factor(EF-Tu) of L.fermentum as the target gene.Twenty-six strains including L.gasseri were tested with specific detection.The sensitivity of various diluted standard strains were determined.The results indicated that the PCR-DHPLC method was specific and sensitive with a detection limit of 100 CFU/ml.
出处 《渔业科学进展》 CSCD 北大核心 2011年第3期111-115,共5页 Progress in Fishery Sciences
基金 国家质检总局课题(2008IK140 2009IK170)资助
关键词 发酵乳酸杆菌 PCR 变性高效液相色谱 检测 Lactobacillus fermentum PCR DHPLC Detection
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