首页> 外文期刊>Journal of Microbiological Methods >Development of a quantitative PCR assay for rapid detection of Lactobacillus plantarum and Lactobacillus fermentum in cocoa bean fermentation
【24h】

Development of a quantitative PCR assay for rapid detection of Lactobacillus plantarum and Lactobacillus fermentum in cocoa bean fermentation

机译:用于快速检测乳酸杆菌和乳杆菌发酵乳杆菌和乳杆菌发酵乳杆菌测定的定量PCR测定

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

To monitor dominant species of lactic acid bacteria during cocoa bean fermentation, i.e. Lactobacillus plantarum and Lactobacillus fermentum, a fast and reliable culture-independent qPCR assay was developed. A modified DNA isolation procedure using a commercial kit followed by two species-specific qPCR assays resulted in 100% sensitivity for L. plantarum and L. fermentum. Kruskal-Wallis and post-hoc analyses of data obtained from experiments with cocoa beans that were artificially spiked with decimal concentrations of L. plantarum and L. fermentum strains allowed the calculation of a regression line suitable for the estimation of both species with a detection limit of 3 to 4 Log cells/g cocoa beans. This process was successfully tested for efficacy through the analyses of samples from laboratory-scale cocoa bean fermentations with both the qPCR assay and a culture-dependent method which resulted in comparable results. (C) 2015 Elsevier B.V. All rights reserved.
机译:为了监测可可豆发酵过程中乳酸菌的显性种类,即乳酸杆菌和乳杆菌乳酸乳杆菌,开发了一种快速且可靠的培养型QPCR测定。 使用商业套件的改性DNA隔离程序,然后使用两种特异性的QPCR测定,导致L.Playarum和L.Fermentum的100%敏感性。 Kruskal-wallis和Hoc型从实验中获得的数据和HOC分析,所述可可豆与L.Playarum和L.Formintum的小数浓度为小数浓度,允许计算适合于估计两种物种的回归线具有检测限 3到4个日志细胞/ g可可豆。 通过从实验室标度可可豆发酵和QPCR测定和培养依赖性方法的分析来成功测试该方法的疗效,并导致结果。 (c)2015 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号