Suppr超能文献

使用实时定量PCR对发酵乳制品中的乳酸菌进行分子定量分析。

Molecular quantification of lactic acid bacteria in fermented milk products using real-time quantitative PCR.

作者信息

Furet Jean-Pierre, Quénée Pascal, Tailliez Patrick

机构信息

Institut National de la Recherche Agronomique, Unité de Recherches Laitières et Génétique Appliquée, Domaine de Vilvert, 78352 Jouy-en-Josas Cedex, France.

出版信息

Int J Food Microbiol. 2004 Dec 15;97(2):197-207. doi: 10.1016/j.ijfoodmicro.2004.04.020.

Abstract

Real-time quantitative PCR assays were developed for the absolute quantification of lactic acid bacteria (LAB) (Streptococcus thermophilus, Lactobacillus delbrueckii, L. casei, L. paracasei, L. rhamnosus, L. acidophilus and L. johnsonii) in fermented milk products. The results of molecular quantification and classic bacterial enumeration did not differ significantly with respect to S. thermophilus and the species of the L. casei group which were detected in the six commercial fermented products tested, thus showing that DNA extraction was efficient and that genomic DNA solutions were free of PCR inhibitors. For L. delbrueckii, the results of bacterial enumeration were generally lower by a factor 10 to 100 than those of PCR quantification, suggesting a loss of viability during storage of the dairy products at 1-8 degrees C for most of the strains in this species. Real-time quantitative assays enabled identification of the species of lactic acid bacterial strains initially present in commercial fermented milk products and their accurate quantification with a detection threshold of 10(3) cells per ml of product.

摘要

开发了实时定量PCR检测方法,用于对发酵乳制品中的乳酸菌(嗜热链球菌、德氏乳杆菌、干酪乳杆菌、副干酪乳杆菌、鼠李糖乳杆菌、嗜酸乳杆菌和约翰逊乳杆菌)进行绝对定量。在测试的六种商业发酵产品中,嗜热链球菌和干酪乳杆菌组各菌种的分子定量结果与传统细菌计数结果差异不显著,这表明DNA提取效率高,基因组DNA溶液不含PCR抑制剂。对于德氏乳杆菌,细菌计数结果通常比PCR定量结果低10到100倍,这表明该菌种的大多数菌株在乳制品于1-8℃储存期间活力有所丧失。实时定量检测能够鉴定商业发酵乳制品中最初存在的乳酸菌菌株种类,并以每毫升产品10³个细胞的检测阈值对其进行准确定量。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验