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通过实时聚合酶链反应直接定量检测和鉴定牛奶和乳清中的乳球菌噬菌体:在法国生羊乳清中检测乳球菌噬菌体的应用

Direct Quantitative Detection and Identification of Lactococcal Bacteriophages from Milk and Whey by Real-Time PCR: Application for the Detection of Lactococcal Bacteriophages in Goat's Raw Milk Whey in France.

作者信息

Ly-Chatain Mai Huong, Durand Loïc, Rigobello Véronique, Vera Annabelle, Demarigny Yann

机构信息

Department of Food Industry and Quality, ISARA-Lyon, 23 Jean Baldassini, 69364 Lyon Cedex 07, France.

出版信息

Int J Microbiol. 2011;2011:594369. doi: 10.1155/2011/594369. Epub 2011 Oct 13.

Abstract

The presence of Lactococcus bacteriophages in milk can partly or completely inhibit milk fermentation. To prevent the problems associated with the bacteriophages, the real-time PCR was developed in this study for direct detection from whey and milk of three main groups of Lactococcus bacteriophages, c2, 936, and P335. The optimization of DNA extraction protocol from complex matrices such as whey and milk was optimized allowed the amplification of PCR without any matrix and nontarget contaminant interference. The real-time PCR program was specific and with the detection limit of 10(2) PFU/mL. The curve slopes were -3.49, -3.69, and -3.45 with the amplification efficiency estimated at 94%, 94%, and 98% and the correlation coefficient (R(2)) of 0.999, 0.999, and 0.998 for c2, 936 and P335 group, respectively. This method was then used to detect the bacteriophages in whey and goat's raw milk coming from three farms located in the Rhône-Alpes region (France).

摘要

牛奶中乳酸乳球菌噬菌体的存在会部分或完全抑制牛奶发酵。为防止与噬菌体相关的问题,本研究开发了实时荧光定量PCR技术,用于直接检测乳清和牛奶中三种主要类型的乳酸乳球菌噬菌体,即c2、936和P335。对从乳清和牛奶等复杂基质中提取DNA的方法进行了优化,使得PCR扩增不受任何基质和非目标污染物的干扰。实时荧光定量PCR程序具有特异性,检测限为10(2) PFU/mL。c2、936和P335组的曲线斜率分别为-3.49、-3.69和-3.45,扩增效率估计分别为94%、94%和98%,相关系数(R(2))分别为0.999、0.999和0.998。然后使用该方法检测来自法国罗纳-阿尔卑斯地区三个农场的乳清和山羊生鲜乳中的噬菌体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bc1/3195528/977574dc7faf/IJMB2011-594369.001.jpg

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