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Rapid Identification of Fermentation Spoilage Microbes Using Molecular Beacons and a Two-Step Direct DNA Amplification Protocol

机译:使用分子信标快速鉴定发酵腐败微生物和两步直接DNA扩增方案

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摘要

Bacterial contamination is a long-standing problem in the brewing and distilling industry. Extant approaches in measuring contamination levels, or for measuring specific microbes, is either slow or expensive. A very rapid ( 1 hr) DNA method using PCR coupled with a fluorescent molecular beacon, showing a sensitivity able to detect levels of a common contaminant (L. delbrueckii), well before sensory signals are triggered, is described. The approach is highly discriminatory, able to differentiate among contaminating strains within a genus, and even in the presence of a considerable excess of desirable strains. The approach implies ways to determine entry points for contamination to help ameliorate the problem and could save a considerable amount of time, resources, and income for the manufacturer.
机译:细菌污染是酿造和蒸馏工业中的长期问题。测量污染水平或测量特异性微生物的现存方法是缓慢或昂贵的。描述了使用PCR与荧光分子标信标的PCR的非常快速(<1小时)DNA方法,显示能够检测普通污染物(L. delbrueckii)的水平的敏感性,并且在触发感觉信号之前。该方法是高度歧视的,能够区分在属中的污染菌株中,甚至在存在相当过量的期望菌株中。该方法意味着确定污染的入口点,以帮助改善问题,可以节省制造商的相当长的时间,资源和收入。

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