Biotechnical use of polymerase chain reaction for microbiological analysis of biological samples.

P G Lantz, W Abu al-Soud, R Knutsson, B Hahn-Hägerdal, P Rådström
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引用次数: 118

Abstract

Since its introduction in the mid-80s, polymerase chain reaction (PCR) technology has been recognised as a rapid, sensitive and specific molecular diagnostic tool for the analysis of micro-organisms in clinical, environmental and food samples. Although this technique can be extremely effective with pure solutions of nucleic acids, it's sensitivity may be reduced dramatically when applied directly to biological samples. This review describes PCR technology as a microbial detection method, PCR inhibitors in biological samples and various sample preparation techniques that can be used to facilitate PCR detection, by either separating the micro-organisms from PCR inhibitors and/or by concentrating the micro-organisms to detectable concentrations. Parts of this review are updated and based on a doctoral thesis by Lantz [1] and on a review discussing methods to overcome PCR inhibition in foods [2].

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聚合酶链反应在生物样品微生物分析中的生物技术应用。
自80年代中期引入以来,聚合酶链反应(PCR)技术已被认为是一种快速,敏感和特异性的分子诊断工具,用于分析临床,环境和食品样品中的微生物。虽然这种技术对核酸的纯溶液非常有效,但当直接应用于生物样品时,它的灵敏度可能会大大降低。本文介绍了PCR技术作为一种微生物检测方法,生物样品中的PCR抑制剂和各种样品制备技术,这些技术可以通过将微生物从PCR抑制剂中分离出来和/或将微生物浓缩到可检测的浓度来促进PCR检测。这篇综述的部分内容是根据Lantz的博士论文[1]和一篇讨论克服食品中PCR抑制方法的综述[2]进行更新的。
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