Nakano Michihiko, Komatsu Jun, Matsuura Shun-ichi, Takashima Kazunori, Katsura Shinji, Mizuno Akira
Department of Ecological Engineering, Toyohashi University of Technology, Tempaku-cho, Toyohashi, Aichi 441-8580, Japan.
J Biotechnol. 2003 Apr 24;102(2):117-24. doi: 10.1016/s0168-1656(03)00023-3.
Polymerase chain reaction (PCR) using a single molecule of DNA is very useful for analysis, detection and cloning of the desired DNA fragment. We developed a simple PCR method utilizing a water-in-oil (W/O) emulsion that included numerous droplets of reaction mixture in bulk oil phase. These droplets, which were stable even at high temperatures, functioned as micro-reactors. This allows the effective concentration of template DNA to be increased, even for low concentrations of template DNA. The present method consists of a two-step thermal cycle. The first step was carried out using the W/O emulsion. During this step, the template DNA was amplified in the limited volume of the droplets in the W/O emulsion. The W/O emulsion was broken and the second PCR step was carried out. This method can be easily applied to amplify a single DNA molecule.
使用单分子DNA的聚合酶链反应(PCR)对于所需DNA片段的分析、检测和克隆非常有用。我们开发了一种简单的PCR方法,该方法利用油包水(W/O)乳液,在大量油相中包含许多反应混合物液滴。这些液滴即使在高温下也很稳定,可作为微反应器。这使得即使对于低浓度的模板DNA,也能提高其有效浓度。本方法包括两步热循环。第一步使用W/O乳液进行。在此步骤中,模板DNA在W/O乳液液滴的有限体积内进行扩增。然后打破W/O乳液并进行第二步PCR。该方法可轻松应用于扩增单个DNA分子。