Department of Molecular and Pharmaceutical Biotechnology, Graduate School of Pharmaceutical Sciences, University of Tokushima, Shomachi 1-78, Tokushima 770-8505, Japan.
J Pharm Biomed Anal. 2010 Jun 5;52(2):323-8. doi: 10.1016/j.jpba.2009.12.023.
We describe the potential of microchip electrophoresis with a Hitachi SV1100, which can be used to determine DNA sizes between 500 and 5000 bp with good quantification (DNA concentration, <8 ng/l) within 5 min, for the analysis of DNA ligation. On analysis of an electropherogram of a ligation mixture of the pTAC1-T vector and a 789 bp PCR-amplified DNA fragment, the presence of recombinant DNA was easily detected by comparison with an electropherogram obtained without ligase. On analysis of a ligation mixture of pUC19/Eco RI without alkaline phosphatase treatment and a 667 bp Eco RI-digested fragment of foreign DNA, several peaks observed in the electropherogram corresponded to the formation of monomeric and polymeric insert DNAs, self-ligated vector DNA, and recombinant DNA. On the other hand, several peaks were also observed in the electropherogram of the ligation mixture of pUC19/Eco RI with alkaline phosphatase treatment and the 667 bp Eco RI-digested fragment of foreign DNA, the fluorescence intensity corresponding to recombinant DNA apparently being increased. These results indicate the potential of microchip electrophoresis for the analysis of DNA ligation, it offering high resolution in a short time.
我们描述了日立 SV1100 微芯片电泳的潜力,它可以在 5 分钟内分析 DNA 连接,用于分析 DNA 连接,能够很好地定量(DNA 浓度,<8ng/l)500bp 至 5000bp 之间的 DNA 大小。在 pTAC1-T 载体和 789bp PCR 扩增 DNA 片段的连接混合物的电泳图谱分析中,通过与没有连接酶的电泳图谱比较,很容易检测到重组 DNA 的存在。在 pUC19/Eco RI 无碱性磷酸酶处理和 667bp Eco RI 消化的外源 DNA 片段的连接混合物的分析中,电泳图谱中观察到的几个峰对应于单体和多聚插入 DNA、自身连接的载体 DNA 和重组 DNA 的形成。另一方面,在 pUC19/Eco RI 用碱性磷酸酶处理和 667bp Eco RI 消化的外源 DNA 片段的连接混合物的电泳图谱中也观察到几个峰,重组 DNA 的荧光强度明显增加。这些结果表明微芯片电泳在 DNA 连接分析中的潜在应用,它在短时间内提供高分辨率。