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SapI/AarI 切口介导的质粒编辑方法的开发。

Development of the SapI/AarI Incision Mediated Plasmid Editing Method.

机构信息

Biology Department, Loyola Marymount University, 1 Loyola Maryount Dr., Los Angeles, CA 90045, United States.

Biochemistry Program, Ohio State University, 1461 Mount Vernon Avenue, Marion, OH 43302, United States.

出版信息

J Mol Biol. 2018 May 11;430(10):1426-1430. doi: 10.1016/j.jmb.2018.03.030. Epub 2018 Apr 5.

Abstract

Plasmid engineering and molecular cloning is a virtually ubiquitous tool in biology. Although various methods have been developed for ligating DNA molecules or targeted mutagenesis of plasmids, each has its limitations. Many of the commonly used laboratory strategies are inefficient, while commercially available kits are quite costly and often specialized for highly specific circumstances. Here, we describe the SapI/AarI incision mediated plasmid editing (SIMPLE) method, which allows users to perform site-directed mutagenesis, deletions, and even short insertions into any plasmid in a single PCR reaction, using just one restriction enzyme. In addition, the SIMPLE method can be adapted to insert any sized DNA fragment into a vector using a two-step PCR approach, and can be used to ligate any number of DNA fragments with non-compatible ends in the specific order desired. The SIMPLE method provides researches an efficient and powerful tool with a broad range of applications for molecular cloning.

摘要

质粒工程和分子克隆是生物学中几乎无处不在的工具。尽管已经开发了各种用于连接 DNA 分子或靶向质粒突变的方法,但每种方法都有其局限性。许多常用的实验室策略效率低下,而商业试剂盒则非常昂贵,并且通常专门针对特定的情况。在这里,我们描述了 SapI/AarI 切口介导的质粒编辑 (SIMPLE) 方法,该方法允许用户在单个 PCR 反应中对任何质粒进行定点诱变、缺失,甚至短插入,只需使用一种限制酶。此外,SIMPLE 方法可以通过两步 PCR 方法将任何大小的 DNA 片段插入载体中,并可用于以所需的特定顺序连接任何数量的具有不兼容末端的 DNA 片段。SIMPLE 方法为研究人员提供了一种高效、强大的工具,具有广泛的分子克隆应用。

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