Yonemoto Isaac T, Weyman Philip D
J. Craig Venter Institute, Synthetic Biology and Bioenergy Group, 4120 Capricorn Lane, La Jolla, CA, 92137, USA.
Methods Mol Biol. 2017;1498:359-366. doi: 10.1007/978-1-4939-6472-7_24.
Site-directed mutagenesis is a commonly used molecular biology technique to manipulate biological sequences, and is especially useful for studying sequence determinants of enzyme function or designing proteins with improved activity. We describe a strategy using Gibson Isothermal DNA Assembly to perform site-directed mutagenesis on large (>~20 kbp) constructs that are outside the effective range of standard techniques such as QuikChange II (Agilent Technologies), but more reliable than traditional cloning using restriction enzymes and ligation.
定点诱变是一种常用的分子生物学技术,用于操纵生物序列,尤其适用于研究酶功能的序列决定因素或设计具有更高活性的蛋白质。我们描述了一种使用吉布森等温DNA组装技术对大型(>~20 kbp)构建体进行定点诱变的策略,这些构建体超出了标准技术(如QuikChange II(安捷伦科技公司))的有效范围,但比使用限制性酶和连接的传统克隆更可靠。