College of Biotechnology, Shenyang Agricultural University, Shenyang, China.
N Biotechnol. 2011 Jul;28(4):320-5. doi: 10.1016/j.nbt.2011.03.001. Epub 2011 Mar 23.
Here we describe a robust method, termed QuikChange shuffling, for efficient site-directed mutagenesis and random recombination of homologous genes. The homologous genes are fragmented, and the random fragments are reassembled in a self-priming polymerase reaction to obtain chimeric genes. The product is then mixed with linearized vector and two pairs of complementary mutagenic primers, followed by assembly of the chimeric genes and linearized vector through QuikChange-like amplification to introduce recombinant plasmids with a site-directed mutation. The method, which can yield 100% chimeric genes after library construction, is more convenient and efficient than current DNA shuffling methods.
在这里,我们描述了一种称为 QuikChange shuffling 的强大方法,用于高效的定点突变和同源基因的随机重组。同源基因被片段化,随机片段在自我启动的聚合酶反应中重新组装,以获得嵌合基因。然后将产物与线性化载体和两对互补诱变引物混合,然后通过类似于 QuikChange 的扩增来组装嵌合基因和线性化载体,以引入具有定点突变的重组质粒。该方法在文库构建后可以产生 100%的嵌合基因,比当前的 DNA shuffling 方法更方便、更高效。