Beyer Hannes M, Gonschorek Patrick, Samodelov Sophia L, Meier Matthias, Weber Wilfried, Zurbriggen Matias D
Faculty of Biology, University of Freiburg, Freiburg, Germany; Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, Germany.
Faculty of Biology, University of Freiburg, Freiburg, Germany.
PLoS One. 2015 Sep 11;10(9):e0137652. doi: 10.1371/journal.pone.0137652. eCollection 2015.
Assembly cloning is increasingly replacing conventional restriction enzyme and DNA-ligase-dependent cloning methods for reasons of efficiency and performance. Here, we describe AQUA (advanced quick assembly), a simple and versatile seamless assembly cloning approach. We demonstrate the applicability and versatility of AQUA Cloning in selected proof-of-principle applications including targeted insertion-, deletion- and site-directed point-mutagenesis, and combinatorial cloning. Furthermore, we show the one pot de novo assembly of multiple DNA fragments into a single circular plasmid encoding a complex light- and chemically-regulated Boolean A NIMPLY B logic operation. AQUA Cloning harnesses intrinsic in vivo processing of linear DNA fragments with short regions of homology of 16 to 32 bp mediated by Escherichia coli. It does not require any kits, enzymes or preparations of reagents and is the simplest assembly cloning protocol to date.
由于效率和性能方面的原因,组装克隆正越来越多地取代传统的依赖限制性内切酶和DNA连接酶的克隆方法。在此,我们描述了AQUA(先进快速组装),一种简单且通用的无缝组装克隆方法。我们在选定的原理验证应用中展示了AQUA克隆的适用性和通用性,这些应用包括靶向插入、缺失和定点诱变,以及组合克隆。此外,我们展示了将多个DNA片段一锅法从头组装成一个单一的环状质粒,该质粒编码一个复杂的光控和化学调控的布尔A NIMPLY B逻辑操作。AQUA克隆利用大肠杆菌介导的具有16至32 bp短同源区域的线性DNA片段的内在体内加工过程。它不需要任何试剂盒、酶或试剂制备,是迄今为止最简单的组装克隆方案。