Rapid Construction of Recombinant Plasmids by QuickStep-Cloning

Methods Mol Biol. 2017:1472:205-14. doi: 10.1007/978-1-4939-6343-0_16.

Abstract

QuickStep-Cloning is a novel molecular cloning technique that builds upon the concepts of asymmetric PCR and megaprimer-based amplification of whole plasmid. It was designed specifically to address the major drawbacks of previously reported cloning methods. The fully optimized protocol allows for a seamless integration of a long DNA fragment into any position within a plasmid of choice, in a time-efficient and cost-effective manner, without the need of a tedious DNA gel purification, a restriction digestion, and an enzymatic ligation. QuickStep-Cloning can be completed in less than 6 h, significantly faster than most of the existing cloning methods, while retaining high efficiency.

Keywords: Ligation-independent cloning; Megaprimer PCR; Metabolic engineering; Plasmid construction; Protein engineering; Recombinant DNA; Synthetic biology.

MeSH terms

  • Cloning, Molecular*
  • DNA, Recombinant / genetics
  • Plasmids / genetics*
  • Polymerase Chain Reaction
  • Recombination, Genetic
  • Transformation, Bacterial

Substances

  • DNA, Recombinant