Uracil Excision for Assembly of Complex Pathways

Mafalda Cavaleiro, Morten Thrane Nielsen, Se Hyeuk Kim, Susanna Seppala, Morten Nørholm

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

Abstract

Despite decreasing prices on synthetic DNA constructs, higher-order assembly of PCR-generated DNA continues to be an important exercise in molecular and synthetic biology. Simplicity and robustness are attractive features met by the uracil excision DNA assembly method, which is one of the most inexpensive technologies available. Here, we describe four different protocols for uracil excision-based DNA editing: one for simple manipulations such as site-directed mutagenesis, one for plasmid-based multigene assembly in Escherichia coli, one for one-step assembly and integration of single or multiple genes into the genome, and a standardized assembly pipeline using benchmarked oligonucleotides for pathway assembly and multigene expression optimization.
Original languageEnglish
Title of host publicationSpringer Protocols Handbooks
Number of pages11
PublisherHumana Press
Publication date2015
DOIs
Publication statusPublished - 2015
SeriesSpringer Protocols Handbooks
ISSN1949-2448

Keywords

  • BioBricks
  • DNA editing
  • Metabolic engineering
  • Molecular cloning
  • Synthetic biology
  • Uracil excision cloning

Cite this

Cavaleiro, M., Nielsen, M. T., Kim, S. H., Seppala, S., & Nørholm, M. (2015). Uracil Excision for Assembly of Complex Pathways. In Springer Protocols Handbooks Humana Press. Springer Protocols Handbooks https://doi.org/10.1007/8623_2015_133