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RapGene: a fast and accurate strategy for synthetic gene assembly in Escherichia coli

The ability to assemble DNA sequences de novo through efficient and powerful DNA fabrication methods is one of the foundational technologies of synthetic biology. Gene synthesis, in particular, has been considered the main driver for the emergence of this new scientific discipline. Here we describe...

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Detalles Bibliográficos
Autores principales: Zampini, Massimiliano, Stevens, Pauline Rees, Pachebat, Justin A., Kingston-Smith, Alison, Mur, Luis A. J., Hayes, Finbarr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462754/
https://www.ncbi.nlm.nih.gov/pubmed/26062748
http://dx.doi.org/10.1038/srep11302
Descripción
Sumario:The ability to assemble DNA sequences de novo through efficient and powerful DNA fabrication methods is one of the foundational technologies of synthetic biology. Gene synthesis, in particular, has been considered the main driver for the emergence of this new scientific discipline. Here we describe RapGene, a rapid gene assembly technique which was successfully tested for the synthesis and cloning of both prokaryotic and eukaryotic genes through a ligation independent approach. The method developed in this study is a complete bacterial gene synthesis platform for the quick, accurate and cost effective fabrication and cloning of gene-length sequences that employ the widely used host Escherichia coli.