| Literature DB >> 27485329 |
Kiavash Mirzadeh1, Stephen Toddo1, Morten H H Nørholm2, Daniel O Daley3.
Abstract
Reengineering a gene with synonymous codons is a popular approach for increasing production levels of recombinant proteins. Here we present a minimalist alternative to this method, which samples synonymous codons only at the second and third positions rather than the entire coding sequence. As demonstrated with two membrane-embedded transporters in Escherichia coli, the method was more effective than optimizing the entire coding sequence. The method we present is PCR based and requires three simple steps: (1) the design of two PCR primers, one of which is degenerate; (2) the amplification of a mini-library by PCR; and (3) screening for high-expressing clones.Entities:
Keywords: Codon optimization; Membrane protein; Protein expression; Synonymous codon
Mesh:
Substances:
Year: 2016 PMID: 27485329 DOI: 10.1007/978-1-4939-3637-3_4
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745