Phosphorothioate-based DNA recombination : an enzyme-free method for the combinatorial assembly of multiple DNA fragments

Rational guided generation of protein chimeras has developed into an attractive approach in protein engineering for tailoring catalytic and biophysical properties of enzymes. Combinatorial recombination of structural elements or whole protein domains is still technically challenging due to sequence...

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Détails bibliographiques
Publié dans:BioTechniques. - 1991. - 52(2012), 5 vom: 01. Mai
Auteur principal: Marienhagen, Jan (Auteur)
Autres auteurs: Dennig, Alexander, Schwaneberg, Ulrich
Format: Article en ligne
Langue:English
Publié: 2012
Accès à la collection:BioTechniques
Sujets:Journal Article Research Support, Non-U.S. Gov't PTRec directed evolution phosphorothioate protein engineering recombination Phosphates phosphorodithioic acid 8056RR93HU plus... DNA 9007-49-2
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Résumé:Rational guided generation of protein chimeras has developed into an attractive approach in protein engineering for tailoring catalytic and biophysical properties of enzymes. Combinatorial recombination of structural elements or whole protein domains is still technically challenging due to sequence dependent biases diminishing the overall quality of resulting chimeric libraries. Since methods for generating such libraries are often limited by a low frequency of crossover points and suffer from challenges in handling, we developed the phosphorothioate-based DNA recombination method (PTRec). PTRec is an enzyme-free method and only requires a short stretch of four amino acids that is identical among the proteins to be recombined in order to define a single crossover point. In a PTRec-generated chimeric library that shuffled five domains of phytase using genes from three different species, 88% of 42 randomly picked and sequenced genes were efficiently recombined. Furthermore, PTRec is a technically simple, fast, and reliable method that can be used for domain- and exon-shuffling or recombination of DNA fragments in general
Description:Date Completed 18.05.2016
Date Revised 26.08.2015
published: Electronic
Citation Status MEDLINE
ISSN:1940-9818
DOI:10.2144/000113865