Lehtonen Soili I, Taskinen Barbara, Ojala Elina, Kukkurainen Sampo, Rahikainen Rolle, Riihimäki Tiina A, Laitinen Olli H, Kulomaa Markku S, Hytönen Vesa P
BioMediTech, FI-33014 University of Tampere, Biokatu 6, Finland.
BioMediTech, FI-33014 University of Tampere, Biokatu 6, Finland Fimlab Laboratories, Biokatu 4, FI-33520 Tampere, Finland.
Protein Eng Des Sel. 2015 Jan;28(1):23-8. doi: 10.1093/protein/gzu050. Epub 2014 Dec 1.
Efficient and robust subcloning is essential for the construction of high-diversity DNA libraries in the field of directed evolution. We have developed a more efficient method for the subcloning of DNA-shuffled libraries by employing recombination cloning (Gateway). The Gateway cloning procedure was performed directly after the gene reassembly reaction, without additional purification and amplification steps, thus simplifying the conventional DNA shuffling protocols. Recombination-based cloning, directly from the heterologous reassembly reaction, conserved the high quality of the library and reduced the time required for the library construction. The described method is generally compatible for the construction of DNA-shuffled gene libraries.
高效且稳健的亚克隆对于定向进化领域中高多样性DNA文库的构建至关重要。我们通过采用重组克隆(Gateway)开发了一种更高效的DNA改组文库亚克隆方法。在基因重新组装反应后直接进行Gateway克隆程序,无需额外的纯化和扩增步骤,从而简化了传统的DNA改组方案。基于重组的克隆直接来自异源重新组装反应,保留了文库的高质量并减少了文库构建所需的时间。所描述的方法通常适用于DNA改组基因文库的构建。