High fidelity one‐pot DNA assembly using orthogonal serine integrases

Background Large serine integrases (LSIs, derived from temperate phages) have been adapted for use in a multipart DNA assembly process in vitro, called serine integrase recombinational assembly (SIRA). The versatility, efficiency, and fidelity of SIRA is limited by lack of a sufficient number of LSIs whose activities have been characterized in vitro. Methods and Major Results In this report, we compared the activities in vitro of 10 orthogonal LSIs to explore their suitability for multiplex SIRA reactions. We found that Bxb1, ϕR4, and TG1 integrases were the most active among the set we studied, but several others were also usable. As proof of principle, we demonstrated high‐efficiency one‐pot assembly of six DNA fragments (made by PCR) into a 7.5 kb plasmid that expresses the enzymes of the β‐carotenoid pathway in Escherichia coli, using six different LSIs. We further showed that a combined approach using a few highly active LSIs, each acting on multiple pairs of att sites with distinct central dinucleotides, can be used to scale up “poly‐part” gene assembly and editing. Conclusions and Implications We conclude that use of multiple orthogonal integrases may be the most predictable, efficient, and programmable approach for SIRA and other in vitro applications. Graphical and Lay Summary There is a need for better DNA assembly technologies for constructing and editing genomes and genetic circuits designed for synthetic biology applications. One such technology involves the use of large serine integrases (LSIs), which are DNA recombinases derived from lysogenic phages. In this work, we have improved the efficiency and fidelity of the technology by using several orthogonal LSIs to assemble a plasmid vector in a one‐pot reaction.