Research Article

j5 DNA Assembly Design Automation Software

Fuels Synthesis Division, Joint BioEnergy Institute, Emeryville, California 94608, United States
Physical Bioscience Division, Lawrence Berkeley National Lab, 1 Cyclotron Road Mail Stop 978R4121, Berkeley, California 94720, United States
§ Department of Chemical & Biomolecular Engineering, Department of Bioengineering, University of California, Berkeley, California 94720, United States
ACS Synth. Biol., 2012, 1 (1), pp 14–21
DOI: 10.1021/sb2000116
Publication Date (Web): December 7, 2011
Copyright © 2011 American Chemical Society
*Tel: +1 510 486 6754. Fax: +1 510 486 4252. E-mail: njhillson@lbl.gov.

 Author Present Address

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.

Abstract

Abstract Image

Recent advances in Synthetic Biology have yielded standardized and automatable DNA assembly protocols that enable a broad range of biotechnological research and development. Unfortunately, the experimental design required for modern scar-less multipart DNA assembly methods is frequently laborious, time-consuming, and error-prone. Here, we report the development and deployment of a web-based software tool, j5, which automates the design of scar-less multipart DNA assembly protocols including SLIC, Gibson, CPEC, and Golden Gate. The key innovations of the j5 design process include cost optimization, leveraging DNA synthesis when cost-effective to do so, the enforcement of design specification rules, hierarchical assembly strategies to mitigate likely assembly errors, and the instruction of manual or automated construction of scar-less combinatorial DNA libraries. Using a GFP expression testbed, we demonstrate that j5 designs can be executed with the SLIC, Gibson, or CPEC assembly methods, used to build combinatorial libraries with the Golden Gate assembly method, and applied to the preparation of linear gene deletion cassettes for E. coli. The DNA assembly design algorithms reported here are generally applicable to broad classes of DNA construction methodologies and could be implemented to supplement other DNA assembly design tools. Taken together, these innovations save researchers time and effort, reduce the frequency of user design errors and off-target assembly products, decrease research costs, and enable scar-less multipart and combinatorial DNA construction at scales unfeasible without computer-aided design.

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Received 4 October 2011
Published online 7 December 2011
Published in print 20 January 2012
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