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Open Access Methodology

Introduction of customized inserts for streamlined assembly and optimization of BioBrick synthetic genetic circuits

Julie E Norville123*, Ratmir Derda456, Saurabh Gupta2, Kelly A Drinkwater12, Angela M Belcher23, Andres E Leschziner7 and Thomas F Knight18

Author Affiliations

1 Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

2 Biological Engineering Division, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

3 Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

4 Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada

5 Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA

6 Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA 02138, USA

7 Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA

8 Ginkgo BioWorks, 7 Tide St., Unit 2B, Boston, MA 02210, USA

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Journal of Biological Engineering 2010, 4:17  doi:10.1186/1754-1611-4-17

Published: 20 December 2010

Abstract

Background

BioBrick standard biological parts are designed to make biological systems easier to engineer (e.g. assemble, manipulate, and modify). There are over 5,000 parts available in the Registry of Standard Biological Parts that can be easily assembled into genetic circuits using a standard assembly technique. The standardization of the assembly technique has allowed for wide distribution to a large number of users -- the parts are reusable and interchangeable during the assembly process. The standard assembly process, however, has some limitations. In particular it does not allow for modification of already assembled biological circuits, addition of protein tags to pre-existing BioBrick parts, or addition of non-BioBrick parts to assemblies.

Results

In this paper we describe a simple technique for rapid generation of synthetic biological circuits using introduction of customized inserts. We demonstrate its use in Escherichia coli (E. coli) to express green fluorescent protein (GFP) at pre-calculated relative levels and to add an N-terminal tag to GFP. The technique uses a new BioBrick part (called a BioScaffold) that can be inserted into cloning vectors and excised from them to leave a gap into which other DNA elements can be placed. The removal of the BioScaffold is performed by a Type IIB restriction enzyme (REase) that recognizes the BioScaffold but cuts into the surrounding sequences; therefore, the placement and removal of the BioScaffold allows the creation of seamless connections between arbitrary DNA sequences in cloning vectors. The BioScaffold contains a built-in red fluorescent protein (RFP) reporter; successful insertion of the BioScaffold is, thus, accompanied by gain of red fluorescence and its removal is manifested by disappearance of the red fluorescence.

Conclusions

The ability to perform targeted modifications of existing BioBrick circuits with BioScaffolds (1) simplifies and speeds up the iterative design-build-test process through direct reuse of existing circuits, (2) allows incorporation of sequences incompatible with BioBrick assembly into BioBrick circuits (3) removes scar sequences between standard biological parts, and (4) provides a route to adapt synthetic biology innovations to BioBrick assembly through the creation of new parts rather than new assembly standards or parts collections.