Emergent Bistability by a Growth-Modulating Positive Feedback Circuit

Tuesday, November 10, 2009: 12:30 PM
Delta Ballroom B (Gaylord Opryland Hotel)

Chee Meng Tan, Biomedical Engineering & Institute for Genome Sciences and Policy, Duke University, Durham, NC
Philippe R. Marguet, Dept. of Biochemistry, Duke University, Durham, NC
Lingchong You, Biomedical Engineering, Duke University, Durham, NC

A synthetic gene circuit is often engineered by considering the host cell as an invariable “chassis”. Circuit activation, however, may modulate host physiology, which in turn can drastically impact circuit behavior. We illustrate this point by a simple circuit consisting of mutant T7 RNA polymerase (T7 RNAP*) that activates its own expression in bacterium Escherichia coli. Although activation by the T7 RNAP* is noncooperative, the circuit caused bistable gene expression. This counterintuitive observation can be explained by growth retardation caused by circuit activation, which resulted in nonlinear dilution of T7 RNAP* in individual bacteria. Predictions made by a model accounting for such effects were verified by further experimental measurements. Our results reveal a novel mechanism of generating bistability and underscore the need to account for host physiology modulation in engineering gene circuits.
Extended Abstract: File Not Uploaded
See more of this Session: Synthetic Systems Biology I
See more of this Group/Topical: Topical A: Systems Biology