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Navigational control of bacteria: the design of a synthetic chemotactic biological system
BMC Systems Biology volume 1, Article number: S14 (2007)
Background
Synthetic Biology is a rapidly developing field, which sees engineering principles applied to natural biological systems with a view to re-engineer them for useful purposes. This study focused on chemotaxis, the natural directed motion of a micro-organism toward environmental conditions it deems attractive, with an aim of demonstrating external navigational control over E. coli bacteria. The concept has potential long-term applications in a range of fields, including biological and environmental sensors, drug discovery and the maintenance or enhancement of human health.
Method
The periplasmic maltose-binding protein (MBP) is essential for maltose transport and taxis. It was placed under external control via synthetic plasmids containing 2 different IPTG-based promoters coupled to the MBP-encoding malE and malE31[1] genes. These were transformed into three engineered ΔmalE E. coli strains allowing for both permanent and temporary reactivation of maltose chemotaxis. The stochastic simulator StochSim [2] was adapted from the standard aspartate model to consider the associated maltose regulon.
Results
The re-engineering of the natural chemotaxis system was successfully demonstrated on both the macro and micro scale using swimming and agarose plug assays. It was shown maltose chemotaxis could be initiated and repressed by an external signal. Stochsim was successfully adapted to model the maltose system, with simulation data for the adaptation and dependence on MBP shown to closely match experimental data [3].
Conclusion
A novel approach demonstrated the feasible control of the sensory system and resultant motile behaviour of synthetically engineered E. coli cells. This provides an appropriate tool for generating experimental data that in turn may feed the computational modelling of chemotaxis. This allows a better understanding of the natural system and how one might go about specifically engineering that system for a useful cause.
References
Sandén AM, Boström M, Markland K, Larsson G: Solubility and proteolysis of the Zb-MalE and Zb-MalE31 proteins during overproduction in Escherichia coli. Biotechnol Bioeng. 2005, 90: 239-247. 10.1002/bit.20433
Morton-Firth CJ, Shimizu TS, Bray D: A free-energy-based stochastic simulation of the tar receptor complex. J Mol Biol. 1999, 286: 1059-1074. 10.1006/jmbi.1999.2535
Manson MD, Boos W, Bassford PJ Jr, Rasmussen BA: Dependence of maltose transport and chemotaxis on the amount of maltose-binding protein. J Biol Chem. 1985, 260: 9727-9733.
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Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Brown, J. Navigational control of bacteria: the design of a synthetic chemotactic biological system. BMC Syst Biol 1 (Suppl 1), S14 (2007). https://doi.org/10.1186/1752-0509-1-S1-S14
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DOI: https://doi.org/10.1186/1752-0509-1-S1-S14