Volume 1 Supplement 1

BioSysBio 2007: Systems Biology, Bioinformatics, Synthetic Biology

Open Access

New tools for self-organized pattern formation

  • Kaj Bernhardt1,
  • Nikhilesh Singh Chand1Email author,
  • Elizabeth Carter1,
  • Jisun Lee2,
  • Yang Xu2,
  • Xueni Zhu2,
  • Duncan Rowe1,
  • JW Ajioka1,
  • JM Goncalves2,
  • J Haseloff1 and
  • G Micklem1
BMC Systems Biology20071(Suppl 1):S10

DOI: 10.1186/1752-0509-1-S1-S10

Published: 8 May 2007

Introduction

Multicellular organisms undergo self-organisation during development. Our aim was to engineer self-organised pattern formation in free-swimming bacteria cells by providing an artificial system for bi-directional communication. E. coli cells would be equipped with genes derived from independent quorum sensing systems from P. aeruginosa and V. fischeri. These systems enable communication between cell populations and can enable regulated switching between competing cell fates. The negotiation of cell fates within bacterial populations can be visualized precisely by the expression of different fluorescent proteins.

Experiments conducted and results obtained

Using Escherichia coli as a model system we have observed how differential cell motility can, in itself, lead to pattern formation. Adapting the experiments of Weiss et al. [1], we have studied the interactions between cell populations in swimming agar with genetically engineered sender and receiver cells. The sender cells express one of two acyl-homoserine lactone (AHL) synthases whereas the receiver cells are capable of responding to the generated AHL signal. Instead of using a differential response to AHL concentrations we employed cell motility as a way to define zones of response (see Figure 1 for an example). In particular we equipped highly motile strains such as E. coli MC1000 with AHL-mediated autoinducing systems based on Vibrio fischeri luxI/luxR [2] and Pseudomonas aeruginosa lasI/lasR [3] cassettes. We had these auto-inducing cassettes synthesized and tested them as depicted. To obtain an enhanced response the coding sequences were codon optimized. (See Figure 2).
https://static-content.springer.com/image/art%3A10.1186%2F1752-0509-1-S1-S10/MediaObjects/12918_2007_Article_78_Fig1_HTML.jpg
Figure 1

Zones of responses defined by cell motility

https://static-content.springer.com/image/art%3A10.1186%2F1752-0509-1-S1-S10/MediaObjects/12918_2007_Article_78_Fig2_HTML.jpg
Figure 2

An enhanced response by codon optimization of the coding sequences

Authors’ Affiliations

(1)
School of Biological Sciences, University of Cambridge
(2)
Department of Engineering, University of Cambridge

References

  1. Basu S: A synthetic multicellular system for programmed pattern formation. Nature. 2005, 434 (7037): 1130-1134. 10.1038/nature03461PubMedView ArticleGoogle Scholar
  2. Dunlap PV: Quorum regulation of luminescence in Vibrio fischeri. J Mol Microbiol Biotechnol. 1999, 1 (1): 5-12.PubMedGoogle Scholar
  3. Venturi V: Regulation of quorum sensing in Pseudomonas. FEMS Microbiol Rev. 2006, 30 (2): 274-291. 10.1111/j.1574-6976.2005.00012.xPubMedView ArticleGoogle Scholar

Copyright

© Bernhardt et al; licensee BioMed Central Ltd. 2007

This article is published under license to BioMed Central Ltd.

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