From 2007.igem.org

The formation of complex scaffolds of extracellular matrix is one of the problems facing the emerging discipline of tissue engineering[1]. One way to produce such scaffolds would be to have them secreeted by cells joined together in a three dimensional structure.

We concieved the idea of using two light sources of different wavelength, impinging on a suspension of cells from differnt directions to induce the cells at their intersection to join to each other and thus create a three dimensional structure. Since we plan to implement the system in Ecoli we called it coliforming. Implementation of this concept requires two new biobricks of more general application and these are the focus of this years submission to the Igem competition.

1. A new light receptor like the Red light receptor, but sensitive to a different wavelength. This is being developed based on work in the Spudich lab with Sensory RhodopsinII [2] and by Alan Grossman with ComP (kinase), ComA(target) and PsfA(promotor) two component signalling system[3]. Implementation is by dirrect sythesis of the required fusion genes, using the Geneart offer.
2. A protein generator for gas vesicles to make the suspension of cells neutrally bouyant. This is based on the work in the Cannon lab[4]. Implemenation is by removal of restriction sites using site dirrected mutagenesis of Maura's plasmid and PCR primer based engineering of biobrick prefix and suffix.

References:

2. Vishwa D. Trivedi and John L. Spudich, Photostimulation of a Sensory Rhodopsin II/HtrII/Tsr Fusion Chimera Activates CheA-Autophosphorylation and CheY-Phosphotransfer in Vitro. Biochemistry 2003, 42, 13887-13892.
4. Li, N. and M.C. Cannon, Gas vesicle genes identified in Bacillus megaterium and functional expression in Escherichia coli. Journal of Bacteriology, 1998. 180(9): p. 2450-2458.