Brown:Bacterial Freeze Tag

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Bacterial Freeze Tag

Overview

This project involves programming bacteria to be able to play a game of freeze tag. Bacteria will be engineered to swim around a microfluidics device until they reach a certain proximity to the 'IT' cell and then they will lose their ability to move. This loss of motility will be combined with a change in color from Green to Blue. When another bacterium, which is moving (not the 'IT' cell), reaches a certain proximity to the 'frozen' bacteria it will again regain its ability to move and turn from Blue to Yellow.

Sender Cell

TetR promoted with LuxI downstream. LuxI is an enzyme that produces AHL and will produce the red fluorescent protein (RFP). The AHL produced is exported from the cell where it then forms a complex with the LuxR protein that is produced by the AHL sensor within the Receiver cell.

AHL Sender Cell

AHL Sensor

The AHL sensor is TetR promoted and forms the LuxR protein which then forms a complex with AHL. This LuxR and AHL complex then activates the pLuxR promoter. Downstream of the pLuxR promoter is the LacI protein. LacI inhibits the pLac promoter on the "Freeze Machine".

AHL Sensor

'Freeze Machine'

A promoter that is regulated by LacI will promote the production of LasI, MotB, and cI. This will subsequently inhibit the production of CFP and LasR. In the presence of LacI, however, MotB, LasI, and cI will not be produced. CFP will therefore be produced along with LasR and LacI. This results in the "freezing" of the cell.

Freeze Machine

"Dr. Unfreeze"

"Dr. Unfreeze" is responsible for short circuiting the freeze machine. When it is activated by AI-1 and LasR it begins producing cI, which will inhibit pcI and allow the cell to begin producing MotB.

Dr. Unfreeze


What we achieved

One of the major issues concerning creating our game of bacterial freeze tag was that we were unsure if a single bacterium ("IT" cell) would be able to send a sufficient AHL signal. In their native environment, bacteria use molecules like AHL as quorum-sensing molecules and therefore the response is based on many bacteria releasing the signalling molecule. In our system, however, we depend on the ability of a single bacterium to be able to communicate with this same signalling molecule. Since we will be using a strong promoter to drive expression of AHL, it is possible that this will be feasible.

To test this, we designed a plan to mix bacterial sender cells (AHL producers) with bacterial receiver cells (AHL receivers) with downstream reporters. In this way, we could easily measure the communication between the senders and the receivers by measuring fluorescent signal. We could experiment with various concentrations of sender cells and determine our key question of whether a single bacterial cell could elicit a response.

Challenges

Future work

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