GFP grid tests with sender cells and wild-type pLux receiver constructs

Figure 1: Scanned image of GFP fluorescence in a hexagonal grid with sender cells in green and wild type pLux GFP receiver cells. Red numbers indicate the numbers of mines surrounding the colony.

Diffusion experiments were performed to study OHHL diffusion from the sender colonies to the receiver colonies. The colonies were placed in a hexagonal grid pattern such that every colony can have zero, one, two or three mine colonies adjacent to it. Depending on the number of mines around a non-mine colony, more OHHL will be processed in the receiver colonies due to the higher number of mines. 1.5μl of the receiver and sender cultures were plated according to a hexagonal grid pattern on an agar plate. We then investigated the diffusion patterns by scanning the plate with a molecular imaging software. Images of the GFP fluorescence were taken at time intervals of 1.5hours after first detection of fluorescence. Images taken after 11 hours showed GFP saturation.

The picture to the right shows the scanned image of GFP fluorescence after 11 hours of incubation. The green circles mark the mine colonies. The receiver colonies are those that process the OHHL that diffused from the sender colonies. The difference in fluorescence in the receiver colonies correlates directly to the number of adjacent mine colonies. The data from this experiment shows almost complete agreement with the spatio-temporal model.

GFP grid tests with sender cells and mutated pluxR promoter receiver constructs

Figure 2: Scanned image of GFP fluorescence in a hexagonal grid with sender cells in green and mutant pLux GFP receiver cells

The wild-type plux promoter was mutated through site-saturation mutagenesis to achieve different high-pass filters with varying OHHL sensitivities. The OHHL sensitivity of the mutated promoter was compared with the wild-type promoter with grid tests as described above. From the grid tests, it observed that the OHHL sensitivity was too low. No induction of the GFP receiver was observed even after 21 hours of incubation. These results are consistent with the model predictions. This result led to the rational design of additional promoter mutants, where either one of the two point mutions was changed back with the goal to recover some of the sensitivity of the wild type.

Optimization of LuxR production regulation to reduce basal reporter activation

Figure 3: Identification of the source of leakiness in the GFP receiver construct.

Already with the GFP reporter we encountered leakiness in the absence of OHHL. We tested the GFP expression of different constructs in liquid culture over time. With a construct without any GFP we defined zero fluorescence. We used a pLuxR-GFP construct without LuxR protein to show the expression that results from the leakiness of the promoter alone. By testing the complete pLac-Lux-pLuxR-GFP receiver construct with and without induction through OHHL we see in addition the activation of pLuxR through LuxR alone. Combining the results we could show that most of the leakiness comes from activation of the pLux promoter through LuxR alone, meaning in the absence of OHHL (Figure 3).

Figure 4: Strategies to reduce basal LuxR expression using positive feedback loops.

Expecting the hydrolase reporter system to be even more sensitive we designed different strategies to reduce the level of LuxR in the uninduced state (Figure 4). The overall idea was to change from a constant expression of LuxR to a OHHL dependent induction. One possibility would be to place the luxR gene under it's own pLuxR promoter. Only upon induction with OHHL LuxR would be produced. Or we could either use a constant LacI expression to inhibit LuxR production in the uninduced state. By placing the lacI gene under a negatively LuxR/OHHL regulated promoter pLuxL a positive feedback loop for LuxR expression is formed.

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