Modelling & Optimization

The modelling component of our project was aimed at optimizing the system and creating a 3D visual to demonstrate the way the device operates. With quantitative modelling, we characterized the reporter using the plate reader. With the plate reader, we measured cell count and fluorescence over night for E. coli transformed with RFP (Red Fluorescent Protein), E. coli transformed with lacZ, and B. subtilis transformed with RFP. In order to make our diagnostic test as fast as possible, our other goal with modelling was to quantify the experiments performed by biology students on the team to determine most optimal conditions for B. subtilis transformation and growth. Modelling and simulations also allowed us to determine the best way to put our physical device together. 3D animation made using Autodesk Maya software was used to explain how the device works. Creating 3D animation allows to visualize how different parts of the system work as well as how they are connected together. A visual also makes it easier for people from different backgrounds to understand what is happening in the device. Our modelling team also created a 3D animation of our device. It shows the physical outline of the device as well as an animation of the biological system. The animation was created using Autodesk Maya 2013 software and ePMV plug in. It serves as a visual to everything taking place in our device making it easier to understand even for general public.

Quantitative Modelling

In order to describe the expression of the potential reporter proteins, we used the plate reader to measure the cell count and fluorescence. Five dilutions were prepared to see how initial cell concentration will affect cell growth and reporter signal. Overnight, 36 measurements were taken with 1800 s (30 min) intervals. Figure 1 shows the results obtained when the plate reader measured cell count (OD @ 600 nm). From the graph, it is evident that E. coli with lacZ grew more rapidly, but reached the flat region (or no growth region) within 6-7 hours. It also reached lower cell count numbers than bacteria culture with RFP.E. coli and B. subtilis with RFP grew less rapidly, but did not reach the flat region within 20 hours. However, from the graph it is evident that it is approaching the flat region. Bacteria cultures with RFP also reached higher cell count than LacZ.

Figure 1: Cell count (OD @ 600 nm) versus Time for E. coli transformed with RFP (left), E. coli with lacZ (middle), and B. subtilis transformed with RFP (right).

Figure 2 shows RFP fluorescence measurements on E. coli transformed with RFP, E. coli transformed with lacZ and B. subtilis transformed with RFP. E. coli with RFP follows the expected trend. Fluorescence values are growing exponentially over time, and higher concentrations reach higher numbers. However, at 18-20 hours, the differences between dilutions are small. Once we determine the threshold level that bacteria in our device will need to reach, we would be able to tell how long it takes based on the graph in figure 2. E. coli with lacZ was expected to be 0. However, one of the controls (media with no culture) is not 0, but instead follows the same curve as bacteria transformed with RFP which suggests it was contaminated. B. subtilis with RFP graph is not as clean as E. coli graph since dilutions overlap. But the graph still shows general trend that we expected to see.

Figure 2: Fluorescence versus Time for E. coli transformed with RFP (left), E. coli with lacZ (middle), and B. subtilis transformed with RFP (right).

We also attempted to measure lacZ fluorescence on E. coli with lacZ using the plate reader. However, the plate reader did not have the settings and required filters to perform such measurements. Our colour sensor might be better at measuring blue colour (lacZ) than the plate reader, so we will set up a similar experiment using the colour sensor. We will leave it overnight and get our colour sensor to measure the colour every 30 minutes. We would only be able to measure one dilution overnight, and will not be able to measure fluorescence directly. Instead, the colour sensor will output the red, green, and blue components allowing us to see how colour changes over time. We will also be able to see how long it takes for bacteria to express detectable colour.