Experiment
In the first part of the experiment, we first determined the parameters of the model that describe the behavior of our cell culture, according to the procedure described in the modeling part.
The first part of the experiment followed a protocol close to the other:
1.0-90 min : this first incubation was done in the dark to let the bacteria grow and produce KillerRed.
2. 90-330 min : a longer 4 hours period with illumination at maximal intensity. After that time, the effects of light were clear, and the parameters of the model were calculated to fit the observable kinetics.
3. 330-450 min : Then our model was used to calculate the light intensity that would stabilize the population of living cells : light was applied at 70% of its maximal intensity.
4. 450-720 min : After 2 hours, we noticed that the fluorescence and the absorbance were slowly drifting away from the predictions. Since the fluorescence was higher than expected and the OD was lower than expected, we reduced the illumination to 50% of its maximal intensity for 2 hours and then at 40% of its maximal intensity.
To sum up
| Time (min) |
0 |
90 |
330 |
450 |
570 |
720 |
| illumination (%) |
0 |
100 |
70 |
50 |
40 |
end |
Step 1: We ran the the experiment to be able to improve the fit of parameters (90 minutes in the dark, then 3 hours at maximal intensity). The predictions below were calculated with parameters of the previous experience, we see that on this one, bacteria are growing slower, and procuce less KillerRed.
Step 2: m+330 fit of parameters, new prediction, look for a light tha will stabiliser the bacterial population, here I=0,7.
Step 3: m+450 the fluorescence and the OD are too low for the prevision, light intensity is decreased at 0,5.
Step 4: m+570 the fluorescence and the OD are still too low for the prevision, light intensity is decreased at 0,4.
Step 5: m+660 we have just obtained a level of more than 5 hours
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