Team:INSA Toulouse/contenu/lab practice/results/carry

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   <h3 class="title3">Experimentation</h3>
   <h3 class="title3">Experimentation</h3>
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  <p class="texte">We realized many experiences in order to measure how AHL diffuses into agar medium. We used a particular bacteria, Chromobacterium violaceum, which is capable to detect presence of AHL by producing a purple pigment, the violacein.<br><br>
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  <p class="texte">We realized different experiences in order to measure how AHL diffuses into agar medium. We used a bacteria with particular habilities, Chromobacterium violaceum. In presence of AHL, the strain starts to produce a purple pigment, the violacein.<br><br>
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Figure 1 shows petri dishes containing eight colonies of bacteria placed at 5, 10, 15, 20, 25, 30, 35 and 40 mm from the center of the box. With this experience we can track the diffusion of the AHL. Also we can see that the colonies are in a spiral disposition. This typical disposition allows us to avoid the problem of utilisation of AHL of the n-1 colony to the n colony.  
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Figure 1 shows petri dishes containing eight colonies of bacteria placed at 5, 10, 15, 20, 25, 30, 35 and 40 mm from the center of the box. With this experience, we can study the diffusion of the AHL. We also can see that colonies are disposed in spiral. This disposition allows us to avoid the problem of utilisation of AHL of the n-1 colony to the n colony.  
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<p class="textecaption"><i>Figure 2: Evolution of AHL diffusion into petri dish.</i></p>
<p class="textecaption"><i>Figure 2: Evolution of AHL diffusion into petri dish.</i></p>
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  <p class="texte">With this experience we can represent on figure 3 the surface of AHL diffusion (surface is a disk) versus time in order to find the diffusion coefficient of AHL into LB agar. The directing coefficient of the regression line gives us the order of magnitude of diffusion coefficient, we find an order of 10<SUP>-8</SUP> m²/s. This coefficient is an important value to develop analytical and numerical modelling.
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  <p class="texte">With this experience, we can represent the surface of AHL diffusion on figure 3(surface is a disk) versus time in order to find the diffusion coefficient of AHL into LB agar. The directing coefficient of the regression line gives us the order of magnitude of diffusion coefficient, we find an order of 10<SUP>-8</SUP> m²/s. This coefficient is an important value to develop analytical and numerical modelling.
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<img style="width:500px" src="https://static.igem.org/mediawiki/2013/0/04/Coefficient_of_diffusivity.PNG" class="imgcontentcaption"/>
<img style="width:500px" src="https://static.igem.org/mediawiki/2013/0/04/Coefficient_of_diffusivity.PNG" class="imgcontentcaption"/>

Revision as of 22:49, 4 October 2013

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Results: Modelling

Experimentation

We realized different experiences in order to measure how AHL diffuses into agar medium. We used a bacteria with particular habilities, Chromobacterium violaceum. In presence of AHL, the strain starts to produce a purple pigment, the violacein.

Figure 1 shows petri dishes containing eight colonies of bacteria placed at 5, 10, 15, 20, 25, 30, 35 and 40 mm from the center of the box. With this experience, we can study the diffusion of the AHL. We also can see that colonies are disposed in spiral. This disposition allows us to avoid the problem of utilisation of AHL of the n-1 colony to the n colony.

Figure 1: Photographs at 25h of petri dishes containing each 8 Chromobacterium violaceum colonies from 5 mm to 40 mm.

Figure 2 represents the evolution of AHL diffusion versus time.

Figure 2: Evolution of AHL diffusion into petri dish.

With this experience, we can represent the surface of AHL diffusion on figure 3(surface is a disk) versus time in order to find the diffusion coefficient of AHL into LB agar. The directing coefficient of the regression line gives us the order of magnitude of diffusion coefficient, we find an order of 10-8 m²/s. This coefficient is an important value to develop analytical and numerical modelling.

Figure 3: Determination of diffusion coefficient of AHL into LB agar medium.

Analytical Model

After the creation of our first model above, which allowed us to find relevant answer for our system, we thought that in terms of modelling we were not really satisfied. That is why we developed a new model based on equation of continuity in cylindrical coordinates. The general equation in our case is the following. Equation of continuity:

Bird, R. B., Stewart, W. E., & Lightfoot, E. N. (1960). Transport phenomena (Vol. 2). New York: Wiley.

In our case we have: No reaction No evolution in z and θ directions dwA/dr=0 because of the mass equation (Dρ/Dt=0) with ρ=cste After simplification:

After simplification and changing the mass in concentration we obtained:

To solve this equation we first thought to use the separation of variables method, but we faced different issues. After more researches, we found a new solution which fits better with our system. This solution corresponds to a Dirac impulsion. This is not the perfect solution but this is the closest analytical solution to our system. The only difference with our system is that the boundary condition for C(0;0), is not exactly the same. For the Dirac impulsion C(0;0)->∞, but this approximation can be acceptable for our system considering that our AHL concentration is high at the beginning of the experiment and the loading surface is really small. This is our analytical solution:

In this case as we consider our system as a dirac impulsion, we cannot be focused on the concentration values (because C(0;0)-> ∞). That is why here, we are working with normalized concentration values. The interest of this model is the evolution of the concentration in time and space and also the determination of the diffusion coefficient D. We tested different diffusivity coefficients to find the one which allows the model with the best experimentation fitting. We found that the coefficient of AHL diffusivity into LBagar medium is around: D = 1.10-8 m²/s On this first chart, we can see the evolution of the concentration for a given distance from the petri dish center. Close to the center the concentration increases really fast and goes down more slowly. More the radius is important more the concentration increase is weak.

Figure 4: Evolution of concentration in time for analytic solution.

On this second chart we can see at different times the concentration profile along the petri dish. With this graph, it is relevant to compare how the concentration profile evolves in time . For instance at 70 min the concentration is still high at r=0 but AHL reached 25 mm, whereas at 20min at r=0 the concentration is 2 times higher but the AHL only reached 10mm.

Figure 5: Evolution of concentration with radius for analytic solution.

This model fits well in terms of evolution with our experimentation. Thanks to this model we can approximately predict the diffusion of AHL into the LB agar. But we have to be careful here because we don’t have the real concentration values and for high time the analytical model isn’t corresponding to the reality.

Numerical Model

The last step of our modeling was to solve on a numerical way our diffusion problem. The aim was to solve the same differential equation presented in the analytical solution part. But here as we solved it with a computer we could use the right boundary condition, and also added a reaction term. Therefore we developed a numerical solution of AHL diffusion into LB agar medium with the software Comsol. We just needed to enter all the physical parameters of our petri dish and the AHL diffusivity. On this first animation, we can see the diffusion of AHL into a petri dish with colonies but without reaction term. We note that the concentration of AHL becomes progressively homogeneous in the medium. This model is closest to the reality than the analytical one because here the boundary conditions are equivalent to the experimental boundary conditions: C(0,0)=cste C(r=R,t->∞)= cste

Figure 6: Diffusion of AHL in LBagar medium with numerical solution.

On these second and third animations we tried to simulate what could be our final system with AHL diffusion from a well 1 to other wells. These following two animations are complementary. The first shows the diffusion of the AHL from well 1, the second allows us to visualize the reach of the AHL in wells 2 and 3.

Figure 7: Diffusion of AHL in LBagar medium with numerical solution from well 1.

Figure 8: Reception of AHL in well 2 and 3.

We can note that the AHL easily reached the well 2, but also 3 after some time. The passage of the AHL from a well n to well n+1 without reaching the point n+2 is really a key point. It is certainly difficult to implement such a system. In addition, it is imperative that the production of AHL is not continuous, because the concentration in the petri reaches all the wells. We need a short pulse in time for transferring the AHL only in well 2. It also requires that the AHL is consumed in well 2 to limit the diffusion in well 3.