Team:Bielefeld-CeBiTec/Results/Modeling
Results
In the following the results of model I and model II are presented.
Model I
The model for the bacterial two hybrid system, model I, needs the affinity value of the bacterial two hybrid complex as an input.
It then simulates the events in the cell which are essential for the bacterial two hybrid system and the resulting production of beta-lactamase.
As an extension the encounter of beta-lactamase and ampicillin, an antibiotic that harms the cell, is modeled. If the beta-lactamase concentration in the cell is too low and the ampicillin concentration is too high, the cell dies. If the proportion of ampicillin does not lead to death a high ampicillin concentration will cause growth inhibitions.
To ensure that our program can deal with all extreme cases, we made a simulation run of three different affinities: an optimal affinity, a moderate affinity and a bad affinity. The time scale for the events in the cell is limited to 20 minutes, because after 20 minutes it is assumed that the cell divides:
To ensure that our program can deal with all extreme cases, we made a simulation run of three different affinities: an optimal affinity, a moderate affinity and a bad affinity. The time scale for the events in the cell is limited to 20 minutes, because after 20 minutes it is assumed that the cell divides:
In figure 1 (A) the beta-lactamase concentrations over time in the periplasm for the 3 affinities are shown.
In the first 200 seconds the beta-lactamase concentration does not rise very strongly, because the products for the bacterial two hybrid complex (B2H) must firstly be produced. When enough products for the B2H complex are present, the probability for the formation of the B2H complex gets high and the reporter gene, here the beta-lactamase gene, is often transcribed. Thus the production of beta-lactamase rises.
After 20 minutes the strain with the optimal affinity comprises a significantly higher beta-lactamase concentration than the other two strains. Furthermore, the beta-lactamase curves for the moderate affinity has an observable higher end concentration then the bad affinity. These results are as assumed, because the change in affinity for the two components of the B2H complex causes a particular expression of the reporter gene, here beta-lactamase. When the bacterial two hybrid complex dissociates quickly, the expression of the reporter gene is lower (bad affinity) than in the cas of a more stable complex (moderate or optimal affinity).
In comparison to the beta-lactamase curves, figure 1 (B) shows the active ampicillin concentrations for the different affinities in the periplasm. For the first 200 seconds, the ampicillin concentration for all affinities extremely rises, because the beta-lactamase concentration is too low at this time and thus the probability for an encounter of beta-lactamase and ampicillin is low. After around 200 seconds the beta-lactamase starts to significantly deactivate ampicillin and the active ampicillin concentration falls. All ampicillin curves have a very strong decline, due to the fact that beta-lactamase is highly active.
As a result our program computes a final concentration of active ampicillin of 1.2682 * 10-6 M for optimal affinity, 2.3616 * 10-6 M for moderate affinity and 5.9811 * 10-6 M for bad affinity. The final active ampicillin concentration is then converted into a reproduction rate for the particular E. coli cell (figure (C)).
After 20 minutes the strain with the optimal affinity comprises a significantly higher beta-lactamase concentration than the other two strains. Furthermore, the beta-lactamase curves for the moderate affinity has an observable higher end concentration then the bad affinity. These results are as assumed, because the change in affinity for the two components of the B2H complex causes a particular expression of the reporter gene, here beta-lactamase. When the bacterial two hybrid complex dissociates quickly, the expression of the reporter gene is lower (bad affinity) than in the cas of a more stable complex (moderate or optimal affinity).
In comparison to the beta-lactamase curves, figure 1 (B) shows the active ampicillin concentrations for the different affinities in the periplasm. For the first 200 seconds, the ampicillin concentration for all affinities extremely rises, because the beta-lactamase concentration is too low at this time and thus the probability for an encounter of beta-lactamase and ampicillin is low. After around 200 seconds the beta-lactamase starts to significantly deactivate ampicillin and the active ampicillin concentration falls. All ampicillin curves have a very strong decline, due to the fact that beta-lactamase is highly active.
As a result our program computes a final concentration of active ampicillin of 1.2682 * 10-6 M for optimal affinity, 2.3616 * 10-6 M for moderate affinity and 5.9811 * 10-6 M for bad affinity. The final active ampicillin concentration is then converted into a reproduction rate for the particular E. coli cell (figure (C)).
Model II
The computed reproduction rates, 1.0532 h-1 for optimal, 0.7248 h-1 for moderate and 0.1569 h-1 for bad affinity from model I are transferred to model II, the competition model. This model simulates how E. colis with the given reproduction rates grow together in one flask.
Furthermore, to model the several successive [inoculation steps] of our project, we simulated a transfer of a determined proportion of every culture after some time, immediately followed by a new cultivation round. In the laboratory, the pipetted amount of culture is assumed to be binomially distributed. Since the assumptions for applying an approximation according to the de Moivre-Laplace theorem are fulfilled (n, corresponding to the number of cells, being large), we use the normal distribution as an approximation to the binomial distribution. The growth behavior under several inoculations is depicted in the following movie:
As a result model II creates a 3D plot that shows how long the cultivation must last and how often an inoculation must be done till the desired proportion of the best adapted E. coli culture is reached. For our system we want to reach a proportion of 95 % of the total culture mix. The 3D plots for our 3 test affinities can be seen below:
Since the pipetting in the inoculation step follows a normal distribution, we get slightly different results when running the program. That's why we take the time period and inoculation number as a result, which reached for all different 3D plots the 95 % mark. For our three affinities the program computes a required cultivation period of … hours and …. Inoculations.
