Difference between revisions of "Team:UESTC-China/Model"

We combined modeling with experiments and human practice to make contributions to our project. For experiments, we established quorum sensing model and degradation optimization model. For human practice, we established the device layout model.

To understand the mechanism better and predict the results of the experiments, we modeled the quorum sensing mechanism from the microscopic point of view, which can help us find the optimal ratio of detection cells and processing cells. So the model can greatly save the cost of our project by using a smaller number of engineered bacteria to achieve greater CrpP production.

To further optimize our experiments, we investigated the external factors affecting the degradation of CIP by engineered bacteria from the macroscopic perspective. Through the reasonable experimental design, we can screen out the main influencing factors and obtain the response surface equation using PB design and Box-Behnken design in the future. Finally, we will find the best external conditions, which improves the degradation rate of CIP.

To make our device applied widely in real life, we established a device layout model from a more macroscopic perspective to provide a scientific solution for human practice and hardware. We completed the work to use a minimum number of devices but achieve the highest efficiency of drugs recycling.

To further understand, predict, and control the behavior of engineered microbial quorum sensing, we modeled the quorum sensing based on the entire process of CrpP enzyme's production and degradation.

The model involves a wide range of biological and physical processes, such as diffusion, binding and so on. Through the establishment and solution of differential equations, we have used this model to predict the connection between the production of CrpP enzyme and the concentration of external AHL, which can help us find the optimal ratio of the detection bacteria and the degrading bacteria in order to save the cost of the device by using a smaller number of engineered bacteria to achieve greater CrpP production.

To further optimize our experiments, we found the factors affecting the degradation rate from papers. We designed a scheme which used the Plackett-Burman design to screen factors. We can get the key factors through experiments in the future. The Box-Behnken design will be used in the experimental design. According to the future experimental results, the response surface equation can be obtained. Then, we can find the optimal external influence factors (eg. PH, temperature) and increase the degradation rate to optimize our experiment. At present, we are working hard to get the experimental data. In the future, we will use our scheme to optimize our experiment and adjust our model with experimental data.