Team:Imperial College London/Major results
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==Simulations: Chemoinduction/Module 1-Output yield of drug of interest== | ==Simulations: Chemoinduction/Module 1-Output yield of drug of interest== |
Revision as of 21:15, 20 October 2009
Major Results
This page contains some, but not all of our major results and highlights of our simulations. This is not complete. More results will be presented at the jamboree.
Simulations: Chemoinduction/Module 1-Output yield of drug of interest
Our simulation results indicate that increasing input amounts of IPTG result in a greater yield of polypeptide drug of interest (See simulation results). We did an experiment to study how different input concentrations of IPTG affect cell growth, and concluded that IPTG has no significant effect on cell growth within the ranges we are using(IPTG growth curves). Therefore, we can conclude that increasing IPTG concentration initially will have a positive contribution to our dosage.
Note: Parameters used in the system are arbitrary. For a justification see the system stability analysis.
Experimental: Module 2 - Encapsulation growth curves
Dependent on lab results today
Experimental: Autoinduction - Diauxic growth curve and CRP GFP
Here we can pick a diauxic growth curve and compare directly to a simulation (if I manage to make one work!! :-S)
Simulations: Module 1 - Enzyme kinetics and dosage control
Many polypeptides of interest are enzymes. This means that detecting how much drug has been produced requires knowledge about their interaction with their respective substrates in the enzymatic assays. Here we assumed that enzymatic activity follows Michaelis-Menten kinetics [7]. This means that we can directly relate enzymatic activity to the required dosage for successful administration of the polypeptide of interest.
Dosage Calculations:
Tianyi upload once we work out activity or whatever is necessary!
Experimental: Module 3 - Thermoinducible promoter
Need Matthieu's latest processed data
Conclusion
Need some inspiration here guys!