Tianjin/FLIP-FLOP

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The logic principle of our design is shown above. Unless the input signal transfer from one stable condition to another ( such as 0 to 1 or 1 to 0), the output signal would change into 1, otherwise it would maintain 0. Thus, the immediate response to emergency (input change) enables our design to detect signal variation in a short time, which is beneficial for process control because of its time-saving character.

2.Construction of Biological Circuit <More details>

Modeling

Based on Ordinary Differential Equations, we construct the Mathematical Model of our flip-flop system to test the result of our design and predict potential key factors deciding the results of our experiment. According to the model,the variation of output signal responding to the input signal matches the typical feature of flip-flop,there would no output signal only at the positive edge and negative edge of the input signal. The influence of AHL to the output signal is also considered. By changing the degradation speed of AHL, the fluoresence intensity exhibit different behaviour which could be explained by principles of flip-flop. Finally, the parameter sensitivity is also tested to explore most significant parameter to output signals and it is discovered that the strength of promoter I, which controls the production of LuxI, the promoter II, which controls the expression of LuxR, exert great effect on the final results.

1. Construction of Mathematical Model

2. Model Result

2.1 Model of the whole system

2.2 Change the degradation speed of AHL

2.3 parameter sensitivity

Experiment

1.Ligation Strategy and Parts Reservoir

Parts used in our design and ligation strategy


2.Experimental Result

Consider the significance of IPTG impulse as the input signal, we designed a series of experiment to search for most suitable condition to produce legible output signals, including the concentration of IPTG (high and low input signal), the time point for addition( exponential phase and stationary phase) and supplement of IPTG.The optimal plan is to add 0.5mM IPTG during the early exponential phase of E.coli cells, and the output signal together with other parameters have been summarized on the same graph which proves that every part of our device works as well as we expected. The slow degrading rate of Green Fluorescence Protein leave our device some space to improve to achieve a more desirable result.