Difference between revisions of "Team:ZJU-China/Design"

    We have achieved information input using light control system, and have decided the transformational rule using oscillation system. The following problem is how to combine these two systems together and we design an AND gate. The main principle we use in the AND gate is using tRNA to identify amber mutation. Protein T7ptag can activate PT7 promoter. When we make two amber mutations on T7ptag, the process of protein translation will be inhibited. After inputting exogenetic tRNA into E.coli, whose feature is to identify amber mutation, these two promoters controlling T7ptag and tRNA have composed the input of AND gate. And the output is the downstream PT7 gene.


    In the light control system, there has Plamada promoter and PcpcG2 promoter. In the oscillation system, there has Plsr promoter and PluxR promoter. Match these promoters together with fluorescence protein reporter gene, we can get four AND gate circuits:
                （1）Plamda+PluxR+GFP
                （2）Plamda+Plsr+RFP
                （3）PcpcG2+PluxR+RFP
                （4）PcpcG2+PluxR+GFP


    When bacteria are expressing AHL, PluxR is turned on continuously, and the inputting optical signal is changed into another light of different color. For example, irradiating with red light will turn on Plamda, resulting in the emission of green light (GFP).
    In practice, If the period of the oscillation system is 1.5h, suppose we irradiate three tubes of bacteria using red light, green light, red light at 14:00 in the afternoon, we can get the feedback of green light (GFP), red light (RFP), red light (RFP), which are the encrypted cipher-text. Then the bacteria will continue oscillation but we could not know their states. When we need to decrypt, irradiate them using green light, red light, red light at 15:30, the bacteria will return to their original states, emitting red light, green light and red light which means we get the original text. By now, we have successfully achieved the process of encryption and decryption.

    Using light-switchable two-component systems as input, and AND gate circuit to manipulate the input signal, we have already achieved the basic function of the cipher machine.

    To realize an independent and dynamic encryption, we use logic gates to combine the light control system and the oscillation system. We use AHL to replace Ara, and DPD to replace IPTG. Thus, with the adjustment by the oscillation system, the second generation of cipher machine could change periodically between two different code books all by itself.

    The effect using red light system to inhibit PopmC is not obvious enough. During the experiment, we integrated the two plasmids mentioned in the original reference into a whole. We suspect that the incoordination happened in the system is due to different copy numbers. In the future, we plan to change the copy numbers and try to find the best effect. Besides, we consider to replace cph8 and RBS before PcyA/ho1.
    Also, we want to adopt the blue light control system used by Uppsala_Sweden2011, and compare its influences with red light and green light systems.
    In order to describe the light control system more in details, we plan to use multi-mode reading machine to take pictures regularly. Thus we could analyze after how much time being irradiated can bacteria produce the initial response, and draw the response curve according to fluorescence intensity.Currently we use LED lights to irradiate bacteria. The luminance of red LED light is 1200MCD, and 5000MCD for green LED light. In the future, we plan to increase the light intensity, to explore the correlation between light intensity and bacteria’s response time.


    In practice, in order to merge several chambers into a whole encryption unit, we have to realize synchronization among chambers instead of within a single one. And this needs strict requirements about the initial bacteria quantity in each chamber and other related factors. So, it has high possibility that desynchronization occurs.
    For realizing synchronization as a whole, besides quorum sensing substances, we hope to apply a new micromolecule which could penetrate the PDMS surface, and coordinate bacteria’s gene expression process. After research and discussion, we find that hydrogen peroxide molecule is a good choice. Through redox signalling by hydrogen peroxide (H2O2) and the native redox sensing machineries of E. Coli, we can apply H2O2 to our oscillation system (Fig.11). Using AHL to activate the production of H2O2 in chambers, letting H2O2 to coordinate gene expression in the whole unit, we then realize a perfect synchronization in the whole unit. (Fig.12, Fig.13)


    For double-period oscillation, we need to find another substance that can be compared with hydrogen peroxide molecules, which requires our further efforts.


    When using hydrogen peroxide as diffusion molecule in oscillation system, we need to modify the microfluidics device. H2O2 can penetrate PDMS material freely. And on a PDMS chip, we need to distinguish different encryption units because each unit has its own oscillation state. So, we have to take measures to block H2O2 from diffusion to different units. We are going to use vertical bonded silicon sheets to achieve this target.


    Promoter leak is still existing. In the combination of arabinose promoter and lactose promoter, lactose promoter leak seriously. So we will do the following experiments for further optimization of the system.
                1.Change the position of Pbad and Plac, to explore the influences on PT7 caused by T7ptag and tRNA.
                2.Replace current promoters with promoters of low leak values, for example, to use salicylate promoter.
                3.Add a weaker RBS before T7ptag, for example, J61100.
                4.Use computer to simulate the position of T7ptag amber mutation, and find the best mutant site to inhibit the expression of T7ptag completely.
                5.Add input and output on plasmids of different copy numbers in order to make our logic gate more precise.