Team:Chiba/System 1


Revision as of 21:43, 27 October 2010 by Hotpotato (Talk | contribs)




Overall Circuit

“Genetic double click system” is based on the ANDgate which is high only when same inputs are given two times in quick succession. This system requires the operations which never happen naturally to turn the switch. So, we believe that this is very safety device. This system requires that a first input is transient in order to allow a second input. Unlike chemical inputs, light inputs are very suitable for this system because it does not remain after inputting. But, there is not light sensor with good sensitivity. So, we produced artificially transient input by AHL inputting and washing. Next, this system is required to memorize the transient first input since this system is based on AND gate. Moreover, this system requires time-limit in genetic sequence between the first and the second input like a computer mouse to recognized double-click and two separated single-clicks as different, so, this system is required to memorize the transient first input temporarily. In our first design, we decided a pulse-generator to memorize the input temporarily. And, we designed the system which is based on combination of a Fast-pulse and a Slow-pulse in principle as shown in the following figure.

This system consists of a pulse-generator and two inverters which can be seemed as a slow pulse.In this system, we also use AHL input and GFP output. This time, we use AHL as an activate signal, so when there is AHL added, Lux promoter will be activated. The transcription factors of output are T7 RNA Polymerase and cI repressor.

Fast Pulse

At initial state, LuxR and cI protein are constitutively generated. cI binds to the operator site of PT7/cI. When 1st input is injected, LuxR-AHL dimmer binds to the Lux-box of the lux promoters so that T7 RNA Polymerase, cI434 and tetR protein are generated at the same time. cI434 gradually accumulates, and gradually repress the transcription of T7 RNA Polymerase so that the expression of T7 RNA Polymerase can be shown as a pulse. At the same time, Transcription of cI is stopped by tetR, cI decomposes and the PT7/cI promoter is unbound. This derepression occurs after the pulse of T7 RNAP has passed. In other words, the operator sites of PT7/cI is repressed by cI when there is pulse of T7 RNA Polymerase. So, it cannot transcribe GFP. TetR creates a time delay here from input to derepression. Because of this time delay and one-time pulse, bacteria can never work by one input.
Slow Pulse

Before injecting 2nd input, we must create none-input-environment. So we choose to wash the 1st input. By washing , tetR protein and cI434 protein will degrade. cI434 protein should disappear so that when there is 2nd input, T7 RNA Polymerase will be shown as a pulse which is the same as the 1st time. cI will begin to generate if tetR protein gets lost. We recognize it as time-limit, when there is enough cI generated (this means cI repression is stronger than T7 RNA Polymerase activation), there will be no GFP output. On the contrary, when there is less cI protein or no cI protein at the moment, T7 RNA Polymerase pulse can accumulate GFP output. By the second injected AHL before the inhibition by cI, T7 RNA Polymerase binds to the PT7/cI promoter and transcribes the downstream GFP.