Team:Bologna
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The device consists of two new BioBricks: | The device consists of two new BioBricks: | ||
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[[Image:project3b.png|center|950px|thumb|<center>Figure 1 - T-Rex device</center>]] | [[Image:project3b.png|center|950px|thumb|<center>Figure 1 - T-Rex device</center>]] | ||
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More details about our work are reported in the [[Team:Bologna/Project|Project]] section. | More details about our work are reported in the [[Team:Bologna/Project|Project]] section. | ||
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= Acknowledgements = | = Acknowledgements = | ||
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Revision as of 18:59, 21 October 2009
HOME | TEAM | PROJECT | SOFTWARE | MODELING | WET LAB | PARTS | HUMAN PRACTICE | JUDGING CRITERIA |
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Project Summary
Our idea
The project aims to design a new device to control the synthesis of a protein in Escherichia coli regardless of the protein to be controlled. This "general-purpose" standard device acts on translation to allow a faster silencing of protein expression if compared to standard regulated promoters. We named this device T-Rex (Trans Repressor of Expression).
How T-Rex works
The device consists of two new BioBricks:
CIS-repressing and TRANS-repressor sequences were seeked by BASER software.
Transcription of the target gene produces a mRNA strand, starting with the Cis element, which is translated into proteins by ribosome (see Fig. 1, right panel). Trans’ promoter induction produces a transcript that binds with the Cis part. The RNA duplex prevents ribosome from binding to RBS, repressing protein synthesis. Thus, the TRANS-repressor amount regulates the gene mRNA translation rate (see Fig. 1, left panel)
How we can test the device
In order to test and characterize our T-REX device, we developed the following genetic circuit (Fig 2):
More details about our work are reported in the Project section.
Acknowledgements
- [http://www.unibo.it/Portale/default.htm University of Bologna]
- [http://serinar.criad.unibo.it Ser.In.Ar. Cesena]
- Cultural Association San Sebastiano