Part:BBa_K510036:Design
Improved Flip Flop (Module II: asRNA)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
As for the different sequences used in our construction, here it is a brief description of each one:
- cI promoter (Part: BBa_R0051): The cI regulated promoter is based on the pR promoter from bacteriophage lambda. The promoter has two DNA binding sites for lambda cI repressor BBa_C0051. cI binding results in repression of transcription. The specific sequence used here is based on the cI repressible promoter used in the Elowitz repressilator.
- RybB asRNA: Taken from Bouvier et al. (2008). The device includes a RBS followed by the RybB asRNA and a terminator.
Source
It's a composite part which comes from different genes forming the bassic flip-flop with anothers improvements. According to Design Notes, the main source was the Registry of Standard Biological Parts although also nbci database was used to the following parts: LacI and SspB. Besides Tag sequences (DAS4, asRNA and OmpN fusion) were obtained from each articles (see references).
References
- Timothy S. G., Charles R. C. & James J. C. (2000). Construction of a genetic toggle switch in Escherichia coli. Nature 403, 339-342.
- McGinness, K.E., Baker, T.A., and Sauer, R.T. (2006). Engineering Controllable Protein Degradation. Molecular Cell 22, 701-707.
- Bouvier, M., Sharma, C.M., Mika, F., Nierhaus, K.H., and Vogel, J. (2008). Small RNA Binding to 5’ mRNA Coding Region Inhibits Translational Initiation. Molecular Cell 32, 827-837.
For further information please vistit our [http://2011.igem.org/Team:UPO-Sevilla wiki] or contact with us at igem@upo.es