Part:BBa_K2066123
Synthetic Enhancer Project: UNS 55as NRII TetR
This part takes the synthetic genetic circuit from Amit et. al. 2011, the NRII promoter and coding region from Amit et. al. 2011 as well as the TetR promoter and coding region from Bba_I739001 and puts it onto a BioBrick backone flanked by the UNS regions. Used for the synthetic enhancer project, this part consists of an enhancer region, that when bound to phosphorylated NRI protein, can bind to the promoter after the DNA loops to allow for these kinetics. The promoter and coding sequence for the NRII protein (which is mutated to be solely a kinase that can phosphorylate and activate the NRI and allow it to bind to the enhancer region) was taken from the Amit et. al. pACT Tet helper plasmid and put the sequence between the UNS 3 sequence. Furthermore, the Bba_I739001 sequence was inserted into the UNS2 region of the insert to let TetR consititutively expressed by the J23105 promoter. NRII and TetR were moved to the same plasmid as the synthetic enhancer to 1. reduce the circuit's dependence on LacI (which is also expressed in the original pACT Tet helper plasmid) as well as decrease the interference of these plasmids after transformations with the current bacterial circuitry and thus reduce the metabolic strain on the bacteria.
Once the bound enhancer loops over and interacts with the sigma 54 poised promoter, transcription of the NRI protein for positive feedback as well as the output flourescent reporter is initiated. This part is from the synthetic enhancer genetic circuits created by Amit et. al where there is a tetR binding cassette with two TetO binding sites in the spacer region between the enhancer and the promoter. The two binding sites allows for three discrete states of output: a repressed, intermediate, and unrepressed state. Small chemical induction with aTc binds to and inactivates available TetR repressor. When a small amount of aTc is present, there isn't enough aTc to find TetR proteins and there is enough repressor available to allow for a constant filling of the two available TetO binding sites. When both TetO sites are bound, the DNA becomes less flexible and makings looping of the enhancer to the promoter extremely difficult, thus not allowing for very minimal transcription of the NRI and reporter proteins. When more aTc is added to the system, more TetR is bound and inactivated and this creates an intermediate step where enough TetR is bound that at any point only one TetR is bound to the teto sites and this increases the rigidity of the DNA and allows for looping and activation and reporter output less frequently. Finally, when aTc conentration is high, you reach a saturation point where almost all TEtR repressors are bound and inactivated and you get maximal amount of looping and thus maximal amount of NRI and reporter transcribed and translated.
Source: The enhancer, tet cassette, glnAp2 synthetic promoter, NRI coding region, and mCherry coding region sequences were derived from Amit, R., Garcia, H. G., Phillips, R. & Fraser, S. E. Building enhancers from the ground up: a synthetic biology approach. Cell146, 105–118 (2011). The NRII2302 coding region and the promoter that it is controlled by is derived from the helper plasmid pACT tet from Amit et. al 2011. The sequence for the TetR controlled by J23105 promoter is from Biobrick part Bba_I739001. The TetR is inserted between the UNS2 sequence and is added to the same plasmid as the synthetic enhancer suite and NRII2302 to reduce the interference with other genetic circuitry in the bacteria and thus decrease overall metabolic strain. The UNS sequences at the ends of the insert are derived from Torella, J. P., Boehm, C. R., Lienert, F., Chen, J. H., Way, J. C., & Silver, P. A. (2013). Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly. Nucleic acids research, gkt860. A huge thanks to all the researchers involved in its original creation!
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 27
Illegal NheI site found at 50
Illegal NheI site found at 194
Illegal NotI site found at 3795 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 973
- 1000COMPATIBLE WITH RFC[1000]
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