Difference between revisions of "Part:BBa K2066121"

Latest revision as of 05:14, 29 October 2016

Synthetic Enhancer Project: 2X TetO Binding Cassette(55aS) + NRII + TetR + sfGFP on UNS

The synthetic enhancer, first characterized by Amit et. al. 2011, allows for a multistate transfer function by modulating the rigidity of the spacer region between the enhancer promoter region, thus affecting the DNA rigidity and hence the kinetic capability of the two components to loop together and initiate transcription. For more information on the mechanism, please refer to: http://2016.igem.org/Team:William_and_Mary/Synthetic_Enhancer.

This part takes the synthetic enhancer circuit with a two TetO binding cassette as, the promoter and coding region of NRII from the helper plasmid of Amit et. al. 2011 circuits as well as constitutively expressed TetR (Bba_I739001) and puts it onto a single BioBrick backbone flanked by the UNS regions. This part allows for a three step output response due to the two TetO binding cassette in the spacer region between the enhancer and promoter. Combining NRII, TetR, and the synthetic enhancer circuit reduces metabolic strain, decouples the system from LacI/IPTG dependence, and allows for an ease of cloning due to the UNS sequences. The number of filled TetO sites influences the rigidity and the thermodynamics of the looping. Furthermore, we included an sfGFP reporter for more pronounced fluorescent signals.

aTc induction should be used to obtain a multistate response curve.

Source: The enhancer, tet cassette, glnAp2 synthetic promoter, and NRI coding region sequences were derived from the synthetic enhancer circuits 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 sfGFP flourescent reporter design is inspired by C. Lou, B. Stanton, Y.-J. Chen, B. Munsky, C. A. Voigt, Ribozyme-based insulator parts buffer synthetic circuits from genetic context. Nat. Biotechnol. 30, 1137 (2012). doi:10.1038/nbt.2401 pmid:23034349. 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

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
INCOMPATIBLE 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 3801
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
INCOMPATIBLE WITH RFC[25]
Illegal AgeI site found at 973
1000
INCOMPATIBLE WITH RFC[1000]
Illegal SapI.rc site found at 1961

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 <partinfo>BBa_K2066121 short</partinfo>
-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.
+The synthetic enhancer, first characterized by Amit et. al. 2011, allows for a multistate transfer function by modulating the rigidity of the spacer region between the enhancer promoter region, thus affecting the DNA rigidity and hence the kinetic capability of the two components to loop together and initiate transcription. For more information on the mechanism, please refer to: http://2016.igem.org/Team:William_and_Mary/Synthetic_Enhancer.
- 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.
+This part takes the synthetic enhancer circuit with a two TetO binding cassette as, the promoter and coding region of NRII from the helper plasmid of Amit et. al. 2011 circuits as well as constitutively expressed TetR (Bba_I739001) and puts it onto a single BioBrick backbone flanked by the UNS regions. This part allows for a three step output response due to the two TetO binding cassette in the spacer region between the enhancer and promoter. Combining NRII, TetR, and the synthetic enhancer circuit reduces metabolic strain, decouples the system from LacI/IPTG dependence, and allows for an ease of cloning due to the UNS sequences. The number of filled TetO sites influences the rigidity and the thermodynamics of the looping. Furthermore, we included an sfGFP reporter for more pronounced fluorescent signals.
+aTc induction should be used to obtain a multistate response curve.
 Source: