Difference between revisions of "Part:BBa K2066117:Design"

 
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===Design Notes===
 
===Design Notes===
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To be completed
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We designed the part to include the synthetic enhancer suite and the NRII helper protein on the same UNS backbone, which allows for the phosphorylation (activation) of the protein product of the synthetic enhancer product (NRI). Making one plasmid reduces the metabolic strain on the cell and further decouples the synthetic enhancer system from LacI/IPTG to allow for minimal inference of our circuits in the complete biological system.
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+
  
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We chose to include UNS overhangs before and after our insert to allow for an ease of clone. UNS sequences are from Torella et. al. Furthermore, the NRII sequence and the synthetic enhancer suite sequences are from Amit et. al.
  
 
===Source===
 
===Source===
  
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To be completed
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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 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!
  
 
===References===
 
===References===

Latest revision as of 03:55, 29 October 2016


Synthetic Enhancer: 2x TetO Binding Cassette + NRII on UNS


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 111
    Illegal NotI site found at 3712
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 890
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We designed the part to include the synthetic enhancer suite and the NRII helper protein on the same UNS backbone, which allows for the phosphorylation (activation) of the protein product of the synthetic enhancer product (NRI). Making one plasmid reduces the metabolic strain on the cell and further decouples the synthetic enhancer system from LacI/IPTG to allow for minimal inference of our circuits in the complete biological system.

We chose to include UNS overhangs before and after our insert to allow for an ease of clone. UNS sequences are from Torella et. al. Furthermore, the NRII sequence and the synthetic enhancer suite sequences are from Amit et. al.

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 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!

References