Difference between revisions of "Part:BBa K4164028"
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− | <p style="text-align: center!important;"><b>Fig.1 Gene circuit based on GFP</b></p> | + | <p style="text-align: center!important;"><b>Fig.1. Gene circuit based on GFP</b></p> |
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<p style="text-align: center;"><img src="https://static.igem.wiki/teams/4164/wiki/part-registry/part-028-2.png"with="1000" height="" width="500" height=""/></p> | <p style="text-align: center;"><img src="https://static.igem.wiki/teams/4164/wiki/part-registry/part-028-2.png"with="1000" height="" width="500" height=""/></p> | ||
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− | <p style="text-align: center!important;"><b>Fig. | + | <p style="text-align: center!important;"><b>Fig.2. Fluorescence intensity/OD using a gradient of CDCA concentrations based on ddRFP.</b></p> |
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===Usage and Biology=== | ===Usage and Biology=== |
Latest revision as of 15:10, 12 October 2022
pCadBA-GFP
This composite part contains the pCadBA promoter (BBa_K3425101) and green fluorescent protein (BBa_E0040). When the CadC domains dimerize, the downstream CadBA promoter will drive green fluorescent protein (GFP) expression.
We recombined pCadBA promoter (BBa_K3425101) and green fluorescent protein (BBa_E0040) by homologous recombination.
With the system above, we selected CadC, promoter CadBA, GFP as our report device. When FXR and RXR dimerize, the linked CadC will be in close proximity and the dimerization occurs, activating promoter CadBA to express GFP.
Finally, we chose FXR and RXR as bile acid sensing receptors, GFP as a signaling device and E. coli BL21 as our chassis organism, hoping to demonstrate the feasibility of our project.
Fig.1. Gene circuit based on GFP
Fig.2. Fluorescence intensity/OD using a gradient of CDCA concentrations based on ddRFP.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 800