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Team:UT Dallas/data
From 2011.igem.org
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<b>Data For Pre-existing Parts</b><br> | <b>Data For Pre-existing Parts</b><br> | ||
| - | <a href="http://partsregistry.org/Part:BBa_K131010:Experience">Experience</a> | + | <a href="http://partsregistry.org/Part:BBa_K131010:Experience">Experience</a>: We grew PcstA-RBS-LuxI-terminator and AHL-inducible ColicinE2-GFP transformed in BL21 E.coli cells. We combined the two cultures in various ratios and either added or did not add glucose. We allowed these samples to continue growing for 2 hours and we took measurements using a fluorescent microscope. |
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Revision as of 02:12, 29 September 2011
Data
Data For Our Favorite New PartsPcstA-RBS-LuxI-terminator, BBa_K569001 (Main Page): This part produces LuxI,an enzyme for creating acyl-homoserine lactones from normal cell metabolites, in the absence of glucose. This part is repressed by glucose.
PyeaR-ToxR-FGFR, BBa_K569013 (Main Page): PyeaR is a nitrate inducible promoter. ToxR+FGFR is a receptor fusion of two dimerizing proteins. FGFR responds to FGF by dimerizing; this causes ToxR to dimerize. When ToxR is dimerized it acts as a transcription factor for the ctx promoter.
SCP-ToxR-FGFR, BBa_K569014 (Main Page): This part constitutively produces the ToxR+FGFR fusion protein. ToxR+FGFR dimerizes in response to FGF and can then activate the ctx promoter from the bacteria Vibrio cholera. ToxR by itself is a transcription factor, while FGFR is a immune system sensor.
Data For Pre-existing Parts
Experience: We grew PcstA-RBS-LuxI-terminator and AHL-inducible ColicinE2-GFP transformed in BL21 E.coli cells. We combined the two cultures in various ratios and either added or did not add glucose. We allowed these samples to continue growing for 2 hours and we took measurements using a fluorescent microscope.
