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Team:UT Dallas/data
From 2011.igem.org
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<b>Data For Our Favorite New Parts</b> | <b>Data For Our Favorite New Parts</b> | ||
| - | <br>PcstA-RBS-LuxI-terminator, BBa_K569001 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569001">Main Page</a>): 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. | + | <br>PcstA-RBS-LuxI-terminator, BBa_K569001 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569001">Main Page</a>): 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.<br> |
| - | <br>PyeaR-ToxR-FGFR, BBa_K569013 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569013">Main Page</a>): 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. | + | <br>PyeaR-ToxR-FGFR, BBa_K569013 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569013">Main Page</a>): 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. <br> |
<br>SCP-ToxR-FGFR, BBa_K569014 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569014">Main Page</a>): 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.<br><br> | <br>SCP-ToxR-FGFR, BBa_K569014 (<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K569014">Main Page</a>): 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.<br><br> | ||
Revision as of 02:14, 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.
