Difference between revisions of "Part:BBa K819007"
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<p style="text-align:center">Figure 1. luminance measurement of different attenuator</p> | <p style="text-align:center">Figure 1. luminance measurement of different attenuator</p> | ||
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Revision as of 07:25, 25 September 2012
Measurement device for Luminesensor
recA408 Promoter + B0030 + GFP + ssrA-tag
A fast degrading GFP ligated to the rear of a sulA promoter in 408 form (only recognizable by our LexA-VVD fusing protein, not by E.coli endogenous LexA). The sulA promoter promotes a gene which express SulA protein, a differentiation inhibitor, and was a member of the SOS regulon family. When co-transformed with our luminesensor plasmid into E.coli cell illuminated by blue light, the light will triger the dimerizaiton of the LexA408-VVD fusion protein and the dimerized LexA408 domain will bind the SOS box in 408 form in the SulA408 promoter to inhibit the transcription of the downstream gene so that no GFP will be expressed; if the environment is dark, the luminesensor will not dimerize and no supression of the promoter will occour, and GFP will be expressed.
Cells exposed to different light intensity expressing Luminesensor showed manifest light-repressed reporter gene transcription. As shown in the figure, all of the cells with dissimilar attenuators showed incredible repression efficiency (figure 1: luminance measurement of different attenuator).
Figure 1. luminance measurement of different attenuator
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 850
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 850
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 850
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 850
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 745