Difference between revisions of "Part:BBa M50499"
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<partinfo>BBa_M50499 SequenceAndFeatures</partinfo> | <partinfo>BBa_M50499 SequenceAndFeatures</partinfo> | ||
− | Constitutive promoter (BBa_S05450, iGEM) | + | Constitutive promoter (BBa_S05450, iGEM) and catabolite activator protein (CAP) binding site (BBa_M36547, iGEM) |
− | catabolite activator protein (CAP) binding site (BBa_M36547, iGEM) | + | |
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 23:47, 11 December 2018
Catabolite Activator Protein (CAP) Repressed Promoter
We placed the constitutive promoter (BBa_S05450, iGEM) immediately upstream from a catabolite activator protein (CAP) binding site (BBa_M36547, iGEM) in Plasmid E.
For our experiments, we placed this part upstream from GFP in order to assay expression levels through fluorescent intensity. This construct is an adaption of the natural lac operon, which is positively regulated by CAP, since the CAP binding site is naturally upstream of the RNA polymerase binding site. In this construct, we put the CAP binding site downstream in order to repress transcription when CAP binds due to steric hindrance.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 1059
Illegal PstI site found at 688
Illegal PstI site found at 849 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 144
Illegal NheI site found at 167
Illegal PstI site found at 688
Illegal PstI site found at 849 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 1059
Illegal PstI site found at 688
Illegal PstI site found at 849 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 1059
Illegal PstI site found at 688
Illegal PstI site found at 849 - 1000COMPATIBLE WITH RFC[1000]
Constitutive promoter (BBa_S05450, iGEM) and catabolite activator protein (CAP) binding site (BBa_M36547, iGEM)