Part:BBa_K4244015
dCas9 double repression system
This plasmid contains a system to control the amount of dCas9 with the amount of rhamnose. Here the amount of dSpyCas9 will decrease when more rhamnose is present. This was accomplished by placing the repressor gene CI under the rhamnose inducible promoter. Due to this, more CI will produced the more rhamnose is present. This CI then represses the pR promoter that controls the expression of dSpyCas9. To check this, a lucifirase protein was fused to dSpyCas9. For this system a titratable inducer was needed. Therefore the experiment must be done in an E. coli strain containing two knock-outs, one for rhamnose transport and one for rhamnose catabolism, these were obtained form papers [1]. This system was tested, by placing cells on different amounts of rhamnose and then measuring luciferase expression (Figure 1)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 33
Illegal EcoRI site found at 1038
Illegal EcoRI site found at 2410 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 33
Illegal EcoRI site found at 1038
Illegal EcoRI site found at 2410
Illegal NheI site found at 2169 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 33
Illegal EcoRI site found at 1038
Illegal EcoRI site found at 2410
Illegal BamHI site found at 4448 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 33
Illegal EcoRI site found at 1038
Illegal EcoRI site found at 2410 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 33
Illegal EcoRI site found at 1038
Illegal EcoRI site found at 2410 - 1000COMPATIBLE WITH RFC[1000]
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