Reporter
Part:BBa_K2150019
Designed by: Jianyi Huang Group: iGEM16_UCAS (2016-10-12)
pT7+pTet+RBS+tetX-GFP(fusion protein)+DT
Two promoters are used, a constitutive promoter pTet and a T7RNAP specific promoter pT7. The fusion protein is tetX and GFP with a 3*GGGGS linker so that the expression level of tetX can be accurately reported by the fluorescence intensity of GFP. By testing the fluorescence intensity, we found that in the absence of T7 promoter, these two promoters exhibit higher efficiency than single pTet; the fluorescence intensity is lower that BBa_K2150018, in which the fusion protein is substituted by single tetX. With pT7, expression of GFP can be amplified while with pTet, expression of GFP can be repressed by tetR.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 670
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1967
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Categories
Parameters
None |