Part:BBa_K3505036
pFliC:RBS-LacI-Terminator- pAndersonJ23115:LacO:RBS-ECFP-terminator
Usage and Biology
2 Trancription Units
- LacI BBa_K3505003regulated by inducible promoter FliC BBa_K2924016which is activated from SFCAs and more specifically from Butyrate
- eCFP BBa_K3505019under control of lac regulated AndersonBBa_K3505013.
This way we take signal in the Absence of SCFAs
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is present in BBa_K3505010 and has overhangs compatible for GoldenBraid cloning.
Verification of cloning
Experimental Use and Experience
Measurements are the average of 9 total replicates (3 biological replicates and 3 technical replicates per biological replicate). Error bars represent standard deviation of biological replicates
Conculusion
There is a slight increase in fluorescence in absence of SCFAs - acetate and propionate - as expected. We hypothesize that the gap will be bigger when adding butyrate, which is the main inducer for pFliC, and which we didn’t have in the lab as per Wiki Freeze date. As far as the cell growth goes, we expected a reduction of the cells, since we add acids that are toxic to the cells. These results indicate that our NOT-Gate system works, regarding these acids but in an expected range.
Sequnce and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1321
Illegal NheI site found at 1344 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
None |