Part:BBa_K3505028
PfliC:RBS-eCFP-terminator
eCFP BBa_K3505019uder control of a SCFAs inducible promoter pFLliC BBa_K2924016.
Usage and Biology
This Trancriscription Unit (TU) is activated form SCFAs and more specifically from Butyrate. Exressing the eCFP protein for report gene, representing the activity of the promoter FliC.
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 cloned in BBa_K3505008 and has overhangs compatible for Golden Braid cloning.
Verification of cloning
Experimental Use and Experinece
Conclusion
The graphs above indicate that adding acetate and propionate can provoke the expression of the reporter genes. However, based on the concentration and the time-point that the measurement is taken, the results change. As time passes, the expression of each fluorescent protein is higher. Furthermore, there is the maximum expression of these three reporter genes when we add 2mM acetate or propionate accordingly, while it is indicated that adding increasing (20mM, 200mM) concentration of acids and, especially, acetate prevents cell growth. That may occur, due to their toxicity to the cells which may lead to unsettling results.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
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