Part:BBa_K1072007
Lux pI+RBS+LuxR+2TM+Lux pR+RBS+LuxI+2TM+Lux pR+RBS+GFP+2TM+Lux pR+RBS+α-ALS+2TM
BBa_K1072007 is a composite divece, including LuxR, LuxI, GFP and α-ALS genes.
LuxR is under control of a constitutive promotor, Lux pI. Produce, LuxR, forms a complex with the quorum sensing molecule AHL and this complex subsequently increases the transcriptional rate of the lux pR promoter while also decreas the transcriptional rate of the lux pL promoter. The other genes are under control of this lux pR promoter.
The generator, Lux pR+RBS+LuxI+B0015, express AHL which will combine with LuxR.
GFP also is under control of Lux pR, presenting as reporter.
α-ALS,as our desire produce, will transcrip activated by LuxR and AHL complex. If co-transforming with B0015, this system will transcript α-ALS periodically.
Finally, this part just is the combination of BBa_K1072000 and BBa_K1072006.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1821
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1101
Illegal BsaI.rc site found at 1970
Illegal BsaI.rc site found at 2697
Illegal BsaI.rc site found at 2916
//chassis/prokaryote/ecoli
//function/reporter/fluorescence
control | (1) R0063 & (2) R0062 & (3) R0062 |
device_type | feedback |
direction | Forward |
latency | Seconds |
protein | (1) LuxR _ (2) GFP (3) luxI-LVA (4) α-ALS |
signalling_molecule | 3OC6HSL (AHL) |
switch_point | (1) 2nM |