Composite
Part:BBa_K396000:Design
Designed by: Ryuji Yamamoto Group: iGEM10_Chiba (2010-10-21)
T7/CI Hybrid Promoter with GFP (composite with LuxR generator)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 783
Illegal NheI site found at 806 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 852
Illegal BamHI site found at 1421
Illegal XhoI site found at 822
Illegal XhoI site found at 1322 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
LuxR generator functions as it is designed. T7/CI hybrid promoter function is checked by using BL21(DE3) strain, resulted in that it works within limited range of the expression of T7 RNA polymerase (IPTG concentration<100μM).
Source
Lambda CI operator sequence (OR1, BBa_R1051) is connected to T7 Promoter (BBa_I719005). LuxR generator is consisted of constitutive promoter (BBa_J23100) and LuxR coding sequence (BBa_C0062).