Composite
Part:BBa_K4432142:Design
Designed by: Paul Weimer Group: iGEM22_Evry_Paris-Saclay (2022-09-26)
Pseudomonas aeruginosa PhzA1-G1 truncated operon under the control of the T5 promoter
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1048
Illegal EcoRI site found at 3670
Illegal PstI site found at 1191
Illegal PstI site found at 4675
Illegal PstI site found at 5224 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1048
Illegal EcoRI site found at 3670
Illegal PstI site found at 1191
Illegal PstI site found at 4675
Illegal PstI site found at 5224 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1048
Illegal EcoRI site found at 3670
Illegal BamHI site found at 397
Illegal BamHI site found at 1603
Illegal XhoI site found at 341
Illegal XhoI site found at 500 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1048
Illegal EcoRI site found at 3670
Illegal PstI site found at 1191
Illegal PstI site found at 4675
Illegal PstI site found at 5224 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1048
Illegal EcoRI site found at 3670
Illegal PstI site found at 1191
Illegal PstI site found at 4675
Illegal PstI site found at 5224
Illegal NgoMIV site found at 263
Illegal NgoMIV site found at 1272
Illegal NgoMIV site found at 1419
Illegal NgoMIV site found at 1437
Illegal NgoMIV site found at 1441
Illegal NgoMIV site found at 2245
Illegal NgoMIV site found at 2419
Illegal AgeI site found at 5513 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 5656
Illegal BsaI.rc site found at 2355
Illegal BsaI.rc site found at 4732
Illegal BsaI.rc site found at 5138
Illegal BsaI.rc site found at 5165
Illegal SapI.rc site found at 4152
Design Notes
T5 promoter (BBa_K4432000) + custom made RBS (BBa_K4432014) + Pseudomonas aeruginosa PhzA1-G1 truncated operon (BBa_I723028)
Source
PCR amplification & Assembly