Translational_Unit
Part:BBa_K3866007
Designed by: Venetios Michelioudakis Group: iGEM21_Thessaly (2021-09-23)
ParaBAD-pta-Terminator
Usage and Biology
This TU includes the Pta gene placed under the control of the arabinosed-induced promoter. The inducible promoter is used because cloning wasn't done. After the constitutive expression, the metabolism went out of balance so no colonies survied to be chosen for screening.
Design Notes
The coding sequence was domesticated . We removed BsmBI and BsaI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in p3 a1 vector and has overhangs compatible for GoldenBraid cloning.
Verification of Cloning
Experimental Use and Experience
This part showed functionality at this part BBa_K3866009
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 2279
Illegal PstI site found at 2825
Illegal PstI site found at 3125
Illegal PstI site found at 3290 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 2279
Illegal PstI site found at 2825
Illegal PstI site found at 3125
Illegal PstI site found at 3290 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1148
Illegal BamHI site found at 2929 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 2279
Illegal PstI site found at 2825
Illegal PstI site found at 3125
Illegal PstI site found at 3290 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 2279
Illegal PstI site found at 2825
Illegal PstI site found at 3125
Illegal PstI site found at 3290
Illegal AgeI site found at 983
Illegal AgeI site found at 1385
Illegal AgeI site found at 1783
Illegal AgeI site found at 3029
Illegal AgeI site found at 3227 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 965
References
- Dittrich, C. R., Bennett, G. N., & San, K. Y. (2005). Characterization of the acetate-producing pathways in Escherichia coli. Biotechnology progress, 21(4), 1062–1067. https://doi.org/10.1021/bp050073s
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Categories
Parameters
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