Part:BBa_K3746011:Design
T7-LacO-DsbAss-FDRA-6His
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 189
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The start codon of basic part FDR-A (BBa_K3746003) is removed in our designed DNA due to a N-terminal signal peptide (DsbAss) is added into this secretory construct.
Source
The sequence of MSMEG_5998 (coding sequence of FDR-A) was identified by a literature review [1] and the sequence was then extracted from NCBI (RefSeq: NZ_CP054795.1:4976460-4976939). Codon optimization for E. coli done by ThermoFisher Scientific GeneArt platform.
The other basic part sequences were identified from the iGEM part registry. The T7 promoter, LacO, RBS, and T7 terminator parts were used in the previous iGEM projects of our team.
We plan to synthesize this composite part by IDT in form of gene fragments and clone it into the pSB1C3 vector by restriction cloning.