Part:BBa_K4321007:Design
Cyt1Aa Cassette
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 264
Illegal PstI site found at 1006 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 264
Illegal PstI site found at 1006
Illegal NotI site found at 1888 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 264
Illegal BglII site found at 1304
Illegal BamHI site found at 683 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 264
Illegal PstI site found at 1006 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 264
Illegal PstI site found at 1006 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Unlike Cyt2Ba, the stability of the Cyt1Aa protein and colony formation in host and E.coli cells are reliant on the co-expression of a P20 helper protein. When trying to express Cyt1Aa, this factor should be considered. For our project we designed this cassette with flanking BsaI sites (included in cassette), for insertion into pCG004. However, desired restriction sites can be added to both ends of the cassette for desired plasmid insertion. Following the digestion with BsaI the last two bases will be lost to yield a 2206 bp fragment.
Source
The cassette was synthesized by IDT. Information on the origin of each part can be found on their respective part pages: P20 helpher protein - BBa_K2938004, Cyt1Aa - BBa_K2938003, RBS - BBa_B0034, mScarlet - BBa_K4321004, Terminator - BBa_K4321008.
References
Soberón, M., López-Díaz, J. A., & Bravo, A. (2013). Cyt toxins produced by bacillus thuringiensis: A protein fold conserved in several pathogenic microorganisms. Peptides, 41, 87–93. https://doi.org/10.1016/j.peptides.2012.05.023
Torres-Quintero, M.-C., Gómez, I., Pacheco, S., Sánchez, J., Flores, H., Osuna, J., Mendoza, G., Soberón, M., & Bravo, A. (2018). Engineering bacillus thuringiensis cyt1aa toxin specificity from dipteran to lepidopteran toxicity. Scientific Reports, 8(1). https://doi.org/10.1038/s41598-018-22740-9
Valtierra-de-Luis, D., Villanueva, M., Berry, C., & Caballero, P. (2020). Potential for bacillus thuringiensis and other bacterial toxins as biological control agents to combat dipteran pests of medical and agronomic importance. Toxins, 12(12), 773. https://doi.org/10.3390/toxins12120773