Part:BBa_K5103001
PCG004 with Cry8Da
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 595
Illegal EcoRI site found at 6398
Illegal EcoRI site found at 8948
Illegal EcoRI site found at 9027
Illegal EcoRI site found at 10439
Illegal EcoRI site found at 11102
Illegal XbaI site found at 11533
Illegal PstI site found at 8079
Illegal PstI site found at 9520 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 595
Illegal EcoRI site found at 6398
Illegal EcoRI site found at 8948
Illegal EcoRI site found at 9027
Illegal EcoRI site found at 10439
Illegal EcoRI site found at 11102
Illegal NheI site found at 6234
Illegal PstI site found at 8079
Illegal PstI site found at 9520 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 595
Illegal EcoRI site found at 6398
Illegal EcoRI site found at 8948
Illegal EcoRI site found at 9027
Illegal EcoRI site found at 10439
Illegal EcoRI site found at 11102
Illegal BglII site found at 66
Illegal BglII site found at 3147
Illegal XhoI site found at 3151
Illegal XhoI site found at 11410 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 595
Illegal EcoRI site found at 6398
Illegal EcoRI site found at 8948
Illegal EcoRI site found at 9027
Illegal EcoRI site found at 10439
Illegal EcoRI site found at 11102
Illegal XbaI site found at 11533
Illegal PstI site found at 8079
Illegal PstI site found at 9520 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 595
Illegal EcoRI site found at 6398
Illegal EcoRI site found at 8948
Illegal EcoRI site found at 9027
Illegal EcoRI site found at 10439
Illegal EcoRI site found at 11102
Illegal XbaI site found at 11533
Illegal PstI site found at 8079
Illegal PstI site found at 9520
Illegal AgeI site found at 9294
Illegal AgeI site found at 10176 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 11524
Illegal BsaI.rc site found at 7949
Illegal BsaI.rc site found at 7962
Illegal BsaI.rc site found at 11537
Illegal SapI.rc site found at 1219
Illegal SapI.rc site found at 5124
Profile
Name: PCG004 with Cry8Da
Base Pairs: 12661 bp
Origin: Add
Properties: High copy number [1]
Usage and Biology
It includes features for selective gene expression in a dropout region that normally contains green fluorescent protein (GFP) flanked by BsaI sites. In this case we replaced GFP with Cry8Da crystal toxin sequences from Bacillus thuringiensis (Bt). Upstream, a lacI sequence encodes the lac repressor and a lac operator (lacO) overlaps with the pGrac promoter. Using this plasmid allows us to induce the expression of Cry8Da when we want using IPTG. This allows transcription of Cry8Da by causing a conformational change in Lac, releasing it from lacO.
This is a composite part (seePart:BBa_K5103000) that includes pCG004, a shuttle plasmid backbone designed for E. coli , with the Cry8Da gene inserted. The Cry8Da gene is under the control of an IPTG-inducible promoter, enabling regulation of protein expression.
This composite part has been demonstrated to work effectively in E. coli DH5α, and the expression of Cry8Da is regulated using the IPTG-inducible promoter.
This system can be used for producing the Cry8Da protein in E. coli for laboratory studies, protein purification, and potential applications in bioinsecticide development.
INSERT INFORMATION ABOUT THE HISTORY OF THE PART
Figure 1 . Streak plate of PCG-Cry8Da transformant colonies grown on ampicillin selective media.
References
[1] Gilbert, C., Howarth, M., Harwood, C. R., & Ellis, T. (2017). Extracellular Self-Assembly of Functional and Tunable Protein Conjugates from Bacillus subtilis. ACS synthetic biology, 6(6), 957–967. https://doi.org/10.1021/acssynbio.6b00292
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