Part:BBa_K5322000:Design
Constitutive Mfp3 Expression System
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 210
Illegal NotI site found at 174 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
To ensure that the animal-derived mussel foot protein Mfp3 can be successfully expressed in BL21(DE3), we performed codon optimization on the Mfp3 sequence.
Source
The plasmid pET29a-J23119-RBS-Mfp3-T7 utilizes the pET29a vector, which is commonly employed for robust gene expression in Escherichia coli. The components used in this design, including the J23119 promoter and Mfp3, are derived from the standard biological parts registry of iGEM ( BBa_J23119, BBa_K4854000), with the mussel foot protein Mfp3 sourced from natural marine mussels. These parts were selected for their validated functionality and compatibility in synthetic biology applications, facilitating controlled expression within bacterial cells under specific conditions.
References
1.Kaoru Takabayashi, Naoki Hosoe, Motohiko Kato, et al. Significance of endoscopic deep small bowel evaluation using balloon-assisted enteroscopy for Crohn's disease in clinical remission[J]. Journal of gastroenterology. 2020, 56(prepublish): 1-9.
2.Zhao Mirabella, Gönczi Lóránt, Lakatos Peter L, et al. The Burden of Inflammatory Bowel Disease in Europe in 2020[J]. Journal of Crohn's and Colitis. 2021, 15(9): 1573-1587.