Part:BBa_K5322007
NO-inducible Mfp53 Expression System
Usage and Biology
The plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7 utilizes the pET29a vector for high-level expression in Escherichia coli. To enhance intestinal mucosal repair, we employed the oxidative stress-responsive SoxR/SoxS promoter system, targeting treatment at the site of intestinal inflammation in a high nitric oxide (NO) environment. The expression of SoxR is controlled by the strong constitutive promoter J23119, which responds to NO and activates the SoxR promoter to regulate the expression of the mussel foot protein Mfp53. The ribosome binding site (RBS) ensures efficient translation of mRNA, while the T7 terminator provides a clean and efficient transcriptional end. This system is designed for the effective expression of Mfp53 in high NO environments associated with intestinal inflammation, facilitating its adhesive properties.
Construction of the plasmid
Due to the lack of endotoxin in Escherichia coli Nissle 1917 (EcN), we chose EcN as the chassis cell to enhance safety. To achieve efficient expression of adhesive proteins, we selected the strong promoter J23119 as the regulatory element and used the protein linker (GGGGS) to connect Mfp3 and Mfp5. To improve intestinal mucosal repair in a high nitric oxide (NO) environment associated with intestinal inflammation, we employed the oxidative stress-responsive SoxR/SoxS promoter system, targeting treatment at the site of intestinal inflammation. As shown in Figure 2-1, we designed the plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7. Through homologous recombination, we transferred this plasmid into EcN, followed by the selection of single colonies from several transformation plates for plasmid extraction. We verified the presence of the target 1333 bp fragment using specific primers in a PCR assay, as depicted in Figure 2-2. Plasmids with correctly positioned bands were sequenced, and the sequencing results in Figure 2-3 confirmed the successful construction of the plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7.
Figure 2-1 Plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7
Figure 2-2 Colony PCR gel electrophoresis of plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7(1333bp)
Figure 2-3 plasmid pET29a-J23119-SoxR-T-pSoxS-RBS-Mfp53-T7 sequencing result
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 603
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 603
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 603
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 603
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 603
Illegal AgeI site found at 585 - 1000COMPATIBLE WITH RFC[1000]
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