Difference between revisions of "Part:BBa K3089021"
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<partinfo>BBa_K3089021 short</partinfo> | <partinfo>BBa_K3089021 short</partinfo> | ||
− | This composite | + | This composite parts is meant to express csgA-linker-mfp5 fusion genes under T7 promoter and purify CsgA-linker-Mfp5 recombinant proteins by His-tag affinity purification. CsgA is an amyloid-like protein encoded on genome of E.coli MG1655 providing mechanical cohesive strength and Mfp5 is a mussel foot protein from Mytilus galloprovincialis responsible for interface adhesion. This recombinant protein would self-assemble into fibrous bundles or films with adhesive properties by displaying the mussel adhesion domains on the surface of amyloid scaffolds, which would be a promising new generation of bio-inspired adhesives for a wide range of applications. This part was designed based on the core part——mfp5, which has been submitted into parts registry by iGEM2015 Tu_delft(BBa_K1583002). |
Revision as of 09:45, 16 October 2019
T7 promoter+csgA-linker-mfp5-His fusion protein
This composite parts is meant to express csgA-linker-mfp5 fusion genes under T7 promoter and purify CsgA-linker-Mfp5 recombinant proteins by His-tag affinity purification. CsgA is an amyloid-like protein encoded on genome of E.coli MG1655 providing mechanical cohesive strength and Mfp5 is a mussel foot protein from Mytilus galloprovincialis responsible for interface adhesion. This recombinant protein would self-assemble into fibrous bundles or films with adhesive properties by displaying the mussel adhesion domains on the surface of amyloid scaffolds, which would be a promising new generation of bio-inspired adhesives for a wide range of applications. This part was designed based on the core part——mfp5, which has been submitted into parts registry by iGEM2015 Tu_delft(BBa_K1583002).
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This part was designed based on the paper "Strong underwater adhesives made by self-assembling multi-protein nanofibres" (Zhong et al, 2014.)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 314
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 314
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 516
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 314
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 314
- 1000COMPATIBLE WITH RFC[1000]