Part:BBa_K2933122
GST+Linker+Fla.103
This part encodes the fusion protein of GST tag and Fla.103 to promote the expression and purification of target protein(Fla.103).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 774
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 774
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1256
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 774
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 774
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 85
Usage and Biology
This composite part is made up with three basic parts, the GST tag, the cutting site of Prescission Protease and our target protein Fla.103. It encodes a protein which is Fla.103 fused with GST tag. The fusion protein is about 54.7 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of Fla.103 and combine the two parts with the cutting site of Prescission Protease. The fusion protein can be cut off at the cutting site by Prescission Protease. It is convenient for us to purify our target protein.
Molecular cloning
First, we used the vector pGEX-6p-1 to construct our expression plasmid. And then we converted the plasmid constructed to E. coli DH5α to expand the plasmid largely.We then extracted plasmids and performed double enzyme digestion verification.
Figure 1. (a) The PCR result of Fla.103. (b) The verification results by enzyme digestion.The 1 is the original plasmid.The 2 is the
results verified by double enzyme digestion.
After verification, it was determined that the construction is successful. We converted the plasmid to E. coli BL21(DE3) for expression and purification.
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