Difference between revisions of "Part:BBa K2933209"
(→Usage and Biology=) |
|||
Line 26: | Line 26: | ||
'''Figure 1.''' The PCR result of PEDO-1. <br> | '''Figure 1.''' The PCR result of PEDO-1. <br> | ||
</p> | </p> | ||
+ | ===References=== | ||
+ | [1]Dereje Dadi Gudeta, Valeria Bortolaia,The Soil Microbiota Harbors a Diversity of Carbapenem-Hydrolyzing β-Lactamases of Potential Clinical Relevance[J],Antimicrobial Agents and chemotherapy,January 2016<br> |
Revision as of 13:48, 23 September 2019
T7 promoter+RBS b+Linker h+His+Linker f+PEDO-1+T7 terminator
This part consists of T7 promoter, RBS and protein coding sequence(His+Linker f+PEDO-1),and the biological module can be built into E.coli for protein expression.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 47
Illegal PstI site found at 741
Illegal PstI site found at 1027 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 169
Illegal PstI site found at 741
Illegal PstI site found at 1027 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 47
Illegal PstI site found at 741
Illegal PstI site found at 1027 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 47
Illegal PstI site found at 741
Illegal PstI site found at 1027 - 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
This composite part is made up with seven basic parts, the His tag, T7 promoter, RBS ,Linker h ,Linker f,T7 terminatorand and our target protein PEDO-1. It encodes a protein which is PEDO-1 fused with His tag. The fusion protein is about 32.2 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of PEDO-1 . It is convenient for us to purify our target protein.
Molecular cloning
First, we used the vector pGEX-28a to construct our expression plasmid. And then we converted the plasmid constructed to E. coli DH5α to expand the plasmid largely.
Figure 1. The PCR result of PEDO-1.
References
[1]Dereje Dadi Gudeta, Valeria Bortolaia,The Soil Microbiota Harbors a Diversity of Carbapenem-Hydrolyzing β-Lactamases of Potential Clinical Relevance[J],Antimicrobial Agents and chemotherapy,January 2016