Difference between revisions of "Part:BBa K2933278"

 
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<partinfo>BBa_K2933278 parameters</partinfo>
 
<partinfo>BBa_K2933278 parameters</partinfo>
 
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===Usage and Biology===
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This composite part is made up with three basic parts, the HiS tag, the thrombin restriction site and our target protein TMB-2. It encodes a protein which is TMB-2 fused with His tag. The fusion protein is about 27.2 kD. It is convenient for us to purify our target protein.
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===Molecular cloning===
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First, we used the vector pET-28a to construct our expression plasmid. And then we converted the plasmid constructed to ''E. coli'' DH5α to expand the plasmid largely.<br>
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<p style="text-align: center;">
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  [[File:TMB PCR.png|200px]]<br>
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'''Figure 1.'''    The PCR result of TMB-2. <br>
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===References===
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[1]Structural Insights into TMB-1 and the Role of Residues 119 and 228 in Substrate and Inhibitor Binding.Skagseth S, Christopeit T, Akhter S, Bayer A, Samuelsen Ø, Leiros HS.Antimicrob Agents Chemother. 2017 Jul 25;61(8).

Revision as of 07:33, 24 September 2019


RBS+Linker h+His+Linker f+TMB-2+T7 terminator

This part consists of RBS, protein coding sequence(His+Linker h+Sumo+Linker f+TMB-2) and T7 terminator,and the biological module can be build into E.coli for protein expression. This part can be prefaced with promoters of different strengths and types to regulate expression function.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 93
    Illegal NheI site found at 874
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This composite part is made up with three basic parts, the HiS tag, the thrombin restriction site and our target protein TMB-2. It encodes a protein which is TMB-2 fused with His tag. The fusion protein is about 27.2 kD. It is convenient for us to purify our target protein.

Molecular cloning

First, we used the vector pET-28a to construct our expression plasmid. And then we converted the plasmid constructed to E. coli DH5α to expand the plasmid largely.

TMB PCR.png
Figure 1. The PCR result of TMB-2.

References

[1]Structural Insights into TMB-1 and the Role of Residues 119 and 228 in Substrate and Inhibitor Binding.Skagseth S, Christopeit T, Akhter S, Bayer A, Samuelsen Ø, Leiros HS.Antimicrob Agents Chemother. 2017 Jul 25;61(8).