Difference between revisions of "Part:BBa K3505039"

 
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<partinfo>BBa_K3505039 short</partinfo>
 
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===Usage and Biology===
 
===Usage and Biology===
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This Trancriscription Unit can overexpress antitoxic proteins in order to to achieve epression of non omologous membrane proteins in E. coli.
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===Design Notes===
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The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is present in <bbpart>BBa_K3505009</bbpart> and has overhangs compatible for Golden Braid cloning.
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===Verification of cloning===
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[[File:T--Thessaly--d1.png|600px|thumb|none|<i><b>Fig.2:</b>Level 0 DjlA U4 C4 Digested with EcoRI, PstI Expected bands  2029, 894</i>]]
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===Sequence and Features===
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K3505039 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K3505039 SequenceAndFeatures</partinfo>
  
  
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===References===
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===Functional Parameters===
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*[1]Gialama, D., Delivoria, D., Michou, M., Giannakopoulou, A. and Skretas, G., 2017. Functional Requirements for DjlA- and RraA-Mediated Enhancement of Recombinant Membrane Protein Production in the Engineered Escherichia coli Strains SuptoxD and SuptoxR. <em>Journal of Molecular Biology</em>, 429(12), pp.1800-1816.
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<partinfo>BBa_K3505039 parameters</partinfo>
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Revision as of 16:42, 24 October 2020


ParaBAD-DjlA-Terminator



Usage and Biology

This Trancriscription Unit can overexpress antitoxic proteins in order to to achieve epression of non omologous membrane proteins in E. coli.


Design Notes

The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is present in BBa_K3505009 and has overhangs compatible for Golden Braid cloning.



Verification of cloning

Fig.2:Level 0 DjlA U4 C4 Digested with EcoRI, PstI Expected bands 2029, 894


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1148
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 983
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 965


References

  • [1]Gialama, D., Delivoria, D., Michou, M., Giannakopoulou, A. and Skretas, G., 2017. Functional Requirements for DjlA- and RraA-Mediated Enhancement of Recombinant Membrane Protein Production in the Engineered Escherichia coli Strains SuptoxD and SuptoxR. Journal of Molecular Biology, 429(12), pp.1800-1816.