Difference between revisions of "Part:BBa K3771033"
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<br>This composite part is a component of the IFN-γ sensing system and is used to express the taurine production enzyme, JJU10.
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<br>This composite part is a component of the IFN-γ sensing system and is used to express the taurine production enzyme, JJU.
 
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<br>The ompA promoter facilitates the constitutive expression of OmpA/OprF. Binding of IFN-γ to the OmpA/OprF chimeric protein induces the response of the phage shock protein (Psp) system, a highly conserved stress response system in enterobacteria[1]. Signal transduction from the outer membrane to the inner membrane activates the <i>pspA</i> promoter, initiating expression of JJU10. JJU10 converts L-cysteine into L-cystate in the taurine synthesis L-cystate pathway.
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  <br>The <i>ompA</i> promoter facilitates the constitutive expression of OmpA/OprF. Binding of IFN-γ to the OmpA/OprF chimeric protein induces the response of the phage shock protein (Psp) system, a highly conserved stress response system in enterobacteria[1]. Signal transduction from the outer membrane to the inner membrane activates the <i>pspA</i> promoter, initiating expression of JJU. JJU converts L-cysteine into L-cystate in the taurine synthesis L-cystate pathway.
 
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<img src="https://2021.igem.org/wiki/images/c/c9/T--NCKU_Tainan--taurine_pathway_1.png" style="width:60%;">
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<p align="center">Fig.1 Taurine pathways in <i>E. coli</i></p>
 
<br><b style="font-size:1.3rem">Usage</b>
 
<br><b style="font-size:1.3rem">Usage</b>
 
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<br>We ligased the NPO-OmpA* fragment and pspA-JJU10-his-tag on the pSU expression vector and transformed it into DH5alpha to complete construction of the plasmid. The his-tag allows for confirmation of JJU10 expression by western blot using the anti-6X his-tag antibody.
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  <br>We ligased the <i>P<sub>ompA</sub>-ompA/oprF</i> fragment and <i>P<sub>pspA</sub>-jju-6xHis</i> on the pSU expression vector and transformed it into DH5α to complete construction of the plasmid. The his-tag allows for confirmation of JJU expression by western blot using the anti-6X his-tag antibody.
 
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<br>Double digestion results are shown in Figure 1.
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<p align="center">Fig. 2. Double digestion check of <i>P<sub>pspA</sub>-jju-6xHis</i></p>
  
 
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<img src="https://2021.igem.org/wiki/images/a/a8/T--NCKU_Tainan--colony_pspAjjuompA.jpg" style="width:40%;">
 
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<p align="center">圖片描述</p>
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<p align="center">Fig. 3. Colony PCR confirmation of the construction</p>
  
 
<br><b style="font-size:1.3rem">References</b>
 
<br><b style="font-size:1.3rem">References</b>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===

Revision as of 21:27, 19 October 2021


PpspA-JJU-6xHis-PompA-OmpA/OprF


Description

This composite part is a component of the IFN-γ sensing system and is used to express the taurine production enzyme, JJU.

Biology

The ompA promoter facilitates the constitutive expression of OmpA/OprF. Binding of IFN-γ to the OmpA/OprF chimeric protein induces the response of the phage shock protein (Psp) system, a highly conserved stress response system in enterobacteria[1]. Signal transduction from the outer membrane to the inner membrane activates the pspA promoter, initiating expression of JJU. JJU converts L-cysteine into L-cystate in the taurine synthesis L-cystate pathway.

Fig.1 Taurine pathways in E. coli


Usage

We ligased the PompA-ompA/oprF fragment and PpspA-jju-6xHis on the pSU expression vector and transformed it into DH5α to complete construction of the plasmid. The his-tag allows for confirmation of JJU expression by western blot using the anti-6X his-tag antibody.

Characterization

Fig. 2. Double digestion check of PpspA-jju-6xHis

Fig. 3. Colony PCR confirmation of the construction


References

1. Darwin AJ. The phage-shock-protein response. Molecular Microbiology. 2005;57(3):621-628. doi:10.1111/j.1365-2958.2005.04694.x https://pubmed.ncbi.nlm.nih.gov/16045608/

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 12
    Illegal BamHI site found at 2485
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]