Difference between revisions of "Part:BBa K3771021"
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<p align="center">Fig.1 Taurine pathways in <i>E. coli</i></p> | <p align="center">Fig.1 Taurine pathways in <i>E. coli</i></p> | ||
<br><b style="font-size:1.3rem">Usage</b><br> | <br><b style="font-size:1.3rem">Usage</b><br> | ||
− | <br>We ligased the <i>jju</i>-6xHis fragment and <i>pspA</i> promoter on the pSU expression vector and transformed it into DH5α to complete construction of the plasmid. The | + | <br>We ligased the <i>jju</i>-6xHis fragment and <i>pspA</i> promoter on the pSU expression vector and transformed it into DH5α to complete construction of the plasmid. The 6xHis allows for confirmation of JJU expression by western blot using the anti-6xHis antibody. <br> |
<br><b style="font-size:1.3rem">Characterization</b> | <br><b style="font-size:1.3rem">Characterization</b> |
Revision as of 20:17, 19 October 2021
PpspA-JJU10-6xHis
Description
This composite part is a component of the IFN-γ sensing system and was used to express the taurine production enzyme, JJU.
Biology
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 jju-6xHis fragment and pspA promoter on the pSU expression vector and transformed it into DH5α to complete construction of the plasmid. The 6xHis allows for confirmation of JJU expression by western blot using the anti-6xHis antibody.
Characterization
Fig. 2. Colony PCR confirmation of the construction
Reference
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