Difference between revisions of "Part:BBa K2336039:Design"

 
 
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<partinfo>BBa_K2336039 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2336039 SequenceAndFeatures</partinfo>
  
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<h1>'''Design Note'''</h1>
  
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===Design Notes===
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We made full use of the two-component system found in Salmonella. We try to change the Iron binding motif to 12 lathanide binding tags in the membrane protein PmrB. Then PmrB can activate PmrA by phosphorylating it. Phosphorylated PmrA is going to activate promoter PmrC and GFP can be expressed. In the end, the sensing system can detect the concentration of lanthanide nearby.
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None.
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<h1>'''Resources'''</h1>
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===Source===
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Our LBT.PmrA-PmrB(Fe).PmrC-GFP were synthesized by IDT. Then we used SOE (splicing by over-lapping extension) to change the Iron binding motif to 12 lathanide binding tags in the membrane protein PmrB. Moreover, we use restriction enzyme and ligase to fuse the PmrA-PmrB(LBT) and PmrC-GFP.
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</h1>'''References'''</h1>
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None.
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Engineering Bacterial Two-Component System PmrA/PmrB to Sense Lanthanide Ions
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===References===
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Latest revision as of 19:37, 31 October 2017


PmrA-PmrB(LBT11)-PmrC-GFP


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2125
    Illegal XhoI site found at 2164
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1713
    Illegal AgeI site found at 2890
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2813
    Illegal SapI.rc site found at 691

Design Note

We made full use of the two-component system found in Salmonella. We try to change the Iron binding motif to 12 lathanide binding tags in the membrane protein PmrB. Then PmrB can activate PmrA by phosphorylating it. Phosphorylated PmrA is going to activate promoter PmrC and GFP can be expressed. In the end, the sensing system can detect the concentration of lanthanide nearby.


Resources

Our LBT.PmrA-PmrB(Fe).PmrC-GFP were synthesized by IDT. Then we used SOE (splicing by over-lapping extension) to change the Iron binding motif to 12 lathanide binding tags in the membrane protein PmrB. Moreover, we use restriction enzyme and ligase to fuse the PmrA-PmrB(LBT) and PmrC-GFP. </h1>References</h1> Engineering Bacterial Two-Component System PmrA/PmrB to Sense Lanthanide Ions