Difference between revisions of "Part:BBa K4244005"

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<partinfo>BBa_K4244005 short</partinfo>
 
<partinfo>BBa_K4244005 short</partinfo>
  
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sfGFP <partinfo>BBa_K4244004</partinfo> was fused to PelB <partinfo>BBa_J32015</partinfo> to secrete sfGFP and use it as an extracellular reporter. It is under an inducible promoter <partinfo>BBa_K914003</partinfo>. For better titration using <partinfo>BBa_K914003</partinfo> we introduced the plasmid in a &Delta; ''rhaB'',&Delta; ''rhaT'' strain [1].
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sfGFP <partinfo>BBa_K4244004</partinfo> was fused to PelB <partinfo>BBa_J32015</partinfo> (fused at the N-terminus) to secrete sfGFP and use it as an extracellular reporter. It is under an inducible promoter <partinfo>BBa_K914003</partinfo>. For better titration using <partinfo>BBa_K914003</partinfo> we introduced the plasmid in a &Delta; ''rhaB'',&Delta; ''rhaT'' strain [1].
  
  

Revision as of 08:44, 12 October 2022


Rhamose inducible sfGFP with OmpA secretion tag

sfGFP BBa_K4244004 was fused to PelB BBa_J32015 (fused at the N-terminus) to secrete sfGFP and use it as an extracellular reporter. It is under an inducible promoter BBa_K914003. For better titration using BBa_K914003 we introduced the plasmid in a Δ rhaB,Δ rhaT strain [1].


Secretion assay

Figure 1: End point measurement of total, pellet and supernatant fraction of sfGFP under the OmpA signal peptide expressed with rhamnose inducible promoter. Measurement was performed 5 hours after rhamnose induction at 500 μM. No significant fluorescence was detected in the supernatant fraction.

Discussion

No secretion was observed in E. coli Nissle. This experiment still need adjustment and fine tuning to prove the secretion of sfGFP.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


References

1. Hjelm A, Karyolaimos A, Zhang Z, Rujas E, Vikström D, Slotboom DJ, et al. Tailoring Escherichia coli for the l -Rhamnose PBAD Promoter-Based Production of Membrane and Secretory Proteins. ACS Synth Biol. 2017;6(6):985–94.