Difference between revisions of "Part:BBa K4195102"

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<b>Fig. 1 Graphic description of the expression gene circuits for display cassette designed in OMEGA project.</b>
 
<b>Fig. 1 Graphic description of the expression gene circuits for display cassette designed in OMEGA project.</b>
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TTPB was fused to the C-terminal of INPNC to surface display for targeting <i>V. parahaemolyticus</i>. Arabinose-inducible system was used in the expression circuit of this part in pSB1C3 then constructed this part. We transformed the constructed plasmid into <i>E. coli</i> BL21(DE3) for further verification of its expression and function on the surface of <i>E. coli</i> and OMVs, including the interaction between TTPB and Vp0980.
 
TTPB was fused to the C-terminal of INPNC to surface display for targeting <i>V. parahaemolyticus</i>. Arabinose-inducible system was used in the expression circuit of this part in pSB1C3 then constructed this part. We transformed the constructed plasmid into <i>E. coli</i> BL21(DE3) for further verification of its expression and function on the surface of <i>E. coli</i> and OMVs, including the interaction between TTPB and Vp0980.
 
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Revision as of 16:31, 10 October 2022


I0500-B0034-INPNC-ttpB-B0015

Biology

INPNC INPNC is a truncated form of ice nucleation protein (INP) consisting of N- and C- terminal domains (1). It is a membrane protein commonly used to displayed protein on the cell surface (2).

TTPB TTPB is tail tubular protein B of podophage 7. It has been found that TTPB serves as ligands that recognizes the conserved Vibrio receptor Vp0980 to mediate phage adsorption. It binds with Vp0980 of Vibrio parahaemolyticus and then mediates phage adsorption and subsequent bacterial lysis(3).

Usage and design

Engineering OMVs for treating and preventing AHPND caused by the pathogen V. parahaemolyticus are a significant part of OMEGA project (Operable Magic to Efficiently Getting over AHPND). Based on the efforts of our previous projects in 2020 (AnTea-Glyphosate[hyperlink]) and 2021 (SALVAGE[hyperlink]), we further developed the surface display system on the OMVs released by the engineered bacteria. The usage of cargo proteins were no more limited to enzymes that are usually utilized to catalyze series bio-chemical reactions, since some receptors or ligands involved in complex protein-protein interaction (PPI) were selected as the cargo candidates. This year, we chose two classic anchor proteins, ClyA and INPNC, to construct the display cassette with various cargo proteins including rFET (receptor), rLvAPN1 (receptor), TTPA (ligand) and TTPB (ligand) (Fig. 1). On one hand, with the receptors displayed, OMVs will gain the function of neutralizing toxins secreted by V. parahaemolyticus. On the other hand, with the assistance of ligands displayed on the surface, OMVs will become a special vector to deliver antimicrobials for the specific pathogen. In summary, we have taken a step closer to the collections of extracellular functional elements (EFE), combining the OMVs, secretion systems and surface display systems which we have been dedicated to since 2020. Learn more information from our Design page.

T--XMU-China--surface display circuit.png

Fig. 1 Graphic description of the expression gene circuits for display cassette designed in OMEGA project.

TTPB was fused to the C-terminal of INPNC to surface display for targeting V. parahaemolyticus. Arabinose-inducible system was used in the expression circuit of this part in pSB1C3 then constructed this part. We transformed the constructed plasmid into E. coli BL21(DE3) for further verification of its expression and function on the surface of E. coli and OMVs, including the interaction between TTPB and Vp0980. Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
    Illegal NheI site found at 1537
    Illegal NheI site found at 1573
    Illegal NheI site found at 3709
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
    Illegal BamHI site found at 1566
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1308
    Illegal NgoMIV site found at 1641
    Illegal NgoMIV site found at 2973
    Illegal AgeI site found at 979
    Illegal AgeI site found at 2059
    Illegal AgeI site found at 2329
    Illegal AgeI site found at 2464
    Illegal AgeI site found at 2884
    Illegal AgeI site found at 3232
    Illegal AgeI site found at 4063
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2962
    Illegal SapI site found at 961
    Illegal SapI site found at 2180