Difference between revisions of "Part:BBa K4195013"
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===Usage and Design=== | ===Usage and Design=== | ||
− | Engineering OMVs for treating and preventing AHPND caused by the pathogen V. parahaemolyticus are a significant part of '''OMEGA''' project (<u>O</u>perable <u>M</u>agic to <u>E</u>fficiently <u>G</u>etting over <u>A</u>HPND). Based on the efforts of our previous projects in 2020([https://2020.igem.org/Team:XMU-China AnTea-Glyphosate])and 2021 ([https://2021.igem.org/Team:XMU-China | + | Engineering OMVs for treating and preventing AHPND caused by the pathogen V. parahaemolyticus are a significant part of '''OMEGA''' project (<u>O</u>perable <u>M</u>agic to <u>E</u>fficiently <u>G</u>etting over <u>A</u>HPND). Based on the efforts of our previous projects in 2020([https://2020.igem.org/Team:XMU-China AnTea-Glyphosate])and 2021 ([https://2021.igem.org/Team:XMU-China SALVAGE]), 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 guiding proteins 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 (guiding protein) and TTPB (guiding protein) (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 guiding proteins 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. |
[[File:T--XMU-China--surface display circuit.png|400px]] | [[File:T--XMU-China--surface display circuit.png|400px]] | ||
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− | '''Fig. 2 DNA gel electrophoresis of the colony PCR products of | + | '''Fig. 2 DNA gel electrophoresis of the colony PCR products of BBa_K4195100_pSB1C3.''' |
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− | 2. | + | ====2. Characterization of displaying cargo proteins==== |
+ | We used <partinfo>BBa_I0500</partinfo> promoter and RBS (<partinfo>BBa_B0034</partinfo>) to express INPNC-TTPB-his protein in ''E. coli'' BL21(DE3). The arabinose-induced overnight culture was then incubated with FITC-labeled anti-His-tag antibody in turn to verify whether the TTPB was displayed on the surface of ''E. coli'' or not. | ||
− | + | [[File:T--XMU-China--ItB.png|300px]] | |
− | + | '''Fig. 3 The results of immunofluorescence to characterize the function of the display system (p = 0.0277).''' | |
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+ | The ratio of fluorescence intensity (''λ''<sub>Ex</sub> = 492 nm, ''λ''<sub>Em</sub> = 518 nm) to OD<sub>600</sub> of positive control (''E. coli'' harboring <partinfo>BBa_K4195100</partinfo>) is higher than that of negative control (''E. coli'' harboring <partinfo>BBa_K4195008</partinfo>) (Fig. 3), which indicates that our surface display system can successfully display TTPB on the surface of ''E. coli''. | ||
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+ | ===Reference=== | ||
+ | 1. E. van Bloois, R. T. Winter, H. Kolmar, M. W. Fraaije, Decorating microbes: surface display of proteins on ''Escherichia coli''. ''Trends. Biotechnol.'' '''29''', 79-86 (2011). | ||
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+ | 2. http://2016.igem.org/Team:TJUSLS_China. | ||
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+ | 3. M. Hu, H. Zhang, D. Gu, Y. Ma, X. Zhou, Identification of a novel bacterial receptor that binds tail tubular proteins and mediates phage infection of ''Vibrio parahaemolyticus''. ''Emerg. Microbes. Infect.'' '''9''', 855-867 (2020). | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K4195013 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4195013 SequenceAndFeatures</partinfo> | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K4195013 parameters</partinfo> | <partinfo>BBa_K4195013 parameters</partinfo> | ||
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Latest revision as of 10:28, 13 October 2022
INPNC-ttpB-his
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)and 2021 (SALVAGE), 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 guiding proteins 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 (guiding protein) and TTPB (guiding protein) (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 guiding proteins 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.
Fig. 1 Graphic description of the expression gene circuits for display cassette designed in OMEGA project.
For this part (INPNC-TTPB-his), 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 composite part BBa_K4195100. 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.
Characterization
1.Identification
When constructing this circuit, colony PCR and gene sequencing were used to verify that the transformatants were correct. Target bands (4706 bp) can be observed at the position around 5000 bp (Fig. 2).
Fig. 2 DNA gel electrophoresis of the colony PCR products of BBa_K4195100_pSB1C3.
2. Characterization of displaying cargo proteins
We used BBa_I0500 promoter and RBS (BBa_B0034) to express INPNC-TTPB-his protein in E. coli BL21(DE3). The arabinose-induced overnight culture was then incubated with FITC-labeled anti-His-tag antibody in turn to verify whether the TTPB was displayed on the surface of E. coli or not.
Fig. 3 The results of immunofluorescence to characterize the function of the display system (p = 0.0277).
The ratio of fluorescence intensity (λEx = 492 nm, λEm = 518 nm) to OD600 of positive control (E. coli harboring BBa_K4195100) is higher than that of negative control (E. coli harboring BBa_K4195008) (Fig. 3), which indicates that our surface display system can successfully display TTPB on the surface of E. coli.
Reference
1. E. van Bloois, R. T. Winter, H. Kolmar, M. W. Fraaije, Decorating microbes: surface display of proteins on Escherichia coli. Trends. Biotechnol. 29, 79-86 (2011).
2. http://2016.igem.org/Team:TJUSLS_China.
3. M. Hu, H. Zhang, D. Gu, Y. Ma, X. Zhou, Identification of a novel bacterial receptor that binds tail tubular proteins and mediates phage infection of Vibrio parahaemolyticus. Emerg. Microbes. Infect. 9, 855-867 (2020).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 469
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2106
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 72
Illegal NgoMIV site found at 405
Illegal NgoMIV site found at 1737
Illegal AgeI site found at 492
Illegal AgeI site found at 823
Illegal AgeI site found at 1093
Illegal AgeI site found at 1648
Illegal AgeI site found at 2062
Illegal AgeI site found at 2506
Illegal AgeI site found at 2827 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 929