Difference between revisions of "Part:BBa K4197021"

 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K4197021 short</partinfo>
 
<partinfo>BBa_K4197021 short</partinfo>
 
OmpA_Ana o 3 fusion + mSCARLET-I with ihfb800 promoter
 
  
 
<html>
 
<html>
  
 
<h2>Introduction</h2>
 
<h2>Introduction</h2>
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<p>The mScarlet-I fluorescent reporter has been added on the plasmid allowing to express the gene of cashew nut Ana o 3 (<a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a>) on the surface of <i>E. coli</i>. Expression of mScarlet-I is driven by the ihfb800 promoter (see <a href="https://parts.igem.org/Part:BBa_K41970022">K41970022</a>).
 +
This red fluorescence is destined to identify the allergen expressing cells by FACS.
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</p>
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 +
 +
 
<p>The part expressing the gene of cashew nut Ana o 3 (<a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a>) has been completed with the ihfb800-mScarlet construction (<a href="https://parts.igem.org/Part:BBa_K41970022">K41970022</a>) to express red  
 
<p>The part expressing the gene of cashew nut Ana o 3 (<a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a>) has been completed with the ihfb800-mScarlet construction (<a href="https://parts.igem.org/Part:BBa_K41970022">K41970022</a>) to express red  
 
fluorescence. This red fluorescence allows sorting of bacteria by FACS. </p>
 
fluorescence. This red fluorescence allows sorting of bacteria by FACS. </p>
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IF4_mSCARLET-I R (atggtttctaaaggtgaagcagtg) primers. The expected size of the amplicon is 699 bp. The fragment was inserted on the linearized plasmid pET21b(+) with  
 
IF4_mSCARLET-I R (atggtttctaaaggtgaagcagtg) primers. The expected size of the amplicon is 699 bp. The fragment was inserted on the linearized plasmid pET21b(+) with  
 
Ana o 3 (<a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a>) by In-Fusion. </p>
 
Ana o 3 (<a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a>) by In-Fusion. </p>
<p>The resulting products were transformed into Stellar cells and positive transformants were selected.</p>
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<p>The resulting products were transformed into Stellar cells and positive transformants were selected. The correct sequence was further assessed by sequencing.</p>
  
 
      
 
      
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<h2>Validation</h2>
 
<h2>Validation</h2>
<p>Successful colonies have shown bright pink fluorescence (Figure 1).</p>
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<p>Successful colonies have shown pink coloring even without excitation light indicating the expression of the mScarlet-I, thus validating the mScarlet-I addition to the construction and its correct expression driven by the <i>ihfB</i> promoter (Figure 1).</p>
 
<div class="center">
 
<div class="center">
 
     <div class="thumb tnone">
 
     <div class="thumb tnone">
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                     <a href="https://static.igem.wiki/teams/4197/wiki/results/facs/fig-56-mscarlet-petri.jpg" class="internal" title="Enlarge"></a>
 
                     <a href="https://static.igem.wiki/teams/4197/wiki/results/facs/fig-56-mscarlet-petri.jpg" class="internal" title="Enlarge"></a>
 
                 </div>
 
                 </div>
                 <b>Figure 2: </b><b>Second plating of pET-21 b (+)_Ara h 2_OmpA_mScarlet-I transformed cells and pET-21 b (+)_Ana o 3_OmpA_mScarlet-I transformed Stellar cells. </b>   
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                 <b>Figure 1: </b><b>Second plating of pET-21 b (+)_Ara h 2_OmpA_mScarlet-I transformed cells and pET-21 b (+)_Ana o 3_OmpA_mScarlet-I transformed Stellar cells. </b>   
                 The colonies were selected on LB-ampicillin plates. Pink coloring indicates the expression of the mScarlet-I.
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                 The colonies were selected on LB-ampicillin plates.
 
             </div>
 
             </div>
 
         </div>
 
         </div>
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</div>
 
</div>
  
   
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<h2>References</h2>
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<h2>DAISY PROJECT</h2>
 
<ol>
 
<ol>
<li> <a href="https://parts.igem.org/Part:BBa_K4197007">K4197007</a> </li>
 
<li> <a href="https://parts.igem.org/Part:BBa_K4197022">K4197022</a> </li>
 
 
<li> <a href="https://2022.igem.wiki/toulouse-insa-ups/index.html"> DAISY (INSA-UPS 2022)</a> </li>
 
<li> <a href="https://2022.igem.wiki/toulouse-insa-ups/index.html"> DAISY (INSA-UPS 2022)</a> </li>
 
</ol>
 
</ol>
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
<partinfo>BBa_K4197003 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K4197021 SequenceAndFeatures</partinfo>
  
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  
 
===Functional Parameters===
 
===Functional Parameters===
<partinfo>BBa_K4197003 parameters</partinfo>
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<partinfo>BBa_K4197021 parameters</partinfo>
 
<!-- -->
 
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Latest revision as of 19:07, 10 October 2022


Ana o 3 expression at the surface of E. coli cells sortable by FACS using mSCARLET-I

Introduction

The mScarlet-I fluorescent reporter has been added on the plasmid allowing to express the gene of cashew nut Ana o 3 (K4197007) on the surface of E. coli. Expression of mScarlet-I is driven by the ihfb800 promoter (see K41970022). This red fluorescence is destined to identify the allergen expressing cells by FACS.

The part expressing the gene of cashew nut Ana o 3 (K4197007) has been completed with the ihfb800-mScarlet construction (K41970022) to express red fluorescence. This red fluorescence allows sorting of bacteria by FACS.

Construction

The ihfb800-mScarlet construction was amplified by PCR with the high-fidelity Phusion polymerase using IF3_mSCARLET-I F (ttatttgtacagttcatccataccacc) and IF4_mSCARLET-I R (atggtttctaaaggtgaagcagtg) primers. The expected size of the amplicon is 699 bp. The fragment was inserted on the linearized plasmid pET21b(+) with Ana o 3 (K4197007) by In-Fusion.

The resulting products were transformed into Stellar cells and positive transformants were selected. The correct sequence was further assessed by sequencing.

Validation

Successful colonies have shown pink coloring even without excitation light indicating the expression of the mScarlet-I, thus validating the mScarlet-I addition to the construction and its correct expression driven by the ihfB promoter (Figure 1).

Figure 1: Second plating of pET-21 b (+)_Ara h 2_OmpA_mScarlet-I transformed cells and pET-21 b (+)_Ana o 3_OmpA_mScarlet-I transformed Stellar cells. The colonies were selected on LB-ampicillin plates.

DAISY PROJECT

  1. DAISY (INSA-UPS 2022)

Sequence and Features


Assembly Compatibility:
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