Difference between revisions of "Team:BNU-China/Results"

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<div id="w_text">
 
<div id="w_text">
 
<h1>Results</h1>
 
<h1>Results</h1>
<h2 id="title1">Microtubule</h2>
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  <h2 id="title1">Microtubule</h2>
<h3>Plasmid construction</h3>
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    <h3>Plasmid construction</h3>
<p>We have accomplished the construction of 6 main parts whose functions are described respectively in previous design page. <a href="https://2017.igem.org/Team:BNU-China/Design#title2">(Microtubule module)</a></p>
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<img src="https://static.igem.org/mediawiki/2017/6/6f/T--BNU-China--results1.png" alt="Sorry, the image is not supported by your browser." width=80% />
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        <p>We have accomplished the construction of 6 main parts whose functions are described respectively in previous design page. <a href="https://2017.igem.org/Team:BNU-China/Design#title2">(Microtubule module)</a>
<h4>Figure 1 The electrophoresis image of these 6 plasmids.</h4>
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        </p>
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        <img src="https://static.igem.org/mediawiki/2017/6/6f/T--BNU-China--results1.png" alt="Sorry, the image is not supported by your browser." width=80% />
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      <h4>Figure 1 The electrophoresis image of these 6 plasmids.</h4>
  
<h3>Protein expression analysis- Fluorescence microscopy</h3>
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    <h3>Protein expression analysis- Fluorescence microscopy</h3>
<p>These are images recorded by the Fluorescence microscope.The engineered yeasts were induced at 30°C for 20 hours. And from the image, we can notice that our engineered yeasts have successfully expressed our recombinant proteins mCherry-αand mCherry. Moreover, the expression rate of mCherry is almost up to 100%. </p>
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        <p>These are images recorded by the Fluorescence microscope.The engineered yeasts were induced at 30°C for 20 hours. And from the image, we can notice that our engineered yeasts have successfully expressed our recombinant proteins mCherry-αand mCherry. Moreover, the expression rate of mCherry is almost up to 100%.  
 +
        </p>
  
 
<img src="https://static.igem.org/mediawiki/2017/1/19/T-BNU-China-results2.png" alt="Sorry, the image is not supported by your browser.">
 
<img src="https://static.igem.org/mediawiki/2017/1/19/T-BNU-China-results2.png" alt="Sorry, the image is not supported by your browser.">
<h4>Figure 2 Induced 20h in SG-Ura medium;<br>
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      <h4>Figure 2 Induced 20h in SG-Ura medium;<br>
 
A,B recipient strain with empty plasmid; <br>
 
A,B recipient strain with empty plasmid; <br>
 
C a bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;<br>
 
C a bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;<br>
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F fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring  pYCα–mCherry;<br></h4>
 
F fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring  pYCα–mCherry;<br></h4>
  
<h3>Protein expression analysis- Western blot</h3>
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    <h3>Protein expression analysis- Western blot</h3>
<p>The image shows the results of a Western blot analysis carried out with an anti-V5 antibody.
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          <p>The image shows the results of a Western blot analysis carried out with an anti-V5 antibody.
The target proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively.</p>
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The target proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively.
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          </p>
 
<img src="https://static.igem.org/mediawiki/2017/2/25/T-BNU-China-results3.png" alt="Sorry, the image is not supported by your browser.">
 
<img src="https://static.igem.org/mediawiki/2017/2/25/T-BNU-China-results3.png" alt="Sorry, the image is not supported by your browser.">
<h4>Figure 3 The results of a Western blot analysis carried out with an anti-V5 antibody.</h4>
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      <h4>Figure 3 The results of a Western blot analysis carried out with an anti-V5 antibody.</h4>
  
<p><br>Our engineered yeasts, containing pYD1-β tubulin vector, have been proved  successfully expressing exogenous βtubulin by Western blot analysis.</p>
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          <p><br>
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          Our engineered yeasts, containing pYD1-β tubulin vector, have been proved  successfully expressing exogenous βtubulin by Western blot analysis.</p>
 
<img src="https://static.igem.org/mediawiki/2017/9/9f/T-BNU-China-results4.png" alt="Sorry, the image is not supported by your browser.">
 
<img src="https://static.igem.org/mediawiki/2017/9/9f/T-BNU-China-results4.png" alt="Sorry, the image is not supported by your browser.">
 
<h4>Figure 4 The partly results of a Western blot analysis carried out with an anti-V5 antibody.</h4>
 
<h4>Figure 4 The partly results of a Western blot analysis carried out with an anti-V5 antibody.</h4>
<h2 id="title2">Flagellar Filament</h2>
 
<h3>Plasmid construction</h3>
 
<p>We have successfully constructed the following 11 parts that have been described in detail in previous design page. <a href="https://2017.igem.org/Team:BNU-China/Design#title3">(Filagellar filament module)</a>The parts are named: , , , , </p>
 
<h4>The electrophoresis image of our parts.</h4>
 
  
<h3>Protein expression analysis- Fluorescence microscopy</h3>
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  <h2 id="title2">Flagellar Filament</h2>
<p>The below image shows the expression of the S. cerevisiae INVSc1 cells harbouring pYCα–FliC(eGFP). The strong fluorescence signal validates the expression of recombinant protein: FilC fused with eGFP.</p>
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    <h3>Plasmid construction</h3>
 +
            <p>We have successfully constructed the following 11 parts that have been described in detail in previous design page. <a href="https://2017.igem.org/Team:BNU-China/Design#title3">(Filagellar filament module)</a>The parts are named: , , , ,
 +
            </p>
 +
      <h4>The electrophoresis image of our parts.</h4>
 +
 
 +
    <h3>Protein expression analysis- Fluorescence microscopy</h3>
 +
            <p>The below image shows the expression of the S. cerevisiae INVSc1 cells harbouring pYCα–FliC(eGFP). The strong fluorescence signal validates the expression of recombinant protein: FilC fused with eGFP.
 +
            </p>
 
<img src="https://static.igem.org/mediawiki/2017/e/e7/T--BNU-China--results5.png" alt="Sorry, the image is not supported by your browser.">
 
<img src="https://static.igem.org/mediawiki/2017/e/e7/T--BNU-China--results5.png" alt="Sorry, the image is not supported by your browser.">
<h4>Figure 5 Fluorescence image of recombinant FliC(eGFP) expressed by the engineered yeast cell.A,B recipient strain EBY100 harbouring pYCα;<br>C  a bright-field micrograph of S. cerevisiae EBY100 cells harbouring pYCα–FliC(eGFP);<br>
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      <h4>Figure 5 Fluorescence image of recombinant FliC(eGFP) expressed by the engineered yeast cell.A,B recipient strain EBY100 harbouring pYCα;<br>C  a bright-field micrograph of S. cerevisiae EBY100 cells harbouring pYCα–FliC(eGFP);<br>
D fluorescence micrograph of S. cerevisiae EBY100 cells harbouring  pYCα–FliC(eGFP)<br></h4>
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D fluorescence micrograph of S. cerevisiae EBY100 cells harbouring  pYCα–FliC(eGFP)<br>
 +
      </h4>
  
<h3>Protein expression analysis- Western blot</h3>
+
    <h3>Protein expression analysis- Western blot</h3>
 
<p>The image shows the results of a Western blot analysis carried out with an anti-His antibody.</p>
 
<p>The image shows the results of a Western blot analysis carried out with an anti-His antibody.</p>
 
<img src="https://static.igem.org/mediawiki/2017/f/fb/T-BNU-China-results6new.png" alt="Sorry, the image is not supported by your browser.">
 
<img src="https://static.igem.org/mediawiki/2017/f/fb/T-BNU-China-results6new.png" alt="Sorry, the image is not supported by your browser.">
<h4>figure 6</h4>
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      <h4>figure 6</h4>
  
 
</div>
 
</div>

Revision as of 03:29, 23 October 2017

BNU-China ">

Results

Microtubule

Plasmid construction

We have accomplished the construction of 6 main parts whose functions are described respectively in previous design page. (Microtubule module)

Sorry, the image is not supported by your browser.

Figure 1 The electrophoresis image of these 6 plasmids.

Protein expression analysis- Fluorescence microscopy

These are images recorded by the Fluorescence microscope.The engineered yeasts were induced at 30°C for 20 hours. And from the image, we can notice that our engineered yeasts have successfully expressed our recombinant proteins mCherry-αand mCherry. Moreover, the expression rate of mCherry is almost up to 100%.

Sorry, the image is not supported by your browser.

Figure 2 Induced 20h in SG-Ura medium;
A,B recipient strain with empty plasmid;
C a bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;
D fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry-α;
E a bright-field micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry;
F fluorescence micrograph of S. cerevisiae INVSc1 cells harbouring pYCα–mCherry;

Protein expression analysis- Western blot

The image shows the results of a Western blot analysis carried out with an anti-V5 antibody. The target proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively.

Sorry, the image is not supported by your browser.

Figure 3 The results of a Western blot analysis carried out with an anti-V5 antibody.


Our engineered yeasts, containing pYD1-β tubulin vector, have been proved successfully expressing exogenous βtubulin by Western blot analysis.

Sorry, the image is not supported by your browser.

Figure 4 The partly results of a Western blot analysis carried out with an anti-V5 antibody.

Flagellar Filament

Plasmid construction

We have successfully constructed the following 11 parts that have been described in detail in previous design page. (Filagellar filament module)The parts are named: , , , ,

The electrophoresis image of our parts.

Protein expression analysis- Fluorescence microscopy

The below image shows the expression of the S. cerevisiae INVSc1 cells harbouring pYCα–FliC(eGFP). The strong fluorescence signal validates the expression of recombinant protein: FilC fused with eGFP.

Sorry, the image is not supported by your browser.

Figure 5 Fluorescence image of recombinant FliC(eGFP) expressed by the engineered yeast cell.A,B recipient strain EBY100 harbouring pYCα;
C a bright-field micrograph of S. cerevisiae EBY100 cells harbouring pYCα–FliC(eGFP);
D fluorescence micrograph of S. cerevisiae EBY100 cells harbouring pYCα–FliC(eGFP)

Protein expression analysis- Western blot

The image shows the results of a Western blot analysis carried out with an anti-His antibody.

Sorry, the image is not supported by your browser.

figure 6

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