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<div id="w_text"> | <div id="w_text"> | ||
<h1>Results</h1> | <h1>Results</h1> | ||
− | <h2 id="title1">Microtubule</h2> | + | <h2 id="title1">Microtubule</h2> |
− | <h3>Plasmid construction</h3> | + | <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> | + | |
− | <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% /> | + | <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> | + | </p> |
+ | <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% /> | ||
+ | <h4>Figure 1 The electrophoresis image of these 6 plasmids.</h4> | ||
− | <h3>Protein expression analysis- Fluorescence microscopy</h3> | + | <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> | + | <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> | + | |
+ | <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> | + | <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. | + | <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> | + | The target proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively. |
+ | </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> | + | <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> | + | <p><br> |
+ | 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> | ||
− | |||
− | |||
− | |||
− | |||
− | <h3>Protein expression analysis- Fluorescence microscopy</h3> | + | <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> | + | <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> | + | <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> | + | 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> | + | <h4>figure 6</h4> |
</div> | </div> |
Revision as of 03:29, 23 October 2017
Results
Microtubule
Plasmid construction
We have accomplished the construction of 6 main parts whose functions are described respectively in previous design page. (Microtubule module)
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%.
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.
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.
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.
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.
figure 6
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