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

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       <h4>The electrophoresis image of our parts.</h4>
 
       <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.
 
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<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>
 
D fluorescence micrograph of S. cerevisiae EBY100 cells harbouring  pYCα–FliC(eGFP)<br>
 
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     <h3>Protein expression analysis- Western blot</h3>
 
     <h3>Protein expression analysis- Western blot</h3>

Revision as of 03:14, 26 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)

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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%.

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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 recombinant proteins are expressed by the engineered yeasts which contain pYCα-alpha, pYCα-beta, pYCα-mCherry and pYCα-mCherry-αtubulin, respectively. After 24h inducing,the recombinant proteins are extracted and analysed by Western blot.

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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.

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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. (Flagellar filament module)The parts are named: , , , ,

The electrophoresis image of our parts.

Protein expression analysis- Western blot

The image shows the results of a Western blot analysis carried out with an anti-His antibody.The recombinant proteins are expressed by S.cerevisiae INVSCi pYCα-FilC(PETase), pYCα-FliC(XynA), respectively. After 24h inducing,the recombinant proteins are extracted and analysed by Western blot.

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figure 6 The results of a Western blot analysis carried out with an anti-His antibody.

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