Difference between revisions of "Team:KUAS Korea/Results"

(Prototype team page)
 
Line 1: Line 1:
{{KUAS_Korea}}
+
{{KUAS_Korea/head}}
 +
{{KUAS_Korea/body/header}}
 
<html>
 
<html>
 +
<style>
 +
font{
 +
font-family: "Avenir",sans-serif;}
 +
</style>
  
 +
<table id="intro-title">
 +
    <tbody>
 +
    <tr>
 +
        <td class="align-middle text-center section-header"><h3>Results</h3></td>
 +
    </tr>
 +
    </tbody>
 +
</table>
  
<div class="column full_size">
+
<br><br>
<h1>Results</h1>
+
<main id="main">
<p>Here you can describe the results of your project and your future plans. </p>
+
    <section id="description">
</div>
+
        <div class="container">
 +
            <header class="section-header">
 +
             
 +
                <h4><strong>1. Beta-glucosidase expression</strong></h4>
  
 
+
              <div style="text-align:justify">
<div class="column third_size" >
+
                <ol><br><br>Cooperator expresses beta-glucosidase with constitutive promoter to degrade cellobiose around it. We had the cell stock of cooperator with pCEL vector containing beta-glucosidase and transformed it into E.coli BW25113. The medium plate contains cellobiose instead of glucose to check whether E.coli that we transformed expresses beta-glucosidase on its surface. The streaking side below shows that cooperator grows on cellobiose containing M9 minimal medium.  
 
+
</ol>
<h3>What should this page contain?</h3>
+
<ul>
+
<li> Clearly and objectively describe the results of your work.</li>
+
<li> Future plans for the project. </li>
+
<li> Considerations for replicating the experiments. </li>
+
</ul>
+
 
</div>
 
</div>
  
 +
<p>
 +
<img src="https://static.igem.org/mediawiki/2018/0/0c/T--KUAS_Korea--BETAGlucosidase_expression.png" width="700px" height="500px" style="float: center;"hspace="" vspace="10">
 +
<br>[Fig 1.] Cultured cooperator on M9 minimal medium with 0.48% cellobiose
 +
</p>
  
 +
<br><br>
  
 
+
</header>
<div class="column two_thirds_size" >
+
            <header class="section-header">
<h3>Describe what your results mean </h3>
+
                <h4><strong>2. GFP expression</strong></h4>
<ul>
+
<div style="text-align:justify">
<li> Interpretation of the results obtained during your project. Don't just show a plot/figure/graph/other, tell us what you think the data means. This is an important part of your project that the judges will look for. </li>
+
                <ol>Cheater expresses GFP when it obtains glucose. We had the cell stock of cheater with the vector encoding GFP as a reporter gene and transformed it firstly into E.coli DH5α and then to E.coli BW25113.  
<li> Show data, but remember all measurement and characterization data must be on part pages in the Registry. </li>
+
</ol>
<li> Consider including an analysis summary section to discuss what your results mean. Judges like to read what you think your data means, beyond all the data you have acquired during your project. </li>
+
</ul>
+
 
</div>
 
</div>
 +
<p>
 +
<img src="https://static.igem.org/mediawiki/2018/4/48/T--KUAS_Korea--GFP_PART1.png" width="700px" height="500px" style="float: center;" hspace="5" vspace="100"
 +
>
 +
<br>[Fig 2.] Cultured cheater on M9 minimal medium with 0.48% glucose
 +
<br><br><br><br><br><br>
 +
<img src="https://static.igem.org/mediawiki/2018/1/1b/T--KUAS_Korea--GFP_PART2.png" width="700px" height="500px" style="float: center;" hspace="5" vspace="100">
 +
<br>[Fig 2-1.] Cultured cheater under fluorescence microscopy showing the GFP activity
 +
</p>
 +
<br><br><br><br><br>
  
 
+
</header>
<div class="clear extra_space"></div>
+
</main>
 
+
 
+
 
+
<div class="column two_thirds_size" >
+
<h3> Project Achievements </h3>
+
 
+
<p>You can also include a list of bullet points (and links) of the successes and failures you have had over your summer. It is a quick reference page for the judges to see what you achieved during your summer.</p>
+
 
+
<ul>
+
<li>A list of linked bullet points of the successful results during your project</li>
+
<li>A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.</li>
+
</ul>
+
 
+
</div>
+
 
+
 
+
 
+
<div class="column third_size" >
+
<div class="highlight decoration_A_full">
+
<h3>Inspiration</h3>
+
<p>See how other teams presented their results.</p>
+
<ul>
+
<li><a href="https://2014.igem.org/Team:TU_Darmstadt/Results/Pathway">2014 TU Darmstadt </a></li>
+
<li><a href="https://2014.igem.org/Team:Imperial/Results">2014 Imperial </a></li>
+
<li><a href="https://2014.igem.org/Team:Paris_Bettencourt/Results">2014 Paris Bettencourt </a></li>
+
</ul>
+
</div>
+
</div>
+
 
+
 
+
 
+
 
+
  
 
</html>
 
</html>
 +
{{KUAS_Korea/body/footer}}
 +
{{KUAS_Korea/foot}}

Revision as of 11:27, 17 October 2018

Results



1. Beta-glucosidase expression



    Cooperator expresses beta-glucosidase with constitutive promoter to degrade cellobiose around it. We had the cell stock of cooperator with pCEL vector containing beta-glucosidase and transformed it into E.coli BW25113. The medium plate contains cellobiose instead of glucose to check whether E.coli that we transformed expresses beta-glucosidase on its surface. The streaking side below shows that cooperator grows on cellobiose containing M9 minimal medium.


[Fig 1.] Cultured cooperator on M9 minimal medium with 0.48% cellobiose



2. GFP expression

    Cheater expresses GFP when it obtains glucose. We had the cell stock of cheater with the vector encoding GFP as a reporter gene and transformed it firstly into E.coli DH5α and then to E.coli BW25113.


[Fig 2.] Cultured cheater on M9 minimal medium with 0.48% glucose






[Fig 2-1.] Cultured cheater under fluorescence microscopy showing the GFP activity






Sponsors