Team:Uppsala

From 2014.igem.org

(Difference between revisions)
 
(130 intermediate revisions not shown)
Line 4: Line 4:
<script type="text/javascript">
<script type="text/javascript">
-
 
function toggleVisibility(selectedTab) {
function toggleVisibility(selectedTab) {
Line 19: Line 18:
               else {
               else {
                     content[i].style.opacity = 0;
                     content[i].style.opacity = 0;
 +
                    setTimeout(function(){$("#cover").hide()}, 1400);
                     var a = content[i];              //must change the variables for setTimeout cuz witchcraft
                     var a = content[i];              //must change the variables for setTimeout cuz witchcraft
Line 31: Line 31:
</script>
</script>
-
 
+
<div id="cover">&nbsp;</div>
-
<div id="intro" class="view">       <!--originally: no id="intro"-->
+
<div id="intro" class="view">
-
 
+
<script type="text/javascript">
-
   
+
$("#cover").show();
 +
</script>
     <div class="nav">
     <div class="nav">
-
    <div class="container">
 
     <ul>
     <ul>
-
     <li><a href="#"> Bactissiles - The future of microbial combat </a></li>
+
     <li><h>Bactissiles - The future of microbial combat </h></li>
     </ul>  
     </ul>  
     </div>
     </div>
 +
    <!-- <a class="info" onclick="toggleVisibility('intro');">Click me twice to hide!</a> -->
 +
    <img src="https://static.igem.org/mediawiki/2014/4/4c/Uppsala2014_comic.png" </img>
     </div>
     </div>
-
    <img class="comic" src="https://static.igem.org/mediawiki/2014/4/4c/Uppsala2014_comic.png" </img>
 
-
        <a class="info" onclick="toggleVisibility('intro');">Hide</a>
 
-
 
 
-
    </div>
 
-
 
<div>
<div>
-
<h2>Project Description</h2>
+
<h2>Bactissiles: The future of microbial combat</h2>
-
<p>With increasing antibiotic resistance in most of the pathogens, it becomes a critical problem to tackle in order to save the people of tomorrow. If we do not find an alternative to the antibiotics now, WHO estimates that the world will be thrown back to the hospital situation of the 1800’s.Considering this problem, the Uppsala iGEM team tries to combat it using the pathogen’s own quorum sensing system  to help probiotic bacteria find and kill that specific pathogen. By acquiring the quorum sensing system from Yersinia enterocolitica, we can sense their presence and use it to control the movement and the expression of a specific bacteriocin in our probiotic. This bacteriocin produced will eliminate the Yersinia enterocolitica, leaving the gut flora intact.</p>
+
<p>Destabilized ecosystems and disturbed gut floras are both consequences of treatments that lack selectivity. More efficient and precise methods are needed. This year we, the Uppsala iGEM team, try to widen the view and find new possibilities with engineered bacteria. By developing a system that homes towards a target and secretes an affectant, we can ensure a specific outcome. Such a system could have applications in a number of different fields, though we have chosen to put this into practice in a pinpointing pathogen-killing approach. In our prototype system, introduced in<i> E. coli </i>, we hijack the quorum sensing system of the gut pathogen <i> Yersinia enterocolitica </i>. Our bacteria will be able to sense the presence of the pathogen, accumulate in its vicinity and emit a target-specific bacteriocin, leaving the remaining gut flora intact. The era of mass destruction is over. Welcome the missile bacteria, the Bactissile!</p><br>
 +
 
 +
<div id="p_containerM">
 +
<table Style="margin:15px;">
 +
<tr><td></td><td><h2>What we have created</h2></td></tr>
 +
<tr><td><img class="schedule" src="https://static.igem.org/mediawiki/2014/e/ea/Sum_up_Uppsala14.png"</img></td>
 +
<td><p>Our creation, the Bactissile, is a missile bacteria, containing a two-mode system. Initially, the Bactissile will be in the <b>Tracking mode</b>, in which it will be producing a lot of the mobility protein, CheZ and a silencing sRNA, which will silence the expression of the Bactissiles weapon, colicin Fy. In this state, the Bactissile will be taking big leaps, randomly searching for its target, <i>Y. enterocolitica</i>. <br><br>When <i>Y. enterocolitica</i> enters the vicinity of the Bactissile, the Bactissile will switch to its <b>Attack mode</b>. In this state, the Bactissile will stop the production of CheZ and the sRNA and initiate the production of its weapon, the bacteriocin colicin Fy. The Bactissile will start tumbling close to the target, emitting its weapon. When the concentration of colicin Fy reaches a threshold value, the dosage will be lethal for <i>Y. enterocolitica</i>. Colicin Fy is only harmful for <i>Y. enterocolitica</i>, which entails that the beneficial gut flora in the Bactissile's surroundings will remain unharmed.</p></td></tr></table>
 +
</div>
 +
<br>
 +
 
 +
<h1>Main Result</h1>
 +
 
 +
<div id="grid_container_sensing">
 +
 
 +
<h2>The Sensing System</h2>
 +
 
 +
<div id="fucking-border">
 +
 
 +
<table>
 +
<tr>
 +
<td>
 +
<p><br><i>Graph 1. The production of the green fluorescence protein GFP in cells containing the following constructs:<br>
 +
1. pSB3C17-yenbox_WT-B0032-GFP<br>
 +
2. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23101-B0034-YenR<br>
 +
3. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23110-B0034-YenR<br>
 +
4. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23102-B0034-YenR</i></p>
 +
</td>
 +
<td>
 +
<img class="main_pic_left" src="https://static.igem.org/mediawiki/2014/b/b3/YenSystem_Char_Uppsala14.png">
 +
</td>
 +
</tr>
 +
</table>
 +
 
 +
<p>The measurement construct yenbox_WT-B0032-GFP  was transformed into strains containing expression cassettes producing the activator YenR. Using a flow cytometer, we managed to show that YenR was working perfectly fine in <i>E. coli</i> and that it recognised the luxbox homolog, the yenbox, and induced the expression level. With the strongest YenR producing expression cassette we succeeded in getting a five-fold increase of the green fluorescence protein GFP production.
 +
</p>
 +
<br>
 +
<a href="https://2014.igem.org/Team:Uppsala/Project_Sensing">Read more about the Sensing System</a>  
</div>
</div>
 +
 +
</div>
 +
 +
<div id="grid_container_targeting">
 +
 +
<h2 class="border_h2_right">The Targeting System</h2>
 +
 +
<div id="fucking-border">
 +
 +
<table>
 +
<tr>
 +
<td>
 +
<img class="main_pic_left" src="https://static.igem.org/mediawiki/2014/9/91/CheZswarmassay_Uppsala14.PNG">
 +
</td>
 +
<td>
 +
<p style="margin-left: 20px;"><br><i>Figure 1. A, B and C show three different swarmplate assays. 1: Motile strain RP437 (positive control), 2: cheZ mutant (negative control), 3: J23100-B0034-cheZ, 4: J23113-B0034-cheZ, 5: J23114-B0034-cheZ</i></p>
 +
</td>
 +
</tr>
 +
</table>
 +
 +
<p>We managed to restore chemotaxis in non-motile mutant strains, by reintroducing the cheZ gene on plasmids into the cheZ-knockout <i>E. coli</i>. Three promoters of different strengths were tested in combination with our construct and were shown to induce different levels of motility.</p>
 +
<br>
 +
<a href="https://2014.igem.org/Team:Uppsala/Project_Targeting">Read more about the Targeting System</a>
 +
 +
 +
 +
</div>
 +
</div>
 +
 +
<div id="grid_container">
 +
 +
<h2>The Killing System</h2>
 +
 +
<div id="fucking-border">
 +
 +
<table>
 +
<tr>
 +
<td>
 +
<p><br><i>Figure 2. The picture shows the result from an experiment to test the killing efficiency of colicin Fy. On the left Y. enterocolitica has been grown in liquid culture together with colicin Fy. The right plate is a negative control, where Y. enterocolitica has grown in the same conditions in liquid culture without any colicin Fy added.</p>
 +
</td>
 +
<td>
 +
<img class="main_pic_left" src="https://static.igem.org/mediawiki/2014/5/55/Uppsala-igem2014-4h_10.jpg">
 +
</td>
 +
</tr>
 +
</table>
 +
 +
<p>We managed to produce the bacteriocin colicin Fy. By fusing it with a His-tag we could perform an SDS-page gel and prove its presence. To analyse the colicin Fy’s killing efficiency, we let <i>Y. enterocolita</i> grow with and without colicin Fy in liquid cultures and compared the result. Fig. 2 shows these two  cultures plated. On the left plate, the <i>Y. enterocolitica</i> had grown with the colicin Fy added, while the right plate is the negative control, where <i>Y. enterocolitica</i> had grown without any colicin Fy. If we compare the two plates, we can see that there is a clear difference in the amount of <i>Y. enterocolitica</i> colonies.
 +
</p>
 +
<br>
 +
<a href="https://2014.igem.org/Team:Uppsala/Project_Killing">Read more about the Killing System</a>
 +
 +
 +
</div>
 +
</div>
 +
</html>
</html>
{{:Team:Uppsala/Templates/bottom_template}}
{{:Team:Uppsala/Templates/bottom_template}}

Latest revision as of 21:26, 17 October 2014

Home

 
  • Bactissiles - The future of microbial combat

Bactissiles: The future of microbial combat

Destabilized ecosystems and disturbed gut floras are both consequences of treatments that lack selectivity. More efficient and precise methods are needed. This year we, the Uppsala iGEM team, try to widen the view and find new possibilities with engineered bacteria. By developing a system that homes towards a target and secretes an affectant, we can ensure a specific outcome. Such a system could have applications in a number of different fields, though we have chosen to put this into practice in a pinpointing pathogen-killing approach. In our prototype system, introduced in E. coli , we hijack the quorum sensing system of the gut pathogen Yersinia enterocolitica . Our bacteria will be able to sense the presence of the pathogen, accumulate in its vicinity and emit a target-specific bacteriocin, leaving the remaining gut flora intact. The era of mass destruction is over. Welcome the missile bacteria, the Bactissile!


What we have created

Our creation, the Bactissile, is a missile bacteria, containing a two-mode system. Initially, the Bactissile will be in the Tracking mode, in which it will be producing a lot of the mobility protein, CheZ and a silencing sRNA, which will silence the expression of the Bactissiles weapon, colicin Fy. In this state, the Bactissile will be taking big leaps, randomly searching for its target, Y. enterocolitica.

When Y. enterocolitica enters the vicinity of the Bactissile, the Bactissile will switch to its Attack mode. In this state, the Bactissile will stop the production of CheZ and the sRNA and initiate the production of its weapon, the bacteriocin colicin Fy. The Bactissile will start tumbling close to the target, emitting its weapon. When the concentration of colicin Fy reaches a threshold value, the dosage will be lethal for Y. enterocolitica. Colicin Fy is only harmful for Y. enterocolitica, which entails that the beneficial gut flora in the Bactissile's surroundings will remain unharmed.


Main Result

The Sensing System


Graph 1. The production of the green fluorescence protein GFP in cells containing the following constructs:
1. pSB3C17-yenbox_WT-B0032-GFP
2. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23101-B0034-YenR
3. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23110-B0034-YenR
4. pSB3C17-yenbox_WT-B0032-GFP + pSB1K3-J23102-B0034-YenR

The measurement construct yenbox_WT-B0032-GFP was transformed into strains containing expression cassettes producing the activator YenR. Using a flow cytometer, we managed to show that YenR was working perfectly fine in E. coli and that it recognised the luxbox homolog, the yenbox, and induced the expression level. With the strongest YenR producing expression cassette we succeeded in getting a five-fold increase of the green fluorescence protein GFP production.


Read more about the Sensing System

The Targeting System


Figure 1. A, B and C show three different swarmplate assays. 1: Motile strain RP437 (positive control), 2: cheZ mutant (negative control), 3: J23100-B0034-cheZ, 4: J23113-B0034-cheZ, 5: J23114-B0034-cheZ

We managed to restore chemotaxis in non-motile mutant strains, by reintroducing the cheZ gene on plasmids into the cheZ-knockout E. coli. Three promoters of different strengths were tested in combination with our construct and were shown to induce different levels of motility.


Read more about the Targeting System

The Killing System


Figure 2. The picture shows the result from an experiment to test the killing efficiency of colicin Fy. On the left Y. enterocolitica has been grown in liquid culture together with colicin Fy. The right plate is a negative control, where Y. enterocolitica has grown in the same conditions in liquid culture without any colicin Fy added.

We managed to produce the bacteriocin colicin Fy. By fusing it with a His-tag we could perform an SDS-page gel and prove its presence. To analyse the colicin Fy’s killing efficiency, we let Y. enterocolita grow with and without colicin Fy in liquid cultures and compared the result. Fig. 2 shows these two cultures plated. On the left plate, the Y. enterocolitica had grown with the colicin Fy added, while the right plate is the negative control, where Y. enterocolitica had grown without any colicin Fy. If we compare the two plates, we can see that there is a clear difference in the amount of Y. enterocolitica colonies.


Read more about the Killing System

Back to Top

Retrieved from "http://2014.igem.org/Team:Uppsala"