Team:Nanjing-China/tran

From 2013.igem.org

(Difference between revisions)
 
(17 intermediate revisions not shown)
Line 7: Line 7:
   <div class="header">
   <div class="header">
     <div class="top"></div>
     <div class="top"></div>
-
     <div class="logo"><a href="https://static.igem.org/mediawiki/2013/6/68/IgemLogo.png" target="_blank"></a></div>
+
     <div class="logo"><a href="https://2013.igem.org/Main_Page" target="_blank" class="bl"></a><a href="https://igem.org/Team.cgi?year=2013&team_name=Nanjing-China" target="_blank" class="bl2"></a></div>
     <div class="gywm"><a href="https://2013.igem.org/Team:Nanjing-China/contact"></a></div>
     <div class="gywm"><a href="https://2013.igem.org/Team:Nanjing-China/contact"></a></div>
     <div class="nav">
     <div class="nav">
Line 31: Line 31:
           <li class="bar">Project</li>
           <li class="bar">Project</li>
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/project">Overall Project</a></li>
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/project">Overall Project</a></li>
-
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/pre">Pre-experiment</a></li>
+
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/pre">Pre-experiments</a></li>
-
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/tran" class="son_hover">Transporter</a></li>
+
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/tran" class="son_hover">Transportation</a></li>
-
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/qs">QS System</a></li>
+
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/rib">Recognition</a></li>
-
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/rib">Ribosome Switch</a></li>
+
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/qs">Aggregation</a></li>
-
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/deg">Degrading Enzyme</a></li>
+
           <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/deg">Degradation</a></li>
         </ul>
         </ul>
   </div>
   </div>
Line 59: Line 59:
       <div class="Project2">
       <div class="Project2">
         <dl>
         <dl>
-
             <dt><a href="###">Transporter</a></dt>
+
             <dt><a href="###">Transportation</a></dt>
             <dd class="dd_1">
             <dd class="dd_1">
-
Currently, Pseudomonas sp. strain ADP seems to be the optimal bacteria strain for atrazine degradations, which appears to be the sole nitrogen source for the bacteria. A study has found that a large plasmid carries all the genes and complex pathways related to atrazine degradation in Pseudomonas sp. strain ADP. We analyzed all the genes in it and finally found a multiple transmembrane protein which we called TRM (Fig. 3-3-1). We hypothesized that the function of transmembrane protein was related to atrazine transportation and thus confirmed it with several experiments.<br/><br/>
+
Currently, Pseudomonas sp. strain ADP seems to be the optimal bacteria strain for atrazine degradation, which appears to be the sole nitrogen source for the bacteria. A study has found that a large plasmid carries all the genes and complex pathways related to atrazine degradation in Pseudomonas sp. strain ADP<sup>[1,2]</sup>. We analyzed all the genes in it and finally found a multiple transmembrane protein which we named TRM (Fig. 3-3-1). We hypothesized that the function of the transmembrane protein was related to atrazine transportation and thus confirmed it with several experiments.<br><br>
-
<img src="https://static.igem.org/mediawiki/2013/d/dd/Fig_3-3-1.jpg"><br/><br/>
+
<p style="text-align:center"><img src="https://static.igem.org/mediawiki/2013/d/dd/Fig_3-3-1.jpg"width="600"></p><br/>
-
Fig. 3-3-1 TMHMM posterior probabilities for WEBSEQUENCE. TRM has 11 trans-membrane domains. In prokaryotes, a protein like this has been considered as a potential transmembrane protein.<br/>
+
<div style="padding:0 50px; font-size:11px"><strong>Fig. 3-3-1</strong> TMHMM posterior probabilities for WEBSEQUENCE. TRM has 11 trans-membrane domains. In prokaryotes, a protein like this is considered as a potential transmembrane protein.</div><br><br>
-
<br/>
+
 
<strong>Experiments and Results</strong><br>
<strong>Experiments and Results</strong><br>
-
+
To prove that TRM is related to the transportation of atrazine, we used HPLC to analyze the concentration of atrazine after incubating engineered bacteria in 500μM atrazine for 24h (Fig. 3-3-2). It is obvious that bacteria with TRM can reduce the concentration of atrazine, suggesting that TRM plays an important role in the transportation of atrazine.<br><br>
-
To prove that TRM is a transmembrane protein, we constructed a circuit where a constant promoter drives the expression of the TRM which is fused with a green fluorescent protein to localize it. And the result of transmembrane protein verification is shown in Fig. 3-3-2, suggesting that TRM is located on the cell membrane.<br/><br/>
+
<p style="text-align:center"><img src="https://static.igem.org/mediawiki/2013/5/52/HPLC_TRM_Col_blue.jpg"width="400"></p><br/>
-
<img src="https://static.igem.org/mediawiki/2013/c/cd/Fig_3-3-2.jpg"><br/><br/>
+
<div style="padding:0 50px; font-size:11px"><strong>Fig. 3-3-2</strong> Atrazine concentration of K-12 with or without TRM. "0h" stands for control group with no atrazine and that the bacteria have been incubated for 0 hour. "Wild Type" stands for Escherichia coli K-12 which is the positive control and "Vector" stands for K-12 containing plasmid-pGFPs which is the negative control. "TRM+" is the experimental group where a plasmid-pGFP carrying TRM was transformed into Escherichia coli K-12. And the result shows that K12 is significantly different from TRM+ in the statistical sense and it also indicates that TRM plays an important role in the transportation of atrazine.</div><br><br>
-
Fig. 3-3-2 The circuit we constructed to verify the function of TRM and subcellular localization of TRM-GFP fusion protein. (A) The circuit we constructed to verify the function of TRM. (B) Fluorescent microscopy image of cells expressing TRM-GFP (green) shows that TRM distributed throughout the cell membrane.<br/><br/>
+
Through all the preliminary experiments, we reached to the conclusion that TRM is closely related to the transportation of atrazine. And therefore the transporter can enhance the absorption of atrazine, which will improve the sensitivity of detection of atrazine. According to this idea, it will enhance degradation of atrazine in the bacteria, which provides a new way for the further study of detection and degradation of atrazine. There is no doubt that it will be an amazing element for our project and synthetic biology.<br/><br/>
-
To prove that TRM is related to transportation of atrazine, we used HPLC to analyze the concentration of atrazine after incubating engineered bacteria in 500μM atrazine for 24h (Fig. 3-3-3).It is obvious that bacteria with TRM can reduce the concentration of atrazine, suggesting that TRM plays an important role in transportation of atrazine.<br/><br/>
+
<strong>Reference</strong><br/>
-
<img src="https://static.igem.org/mediawiki/2013/4/44/Fig_3-3-3.jpg"><br/><br/>
+
[1] Betsy Martinez, et al. Complete Nucleotide Sequence and Organization of the Atrazine Catabolic Plasmid pADP-1 from Pseudomonas sp. Strain ADP. Journal of Bacteriology, 2001, 183 (19): 5684-5697.<br/>
-
Fig. 3-3-3 Atrazine concentration of K-12 with or without TRM. "0h" stands for control group with no atrazine and the bacteria have been incubated for 0 hour. "Wild Type" stands for Escherichia coli K-12 which ispositive control and "Vector" stands for K-12 which contains a plasmid-pGFP which is negative control. "TRM+" is the experimental group where a plasmid-pGFP which carries TRM was transformed into Escherichia coli K-12. And the result shows that K12 is significantly different from TRM+ in the statistical sense and it also indicates that TRM plays an important role in transportation of atrazine.<br/>      
+
[2] Platero AI, et al. Transcriptional organization and regulatory elements of a Pseudomonas sp. strain ADP operon encoding a LysR-type regulator and a putative solute transport system. Journal of bacteriology, 2012, 194 (23): 6560-6573.
             </dd>
             </dd>
         </dl>         
         </dl>         
Line 98: Line 98:
     </div>
     </div>
     <div class="p1">Team NANJING UNIVERSITY All Rights Reserved.</div>
     <div class="p1">Team NANJING UNIVERSITY All Rights Reserved.</div>
 +
<style>
 +
            #tbox{width:64px; height:73px; float:right; position:fixed;
 +
_position:absolute;
 +
_bottom:auto;
 +
_top:expression(eval(document.documentElement.scrollTop+document.documentElement.clientHeight-this.offsetHeight-(parseInt(this.currentStyle.marginTop,200)||0)-(parseInt(this.currentStyle.marginBottom,200)||0)));
 +
_margin-bottom:10px;
 +
}/*解决IE6下不兼容 position:fixed 的问题*/
 +
#gotop{ width:64px; height:64px; background:url(https://static.igem.org/mediawiki/2013/6/62/Top.gif) no-repeat; position:absolute; top:0px; display:none; cursor:pointer}
 +
        </style>
 +
        <script type="text/javascript" src="http://www.11ml.cn/templets/default/js/jquery-1.4.2.min.js"></script>
 +
        <script type="text/javascript" src="http://www.11ml.cn/templets/default/js/js.js"></script>
 +
        <div id="tbox"><a id="gotop" href="javascript:void(0)"></a></div>
</div>
</div>
<!--//footer-->
<!--//footer-->
</html>
</html>

Latest revision as of 02:50, 28 September 2013

Transportation
Currently, Pseudomonas sp. strain ADP seems to be the optimal bacteria strain for atrazine degradation, which appears to be the sole nitrogen source for the bacteria. A study has found that a large plasmid carries all the genes and complex pathways related to atrazine degradation in Pseudomonas sp. strain ADP[1,2]. We analyzed all the genes in it and finally found a multiple transmembrane protein which we named TRM (Fig. 3-3-1). We hypothesized that the function of the transmembrane protein was related to atrazine transportation and thus confirmed it with several experiments.


Fig. 3-3-1 TMHMM posterior probabilities for WEBSEQUENCE. TRM has 11 trans-membrane domains. In prokaryotes, a protein like this is considered as a potential transmembrane protein.


Experiments and Results
To prove that TRM is related to the transportation of atrazine, we used HPLC to analyze the concentration of atrazine after incubating engineered bacteria in 500μM atrazine for 24h (Fig. 3-3-2). It is obvious that bacteria with TRM can reduce the concentration of atrazine, suggesting that TRM plays an important role in the transportation of atrazine.


Fig. 3-3-2 Atrazine concentration of K-12 with or without TRM. "0h" stands for control group with no atrazine and that the bacteria have been incubated for 0 hour. "Wild Type" stands for Escherichia coli K-12 which is the positive control and "Vector" stands for K-12 containing plasmid-pGFPs which is the negative control. "TRM+" is the experimental group where a plasmid-pGFP carrying TRM was transformed into Escherichia coli K-12. And the result shows that K12 is significantly different from TRM+ in the statistical sense and it also indicates that TRM plays an important role in the transportation of atrazine.


Through all the preliminary experiments, we reached to the conclusion that TRM is closely related to the transportation of atrazine. And therefore the transporter can enhance the absorption of atrazine, which will improve the sensitivity of detection of atrazine. According to this idea, it will enhance degradation of atrazine in the bacteria, which provides a new way for the further study of detection and degradation of atrazine. There is no doubt that it will be an amazing element for our project and synthetic biology.

Reference
[1] Betsy Martinez, et al. Complete Nucleotide Sequence and Organization of the Atrazine Catabolic Plasmid pADP-1 from Pseudomonas sp. Strain ADP. Journal of Bacteriology, 2001, 183 (19): 5684-5697.
[2] Platero AI, et al. Transcriptional organization and regulatory elements of a Pseudomonas sp. strain ADP operon encoding a LysR-type regulator and a putative solute transport system. Journal of bacteriology, 2012, 194 (23): 6560-6573.

Retrieved from "http://2013.igem.org/Team:Nanjing-China/tran"