Team:Fudan Lux/Notebook

From 2012.igem.org

(Difference between revisions)
(Undo revision 173439 by GemmaA (talk))
 
(34 intermediate revisions not shown)
Line 6: Line 6:
background-image: none;
background-image: none;
}
}
-
#img{
+
 
-
margin:20px;
+
img.myimg {
 +
 
 +
-webkit-box-shadow: 0px 0px 17px #999;
 +
 
}
}
#p-logo {
#p-logo {
Line 215: Line 218:
<div id="header">  
<div id="header">  
   <!-- wrapper-header -->
   <!-- wrapper-header -->
-
   <div class="wrapper"> <a href="http://luiszuno.com/themes/nova/index.html"><img id="logo" src="https://static.igem.org/mediawiki/2012/5/5d/Logo_64px.png" alt="Nova"></a>  
+
   <div class="wrapper"> <a href="https://2012.igem.org/Team:Fudan_Lux><img id="logo" src="https://static.igem.org/mediawiki/2012/5/5d/Logo_64px.png" alt="Nova"></a>  
-
    <!-- search -->
+
      <!-- search -->
     <div class="top-search">
     <div class="top-search">
-
       <form method="get" id="searchform" action="#">
+
       <form method="get" id="searchform" action="https://2012.igem.org/Special:Search">
         <div>
         <div>
-
           <input type="text" value="Search..." name="s" id="s" onFocus="defaultInput(this)" onBlur="clearInput(this)">
+
           <input type="text" value="Search..." name="search" id="s" onfocus="defaultInput(this)" onblur="clearInput(this)">
           <input type="submit" id="searchsubmit" value=" ">
           <input type="submit" id="searchsubmit" value=" ">
         </div>
         </div>
Line 244: Line 247:
         <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/project_introduction">Project<span class="subheader">Cool</span></a>
         <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/project_introduction">Project<span class="subheader">Cool</span></a>
           <ul style="display: none; visibility: hidden; ">
           <ul style="display: none; visibility: hidden; ">
-
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/project_introduction">Introduction</a></li>
+
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/project_introduction">Overview</a></li>
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/biowave">Project Biowave</a></li>
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/biowave">Project Biowave</a></li>
-
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/nanotube">nanotubling</a></li>
+
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/nanotube">Project Bacto-Trafficking</a></li>
-
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/result">Result</a></li>
+
             <li><a href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/result">Results</a></li>
           </ul>
           </ul>
         </li>
         </li>
Line 257: Line 260:
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/labcloud">Project Labcloud</a></li>
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/labcloud">Project Labcloud</a></li>
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/Associations">Associations</a></li>
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/Associations">Associations</a></li>
-
            <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/tianmu">Tianmu mountain</a></li>
 
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/other practise">Other Practise</a></li>
             <li><a href="href="https://2012.igem.org/wiki/index.php?title=Team:Fudan_Lux/other practise">Other Practise</a></li>
           </ul>
           </ul>
Line 292: Line 294:
<div id="page-title">
<div id="page-title">
<span class="title">Note Book</span>
<span class="title">Note Book</span>
-
<span class="subtitle">Tabs</span>
+
<span class="subtitle">Record iGEMers in summer.</span>
</div>
</div>
<!-- ENDS title -->
<!-- ENDS title -->
Line 302: Line 304:
<!-- the tabs -->
<!-- the tabs -->
<ul class="tabs">
<ul class="tabs">
-
<li><a href="#"><span>March</span></a></li>
+
<li><a href="#"><span>week 1</span></a></li>
-
<li><a href="#"><span>April</span></a></li>
+
<li><a href="#"><span>week 2</span></a></li>
-
<li><a href="#"><span>May</span></a></li>
+
<li><a href="#"><span>week 3~week 4</span></a></li>
-
<li><a href="#"><span>June</Span></a></li>
+
<li><a href="#"><span>week 5</Span></a></li>
-
<li><a href="#"><span>July~August</span></a></li>
+
<li><a href="#"><span>week 6~week 10</span></a></li>
-
<li><a href="#"><span>September</Span></a></li>
+
<li><a href="#"><span>week 11</Span></a></li>
-
<li><a href="#"><span>October</span></a></li>
+
<li><a href="#"><span>week 12</span></a></li>
</ul>
</ul>
Line 317: Line 319:
<!-- tab 1 content  -->
<!-- tab 1 content  -->
<div>
<div>
-
<p>We summarized our recent brain storm result. At last we chose to make a light-signal oscillator <img  src="https://static.igem.org/mediawiki/2012/1/1d/Discussion.jpg" style="float:right;width:300px;"alt="test">in E.coli and possibilities to use nanotubes.
+
<p>We summarized our recent brain storm result. At last we chose to make a light-signal oscillator <img  src="https://static.igem.org/mediawiki/2012/1/1d/Discussion.jpg" style="float:right;width:300px;"alt="test" class="myimg">in E.coli and possibilities to use nanotubes.
The first thing for the next week is to find an efficient light sensor and a stable lighting part.
The first thing for the next week is to find an efficient light sensor and a stable lighting part.
</p>
</p>
Line 328: Line 330:
       
       
-
<p>Discuss the establishment of the gene circuits.</p><img src="https://static.igem.org/mediawiki/2012/6/64/Gene_circuits1.jpg" style="width:300px;"alt="test"><br>
+
<p>Discuss the establishment of the gene circuits.</p>
 +
<img src="https://static.igem.org/mediawiki/2012/6/64/Gene_circuits1.jpg" style="width:400px;"alt="test" class="myimg">
 +
<img src="https://static.igem.org/mediawiki/igem.org/d/da/Gene_circuits2.jpg" style="width:400px;"alt="test" class="myimg"><br><br>
<p>Get lux without operon and promoter from k325909 by PCR.
<p>Get lux without operon and promoter from k325909 by PCR.
We used longPCR Enzyme and Overlapping PCR.
We used longPCR Enzyme and Overlapping PCR.
</p><br>
</p><br>
<p>Measure the growth curve of dH5a transformed by lux with araBAD (k325909)</p>
<p>Measure the growth curve of dH5a transformed by lux with araBAD (k325909)</p>
-
<img src="http://partsregistry.org/wiki/images/4/4c/Growth_curve_of_K325909.jpg" style="width:300px;"alt="test"><br>
+
<img src="http://partsregistry.org/wiki/images/4/4c/Growth_curve_of_K325909.jpg" style="width:500px;"alt="test" class="myimg"><br><br>
<p>Transform tetR (<a href="http://partsregistry.org/Part:BBa_C0040">C0040</a>) from the kit. Transfer araBAD (<a href=" http://partsregistry.org/Part:BBa_I0500">I0500</a>) and tetR (<a href="http://partsregistry.org/Part:BBa_C0040">C0040</a>) with RBS into pSB1C3 by 3A ligation. Transform it into dH5a.</p><br><p>Transfer tetR with promoter and RFP with ptetO as promoter (<a href="http://partsregistry.org/Part:BBa_J61002">J61002</a>) into pSB1C3 by 3A ligation. Transform it into dH5a.</p><br>
<p>Transform tetR (<a href="http://partsregistry.org/Part:BBa_C0040">C0040</a>) from the kit. Transfer araBAD (<a href=" http://partsregistry.org/Part:BBa_I0500">I0500</a>) and tetR (<a href="http://partsregistry.org/Part:BBa_C0040">C0040</a>) with RBS into pSB1C3 by 3A ligation. Transform it into dH5a.</p><br><p>Transfer tetR with promoter and RFP with ptetO as promoter (<a href="http://partsregistry.org/Part:BBa_J61002">J61002</a>) into pSB1C3 by 3A ligation. Transform it into dH5a.</p><br>
<p>Sorry to find the ligation is failed. But fortunately, we decide to change the reporter into GFP (<a href="http://partsregistry.org/Part:BBa_I13522">I13522</a>). Transform the plasmid from the kit into dH5a.</p><br>
<p>Sorry to find the ligation is failed. But fortunately, we decide to change the reporter into GFP (<a href="http://partsregistry.org/Part:BBa_I13522">I13522</a>). Transform the plasmid from the kit into dH5a.</p><br>
-
<p>Design protein composed by lov domain and modified helix turn helix (abbr. lov-HTH).</p>
+
<p>Design protein composed by lov domain and modified helix turn helix (abbr. <a href="http://partsregistry.org/Part:BBa_K785004">lov-HTH</a>).</p>
-
<img src="https://static.igem.org/mediawiki/2012/f/fd/Lov_demestration.jpg" style="width:300px;"alt="test"><br>
+
<img src="https://static.igem.org/mediawiki/2012/f/fd/Lov_demestration.jpg" style="width:500px;"alt="test" class="myimg"><br>
       
       
-
+
Line 354: Line 358:
<p>Send the synthetic orders to the gene synthesis company.</p><br>
<p>Send the synthetic orders to the gene synthesis company.</p><br>
<p>Half of our members went to Tianmu Mount, Zhejiang Province. They spent a week there to participate a fieldwork organized by the Life Science Institute. During the fieldwork, they paid a lot of attention to a China’s specific firefly, Qiongyuying. They observed the behavior of Qiongyuying, especially the synchrony.</p>
<p>Half of our members went to Tianmu Mount, Zhejiang Province. They spent a week there to participate a fieldwork organized by the Life Science Institute. During the fieldwork, they paid a lot of attention to a China’s specific firefly, Qiongyuying. They observed the behavior of Qiongyuying, especially the synchrony.</p>
-
<img src="https://static.igem.org/mediawiki/2012/c/cf/Firefly1.jpg" style="width:300px;"alt="test"><br><br>
+
<img src="https://static.igem.org/mediawiki/2012/c/cf/Firefly1.jpg" style="width:300px;"alt="test" class="myimg"><br><br>
<p>Our instructor and four of our members went to meet Richard J Roberts after the reward ceremony of COMBREX, a project to accelerate the functional annotation of prokaryotic genomes. They talked for about an hour and we presented our project to him. Richard advised that we should make our project more practical and functional.</p>
<p>Our instructor and four of our members went to meet Richard J Roberts after the reward ceremony of COMBREX, a project to accelerate the functional annotation of prokaryotic genomes. They talked for about an hour and we presented our project to him. Richard advised that we should make our project more practical and functional.</p>
-
<img src="https://static.igem.org/mediawiki/2012/c/c6/Richard.jpg" style="width:400px;"alt="test"><br><br>
+
<img src="https://static.igem.org/mediawiki/2012/c/c6/Richard.jpg" style="width:400px;"alt="test"class=“myimg"><br><br>
<p>After negotiating with the principal of volunteer teaching program in our institute, one of our members, with all members of Fudan_Lux’s hope and responsibility on his shoulders, went to Shangrao, Jiangxi Province to do the volunteer teaching.</p>
<p>After negotiating with the principal of volunteer teaching program in our institute, one of our members, with all members of Fudan_Lux’s hope and responsibility on his shoulders, went to Shangrao, Jiangxi Province to do the volunteer teaching.</p>
-
<div><img src="https://static.igem.org/mediawiki/2012/8/87/VT1.jpg" style="width:250px;"alt="test">
+
<div><img src="https://static.igem.org/mediawiki/2012/8/87/VT1.jpg" style="width:250px;"alt="test class="myimg"">
-
<img src="https://static.igem.org/mediawiki/2012/3/3b/VT2.jpg" style="width:250px;"alt="test"></div><br>
+
<img src="https://static.igem.org/mediawiki/2012/3/3b/VT2.jpg" style="width:250px;"alt="test" class="myimg"></div><br>
<p>Make an appointment with Li Jin, Hongyan Wang etc. to show our projects.</p><br>
<p>Make an appointment with Li Jin, Hongyan Wang etc. to show our projects.</p><br>
<p>Receive lov-HTH in nonstandard vector.</p><br>
<p>Receive lov-HTH in nonstandard vector.</p><br>
Line 379: Line 383:
<div>
<div>
<p>The double digestion and the ligation held us for more than 4 weeks!</p>
<p>The double digestion and the ligation held us for more than 4 weeks!</p>
-
<img src="https://static.igem.org/mediawiki/2012/8/86/YuAn.jpg" style="width:500px;"alt="test"></div><br>
+
<img src="https://static.igem.org/mediawiki/2012/8/86/YuAn.jpg" style="width:400px;"alt="test" class="myimg"><br><br>
-
<p>We hope to establish 54 gene circuits:
+
<p>In order to do the ligation more efficiently, we decide to do the ligation according to this table.</p>
-
1. araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP
+
<table style="border-collapse:collapse;" width="96%" align="center" border="1" cellspace="0" cellpadding="3"><tbody>
-
2. araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP
+
<tr><td valign="top">NO.&nbsp;<br>
-
3. araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP
+
</td><td valign="top">Composition
-
4. araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP
+
</td><td valign="top">Backbone
-
5. araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP
+
</td><td valign="top">Code
-
6. araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP
+
</td></tr>
-
7. araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP
+
<tr><td valign="top">P1 14N
-
8. araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP
+
</td><td valign="top">araBAD
-
9. araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP
+
</td><td valign="top">pSB2K3
-
10. araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP
+
</td><td valign="top">I0050
-
11. araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP
+
</td></tr>
-
12. araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP
+
<tr><td valign="top">P1 6G
-
13. araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux
+
</td><td valign="top">pLac
-
14. araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO- lux
+
</td><td valign="top">pSB1A2
-
15. araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO- lux
+
</td><td valign="top">R0011
-
16. araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO- lux
+
</td></tr>
-
17. araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO- lux  
+
<tr><td valign="top">P1 6N
-
18. araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO- lux
+
</td><td valign="top">T7 promoter
-
19. pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP
+
</td><td valign="top">pSB1AK8
-
20. pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP
+
</td><td valign="top">I712074
-
21. pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP
+
</td></tr>
-
22. pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP
+
<tr><td valign="top">P1 2M
-
23. pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP
+
</td><td valign="top">Rbs(1.0)
-
24. pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP
+
</td><td valign="top">pSB1A2
-
25. pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP
+
</td><td valign="top">B0034
-
26. pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP
+
</td></tr>
-
27. pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP
+
<tr><td style="">P1 2I</td><td style="">Rbs(0.3)</td><td style="">pSB1A2&nbsp;&nbsp;</td><td style="">B0032&nbsp;</td></tr>
-
28. pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP
+
<tr><td style="">P1 2G&nbsp;</td><td style="">Rbs(0.07)</td><td style="">pSB1A2&nbsp;&nbsp;</td><td style="">B0031&nbsp;</td></tr></tbody></table>
-
29. pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP
+
<p>1.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP</p>
-
30. pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP
+
<p>2.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP</p>
-
31. pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO- lux
+
<p>3.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP</p>
-
32. pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux
+
<p>4.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP</p>
-
33. pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux
+
<p>5.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP</p>
-
34. pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux
+
<p>6.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP</p>
-
35. pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux
+
<p>7.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP</p>
-
36. pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux
+
<p>8.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP</p>
-
37. T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP
+
<p>9.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP</p>
-
38. T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP
+
<p>10.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP</p>
-
39. T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP
+
<p>11.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP</p>
-
40. T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP
+
<p>12.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP</p>
-
41. T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP
+
<p>13.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux</p>
-
42. T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP
+
<p>14.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO- lux</p>
-
43. T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP
+
<p>15.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO- lux</p>
-
44. T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP
+
<p>16.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO- lux</p>
-
45. T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP
+
<p>17.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO- lux&nbsp;</p>
-
46. T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP
+
<p>18.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO- lux</p>
-
47. T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP
+
<p>19.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP</p>
-
48. T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP
+
<p>20.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP</p>
-
49. T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux
+
<p>21.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP</p>
-
50. T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux
+
<p>22.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP</p>
-
51. T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux
+
<p>23.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP</p>
-
52. T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux
+
<p>24.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP</p>
-
53. T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux
+
<p>25.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP</p>
-
54. T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux
+
<p>26.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP</p>
-
</p><br>
+
<p>27.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP</p>
 +
<p>28.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP</p>
 +
<p>29.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP</p>
 +
<p>30.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP</p>
 +
<p>31.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO- lux</p>
 +
<p>32.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux</p>
 +
<p>33.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux</p>
 +
<p>34.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux</p>
 +
<p>35.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux</p>
 +
<p>36.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux</p>
 +
<p>37.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP</p>
 +
<p>38.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP</p>
 +
<p>39.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP</p>
 +
<p>40.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP</p>
 +
<p>41.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP</p>
 +
<p>42.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP</p>
 +
<p>43.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP</p>
 +
<p>44.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP</p>
 +
<p>45.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP</p>
 +
<p>46.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP</p>
 +
<p>47.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP</p>
 +
<p>48.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP</p>
 +
<p>49.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux</p>
 +
<p>50.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux</p>
 +
<p>51.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux</p>
 +
<p>52.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux</p>
 +
<p>53.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux</p>
 +
<p>54.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux</p>
<p>Transform the parts mentioned in the box into dH5a.</p><br>
<p>Transform the parts mentioned in the box into dH5a.</p><br>
<p>Pick colonies to cultivate. And extract plasmids.</p><br>
<p>Pick colonies to cultivate. And extract plasmids.</p><br>
-
<p>Do all the double digestions and ligations together for the first time. The order is:
+
<p>Do all the double digestions and ligations together for the first time. The order is:</p>
-
1. Promoter + Rbs & Terminator + Reporter
+
<p>1.Promoter + Rbs & Terminator + Reporter</p>
-
2. Promoter-Rbs + modified protein
+
<p>2.Promoter-Rbs + modified protein</p>
-
3. Promoter-Rbs-modified protein + Terminator-Reporter
+
<p>3.Promoter-Rbs-modified protein + Terminator-Reporter</p>
-
</p><br>
+
<br>
<p>Transform fails for several ligation products.</p><br>
<p>Transform fails for several ligation products.</p><br>
-
<p>At last, we choose 3 gene circuits for further investigation:
+
<p>At last, we choose 3 gene circuits for further investigation:</p>
-
1. araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP
+
<p>1.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP</p>
-
2. T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP
+
<p>2.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP</p>
-
3. araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP
+
<p>3.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP</p>
-
4. araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux
+
<p>4.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux</p>
-
5. T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-lux
+
<p>5.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-lux<p>
-
6. araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-lux
+
<p>6.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-lux</p>
-
</p><br>
+
<br>
<p>We run a SDS-PAGE gel to confirm the expression of the modified protein. The result is positive. </p><br>
<p>We run a SDS-PAGE gel to confirm the expression of the modified protein. The result is positive. </p><br>
<p>In order to verify the modified protein’s characteristic, Juntao Mai does the western-blot. The result is partly positive. Under equal quantity induction of arabinose (0.3%), samples under 450nm wavelength light shows a 30% GFP decay compared with samples incubated in the dark.</p><br>
<p>In order to verify the modified protein’s characteristic, Juntao Mai does the western-blot. The result is partly positive. Under equal quantity induction of arabinose (0.3%), samples under 450nm wavelength light shows a 30% GFP decay compared with samples incubated in the dark.</p><br>
<p>We detected the lov-HTH, whose HTH part is modified, by reversed transcription PCR. We‘ve done a series of RT PCR with samples induced by 0.3% arabinose during their incubation and samples incubated without arabinose at the first place. In order to get rid of the effect of light, we incubated all the cells in the dark. We can easily find lov-HTH (modified) mRNA in samples induced by arabinose.</p><br>
<p>We detected the lov-HTH, whose HTH part is modified, by reversed transcription PCR. We‘ve done a series of RT PCR with samples induced by 0.3% arabinose during their incubation and samples incubated without arabinose at the first place. In order to get rid of the effect of light, we incubated all the cells in the dark. We can easily find lov-HTH (modified) mRNA in samples induced by arabinose.</p><br>
<p>We investigated the time course of the transcription of the arabinose-induced GFP using quantitative real-time PCR. We combined different conditions together and did a series of QRT PCR. We can get the detail in this table.</p>
<p>We investigated the time course of the transcription of the arabinose-induced GFP using quantitative real-time PCR. We combined different conditions together and did a series of QRT PCR. We can get the detail in this table.</p>
-
<img src="https://static.igem.org/mediawiki/2012/9/9b/QRTPCR.JPG" style="width:250px;"alt="test"><br>
+
<img src="https://static.igem.org/mediawiki/2012/9/9b/QRTPCR.JPG" style="width:500px;"alt="test" class="myimg"><br><br>
<p>We decide to use EMSA (Electrophoretic Mobility Shift Assay) to verify if the modified protein can be efficient binding the specific part in ptetO.</p><br>
<p>We decide to use EMSA (Electrophoretic Mobility Shift Assay) to verify if the modified protein can be efficient binding the specific part in ptetO.</p><br>
<p>Considering the time, cost and the possibility, we give up EMSA.</p><br>
<p>Considering the time, cost and the possibility, we give up EMSA.</p><br>
Line 468: Line 499:
<!-- tab 6 content  -->
<!-- tab 6 content  -->
<div>
<div>
-
+
<p>With one of our classmates’ help, Zining Hou make a wood box for shooting pictures in the dark.</p>
 +
<img src="https://static.igem.org/mediawiki/igem.org/0/03/Wood_box.jpg" style="width:300px;"alt="test" class="myimg"><br><br>
 +
<p>We make our first double layer disk to shoot.</p><br>
 +
<p>Our instructor helps us make a single colony mathematic model.</p>
 +
<img src="https://static.igem.org/mediawiki/igem.org/a/a5/Stimulation.jpg" style="width:500px;"alt="test" class="myimg"><br><br>
 +
<p>We get a series of photos which show a positive result.
 +
(araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux)
 +
</p><br>
 +
<p>We compare araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux, araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-lux and T7 promoter-Rbs(0.3)-lov-HTH-Terminator-ptetO-lux by putting four double layer disks together (we use ptetO-lux as control).
 +
Unfortunately, the light emitted from different disks interfere each other. So we couldn’t get a usable result. But good news is that we assure the light emitted by lux is strong enough to be a signal.
 +
</p><br>
 +
<p>Organize our first association recruiting with <a href="https://2012.igem.org/Team:Fudan_D">Fudan_D</a>, our cooperating team.</p>
 +
<img src="https://static.igem.org/mediawiki/2012/c/cf/Association.jpg" style="width:500px;"alt="test" class="myimg"><br><br>
 +
<p>Build the wiki</p><br>
</div>
</div>
Line 488: Line 532:
<!-- ENDS MAIN -->
<!-- ENDS MAIN -->
-
<!-- Twitter -->
+
<!-- Twitter -->
<div id="twitter">
<div id="twitter">
-
<div class="wrapper">
+
-
<a href="#" id="prev-tweet"></a>
+
-
<a href="#" id="next-tweet"></a>
+
-
<img id="bird" src="img/bird.png" alt="Tweets" />
+
-
<div id="tweets">
+
-
<ul class="tweet_list"></ul>
+
-
</div>
+
-
</div>
+
</div>
</div>
<!-- ENDS Twitter -->
<!-- ENDS Twitter -->
Line 508: Line 545:
<!-- footer-cols -->
<!-- footer-cols -->
<ul id="footer-cols">
<ul id="footer-cols">
-
<li class="col">
+
-
<h6>Pages</h6>
+
-
<ul>
+
-
<li class="page_item"><a href="index.html">Home</a></li>
+
-
<li class="page_item"><a href="features.html">Features</a></li>
+
-
<li class="page_item"><a href="blog.html">Blog</a></li>
+
-
<li class="page_item"><a href="portfolio.html">Portfolio</a></li>
+
-
<li class="page_item"><a href="gallery.html">Gallery</a></li>
+
-
<li class="page_item"><a href="contact.html">Contact</a></li>
+
-
</ul>
+
-
</li>
+
<li class="col">
<li class="col">
-
<h6>Categories</h6>
+
<h6>About the Team</h6>
-
<ul>
+
He he he he!
-
<li><a href="#">Webdesign projects senectus</a></li>
+
-
<li><a href="#/">Wordpress projects senectus</a></li>
+
-
<li><a href="#">Vestibulum tortor quam</a></li>
+
-
<li><a href="#">Code projects amet quam egestas</a></li>
+
-
<li><a href="#">Web design projects senectus</a></li>
+
-
<li><a href="#/">Marketplace projects</a></li>
+
-
<li><a href="#">Writting projects senectus</a></li>
+
-
<li><a href="#">Drawings projects fames Aenean</a></li>
+
-
<li><a href="#/">Wordpress projects Aenean ultricies</a></li>
+
-
</ul>
+
-
</li>
+
-
<li class="col">
+
-
<h6>About the theme</h6>
+
-
Pellentesque habitant morbi tristique senectus et netus et malesuada fames ac turpis egestas. Vestibulum tortor quam, feugiat vitae, ultricies eget, tempor sit amet, ante. Donec eu libero sit amet quam egestas semper. Aenean ultricies mi vitae est. Mauris placerat eleifend leo. Cursus faucibus, tortor neque egestas augue, eu vulputate magna eros.
+
</li>
</li>
Line 551: Line 565:
<!-- wrapper-bottom -->
<!-- wrapper-bottom -->
<div class="wrapper">
<div class="wrapper">
-
<div id="bottom-text">2011 Nova all rights reserved. <a href="http://www.luiszuno.com"> Luiszuno.com</a> </div>
+
<div id="bottom-text">All rights reserved. Tempalate Edit by Fudan-lux team <a href="http://www.luiszuno.com">Powered By Luiszuno.com</a> </div>
<!-- Social -->
<!-- Social -->
-
<ul class="social ">
+
-
<li><a href="http://www.facebook.com" class="poshytip  facebook" title="Become a fan"></a></li>
+
-
<li><a href="http://www.twitter.com" class="poshytip twitter" title="Follow our tweets"></a></li>
+
-
<li><a href="http://www.dribbble.com" class="poshytip dribbble" title="View our work"></a></li>
+
-
<li><a href="http://www.addthis.com" class="poshytip addthis" title="Tell everybody"></a></li>
+
-
<li><a href="http://www.vimeo.com" class="poshytip vimeo" title="View our videos"></a></li>
+
-
<li><a href="http://www.youtube.com" class="poshytip youtube" title="View our videos"></a></li>
+
-
</ul>
+
<!-- ENDS Social -->
<!-- ENDS Social -->
<div id="to-top" class="poshytip" title="To top"></div>
<div id="to-top" class="poshytip" title="To top"></div>
Line 567: Line 574:
</div>
</div>
<!-- ENDS Bottom -->
<!-- ENDS Bottom -->
-
 
-
</body>
 
-
</html>
 

Latest revision as of 22:52, 26 September 2012

NOVA

Note Book Record iGEMers in summer.

We summarized our recent brain storm result. At last we chose to make a light-signal oscillator testin E.coli and possibilities to use nanotubes. The first thing for the next week is to find an efficient light sensor and a stable lighting part.

Discuss the establishment of the gene circuits.

test test

Get lux without operon and promoter from k325909 by PCR. We used longPCR Enzyme and Overlapping PCR.


Measure the growth curve of dH5a transformed by lux with araBAD (k325909)

test

Transform tetR (C0040) from the kit. Transfer araBAD (I0500) and tetR (C0040) with RBS into pSB1C3 by 3A ligation. Transform it into dH5a.


Transfer tetR with promoter and RFP with ptetO as promoter (J61002) into pSB1C3 by 3A ligation. Transform it into dH5a.


Sorry to find the ligation is failed. But fortunately, we decide to change the reporter into GFP (I13522). Transform the plasmid from the kit into dH5a.


Design protein composed by lov domain and modified helix turn helix (abbr. lov-HTH).

test

Design protein composed by lov domain and tetR (abbr. lov-tetR).


Send the synthetic orders to the gene synthesis company.


Half of our members went to Tianmu Mount, Zhejiang Province. They spent a week there to participate a fieldwork organized by the Life Science Institute. During the fieldwork, they paid a lot of attention to a China’s specific firefly, Qiongyuying. They observed the behavior of Qiongyuying, especially the synchrony.

test

Our instructor and four of our members went to meet Richard J Roberts after the reward ceremony of COMBREX, a project to accelerate the functional annotation of prokaryotic genomes. They talked for about an hour and we presented our project to him. Richard advised that we should make our project more practical and functional.

test

After negotiating with the principal of volunteer teaching program in our institute, one of our members, with all members of Fudan_Lux’s hope and responsibility on his shoulders, went to Shangrao, Jiangxi Province to do the volunteer teaching.

test class= test

Make an appointment with Li Jin, Hongyan Wang etc. to show our projects.


Receive lov-HTH in nonstandard vector.


Design primers to make clones of lov-HTH, and transfer lov-HTH with double terminators into pSB1C3.


Receive lov-tetR in nonstandard vector.


Do double digestion by E.coliI HF and SpeI, and transfer lov-tetR into pSB1C3.


Make an appointment with prof. Guoping Zhao, who establishes China’s first synthesis biology laboratory in Shanghai. He talked directly about the impropriation of our tumor project and the lack of application about our biowave project.


The double digestion and the ligation held us for more than 4 weeks!

test

In order to do the ligation more efficiently, we decide to do the ligation according to this table.

NO. 
Composition Backbone Code
P1 14N araBAD pSB2K3 I0050
P1 6G pLac pSB1A2 R0011
P1 6N T7 promoter pSB1AK8 I712074
P1 2M Rbs(1.0) pSB1A2 B0034
P1 2IRbs(0.3)pSB1A2  B0032 
P1 2G Rbs(0.07)pSB1A2  B0031 

1.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP

2.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP

3.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP

4.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP

5.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP

6.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP

7.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP

8.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP

9.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP

10.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP

11.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP

12.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP

13.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux

14.araBAD-Rbs(0.3)-lov-HTH-Terminator-ptetO- lux

15.araBAD-Rbs(0.07)-lov-HTH-Terminator-ptetO- lux

16.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO- lux

17.araBAD-Rbs(0.3)-lov- tetR -Terminator-ptetO- lux 

18.araBAD-Rbs(0.07)-lov- tetR -Terminator-ptetO- lux

19.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP

20.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP

21.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP

22.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP

23.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP

24.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP

25.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP

26.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP

27.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP

28.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP

29.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP

30.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP

31.pLac-Rbs(1.0)-lov-HTH-Terminator-ptetO- lux

32.pLac -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux

33.pLac -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux

34.pLac -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux

35.pLac -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux

36.pLac -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux

37.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP

38.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP

39.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-GFP

40.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP

41.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-GFP

42.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-GFP

43.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-CFP

44.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-CFP

45.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO-CFP

46.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO-CFP

47.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO-CFP

48.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO-CFP

49.T7 promoter-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux

50.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO- lux

51.T7 promoter -Rbs(0.07)-lov-HTH-Terminator-ptetO- lux

52.T7 promoter -Rbs(1.0)-lov-tetR-Terminator-ptetO- lux

53.T7 promoter -Rbs(0.3)-lov- tetR -Terminator-ptetO- lux

54.T7 promoter -Rbs(0.07)-lov- tetR -Terminator-ptetO- lux

Transform the parts mentioned in the box into dH5a.


Pick colonies to cultivate. And extract plasmids.


Do all the double digestions and ligations together for the first time. The order is:

1.Promoter + Rbs & Terminator + Reporter

2.Promoter-Rbs + modified protein

3.Promoter-Rbs-modified protein + Terminator-Reporter


Transform fails for several ligation products.


At last, we choose 3 gene circuits for further investigation:

1.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-GFP

2.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-GFP

3.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-GFP

4.araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux

5.T7 promoter -Rbs(0.3)-lov-HTH-Terminator-ptetO-lux

6.araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-lux


We run a SDS-PAGE gel to confirm the expression of the modified protein. The result is positive.


In order to verify the modified protein’s characteristic, Juntao Mai does the western-blot. The result is partly positive. Under equal quantity induction of arabinose (0.3%), samples under 450nm wavelength light shows a 30% GFP decay compared with samples incubated in the dark.


We detected the lov-HTH, whose HTH part is modified, by reversed transcription PCR. We‘ve done a series of RT PCR with samples induced by 0.3% arabinose during their incubation and samples incubated without arabinose at the first place. In order to get rid of the effect of light, we incubated all the cells in the dark. We can easily find lov-HTH (modified) mRNA in samples induced by arabinose.


We investigated the time course of the transcription of the arabinose-induced GFP using quantitative real-time PCR. We combined different conditions together and did a series of QRT PCR. We can get the detail in this table.

test

We decide to use EMSA (Electrophoretic Mobility Shift Assay) to verify if the modified protein can be efficient binding the specific part in ptetO.


Considering the time, cost and the possibility, we give up EMSA.


With propose of testing the protein’s repression ability, we do a fluorescence intensity test. Under an arabinose induction gradient between 0 to 0.3%, we investigate the time course of the two groups of cells’ GFP fluorescence intensity and the absorbance of OD600 at the same time. One group of them is incubated in the 470nm wavelength light and the other one was incubated in the dark. The two curves of RFU per OD600 present 30% differences which is positive.


With one of our classmates’ help, Zining Hou make a wood box for shooting pictures in the dark.

test

We make our first double layer disk to shoot.


Our instructor helps us make a single colony mathematic model.

test

We get a series of photos which show a positive result. (araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux)


We compare araBAD-Rbs(1.0)-lov-HTH-Terminator-ptetO-lux, araBAD-Rbs(1.0)-lov-tetR-Terminator-ptetO-lux and T7 promoter-Rbs(0.3)-lov-HTH-Terminator-ptetO-lux by putting four double layer disks together (we use ptetO-lux as control). Unfortunately, the light emitted from different disks interfere each other. So we couldn’t get a usable result. But good news is that we assure the light emitted by lux is strong enough to be a signal.


Organize our first association recruiting with Fudan_D, our cooperating team.

test

Build the wiki


All rights reserved. Tempalate Edit by Fudan-lux team Powered By Luiszuno.com

Retrieved from "http://2012.igem.org/Team:Fudan_Lux/Notebook"