Calgary/final result

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  E.co Lisa Final Results Page
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     <td><a href="https://2007.igem.org/Calgary"><img style="border:none" src="https://static.igem.org/mediawiki/2007/3/34/BackToHome.gif" alt="back to U of C Homepage"></a></td>
     <td><a href="https://2007.igem.org/Calgary"><img style="border:none" src="https://static.igem.org/mediawiki/2007/3/34/BackToHome.gif" alt="back to U of C Homepage"></a></td>
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     <td align="right"><a href=""><img img style="border:none" src="https://static.igem.org/mediawiki/2007/2/29/CheckOutevoGEM.gif" alt="Check out evoGEM"></a></td>
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     <td align="right"><a href="https://2007.igem.org/Calgary/evoGEM_introduction"><img img style="border:none" src="https://static.igem.org/mediawiki/2007/2/29/CheckOutevoGEM.gif" alt="Check out evoGEM"></a></td>
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     <td align="center"  ><a class="mainLinks" href="https://2007.igem.org/Calgary/choosing_our_project" title="choosing our project" >Projects</a> </td>
     <td align="center"  ><a class="mainLinks" href="https://2007.igem.org/Calgary/choosing_our_project" title="choosing our project" >Projects</a> </td>
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/design" title="designing our project">Project Design: Wet Lab</a> </td>
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/design" title="designing our project - wetlab">Design: Wet Lab</a> </td>
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/constructing_printer" title="constructing our project - printer and software" >Project Design: Printer and Software</a> </td>  
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/constructing_printer" title="designing our project - printer" >Design: Printer</a> </td>
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    <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/software" title="designing our project - printer" >Design: Software</a> </td>
     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/testing" title="testing our parts and primers" >Testing</a> </td>
     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/testing" title="testing our parts and primers" >Testing</a> </td>
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/constructing_wetlab" title="constructing our project" >Constructing our Project: The Wetlab</a> </td>
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     <td align="center" ><a class="mainLinks" href="https://2007.igem.org/Calgary/constructing_wetlab" title="constructing our project" >Construction: The Wetlab</a> </td>
     <td align="center"  valign="top"><a class="mainLinks" href="https://2007.igem.org/Calgary/protocols" title="protocols" >Protocols</a> </td>
     <td align="center"  valign="top"><a class="mainLinks" href="https://2007.igem.org/Calgary/protocols" title="protocols" >Protocols</a> </td>
     <td align="center" bgcolor="#006633"><a class="mainLinks" href="https://2007.igem.org/Calgary/final_result" title="final results" >Final Result of E.co Lisa</a> </td>
     <td align="center" bgcolor="#006633"><a class="mainLinks" href="https://2007.igem.org/Calgary/final_result" title="final results" >Final Result of E.co Lisa</a> </td>
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  Final state of project
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<p>At the time of the Jamboree the final state of our project is unfortunately unfinished. We were unable to complete our bacterial printer system. However, even without the fully working printer system our team still has many acheivements to present.  This section summarizes the final results of our work with <em>E. co</em>Lisa.</p>
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    <td valign="top"  width="33%"><p><a style="font-size:15px; font-family:Verdana, Arial, Helvetica, sans-serif;" href="#contributions" title="See our contributions to the Registry" >Contributions To The Registry</a></td>
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    <td valign="top"  width="33%"><p><a style="font-size:15px; font-family:Verdana, Arial, Helvetica, sans-serif;" href="#agarase" title="Sequencing of Agarase" >Sequencing of Agarase</a></td>
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    <td valign="top"  width="33%"><p> <a style="font-size:15px; font-family:Verdana, Arial, Helvetica, sans-serif;" href="#logic" title="Sequencing of Logic Circut" >Sequencing of Logic Circut </a></td>
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  Table summarizing the parts contributed to the registry
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    <td style="width:85%;"><p style="font-size:20px; font-weight:bold;"><a style="text-decoration:none" name="contributions"> Our Contributions To The Registry</a></p></td>
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    <td width="15%"><a style="float:right;" href="#top" title="return to top">return to top</a> </td>
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    <td><strong>Number</strong></td>
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    <td><strong> Parts</strong></td>
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    <td><strong>Plasmid</strong></td>
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    <td><strong>New part name</strong></td>
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    <td><strong>Type</strong></td>
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    <td ><strong>Notes</strong></td>
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    <td>1</td>
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    <td>agarase</td>
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    <td>pSB1A2</td>
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    <td>i737020</td>
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    <td >Basic Part</td>
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    <td>2</td>
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    <td>R0084 . A340620 . S01414 . I13504</td>
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    <td>pSB1AK3</td>
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    <td>I737010</td>
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    <td>Project</td>
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    <td>3</td>
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    <td>R0083 . A340620 . S01414 . I13504</td>
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    <td>pSB1AK3</td>
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    <td>I737012</td>
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    <td>Project</td>
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    <td>4</td>
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    <td>R0082 . A340620 . S01414 . I13504</td>
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    <td>pSB1AK3</td>
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    <td>I737014</td>
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    <td>Project</td>
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    <td>5</td>
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    <td>R0040 . A340620 . I13504</td>
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    <td>pSB1AC3</td>
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    <td>S03868</td>
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    <td>Intermediate</td>
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    <td>Entered as part I13553 and J26010, not available or experience</td>
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    <td>6</td>
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    <td>R0040 . J01010 . I13401</td>
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    <td>pSB1AC3</td>
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    <td>S03867</td>
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    <td>Intermediate</td>
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    <td>Entered as part I714081, but not available</td>
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    <td>7</td>
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    <td>R0040 . J01008 . B0015</td>
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    <td>pSB1AC3</td>
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    <td>S03863</td>
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    <td>Intermediate</td>
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    <td>Is S03862 . B0015</td>
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    <td>8</td>
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    <td>R0040 . J01080 . I13401</td>
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    <td>pSB1AC3</td>
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    <td>S03864</td>
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    <td>Intermediate</td>
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    <td>Is J01109 . I13401</td>
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    <td>9</td>
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    <td>R0040 . J23008 . B0015</td>
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    <td>pSB1AC3</td>
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    <td>S03866</td>
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    <td>Intermediate</td>
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    <td>Is S03865 . B0015</td>
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    <td>10</td>
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    <td>R0040 . J01010 . E0040 . S01414 .    B0015</td>
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    <td>pSB1AK3</td>
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    <td>S03871</td>
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    <td>Intermediate</td>
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    <td>Is S03870 . I0462</td>
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    <td >11</td>
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    <td >S01414 . I13504</td>
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    <td>pSB1AK3</td>
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    <td>S03869</td>
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    <td >Intermediate</td>
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    <td >12</td>
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    <td >R0040 . A340620 . J23008 . B0015</td>
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    <td>pSB1AK3</td>
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    <td>S03872</td>
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    <td>Intermediate</td>
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    <td>Is F2620 . J23021</td>
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  </tr>
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    <td >13</td>
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    <td>R0040 . J06801</td>
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    <td>pSB2K3</td>
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    <td>S03743</td>
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    <td >Intermediate</td>
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<p style="margin-bottom:40px">Our team is pleased to report that we have submitted 13 unique parts to the iGEM registry. These parts include the β-agarase gene, our logic circut and several of the intermediate parts we constructed. </p>
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  Sequencing information for beta Agarase
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    <td style="width:85%;"><p style="font-size:20px; font-weight:bold;"><a style="text-decoration:none" name="agarase"> Sequencing of Agarase</a></p></td>
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    <td width="15%"><a style="float:right;" href="#top" title="return to top">return to top</a> </td>
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<p> We were able to sucessfully isolate β-agarase gene from the <em>Pseudoalteromonas atlantica</em> genome. Here are the results we obtained from sequencing the isolated β-agarase gene. Click on the image below to see the full sequencing information for β-agarase in pdf format. </p>
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    <td><a href="https://static.igem.org/mediawiki/2007/8/85/Agaraseclone_sequence.pdf" target="_blank"><img style="border:#CCCCCC thin outset" src="https://static.igem.org/mediawiki/2007/9/9f/AgaraseSequencingThumb.gif" atl="sequencing information from β-agarase gene" /></a> </td>
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    <td> The sequencing information obtained confirms that we have indeed isolated the β-agarase gene and it is present in the plasmid. </td>
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    <td><img src="https://static.igem.org/mediawiki/2007/b/b6/AgaraseChromatogramForward.jpg" alt="Reverse Chromatogram from aragase" /> </td>
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    <td><p> This is the Reverse Chromatogram from the sequencing of our β-agarase containing plasmid. The results confirm that β-agarase is present in the plasmid</p></td>
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    <td><img src="https://static.igem.org/mediawiki/2007/7/7a/AgaraseChromatogramForward2%28actuallyForward%29.jpg" atl="Forward Chromatogram from agarase" /> </td>
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    <td><p> This is the Forward Chromatogram from the sequencing of our β-agarase containing plasmid. The results confirm that β-agarase is present in the plasmid</p></td>
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  Sequencing informatio for the logic circut
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    <td style="width:85%;"><p style="font-size:20px; font-weight:bold;"><a style="text-decoration:none" name="logic"> Sequencing of Logic Circut</a></p></td>
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    <td width="15%"><a style="float:right;" href="#top" title="return to top">return to top</a> </td>
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<p> There were three seperate logic ciructs prepared. Each differed only in the initial promotorer being used. The first circut used part R0084 a promter that is activated by phosphorylated <em>ompR</em> while the other two R0082 and R0083 are repressed by phosphorylated <em>ompR</em> </p>
 +
<p> Our team synthesized plasmids containing our logic circut using each of these promoters. The links below connect to pdf's showing the result of the sequencing for each of these plasmids. The sequencing information confirmed that our logic circut was present in the plasmids. </p>
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    <td>|<a href="https://static.igem.org/mediawiki/2007/5/55/R82akgv.pdf" title="R0082 Logic Circut">R0082 Logic Circut</a>| </td>
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    <td> |<a href="https://static.igem.org/mediawiki/2007/3/3a/R83AKVF5FR83AKVR.pdf" title="R0083 Logic Circut">R0083 Logic Circut</a>|</td>
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    <td>|<a href="https://static.igem.org/mediawiki/2007/a/aa/R84AKGB.pdf" title="R0084 Logic Circut">R0084 Logic Circut</a>|</td>
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Latest revision as of 06:54, 19 December 2007

back to U of C Homepage Check out evoGEM
Projects Design: Wet Lab Design: Printer Design: Software Testing Construction: The Wetlab Protocols Final Result of E.co Lisa

At the time of the Jamboree the final state of our project is unfortunately unfinished. We were unable to complete our bacterial printer system. However, even without the fully working printer system our team still has many acheivements to present. This section summarizes the final results of our work with E. coLisa.

Contributions To The Registry

Sequencing of Agarase

Sequencing of Logic Circut

Our Contributions To The Registry

 return to top
Number Parts Plasmid New part name Type Notes
1 agarase pSB1A2 i737020 Basic Part
2 R0084 . A340620 . S01414 . I13504 pSB1AK3 I737010 Project
3 R0083 . A340620 . S01414 . I13504 pSB1AK3 I737012 Project
4 R0082 . A340620 . S01414 . I13504 pSB1AK3 I737014 Project
5 R0040 . A340620 . I13504 pSB1AC3 S03868 Intermediate Entered as part I13553 and J26010, not available or experience
6 R0040 . J01010 . I13401 pSB1AC3 S03867 Intermediate Entered as part I714081, but not available
7 R0040 . J01008 . B0015 pSB1AC3 S03863 Intermediate Is S03862 . B0015
8 R0040 . J01080 . I13401 pSB1AC3 S03864 Intermediate Is J01109 . I13401
9 R0040 . J23008 . B0015 pSB1AC3 S03866 Intermediate Is S03865 . B0015
10 R0040 . J01010 . E0040 . S01414 . B0015 pSB1AK3 S03871 Intermediate Is S03870 . I0462
11 S01414 . I13504 pSB1AK3 S03869 Intermediate
12 R0040 . A340620 . J23008 . B0015 pSB1AK3 S03872 Intermediate Is F2620 . J23021
13 R0040 . J06801 pSB2K3 S03743 Intermediate

Our team is pleased to report that we have submitted 13 unique parts to the iGEM registry. These parts include the β-agarase gene, our logic circut and several of the intermediate parts we constructed.

Sequencing of Agarase

 return to top

We were able to sucessfully isolate β-agarase gene from the Pseudoalteromonas atlantica genome. Here are the results we obtained from sequencing the isolated β-agarase gene. Click on the image below to see the full sequencing information for β-agarase in pdf format.

The sequencing information obtained confirms that we have indeed isolated the β-agarase gene and it is present in the plasmid.
Reverse Chromatogram from aragase

This is the Reverse Chromatogram from the sequencing of our β-agarase containing plasmid. The results confirm that β-agarase is present in the plasmid

This is the Forward Chromatogram from the sequencing of our β-agarase containing plasmid. The results confirm that β-agarase is present in the plasmid

Sequencing of Logic Circut

 return to top

There were three seperate logic ciructs prepared. Each differed only in the initial promotorer being used. The first circut used part R0084 a promter that is activated by phosphorylated ompR while the other two R0082 and R0083 are repressed by phosphorylated ompR

Our team synthesized plasmids containing our logic circut using each of these promoters. The links below connect to pdf's showing the result of the sequencing for each of these plasmids. The sequencing information confirmed that our logic circut was present in the plasmids.

|R0082 Logic Circut| |R0083 Logic Circut| |R0084 Logic Circut|

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