Team:iHKU/design
From 2008.igem.org
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<h3 class="style7"><strong><a name="1" id="1"></a></strong>Our Aim</h3> | <h3 class="style7"><strong><a name="1" id="1"></a></strong>Our Aim</h3> | ||
<p>We endeavor our strains to grow into patterns by arranging themselves in a synchronous, self-organised manner, “just as in organisms in nature which all are able to develop shapes and patterns.” Implementing such idea on bacteria sheds light to a mechanism involving cell-cell communication that would produce a key response, predominately a respond affecting cell motility. The characteristics of the response logically should be critical towards the formation overall pattern. </p> | <p>We endeavor our strains to grow into patterns by arranging themselves in a synchronous, self-organised manner, “just as in organisms in nature which all are able to develop shapes and patterns.” Implementing such idea on bacteria sheds light to a mechanism involving cell-cell communication that would produce a key response, predominately a respond affecting cell motility. The characteristics of the response logically should be critical towards the formation overall pattern. </p> | ||
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<h3><strong><a name="2" id="2"></a>Chassis selection</strong></h3> | <h3><strong><a name="2" id="2"></a>Chassis selection</strong></h3> | ||
<p>Past chemotaxis studies have provided the molecular basis of cellular motility regulation, <em>Escherichia coli</em> and Bacillus subtilis are notably the well-understood strains which are ideal to be the chassis of our designed genetic circuit. We chose <em>E.coli</em> as our chassis for the project reasoning that cell-cell communications will require the use of a signaling molecule, which are often density related. <em>E.coli</em> is known to be less motile than <em>Bacillus</em> in terms of speed, thus would ease the accumulation of the signaling molecule. We hope the subsequent pattern generated by using <em>E.coli</em> as chassis would be finer and more interesting.</p> | <p>Past chemotaxis studies have provided the molecular basis of cellular motility regulation, <em>Escherichia coli</em> and Bacillus subtilis are notably the well-understood strains which are ideal to be the chassis of our designed genetic circuit. We chose <em>E.coli</em> as our chassis for the project reasoning that cell-cell communications will require the use of a signaling molecule, which are often density related. <em>E.coli</em> is known to be less motile than <em>Bacillus</em> in terms of speed, thus would ease the accumulation of the signaling molecule. We hope the subsequent pattern generated by using <em>E.coli</em> as chassis would be finer and more interesting.</p> | ||
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<p></p> | <p></p> | ||
<h3><strong><a name="3" id="3"></a>Genetic Circuit Design</strong></h3> | <h3><strong><a name="3" id="3"></a>Genetic Circuit Design</strong></h3> | ||
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<p>Predicted Pattern:</p> | <p>Predicted Pattern:</p> | ||
<h1 align="center"><img src="/wiki/images/thumb/1/1e/Design_pic3.png/800px-Design_pic3.png" width="465" height="230" /></h1> | <h1 align="center"><img src="/wiki/images/thumb/1/1e/Design_pic3.png/800px-Design_pic3.png" width="465" height="230" /></h1> | ||
- | <p> </p> | + | <p align="center"> </p> |
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<h3><strong><a name="4" id="4"></a>Plasmids and strains</strong></h3> | <h3><strong><a name="4" id="4"></a>Plasmids and strains</strong></h3> | ||
</td> | </td> | ||
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<th width="2%" scope="row"> </th> | <th width="2%" scope="row"> </th> | ||
<td width="95%"><div align="center"> | <td width="95%"><div align="center"> | ||
- | <img src="/wiki/images/5/5d/Design_tab1.png" width="538" height="551" /></br> | + | <p><img src="/wiki/images/5/5d/Design_tab1.png" width="538" height="551" /></br> |
- | <img src="/wiki/images/7/7d/Design_tab2.png" width="538" height="430" /></div></td> | + | <img src="/wiki/images/7/7d/Design_tab2.png" width="538" height="430" /></p> |
+ | <p align="right"><a href="#top">[Back to Top]</a></p> | ||
+ | </div></td> | ||
</tr> | </tr> | ||
</table> | </table> |
Revision as of 16:35, 29 October 2008