Template:Imperial/09/Overview

From 2009.igem.org

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<dd id="ph"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="ph"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<span><div class="first">Growth</div>
<span><div class="first">Growth</div>
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<div class="rest">The cells are grown to a critical cell density, before the system is started. This allows the culture to reach a sufficient stage of growth before the triggering the cells to begin protein which can slow cell growth. </div></span>
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<div class="rest">The cells are grown to a critical cell density, before the system is started. It allows the culture to reach a sufficient cell number before the the cells are triggered to begin protein production. This is because protein production can slow cell growth. </div></span>
</a></dd>
</a></dd>
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<dd id="at"><a href="https://2009.igem.org/Team:Imperial_College_London/M1" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="at"><a href="https://2009.igem.org/Team:Imperial_College_London/M1" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<span><div class="first">Module 1: Protein Production</div>
<span><div class="first">Module 1: Protein Production</div>
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<div class="rest">The first module is induced with IPTG and triggers the production of the protein of interest. As part of this project we have looked into two proteins and a peptide of interest. </div></span>
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<div class="rest">The first module is induced with IPTG, which triggers the production of the protein of interest. As part of this project we have looked into two proteins and a peptide of interest. </div></span>
</a></dd>
</a></dd>
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<dd id="u"><a href="https://2009.igem.org/Team:Imperial_College_London/M2" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="u"><a href="https://2009.igem.org/Team:Imperial_College_London/M2" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<span><div class="first">Module 2: Encapsulation</div>
<span><div class="first">Module 2: Encapsulation</div>
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<div class="rest">This second module is where the bacterium, after having produced the peptide of interest, produces colanic acid thus creating a protecting layer around itself to shelter it from the acidity of the stomach.</div></span>
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<div class="rest">The second module is where the cell, after having produced the peptide of interest, produces colanic acid. This creates a protecting layer around teh bacterium to shelter it from the acidity of the stomach.</div></span>
</a></dd>
</a></dd>
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<dd id="g"><a href="https://2009.igem.org/Team:Imperial_College_London/M3" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="g"><a href="https://2009.igem.org/Team:Imperial_College_London/M3" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<span><div class="first">Module 3: Genome deletion</div>
<span><div class="first">Module 3: Genome deletion</div>
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<div class="rest">Module 3 occurs after encapsulation of the bacterium containing the produced peptide of interest. This module has the purpose of making the bacterium non viable. It does so by over-expressing restriction enzymes which subsequently cleave the genomic DNA into small fragments. The bacterium is thus unable to produce any proteins and therefore unable to survive.</div></span>
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<div class="rest">Module 3 occurs after encapsulation of the cell containing the produced peptide of interest. This module makes the bacterium non-viable. It does so by over-expressing restriction enzymes which subsequently cleave the genomic DNA into small fragments. The cell is thus unable to produce any proteins and therefore unable to survive.</div></span>
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</a></dd>
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<dd id="p"><a href="https://2009.igem.org/Team:Imperial_College_London/Manufacturing_Considerations" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="p"><a href="https://2009.igem.org/Team:Imperial_College_London/Manufacturing_Considerations" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<span><div class="first">Secondary Encapsulation</div>
<span><div class="first">Secondary Encapsulation</div>
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<div class="rest"> Several manufacturing considerations regarding the postprocessing of the culture have been investigated. Postprocessing of the culture allows the polypeptide filled cells to be converted into a pharmaceutical tablet, that can be taken orally. </div></span>
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<div class="rest"> Several manufacturing considerations regarding the post-processing of the culture have been investigated. Post-processing of the culture allows the polypeptide filled cells to be converted into a pharmaceutical tablet, that can be taken orally. </div></span>
</a></dd>
</a></dd>
<dt>Chemoinduction</dt>
<dt>Chemoinduction</dt>
<dd id="time"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="time"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
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<span><div class="first">Chemoinduction</div>
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<span><div class="first">Module Integration: Chemoinduction</div>
<div class="rest"> <b>Module 1</b> is induced by the addition of a compound, IPTG. This allows the user to 'kickstart' the system once the culture has reached a sufficiently high cell density.</div></span>
<div class="rest"> <b>Module 1</b> is induced by the addition of a compound, IPTG. This allows the user to 'kickstart' the system once the culture has reached a sufficiently high cell density.</div></span>
</a></dd>
</a></dd>
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         <dt>Autoinduction</dt>
         <dt>Autoinduction</dt>
<dd id="ci"><a href="https://2009.igem.org/Team:Imperial_College_London/Autoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="ci"><a href="https://2009.igem.org/Team:Imperial_College_London/Autoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
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<span><div class="first">Autoinduction</div>
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<span style="height:235px"><div class="first">Module Integration: Autoinduction</div>
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<div class="rest"> <b>Module 2</b> is triggered by a switch to a secondary carbon source. When the initial preferential carbon source (glucose) is exhausted, the system will metabolise the secondary carbon source that is available. This switch triggers the promoter that controls the start of <b>Module 2</b>. By knowing the initial concentrations of each carbon source, this acts as a programmable time delay system for the activation of encapsulation.</div></span>
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<div class="rest"><b>Module 2</b> is triggered by a switch from glucose consumption to a secondary carbon source consumption. When the initial preferential carbon source (glucose) is exhausted, the system will metabolise the secondary carbon source that is available. This switch triggers the promoter that controls the start of <b>Module 2</b>. By knowing the initial concentrations of each carbon source, this acts as a programmable time delay system for the activation of encapsulation.</div></span>
</a></dd>
</a></dd>
         <dt>Thermoinduction</dt>
         <dt>Thermoinduction</dt>
<dd id="t5"><a href="https://2009.igem.org/Team:Imperial_College_London/Thermoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
<dd id="t5"><a href="https://2009.igem.org/Team:Imperial_College_London/Thermoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();">
-
<span><div class="first">Thermoinduction</div>
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<span><div class="first">Module Integration: Thermoinduction</div>
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<div class="rest"><b>Module 3</b> is initiated upon an increase in temperature. The system is initially grown at 28 degrees, at which point <b>Module 3</b> is repressed. When the temperature is raised to 42 degrees, this repression is blocked, triggering the start of <b>Module 3</b>. This temperature sensitive system was chosen as after encapsulation chemical induction may be less effective due to limited diffusion.</div></span>
+
<div class="rest"><b>Module 3</b> is initiated upon an increase in temperature. The system is initially grown at 28°C, at which point <b>Module 3</b> is repressed. When the temperature is raised to 42°C, this repression is blocked, triggering the start of <b>Module 3</b>. This temperature sensitive system was chosen as after encapsulation, chemical induction may be less effective due to limited diffusion.</div></span>
</a></dd>
</a></dd>
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Latest revision as of 02:49, 22 October 2009

Growth
Growth
The cells are grown to a critical cell density, before the system is started. It allows the culture to reach a sufficient cell number before the the cells are triggered to begin protein production. This is because protein production can slow cell growth.
Module 1: Protein Production
Module 1: Protein Production
The first module is induced with IPTG, which triggers the production of the protein of interest. As part of this project we have looked into two proteins and a peptide of interest.
Module 2: Encapsulation
Module 2: Encapsulation
The second module is where the cell, after having produced the peptide of interest, produces colanic acid. This creates a protecting layer around teh bacterium to shelter it from the acidity of the stomach.
Module 3: Genome deletion
Module 3: Genome deletion
Module 3 occurs after encapsulation of the cell containing the produced peptide of interest. This module makes the bacterium non-viable. It does so by over-expressing restriction enzymes which subsequently cleave the genomic DNA into small fragments. The cell is thus unable to produce any proteins and therefore unable to survive.
Secondary Encapsulation
Secondary Encapsulation
Several manufacturing considerations regarding the post-processing of the culture have been investigated. Post-processing of the culture allows the polypeptide filled cells to be converted into a pharmaceutical tablet, that can be taken orally.
Chemoinduction
Module Integration: Chemoinduction
Module 1 is induced by the addition of a compound, IPTG. This allows the user to 'kickstart' the system once the culture has reached a sufficiently high cell density.
Autoinduction
Module Integration: Autoinduction
Module 2 is triggered by a switch from glucose consumption to a secondary carbon source consumption. When the initial preferential carbon source (glucose) is exhausted, the system will metabolise the secondary carbon source that is available. This switch triggers the promoter that controls the start of Module 2. By knowing the initial concentrations of each carbon source, this acts as a programmable time delay system for the activation of encapsulation.
Thermoinduction
Module Integration: Thermoinduction
Module 3 is initiated upon an increase in temperature. The system is initially grown at 28°C, at which point Module 3 is repressed. When the temperature is raised to 42°C, this repression is blocked, triggering the start of Module 3. This temperature sensitive system was chosen as after encapsulation, chemical induction may be less effective due to limited diffusion.

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