Template:Imperial/09/Overview
From 2009.igem.org
(Difference between revisions)
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<dd id="p"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | <dd id="p"><a href="https://2009.igem.org/Team:Imperial_College_London/Chemoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | ||
<span><div class="first">Chemoinduction</div> | <span><div class="first">Chemoinduction</div> | ||
- | <div class="rest"> | + | <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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<dd id="time"><a href="https://2009.igem.org/Team:Imperial_College_London/Autoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | <dd id="time"><a href="https://2009.igem.org/Team:Imperial_College_London/Autoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | ||
<span><div class="first">Autoinduction</div> | <span><div class="first">Autoinduction</div> | ||
- | <div class="rest"> | + | <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> |
</a></dd> | </a></dd> | ||
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<dd id="ci"><a href="https://2009.igem.org/Team:Imperial_College_London/Thermoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | <dd id="ci"><a href="https://2009.igem.org/Team:Imperial_College_London/Thermoinduction" onmouseover="haxbackground();" onmouseout="unhaxbackground();"> | ||
<span><div class="first">Thermoinduction</div> | <span><div class="first">Thermoinduction</div> | ||
- | <div class="rest"> | + | <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> |
</a></dd> | </a></dd> | ||
Revision as of 14:00, 20 October 2009
- Growth
-
GrowthWe are growing the cells to a desired OD of 0.7 in order to ensure that there are enough cells to produce a wanted amount of proteins
- Module 1: Protein Production
-
Module 1: Protein ProductionThe 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.
- Module 2: Encapsulation
-
Module 2: EncapsulationThis 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.
- Module 3: Genome deletion
-
Module 3: Genome deletionModule 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.
- Chemoinduction
-
ChemoinductionModule 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
-
AutoinductionModule 2 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 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
-
ThermoinductionModule 3 is initiated upon an increase in temperature. The system is initially grown at 28 degrees, at which point Module 3 is repressed. When the temperature is raised to 42 degrees, 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.
- Another
-
Time RegulationUsing oscillators to measure time, it enables detachment from the small intestine after a certain amount of time.