Team:Imperial College London/Temporal Control/Thermoinduction

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<font face='Calibri' size='5'>Thermoinduction</font><br><br>
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=Thermoinduction=
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[[Image:II09_MapIndicator_Thermoinduction.png]]
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===Overview===
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This part of temporal control is responsible for triggering genomic deletion, after encapsulation has taken place.
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*When the <b>temperature</b> is <b>low</b>, restriction enzymes are inhibited and <b>DNA is protected</b>.
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*When the <b>temperature</b> is <b>high</b>, restriction enzymes are produced and <b>DNA is digested</b>.
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[[Image:II09_hitemp_lotemp.jpg|400px|centre]]
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Thermoinduction means using a change in temperature to cause a biological change to the system. One way this can be done is by increasing temperatures of the system. Thermal denaturation will occur and this results in decreased binding efficiency of the substrate with the enzyme. Therefore a biological change will be induced.
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Thermoinduction means using a change in temperature to cause a biological change to the system. One way this can be done is by increasing temperatures of the system. Thermal denaturation will occur and this results in a decrease in  binding efficiency of the substrate with the enzyme. This will induce the intended biological change.
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<font face='Calibri' size='3'><b>Relevance to our project</b></font>
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<html><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Thermoinduction/System"><img style="vertical-align:bottom;" width=50px align="left" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Learnmore.png"></a></html>&nbsp; <b><i>About the thermoinduction system.</i></b> <br>
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<br>
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We made use of thermoinduction in Module 3 – genome deletion, in our E.ncapsulator.
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<font face='Calibri' size='3'><b>Relevance to our project</b></font><br>
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In short, thermoinduction is used to start genome deletion when sufficient drug protein of interest has been produced, and encapsulation is complete. Genome deletion then induced by manually raising the temperatures from 28°C to 42°C. This would cause de-repression of the pLambda promoter. Restriction enzymes DpnII and TaqI will be produced. They are the ones who carry out DNA restriction, and cause cell death.
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[[Image:ii09_thermo.png|right|350px]]
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In this case, we have used BBa_K098995 (Harvard 2008). This BioBrick consists of the heat sensitive cI857 with a strong promoter. This temperature sensitive cI857 protein repressor, has a significantly decreased binding efficiency with the cI promoter between 35°C to 42°C. Therefore when temperatures are increased, the cI protein repressor would have a decreased probability of binding with the cI promoter, due to thermal denaturation. We can now say that will be a de-repression at higher temperatures.
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We made use of thermoinduction in Module 3 – genome deletion.
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Thermoinduction is used to start genome deletion when sufficient drug protein of interest has been produced, and encapsulation is complete. Genome deletion is induced by manually raising the temperatures from 28°C to 42°C. In our case, we have used BBa_K098995 (Harvard 2008). This BioBrick consists of the heat sensitive cI857 with a strong promoter. This temperature sensitive cI857 protein repressor, has a significantly decreased binding efficiency with the cI promoter between 35°C to 42°C. This would cause de-repression of the pLambda promoter. Restriction enzymes DpnII and TaqI will be produced. They are the ones who carry out DNA restriction, and cause cell death.
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{{Imperial/09/Division}}
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===Temporal Control: Thermoinduction===
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<html><center><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Chemical_Induction"><img style="vertical-align:bottom;" width="20%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Drylabmainimage1.png"></a><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Autoinduction"><img style="vertical-align:bottom;" width="20%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Drylabmainimage2.png"></a><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Thermoinduction "><img style="vertical-align:bottom;" width="20%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Drylabmainimage3.png"></a><a href="https://2009.igem.org/Team:Imperial_College_London/Drylab"><img style="vertical-align:bottom;" width="20%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Drylabmainimage4.png"></a><a href="https://2009.igem.org/Team:Imperial_College_London/Wetlab"><img style="vertical-align:bottom;" width="20%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Drylabmainimage5.png"></a></center></html>
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<html><table border="0" style="background-color:transparent;" width="100%">
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<tr><td width="0%">&nbsp;</td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Chemical_Induction"><b>Chemical Induction</b></a></center></td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Autoinduction"><b>Autoinduction</b></a></center></td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control/Thermoinduction"><b>Thermoinduction</b></a></center></td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Drylab"><b>Modelling</b></a></center></td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Wetlab"><b>Results</b></a></center></td>
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<td width="1%"></td>
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</tr></table></html>
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<br>
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<html><center><a href="https://2009.igem.org/Team:Imperial_College_London/Temporal_Control#Temporal_Control_Contents"><img width=150px src="https://static.igem.org/mediawiki/2009/1/10/II09_TourArrow.png"></a>
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</html>
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{{Imperial/09/TemplateBottom}}

Latest revision as of 02:26, 22 October 2009

Thermoinduction

II09 MapIndicator Thermoinduction.png

Overview

This part of temporal control is responsible for triggering genomic deletion, after encapsulation has taken place.

  • When the temperature is low, restriction enzymes are inhibited and DNA is protected.
  • When the temperature is high, restriction enzymes are produced and DNA is digested.
II09 hitemp lotemp.jpg

Thermoinduction means using a change in temperature to cause a biological change to the system. One way this can be done is by increasing temperatures of the system. Thermal denaturation will occur and this results in a decrease in binding efficiency of the substrate with the enzyme. This will induce the intended biological change.

  About the thermoinduction system.

Relevance to our project

Ii09 thermo.png

We made use of thermoinduction in Module 3 – genome deletion.

Thermoinduction is used to start genome deletion when sufficient drug protein of interest has been produced, and encapsulation is complete. Genome deletion is induced by manually raising the temperatures from 28°C to 42°C. In our case, we have used BBa_K098995 (Harvard 2008). This BioBrick consists of the heat sensitive cI857 with a strong promoter. This temperature sensitive cI857 protein repressor, has a significantly decreased binding efficiency with the cI promoter between 35°C to 42°C. This would cause de-repression of the pLambda promoter. Restriction enzymes DpnII and TaqI will be produced. They are the ones who carry out DNA restriction, and cause cell death.



Temporal Control: Thermoinduction

 
Chemical Induction
Autoinduction
Thermoinduction
Modelling
Results


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