Team:Imperial College London/M3

From 2009.igem.org

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(40pxModule 3 Overview)
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[[Image: II09_gmo fears.jpg| right| 200px]]
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Module 3 is the final module of the system. This programs the E.ncapsulator to destroy its genetic material after encapsulation has finished.    This prevents any possible pathogenic effects, and also allays health concerns of eating genetically modified organisms. <br>
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Module 3 is the final module of the system. It programs the E.ncapsulator to destroy its genetic material after encapsulation has finished.    This prevents any possible pathogenic effects, and also allays health concerns of eating genetically modified organisms. <br>
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10th International Symposium on the Biosafety of Genetically Modified Organisms (GM Biosafety Symposium)<br>
10th International Symposium on the Biosafety of Genetically Modified Organisms (GM Biosafety Symposium)<br>
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Module 3 consists of 2 parts: <br>
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1) Thermoinduction <br>
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2) Killing by Restriction Enzymes<br>
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<br>
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A distinct advantage of using restriction enzymes for our 'killing' mechanism is that the cell membrane is left intact afterwards, and the protein of interest will still be protected by the encapsulated cell.  This renders the bacterium no more than an inanimate shell containing our protein drug of choice. <br>
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[[Image: inanimate shell.jpg| center]]
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<br>
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==Thermoinduction==
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After Module 2 has been completed, genome deletion is triggered by raising the temperature. This is especially suitable since it is difficult for normal chemical induction to penetrate the colanic acid coating. <br>(see [[Team:Imperial_College_London/Temporal_Control/Thermoinduction| thermoinduction under temporal control]]) <br>
After Module 2 has been completed, genome deletion is triggered by raising the temperature. This is especially suitable since it is difficult for normal chemical induction to penetrate the colanic acid coating. <br>(see [[Team:Imperial_College_London/Temporal_Control/Thermoinduction| thermoinduction under temporal control]]) <br>
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To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli [[Team:Imperial_College_London/M1/Dam| Dam methylase protection system]]. This methylates DNA.  Therefore, only high levels of restriction enzyme (ie. after thermal triggering) will cleave the DNA.<br>
To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli [[Team:Imperial_College_London/M1/Dam| Dam methylase protection system]]. This methylates DNA.  Therefore, only high levels of restriction enzyme (ie. after thermal triggering) will cleave the DNA.<br>
<br>
<br>
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A distinct advantage of using restriction enzymes for our 'killing' mechanism is that the cell membrane is left intact afterwards, and the protein of interest will still be protected by the encapsulated cell.  This renders the bacterium no more than an inanimate shell containing our protein drug of choice. <br>
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[[Image: inanimate shell.jpg| center]]
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Revision as of 22:40, 16 September 2009

II09 Thumb m3.pngModule 3 Overview

II09 TimelineM3.png
II09 gmo fears.jpg

Module 3 is the final module of the system. It programs the E.ncapsulator to destroy its genetic material after encapsulation has finished. This prevents any possible pathogenic effects, and also allays health concerns of eating genetically modified organisms.
10th International Symposium on the Biosafety of Genetically Modified Organisms (GM Biosafety Symposium)


Module 3 consists of 2 parts:
1) Thermoinduction
2) Killing by Restriction Enzymes

A distinct advantage of using restriction enzymes for our 'killing' mechanism is that the cell membrane is left intact afterwards, and the protein of interest will still be protected by the encapsulated cell. This renders the bacterium no more than an inanimate shell containing our protein drug of choice.

Inanimate shell.jpg


Thermoinduction

After Module 2 has been completed, genome deletion is triggered by raising the temperature. This is especially suitable since it is difficult for normal chemical induction to penetrate the colanic acid coating.
(see thermoinduction under temporal control)

The cell then produces the restriction enzymes DpnII and TaqI which specifically target and cut DNA sequences, in order to destroy all genetic material contained within the cell.

II09 cut dna.jpg

To protect against DNA destruction due to basal levels of restriction enzyme production, we have made use of the native E. coli Dam methylase protection system. This methylates DNA. Therefore, only high levels of restriction enzyme (ie. after thermal triggering) will cleave the DNA.


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