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*Induced when T°>42°C | *Induced when T°>42°C | ||
<p style="text-align:right;"> [http://2011.igem.org/Team:METU-Ankara#project5 Read More] </p> | <p style="text-align:right;"> [http://2011.igem.org/Team:METU-Ankara#project5 Read More] </p> | ||
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| <center> Caltech </center> | |||
| <center> 2011 </center> | |||
| <center> [http://2011.igem.org/Team:Caltech Bioremediation of Endocrine Disruptors Using Genetically Modified Escherichia Coli] </center> | |||
| Endocrine-disrupting chemicals (EDCs) are chemicals that interact with the endocrine system by binding to hormone receptors, causing problems in sexual development and reproduction of organisms | |||
| Biosafety ideas: | |||
*Water filtration system for containment of microbes (filters all microbes, does not retain free DNA). | |||
*Use the ccdB gene (BBa_P1016 and BBa_P1010)on a plasmid in conjunction with an E. coli strain such as DB3.1 (BBa_V1005). The plasmid will code for the “death gene” which will kill any cell that does not code for immunity in its genome. If a native microorganism would uptake this man-made plasmid, it would die, preventing the propagation of the recombinant DNA in the environment (Featured Parts: Cell Death). | |||
*Another similar “suicide” containment system uses streptavidin (BBa_J36841) (Kaplan, Mello et al. 1999; Urgun-Demirtas, Stark et al. 2006). This protein binds very tightly to biotin, a required co-enzyme for many metabolic pathways. This makes biotin unavailable and causes cell death. Kaplan et al. reported cell counts were reduced 99.9% in eight hours after their system was activated by absence of pollutant to degrade. | |||
<p style="text-align:right;"> [http://2011.igem.org/Team:Caltech/Biosafety Read More] </p> | |||
|- | |||
| <center> Berkeley</center> | |||
| <center> 2010 </center> | |||
| <center> [http://2011.igem.org/Team:Caltech Bioremediation of Endocrine Disruptors Using Genetically Modified Escherichia Coli] </center> | |||
| Choa Choa's Delivery Service | |||
| Clotho Framework: | |||
Clotho implements the current biosafety standards as outlined by the NIH and the CDC. Whenever a new part is instantiated, Clotho BLAST's its sequence against a databank of known virulence factors and pathogens and returns the RG number of the highest match. This framework ensures that every part in Clotho has a RG value associated with it. In addition, when composite parts are made by joining basic parts, the composite part is also assigned a BSL number. Finally, all strains in Clotho have a risk group. | |||
<p style="text-align:right;"> [http://2011.igem.org/Team:Caltech/Biosafety Read More] </p> | |||
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| <center> | | <center> Johns Hopkins </center> | ||
| <center> 2011 </center> | | <center> 2011 </center> | ||
| <center> [http://2011.igem.org/Team: | | <center> [http://2011.igem.org/Team:Johns_Hopkins VitaYeast] </center> | ||
| | | They want to make bread with yeast producing Vitamin | ||
| | | their yeast strain lacks functional pathways for '''seven''' essential aa. | ||
<p style="text-align:right;"> [http://2011.igem.org/Team:Johns_Hopkins/Safety Read More] </p> | |||
<p style="text-align:right;"> [http://2011.igem.org/Team: | |||
|- | |- | ||
| <center> | | <center> Kyoto </center> | ||
| <center> | | <center> 2009 </center> | ||
| <center> [http:// | | <center> [http://2009.igem.org/Team:Kyoto/GSDD p1 : Gene Switch Depending on Duplication] </center> | ||
| | | How to express a gene after a certain lifespan. The use Linear DNA, in which a repressor will be degraded after few cell division. | ||
| | | "they want to control exact cell’s life time (or '''death time''') depending on the number of cell division times. | ||
They get rid of the exonucelase problem by inserting multiple protein binding site that will be degraded when division occurs, but not with exonucleases. The repressor gene is degraded after a certain time." | |||
<p style="text-align:right;"> [http:// | <p style="text-align:right;"> [http://2009.igem.org/wiki/images/5/5f/Kyoto_GEDD_2_kai.png Read More] </p> | ||
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