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<h3>Safety</h3> | <h3>Safety</h3> | ||
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− | <p1> Our genetic circuit is activated/deactivated by the redox state of the transcription factor (SoxR). SoxR oxidation is modulated by small redox molecules, such as the redox-cycling drug pyocyanin. We realized that using another cheaper redox molecule could not only replace inducer molecules such as IPTG due to their price, but also make our system cheaper to use. Using PMS which is a small redox molecule, we can activate a gene much like IPTG would with p<i>lac</i>. Not only is PMS far cheaper than both pyocyanin and IPTG, it is also non-toxic and makes our system more applicable for real world applications. | + | <p1> Our genetic circuit is activated/deactivated by the redox state of the transcription factor (SoxR). SoxR oxidation is modulated by small redox molecules, such as the redox-cycling drug pyocyanin. Pyocyanin is also a toxin synthesised by the gram-negative pathogen Pseudomonas aeruginosa. This significantly limits the safety and potential applications of our system. We realized that using another cheaper redox molecule could not only replace inducer molecules such as IPTG due to their price, but also make our system cheaper to use. Using PMS which is a small redox molecule, we can activate a gene much like IPTG would with p<i>lac</i>. Not only is PMS far cheaper than both pyocyanin and IPTG, it is also non-toxic and makes our system more applicable for real world applications. |
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<h4>Toxicity comparison between Pyocyanin and PMS</h4></br> | <h4>Toxicity comparison between Pyocyanin and PMS</h4></br> |
Revision as of 00:52, 16 October 2018