Difference between revisions of "Team:Imperial College/IHP"

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The primary aim of our project was to prove how to control bacterial gene expression using electricity in a spatial manner. In the process of designing our system, through discussion, we discovered new ways we could apply our system to solve different problems as well as new applications which our system could potentially solve.
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<p2>The primary aim of our project was to prove how to control bacterial gene expression using electricity in a spatial manner. In the process of designing our system, through discussion, we discovered new ways we could apply our system to solve different problems as well as new applications which our system could potentially solve.</pr>
 
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<b>Team Communication App (Let’s Talk about It!)</b>
 
<b>Team Communication App (Let’s Talk about It!)</b>

Revision as of 16:08, 13 October 2018


Integrated HP



The primary aim of our project was to prove how to control bacterial gene expression using electricity in a spatial manner. In the process of designing our system, through discussion, we discovered new ways we could apply our system to solve different problems as well as new applications which our system could potentially solve.
Team Communication App (Let’s Talk about It!)
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PMS
Inducer molecules such as IPTG or AHLs are prohibitively expensive considering how essential they are for life science research. Since our system uses a transcription factor (SoxR) that activates in the presence of small redox molecules such as pyocyanin (which is also prohibitively expensive), 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 plac. 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.
Sulfite biosensor
To maintain a reducing plate in an oxidizing atmosphere, we used sulfite, which is a reducing molecule, to ensure that our system does not oxidize in air. Sulfite is also a common ingredient in many preserved foods, such as wine or canned goods, by maintaining reducing environment that is unfavorable for pathogenic growth, unfortunately some people are allergic to sulfite and, especially in wine, can have an adverse effect on taste. However, if we reverse the application of our system, we realized that our construct is an effective way of detecting redox levels, where oxidizing environments cause our bacteria to turn green while reducing environments do the opposite. This may prove helpful for the food industry where a compromise between food preservation and taste needs to be determined. (CHECK IF WE HAVE DATA, IF NOT SCRAP IT)
Biocontainment
A big socio-ethical issue with using genetically engineered organisms is the issue of biocontainment. We recognized this as an issue from our survey data. These organisms should not be released where they could potentially cause ecological damage by outcompeting or harming native species. While some may debate the impact of this ecological damage, it would be easier to persuade governments and its people to use GMOs when proper biocontainment measures are in place. This is especially true for our project. By transcribing growth retardants or toxins, like gp2 and MazF respectively, we can control where our bacteria will live and thus add a layer of biocontainment. This application has been shown to work experimentally.
Biopatterning print
In preparation for our art exhibition, we discussed the integration of science and art with a student from the RCA. She mentioned that in fashion, chemical pollution as a result of the usage of dyes is prominent. We realized that using bacteria to synthesize dyes could provide for an ecologically friendly solution. Moreover, with the ability to pattern using our electrode array, we can design simple prints using MelA which is a step in the right direction for the fashion industry. We have also succeeded in cloning the MelA gene into our construct design.