Team:UCL London/Future Vision

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The current method of monitoring the dissolved oxygen in a fermenter is placing several dissolved oxygen probes in different locations of the fermenter. Using the green dye gene, we can reduce the number of probes needed, and depend on a more "live" visual technique!
The current method of monitoring the dissolved oxygen in a fermenter is placing several dissolved oxygen probes in different locations of the fermenter. Using the green dye gene, we can reduce the number of probes needed, and depend on a more "live" visual technique!
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=Maybe one day...=
=Maybe one day...=

Revision as of 12:08, 26 October 2010

UCL IGEM 2010

RETURN TO IGEM 2010

FUTURE VISION

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At this stage, our main aim is to show that our circuit does in fact react in the way it does to hypoxia. Pending this achievable target, we have high hopes of our Principle being implemented in a potentially infinite number of ways. We have split them into the following main categories just to give you an idea.



Health & Medicine

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Imagine if the bacteria as we know it today could drive protein expression with the lack of oxygen. Synthetic biology through biochemical engineering can create the potential at which Escherichia coli cells- and we all know how harmful to humans can specific strains be- used in a twisted yet beautifully way as an expression system for the production of biopharmaceuticals. The project is based on the engineering modification of the cells and the construction of a self-induced biological circuit that allows an automated protein expression



Manufacturing

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The pharmaceutical industry is a trillion dollar industry. Most of the money is wasted because of the inefficiency of the processes. There are still plenty of rooms of improvement on several frontiers which could potentially lead to a decrease in cost. Our project has successfully introduced a new way of increasing the reliability of batches, and removing the need for chemicals and their storage. The application of this at industrial level can reduce the cost of a bio-pharmaceutical drug, making it available to more people.



Online/Real time monitoring

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The current method of monitoring the dissolved oxygen in a fermenter is placing several dissolved oxygen probes in different locations of the fermenter. Using the green dye gene, we can reduce the number of probes needed, and depend on a more "live" visual technique!

Maybe one day...

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Hypoxia induced cells can be key in solving several issues, particularly when it comes to aquatic ecosystems where the lack of oxygen caused by an external factor can be countered by the production of a suitable protein capable of reversing or at least minimising the damage that is limiting the oxygen in water.

The first example, and a huge concern now, are oil spills. Oil floats on water creating a barrier between the air and water. Fish and plants living in the ocean use up the little oxygen left in the water reducing the dissolved oxygen levels. Genetically engineered E. coli can be made so that hypoxia triggers the production of an enzyme that breaks down hydrocarbon and carbon-carbon bonds.

Another problem that could be addressed is the excessive use of fertilisers by farmers. The nitrates and phosphates that fin their way to nearby ponds and lakes covered cause eutrophication. Algae grows on the surface of the water, and blocks the sunlight from reaching photosynthetic organisms that live in the lake. During the night time, algae consumes large quantities of oxygen. This causes anoxia of the lake, and aquatic life that inhabits that lake would suffocate. Using hypoxia triggered E.coli that can synthesise a protein toxic to the algae can limit their growth and refresh the ecosystem of the water body. Similarly, such E.coli can be used for waste water treatment, and as biofilters.

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In a more medical approach, the hypoxia gene can be introduced into mammalian cells, where they can be a key factor in stem cell therapy; in cardiovascular diseases for instance. Once stem cells are injected into an area deprived or not receiving sufficient oxygen, the low level of oxygen would trigger the cells into synthesising the co-factors needed for cell differentiation into vessels. This technique can be exploited and remodelled so as to have a completely independent single-injection stem cell therapy.





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