Team:UCL London/Future Vision

From 2010.igem.org

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Cells go through different phases before reaching their maximum number. There is no way of telling how long the lag phase would be, or when the oxygen spike would occur. (We experienced a four day lag phase in one of our four fermentations where the cells were not dead, but not growing! This can get frustrating, and can give some ''Steve, the guardian of the fermenters'' horrible ideas like killing the cells and starting again!)
Cells go through different phases before reaching their maximum number. There is no way of telling how long the lag phase would be, or when the oxygen spike would occur. (We experienced a four day lag phase in one of our four fermentations where the cells were not dead, but not growing! This can get frustrating, and can give some ''Steve, the guardian of the fermenters'' horrible ideas like killing the cells and starting again!)

Revision as of 00:18, 11 October 2010

UCL IGEM 2010

RETURN TO IGEM 2010

FUTURE VISION

UCL-brainsotrm.JPG


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

UCL-blue.JPG

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

UCL-manufacture.JPG


Cells need constant monitoring for a "oxygen spike". This peak occurs when cells have reached their maximum growth capacity in the fermenter, and are competing for nutrients in the fermenter. At that point, an operator has to introduce a predetermined volume of IPTG (chemical) into the fermenter to stop the cell growth and channel the energy into transcription of a certain gene. This is how the cells are made to produce pharmaceuticals!

Reliability

UCL-fao.gif

Cells go through different phases before reaching their maximum number. There is no way of telling how long the lag phase would be, or when the oxygen spike would occur. (We experienced a four day lag phase in one of our four fermentations where the cells were not dead, but not growing! This can get frustrating, and can give some Steve, the guardian of the fermenters horrible ideas like killing the cells and starting again!)

What if the oxygen spike happens on a weekend, or falls somewhere outside the 8-hour-shift? This is where auto-induction becomes useful. The cells would automatically realise the oxygen spike and change from growth to manufacturing automatically!

Cost

Not only does auto-induction save money on IPTG, it can eliminate the need of IPTG storage saving massive amounts of money on refrigeration in a sterile environment(IPTG must be stored at -20 degrees). Also, there is no more risks of contamination of the IPTG, or of the batch when introducing the IPTG! That means that less batches are wasted, and there is therefore a lower chance of batch failure per year. So with more batches produced per annum, the cost of the drug would decrease giving more people access to it!

Environmental

As mentioned above, IPTG needs to be stored at -20 degrees. Not using IPTG would eliminate the need for refrigerators, making the pharmaceutical industry a little greener.

Online/Real time monitoring

UCL-Green.JPG


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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