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Team:Edinburgh/Conclusions
From 2011.igem.org
Revision as of 10:42, 12 September 2011 by Allancrossman (Talk | contribs)
In our abstract, we asked a number of questions that our feasibility study was intended to answer.
Would the efficiency of cellulases be increased by having different types close together?
- Very probably. Our C model and Kappa model showed that synergy makes sense in silico.
Could this be done by displaying them on a cell outer membrane?
- This seems a promising approach. <partinfo>BBa_K265008</partinfo> seems a promising carrier for placing enzymes at high copy number on the E. coli outer membrane.
Could it be done by displaying them on a phage?
- Further work is needed to answer this question. There are theoretical reasons to expect that this is a challenging problem.
Does the BioSandwich DNA assembly method work properly?
How would a biorefinery involving either system actually be constructed?
Would such a biorefinery be economically viable?
What are the social implications of creating such a biorefinery?
What are people's thoughts and feelings regarding this project?
Should we (meaning society) actually build such a biorefinery?
