1. Targeted bioengineering of E. coli MG1655 to utilize PET as a carbon source. We seek to this by introducing a couple different modules to the strain. The first module encodes a cutinase gene which has been found to degrade PET into ethylene glycol and terephthalic acid. The second encodes the first two enzymes in a pathway that has been found to feed ethylene glycol into the TCA cycle.
2. Rational protein engineering to increase the enzymatic activity of cutinase to degrade PET.
3. Directed evolution of the ethylene glycol degradation pathway to increase its efficiency of ethylene glycol metabolism in E. coli cultures. Reintroduction of the glycolaldehyde reductase and glycolaldehyde dehydrogenase enzymes in various constructs to MG1655 and E-15 EG3 to increase the ethylene glycol consumption beyond E-15 EG3’s original capabilities.