Team:UC Davis/Project/Catalyst
From 2012.igem.org
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- | + | We began the summer looking for a way to engineer <i>E. coli</i> to degrade plastics. We focused our attention on PET once we came across a paper that conducted a metagenomic analysis of leaf-branch compost, identified a cutinase homolog, and demonstrated its PET-degrading activity [1]. It was also found that the PET was broken down into two by-products: ethylene glycol and terepthalic acid (TPA). | |
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Revision as of 22:34, 10 August 2012
Cutinase
We decided to use pelB as a leading sequence on the cutinase gene since it has been shown to direct the enzyme to the periplasmic space [1] . Once the enzyme is led towards the membrane, there is a leakage that helps it be secreted into the extracellular matrix [1]. We hoped that this sequence would help the enzyme be secreted so the PET would more easily be degraded. When we ordered the cutinase sequence, we added pelB to the front of the sequence, in hopes of repeating the secretion shown in previous results.