| Literature DB >> 33865980 |
Till Tiso1, Tanja Narancic2, Ren Wei3, Eric Pollet4, Niall Beagan5, Katja Schröder1, Annett Honak3, Mengying Jiang6, Shane T Kenny7, Nick Wierckx8, Rémi Perrin9, Luc Avérous4, Wolfgang Zimmermann3, Kevin O'Connor10, Lars M Blank11.
Abstract
Over 359 million tons of plastics were produced worldwide in 2018, with significant growth expected in the near future, resulting in the global challenge of end-of-life management. The recent identification of enzymes that degrade plastics previously considered non-biodegradable opens up opportunities to steer the plastic recycling industry into the realm of biotechnology. Here, the sequential conversion of post-consumer polyethylene terephthalate (PET) into two types of bioplastics is presented: a medium chain-length polyhydroxyalkanoate (PHA) and a novel bio-based poly(amide urethane) (bio-PU). PET films are hydrolyzed by a thermostable polyester hydrolase yielding highly pure terephthalate and ethylene glycol. The obtained hydrolysate is used directly as a feedstock for a terephthalate-degrading Pseudomonas umsongensis GO16, also evolved to efficiently metabolize ethylene glycol, to produce PHA. The strain is further modified to secrete hydroxyalkanoyloxy-alkanoates (HAAs), which are used as monomers for the chemo-catalytic synthesis of bio-PU. In short, a novel value-chain for PET upcycling is shown that circumvents the costly purification of PET monomers, adding technological flexibility to the global challenge of end-of-life management of plastics.Entities:
Keywords: Biopolymers; Metabolic engineering; Polyethylene terephthalate (PET) degradation; Pseudomonas putida; Synthetic biology
Year: 2021 PMID: 33865980 DOI: 10.1016/j.ymben.2021.03.011
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783