4.6 Article

QM/MM Investigation to Identify the Hallmarks of Superior PET Biodegradation of PETase over Cutinase

Journal

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.2c04913

Keywords

plastic biodegradation; catalytic mechanism; clean environment; cutinase; QM; MM

Funding

  1. NSERC Discovery Grant [RGPIN-2022-03348]
  2. University of Waterloo NSERC RIF fund

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Polyethylene terephthalate (PET), a widely used plastic, is a significant contributor to global plastic pollution. This study investigates the enzymatic biodegradation of PET and identifies key factors for efficient PET hydrolysis. The results provide insights into the reaction mechanism and molecular features of PETase and cutinase enzymes, which can be useful for designing more efficient enzymes for PET hydrolysis.
Polyethylene terephthalate (PET), the most extensively used plastic, is one of the significant contributors to global plastic pollution. Enzymatic biodegradation of PET using different hydrolases has been previously reported as a promising biodegradation strategy for closed-loop recycling. Among the different hydrolases known to depolymerize PET to its soluble building blocks, the PETase and cutinase family of enzymes have notable PET biodegradation activities. In fact, they exhibit different thermostabilities and efficiencies in hydrolyzing PET polyesters despite sharing high structural similarities. Herein, we employed quantum mechanics/molecular mechanics calculations to identify the key factors necessary for efficient PET hydrolysis. Our results show that in both PETase and cutinase (Tfcut2 as a model system), the PET hydrolysis reaction pathway proceeds through a multi -step process with rate-limiting steps having energy barriers of similar to 18.0 and similar to 20 kcal/mol for PETase and Tf Cut2, respectively, which agrees well with the experimental data. A deeper inspection of the structural complexes revealed that the bent conformation adopted by PET and the tighter H-bond interaction between the catalytic triad residues, mediated by the unique disulfide bridge, contribute to the lower barrier (i.e., better catalytic performance) of PETase. The intrinsic molecular features identified in this work will also be useful for rational engineering of more efficient cutinases for PET hydrolysis.

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