Affiliation:
1. Centre for Enzyme Innovation School of Biological Sciences Institute of Biological and Biomedical Sciences University of Portsmouth Portsmouth PO1 2DY United Kingdom
2. BOTTLE Consortium Golden CO 80401 United States
3. Institute of Biochemistry Department of Biotechnology & Enzyme Catalysis University of Greifswald D-17487 Greifswald Germany
4. Renewable Resources and Enabling Sciences Center National Renewable Energy Laboratory Golden CO 80401 United States
Abstract
AbstractEnzyme‐based depolymerization is a viable approach for recycling of poly(ethylene terephthalate) (PET). PETase from Ideonella sakaiensis (IsPETase) is capable of PET hydrolysis under mild conditions but suffers from concentration‐dependent inhibition. In this study, this inhibition is found to be dependent on incubation time, the solution conditions, and PET surface area. Furthermore, this inhibition is evident in other mesophilic PET‐degrading enzymes to varying degrees, independent of the level of PET depolymerization activity. The inhibition has no clear structural basis, but moderately thermostable IsPETase variants exhibit reduced inhibition, and the property is completely absent in the highly thermostable HotPETase, previously engineered by directed evolution, which simulations suggest results from reduced flexibility around the active site. This work highlights a limitation in applying natural mesophilic hydrolases for PET hydrolysis and reveals an unexpected positive outcome of engineering these enzymes for enhanced thermostability.
Funder
U.S. Department of Energy
Office of Energy Efficiency and Renewable Energy
Subject
General Energy,General Materials Science,General Chemical Engineering,Environmental Chemistry
Cited by
17 articles.
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