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Enhanced Poly(ethylene terephthalate) Hydrolase Activity by Protein Engineering

Open access
Ma, Yuan, Yao, Mingdong, Li, Bingzhi, Ding, Mingzhu, He, Bo, Chen, Si, Zhou, Xiao, Yuan, Yingjin·2018·Engineering

Abstract

Poly(ethylene terephthalate) hydrolase (PETase) from Ideonella sakaiensis exhibits a strong ability to degrade poly(ethylene terephthalate) (PET) at room temperature, and is thus regarded as a potential tool to solve the issue of polyester plastic pollution. Therefore, we explored the interaction between PETase and the substrate (a dimer of the PET monomer ethylene terephthalate, 2PET), using a model of PETase and its substrate. In this study, we focused on six key residues around the substrate-binding groove in order to create novel high-efficiency PETase mutants through protein engineering. These PETase mutants were designed and tested. The enzymatic activities of the R61A, L88F, and I179F mutants, which were obtained with a rapid cell-free screening system, exhibited 1.4 fold, 2.1 fold, and 2.5 fold increases, respectively, in comparison with wild-type PETase. The I179F mutant showed the highest activity, with the degradation rate of a PET film reaching 22.5 mg per μmol·L−1 PETase per day. Thus, this study has created enhanced artificial PETase enzymes through the rational protein engineering of key hydrophobic sites, and has further illustrated the potential of biodegradable plastics.

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Metadata

Authors
Ma, Y., Yao, M., Li, B., Ding, M., He, B., Chen, S., Zhou, X., & Yuan, Y.
Venue
Engineering
Publisher
Elsevier BV
Published
2018-12
Volume
4
Issue
6
Pages
888-893
ISSN
2095-8099 (ISSN-L)
OpenAlex
W2889859816
Cited by
229
References
1
FWCI
5.18
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Enhanced Poly(ethylene terephthalate) Hydrolase Activity by Protein Engineering. https://app.cochat.ai/papers/10.1016/j.eng.2018.09.007
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Ma, Y., Yao, M., Li, B., Ding, M., He, B., Chen, S., Zhou, X., & Yuan, Y. (2018). Enhanced Poly(ethylene terephthalate) Hydrolase Activity by Protein Engineering. Engineering. https://doi.org/10.1016/j.eng.2018.09.007

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