4.8 Article

Multiple Substrate Binding Mode-Guided Engineering of a Thermophilic PET Hydrolase

Journal

ACS CATALYSIS
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c02275

Keywords

polyethylene terephthalate (PET); PET hydrolysis; thermophilic polyester hydrolase; enzyme engineering; crystallization; molecular dynamics; binding modes; kinetics

Funding

  1. National Key Research and Development Program of China [2021YFC2103600, 2021YFA0910200]
  2. European Union's Horizon 2020 research and innovation program [870294, 953214, 857560]
  3. Czech Ministry of Education [CZ.02.1.01/0.0/0.0/16_026/0008451]
  4. German Federal Environmental Foundation
  5. Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project [TSBICIP-PTJJ-008, TSBICIP-IJCP-003, TSBICIP-KJGG-009-01, TSBI-CIP-KJGG-002-06]
  6. Youth Innovation Promotion Associ-ation CAS
  7. China Scholarship Council
  8. National Natural Science Foundation of China [31961133017]

Ask authors/readers for more resources

Thermophilic polyester hydrolases (PES-H) play a crucial role in the biocatalytic recycling of synthetic polyester polyethylene terephthalate (PET). By studying the crystal structures of two enzymes derived from metagenomes, researchers gained insights into the mechanism of enzymatic PET hydrolysis. Mutations in key residues resulted in improved hydrolytic activity of certain variants, making them potential candidates for industrial plastic recycling processes.
Thermophilic polyester hydrolases (PES-H) have recently enabled biocatalytic recycling of the mass-produced synthetic polyester polyethylene terephthalate (PET), which has found widespread use in the packaging and textile industries. The growing demand for efficient PET hydrolases prompted us to solve high-resolution crystal structures of two metagenome-derived enzymes (PES-H1 and PES-H2) and notably also in complex with various PET substrate analogues. Structural analyses and computational modeling using molecular dynamics simulations provided an understanding of how product inhibition and multiple substrate binding modes influence key mechanistic steps of enzymatic PET hydrolysis. Key residues involved in substrate binding and those identified previously as mutational hotspots in homologous enzymes were subjected to mutagenesis. At 72 ?, the L92F/Q94Y variant of PES-H1 exhibited 2.3-fold and 3.4-fold improved hydrolytic activity against amorphous PET films and pretreated real-world PET waste, respectively. The R204C/S250C variant of PES-H1 had a 6.4 ? higher melting temperature than the wild-type enzyme but retained similar hydrolytic activity. Under optimal reaction conditions, the L92F/Q94Y variant of PES-H1 hydrolyzed low-crystallinity PET materials 2.2-fold more efficiently than LCC ICCG, which was previously the most active PET hydrolase reported in the literature. This property makes the L92F/Q94Y variant of PES-H1 a good candidate for future applications in industrial plastic recycling processes.

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