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Rate Response of Poly(Ethylene Terephthalate)-Hydrolases to Substrate Crystallinity: Basis for Understanding the Lag Phase.
Thomsen, Thore B; Schubert, Sune; Hunt, Cameron J; Borch, Kim; Jensen, Kenneth; Brask, Jesper; Westh, Peter; Meyer, Anne S.
Afiliação
  • Thomsen TB; Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads, DK-2800, Kgs. Lyngby, Denmark.
  • Schubert S; Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads, DK-2800, Kgs. Lyngby, Denmark.
  • Hunt CJ; Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads, DK-2800, Kgs. Lyngby, Denmark.
  • Borch K; Novozymes A/S, Biologiens Vej 2, 2800, Kgs. Lyngby, Denmark.
  • Jensen K; Novozymes A/S, Biologiens Vej 2, 2800, Kgs. Lyngby, Denmark.
  • Brask J; Novozymes A/S, Biologiens Vej 2, 2800, Kgs. Lyngby, Denmark.
  • Westh P; Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads, DK-2800, Kgs. Lyngby, Denmark.
  • Meyer AS; Department of Biotechnology and Biomedicine, Technical University of Denmark, Søltofts Plads, DK-2800, Kgs. Lyngby, Denmark.
ChemSusChem ; 16(13): e202300291, 2023 Jul 07.
Article em En | MEDLINE | ID: mdl-37073816
ABSTRACT
The rate response of poly(ethylene terephthalate) (PET)-hydrolases to increased substrate crystallinity (XC ) of PET manifests as a rate-lowering effect that varies significantly for different enzymes. Herein, we report the influence of XC on the product release rate of six thermostable PET-hydrolases. All enzyme reactions displayed a distinctive lag phase until measurable product formation occurred. The duration of the lag phase increased with XC . The recently discovered PET-hydrolase PHL7 worked efficiently on "amorphous" PET disks (XC ≈10 %), but this enzyme was extremely sensitive to increased XC , whereas the enzymes LCCICCG , LCC, and DuraPETase had higher tolerance to increases in XC and had activity on PET disks having XC of 24.4 %. Microscopy revealed that the XC -tolerant hydrolases generated smooth and more uniform substrate surface erosion than PHL7 during reaction. Structural and molecular dynamics analysis of the PET-hydrolyzing enzymes disclosed that surface electrostatics and enzyme flexibility may account for the observed differences.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Ftálicos / Hidrolases Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Ftálicos / Hidrolases Idioma: En Ano de publicação: 2023 Tipo de documento: Article