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Enhancing PET Degrading Enzymes: A Combinatory Approach.
Joho, Yvonne; Royan, Santana; Caputo, Alessandro T; Newton, Sophia; Peat, Thomas S; Newman, Janet; Jackson, Colin; Ardevol, Albert.
Afiliação
  • Joho Y; Manufacturing, Commonwealth Scientific and Industrial Research Organisation, Clayton, Victoria, 3168, Australia.
  • Royan S; Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.
  • Caputo AT; CSIRO Advanced Engineering Biology Future Science Platform, GPO Box 1700, Canberra, ACT 2601, Australia.
  • Newton S; Manufacturing, Commonwealth Scientific and Industrial Research Organisation, Clayton, Victoria, 3168, Australia.
  • Peat TS; Manufacturing, Commonwealth Scientific and Industrial Research Organisation, Clayton, Victoria, 3168, Australia.
  • Newman J; Manufacturing, Commonwealth Scientific and Industrial Research Organisation, Clayton, Victoria, 3168, Australia.
  • Jackson C; School of Biotechnology & Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
  • Ardevol A; School of Biotechnology & Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Chembiochem ; 25(10): e202400084, 2024 May 17.
Article em En | MEDLINE | ID: mdl-38584134
ABSTRACT
Plastic waste has become a substantial environmental issue. A potential strategy to mitigate this problem is to use enzymatic hydrolysis of plastics to depolymerize post-consumer waste and allow it to be reused. Over the last few decades, the use of enzymatic PET-degrading enzymes has shown promise as a great solution for creating a circular plastic waste economy. PsPETase from Piscinibacter sakaiensis has been identified as an enzyme with tremendous potential for such applications. But to improve its efficiency, enzyme engineering has been applied aiming at enhancing its thermal stability, enzymatic activity, and ease of production. Here, we combine different strategies such as structure-based rational design, ancestral sequence reconstruction and machine learning to engineer a more highly active Combi-PETase variant with a melting temperature of 70 °C and optimal performance at 60 °C. Furthermore, this study demonstrates that these approaches, commonly used in other works of enzyme engineering, are most effective when utilized in combination, enabling the improvement of enzymes for industrial applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia de Proteínas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia de Proteínas Idioma: En Ano de publicação: 2024 Tipo de documento: Article