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A novel approach to analyze the impact of lytic polysaccharide monooxygenases (LPMOs) on cellulosic fibres.
Sulaeva, Irina; Budischowsky, David; Rahikainen, Jenni; Marjamaa, Kaisa; Støpamo, Fredrik Gjerstad; Khaliliyan, Hajar; Melikhov, Ivan; Rosenau, Thomas; Kruus, Kristiina; Várnai, Anikó; Eijsink, Vincent G H; Potthast, Antje.
Afiliação
  • Sulaeva I; Core Facility "Analysis of Lignocellulosics" (ALICE), University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria.
  • Budischowsky D; Institute of Chemistry of Renewable Resources, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria.
  • Rahikainen J; Solutions for Natural Resources and Environment, VTT Technical Research Centre of Finland Ltd, Tietotie 2, FI-02044 Espoo, Finland.
  • Marjamaa K; Solutions for Natural Resources and Environment, VTT Technical Research Centre of Finland Ltd, Tietotie 2, FI-02044 Espoo, Finland.
  • Støpamo FG; Faculty of Chemistry, Biotechnology and Food Science, NMBU - Norwegian University of Life Sciences, 1432 Ås, Norway.
  • Khaliliyan H; Institute of Chemistry of Renewable Resources, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria.
  • Melikhov I; Institute of Chemistry of Renewable Resources, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria.
  • Rosenau T; Institute of Chemistry of Renewable Resources, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria.
  • Kruus K; Solutions for Natural Resources and Environment, VTT Technical Research Centre of Finland Ltd, Tietotie 2, FI-02044 Espoo, Finland; School of Chemical Engineering, Aalto University, P.O. Box 16100, Espoo 00076 AALTO, Finland.
  • Várnai A; Faculty of Chemistry, Biotechnology and Food Science, NMBU - Norwegian University of Life Sciences, 1432 Ås, Norway.
  • Eijsink VGH; Faculty of Chemistry, Biotechnology and Food Science, NMBU - Norwegian University of Life Sciences, 1432 Ås, Norway.
  • Potthast A; Institute of Chemistry of Renewable Resources, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz-Straße 24, A-3430 Tulln an der Donau, Austria. Electronic address: antje.potthast@boku.ac.at.
Carbohydr Polym ; 328: 121696, 2024 Mar 15.
Article em En | MEDLINE | ID: mdl-38220335
ABSTRACT
Enzymatic treatment of cellulosic fibres is a green alternative to classical chemical modification. For many applications, mild procedures for cellulose alteration are sufficient, in which the fibre structure and, therefore, the mechanical performance of cellulosic fibres are preserved. Lytic polysaccharide monooxygenases (LPMOs) bear a great potential to become a green reagent for such targeted cellulose modifications. An obstacle for wide implementation of LPMOs in tailored cellulose chemistry is the lack of suitable techniques to precisely monitor the LPMO impact on the polymer. Soluble oxidized cello-oligomers can be quantified using chromatographic and mass-spectrometric techniques. A considerable portion of the oxidized sites, however, remain on the insoluble cellulose fibres, and their quantification is difficult. Here, we describe a method for the simultaneous quantification of oxidized sites on cellulose fibres and changes in their molar mass distribution after treatment with LPMOs. The method is based on quantitative, heterogeneous, carbonyl-selective labelling with a fluorescent label (CCOA) followed by cellulose dissolution and size-exclusion chromatography (SEC). Application of the method to reactions of seven different LPMOs with pure cellulose fibres revealed pronounced functional differences between the enzymes, showing that this CCOA/SEC/MALS method is a promising tool to better understand the catalytic action of LPMOs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissacarídeos / Oxigenases de Função Mista Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissacarídeos / Oxigenases de Função Mista Idioma: En Ano de publicação: 2024 Tipo de documento: Article