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Glycoside Phosphorylase Catalyzed Cellulose and β-1,3-Glucan Synthesis Using Chromophoric Glycosyl Acceptors

    • Aalto University

    Research output: Contribution to journal › Article › Scientific › peer-review

    Abstract

    Glycoside phosphorylases are enzymes that are frequently used for polysaccharide synthesis. Some of these enzymes have broad substrate specificity, enabling the synthesis of reducing-end-functionalized glucan chains. Here, we explore the potential of glycoside phosphorylases in synthesizing chromophore-conjugated polysaccharides using commercially available chromophoric model compounds as glycosyl acceptors. Specifically, we report cellulose and β-1,3-glucan synthesis using 2-nitrophenyl β-d-glucopyranoside, 4-nitrophenyl β-d-glucopyranoside, and 2-methoxy-4-(2-nitrovinyl)phenyl β-d-glucopyranoside with Clostridium thermocellum cellodextrin phosphorylase and Thermosipho africanus β-1,3-glucan phosphorylase as catalysts. We demonstrate activity for both enzymes with all assayed chromophoric acceptors and report the crystallization-driven precipitation and detailed structural characterization of the synthesized polysaccharides, i.e., their molar mass distributions and various structural parameters, such as morphology, fibril diameter, lamellar thickness, and crystal form. Our results provide insights for the studies of chromophore-conjugated low molecular weight polysaccharides, glycoside phosphorylases, and the hierarchical assembly of crystalline cellulose and β-1,3-glucan.

    Original languageEnglish
    Pages (from-to)5048-5057
    Number of pages10
    JournalBiomacromolecules
    Volume25
    Issue number8
    DOIs
    Publication statusPublished - 12 Aug 2024
    MoE publication typeA1 Journal article-refereed

    Funding

    This work was supported by the Jenny and Antti Wihuri Foundation (Center for Young Synbio Scientists), the Academy of Finland Center of Excellence Program in Life-Inspired Hybrid Materials (LIBER) project 346106, and the Academy of Finland project 348628. The authors acknowledge the provision of facilities and technical support by Aalto University at the OtaNano Nanomicroscopy Center (Aalto-NMC) and thank Atte Mikkelson for SEC measurements.

    Keywords

    • Cellulose/chemistry
    • beta-Glucans/chemistry
    • Glucosyltransferases/chemistry
    • Clostridium thermocellum/enzymology
    • Phosphorylases/metabolism

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