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 language | English |
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Pages (from-to) | 5048-5057 |
Number of pages | 10 |
Journal | Biomacromolecules |
Volume | 25 |
Issue number | 8 |
DOIs | |
Publication status | Published - 12 Aug 2024 |
MoE publication type | A1 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