A unique Equisetum enzyme, hetero-trans-β-glucanase (HTG), enhances industrially and environmentally important cellulose-rich materials

Gigatons of cellulose are synthesised and degraded annually. Under-utilised cellulose, e.g. from sugar-beet pulp ('Curran') and recycled paper, could be valorised by Equisetum hetero-trans-β-glucanase (HTG), the only known enzyme modifying cellulose non-destructively. It catalyses hetero-transglycosylation, with cellulose as donor substrate and xyloglucan oligosaccharides (XGOs) as acceptor, creating cellulose-XGO covalent bonds. Interestingly, XGOs participate in this reaction even if linked to a biotechnologically-valuable 'cargo', e.g. a dye, fluorophore, cation, anion, hydrophobic compound or antibiotic, beneficially functionalising the cellulose. Here, we tested whether HTG acts on intransigent agricultural/industrial celluloses. Curran was found to be a pectin- and hemicellulose-poor, but cellulose-rich product, thus potentially enhanceable by HTG technology. To generate industrial quantities of HTG, we explored Equisetum extraction methods, comparing extractants (buffers versus tap-water), extractant ratios, homogenisation technique, work-up (centrifugation versus filtration) and salting out. Pleasingly, simplified 'industrial' methods were 75-85 % as effective as laboratory methods. Up-scaled heterologous expression in Pichia also yielded plentiful EfHTG. Thus diverse methods enabled bulk HTG production. All HTG preparations tested acted on pure cellulose (Whatman filter-paper; donor substrate) and radioactive or fluorescent cargo-bearing XGOs ([<sup>3</sup>H]XXXGol or XXXGol-sulphorhodamine respectively; model acceptor substrates). Diverse HTG preparations acted on potentially 'intractable' celluloses, e.g. Curran and crude recycled brown card, at rates comparable to those on pure celluloses (filter-paper and virgin white never-dried pulp). Where necessary, coarse industrial celluloses were H<sub>2</sub>SO<sub>4</sub>-hydrolysed to expose underestimated signal from incorporated but 'masked' radioactive substrate. Unlike surface-finish modifications, HTG-catalysed bonding of cargoes to cellulose is covalent (thus highly stable) and environmentally friendly (green sustainable technology).

Authors

Institutions

Publication Details

Journal
Environmental Research
Published
2025-04-08
DOI
https://doi.org/10.1016/j.envres.2025.121558
Citations
1
Primary Topic
Polysaccharides and Plant Cell Walls
Type
article
Field-Weighted Citation Impact
1.75

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A unique Equisetum enzyme, hetero-trans-β-glucanase (HTG), enhances industrially and environmentally important cellulose-rich materials

Eric Whale, Lenka Franková, David Hepworth, Stephen C. Fry
1 citations
Environmental Research
Polysaccharides and Plant Cell Walls
1.75
article

A unique Equisetum enzyme, hetero-trans-β-glucanase (HTG), enhances industrially and environmentally important cellulose-rich materials

Eric Whale, Lenka Franková, David Hepworth, Stephen C. Fry
article en
1 citations

Abstract

Gigatons of cellulose are synthesised and degraded annually. Under-utilised cellulose, e.g. from sugar-beet pulp ('Curran') and recycled paper, could be valorised by Equisetum hetero-trans-β-glucanase (HTG), the only known enzyme modifying cellulose non-destructively. It catalyses hetero-transglycosylation, with cellulose as donor substrate and xyloglucan oligosaccharides (XGOs) as acceptor, creating cellulose-XGO covalent bonds. Interestingly, XGOs participate in this reaction even if linked to a biotechnologically-valuable 'cargo', e.g. a dye, fluorophore, cation, anion, hydrophobic compound or antibiotic, beneficially functionalising the cellulose. Here, we tested whether HTG acts on intransigent agricultural/industrial celluloses. Curran was found to be a pectin- and hemicellulose-poor, but cellulose-rich product, thus potentially enhanceable by HTG technology. To generate industrial quantities of HTG, we explored Equisetum extraction methods, comparing extractants (buffers versus tap-water), extractant ratios, homogenisation technique, work-up (centrifugation versus filtration) and salting out. Pleasingly, simplified 'industrial' methods were 75-85 % as effective as laboratory methods. Up-scaled heterologous expression in Pichia also yielded plentiful EfHTG. Thus diverse methods enabled bulk HTG production. All HTG preparations tested acted on pure cellulose (Whatman filter-paper; donor substrate) and radioactive or fluorescent cargo-bearing XGOs ([<sup>3</sup>H]XXXGol or XXXGol-sulphorhodamine respectively; model acceptor substrates). Diverse HTG preparations acted on potentially 'intractable' celluloses, e.g. Curran and crude recycled brown card, at rates comparable to those on pure celluloses (filter-paper and virgin white never-dried pulp). Where necessary, coarse industrial celluloses were H<sub>2</sub>SO<sub>4</sub>-hydrolysed to expose underestimated signal from incorporated but 'masked' radioactive substrate. Unlike surface-finish modifications, HTG-catalysed bonding of cargoes to cellulose is covalent (thus highly stable) and environmentally friendly (green sustainable technology).

Environmental ResearchVol. 277
Cellucomp (United Kingdom) (GB), University of Edinburgh (GB)
Industrial Biotechnology Innovation Centre, Biotechnology and Biological Sciences Research Council, Innovate UK
Responsible consumption and production
Openalex Percentile: Top 16%
Polysaccharides and Plant Cell Walls
1.75
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.