Evidence map›Paper›PMID 40877455›Full record

ArticleCommunications biology2025

Structural and biochemical basis for activity of Aspergillus nidulans α-1,3-glucanases from glycoside hydrolase family 71.

Scott Mazurkewich, Tove Widén, Hampus Karlsson, Lars Evenäs, Poornima Ramamohan, Jakob Wohlert, Gisela Brändén, Johan Larsbrink

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Scott MazurkewichDepartment of Life Sciences, Chalmers University of Technology, Gothenburg, Sweden. scott.mazurkewich@chalmers.se.ORCID http://orcid.org/0000-0002-9238-0615
Tove WidénDepartment of Life Sciences, Chalmers University of Technology, Gothenburg, Sweden.ORCID http://orcid.org/0009-0001-6830-9608
Hampus KarlssonWallenberg Wood Science Center, Chalmers University of Technology, Gothenburg, Sweden.
Lars EvenäsWallenberg Wood Science Center, Chalmers University of Technology, Gothenburg, Sweden.ORCID http://orcid.org/0000-0002-6580-0610
Poornima RamamohanWallenberg Wood Science Center, Chalmers University of Technology, Gothenburg, Sweden.
Jakob WohlertWallenberg Wood Science Center, Chalmers University of Technology, Gothenburg, Sweden.
Gisela BrändénDepartment of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-5615-7187
Johan LarsbrinkDepartment of Life Sciences, Chalmers University of Technology, Gothenburg, Sweden. johan.larsbrink@chalmers.se.ORCID http://orcid.org/0000-0001-8386-2914

Funding

Vetenskapsrådet (Swedish Research Council) 2020-03618
6 · The paper itself

Abstract

The microbial polysaccharide α-1,3-glucan is an important component of fungal cell walls and dental plaque biofilms, contributing to microbial virulence and biofilm resilience. Glycoside hydrolase family 71 (GH71) includes α-1,3-glucan degrading enzymes which could be exploited for biotechnological applications; however, the family is presently poorly understood. To increase our understanding of GH71, we have performed a phylogenetic analysis of the family and detailed biochemical analysis of two of the five GH71 enzymes encoded by Aspergillus nidulans (AnGH71B and -C). Both are active on soluble α-1,3-glucooligosaccharides but surprisingly only minimally on water-insoluble α-1,3-glucan. Assays on intact and milled A. nidulans biomass indicate that the enzymes act on fungal cell wall glycosidic linkages, likely having roles in cell wall remodelling. Both enzymes utilize an inverting mechanism but differ in specificity and product profiles indicating exo- and endo-like activity for AnGH71B and AnGH71C, respectively. We present the first structure of a GH71 protein, AnGH71C, including structures with carbohydrate ligands. These structures revealed a conserved acidic dyad (DxxE), found to be crucial for activity, and active site water coordination consistent with a classical inverting GH mechanism. This work provides new insights into GH71, highlighting its functional diversity and the enzymes roles in fungal physiology.

Indexed as

Aspergillus nidulansCell WallGlycoside HydrolasesBacteriaBiofilmsGlucansOligosaccharidesSubstrate SpecificityGlucansGlycoside HydrolasesOligosaccharides

Identifiers

PMID40877455
PMCPMC12394665

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.