Evidence map›Paper›PMID 37227091›Full record

ArticleActa crystallographica. Section D, Structural biology2023

Structural and functional investigation of a fungal member of carbohydrate esterase family 15 with potential specificity for rare xylans.

Scott Mazurkewich, Karoline C Scholzen, Rikke H Brusch, Jens Christian N Poulsen, Yusuf Theibich, Silvia Hüttner, Lisbeth Olsson, Johan Larsbrink, Leila Lo Leggio

Open access · hybridAbstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 33% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Scott MazurkewichWallenberg Wood Science Center, Division of Industrial Biotechnology, Department of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0000-0002-9238-0615
Karoline C ScholzenDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark.ORCID 0000-0002-5403-0411
Rikke H BruschDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark.ORCID 0000-0003-0646-7018
Jens Christian N PoulsenDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark.ORCID 0000-0002-3553-0015
Yusuf TheibichDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark.ORCID 0000-0002-0073-0842
Silvia HüttnerWallenberg Wood Science Center, Division of Industrial Biotechnology, Department of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0000-0002-7096-9680
Lisbeth OlssonWallenberg Wood Science Center, Division of Industrial Biotechnology, Department of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0000-0002-0827-5442
Johan LarsbrinkWallenberg Wood Science Center, Division of Industrial Biotechnology, Department of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0000-0001-8386-2914
Leila Lo LeggioDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark.ORCID 0000-0002-5135-0882
University of Copenhagen · DKWallenberg Wood Science Center · SE

Funding

Novo Nordisk Fonden NNF17OC0027698Novo Nordisk Fonden NNF21OC0071611
6 · The paper itself

Abstract

In plant cell walls, covalent bonds between polysaccharides and lignin increase recalcitrance to degradation. Ester bonds are known to exist between glucuronic acid moieties on glucuronoxylan and lignin, and these can be cleaved by glucuronoyl esterases (GEs) from carbohydrate esterase family 15 (CE15). GEs are found in both bacteria and fungi, and some microorganisms also encode multiple GEs, although the reason for this is still not fully clear. The fungus Lentithecium fluviatile encodes three CE15 enzymes, of which two have previously been heterologously produced, although neither was active on the tested model substrate. Here, one of these, LfCE15C, has been investigated in detail using a range of model and natural substrates and its structure has been solved using X-ray crystallography. No activity could be verified on any tested substrate, but biophysical assays indicate an ability to bind to complex carbohydrate ligands. The structure further suggests that this enzyme, which possesses an intact catalytic triad, might be able to bind and act on more extensively decorated xylan chains than has been reported for other CE15 members. It is speculated that rare glucuronoxylans decorated at the glucuronic acid moiety may be the true targets of LfCE15C and other CE15 family members with similar sequence characteristics.

Indexed as

EsterasesLigninGlucuronic AcidPolysaccharidesSubstrate SpecificityXylansEsterasesGlucuronic AcidLigninPolysaccharidesXylansbiomass conversionglucuronyl esteraseshemicelluloseLentithecium fluviatilelignocellulose degradationrare xylansα/β hydrolases

Identifiers

PMID37227091
PMCPMC10233622
OpenAlexW4378173087

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.