Evidence map›Paper›PMID 39913342›Full record

ArticleThe ISME journal2025

Metabolism of hemicelluloses by root-associated Bacteroidota species.

Hannah Martin, Lucy A Rogers, Laila Moushtaq, Amanda A Brindley, Polly Forbes, Amy R Quinton, Andrew R J Murphy, Helen Hipperson, Tim J Daniell, Didier Ndeh and 3 more

Abstract read
In one paragraph

Article in The ISME journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Response ofApplied and environmental microbiology · 2026
    Article
  4. Article
  5. Review
  6. International journal of molecular sciences · 2026
    Article
  7. Article
  8. Article
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  11. Article
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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

13 authors.

Hannah MartinMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Lucy A RogersMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Laila MoushtaqMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Amanda A BrindleyPlants, Photosynthesis and Soil, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Polly ForbesMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Amy R QuintonMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Andrew R J MurphySchool of Life Sciences, The University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, West Midlands, United Kingdom.
Helen HippersonPlants, Photosynthesis and Soil, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Tim J DaniellPlants, Photosynthesis and Soil, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Didier NdehSchool of Life Sciences, University of Dundee, Dow Street, Dundee, DD1 5EH, Scotland, United Kingdom.
Sam AmsburyPlants, Photosynthesis and Soil, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Andrew HitchcockMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.
Ian D E A LidburyMolecular Microbiology - Biochemistry and Disease, School of Biosciences, The University of Sheffield, Western Bank, Sheffield, S10 2TN, South Yorkshire, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteroidota species are enriched in the plant microbiome and provide several beneficial functions for their host, including disease suppression. Determining the mechanisms that enable bacteroidota to colonise plant roots may therefore provide opportunities for enhancing crop production through microbiome engineering. By focusing on nutrient acquisition mechanisms, we discovered Bacteroidota species lack high affinity ATP-binding cassette transporters common in other plant-associated bacteria for capturing simple carbon exudates. Instead, bacteroidota possess TonB-dependent transporters predicted to import glycans produced by plant polysaccharide breakdown. Metatranscriptomics (oat rhizosphere) identified several TonB-dependent transporters genes that were highly expressed in Flavobacterium (phylum Bacteroidota). Using Flavobacterium johnsoniae as the model, we experimentally validated the function of one highly expressed TonB-dependent transporter, identifying a conserved Xyloglucan utilisation loci conferring the ability to import and degrade xyloglucan, the major hemicellulose secreted from plant roots. Xyloglucan utilisation loci harbour an endoxyloglucanase related to family 5 subfamily 4 subclade 2D glycoside hydrolases carrying a mutation that we demonstrate is required for full activity towards xyloglucan. Based on analysing 700 soil metagenomes, subclade 2D glycoside hydrolases have radiated in soil and are prevalent among plant-associated bacteroidota and certain taxa affiliated with Gammaproteobacteria. In bacteroidota, particularly Flavobacterium species, xyloglucan utilisation loci organisation was highly conserved, which may increase their competitive ability to utilise xyloglucan. Given bacteroidota lack high-affinity nutrient transporters for simple carbon, instead possessing xyloglucan utilisation loci and similar gene clusters, our data suggests hemicellulose exudates provide them with an important carbon source in the rhizosphere.

Indexed as

BacteroidetesPlant RootsPolysaccharidesATP-Binding Cassette TransportersFlavobacteriumGene Expression ProfilingGlucansGlycoside HydrolasesRhizosphereSoil MicrobiologyXylansATP-Binding Cassette TransportersGlucansGlycoside HydrolaseshemicellulosePolysaccharidesXylansxyloglucanBacteroidotaFlavobacteriumGlycobiologyPlant microbiomePolysaccharide utilisation lociRhizosphereRoot exudates

Identifiers

PMID39913342
PMCPMC11892949

What OpenQuestion holds

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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.