Evidence map›Paper›PMID 25043916›Full record

ArticleBMC genomics2014

Elucidating how the saprophytic fungus Aspergillus nidulans uses the plant polyester suberin as carbon source.

Isabel Martins, Diego O Hartmann, Paula C Alves, Celso Martins, Helga Garcia, Céline C Leclercq, Rui Ferreira, Ji He, Jenny Renaut, Jörg D Becker and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.1field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 47 citations in OpenAlex.

  1. FAMeDB: A Curated Database for the Analysis of Fungal Aromatic Compound Metabolism.Computational and structural biotechnology journal · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Lipids and Lipid-Mediated Signaling in Plant-Pathogen Interactions.International journal of molecular sciences · 2024
    Review
  6. Microorganisms · 2022
    Review
  7. Article
  8. Visualization of Suberization and Lignification in Sugarcane.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

11 authors at 5 institutions in 3 countries.

Isabel Martins
Diego O Hartmann
Paula C Alves
Celso Martins
Helga Garcia
Céline C Leclercq
Rui Ferreira
Ji He
Jenny Renaut
Jörg D Becker
Cristina Silva PereiraInstituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Av, da República, 2780-157 Oeiras, Portugal. spereira@itqb.unl.pt.
Universidade Nova de Lisboa · PTInstituto de Biologia Experimental e Tecnológica · PTNational Library of Luxembourg · LUInstituto Gulbenkian de Ciência · PTNational Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipid polymers in plant cell walls, such as cutin and suberin, build recalcitrant hydrophobic protective barriers. Their degradation is of foremost importance for both plant pathogenic and saprophytic fungi. Regardless of numerous reports on fungal degradation of emulsified fatty acids or cutin, and on fungi-plant interactions, the pathways involved in the degradation and utilisation of suberin remain largely overlooked. As a structural component of the plant cell wall, suberin isolation, in general, uses harsh depolymerisation methods that destroy its macromolecular structure. We recently overcame this limitation isolating suberin macromolecules in a near-native state.

resultsSuberin macromolecules were used here to analyse the pathways involved in suberin degradation and utilisation by Aspergillus nidulans. Whole-genome profiling data revealed the complex degrading enzymatic machinery used by this saprophytic fungus. Initial suberin modification involved ester hydrolysis and ω-hydroxy fatty acid oxidation that released long chain fatty acids. These fatty acids were processed through peroxisomal β-oxidation, leading to up-regulation of genes encoding the major enzymes of these pathways (e.g. faaB and aoxA). The obtained transcriptome data was further complemented by secretome, microscopic and spectroscopic analyses.

conclusionsData support that during fungal growth on suberin, cutinase 1 and some lipases (e.g. AN8046) acted as the major suberin degrading enzymes (regulated by FarA and possibly by some unknown regulatory elements). Suberin also induced the onset of sexual development and the boost of secondary metabolism.

Indexed as

Aspergillus nidulansCarbonCarboxylic Ester HydrolasesCell WallFatty AcidsFungal ProteinsGenome, FungalLipaseLipidsOxidation-ReductionPolyestersTranscriptomeCarbonCarboxylic Ester HydrolasescutinaseFatty AcidsFungal ProteinsLipaseLipidsPolyesterssuberin

Identifiers

PMID25043916
PMCPMC4117967
OpenAlexW1972912205

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.