Evidence map›Paper›PMID 27990770›Full record

ArticleMicrobial biotechnology2017

Bioactive secondary metabolites with multiple activities from a fungal endophyte.

Catherine W Bogner, Ramsay S T Kamdem, Gisela Sichtermann, Christian Matthäus, Dirk Hölscher, Jürgen Popp, Peter Proksch, Florian M W Grundler, Alexander Schouten

Abstract read
In one paragraph

Article in Microbial biotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Synthesis, Anthelmintic Activity, and Mechanism of Action of 5-Aryl-1Journal of agricultural and food chemistry · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Potent Bioactivity of Endophytic Fungi Isolated fromBioMed research international · 2022
    Article
  16. Article
  17. Diverse roles of microbial indole compounds in eukaryotic systems.Biological reviews of the Cambridge Philosophical Society · 2021
    Review
  18. Article
  19. Article
  20. 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

9 authors.

Catherine W BognerInstitute of Crop Science and Resource Conservation (INRES), Department of Molecular Phytomedicine, University of Bonn, Karlrobert-Kreiten Str. 13, 53115, Bonn, Germany.
Ramsay S T KamdemInstitute of Pharmaceutical Biology and Biotechnology, Heinrich-Heine-University Düsseldorf, Universitäts Str. 1. Building. 26.23, 40225, Düsseldorf, Germany.
Gisela SichtermannInstitute of Crop Science and Resource Conservation (INRES), Department of Molecular Phytomedicine, University of Bonn, Karlrobert-Kreiten Str. 13, 53115, Bonn, Germany.
Christian MatthäusInstitute of Photonic Technology, Workgroup Spectroscopy/Imaging, Albert-Einstein-Str. 9, 07745, Jena, Germany.
Dirk HölscherResearch Group Biosynthesis/NMR, Max Planck Institute for Chemical Ecology, Hans-Knöll-Str. 8, 07745, Jena, Germany.
Jürgen PoppInstitute of Photonic Technology, Workgroup Spectroscopy/Imaging, Albert-Einstein-Str. 9, 07745, Jena, Germany.
Peter ProkschInstitute of Pharmaceutical Biology and Biotechnology, Heinrich-Heine-University Düsseldorf, Universitäts Str. 1. Building. 26.23, 40225, Düsseldorf, Germany.
Florian M W GrundlerInstitute of Crop Science and Resource Conservation (INRES), Department of Molecular Phytomedicine, University of Bonn, Karlrobert-Kreiten Str. 13, 53115, Bonn, Germany.
Alexander SchoutenInstitute of Crop Science and Resource Conservation (INRES), Department of Molecular Phytomedicine, University of Bonn, Karlrobert-Kreiten Str. 13, 53115, Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to replace particularly biohazardous nematocides, there is a strong drive to finding natural product-based alternatives with the aim of containing nematode pests in agriculture. The metabolites produced by the fungal endophyte Fusarium oxysporum 162 when cultivated on rice media were isolated and their structures elucidated. Eleven compounds were obtained, of which six were isolated from a Fusarium spp. for the first time. The three most potent nematode-antagonistic compounds, 4-hydroxybenzoic acid, indole-3-acetic acid (IAA) and gibepyrone D had LC

Indexed as

AnimalsAntinematodal AgentsBiological ProductsCulture MediaEndophytesFusariumMicroscopyMolecular StructureSurvival AnalysisTylenchoideaAntinematodal AgentsBiological ProductsCulture Media

Identifiers

PMID27990770
PMCPMC5270730

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.