Evidence map›Paper›PMID 25808147›Full record

ArticleMolecules (Basel, Switzerland)2015

Secondary metabolite localization by autofluorescence in living plant cells.

Pascale Talamond, Jean-Luc Verdeil, Geneviève Conéjéro

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Article
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  3. Article
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  5. Article
  6. Unveiling the Pharmacognostic Potential ofPlants (Basel, Switzerland) · 2025
    Article
  7. Article
  8. Supercritical COPlants (Basel, Switzerland) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. The Content of Anthocyanins in Cowpea (Plants (Basel, Switzerland) · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Geographical Classification of Saffron (Foods (Basel, Switzerland) · 2023
    Article
  18. Article
  19. Article
  20. Histochemical Analysis of Plant Secretory Structures.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
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

3 authors.

Pascale TalamondInstitut des Sciences de l'Evolution Montpellier ISE-M, Université Montpellier, CNRS, IRD, EPHE, CC 065, Place Eugène Bataillon, 34095 Montpellier, France. pascale.talamond@ird.fr.
Jean-Luc VerdeilHistocytology and Plant Cell Imaging platform PHIV, UMR AGAP (CIRAD, INRA, SupAgro)-UMR B&PMP (INRA, CNRS, SupAgro, Montpellier University), 34095 Montpellier, France. verdeil@cirad.fr.
Geneviève ConéjéroHistocytology and Plant Cell Imaging platform PHIV, UMR AGAP (CIRAD, INRA, SupAgro)-UMR B&PMP (INRA, CNRS, SupAgro, Montpellier University), 34095 Montpellier, France. genevieve.conejero@supagro.inra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autofluorescent molecules are abundant in plant cells and spectral images offer means for analyzing their spectra, yielding information on their accumulation and function. Based on their fluorescence characteristics, an imaging approach using multiphoton microscopy was designed to assess localization of the endogenous fluorophores in living plant cells. This method, which requires no previous treatment, provides an effective experimental tool for discriminating between multiple naturally-occurring fluorophores in living-tissues. Combined with advanced Linear Unmixing, the spectral analysis extends the possibilities and enables the simultaneous detection of fluorescent molecules reliably separating overlapping emission spectra. However, as with any technology, the possibility for artifactual results does exist. This methodological article presents an overview of the applications of tissular and intra-cellular localization of these intrinsic fluorophores in leaves and fruits (here for coffee and vanilla). This method will provide new opportunities for studying cellular environments and the behavior of endogenous fluorophores in the intracellular environment.

Indexed as

Secondary MetabolismCoffeaFruitImage Processing, Computer-AssistedMicroscopy, Fluorescence, MultiphotonPhenolsPlant CellsPlant LeavesVanillaPhenols

Identifiers

PMID25808147
PMCPMC6272479

What OpenQuestion holds

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LicenceCC BY
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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.