Evidence map›Paper›PMID 35064799›Full record

ArticlePlant cell reports2022

Color recycling: metabolization of apocarotenoid degradation products suggests carbon regeneration via primary metabolic pathways.

Julian Koschmieder, Saleh Alseekh, Marzieh Shabani, Raymonde Baltenweck, Veronica G Maurino, Klaus Palme, Alisdair R Fernie, Philippe Hugueney, Ralf Welsch

Open access · hybridAbstract read
In one paragraph

Article in Plant cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Cysteine Signalling in Plant Pathogen Response.Plant, cell & environment · 2025
    Article
  2. Article
  3. Desiccation tolerance in the resurrection plantFrontiers in plant science · 2024
    Article
  4. Article
  5. 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 at 4 institutions in 4 countries.

Julian KoschmiederFaculty of Biology II, University of Freiburg, 79104, Freiburg, Germany.
Saleh AlseekhMax-Planck-Institute for Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam, Germany.
Marzieh ShabaniFaculty of Biology II, University of Freiburg, 79104, Freiburg, Germany.
Raymonde BaltenweckUniversité de Strasbourg, INRAE, SVQV UMR-A 1131, 68000, Colmar, France.
Veronica G MaurinoDepartment of Molecular Plant Physiology, Institute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Kirschallee 1, 53115, Bonn, Germany.
Klaus PalmeFaculty of Biology II, University of Freiburg, 79104, Freiburg, Germany.
Alisdair R FernieMax-Planck-Institute for Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam, Germany.
Philippe HugueneyUniversité de Strasbourg, INRAE, SVQV UMR-A 1131, 68000, Colmar, France.
Ralf WelschFaculty of Biology II, University of Freiburg, 79104, Freiburg, Germany. ralf.welsch@biologie.uni-freiburg.de.ORCID http://orcid.org/0000-0002-2865-2743
University of Freiburg · DECenter of Plant Systems Biology and Biotechnology · BGInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRUniversity of Bonn · DE

Funding

deutsche forschungsgemeinschaft WE4731/3horizon 2020 739582
6 · The paper itself

Abstract

key messageAnalysis of carotenoid-accumulating roots revealed that oxidative carotenoid degradation yields glyoxal and methylglyoxal. Our data suggest that these compounds are detoxified via the glyoxalase system and re-enter primary metabolic pathways. Carotenoid levels in plant tissues depend on the relative rates of synthesis and degradation. We recently identified redox enzymes previously known to be involved in the detoxification of fatty acid-derived reactive carbonyl species which were able to convert apocarotenoids into corresponding alcohols and carboxylic acids. However, their subsequent metabolization pathways remain unresolved. Interestingly, we found that carotenoid-accumulating roots have increased levels of glutathione, suggesting apocarotenoid glutathionylation to occur. In vitro and in planta investigations did not, however, support the occurrence of non-enzymatic or enzymatic glutathionylation of β-apocarotenoids. An alternative breakdown pathway is the continued oxidative degradation of primary apocarotenoids or their derivatives into the shortest possible oxidation products, namely glyoxal and methylglyoxal, which also accumulated in carotenoid-accumulating roots. In fact, combined transcriptome and metabolome analysis suggest that the high levels of glutathione are most probably required for detoxifying apocarotenoid-derived glyoxal and methylglyoxal via the glyoxalase pathway, yielding glycolate and D-lactate, respectively. Further transcriptome analysis suggested subsequent reactions involving activities associated with photorespiration and the peroxisome-specific glycolate/glyoxylate transporter. Finally, detoxified primary apocarotenoid degradation products might be converted into pyruvate which is possibly re-used for the synthesis of carotenoid biosynthesis precursors. Our findings allow to envision carbon recycling during carotenoid biosynthesis, degradation and re-synthesis which consumes energy, but partially maintains initially fixed carbon via re-introducing reactive carotenoid degradation products into primary metabolic pathways.

Indexed as

CarbonPyruvaldehydeCarotenoidsGlutathioneMetabolic Networks and PathwaysCarbonCarotenoidsGlutathionePyruvaldehydeApocarotenoidsCarotenoid degradationGlutathioneGlyoxalGlyoxalaseMethylglyoxal

Identifiers

PMID35064799
PMCPMC9035014
OpenAlexW4207038147

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.