Evidence map›Paper›PMID 18522943›Full record

ArticleThe Journal of biological chemistry2008

Catabolism of glutathione conjugates in Arabidopsis thaliana. Role in metabolic reactivation of the herbicide safener fenclorim.

Melissa Brazier-Hicks, Kathryn M Evans, Oliver D Cunningham, David R W Hodgson, Patrick G Steel, Robert Edwards

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Herbicidal safening activity ofFrontiers in plant science · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Metabolism and Photolysis of 2,4-Dinitroanisole in Arabidopsis.Environmental science & technology · 2017
    Article
  9. Article
  10. Article
  11. Protective responses induced by herbicide safeners in wheat.Environmental and experimental botany · 2013
    Article
  12. Article
  13. Glutathione.The arabidopsis book · 2011
    Article
  14. Review
  15. Article
  16. The C-glycosylation of flavonoids in cereals.The Journal of biological chemistry · 2009
    Article
  17. 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

6 authors at 1 institution in 1 country.

Melissa Brazier-HicksCentre for Bioactive Chemistry, Department of Chemistry, Durham University, Durham, United Kingdom.
Kathryn M Evans
Oliver D Cunningham
David R W Hodgson
Patrick G Steel
Robert Edwards
Durham University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D005620/1
6 · The paper itself

Abstract

The safener fenclorim (4,6-dichloro-2-phenylpyrimidine) increases tolerance to chloroacetanilide herbicides in rice by enhancing the expression of detoxifying glutathione S-transferases (GSTs). Fenclorim also enhances GSTs in Arabidopsis thaliana, and while investigating the functional significance of this induction in suspension cultures, we determined that these enzymes glutathionylated the safener. The resulting S-(fenclorim)-glutathione conjugate was sequentially processed to S-(fenclorim)-gamma-glutamyl-cysteine and S-(fenclorim)-cysteine (FC), the latter accumulating in both the cells and the medium. FC was then either catabolized to 4-chloro-6-(methylthio)-phenylpyrimidine (CMTP) or N-acylated with malonic acid. These cysteine derivatives had distinct fates, with the enzymes responsible for their formation being induced by fenclorim and FC. Fenclorim-N-malonylcysteine was formed from FC by the action of a malonyl-CoA-dependent N-malonyltransferase. A small proportion of the fenclorim-N-malonylcysteine then underwent decarboxylation to yield a putative S-fenclorim-N-acetylcysteine intermediate, which underwent a second round of GST-mediated S-glutathionylation and subsequent proteolytic processing. The formation of CMTP was catalyzed by the concerted action of a cysteine conjugate beta-lyase and an S-methyltransferase, with the two activities being coordinately regulated. Although the fenclorim conjugates tested showed little GST-inducing activity in Arabidopsis, the formation of CMTP resulted in metabolic reactivation, with the product showing good enhancing activity. In addition, CMTP induced GSTs and herbicide-safening activity in rice. The bioactivated CMTP was in turn glutathione-conjugated and processed to a malonyl cysteine derivative. These results reveal the surprisingly complex set of competing catabolic reactions acting on xenobiotics entering the S-glutathionylation pathway in plants, which can result in both detoxification and bioactivation.

Indexed as

Gene Expression RegulationGene Expression Regulation, PlantArabidopsisArabidopsis ProteinsGlutathioneGlutathione TransferaseHerbicidesMass SpectrometryModels, BiologicalModels, ChemicalOryzaPlant Physiological PhenomenaProteomicsPyrimidinesTime FactorsArabidopsis ProteinsfenclorimGlutathioneGlutathione TransferaseHerbicidesPyrimidines

Identifiers

PMID18522943
PMCPMC3258958
OpenAlexW1990425731

What OpenQuestion holds

Textmetadata
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.