Evidence map›Paper›PMID 25870290›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Activation of cyclic electron flow by hydrogen peroxide in vivo.

Deserah D Strand, Aaron K Livingston, Mio Satoh-Cruz, John E Froehlich, Veronica G Maurino, David M Kramer

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing 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

63 citing papers in PubMed.

  1. Article
  2. Article
  3. The ascorbate-glutathione cycle coming of age.Journal of experimental botany · 2024
    Review
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  18. Article
  19. Photosynthesis: a multiscopic view.Journal of plant research · 2021
    Review
  20. Review

3 more citing papers are in PubMed but not listed here.

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.

Deserah D StrandPlant Research Laboratory and Departments of Plant Biology and.
Aaron K LivingstonSchool of Molecular Biosciences and Institute for Biological Chemistry, Washington State University, Pullman, WA 99164; and.
Mio Satoh-CruzPlant Research Laboratory and.
John E FroehlichPlant Research Laboratory and Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824;
Veronica G MaurinoInstitute of Developmental and Molecular Biology of Plants, Plant Molecular Physiology and Biotechnology Group, Heinrich-Heine-Universität, Cluster of Excellence on Plant Sciences (CEPLAS), 40225 Düsseldorf, Germany.
David M KramerPlant Research Laboratory and Departments of Plant Biology and Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824; kramerd8@msu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclic electron flow (CEF) around photosystem I is thought to balance the ATP/NADPH energy budget of photosynthesis, requiring that its rate be finely regulated. The mechanisms of this regulation are not well understood. We observed that mutants that exhibited constitutively high rates of CEF also showed elevated production of H2O2. We thus tested the hypothesis that CEF can be activated by H2O2 in vivo. CEF was strongly increased by H2O2 both by infiltration or in situ production by chloroplast-localized glycolate oxidase, implying that H2O2 can activate CEF either directly by redox modulation of key enzymes, or indirectly by affecting other photosynthetic processes. CEF appeared with a half time of about 20 min after exposure to H2O2, suggesting activation of previously expressed CEF-related machinery. H2O2-dependent CEF was not sensitive to antimycin A or loss of PGR5, indicating that increased CEF probably does not involve the PGR5-PGRL1 associated pathway. In contrast, the rise in CEF was not observed in a mutant deficient in the chloroplast NADPH:PQ reductase (NDH), supporting the involvement of this complex in CEF activated by H2O2. We propose that H2O2 is a missing link between environmental stress, metabolism, and redox regulation of CEF in higher plants.

Indexed as

Alcohol OxidoreductasesArabidopsisArabidopsis ProteinsChloroplastsElectron TransportHydrogen PeroxideMembrane ProteinsMutationOxidantsPhotosynthetic Reaction Center Complex ProteinsPhotosystem I Protein ComplexQuinone ReductasesStress, PhysiologicalAlcohol OxidoreductasesArabidopsis Proteinsglycollate oxidaseHydrogen PeroxideMembrane ProteinsNADPH - phenanthrenequinone oxidoreductaseOxidantsPGR5 protein, ArabidopsisPGRL1 protein, ArabidopsisPhotosynthetic Reaction Center Complex ProteinsPhotosystem I Protein ComplexQuinone Reductasescyclic electron flowhydrogen peroxidephotosynthesisreactive oxygen speciesstress

Identifiers

PMID25870290
PMCPMC4418880

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.