The DOI matches its Crossref record; 165 of the 165 references it cites were found in a registry or an index.
Hydrogen peroxide metabolism and functions in plants
Open accessAbstract
Contents Summary 1197 I. Introduction 1198 II. Measurement and imaging of H 2 O 2 1198 III. H 2 O 2 and O 2·− toxicity 1199 IV. Production of H 2 O 2: enzymes and subcellular locations 1200 V. H 2 O 2 transport 1205 VI. Control of H 2 O 2 concentration: how and where? 1205 VII. Metabolic functions of H 2 O 2 1207 VIII. H 2 O 2 signalling 1207 IX. Where next? 1209 Acknowledgements 1209 References 1209 Summary: Hydrogen peroxide (H 2 O 2) is produced, via superoxide and superoxide dismutase, by electron transport in chloroplasts and mitochondria, plasma membrane NADPH oxidases, peroxisomal oxidases, type III peroxidases and other apoplastic oxidases. Intracellular transport is facilitated by aquaporins and H 2 O 2 is removed by catalase, peroxiredoxin, glutathione peroxidase‐like enzymes and ascorbate peroxidase, all of which have cell compartment‐specific isoforms. Apoplastic H 2 O 2 influences cell expansion, development and defence by its involvement in type III peroxidase‐mediated polymer cross‐linking, lignification and, possibly, cell expansion via H 2 O 2‐derived hydroxyl radicals. Excess H 2 O 2 triggers chloroplast and peroxisome autophagy and programmed cell death. The role of H 2 O 2 in signalling, for example during acclimation to stress and pathogen defence, has received much attention, but the signal transduction mechanisms are poorly defined. H 2 O 2 oxidizes specific cysteine residues of target proteins to the sulfenic acid form and, similar to other organisms, this modification could initiate thiol‐based redox relays and modify target enzymes, receptor kinases and transcription factors. Quantification of the sources and sinks of H 2 O 2 is being improved by the spatial and temporal resolution of genetically encoded H 2 O 2 sensors, such as HyPer and ro GFP 2‐Orp1. These H 2 O 2 sensors, combined with the detection of specific proteins modified by H 2 O 2, will allow a deeper understanding of its signalling roles.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Seed dormancy and the control of germination
Finch‐Savage, W. E., & Leubner‐Metzger, G. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01787.x · Cited by 3,177
Imlay, J. A. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro3032 · Cited by 1,684
Cellular Defenses against Superoxide and Hydrogen Peroxide
Imlay, J. A. (2008) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.77.061606.161055 · Cited by 1,563
Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants
Willekens, H. (1997) · The EMBO Journal · doi:10.1093/emboj/16.16.4806 · Cited by 1,267
Genetically encoded fluorescent indicator for intracellular hydrogen peroxide
Belousov, V. V., Fradkov, A. F., Lukyanov, K. A., Staroverov, D. B., Shakhbazov, K. S., Terskikh, A. V., & Lukyanov, S. (2006) · Nature Methods · doi:10.1038/nmeth866 · Cited by 1,258
The Plant NADPH Oxidase RBOHD Mediates Rapid Systemic Signaling in Response to Diverse Stimuli
Miller, G., Schlauch, K., Tam, R., Cortes, D., Torres, M. A., Shulaev, V., Dangl, J. L., & Mittler, R. (2009) · Science Signaling · doi:10.1126/scisignal.2000448 · Cited by 1,141
Methionine residues as endogenous antioxidants in proteins
Levine, R. L., Mosoni, L., Berlett, B. S., & Stadtman, E. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15036 · Cited by 1,041
Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity
Kadota, Y., Sklenář, J., Derbyshire, P., Stransfeld, L., Asai, S., Ntoukakis, V. E., Jones, J. D. G., Shirasu, K., Menke, F. L. H., Jones, A. M. E., et al. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.02.021 · Cited by 987
Real-time imaging of the intracellular glutathione redox potential
Gutscher, M., Pauleau, A.-L., Marty, L., Brach, T., Wabnitz, G. H., Samstag, Y., Meyer, A. J., & Dick, T. P. (2008) · Nature Methods · doi:10.1038/nmeth.1212 · Cited by 894
Systemic Signaling and Acclimation in Response to Excess Excitation Energy in Arabidopsis
Karpinski, S., Reynolds, H., Karpinska, B., Wingsle, G., Creissen, G., & Mullineaux, P. (1999) · Science · doi:10.1126/science.284.5414.654 · Cited by 875
Cited by
Reactive oxygen species signalling in plant stress responses
Mittler, R., Zandalinas, S. I., Fichman, Y., & Van Breusegem, F. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00499-2 · Cited by 2,351
Mechanisms of ROS Regulation of Plant Development and Stress Responses
Huang, H., Ullah, F., Zhou, D.-X., Yi, M., & Zhao, Y. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00800 · Cited by 1,468
Zhu, J., Cai, Y., Wakisaka, M., Yang, Z., Yin, Y., Fang, W., Xu, Y., Omura, T., Yu, R., & Zheng, A. L. T. (2023) · Science of The Total Environment · doi:10.1016/j.scitotenv.2023.165200 · Cited by 135
Oxygen Is Instrumental for Biological Signaling: An Overview
Hancock, J. T. (2021) · Oxygen · doi:10.3390/oxygen1010002 · Cited by 24
Metadata
- Authors
- Smirnoff, N., & Arnaud, D.
- Venue
- New Phytologist
- Publisher
- Wiley
- Published
- 2018-10-13
- Volume
- 221
- Issue
- 3
- Pages
- 1197-1214
- ISSN
- 0028-646X (ISSN-L)
- 1469-8137
- OpenAlex
- W2890213458
- Cited by
- 985
- References
- 165
- FWCI
- 56.44
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Hydrogen peroxide metabolism and functions in plants. https://app.cochat.ai/papers/10.1111/nph.15488
- The paper
- Smirnoff, N., & Arnaud, D. (2019). Hydrogen peroxide metabolism and functions in plants. New Phytologist. https://doi.org/10.1111/nph.15488
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.