The DOI matches its Crossref record; 73 of the 73 references it cites were found in a registry or an index.
Redox- and Reactive Oxygen Species-Dependent Signaling into and out of the Photosynthesizing Chloroplast
Open accessAbstract
Photosynthesis is a high-rate redox metabolic process that is subjected to rapid changes in input parameters, particularly light. Rapid transients of photon capture, electron fluxes, and redox potentials during photosynthesis cause reactive oxygen species (ROS) to be released, including singlet oxygen, superoxide anion radicals, and hydrogen peroxide. Thus, the photosynthesizing chloroplast functions as a conditional source of important redox and ROS information, which is exploited to tune processes both inside the chloroplast and, following retrograde release or processing, in the cytosol and nucleus. Analyses of mutants and comparative transcriptome profiling have led to the identification of these processes and associated players and have allowed the specificity and generality of response patterns to be defined. The release of ROS and oxidation products, envelope permeabilization (for larger molecules), and metabolic interference with mitochondria and peroxisomes produce an intricate ROS and redox signature, which controls acclimation processes. This photosynthesis-related ROS and redox information feeds into various pathways (e.g. the mitogen-activated protein kinase and OXI1 signaling pathways) and controls processes such as gene expression and translation.
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Cites
Reactive oxygen species: Metabolism, oxidative stress, and signal transduction
Apel, K., & Hirt, H. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141701 · Cited by 11,723
MAPK Cascades in Plant Disease Resistance Signaling
Meng, X., & Zhang, S. (2013) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-082712-102314 · Cited by 1,367
Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis[W]
op den Camp, R. G. L., Przybyla, D., Ochsenbein, C., Laloi, C., Kim, C., Danon, A., Wagner, D., Hideg, E., Göbel, C., Feussner, I., et al. (2003) · The Plant Cell · doi:10.1105/tpc.014662 · Cited by 748
Transcriptomic Footprints Disclose Specificity of Reactive Oxygen Species Signaling in Arabidopsis
Gadjev, I., Vanderauwera, S., Gechev, T. S., Laloi, C., Minkov, I. N., Shulaev, V., Apel, K., Inzé, D., Mittler, R., & Van Breusegem, F. (2006) · Plant Physiology · doi:10.1104/pp.106.078717 · Cited by 734
Aquaporin-facilitated transmembrane diffusion of hydrogen peroxide
Bienert, G. P., & Chaumont, F. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.09.017 · Cited by 732
Ramel, F., Birtic, S., Ginies, C., Soubigou-Taconnat, L., Triantaphylidès, C., & Havaux, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1115982109 · Cited by 723
OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis
Rentel, M. C., Lecourieux, D., Ouaked, F., Usher, S. L., Petersen, L., Okamoto, H., Knight, H., Peck, S. C., Grierson, C. S., Hirt, H., et al. (2004) · Nature · doi:10.1038/nature02353 · Cited by 612
Learning the Languages of the Chloroplast: Retrograde Signaling and Beyond
Chan, K. X., Phua, S. Y., Crisp, P., McQuinn, R., & Pogson, B. J. (2016) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043015-111854 · Cited by 582
Singlet oxygen production in photosystem II and related protection mechanism
Krieger-Liszkay, A., Fufezan, C., & Trebst, A. (2008) · Photosynthesis Research · doi:10.1007/s11120-008-9349-3 · Cited by 569
Self-citationEstavillo, G. M., Crisp, P. A., Pornsiriwong, W., Wirtz, M., Collinge, D., Carrie, C., Giraud, E., Whelan, J., David, P., Javot, H., et al. (2011) · The Plant Cell · doi:10.1105/tpc.111.091033 · Cited by 553
Cited by
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
Oxidative Stress and Antioxidant Metabolism under Adverse Environmental Conditions: a Review
García-Caparrós, P., De Filippis, L., Gul, A., Hasanuzzaman, M., Ozturk, M., Altay, V., & Lao, M. T. (2021) · The Botanical Review · doi:10.1007/s12229-020-09231-1 · Cited by 555
The lipid biochemistry of eukaryotic algae
Li-Beisson, Y., Thelen, J. J., Fedosejevs, E., & Harwood, J. L. (2019) · Progress in Lipid Research · doi:10.1016/j.plipres.2019.01.003 · Cited by 453
Variables Governing Photosynthesis and Growth in Microalgae Mass Cultures
Masojídek, J., Ranglová, K., Lakatos, G. E., Silva Benavides, A. M., & Torzillo, G. (2021) · Processes · doi:10.3390/pr9050820 · Cited by 154
The ‘stress’ concept in microalgal biology—homeostasis, acclimation and adaptation
Borowitzka, M. A. (2018) · Journal of Applied Phycology · doi:10.1007/s10811-018-1399-0 · Cited by 152
Metadata
- Authors
- Dietz, K.-J., Turkan, I., & Krieger-Liszkay, A.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2016-06-02
- Volume
- 171
- Issue
- 3
- Pages
- 1541-1550
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2412650228
- Cited by
- 448
- References
- 73
- FWCI
- 18.36
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Dietz, K.-J., Turkan, I., & Krieger-Liszkay, A. (2016). Redox- and Reactive Oxygen Species-Dependent Signaling into and out of the Photosynthesizing Chloroplast. Plant Physiology. https://doi.org/10.1104/pp.16.00375
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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