Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks

Oelze M-L, Kandlbinder A, Dietz K-J (2008)
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS 1780(11): 1261-1272.

Journal Article | Published | English

No fulltext has been uploaded

Abstract
Regulation of the photosynthetic apparatus between efficient energy conversion at low light and avoidance of overreduction and damage development at excess light resembles dangerous navigating between Scylla and Charybdis. Photosynthesis is a high rate redox metabolic pathway that generates redox intermediates with extreme redox potentials and eventually reactive oxygen species and oxidative stress. Therefore it is not surprising that the states of defined redox reactions in the chloroplast provide the predominant information and thus directly or indirectly the decisive signals for the multilevel control of cell activities in the chloroplast, cytoplasm, mitochondrion and nucleus. This review elaborates on the diversity of photosynthesis-derived redox signals such as the plastoquinone and thiol redox state that regulate and coordinate light use efficiency, electron transport activity, metabolic reactions, gene transcription and translation not only in the chloroplast but through retrograde signaling also essentially in all other cell compartments. The synergistic and antagonistic interrelations between the redox-dependent signaling pathways and their interactions with other signals such as abscisic acid and tetrapyrol intermediates constitute a redundant and probably buffered regulatory network to optimize performance of photosynthesis on the cellular and whole leaf level. (C) 2008 Elsevier B.V. All rights reserved.
Publishing Year
ISSN
PUB-ID

Cite this

Oelze M-L, Kandlbinder A, Dietz K-J. Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS. 2008;1780(11):1261-1272.
Oelze, M. - L., Kandlbinder, A., & Dietz, K. - J. (2008). Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1780(11), 1261-1272.
Oelze, M. - L., Kandlbinder, A., and Dietz, K. - J. (2008). Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS 1780, 1261-1272.
Oelze, M.-L., Kandlbinder, A., & Dietz, K.-J., 2008. Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1780(11), p 1261-1272.
M.-L. Oelze, A. Kandlbinder, and K.-J. Dietz, “Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks”, BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, vol. 1780, 2008, pp. 1261-1272.
Oelze, M.-L., Kandlbinder, A., Dietz, K.-J.: Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS. 1780, 1261-1272 (2008).
Oelze, Marie-Luise, Kandlbinder, Andrea, and Dietz, Karl-Josef. “Redox regulation and overreduction control in the photosynthesizing cell: Complexity in redox regulatory networks”. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS 1780.11 (2008): 1261-1272.
This data publication is cited in the following publications:
This publication cites the following data publications:

17 Citations in Europe PMC

Data provided by Europe PubMed Central.

Impacts of high ATP supply from chloroplasts and mitochondria on the leaf metabolism of Arabidopsis thaliana.
Liang C, Zhang Y, Cheng S, Osorio S, Sun Y, Fernie AR, Cheung CY, Lim BL., Front Plant Sci 6(), 2015
PMID: 26579168
System responses to equal doses of photosynthetically usable radiation of blue, green, and red light in the marine diatom Phaeodactylum tricornutum.
Valle KC, Nymark M, Aamot I, Hancke K, Winge P, Andresen K, Johnsen G, Brembu T, Bones AM., PLoS ONE 9(12), 2014
PMID: 25470731
Light acclimation in diatoms: from phenomenology to mechanisms.
Wilhelm C, Jungandreas A, Jakob T, Goss R., Mar Genomics 16(), 2014
PMID: 24412570
Sugarcane genes differentially expressed in response to Puccinia melanocephala infection: identification and transcript profiling.
Oloriz MI, Gil V, Rojas L, Portal O, Izquierdo Y, Jimenez E, Hofte M., Plant Cell Rep. 31(5), 2012
PMID: 22212461
Abiotic stress and the plant circadian clock.
Sanchez A, Shin J, Davis SJ., Plant Signal Behav 6(2), 2011
PMID: 21325898
Peroxiredoxins in plants and cyanobacteria.
Dietz KJ., Antioxid. Redox Signal. 15(4), 2011
PMID: 21194355
The chloroplastic 2-oxoglutarate/malate transporter has dual function as the malate valve and in carbon/nitrogen metabolism.
Kinoshita H, Nagasaki J, Yoshikawa N, Yamamoto A, Takito S, Kawasaki M, Sugiyama T, Miyake H, Weber AP, Taniguchi M., Plant J. 65(1), 2011
PMID: 21175886
The PedR transcriptional regulator interacts with thioredoxin to connect photosynthesis with gene expression in cyanobacteria.
Horiuchi M, Nakamura K, Kojima K, Nishiyama Y, Hatakeyama W, Hisabori T, Hihara Y., Biochem. J. 431(1), 2010
PMID: 20662766
Subcellular compartmentation of glutathione in dicotyledonous plants.
Zechmann B, Muller M., Protoplasma 246(1-4), 2010
PMID: 20186447
PGRL1 participates in iron-induced remodeling of the photosynthetic apparatus and in energy metabolism in Chlamydomonas reinhardtii.
Petroutsos D, Terauchi AM, Busch A, Hirschmann I, Merchant SS, Finazzi G, Hippler M., J. Biol. Chem. 284(47), 2009
PMID: 19783661
Sensing and responding to excess light.
Li Z, Wakao S, Fischer BB, Niyogi KK., Annu Rev Plant Biol 60(), 2009
PMID: 19575582

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Sources

PMID: 18439433
PubMed | Europe PMC

Search this title in

Google Scholar