Cyclic electron flow: facts and hypotheses

Cyclic electron flow around photosystem I is essential for photosynthesis

Munekage, Y. N., Hashimoto, M., Miyake, C., Tomizawa, K., Endo, T., Tasaka, M., & Shikanai, T. (2004) · Nature · doi:10.1038/nature02598 · Cited by 913 · see citing works

Cyclic Electron Transport Around Photosystem I: Genetic Approaches

Shikanai, T. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.58.091406.110525 · Cited by 567 · see citing works

Isolation of the elusive supercomplex that drives cyclic electron flow in photosynthesis

Iwai, M., Takizawa, K., Tokutsu, R., Okamuro, A., Takahashi, Y., & Minagawa, J. (2010) · Nature · doi:10.1038/nature08885 · Cited by 417 · see citing works

Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms

Bailleul, B., Berne, N., Murik, O., Petroutsos, D., Prihoda, J., Tanaka, A., Villanova, V., Bligny, R., Flori, S., Falconet, D., et al. (2015) · Nature · doi:10.1038/nature14599 · Cited by 381 · see citing works

C HLORORESPIRATION

Peltier, G., & Cournac, L. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.100301.135242 · Cited by 379 · see citing works

Cyclic electron transfer in plant leaf

Joliot, P. A., & Joliot, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.102306999 · Cited by 370 · see citing works

Photosynthesis of ATP—Electrons, Proton Pumps, Rotors, and Poise

Allen, J. F. (2002) · Cell · doi:10.1016/s0092-8674(02)00870-x · Cited by 318 · see citing works

NDH-1 and NDH-2 Plastoquinone Reductases in Oxygenic Photosynthesis

Peltier, G., Aro, E., & Shikanai, T. (2016) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043014-114752 · Cited by 304 · see citing works

Alternative Electron Flows (Water–Water Cycle and Cyclic Electron Flow Around PSI) in Photosynthesis: Molecular Mechanisms and Physiological Functions

Miyake, C. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq173 · Cited by 303 · see citing works

Physiology of PSI cyclic electron transport in higher plants

Johnson, G. N. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.11.009 · Cited by 278 · see citing works

Regulation of Photosynthetic Electron Transport and Photoinhibition

Roach, T., & Krieger‐Liszkay, A. (2014) · Current Protein and Peptide Science · doi:10.2174/1389203715666140327105143 · Cited by 270 · see citing works

Electrochromism: a useful probe to study algal photosynthesis

Bailleul, B., Cardol, P., Breyton, C., & Finazzi, G. (2010) · Photosynthesis Research · doi:10.1007/s11120-010-9579-z · Cited by 241 · see citing works

Calcium-dependent regulation of photosynthesis

Hochmal, A. K., Schulze, S., Trompelt, K., & Hippler, M. (2015) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2015.02.010 · Cited by 217 · see citing works

An Arabidopsis Mutant with High Cyclic Electron Flow around Photosystem I (hcef) Involving the NADPH Dehydrogenase Complex

Livingston, A. K., Cruz, J. A., Kohzuma, K., Dhingra, A., & Kramer, D. (2010) · The Plant Cell · doi:10.1105/tpc.109.071084 · Cited by 201 · see citing works

The Plastid Terminal Oxidase: Its Elusive Function Points to Multiple Contributions to Plastid Physiology

Nawrocki, W. J., Tourasse, N. J., Taly, A., Rappaport, F., & Wollman, F.-A. (2015) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043014-114744 · Cited by 187 · see citing works

Regulation of electron transport in microalgae

Cardol, P., Forti, G. C., & Finazzi, G. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.12.004 · Cited by 176 · see citing works

Quantification of cyclic and linear flows in plants

Joliot, P. A., & Joliot, A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501268102 · Cited by 174 · see citing works

State transitions, cyclic and linear electron transport and photophosphorylation in Chlamydomonas reinhardtii

Finazzi, G., Furia, A., Barbagallo, R. P., & Forti, G. C. (1999) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(99)00089-4 · Cited by 173 · see citing works

PGR5-PGRL1-Dependent Cyclic Electron Transport Modulates Linear Electron Transport Rate in Arabidopsis thaliana

Suorsa, M., Rossi, F., Tadini, L., Labs, M., Colombo, M., Jahns, P., Kater, M. M., Leister, D., Finazzi, G., Aro, E., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2015.12.001 · Cited by 143 · see citing works

Activation of cyclic electron flow by hydrogen peroxide in vivo

Strand, D. D., Livingston, A. K., Satoh-Cruz, M., Froehlich, J. E., Maurino, V. G., & Kramer, D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418223112 · Cited by 130 · see citing works

Alternative photosynthetic electron transport pathways during anaerobiosis in the green alga Chlamydomonas reinhardtii

Hemschemeier, A., & Happe, T. (2011) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2011.02.010 · Cited by 129 · see citing works

Redox Modulation of Cyclic Electron Flow around Photosystem I in C3 Plants

Breyton, C., Nandha, B., Johnson, G. N., Joliot, P. A., & Finazzi, G. (2006) · Biochemistry · doi:10.1021/bi061439s · Cited by 129 · see citing works

Dependence of plastoquinol diffusion on the shape, size, and density of integral thylakoid proteins

Tremmel, I., Kirchhoff, H., Weis, E., & Farquhar, G. D. (2003) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2003.09.004 · Cited by 100 · see citing works

Vitamin K as a cofactor of photosynthetic phosphorylation

Arnon, D. I., Whatley, F. R., & Allen, M. B. (1955) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(55)90295-x · Cited by 100 · see citing works

The Water to Water Cycles in Microalgae

Curien, G., Flori, S., Villanova, V., Magneschi, L., Giustini, C., Forti, G. C., Matringe, M., Petroutsos, D., Kuntz, M., & Finazzi, G. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw048 · Cited by 99 · see citing works

Induction events and short-term regulation of electron transport in chloroplasts: an overview

Tikhonov, A. N. (2015) · Photosynthesis Research · doi:10.1007/s11120-015-0094-0 · Cited by 96 · see citing works

Adjustments of embryonic photosynthetic activity modulate seed fitness in A rabidopsis thaliana

Allorent, G., Osorio, S., Vu, J. L., Falconet, D., Jouhet, J., Kuntz, M., Fernie, A. R., Lerbs‐Mache, S., Macherel, D., Courtois, F., et al. (2014) · New Phytologist · doi:10.1111/nph.13044 · Cited by 86 · see citing works

The End of the Line: Can Ferredoxin and Ferredoxin NADP(H) Oxidoreductase Determine the Fate of Photosynthetic Electrons?

Goss, T., & HANKE, G. T. (2014) · Current Protein and Peptide Science · doi:10.2174/1389203715666140327113733 · Cited by 75 · see citing works

Cyclic electron flow provides acclimatory plasticity for the photosynthetic machinery under various environmental conditions and developmental stages

Suorsa, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00800 · Cited by 74 · see citing works

Regulatory network of proton motive force: contribution of cyclic electron transport around photosystem I

Shikanai, T. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0227-0 · Cited by 68 · see citing works

Redox regulation of the antimycin A sensitive pathway of cyclic electron flow around photosystem I in higher plant thylakoids

Strand, D. D., Fisher, N. E., Davis, G. A., & Kramer, D. (2015) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2015.07.012 · Cited by 66 · see citing works

Obstacles in the quantification of the cyclic electron flux around Photosystem I in leaves of C3 plants

Fan, D., Fitzpatrick, D., Oguchi, R., Ma, W., Kou, J., & Chow, W. S. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0223-4 · Cited by 59 · see citing works

The antimycin A-sensitive pathway of cyclic electron flow: from 1963 to 2015

Labs, M., Rühle, T., & Leister, D. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0217-2 · Cited by 59 · see citing works

Complexities and protein complexes in the antimycin A-sensitive pathway of cyclic electron flow in plants

Leister, D., & Shikanai, T. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00161 · Cited by 56 · see citing works

Photoacclimation of photosynthesis in the Eustigmatophycean Nannochloropsis gaditana

Meneghesso, A., Simionato, D., Gerotto, C., Rocca, N. L., Finazzi, G., & Morosinotto, T. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0297-z · Cited by 49 · see citing works

Cytochrome b 6 f function and localization, phosphorylation state of thylakoid membrane proteins and consequences on cyclic electron flow

Dumas, L., Chazaux, M., Peltier, G., Johnson, X., & Alric, J. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0298-y · Cited by 49 · see citing works

Accumulation of the components of cyclic electron flow around photosystem I in C4 plants, with respect to the requirements for ATP

Ishikawa, N., Takabayashi, A., Sato, F., & Endo, T. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0251-0 · Cited by 36 · see citing works

Regulation of Electron Transport in Photosynthesis

Johnson, G. N., Cardol, P., Minagawa, J., & Finazzi, G. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1136-3_16 · Cited by 11 · see citing works

Far‐red photons have equivalent efficiency to traditional photosynthetic photons: Implications for redefining photosynthetically active radiation

Zhen, S., & Bugbee, B. G. (2020) · Plant Cell & Environment · doi:10.1111/pce.13730 · Cited by 279 · see citing works

Evolution of the Z-scheme of photosynthesis: a perspective

Jee, G., Shevela, D., & Björn, L. O. (2017) · Photosynthesis Research · doi:10.1007/s11120-016-0333-z · Cited by 149 · see citing works

Leaf Energy Balance Requires Mitochondrial Respiration and Export of Chloroplast NADPH in the Light

Shameer, S., Ratcliffe, R. G., & Sweetlove, L. J. (2019) · Plant Physiology · doi:10.1104/pp.19.00624 · Cited by 118 · see citing works

Hunting the main player enabling Chlamydomonas reinhardtii growth under fluctuating light

Jokel, M., Johnson, X., Peltier, G., Aro, E., & Allahverdiyeva, Y. (2018) · The Plant Journal · doi:10.1111/tpj.13897 · Cited by 118 · see citing works

Photosynthesis in sun and shade: the surprising importance of far‐red photons

Zhen, S., van Iersel, M. W., & Bugbee, B. G. (2022) · New Phytologist · doi:10.1111/nph.18375 · Cited by 94 · see citing works

Imaging the Photosystem I/Photosystem II chlorophyll ratio inside the leaf

Wientjes, E., Philippi, J., Borst, J. W., & van Amerongen, H. (2017) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2017.01.008 · Cited by 89 · see citing works

ATP compartmentation in plastids and cytosol of <i>Arabidopsis thaliana</i> revealed by fluorescent protein sensing

Voon, C. P., Guan, X., Sun, Y., Sahu, A., Chan, M. N., Gardeström, P., Wagner, S., Fuchs, P., Nietzel, T., Versaw, W. K., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1711497115 · Cited by 86 · see citing works

Antioxidant protection and PSII regulation mitigate photo-oxidative stress induced by drought followed by high light in cashew plants

de Lima, C. S., Ferreira‐Silva, S. L., Carvalho, F. E. L., Neto, M. C. L., de Aragão, R. M., da Silva, E. N., Sousa, R. M. J., & da Silveira, J. A. G. (2018) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2018.02.001 · Cited by 70 · see citing works

A Holistic Approach to Study Photosynthetic Acclimation Responses of Plants to Fluctuating Light

Gjindali, A., Herrmann, H. A., Schwartz, J., Johnson, G. N., & Calzadilla, P. I. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.668512 · Cited by 42 · see citing works

Sublocalization of Cytochrome b6f Complexes in Photosynthetic Membranes

Kirchhoff, H., Li, M., & Puthiyaveetil, S. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2017.04.004 · Cited by 40 · see citing works

The plastid-encoded PsaI subunit stabilizes photosystem I during leaf senescence in tobacco

Schöttler, M. A., Thiele, W., Belkius, K., Bergner, S. V., Flügel, C., Wittenberg, G., Agrawal, S., Stegemann, S., Ruf, S., & Bock, R. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx009 · Cited by 36 · see citing works

The regulation of P700 is an important photoprotective mechanism to NaCl‐salinity in Jatropha curcas

Cerqueira, J. V. A., Silveira, J. A. G., Carvalho, F. E. L., Cunha, J. R., & Neto, M. C. L. (2019) · Physiologia Plantarum · doi:10.1111/ppl.12908 · Cited by 34 · see citing works

Effects of thinning on the understory light environment of different stands and the photosynthetic performance and growth of the reforestation species Phoebe bournei

Su, S., Jin, N., & Wei, X. (2023) · Journal of Forestry Research · doi:10.1007/s11676-023-01651-0 · Cited by 29 · see citing works

Proteomic and physiological approaches reveal new insights for uncover the role of rice thylakoidal APX in response to drought stress

Cunha, J. R., Carvalho, F. E. L., Neto, M. C. L., Messeder, D. J., Cerqueira, J. V. A., Martins, M. O., Fontenele, A. V., Margis-Pinheiro, M. M. A. N., Komatsu, S., & da Silveira, J. A. G. (2018) · Journal of Proteomics · doi:10.1016/j.jprot.2018.08.014 · Cited by 25 · see citing works

Coupling physiological analysis with proteomic profile to understand the photosynthetic responses of young Euterpe oleracea palms to drought

de Oliveira, H. O., de Castro, G. L. S., Correa, L. O., Silvestre, W. V. D., do Nascimento, S. V., Valadares, R. B. D. S., Oliveira, G., Santos, R. I. N., Festucci-Buselli, R. A., & Pinheiro, H. A. (2018) · Photosynthesis Research · doi:10.1007/s11120-018-0597-6 · Cited by 23 · see citing works

An effector protein of Fusarium graminearum targets chloroplasts and suppresses cyclic photosynthetic electron flow

Jin, M., Hu, S. J., Wu, Q., Feng, X., Zhang, Y., Jiang, Q., Ma, J., Qi, P., Chen, G., Jiang, Y., et al. (2024) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiae538 · Cited by 19 · see citing works

Functional consequences of modification of the photosystem I/photosystem II ratio in the cyanobacterium Synechocystis sp. PCC 6803

Moore, V., & Vermaas, W. F. J. (2024) · Journal of Bacteriology · doi:10.1128/jb.00454-23 · Cited by 19 · see citing works

Photosynthetic Electron Flows and Networks of Metabolite Trafficking to Sustain Metabolism in Photosynthetic Systems

Fakhimi, N., & Grossman, A. R. (2024) · Plants · doi:10.3390/plants13213015 · Cited by 11 · see citing works

Opposite domination of cyclic and pseudocyclic electron flows in short-illuminated dark-adapted leaves of angiosperms and gymnosperms

Noridomi, M., Nakamura, S., Tsuyama, M., Futamura, N., & Vladkova, R. S. (2017) · Photosynthesis Research · doi:10.1007/s11120-017-0419-2 · Cited by 9 · see citing works

Development of a minimized model structure and a feedback control framework for regulating photosynthetic activities

Fu, L., Govindjee, G., Tan, J., & Guo, Y. (2019) · Photosynthesis Research · doi:10.1007/s11120-019-00690-1 · Cited by 9 · see citing works

Descriptive Table of Contents

(2017) · Functional Plant Biology · doi:10.1071/fpv44n10toc

Physiological Role of Cyclic Electron Flow in Higher Plants

Huang, W., Zhang, S., & Cao, K. (2012) · JOURNAL OF WUHAN BOTANICAL RESEARCH · doi:10.3724/sp.j.1142.2012.10100 · Cited by 4 · see citing works

Cyclic electron flow around photosystem I is essential for photosynthesis

Munekage, Y. N., Hashimoto, M., Miyake, C., Tomizawa, K., Endo, T., Tasaka, M., & Shikanai, T. (2004) · Nature · doi:10.1038/nature02598 · Cited by 913 · see citing works

Cyclic electron transfer in plant leaf

Joliot, P. A., & Joliot, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.102306999 · Cited by 370 · see citing works

The function of cyclic electron transport in photosynthesis

(1978) · FEBS Letters · doi:10.1016/0014-5793(78)80136-7 · Cited by 45 · see citing works