The DOI matches its Crossref record; 185 of the 185 references it cites were found in a registry or an index.
Evolution of Photosynthesis
Abstract
Energy conversion of sunlight by photosynthetic organisms has changed Earth and life on it. Photosynthesis arose early in Earth's history, and the earliest forms of photosynthetic life were almost certainly anoxygenic (non-oxygen evolving). The invention of oxygenic photosynthesis and the subsequent rise of atmospheric oxygen approximately 2.4 billion years ago revolutionized the energetic and enzymatic fundamentals of life. The repercussions of this revolution are manifested in novel biosynthetic pathways of photosynthetic cofactors and the modification of electron carriers, pigments, and existing and alternative modes of photosynthetic carbon fixation. The evolutionary history of photosynthetic organisms is further complicated by lateral gene transfer that involved photosynthetic components as well as by endosymbiotic events. An expanding wealth of genetic information, together with biochemical, biophysical, and physiological data, reveals a mosaic of photosynthetic features. In combination, these data provide an increasingly robust framework to formulate and evaluate hypotheses concerning the origin and evolution of photosynthesis.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The development of photosynthesis (photosystem I) ensued with solar photons exciting electrons from reaction centers in molecules like bacteriochlorophyll to split hydrogen sulfide, producing sulfur as a byproduct [24].”
From Opinion: The Key Steps in the Origin of Life to the Formation of the Eukaryotic Cell (2024) · cites this paper as [24]
Citations
Cites
Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism
MITCHELL, P. (1961) · Nature · doi:10.1038/191144a0 · Cited by 4,704
Methanogenic archaea: ecologically relevant differences in energy conservation
Thauer, R. K., Kaster, A.-K., Seedorf, H., Buckel, W., & Hedderich, R. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1931 · Cited by 2,184
Meteorites and the early solar system
(1989) · Choice Reviews Online · doi:10.5860/choice.26-4478 · Cited by 1,976
Nitrite-driven anaerobic methane oxidation by oxygenic bacteria
Ettwig, K. F., Butler, M. K., Paslier, D. L., Pelletier, É., Mangenot, S., Kuypers, M. M. M., Schreiber, F., Dutilh, B. E., Zedelius, J., de Beer, D., et al. (2010) · Nature · doi:10.1038/nature08883 · Cited by 1,864
Wilde, S. A., Valley, J. W., Peck, W. H., & Graham, C. M. (2001) · Nature · doi:10.1038/35051550 · Cited by 1,744 · cited 1×
“4 Gya to allow for rock formation (179).”
BackgroundThe oxygenation of the atmosphere and oceans
Holland, H. D. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1838 · Cited by 1,535
Bacterial Rhodopsin: Evidence for a New Type of Phototrophy in the Sea
Béjà, O., Aravind, L., Koonin, E. V., Suzuki, M. T., Hadd, A. G., Nguyen, L. P., Jovanovich, S. B., Gates, C. M., Feldman, R. A., Spudich, J. L., et al. (2000) · Science · doi:10.1126/science.289.5486.1902 · Cited by 1,532
Structure, function, and formation of biological iron-sulfur clusters
Johnson, D. C., Dean, D. R., Smith, A. D., & Johnson, M. K. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133518 · Cited by 1,438 · cited 1×
“FeS clusters (90) mediate electron transport in photosynthesis and respiration, including ferredoxins (4Fe-4S, 3Fe-4S, 2Fe-2S) and Rieske FeS clusters.”
BackgroundMargulis, L. (1981) · Cited by 1,399
A microbial consortium couples anaerobic methane oxidation to denitrification
Raghoebarsing, A. A., Pol, A., van de Pas-Schoonen, K. T., Smolders, A. J. P., Ettwig, K. F., Rijpstra, W. I. C., Stefan Schouten, A., Damsté, J. S. S., den Camp, H. J. M. O., Jetten, M. S. M., et al. (2006) · Nature · doi:10.1038/nature04617 · Cited by 1,364
Research works printed but not linked: 6
- Harrison JF, 2010, Philos. Trans. R. Soc. Lond. B, 277, 1937
- Martin W, 1999, Eur. J. Phycol., 34, 287
- Mereschkowsky C., 1905, Biol. Centralbl., 25, 593
- Meyer A., 1883, Bot. Zeit., 39, 841
- Oparin AI., 1924, Origins of Life: The Central Concepts, 31
- Schimper AFW., 1883, Bot. Zeit., 41, 105
Cited by
Sorted by citations
Items 501–600 of 744
Strieth, D., Kollmen, J., Stiefelmaier, J., Mehring, A., & Ulber, R. (2024) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2023_247 · Cited by 5
The Early Earth as an Analogue for Exoplanetary Biogeochemistry
Stüeken, E. E., Olson, S. L., Moore, E. K., & Foley, B. J. (2024) · Reviews in Mineralogy and Geochemistry · doi:10.2138/rmg.2024.90.14 · Cited by 5
Photosystem II Assembly from Scratch
Rühle, T., & Leister, D. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01234 · Cited by 5
Photosynthetic Light Harvesting
Mirkovic, T., & Scholes, G. D. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1468-5_17 · Cited by 6
Remembering John M. Olson (1929–2017)
Blankenship, R. E., Brune, D. C., & Olson, J. C. (2018) · Photosynthesis Research · doi:10.1007/s11120-018-0489-9 · Cited by 5
Self-citationProteome analysis of response to different spectral light irradiation in Synechocystis sp. PCC 6803
Toyoshima, M., Sakata, M., Ueno, Y., Toya, Y., Matsuda, F., Akimoto, S., & Shimizu, H. (2021) · Journal of Proteomics · doi:10.1016/j.jprot.2021.104306 · Cited by 5
Oxygen production potential of trees in urban areas: a reality check?
Ramanan, S. S., Osman, M., Shanker, A. K., & Sridhar, K. B. (2021) · Current Science · doi:10.18520/cs/v121/i5/622-625 · Cited by 5
Biogeochemistry and Global Change
Huertos, M. L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814266-0.00025-8 · Cited by 5
Gruszecki, W. I. (2013) · Advances in protein chemistry and structural biology · doi:10.1016/b978-0-12-416596-0.00003-8 · Cited by 5
Origin of Oxygenic Photosynthesis from Anoxygenic Type I and Type II Reaction Centers
Allen, J. F. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1148-6_14 · Cited by 5
A Timescale for the Radiation of Photosynthetic EukaryotesPreprint
Evanovich, E., Mattos, P. J. D. S. M., & Guerreiro, J. F. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.18.047969 · Cited by 5
Origin and Early Evolution of Photosynthesis: A Brief Historical AccountPreprint
Cardona, T. (2022) · Preprints.org · doi:10.20944/preprints202202.0031.v1 · Cited by 5
Brzezowski, P., & Grimm, B. (2013) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0020084.pub2 · Cited by 5
Ainsworth, E. A. (2018) · Agronomy monograph/Agronomy · doi:10.2134/agronmonogr60.2014.0035 · Cited by 6
Wang, L., Liu, H., Sun, Y., Wang, W., Li, C., Liu, Y., Liu, Z., Ji, R., Huang, S., Qu, G., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020732 · Cited by 4
Auderset, A., Smart, S. M., Ryu, Y., Marconi, D., Ren, H., Heins, L., Vonhof, H., Schiebel, R., Repschläger, J., Sigman, D. M., et al. (2025) · Biogeosciences · doi:10.5194/bg-22-1887-2025 · Cited by 4
Szymanski, E. A. (2023) · doi:10.1093/oso/9780197640319.001.0001 · Cited by 4
Stress on the Endoplasmic Reticulum Impairs the Photosynthetic Efficiency of Chlamydomonas
Chen, S., Li, S., Qian, S., Xing, J., Liao, J., & Guo, Z. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413304 · Cited by 4
Ecological diversity and metabolic strategies of widespread Marinisomatota in global oceans
Xiang, S., Li, J., Chen, Z., Cheng, R., Wang, L., Yu, L., Wei, G., Guan, X., Briggs, B. R., King, G. M., et al. (2025) · Marine Life Science & Technology · doi:10.1007/s42995-025-00293-x · Cited by 4
Coupling of the energetic and purinergic activities of ATP in ischemic and hypoxic disease states
Ehringer, W. D., & Smith, K. H. (2025) · Biosystems · doi:10.1016/j.biosystems.2025.105544 · Cited by 4
Effects of light regimes on circadian gene co‐expression networks in Arabidopsis thaliana
Rivière, Q., Raskin, V., de Melo, R., Boutet‐Mercey, S., Corso, M., Defrance, M., Webb, A. A. R., Verbruggen, N., & Anoman, A. D. (2024) · Plant Direct · doi:10.1002/pld3.70001 · Cited by 11
Facchinelli, F., & Weber, A. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1303-5_4 · Cited by 3
Perspectives for Photobiology in Molecular Solar Fuels
Hingorani, K., & Hillier, W. (2012) · Australian Journal of Chemistry · doi:10.1071/ch12096 · Cited by 4
Exploring the effects of photon correlations from thermal sources on bacterial photosynthesis
Manrique, P. D., Caycedo‐Soler, F., Mendoza, A. M. D., Rodríguez, F. J., Quiroga, L., & Johnson, N. F. (2016) · Results in Physics · doi:10.1016/j.rinp.2016.11.024 · Cited by 4
Chapter 5: Major Biological Innovations in the History of Life on Earth
Bozdag, G. O., Szeinbaum, N., Conlin, P. L., Chen, I. K., Fos, S. M., Garcia, A. K., Penev, P. I., Schaible, G. A., & Trubl, G. (2024) · Astrobiology · doi:10.1089/ast.2021.0119 · Cited by 5
Plastid Autonomy vs Nuclear Control Over Plastid Function
de Vries, J., & Archibald, J. M. (2017) · Advances in botanical research · doi:10.1016/bs.abr.2017.11.011 · Cited by 4
Astrobiologia: uma ciência emergente
Galante, D., Silva, E. P., Rodrigues, F., Horvath, J. E., & de Avellar, M. G. B. (2023) · doi:10.11606/9788566241037 · Cited by 5
Das, R. (2020) · Springer eBooks · doi:10.1007/978-3-030-11155-7_132-1 · Cited by 4
Global Self‐Similar Scaling of Terrestrial Carbon With Aridity
Yin, J., & Porporato, A. M. (2023) · Geophysical Research Letters · doi:10.1029/2022gl101040 · Cited by 4
Structure-based Hamiltonian model for IsiA uncovers a highly robust pigment–protein complex
Schoffman, H., Brown, W. M., Paltiel, Y., Keren, N., & Gauger, E. M. (2020) · Journal of The Royal Society Interface · doi:10.1098/rsif.2020.0399 · Cited by 4
Molecular Tools for Targeted Control of Nerve Cell Electrical Activity. Part I
Kolesov, D. V., Sokolinskaya, E. L., Lukyanov, K. A., & Bogdanov, A. M. (2021) · Acta Naturae · doi:10.32607/actanaturae.11414 · Cited by 4
A Hybrid Hmm/Autoregressive Time-Delay Neural Network Automatic Speech Recognition System
Selouani, S., & O’Shaughnessy, D. D. (2002) · INFM-OAR (INFN Catania) · doi:10.5281/zenodo.37758 · Cited by 4
Universal features shaping organelle gene retentionPreprint
Giannakis, K., Arrowsmith, S., Richards, L., Gasparini, S., Chustecki, J. M., Røyrvik, E., & Johnston, I. G. (2021) · bioRxiv · doi:10.1101/2021.10.27.465964 · Cited by 3
Cyanobacteria—the pioneering photoautotrophs
Sonam, S., & Dadheech, P. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13231-5.00019-2 · Cited by 3
Rathod, A. K., Shandul, A., & Manna, M. (2025) · Springer eBooks · doi:10.1007/978-981-97-9427-0_20 · Cited by 3
Рудольфовна, Л. Е., & Semin, B. К. (2022) · Origins of Life and Evolution of Biospheres · doi:10.1007/s11084-022-09625-8 · Cited by 3
Zhang, C., Wei, G., & Shu, D. (2022) · Applied Soil Ecology · doi:10.1016/j.apsoil.2022.104604 · Cited by 3
Ecophysiological characteristics of Rosa rugosa under different environmental factors
Kim, Y.-B., Yim, S.-H., Sim, Y. S., & Choo, Y. (2023) · Journal of Ecology and Environment · doi:10.5141/jee.23.040 · Cited by 3
Geographic and Ecological Diversity of Green Sulfur Bacteria in Hot Spring Mat Communities
Bedard, D. L., Slyke, G. V., Nübel, U., Bateson, M. M., Brumfield, S., An, Y. J., Becraft, E. D., Wood, J. M., Thiel, V., & Ward, D. M. (2023) · Microorganisms · doi:10.3390/microorganisms11122921 · Cited by 3
Huang, C., Liu, Y., Lü, J., Deng, X., Liu, Z., Molloy, D. P., Xiao, L., & Luo, Z. (2025) · Environmental Pollution · doi:10.1016/j.envpol.2025.126530 · Cited by 3
Survivability of Photosynthetic Bacteria In Non-Terrestrial Light
PD, J. N. M. (2015) · Journal of Astrobiology & Outreach · doi:10.4172/2332-2519.1000124 · Cited by 3
Insights into soybean with high photosynthetic efficiency
Xu, Q., Liu, X., Zhang, C., Weiguang, D., Guan, Y., & Yang, W. (2022) · Advances in botanical research · doi:10.1016/bs.abr.2022.02.019 · Cited by 3
A mini review on microwave and contemporary based biohydrogen production technologies: a comparison
Saxena, S., Rawat, S., Sasmal, S., & Shadangi, K. P. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-022-21979-0 · Cited by 3
A New Ecological and Evolutionary Perspective on the Emergence of Oxygenic Photosynthesis
Stevenson, D. S. (2022) · Astrobiology · doi:10.1089/ast.2021.0165 · Cited by 3
El papel de los azúcares como moléculas de señalización en las plantas
Hernández-Bernal, A. F., Gregorio-Jorge, J., & León, P. (2022) · TIP Revista Especializada en Ciencias Químico-Biológicas · doi:10.22201/fesz.23958723e.2022.519 · Cited by 4
Microalgae: A Solution for Food Security and Multiplanetary Farming
Xie, X., Zhan, J., & Ren, M. (2025) · Food Frontiers · doi:10.1002/fft2.70020 · Cited by 3
Heureux, A., Matsumoto, T. K., & Keith, L. M. W. (2022) · Algal Research · doi:10.1016/j.algal.2022.102640 · Cited by 3
Artificial respiration in severe COVID-19 cases - A beneficial or deleterious treatment
Müller, K. E. (2021) · Clinical Microbiology and Infectious Diseases · doi:10.15761/cmid.1000186 · Cited by 3
The Diversity of Photosynthetic Cytochromes
Majumder, E. L.-W., & Blankenship, R. E. (2016) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-7481-9_3 · Cited by 3
Self-citationUnique photosynthetic electron transport tuning and excitation distribution in heterokont algae
Røkke, G. B., Melø, T. B., Mühlroth, A., Vadstein, Ô., Bones, A. M., & Hohmann‐Marriott, M. F. (2019) · PLoS ONE · doi:10.1371/journal.pone.0209920 · Cited by 3
Self-citationMoving to the Light: The Evolution of Photosynthesis
Ligrone, R. (2019) · Springer eBooks · doi:10.1007/978-3-030-16057-9_4 · Cited by 3
Light-Regulated Nucleotide Second Messenger Signaling in Cyanobacteria
Enomoto, G., Wilde, A., & Ikeuchi, M. (2020) · Springer eBooks · doi:10.1007/978-3-030-33308-9_19 · Cited by 3
El‐Azazy, M., El‐Mammli, M. Y., Shalaby, A., & Ayad, M. M. (2008) · Chemia Analityczna · Cited by 3
Tuning the Photophysical Features of Self-Assembling Photoactive Polypeptides for Light-Harvesting
Michalik, M., Zbyradowski, M., Heriyanto, H., & Fiedor, L. (2019) · Materials · doi:10.3390/ma12213554 · Cited by 3
The Multifaceted Connections Between Photosynthesis and Respiratory Metabolism
da Fonseca‐Pereira, P., Batista‐Silva, W., Nunes‐Nesi, A., Zsögön, A., & Araújo, W. L. (2020) · Springer eBooks · doi:10.1007/978-981-15-5228-1_3 · Cited by 3
Zabret, J., & Nowaczyk, M. M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.28.450235 · Cited by 3
Substrate water binding to the oxygen-evolving complex in photosystem II
Nilsson, H. (2014) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 3
How to build a water-splitting machine: structural insights into photosystem II assemblyPreprint
Zabret, J., Bohn, S., Schuller, S. K., Arnolds, O., Möller, M., Meier‐Credo, J., Liauw, P., Chan, A., Tajkhorshid, E., Langer, J. D., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.14.294884 · Cited by 3
The Critical Impact of Photosynthetic Pathway of Plants on the Performance of PMFC
Gómora-Hernández, J. C., Flores‐Alamo, N., Díaz‐Colín, L. A., Ventura-Cruz, S., & Jiménez‐Cedillo, M. J. (2024) · doi:10.1002/9781394172337.ch5 · Cited by 3
Function, Structure and Organization of Light‐Harvesting Proteins in Diatoms
Volpe, C., & Büchel, C. (2024) · doi:10.1002/9781119842156.ch6 · Cited by 3
Simkovsky, R., & Carcellar, F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99982-3.00002-x · Cited by 2
The regulatory impact of serine/threonine-specific protein phosphorylation among cyanobacteria
Barske, T., & Hagemann, M. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1540914 · Cited by 2
Anoxygenic photoautotrophy driven by humus and microplastics in a photosynthetic bacterium
Li, Y., Qu, K., Yang, J., Wang, S., & Yan, Z. (2025) · ISME Communications · doi:10.1093/ismeco/ycaf067 · Cited by 2
Moran, J., Ilhardt, P. D., Couvillion, S., Lipton, M. S. W., Metz, T., Tolić, N., Bryant, D. A., & Ward, D. M. (2025) · Applied and Environmental Microbiology · doi:10.1128/aem.00909-25 · Cited by 4
The origin and evolution of HKT proteins with TrkH domain from aquatic plants to flowering plants
Li, P., Hu, R., Zhao, Y., Liu, W., Zhang, Q., Zheng, T., Wu, Y., & Huang, Y. (2025) · Horticulture Research · doi:10.1093/hr/uhaf245 · Cited by 2
Westall, F., Purvis, G., Sano, N., Sheriff, J., Clodoré, L., Foucher, F., & Milojević, T. (2025) · Nature Astronomy · doi:10.1038/s41550-025-02661-0 · Cited by 4
Russell, B. P., Kurashov, V. N., Iwig, D. F., Landry, P., Johnson, W., van der Est, A., Golbeck, J. H., Vinyard, D. J., & Lakshmi, K. V. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110827 · Cited by 2
Nanozymes to Enhance Plant Photosynthesis: Mechanisms, Applications, and Future Prospects
Zhang, Y., Tian, G., Lin, J. F., Fu, Y., & Li, Y. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c12837 · Cited by 2
Liu, X., Hu, Y.-Y., Li, K., Chen, M., & Wang, P. (2023) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2023.104600 · Cited by 2
The origins of photosynthetic systems: Clues from the phosphorus and sulphur chemical scenarios
Freire, M. Á. (2023) · Biosystems · doi:10.1016/j.biosystems.2023.104873 · Cited by 2
Past, Present and Future of Inorganic Carbon Assimilation
Wu, Y., & Rao, S. (2023) · Springer eBooks · doi:10.1007/978-981-99-4125-4_1 · Cited by 2
Gong, H., Zhou, Z., Bu, C., Zhang, D., Fang, Q., Zhang, X., & Song, Y. (2024) · BMC Genomics · doi:10.1186/s12864-024-09968-8 · Cited by 2
Subramanyam, R., Tomo, T., Eaton‐Rye, J. J., Yilmaz, G., & Allakhverdiev, S. I. (2024) · Photosynthesis Research · doi:10.1007/s11120-024-01087-5 · Cited by 2
The Evolutionary Origin of Primary Plastids
Lhee, D., Bhattacharya, D., & Yoon, H. S. (2024) · Springer eBooks · doi:10.1007/978-3-031-57446-7_1 · Cited by 2
Living to Lithified: Construction and Preservation of Silicified Biomarkers
Rasmussen, K. L., Thieringer, P. H., Nevadomski, S., Martinez, A. M., Dawson, K. S., Corsetti, F. A., Zheng, X., Lv, Y., Chen, X., Celestian, A. J., et al. (2024) · Geobiology · doi:10.1111/gbi.12620 · Cited by 2
Kwon, D. Y., Lee, S. H., Khim, J. S., Xu, X., Kim, B., Choi, I., Yoo, Y., & Kim, J. (2024) · Antonie van Leeuwenhoek · doi:10.1007/s10482-024-02044-x · Cited by 2
Li, Z., Yang, X., Yu, F., Jia, Y., Shu, R., Li, Y., Meng, X., Fei, J., Xu, X., & Li, J. (2025) · Small · doi:10.1002/smll.202504713 · Cited by 2
Li, Y., Li, S., Qu, K.-A., Yang, J., Wang, S., & Yan, Z. (2025) · Journal of Environmental Sciences · doi:10.1016/j.jes.2025.07.037 · Cited by 2
The photoaerogens: algae and plants reunited conceptually
Sanders, W. B. (2022) · American Journal of Botany · doi:10.1002/ajb2.1828 · Cited by 2
The C-Terminal Extension of Chloroplast 2-Cys Peroxiredoxin Is Critical for Interaction with ATP
Ferrero, D. S., Arán, M., Rimmaudo, L., & Wolosiuk, R. A. (2012) · Biochemistry · doi:10.1021/bi201843b · Cited by 2
Photosynthetic Apparatus in Cyanobacteria and Microalgae
Moro, I., Rocca, N. L., & Rascio, N. (2016) · Books in soils, plants, and the environment · doi:10.1201/b19498-27 · Cited by 2
Meehan, B. M., & Beckwith, J. R. (2017) · InTech eBooks · doi:10.5772/63342 · Cited by 3
Architecture, Structure and Function of the Energy Conversion Centers
Brinkert, K. (2018) · Springer series in chemical physics · doi:10.1007/978-3-319-77980-5_3 · Cited by 2
Ragni, R., Leone, G., Rizzo, G., la Gatta, S., Milano, F., Trotta, M., & Farinola, G. M. (2019) · MRS Advances · doi:10.1557/adv.2019.68 · Cited by 2
Structure and Function of Plant Light System
葛, 倩. (2019) · Botanical Research · doi:10.12677/br.2019.82023 · Cited by 2
Changes in ATP Sulfurylase Activity in Response to Altered Cyanobacteria Growth Conditions
Gastoldi, L., Ward, L. M., Nakagawa, M., Giordano, M., & McGlynn, S. E. (2021) · Microbes and Environments · doi:10.1264/jsme2.me20145 · Cited by 2
Barsanti, L., & Gualtieri, P. (2014) · CRC Press eBooks · doi:10.1201/b16544-4 · Cited by 2
Das, R. (2021) · Springer eBooks · doi:10.1007/978-3-030-36268-3_132 · Cited by 2
Grettenberger, C. L., Sumner, D. Y., Wall, K., Brown, C. T., Eisen, J. A., Mackey, T., Hawes, I., & Jungblut, A. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/334458 · Cited by 2
Structure of green type Rubisco activase from Nicotiana tabacum
Stotz, M. (2012) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.14494 · Cited by 2
Thinking Twice about the Evolution of PhotosynthesisPreprint
Cardona, T. (2018) · Preprints.org · doi:10.20944/preprints201812.0087.v1 · Cited by 3
Photosynthesis | The Phycobilisome
Adir, N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.21539-2 · Cited by 2
The Origin of Phototrophy Reveals the Importance of Priority Effects for Evolutionary InnovationPreprint
Burnetti, A., & Ratcliff, W. (2022) · Preprints.org · doi:10.20944/preprints202011.0700.v4 · Cited by 2
Харчук, И. А. (2019) · Issues of modern algology (Вопросы современной альгологии) · doi:10.33624/2311-0147-2019-3(21)-1-27 · Cited by 1
The diversity of physiology and metabolism in chlorophototrophic bacteria
White, I. S., Canniffe, D. P., & Hitchcock, A. (2025) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2025.02.003 · Cited by 2
Metabolomics: An Approach to Improve Production of Cyanobacterial Natural Products
Singh, V. K., Jha, S., Rana, P., Singh, A. P., Tripathi, R., Kumari, N., Häder, D., & Sinha, R. P. (2025) · Springer eBooks · doi:10.1007/978-981-96-7067-3_19 · Cited by 1
Ebadirad, S., Lyons, T. W., & Fournier, G. P. (2025) · Elsevier eBooks · doi:10.1016/b978-0-323-95547-8.00030-6 · Cited by 3
Secondary Metabolites of Cyanobacteria: A Focus on Nostoc Culture and Applications
Singh, S., & Srivastava, P. (2026) · Reference series in phytochemistry · doi:10.1007/978-3-031-80866-1_42-1 · Cited by 1
Guo, J.-P., Xu, F., Mao, R.-C., Bie, L., Liu, L., & Gao, J. (2026) · Physical Chemistry Chemical Physics · doi:10.1039/d5cp03498a · Cited by 1
Unlocking the potential of cyanobacterial metabolites: Novel antifungal therapies for the future
Kaviraj, M., Jayappriyan, K. R., & Raja, R. (2026) · Pharmacological Research - Natural Products · doi:10.1016/j.prenap.2026.100609 · Cited by 1
Metadata
- Authors
- Hohmann-Marriott, M. F., & Blankenship, R. E.
- Affiliations
- Department of Biochemistry, University of Otago, Dunedin 9016, New Zealand
- Washington University in St. Louis (US)
- Venue
- Annual Review of Plant Biology
- Publisher
- Annual Reviews
- Published
- 2011-06-02
- Volume
- 62
- Issue
- 1
- Pages
- 515-548
- ISSN
- 1543-5008 (ISSN-L)
- 1545-2123
- OpenAlex
- W2133071735
- Cited by
- 744
- References
- 185
- Citations by year
- 2026: 27 · 2025: 40 · 2024: 54 · 2023: 67 · 2022: 48 · 2021: 48 · 2020: 61 · 2019: 50 · 2018: 53 · 2017: 52 · 2016: 59 · 2015: 39 · 2014: 44 · 2013: 40 · 2012: 46
- FWCI
- 4.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Plant Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Metalloenzymes and iron-sulfur proteins
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
- Keywords
- evolution of photosynthesis, oxygenic photosynthesis, anoxygenic photosynthesis, Great Oxidation, electron carriers, photosynthetic pigments, photosynthetic carbon fixation, horizontal gene transfer, endosymbiosis, origin of photosynthesis, photosynthetic organisms
- MeSH terms
- Bacteria, Carbon, Chlorophyll, Electron Transport, Biological Evolution, Iron-Sulfur Proteins, Photosynthesis, Plant Proteins, Plants, Quinones, Sunlight, Symbiosis, Sensory Rhodopsins, Photosynthetic Reaction Center Complex Proteins
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