Cited by 1,015Photosynthetic Processes and MechanismsAquatic Ecosystems and Phytoplankton DynamicsBiocrusts and Microbial Ecology

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PHOTOTROPHIC PROKARYOTES: THE CYANOBACTERIA

Stanier, R. Y., Cohen-Bazire, G.·1977·Annual Review of Microbiology

DOI 10.1146/annurev.mi.31.100177.001301

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Human coronavirus (HCoV) infection causes respiratory diseases with mild to severe outcomes. In the last 15 years, we have witnessed the emergence of two zoonotic, highly pathogenic HCoVs: severe acute respiratory syndrome coronavirus (SARS-CoV) and ...Read More

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Crossref · 10.1146/annurev.mi.31.100177.001301

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Purification and properties of NADP‐isocitrate dehydrogenase from the unicellular cyanobacterium Synechocystis sp. PCC 6803
MURO‐PASTOR, M. I., & FLORENCIO, F. J. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb19833.x · Cited by 74
Photosynthetic Acclimation of the Filamentous Cyanobacterium, Plectonema boryanum UTEX 485, to Temperature and Light
Miskiewicz, E. I., Ivanov, A. G., Williams, J. P., Khan, M. U., Falk, S., & Hüner, N. P. A. (2000) · Plant and Cell Physiology · doi:10.1093/pcp/41.6.767 · Cited by 73
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“CM Cyanobacteria are oxygenic photoautotrophic organisms adapted to a wide range of environments (Stanier and Cohen-Bazire, 1977).”
Background
Chloroplast-encoded chlB is required for light-independent protochlorophyllide reductase activity in Chlamydomonas reinhardtii.
Li, J., Goldschmidt‐Clermont, M., & Timko, M. P. (1993) · The Plant Cell · doi:10.1105/tpc.5.12.1817 · Cited by 73
The Developmental Biology of Heterocyst and Akinete Formation in Cyanobacteria
Adams, D. G., Carr, N. G., & Wilcox, M. (1981) · CRC Critical Reviews in Microbiology · doi:10.3109/10408418109104486 · Cited by 73
The role of carbohydrate accumulation in the growth of planktonic Oscillatoria species
Foy, R. H., & Smith, R. V. (1980) · British Phycological Journal · doi:10.1080/00071618000650161 · Cited by 76
Complementary iTRAQ proteomics and RNA-seq transcriptomics reveal multiple levels of regulation in response to nitrogen starvation in Synechocystis sp. PCC 6803
Huang, S., Chen, L., Te, R., Qiao, J., Wang, J., & Zhang, W. (2013) · Molecular BioSystems · doi:10.1039/c3mb70188c · Cited by 72
In vitro ferredoxin-dependent desaturation of fatty acids in cyanobacterial thylakoid membranes
Wada, H., Schmidt, H., Heinz, E., & Murata, N. (1993) · Journal of Bacteriology · doi:10.1128/jb.175.2.544-547.1993 · Cited by 72
“Since the structure and the lipid composition of cyanobacterial and chloroplast thylakoids are similar (11, 19), one might assume that Fd, Fd-NADP+ oxidoreductase, and NADPH constitute the electron-donating system for the desaturation of fatty acids in cyanobacteria.”
Background
Identification of a metabolic network structure representative of arthrospira (spirulina) platensis metabolism
Cogne, G., Gros, J. ‐., & Dussap, C. ‐. (2003) · Biotechnology and Bioengineering · doi:10.1002/bit.10808 · Cited by 71
“All the enzymes that mediate the reactions shown are synthesized under both light and dark growth conditions (Stanier and Cohen-Bazire, 1977).”
Background
The NADP+-isocitrate dehydrogenase gene (icd) is nitrogen regulated in cyanobacteria
Muro‐Pastor, M. I., Reyes, J. C., & Florencio, F. J. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.14.4070-4076.1996 · Cited by 71
“Cyanobacteria are photosynthetic prokaryotes that have an incomplete tricarboxylic acid cycle, lacking a-ketoglutarate dehydrogenase and succinyl-coenzyme A synthetase activities (46, 54).”
Background
Biogenically Formed Aragonite Concretions in Marine Rivularia
Golubić, S., & Campbell, S. E. (1981) · Springer eBooks · doi:10.1007/978-3-642-67913-1_16 · Cited by 72
Photosynthetic Characteristics of Picoplankton Compared with Those of Larger Phytoplankton Populations, in Various Water Masses in the Gulf of Maine
Glover, H. E., Phinney, D. A., & Yentsch, C. S. (2013) · Biological Oceanography · doi:10.1080/01965581.1985.10749474 · Cited by 71
Assembly of cyanobacterial and higher plant ribulose bisphosphate carboxylase subunits into functional homologous and heterologous enzyme molecules in Escherichia coli
van der Vies, S. M., Bradley, D., & Gatenby, A. A. (1986) · The EMBO Journal · doi:10.1002/j.1460-2075.1986.tb04519.x · Cited by 71
Effects of light on the electrical output of bioelectrochemical fuel‐cells containing Anabaena variabilis M‐2: Mechanism of the post‐illumination burst
Tanaka, K., Kashiwagi, N., & Ogawa, T. (1988) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.280420307 · Cited by 70
Evidence for plastoquinol-cytochrome fb-563 reductase as a common electron donor to P700 and cytochrome oxidase in cyanobacteria
Peschek, G. A., & Schmetterer, G. (1982) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(82)92126-x · Cited by 70
Respiration and photosynthesis in energy-transducing membranes of cyanobacteria
Binder, A. (1982) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf00743057 · Cited by 70
Simultaneous heterolactic and acetate fermentation in the marine cyanobacterium Oscillatoria limosa incubated anaerobically in the dark
Heyer, H., Stal, L. J., & Krumbein, W. E. (1989) · Archives of Microbiology · doi:10.1007/bf00454875 · Cited by 69
“The predominant mode of cyanobacterial metabolism is oxygenic photosynthesis ( Stanier and Cohen-Bazire 1977 ).”
Background
Nitrogen limitation and recovery in the cyanobacterium Aphanocapsa 6308
Allen, M. M., & Hutchison, F. (1980) · Archives of Microbiology · doi:10.1007/bf00422297 · Cited by 68
“It is possible that some CGP may serve as an energy reserve capable of providing ATP (Stanier and Cohen-Bazire, 1977) since the arginine dihydrolase pathway producing ATP, CO2, NH3 and ornithine from arginine has been shown to be present in Aphanocapsa 6308 (Weathers et al.”
Background
Effect of UV-B on Enzymes of Nitrogen Metabolism in the Cyanobacterium Nostoc calcicola
Kumar, A., Sinha, R. P., & Häder, D. (1996) · Journal of Plant Physiology · doi:10.1016/s0176-1617(96)80298-7 · Cited by 69
Studies on well coupled Photosystem I-enriched subchloroplast vesicles. Content and redox properties of electron-transfer components
Peters, F. A. L. J., Wielink, J. E. V., Sang, H. W. W. F., et al. (1983) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(83)90062-2 · Cited by 69
Biotechnological applications of cyanobacterial phycobiliproteins
Pandey, V., Pandey, A., & Sharma, V. (2013) · Cited by 68
Proteome Mapping of a Cyanobacterium Reveals Distinct Compartment Organization and Cell-Dispersed Metabolism
Baers, L. L., Breckels, L. M., Mills, L. A., Gatto, L., Deery, M. J., Stevens, T. J., Howe, C. J., Lilley, K. S., & Lea‐Smith, D. J. (2019) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.00897 · Cited by 67
“59 The cell envelope is similar to other Gram-negative bacteria, consisting of the PM, 60 peptidoglycan layer and outer membrane (OM) (Stanier and Cohen-Bazire, 1977) 61 (Fig.”
Background
Roles for heme–copper oxidases in extreme high-light and oxidative stress response in the cyanobacterium Synechococcus sp. PCC 7002
Nomura, C. T., Sakamoto, T., & Bryant, D. A. (2006) · Archives of Microbiology · doi:10.1007/s00203-006-0107-7 · Cited by 68
“Cyanobacteria are photosynthetic, oxygen-evolving prokaryotes that share some electron transport proteins for both photosynthesis and respiration, and have adapted to a wide range of ecological niches (Stanier and Cohen-Bazire 1977).”
Background
Tissue loss (white syndrome) in the coral Montipora capitata is a dynamic disease with multiple host responses and potential causes
Work, T. M., Russell, R. E., & Aeby, G. S. (2012) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2012.1827 · Cited by 67
Enzyme Activities Related to Cyanophycin Metabolism in Heterocysts and Vegetative Cells of Anabaena spp.
GUPTA, M., & Carr, N. G. (1981) · Microbiology · doi:10.1099/00221287-125-1-17 · Cited by 67
The Structure of Bacteria
Beveridge, T. J. (1989) · Springer eBooks · doi:10.1007/978-1-4613-0803-4_1 · Cited by 71
Mycosporine-like amino acids (MAAs) profile of a rice-field cyanobacterium Anabaena doliolum as influenced by PAR and UVR
Singh, S. P., Sinha, R. P., Klisch, M., & Häder, D. (2008) · Planta · doi:10.1007/s00425-008-0822-1 · Cited by 66
Insights into isoprene production using the cyanobacterium Synechocystis sp. PCC 6803
Pade, N., Erdmann, S., Enke, H., Dethloff, F., Dühring, U., Georg, J., Wambutt, J., Kopka, J., Hess, W. R., Zimmermann, R., et al. (2016) · Biotechnology for Biofuels · doi:10.1186/s13068-016-0503-4 · Cited by 64
“In addition to sunlight as an energy source for carbon assimilation, cyanobacteria require only water and inorganic and trace nutrients for growth [2].”
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Composition and biological properties of lipopolysaccharides isolated from Schizothrix calcicola (Ag.) Gomont (Cyanobacteria)
Keleti, G., Sýkora, J., Lippy, E. C., et al. (1979) · Applied and Environmental Microbiology · doi:10.1128/aem.38.3.471-477.1979 · Cited by 66
“Even though Stanier and Cohen-Bazire (23) have shown that cyanobacterial cells contain a peptidoglycan layer which varies in width with different species, our data indicate that this constituent probably occurs in S.”
Background
New trends in photobiology
Reuter, W., & Müller, C. (1993) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/1011-1344(93)80159-7 · Cited by 66
The Effects of Methyl Viologen on Gloeocapsa sp. LB795 and Their Relationship to the Inhibition of Acetylene Reduction (Nitrogen Fixation) by Oxygen
Tozum, S. R. D., & Gallon, J. (1979) · Journal of General Microbiology · doi:10.1099/00221287-111-2-313 · Cited by 66
Photosynthetic Accessory Proteins with Bilin Prosthetic Groups
Glazer, A. N. (1981) · Elsevier eBooks · doi:10.1016/b978-0-12-675408-7.50008-2 · Cited by 66
The research progress of CO2 sequestration by algal bio-fertilizer in China
Wang, R., Peng, B., & Huang, K. (2015) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2015.01.007 · Cited by 65
The ultrastructure of Spirulina platensis in relation to temperature and light intensity
van Eykelenburg, C. (1979) · Antonie van Leeuwenhoek · doi:10.1007/bf00443277 · Cited by 66
Different organization of nif genes in nonheterocystous and heterocystous cyanobacteria
Kallas, T., Coursin, T., & Rippka, R. (1985) · Plant Molecular Biology · doi:10.1007/bf00020630 · Cited by 65
“Cyanobacteria (blue-green algae) are a diverse and ancient group of prokaryotes that perform oxygenic ('higher-plant style') photosynthesis for their generation of energy and reducing power ( 30 ).”
Background
Magnesium chelatase from Rhodobacter sphaeroides: initial characterization of the enzyme using purified subunits and evidence for a BchI–BchD complex
Gibson, L. C. D., Jensen, P. E., & Hunter, C. N. (1999) · Biochemical Journal · doi:10.1042/bj3370243 · Cited by 65
Electron Transport Regulates Cellular Differentiation in the Filamentous Cyanobacterium Calothrix.
Campbell, D. A., Houmard, J., & de Marsac, N. T. (1993) · The Plant Cell · doi:10.1105/tpc.5.4.451 · Cited by 65
“The cyanobacteria are an ancient group of oxygenic photoautotrophic prokaryotes (Stanier and Cohen-Bazire, 1977).”
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Cyanospira rippkae and Cyanospira capsulata (gen. nov. and spp. nov.): new filamentous heterocystous cyanobacteria from Magadi lake (Kenya)
Florenzano, G., Sili, C., Pelosi, E., & VINCENZINI, M. T. (1985) · Archives of Microbiology · doi:10.1007/bf00446967 · Cited by 64
Genomic analysis of protein kinases, protein phosphatases and two-component regulatory systems of the cyanobacterium Anabaena sp. strain PCC 7120
Wang, L., Sun, Y., Chen, W., Li, J., & Zhang, C. (2002) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2002.tb11469.x · Cited by 66
“Among prokaryotes, many ¢lamentous cyanobacteria are exceptional in their ability to carry out a variety of important biological functions, including plant-like photosynthesis, nitrogen ¢xation, multicellular behavior and signaling, and cell di¡erentiation [1].”
Background
The Co-Evolution Aspects of the Biogeochemical Role of Phytoplankton in Aquatic Ecosystems: A Review
Lobus, N. V., & Kulikovskiy, M. S. (2023) · Biology · doi:10.3390/biology12010092 · Cited by 67
“Therefore, the content of Fe in the aquatic environment and its bioavailability for diazotrophs are important for the functioning of both aquatic and global biogeochemical nitrogen cycles [45,46].”
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The biological functions of microcystins
Wei, N., Hu, C., Dittmann, E., Song, L., & Gan, N. (2024) · Water Research · doi:10.1016/j.watres.2024.122119 · Cited by 72
ABC‐type amino acid uptake transporters Bgt and N‐II of Anabaena sp. strain PCC 7120 share an ATPase subunit and are expressed in vegetative cells and heterocysts
Pernil, R., Picossi, S., Mariscal, V., Antonia Herrero, B., & Flores, E. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06107.x · Cited by 63
Toxin Release of Cyanobacterium Microcystis aeruginosa after Exposure to Typical Tetracycline Antibiotic Contaminants
Ye, J., Du, Y., Wang, L., Qian, J., Chen, J., Wu, Q., & Hu, X. (2017) · Toxins · doi:10.3390/toxins9020053 · Cited by 63
“Because their cell structure is similar to bacteria [12], cyanobacteria are generally more sensitive to antibiotic contaminants compared with other algal species, and it can be served as an indicator species of water toxicity [13].”
Background
A Panoply of Phototrophs: An Overview of the Thermophilic Chlorophototrophs of the Microbial Mats of Alkaline Siliceous Hot Springs in Yellowstone National Park, WY, USA
Tank, M., Thiel, V., Ward, D. M., & Bryant, D. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-46261-5_3 · Cited by 69
Nucleotide sequence and further characterization of the Synechococcus sp. strain PCC 7002 recA gene: complementation of a cyanobacterial recA mutation by the Escherichia coli recA gene
Murphy, R. C., Gasparich, G. E., Bryant, D. A., & Porter, R. D. (1990) · Journal of Bacteriology · doi:10.1128/jb.172.2.967-976.1990 · Cited by 64
“some species are able to fix atmospheric nitrogen (43).”
Background
Increased ethylene production by overexpressing phosphoenolpyruvate carboxylase in the cyanobacterium Synechocystis PCC 6803
Durall, C., Lindberg, P., Yu, J., & Lindblad, P. C. (2020) · Biotechnology for Biofuels · doi:10.1186/s13068-020-1653-y · Cited by 62
Ultraviolet-B-induced DNA damage and photorepair in the cyanobacterium Anabaena variabilis PCC 7937
Rastogi, R. P., Singh, S. P., Häder, D., & Sinha, R. P. (2011) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2011.06.010 · Cited by 62
Chromatic photoacclimation extends utilisable photosynthetically active radiation in the chlorophyll d-containing cyanobacterium, Acaryochloris marina
Duxbury, Z., Schliep, M., Ritchie, R. J., Larkum, A. W. D., & Chen, M. (2009) · Photosynthesis Research · doi:10.1007/s11120-009-9466-7 · Cited by 62
“Cyanobacteria are oxygenic photosynthetic prokaryotes and typically contain Chl a as their only chlorophyll pigment, as well as carotenoids and phycobilins as accessory pigments (Stanier and Bazine 1977; Blankenship 2002).”
Background
7 Lipid Analysis and the Relationship to Chemotaxonomy
Tornabene, T. G. (1985) · Methods in microbiology · doi:10.1016/s0580-9517(08)70476-8 · Cited by 62
Cyclic appearance of aerobic nitrogenase activity during synchronous growth of unicellular cyanobacteria
León, C., Kumazawa, S., & Mitsui, A. (1986) · Current Microbiology · doi:10.1007/bf01568510 · Cited by 62
Cyanobacteria as Photosynthetic Biocatalysts: A Systems Biology Perspective
Gudmundsson, S., & Nogales, J. (2014) · Molecular BioSystems · doi:10.1039/c4mb00335g · Cited by 61
Interaction of fructose with the glucose permease of the cyanobacterium Synechocystis sp. strain PCC 6803
Flores, E., & Schmetterer, G. (1986) · Journal of Bacteriology · doi:10.1128/jb.166.2.693-696.1986 · Cited by 61
“Photoheterotrophy is best demonstrated by growing sugar-supplemented cultures in the presence of the herbicide dichlorophenyl dimethylurea (DCMU), which, at appropriate concentrations, completely blocks the activity of photosystem II but leaves photosystem I functional (14, 19).”
Background
DIFFERENTIAL EFFECT OF ULTRAVIOLET‐B RADIATION ON CERTAIN METABOLIC PROCESSES IN A CHROMATICALLY ADAPTING Nostoc
Tyagi, R., Srinivas, G., Vyas, D., Kumar, A., & Kumar, H. D. (1992) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1992.tb04254.x · Cited by 61
“Nitrogenase activity was measured by the acetylene reduction technique (Stewart era/., 1968). The ethylene formed was determined at intervals lasting up to 3 h in a CIC (Baroda) gas chromatograph fitted with a Porapak-R column and flame ionization detector. Nitrate reductase activity. I n vivo nitrate reductase activi…”
MethodInfluential
Late D evonian marine anoxia challenged by benthic cyanobacterial mats
Kaźmierczak, J., Kremer, B., & Racki, G. (2012) · Geobiology · doi:10.1111/j.1472-4669.2012.00339.x · Cited by 60
Transcriptional analysis of the cyanobacterial gvpABC operon in differentiated cells: occurrence of an antisense RNA complementary to three overlapping transcripts
Csiszár, K., Houmard, J., Damerval, T., et al. (1987) · Gene · doi:10.1016/0378-1119(87)90210-1 · Cited by 60
Analogous microbial forms in recent subaerial habitats and in Precambrian cherts: Gloethece coerulea Geitler and Eosynechococcus moorei Hofmann
Golubić, S., & Campbell, S. E. (1979) · Precambrian Research · doi:10.1016/0301-9268(79)90029-9 · Cited by 60
Characterization of the cytochrome c oxidase in isolated and purified plasma membranes from the cyanobacterium Anacystis nidulans
Peschek, G. A., Wastyn, M., Trnka, M., et al. (1989) · Biochemistry · doi:10.1021/bi00433a048 · Cited by 60
Nitrogen Fixation in Cyanobacteria
Stal, L. J. (2015) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0021159.pub2 · Cited by 60
Gliding movements in Myxococcus xanthus
Spormann, A. M., & Kaiser, A. D. (1995) · Journal of Bacteriology · doi:10.1128/jb.177.20.5846-5852.1995 · Cited by 59
“Gliding, the movement of a bacterial cell in the direction of its long axis on a surface (14), is found in many distantly related microbes like cyanobacteria (39), green sulfur bacteria (33), and chemoheterotrophic bacteria (9, 35).”
Background
The ferredoxin/thioredoxin system of enzyme regulation in a cyanobacterium
Yee, B. C., de la Torre, A., Crawford, N. A., et al. (1981) · Archives of Microbiology · doi:10.1007/bf00527065 · Cited by 59
Supramolecular structure of stacked and unstacked regions of the photosynthetic membranes of Prochloron sp., a prokaryote
Giddings, T. H., Withers, N. W., & Staehelin, L. A. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.1.352 · Cited by 59
Cyanobacterial plasmids: Their widespread occurrence, and the existence of regions of homology between plasmids in the same and different species
Lau, R. H., Sapienza, C., & Doolittle, W. F. (1980) · Molecular and General Genetics MGG · doi:10.1007/bf00267230 · Cited by 59
“Although cyanobacterial physiology and ecology are well-developed academic disciplines, cyanobacterial molecular biology and genetics are not (for reviews see Carr and Whitton, 1973 ; Fogg et al., 1973 ; Delaney et al., 1976 ;Stanier and Cohen-Bazire, 1977 ; Doolittle, 1979).”
Background
Live-cell imaging of cyanobacteria
Yokoo, R., Hood, R. D., & Savage, D. F. (2014) · Photosynthesis Research · doi:10.1007/s11120-014-0049-x · Cited by 54
Photoautotrophic Polyhydroxybutyrate Granule Formation Is Regulated by Cyanobacterial Phasin PhaP in Synechocystis sp. Strain PCC 6803
Hauf, W., Watzer, B., Roos, N., Klotz, A., & Forchhammer, K. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00604-15 · Cited by 58
“ATP and reduction equivalents derived from photosynthetic electron flow are utilized to fix carbon dioxide and generate 3-phosphoglycerate (1).”
Method
An increase in the level of 2-oxoglutarate promotes heterocyst development in the cyanobacterium Anabaena sp. strain PCC 7120
Li, J., Laurent, S., Konde, V. B., et al. (2003) · Microbiology · doi:10.1099/mic.0.26462-0 · Cited by 58
Molecular Characterization of a Thermostable Cyanophycin Synthetase from the Thermophilic Cyanobacterium Synechococcus sp. Strain MA19 and In Vitro Synthesis of Cyanophycin and Related Polyamides
Hai, T., Oppermann‐Sanio, F. B., & Steinbüchel, A. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.1.93-101.2002 · Cited by 58
“Under strictly anaerobic conditions ATP is formed during ornithine formation from arginine (33).”
Background
An iTRAQ-Based Quantitative Analysis To Elaborate the Proteomic Response of Nostoc sp. PCC 7120 under N2 Fixing Conditions
Stensjö, K., Ow, S. Y., Barrios-Llerena, M. E., et al. (2007) · Journal of Proteome Research · doi:10.1021/pr060517v · Cited by 58
Prokaryotic and Highly-Repetitive WD40 Proteins: A Systematic Study
Hu, X.-J., Li, T., Wang, Y., Xiong, Y., Wu, X., Zhang, D., Ye, Z., & Wu, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-11115-1 · Cited by 55
Active transport of ferric schizokinen in Anabaena sp
Lammers, P. J., & Sanders–Loehr, J. (1982) · Journal of Bacteriology · doi:10.1128/jb.151.1.288-294.1982 · Cited by 57
“Because membrane level phosphorylation is the only known mechanism for ATP synthesis in cyanobacteria (25), it has not been possible to determine whether the inhibition caused by uncouplers and electron transport inhibitors is due only to interference with ATP formation or whether a membrane potential is also required…”
Background
Phosphorus-31 nuclear magnetic resonance analysis of internal pH during photosynthesis in the cyanobacterium Synechococcus
Kallas, T., & Dahlquist, F. W. (1981) · Biochemistry · doi:10.1021/bi00523a038 · Cited by 57
Recent advances in in situ oxygen-generating and oxygen-replenishing strategies for hypoxic-enhanced photodynamic therapy
Qin, S., Xu, Y., Li, H., Chen, H., & Yuan, Z. (2022) · Biomaterials Science · doi:10.1039/d1bm00317h · Cited by 56
Genome-wide comparative analysis of metacaspases in unicellular and filamentous cyanobacteria
Jiang, Q., Qin, S., & Wu, Q. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-198 · Cited by 56
“5 billion years, based on the fossil evidence [1].”
Background
Gene Expression during Heterocyst Differentiation
Herrero, A., Picossi, S., & Flores, E. (2012) · Advances in botanical research · doi:10.1016/b978-0-12-394313-2.00008-1 · Cited by 56
Identification of facultatively heterotrophic, N2-fixing cyanobacteria able to receive plasmid vectors from Escherichia coli by conjugation
Flores, E., & Wölk, C. P. (1985) · Journal of Bacteriology · doi:10.1128/jb.162.3.1339-1341.1985 · Cited by 56
“Cyanobacteria are unique in that they are procaryotes that are able to perform oxygenic photosynthesis (14, 15).”
Background
Genes encoding core components of the phycobilisome in the cyanobacterium Calothrix sp. strain PCC 7601: occurrence of a multigene family
Houmard, J., Capuano, V., Coursin, T., et al. (1988) · Journal of Bacteriology · doi:10.1128/jb.170.12.5512-5521.1988 · Cited by 56
“Tyr UAC 88 (61) 8 (100) 7 (87) 11 (92) 1 (100) UAU 56 (39) 0 1 (12) 1 (8) 0”
Background
The pyruvate: Ferredoxin oxidoreductase in heterocysts of the cyanobacteriuim Anabaena cylindrica
Neuer, G., & Bothe, H. (1982) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/0304-4165(82)90028-9 · Cited by 56
Stimulation effects of ciprofloxacin and sulphamethoxazole in Microcystis aeruginosa and isobaric tag for relative and absolute quantitation‐based screening of antibiotic targets
Liu, Y., Chen, S., Zhang, J., et al. (2016) · Molecular Ecology · doi:10.1111/mec.13934 · Cited by 55
“With a Gram-negative bacteria-like structure (Stanier & Cohen-Bazire 1977), the prokaryotic microalgae cyanobacteria are the most vulnerable to antibiotic exposure.”
Background
The Cyanobacteria—Ecology, Physiology and Molecular Genetics
Cohen, Y., & Gurevitz, M. (2006) · Springer eBooks · doi:10.1007/0-387-30744-3_39 · Cited by 55
Growth Phase-dependent Activation of Nitrogen-related Genes by a Control Network of Group 1 and Group 2 σ Factors in a Cyanobacterium
Imamura, S., Tanaka, K., Shirai, M., & Asayama, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509639200 · Cited by 55
Identification of PamA as a PII-binding Membrane Protein Important in Nitrogen-related and Sugar-catabolic Gene Expression in Synechocystis sp. PCC 6803
Osanai, T., Sato, S., Tabata, S., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507489200 · Cited by 55
Occurrence and distribution of gas vesicle genes among cyanobacteria
Damerval, T., Castets, A. M., Guglielmi, G., et al. (1989) · Journal of Bacteriology · doi:10.1128/jb.171.3.1445-1452.1989 · Cited by 55
“Depending on environmental conditions, vegetative filaments of the latter can differentiate into hormogonia which are distinguishable from mature trichomes by their size and cell shape and, in many strains, by their gliding motility and the transient production of GV (23, 25, 28).”
Background
PIGMENT AND PHOTOSYNTHETIC RESPONSES OF OSCILLATORIA AGARDHII (CYANOPHYTA) TO PHOTON FLUX DENSITY AND SPECTRAL QUALITY1
Millie, D. F., Ingram, D. A., & Dionigi, C. P. (1990) · Journal of Phycology · doi:10.1111/j.0022-3646.1990.00660.x · Cited by 55
Electron transport reactions in respiratory particles of hydrogenase-induced Anacystis nidulans
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Iron isotope fractionation during Fe(II) and Fe(III) adsorption on cyanobacteria
Mulholland, D. S., Poitrasson, F., Shirokova, L. S., González, A. G., Сергеевич, П. О., Boaventura, G. R., & Vieira, L. C. (2015) · Chemical Geology · doi:10.1016/j.chemgeo.2015.01.017 · Cited by 54
Lipid and lipopolysaccharide constituents of cyanobacterium Spirulina platensis (Cyanophyceae, Nostocales)
Tornabene, T. G., Bourne, T., Raziuddin, S., & Ben‐Amotz, A. (1985) · Marine Ecology Progress Series · doi:10.3354/meps022121 · Cited by 54
“They contain lipopolysaccharides (LPS) (Weise et al. 1970, Weckesser et al. 1974, Stanier & Cohen-Bazire 1977, Weckesser et al. 1979, Keleti et al. 1981) that are characteristic of most Gram-negative bacteria and well recognized as an endotoxic and antigenic component of the cell wall.”
Background
The Oceanic Cyanobacterial Picoplankton
Carr, N. G., & Mann, N. H. (1994) · Springer eBooks · doi:10.1007/978-94-011-0227-8_2 · Cited by 54
“It is in marked contrast to the wide range found among the freshwater plankton and represents only a tiny proportion of the ‘largest and most diverse group of prokaryotes’ to use the now well known phrase of Stanier and Cohen-Bazire (1977) .”
Background
Cytochrome c-553 is not required for photosynthetic activity in the cyanobacterium Synechococcus.
Laudenbach, D. E., Herbert, S., McDowell, C., et al. (1990) · The Plant Cell · doi:10.1105/tpc.2.9.913 · Cited by 54
Day and Night: Metabolic Profiles and Evolutionary Relationships of Six Axenic Non-Marine Cyanobacteria
Will, S. E., Henke, P., Boedeker, C., Huang, S., Brinkmann, H., Rohde, M., Jarek, M., Friedl, T., Seufert, S., Schumacher, M., et al. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy275 · Cited by 53
AKINETE GERMINATION IN ANABAENA CIRCINALIS (CYANOPHTA)
van Dok, W., & Hart, B. T. (1997) · Journal of Phycology · doi:10.1111/j.0022-3646.1997.00012.x · Cited by 53
The isocitrate dehydrogenase from cyanobacteria
Papen, H., Neuer, G., Refaian, M., et al. (1983) · Archives of Microbiology · doi:10.1007/bf00429411 · Cited by 53
“The citric acid cycle is incomplete as an enzyme catalyzing the cleavage of oxoglutarate is absent in these organisms (Stanier and Cohen-Bazire 1977).”
Background
Aerobic hydrogenase activity in Anacystis Nidulans The oxyhydrogen reaction
Peschek, G. A. (1979) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(79)90129-4 · Cited by 53
Cyanobacteria-Based Bio-Oxygen Pump Promoting Hypoxia-Resistant Photodynamic Therapy
Sun, T., Zhang, Y., Zhang, C., Wang, H., Pan, H., Liu, J., Li, Z., Chen, L., Chang, J. K., & Zhang, W. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00237 · Cited by 54
“Cyanobacteria are the only prokaryote microorganism capable of oxygenic photosynthesis via respectively taking sunlight and CO2 as the sole energy and carbon source (Stanier and Bazine, 1977).”
Background
Isolated and purified plasma and thylakoid membranes of the cyanobacteriumAnacystis nidulans contain immunologically cross-reactive aa3-type cytochrome oxidase
Molitor, V., Trnka, M., & Peschek, G. A. (1987) · Current Microbiology · doi:10.1007/bf01568134 · Cited by 52
“The second major type of membrane in this peculiar group of oxygenic phototrophic prokaryotes [24] is the chlorophyll-containing intracytoplasmic (or thylakoid) membrane, which houses the photosynthetic electron transport components [7]; part of the latter may be able to participate in respiratory electron transport a…”
Background
Proteomic analysis of heterotrophy in Synechocystis sp. PCC 6803
Kurian, D., Jansén, T., & Mäenpää, P. (2006) · PROTEOMICS · doi:10.1002/pmic.200500413 · Cited by 51
Adaptive Variations in Phycobilisome Structure
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Oligotyping reveals differences between gut microbiomes of free-ranging sympatric Namibian carnivores (Acinonyx jubatus, Canis mesomelas) on a bacterial species-like level
Menke, S., Wasimuddin, Meier, M., Melzheimer, J., Mfune, J. K. E., Heinrich, S. K., Thalwitzer, S., Wachter, B., & Sommer, S. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00526 · Cited by 51
The Black Band Disease of Atlantic Reef Corals.
Taylor, D. L. (1983) · Marine Ecology · doi:10.1111/j.1439-0485.1983.tb00117.x · Cited by 50
Thioredoxins and the redox modulation of glucose-6-phosphate dehydrogenase in Anabaena sp. strain PCC 7120 vegetative cells and heterocysts
Udvardy, J., Borbély, G., Juhász, A., et al. (1984) · Journal of Bacteriology · doi:10.1128/jb.157.2.681-683.1984 · Cited by 50
“49) is the regulatory enzyme of the oxidative pentose phosphate pathway, the only route of carbohydrate breakdown in cyanobacteria (11, 16).”
Background
Occurrence of cytochrome aa3 in Anacystis nidulans
Peschek, G. A. (1981) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(81)90106-7 · Cited by 50
Protein Phosphorylation on Ser, Thr and Tyr Residues in Cyanobacteria
Zhang, C., Jang, J., Sakr, S., & Wang, L. (2005) · Microbial Physiology · doi:10.1159/000089644 · Cited by 49

Authors: Stanier, R. Y., & Cohen-Bazire, G.
Venue: Annual Review of Microbiology
Publisher: Annual Reviews
Published: 1977-10
Volume: 31
Issue: 1
Pages: 225-274
ISSN: 0066-4227 (ISSN-L)
1545-3251
DOI: 10.1146/annurev.mi.31.100177.001301
OpenAlex: W2016267544
Cited by: 1,015
References: 0
Citations by year: 2026: 13 · 2025: 8 · 2024: 17 · 2023: 29 · 2022: 24 · 2021: 33 · 2020: 37 · 2019: 31 · 2018: 26 · 2017: 20 · 2016: 22 · 2015: 22 · 2014: 22 · 2013: 27 · 2012: 28
FWCI: 14.41
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Microbiology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Physical Sciences › Environmental Science › Environmental Chemistry › Aquatic Ecosystems and Phytoplankton Dynamics
Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Biocrusts and Microbial Ecology
Keywords: cyanobacteria, photosynthesis, SARS-CoV, human coronaviruses, zoonotic coronaviruses, respiratory diseases
MeSH terms: Cyanobacteria, Anaerobiosis, Bacterial Proteins, Bacteriochlorophylls, Cell Membrane, Cell Wall, Chloroplasts, Darkness, DNA, Bacterial, Genes, Light, Lipids, Movement, Nitrogen, Organoids, Oxygen Consumption, Photosynthesis, Transcription, Genetic, Protein Biosynthesis

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PHOTOTROPHIC PROKARYOTES: THE CYANOBACTERIA

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