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PHOTOTROPHIC PROKARYOTES: THE CYANOBACTERIA
Abstract
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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“Nevertheless, cyanobacteria grown in the dark have shown lower growth rates than when grown under light conditions (Stanier and Cohenbazire 1977).”
From Renewable energy from Cyanobacteria: energy production optimization by metabolic pathway engineering (2011) · cites this paper as Stanier and Cohenbazire 1977
In the citing paper
“In addition, low RuBP levels significatively reduce this enzyme activity (Kaplan et al. 2008; Stanier and Cohenbazire 1977; Vanderoost et al. 1989).”
From Renewable energy from Cyanobacteria: energy production optimization by metabolic pathway engineering (2011) · cites this paper as Stanier and Cohenbazire 1977
In the citing paper
“However, cyanobacteria possess an incomplete TCA cycle unable to work properly as a respiratory chain (discussed in the next section) (Stanier and Cohenbazire 1977).”
From Renewable energy from Cyanobacteria: energy production optimization by metabolic pathway engineering (2011) · cites this paper as Stanier and Cohenbazire 1977
In the citing paper
“As stated above, cyanobacteria possess an incomplete TCA cycle where two key enzymes are missing, the 2-oxoglutarate dehydrogenase (ogdh, EC 1.2.4.2), involved in the transformation of 2-OG into succinyl-CoA, and the succinyl-CoA synthetase (sucL, EC 6.2.1.4, 6.2.1.5), for the formation of succinate (Pearce et al. 1969; Stanier and Cohenbazire 1977).”
From Renewable energy from Cyanobacteria: energy production optimization by metabolic pathway engineering (2011) · cites this paper as Stanier and Cohenbazire 1977
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Items 701–800 of 1,001
pH‐jump‐induced phosphorylation of ADP in the cyanobacterium Anacystis nidulans
Muchl, R., & Peschek, G. A. (1983) · FEBS Letters · doi:10.1016/0014-5793(83)80031-3 · Cited by 9
Formal Taxonomic Treatment of Cyanophytes
Lewin, R. A. (1979) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-29-4-411 · Cited by 9
Effect of lipids on the membrane-bound cytochrome oxidase of cyanobacteria
Peschek, G. A., & Schmetterer, G. (1981) · Die Naturwissenschaften · doi:10.1007/bf00401673 · Cited by 9
Studies Concerning Enzyme Activities in Salt-loaded Cells of the Cyanobacterium Microcystis firma
Hagemann, M., Erdmann, N., & Wittenburg, E. (1989) · Biochemie und Physiologie der Pflanzen · doi:10.1016/s0015-3796(89)80127-1 · Cited by 9
Juhász, A., Csizmadia, V., Borbély, G., et al. (1986) · FEBS Letters · doi:10.1016/0014-5793(86)80062-x · Cited by 9
New easy lab methods for the extraction of phycobiliproteins and pigments from cyanobacteria
Kollmen, J., Rech, M., Lorig, F., Nonno, S. D., Stiefelmaier, J., & Strieth, D. (2025) · Journal of Applied Phycology · doi:10.1007/s10811-024-03414-8 · Cited by 10
“Most cyanobacteria exhibit heterotrophic, phototrophic, and mixotrophic growth capabilities (Stanier and Cohen-Bazire 1977).”
Zhang, J., Zou, J., Bao, Q., et al. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.1.245-251.2006 · Cited by 8
“Although Arthrospira platensis is found in freshwater environments, this strain is highly resistant to salt and can even be grown in marine water (13, 26).”
BackgroundEvolution of mechanical stability from lipid layers to complex bacterial envelope structures
Pandur, Ž., & Stopar, D. (2020) · Advances in biomembranes and lipid self-assembly · doi:10.1016/bs.abl.2020.09.005 · Cited by 6
Heterocyst and akinete induction with altered pattern in Anabaena cylindrica, caused by neo-peptone
Sharma, P. K. (1984) · Archives of Microbiology · doi:10.1007/bf00401999 · Cited by 8
Development of Oxygen Microsensors for Monitoring Cyanobacterial Photosynthesis in Roman Hypogea
Compagnone, D., Carlo, V. D., Bruno, L., et al. (1999) · Analytical Letters · doi:10.1080/00032719908542816 · Cited by 8
PII, the key regulator of nitrogen metabolism in the cyanobacteria
Zhang, Y., & Zhao, J. (2008) · Science in China Series C Life Sciences · doi:10.1007/s11427-008-0148-z · Cited by 8
Are Cyanobacterial Mats Precursors of Stromatolites?
Elizabeth, C. B., Berrendero, E., Montejano, G., Barrera, J. M. M., & Sánchez-Ramos, M. A. (2011) · Cellular origin and life in extreme habitats · doi:10.1007/978-94-007-0397-1_14 · Cited by 8
Synthesis of new tetronamides displaying inhibitory activity against bloom‐forming cyanobacteria
Acosta, J. A. M., Karak, M., Barbosa, L. C. A., et al. (2019) · Pest Management Science · doi:10.1002/ps.5580 · Cited by 8
Poly(hydroxyalkanoate) in cyanobacteria: an overview
Stal, L. J. (1992) · FEMS Microbiology Letters · doi:10.1016/0378-1097(92)90307-a · Cited by 8
Price, S., & Anandan, S. (2013) · Journal of Phycology · doi:10.1111/jpy.12086 · Cited by 8
“…secondary antibody to distinguish between the fluorescence signal from labeled TrpA, our protein of interest, and the cytosolic autofluorescence from photosynthetic pigments such as phycoerythrin present in T. erythraeum that fluoresce in the 495–565 nm range (Subramaniam et al. 1999).”
Background[25] Rapid permeabilization of Anacystis nidulans to electrolytes
Papageorgiou, G. C. (1988) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(88)67028-5 · Cited by 8
Ammonium Transport in Unicellular Cyanobacterium Anacystis nidulans
Kashyap, A. K., & Singh, D. P. (1985) · Journal of Plant Physiology · doi:10.1016/s0176-1617(85)80025-0 · Cited by 8
Glutamine and Glutamate Transport in Cyanophora paradoxa
Kloos, K., Schlichting, R., Zimmer, W., et al. (1993) · Botanica Acta · doi:10.1111/j.1438-8677.1993.tb00771.x · Cited by 8
Matthijs, H. C. P., Steenbergen, J. M. V., & Kraayenhof, R. (1985) · Photosynthesis Research · doi:10.1007/bf00032922 · Cited by 8
“Cyanobacteria (blue-green algae) mainly depend on their photosynthetic apparatus for their energy requirements [1].”
BackgroundDr.Varaprasad, P. (2013) · ADVANCED SCIENCES INDEX · Cited by 8
Xu, W., & Wang, Y. (2020) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-020-03435-2 · Cited by 7
Molecular Mechanisms of Stress Tolerance in Cyanobacteria
Rosic, N. N. (2021) · Springer eBooks · doi:10.1007/978-981-16-4873-1_7 · Cited by 8
Wang, Y., Ge, H., Xiao, Z., Huang, C., Wang, G., Duan, X., Zheng, L., Dong, J., Huang, X., Zhang, Y., et al. (2023) · Journal of Proteome Research · doi:10.1021/acs.jproteome.2c00759 · Cited by 7
Huang, H., Song, C., Yang, Z., et al. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01370 · Cited by 7
“Cyanobacteria, also called blue–green bacteria, blue–green algae, cyanophyceae, or cyanophytes, represent a large and widespread group of photoautotrophic microorganisms (Stanier and Bazine, 1977; Whitton and Potts, 2012).”
BackgroundAyiti, O. E., Ayangbenro, A. S., & Babalola, O. O. (2022) · Archives of Microbiology · doi:10.1007/s00203-022-02857-2 · Cited by 7
Carbonate precipitation and nitrogen fixation in AMG (Artificial Martian Ground) by cyanobacteria
Tarasashvili, M. V., Elbakidze, K., Doborjginidze, N. D., & Gharibashvili, N. D. (2023) · Life Sciences in Space Research · doi:10.1016/j.lssr.2023.03.002 · Cited by 7
Lineage-Specific Domain Fusion in the Evolution of Purine Nucleotide Cyclases in Cyanobacteria
Wu, J., Bai, J., Bao, Q., et al. (2008) · Journal of Molecular Evolution · doi:10.1007/s00239-008-9127-z · Cited by 7
“Cyanobacteria are an ancient group of gram-negative photoautotrophic bacteria, which exhibit extraordinary diversities in terms of physiological properties, ecological niches, and morphologies (Stanier and Cohen-Bazire 1977).”
BackgroundMoreno-Cabezuelo, J. Á., López‐Lozano, A., Díez, J., et al. (2019) · PeerJ · doi:10.7717/peerj.6248 · Cited by 7
Stress response in cyanobacteria
Rezayian, M., Niknam, V., & Ebrahimzadeh, H. (2019) · doi:10.22034/ijpp.2019.666767 · Cited by 7
Hassan, N., Anesio, A. M., Rafiq, M., Holtvoeth, J., Bull, I. D., Williamson, C. J., & Hasan, F. (2019) · Extremophiles · doi:10.1007/s00792-019-01141-4 · Cited by 7
Xie, C., Li, Z., Li, Z., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0239372 · Cited by 7
Phylogenetic diversity of prokaryotes on the snow-cover of Lewis glacier in Mount Kenya
Josiah, O. K., Huxley, M. M., Hamadi, I. B., et al. (2018) · African Journal of Microbiology Research · doi:10.5897/ajmr2017.8750 · Cited by 7
“Lewis glacier snowpack is not colonized by the phototrophic prokaryotes as usual to other glaciers worldwide (Stanier and Bazine, 1977; Harding et al., 2011).”
BackgroundZhang, R., Ni, S., & Kennedy, M. A. (2020) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.25882 · Cited by 7
Karakaya, H., Ay, M. T., Özkul, K., et al. (2008) · Annals of Microbiology · doi:10.1007/bf03175330 · Cited by 7
“…dehydrogenase (G6PDH) (EC 1.1.1.49) has long been regarded as the key regulatory point of the pathway and the activity of the enzyme is modulated in response to dark or light conditions (Stanier and Cohen-Bazire, 1977; Smith, 1982; Udvardy et al., 1984; Copeland and Turner, 1987).”
BackgroundInfluentialTeklemariam, T. A., Demeter, S., Deák, Z., et al. (1990) · FEBS Letters · doi:10.1016/0014-5793(90)81270-x · Cited by 7
Rock-dwelling cyanobacteria: survival strategies and biodeterioration of monuments
Pandey, V. (2013) · Cited by 7
UV-MEDIATED STRESS AND ITS MITIGATION IN CYANOBACTERIA
RICHA, R., & Sinha, R. P. (2011) · International Journal of Plant Animal and Environmental Sciences · Cited by 7
LIPIDS AS A PRINCIPLE FOR THE IDENTIFICATION OF ARCHAEBACTERIA
Tornabene, T. G., Lloyd, R., Holzer, G., & Oro, J. A. (1980) · Elsevier eBooks · doi:10.1016/b978-0-08-024436-5.50016-0 · Cited by 7
CAROTENOIDS IN RELATION TO CHLOROPLASTS AND OTHER ORGANELLES
Schiff, J. A., Cunningham, F. X., & Green, M. S. (1982) · Elsevier eBooks · doi:10.1016/b978-0-08-026224-6.50027-9 · Cited by 7
Double-stranded gap repair in the photosynthetic prokaryote Synechococcus R2
Kolowsky, K. S., & Szalay, A. A. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.15.5578 · Cited by 7
Kalosaka, K., & Papageorgiou, G. C. (1984) · Springer eBooks · doi:10.1007/978-94-017-6368-4_160 · Cited by 7
Singh, S. P. (2009) · OPUS FAU (Kooperativer Bibliotheksverbund Berlin-Brandenburg (KOBV), on behalf of the Universitätsbibliothek Erlangen-Nürnberg) · Cited by 7
Cartap hydrochloride induced stress response in Anabaena variabilis ARM 441
Kaur, I., & Goyal, D. (2021) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2021.104904 · Cited by 6
Min, X., Hua, H., Sun, B., Dai, Q., & Luo, J.-Z. (2024) · Palaeogeography, Palaeoclimatology, Palaeoecology · doi:10.1016/j.palaeo.2024.112057 · Cited by 6
Sen, S., Agrawal, C., Mishra, Y., et al. (2015) · Journal of Proteomics · doi:10.1016/j.jprot.2015.07.022 · Cited by 6
Sakamoto, T., Inoue‐Sakamoto, K., Persson, S., et al. (2008) · Phycological Research · doi:10.1111/j.1440-1835.2008.00504.x · Cited by 6
“All cyanobacteria can use carbon dioxide as their primary oxidizing agent and carbon source and most can use nitrate as their sole nitrogen source (Stanier & Cohen-Bazire 1977), although reduced nitrogen sources, such as ammonia and urea, can sometimes be used preferen- tially (Flores & Herrero…”
BackgroundSingh, H., Ahluwalia, A. S., & Khattar, J. S. (2013) · Vegetos · doi:10.5958/j.2229-4473.26.1.041 · Cited by 6
Boussiba, S., Wu, X., & Zarka, A. (2000) · Springer eBooks · doi:10.1007/978-94-011-4269-4_15 · Cited by 8
Purification and characterization of 6-phosphogluconate dehydrogenase from Phormidium sp.
Sawa, Y., Suzuki, K., & Ochiai, H. (1985) · Agricultural and Biological Chemistry · doi:10.1271/bbb1961.49.2543 · Cited by 6
Ultramorphological Studies on Spirulina sp.
Palińska, K. A., Krumbein, W. E., & Schlemminger, U. (1998) · Botanica Marina · doi:10.1515/botm.1998.41.1-6.349 · Cited by 6
Production of ammonium dependent on basicL-amino acids byAnacystic nidulans
Flores, E., Herrero, A., & Guerrero, M. G. (1982) · Archives of Microbiology · doi:10.1007/bf01053987 · Cited by 6
Characterization of a malate dehydrogenase in the cyanobacterium Coccochloris peniocystis
Norman, E. G., & Colman, B. (1991) · Archives of Microbiology · doi:10.1007/bf00418183 · Cited by 6
NITROGENASE AND ASPECTS OF ITS REGULATION IN CYANOBACTERIA
Stewart, W. D. P., Rowell, P. P., Hawkesford, M. J., et al. (2013) · Israel journal of botany. Basic and applied plant sciences · Cited by 6
Heterocyst Metabolism and Development
Wölk, C. P., Ernst, A., & Elhai, J. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-48205-3_27 · Cited by 6
Wisén, S., Bergman, B., & Mannervik, B. (2004) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/j.bbaexp.2004.06.003 · Cited by 6
N2‐Fixing Cyanobacteria as Biofertilizers in Rice Fields
Roger, P. A. (2003) · doi:10.1002/9780470995280.ch22 · Cited by 6
“as Biofertilizers in Rice Fields Pierre Roger Cyanobacteria constitute the largest, most diverse, and most widely distributed group of photosynthetic prokaryotes (Stanier & Cohen-Bazire, 1977).”
BackgroundPrasad, P., & Kashyap, A. K. (1990) · Journal of Plant Physiology · doi:10.1016/s0176-1617(11)81657-3 · Cited by 6
Cultivation of Cyanobacteria on Sustainable Dried Luffa cylindrica
Kollmen, J., Stiefelmaier, J., Mofrad, R., & Strieth, D. (2023) · Phycology · doi:10.3390/phycology3040032 · Cited by 5
Modern brackish bryostromatolites (“bryoliths”) from Zeeland (Netherlands)
Harrison, G. W. M., Claussen, A. L., Schulbert, C., & Munnecke, A. (2021) · Palaeobiodiversity and Palaeoenvironments · doi:10.1007/s12549-021-00490-3 · Cited by 5
“The boring microbes had a distinctly cyanobacterial morphology in thin section (Stanier and Cohen-Bazire 1977) and cyanobacteria are known to bore into shells (Pantazidou et al.”
BackgroundSwanson, E., Sbissi, I., Ktari, A., Cherif‐Silini, H., Ghodhbane‐Gtari, F., Tisa, L. S., & Gtari, M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1027317 · Cited by 5
“These photosynthetic and for some of them diazotrophic bacteria are wide-spread and aid the health and growth of many plant species (Stanier and Cohen-Bazire, 1977; Ringelberg et al., 2012).”
BackgroundBozan, M., Schmidt, M., Musat, N., Schmid, A., Adrian, L., & Bühler, K. (2023) · mSystems · doi:10.1128/msystems.00302-23 · Cited by 5
“C yanobacteria are photosynthetic bacteria performing oxygenic photosynthesis (1) and several species can fix atmospheric nitrogen (2).”
BackgroundLobakova, E. S., Selyakh, I., Semenova, L. R., Chivkunova, O. B., Scherbakov, P. N., & Solovchenko, A. E. (2016) · Moscow University Biological Sciences Bulletin · doi:10.3103/s009639251602005x · Cited by 5
“The modified media were the nitrogen-free media (BG-110 [15], Goldberg), the media with added seawater in a 1 : 1 ratio by volume (BG-11, BG-110, Goldberg media with the mineral nitrogen and nitrogenfree), Prat medium diluted by the distilled water (1 : 1 ratio by volume), and Prat medium with and without microelement…”
MethodNew records of benthic coastal cyanobacteria observed from the Southern Islands of Singapore
Curren, E. E.-M., & Leong, S. C. Y. (2018) · Algological Studies · doi:10.1127/algol_stud/2018/0302 · Cited by 5
Reddy, Y. P., Yadav, R. K., Tripathi, K., et al. (2019) · Journal of Basic Microbiology · doi:10.1002/jobm.201800447 · Cited by 5
“doliolum and the cyanobacterium was routinely maintained in BG-11 medium without added nitrogen [19].”
Arora, N., Jaiswal, D., Sengupta, S., & Wangikar, P. P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818305-2.00008-5 · Cited by 7
Redox cycle: signaling and metabolic cross-talks in cyanobacteria
Sharma, S., Mishra, A., Priyanka, P., & Singh, S. S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13231-5.00011-8 · Cited by 7
Bakr, A. A. (2022) · Egyptian Journal of Botany · doi:10.21608/ejbo.2022.122445.1914 · Cited by 5
GENETIC STARTEGIES FOR STUDYING BACTERIAL DIFFERENTIATION
Piggot, P. J. (1979) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.1979.tb00841.x · Cited by 5
Tanniche, I., Collakova, E., Denbow, C. J., & Senger, R. S. (2020) · PeerJ · doi:10.7717/peerj.8585 · Cited by 5
The effect of glyoxylate on nitrogenase‐catalyzed hydrogen formation in Anabaena cylindrica
Smith, G. D., Daday, A., Newbigin, E., et al. (1982) · FEBS Letters · doi:10.1016/0014-5793(82)80641-8 · Cited by 5
Control of a locus that is required for growth ofAnabaena PCC7120 at low temperature
Panoff, J.-M. (1993) · Current Microbiology · doi:10.1007/bf01575991 · Cited by 5
“Cyanobacteria are prokaryotic algae that perform oxygenic photosynthesis [17].”
BackgroundMembranes of Phototrophic Bacteria
Oelze, J., & Drews, G. (2018) · CRC Press eBooks · doi:10.1201/9781351075244-4 · Cited by 5
Sparsification of large ultrametric matrices: insights into the microbial Tree of Life
Gorman, E. D., & Lladser, M. E. (2023) · Proceedings of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rspa.2022.0847 · Cited by 4
Cui, J., Chen, R.-Z., Sun, H., Xue, Y., Diao, Z., Song, J.-Y., Wang, X.-H., Zhang, J., Wang, C., Ma, B., et al. (2023) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2023.11.001 · Cited by 5
“Cyanobacteria are the only group of prokaryotes that perform oxygen-generating photosynthesis, thus they serve as an important source of primary productivity in the biosphere [1].”
Vaz, M. G. M. V., Almeida, A. V. M., de Castro, N. V., Nunes‐Nesi, A., & Araújo, W. L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818305-2.00015-2 · Cited by 6
Singh, S. K., Kaur, R., Rahman, M. A., Mishra, M., & Sundaram, S. (2021) · 3 Biotech · doi:10.1007/s13205-021-02945-y · Cited by 4
Gonzalez, L., Basso, O., Bédu, S., et al. (2001) · Springer eBooks · doi:10.1007/978-94-015-9835-4_19 · Cited by 4
The Photosynthetic Apparatus of Prochloron-Like Cyanobacteria
MARQUARDT, J., & Mörschel, E. (1999) · Springer eBooks · doi:10.1007/978-94-011-4788-0_6 · Cited by 4
Yan, R., Zhang, Z., Zeng, Q., et al. (2011) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-010-0102-3 · Cited by 4
“The tricarboxylic acid (TCA) cycle: In cyanobacteria, the α-ketoglutarate dehydrogenase activity is lacking [26,27].”
BackgroundMaio, R. C., Cosentino, M., Rossetti, C., et al. (2010) · International Immunopharmacology · doi:10.1016/j.intimp.2010.11.017 · Cited by 4
“Cyanobacteria, also termed blue-green algae, are a large group of photosynthetic oxygenic procaryotes with a high degree of biological adaptation, which represent one of the oldest forms of life on earth [1], as well as a rich source of bioactive metabolites endowed with attractive pharmacological activities, includin…”
BackgroundMicroorganisms, infection and the role of medical textiles
Rahman, M. S., Mondal, M. I. H., Hasan, M. S., Alom, J., Ahmed, M. B., & Ahmed, F. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821485-5.00004-4 · Cited by 7
Xie, H., Kukil, K., Lindberg, P., Miao, R., & Lindblad, P. C. (2022) · Clean Energy Production Technologies · doi:10.1007/978-981-16-8090-8_3 · Cited by 4
Using Cyanobacteria (Nostoc spp.) in the Biological Control of Damping off Disease in Cotton
Afify, A., & Ashour, A. Z. A. (2023) · Journal of Agricultural Chemistry and Biotechnology · doi:10.21608/jacb.2023.220778.1058 · Cited by 5
Paerl, H. W., Justić, D., & Paerl, R. W. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-90798-9.00005-6 · Cited by 5
High-Quality Draft Genome Sequence of Pantanalinema sp. GBBB05, a Cyanobacterium From Cerrado Biome
Ferreira, L. S. D. S., Butarelli, A. C. D. A., Sousa, R. D. C., et al. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.639852 · Cited by 4
“Aerobic cultivation was performed in the BG-11 medium (Stanier and Cohen-Bazire, 1977) under the illumination of 3–15 μmol photons m−2 s−1 for 4 weeks at 28C.”
MethodCharacterization of a ribonuclease from Anacystis nidulans infected with cyanophage as-1
Lehmann, J., Völkl, W., Udvardy, J., et al. (1979) · Phytochemistry · doi:10.1016/s0031-9422(00)84256-9 · Cited by 4
Chemiosmotic coupling in cyanobacteria: ATP synthesis in a two-membrane system
Nitschmann, W. H. (1986) · Journal of Theoretical Biology · doi:10.1016/s0022-5193(86)80182-5 · Cited by 4
Investigation of C-phycoerythrin from the cyanobacterium Pseudanabaena W 1174
R�diger, W., Wagenmann, R., & Muckle, G. (1980) · Archives of Microbiology · doi:10.1007/bf00427201 · Cited by 4
Cyanophycin granule polypeptide in a facultatively heterotrophic cyanobacterium
Newton, J. W., & Tyler, D. D. (1987) · Current Microbiology · doi:10.1007/bf01577532 · Cited by 4
“These results suggest that, in addition to serving as a nitrogen reserve, CGP may also be an important reserve for carbon and/or ATP formation, as was suggested by Stanier and Cohen-Bazire [25].”
BackgroundUn mundo dominado por los microorganismos. Ecología microbiana de los lagos antárticos.
Camacho, A., & Fernández‐Valiente, E. (2005) · Ecosistemas · Cited by 4
Bagchi, S. N., Singh, D., & Singh, H. N. (1986) · New Phytologist · doi:10.1111/j.1469-8137.1986.tb00797.x · Cited by 4
Nath, A., & Kyndiah, O. (2007) · Cited by 4
FLORISTIC STUDY ON CYANOPHYTA OF THREE HOT SPRINGS OF HORMOZGAN PROVINCE, IRAN
Arman, M., Riahi, H., Yousefzadi, M., et al. (2014) · Cited by 4
Purification and Characterization of 6-Phosphogluconate Dehydrogenase fromPhormidiumsp.
Sawa, Y., Suzuki, K., & Ochiai, H. (1985) · Agricultural and Biological Chemistry · doi:10.1080/00021369.1985.10867131 · Cited by 4
SOME POSSIBLE CHEMOTAXONOMIC APPROACHES TO UNDERSTANDING CYANOBACTERIAL TAXONOMY AND PHYLOGENY
Holton, R. W. (1981) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1981.tb46534.x · Cited by 4
DNA Transformation in Cyanobacteria, Algae and Fungi: Trends and Perspectives
Kück, U., & Mulligan, B. J. (1984) · Springer eBooks · doi:10.1007/978-3-642-69985-6_13 · Cited by 4
Collection, Purification, and Culture of Cyanobacteria
Court, G. J., Kycia, J. H., & Siegelman, H. W. (1981) · Springer eBooks · doi:10.1007/978-1-4613-3267-1_13 · Cited by 4
Generation and isolation of cyanobacterial inside-out thylakoid vesicles
Nilsson, F. Y., Simpson, D. J. W., Stewart, A. C., et al. (1988) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(88)90134-8 · Cited by 4
Waters, M. F., McLennan, A. G., & Carr, N. G. (1989) · Microbiology · doi:10.1099/00221287-135-7-2045 · Cited by 4
Stone, B. B., Boussiba, S., & Gibson, J. (1988) · Microbiology · doi:10.1099/00221287-134-11-2951 · Cited by 4
Metadata
- 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
- 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
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 ›
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