Rastogi, R. P. et al. Ultraviolet radiation and cyanobacteria. J. Photochem. Photobiol. B. 141, 154–169 (2014).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Komárek, J. Süßwasserfora von Mitteleuropa. Cyanoprokaryota: 3 Teil/Part 3: Heterocystous genera (Springer, 2013).Dabravolski, S. A. & Isayenkov, S. V. Metabolites facilitating adaptation of desert cyanobacteria to extremely arid environments. Plants. 11, 3225 (2022).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Pathak, J. et al. Genetic regulation of scytonemin and mycosporine-like amino acids (MAAs) biosynthesis in cyanobacteria. Plant Gene. 17, 100172 (2019).ArticleÂ
CASÂ
Google ScholarÂ
Phukan, T., Rai, A. N. & Syiem, M. B. Dose dependent variance in UV-C radiation induced effects on carbon and nitrogen metabolism in the cyanobacterium Nostoc muscorum Meg1. Ecotoxicol. Environ. Saf. 155, 171–179 (2018).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Singh, S. P., Häder, D. P. & Sinha, R. P. Cyanobacteria and ultraviolet radiation (UVR) stress: mitigation strategies. Ageing Res. Rev. 9, 79–90 (2010).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Jain, S. et al. Cyanobacteria as efficient producers of mycosporine-like amino acids. J. Basic Microbiol. 57, 715–727 (2017).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Liu, Y. et al. Non-random genetic alterations in the cyanobacterium Nostoc sp. exposed to space conditions. Sci Rep. 12, 12580. https://doi.org/10.1038/s41598-022-16789-w (2022).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Durai, P., Batool, M. & Choi, S. Structure and effects of cyanobacterial lipopolysaccharides. Mar. Drugs. 13, 4217–4230 (2015).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Kehr, J. C. & Dittmann, E. Biosynthesis and function of extracellular glycans in cyanobacteria. Life 5, 164–180 (2015).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Belton, S., McCabe, P. F. & Ng, C. K. Y. The cyanobacterium, Nostoc punctiforme can protect against programmed cell death and induce defence genes in Arabidopsis thaliana. J. Plant Interact. 16, 64–74 (2021).ArticleÂ
CASÂ
Google ScholarÂ
Raetz, C. R. & Whitfield, C. Lipopolysaccharide endotoxins. Annu. Rev. Biochem. 71, 635–700 (2002).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Bertani, B. & Ruiz, N. Function and Biogenesis of Lipopolysaccharides. EcoSal Plus https://doi.org/10.1128/ecosalplus.esp-0001-2018 (2018).ArticleÂ
PubMedÂ
Google ScholarÂ
Singh, S., Verma, E., Niveshika Tiwari, B. & Mishra, A. K. Exopolysaccharide production in Anabaena sp. PCC 7120 under different CaCl2 regimes. Physiol Mol Biol Plants 22, 557–566 (2016).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Xiao, R. et al. Investigation of composition, structure and bioactivity of extracellular polymeric substances from original and stress-induced strains of Thraustochytrium striatum. Carbohydr. Polym. 195, 515–524 (2018).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Cruz, D., Vasconcelos, V., Pierre, G., Michaud, P. & Delattre, C. Exopolysaccharides from cyanobacteria: Strategies for bioprocess development. Appl. Sci. 10, 3763 (2020).ArticleÂ
CASÂ
Google ScholarÂ
Sinha, R. & Häder, D. Natural bioactive compounds: Technological advancements (Elsevier, Amsterdam, 2021).
Google ScholarÂ
Abdulla, M. H. & Sumayya, N. S. Antioxidants from marine cyanobacteria (Elsevier, Amsterdam, 2023).
Google ScholarÂ
Gao, X., Jing, X., Liu, X. & Lindblad, P. Biotechnological production of the sunscreen pigment scytonemin in cyanobacteria: Progress and strategy. Nat. Rev. Microbiol. 19, 791–802 (2021).
Google ScholarÂ
Soule, T., Garcia-Pichel, F. & Stout, V. Gene expression patterns associated with the biosynthesis of the sunscreen scytonemin in Nostoc punctiforme ATCC 29133 in response to UVA radiation. J. Bacteriol. 191, 4639–4646 (2009).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Rosic, N. N. Mycosporine-like amino acids: Making the foundation for organic personalised sunscreens. Mar. Drugs. 17, 638 (2019).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Janknegt, P. J., Van De Poll, W. H., Visser, R. J., Rijstenbil, J. W. & Buma, A. G. Oxidative stress responses in the marine Antarctic diatom Chaetocerosbrevis (Bacillariophyceae) during photoacclimation. J. Phycol. 44, 957–966 (2008).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Wang, G. et al. The response of antioxidant systems in Nostoc sphaeroides against UV-B radiation and the protective effects of exogenous antioxidants. Adv. Space Res. 39, 1034–1042 (2007).ArticleÂ
ADSÂ
CASÂ
Google ScholarÂ
Monsalves, M. T., Amenábar, M. J., Ollivet-Besson, G. P. & Blamey, J. M. Effect of UV radiation on a thermostable superoxide dismutase purified from a thermophilic bacterium isolated from a sterilization drying oven. Protein pept. lett. 20, 749–754 (2013).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Correa-Llantén, D. N., Amenábar, M. J. & Blamey, J. M. Antioxidant capacity of novel pigments from an Antarctic bacterium. J. Microbiol. 50, 374–379 (2012).ArticleÂ
PubMedÂ
Google ScholarÂ
Pattanaik, B., Schumann, R. & Karsten, U. Effects of ultraviolet radiation on cyanobacteria and their protective mechanisms 29–45 (Springer, Berlin, 2007).
Google ScholarÂ
Singh, V. K. et al. Resilience and mitigation strategies of cyanobacteria under ultraviolet radiation stress. Int. J. Mol. Sci. 24, 12381. https://doi.org/10.3390/ijms241512381 (2023).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Feng, Y. N., Zhang, Z. C., Feng, J. L. & Qiu, B. S. Effects of UV-B radiation and periodic desiccation on the morphogenesis of the edible terrestrial cyanobacterium Nostoc flagelliforme. Appl. Environ. Microbiol. 78, 7075–7081 (2012).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Mansouri, H. & Talebizadeh, R. The effects of UVB on growth and anti-UV compounds contents in cyanobacteria Nostoc linckia. J. oceanogr. 12, 1–12 (2022).
Google ScholarÂ
Yu, H. & Liu, R. Effect of UV-B radiation on the synthesis of UV-absorbing compounds in a terrestrial cyanobacterium. Nostoc flagelliforme. J. Appl. Phycol. 25, 1441–1446 (2013).ArticleÂ
CASÂ
Google ScholarÂ
Sheeba, Ruhil, K. & Prasad, S. M. Nostoc muscorum and Phormidium foveolarum differentially respond to butachlor and UV-B stress. Physiol. Mol. Biol. Plants. 26, 841–856 (2020).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Yu, H., Pang, S. & Liu, R. Effects of UV-B and UV-C radiation on the accumulation of scytonemin in a terrestrial cyanobacterium, Nostoc flagelliforme. Preprint at https://ieeexplore.ieee.org/document/6098596 (2011).de Sousa, E. B. et al. Effect of ultraviolet-C radiation on the morphology of cyanobacteria nostoc sp. LBALBR-2 isolated from supply reservoir (Belém, Pará, Brazil). Res. Soc. Dev. 11, e447111234391. https://doi.org/10.33448/rsd-v11i12.34391 (2022).ArticleÂ
Google ScholarÂ
Khalili, A., Bazrafshan, J. & Chraghalizadeh, M. A Comparative study on climate maps of Iran in extended de Martonne classification and application of the method for world climate zoning. J Agricul. Meteorol. 10, 3–16 (2022).
Google ScholarÂ
Feizi, V., Mollashahi, M., Farajzadeh, M. & Azizi, G. Spatial and temporal trend analysis of temperature and precipitation in Iran. Ecopersia 2, 727–742 (2014).
Google ScholarÂ
Etemadi-Khah, A., Pourbabaee, A., Noroozi, M., Alikhani, H. & Bruno, L. Biodiversity of Isolated Cyanobacteria from Desert Soils in Iran. Geomicrobiol. J. 34, 90546809. https://doi.org/10.1080/01490451.2016.1271064 (2017).ArticleÂ
CASÂ
Google ScholarÂ
Ahmad, F. A. Valuation of solar power generating potential in Iran desert areas. J. Appl. Sci. Environ. Manag. 22, 6. https://doi.org/10.4314/jasem.v22i6.21 (2018).ArticleÂ
Google ScholarÂ
Irankhahi, P., Riahi, H., Shariatmadari, Z. & Shariatmadari, Z. A. Diversity and distribution of heterocystous cyanobacteria across solar radiation gradient in terrestrial habitats of Iran. Rostaniha 23, 264–281 (2022).
Google ScholarÂ
Aghashariatmadari, Z. Evaluation of model for estimating total solar radiation at horizontal surfaces based on meteorological data, with emphasis on the performance of the angstrom model over Iran (Tehran University, 2011).Rangaswami, G. Agricultural microbiology (Asia Publishing House, Mumbai, 2011).
Google ScholarÂ
Stanier, R. Y., Kunisawa, R., Mandel, M. & Cohen-Bazire, G. Purification and properties of unicellular blue-green algae (order Chroococcales). Bacteriolo. Rev. 35, 171–205 (1971).ArticleÂ
CASÂ
Google ScholarÂ
Andersen, R. A. Algal culturing techniques (Elsevier Science, Amsterdam, 2005).
Google ScholarÂ
Wehr, J., Sheath, R. & Kociolek, P. Freshwater Algae of North America: Ecology and Classification (Elsevier, Amsterdam, 2015).
Google ScholarÂ
John, D. M., Whitton, B. A. & Brook, A. The freshwater algal flora of the British Isles: an identification guide to freshwater and terrestrial algae (Cambridge University Press, Cambridge, 2002).
Google ScholarÂ
Hauer, T. & Komárek, J. CyanoDB 2.0 – On-line database of cyanobacterial genera. http://www.cyanodb.cz (2022).Dos Santos, H. R. M., Argolo, C. S., Argôlo-Filho, R. C. & Loguercio, L. L. A 16S rDNA PCR-based theoretical to actual delta approach on culturable mock communities revealed severe losses of diversity information. BMC Microbiol. 19, 74 (2019).ArticleÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Nübel, U., Garcia-Pichel, F. & Muyzer, G. PCR primers to amplify 16S rRNA genes from cyanobacteria. Appl. Environ. Microbiol. 63, 3327–3332 (1997).ArticleÂ
ADSÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Sanger, F. & Coulson, A. R. A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. J. Mol. Biol. 94, 441–448 (1975).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Hall, T. A. BioEdit: A user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucl. Acids Symp. Ser. 41, 95–98 (1999).CASÂ
Google ScholarÂ
Monsalves, M. T., Ollivet-Besson, G. P., Amenabar, M. J. & Blamey, J. M. Isolation of a psychrotolerant and UV-C-resistant bacterium from Elephant Island, Antarctica with a highly thermoactive and thermostable catalase. Microorganisms 8, 95 (2020).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Richa Sinha, R. P. Sensitivity of two Nostoc species harbouring diverse habitats to ultraviolet-B radiation. Microbiology 84, 398–4075 (2015).ArticleÂ
Google ScholarÂ
Han, P. et al. Applying the strategy of light environment control to improve the biomass and polysaccharide production of Nostoc flagelliforme. J. Appl. Phycol. 29, 55–65 (2017).ArticleÂ
ADSÂ
CASÂ
Google ScholarÂ
Wellburn, A. R. The spectral determination of chlorophylls a and b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution. J. Plant Physiol. 144, 307–313 (1994).ArticleÂ
CASÂ
Google ScholarÂ
Mushir, S. & Fatma, T. Ultraviolet Radiation-absorbing Mycosporine-like Amino Acids in cyanobacterium Aulosira fertilissima: environmental perspective and characterization. Curr. Res. J. Biol. Sci. 3, 165–171 (2011).CASÂ
Google ScholarÂ
Mushir, S. & Fatma, T. Monitoring stress responses in cyanobacterial scytonemin – screening and characterization. Environ. Technol. 33, 153–157 (2012).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Garcia-Pichel, F. & Castenholz, R. W. Occurrence of UV-absorbing, mycosporine-like compounds among cyanobacterial isolates and an estimate of their screening capacity. Appl. Environ. Microbiol. 59, 163–169 (1993).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
DuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A. & Smith, F. Colorimetric method for determination of sugars and related substances. Anal. Chem. 28, 350–356 (1956).ArticleÂ
CASÂ
Google ScholarÂ
Chairat, B., Pongprasert, N. & Srilaong, V. Effect of UV-C treatment on chlorophyll degradation, antioxidant enzyme activities and senescence in Chinese kale (Brassica oleracea var. alboglabra). Int. Food Res. J. 20, 623–628 (2013).CASÂ
Google ScholarÂ
Aebi, H. Catalase in vitro. Meth. Enzymol. 105, 121–126 (1984).ArticleÂ
CASÂ
Google ScholarÂ
Giannopolitis, C. N. & Ries, S. K. Superoxide dismutases: I. occurrence in higher plants. Plant Physiol. 59, 309–314 (1977).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Bradford, M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254 (1976).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Pfaffl, M. W. A new mathematical model for relative quantification in real-time RT-PCR. Nucl. Acids Res. 29, e45. https://doi.org/10.1093/nar/29.9.e45 (2001).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Jo, S. et al. Lipopolysaccharide membrane building and simulation. Methods Mol. Biol. 1273, 391–406 (2015).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Garcia-Pichel, F. & Belnap, J. Microenvironments and microscale productivity of cyanobacterial desert crusts. J. Phycol. 32, 774–782 (2008).ArticleÂ
Google ScholarÂ
Wu, H., Gao, K., Villafañe, V. E., Watanabe, T. & Helbling, E. W. Effects of solar UV radiation on morphology and photosynthesis of filamentous cyanobacterium Arthrospira platensis. Appl. Environ. Microbiol. 71, 5004–5013 (2005).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Mloszewska, A. M. et al. UV radiation limited the expansion of cyanobacteria in early marine photic environments. Nat. Commun. 9, 3088 (2018).ArticleÂ
ADSÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Tamaru, Y., Takani, Y., Yoshida, T. & Sakamoto, T. Crucial role of extracellular polysaccharides in desiccation and freezing tolerance in the terrestrial cyanobacterium Nostoc commune. Appl. Environ. Microbiol. 71, 7327–7333 (2005).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Helm, R. F. et al. Structural characterization of the released polysaccharide of desiccation-tolerant Nostoc commune DRH-1. J. Bacteriol. 182, 974–982 (2000).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Sakamoto, T. et al. The extracellular-matrix-retaining cyanobacterium Nostoc verrucosum accumulates trehalose, but is sensitive to desiccation. FEMS Microbiol. Ecol. 77, 385–394 (2011).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Li, H. et al. Antioxidant and moisture-retention activities of the polysaccharide from Nostoc commune. Carbohydr. Polym. 83, 1821–1827 (2011).ArticleÂ
CASÂ
Google ScholarÂ
Han, P. P., Sun, Y., Jia, S. R., Zhong, C. & Tan, Z. L. Effects of light wavelengths on extracellular and capsular polysaccharide production by Nostoc flagelliforme. Carbohydr. Polym. 105, 145–151 (2014).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Chandra, R., Fernanda, P. F., Parra-SaldÃvar, R. & Rittmann, B. E. Effect of ultra-violet exposure on production of mycosporine-like amino acids and lipids by Lyngbya purpurem. Biomass Bioenergy 134, 105475 (2020).ArticleÂ
CASÂ
Google ScholarÂ
Sinha, R. P., Klisch, M., Helbling, E. W. & Häder, D. Induction of mycosporine-like amino acids (MAAs) in cyanobacteria by solar ultraviolet-B radiation. J. Photochem. Photobiol. B. 60, 129–135 (2001).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Soule, T., Stout, V., Swingley, W. D., Meeks, J. C. & Garcia-Pichel, F. Molecular genetics and genomic analysis of scytonemin biosynthesis in Nostoc punctiforme ATCC 29133. J. Bacteriol. 189, 4465–4472 (2007).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Orellana, G., Gómez-Silva, B., Urrutia, M. & Galetović, A. UV-A irradiation increases scytonemin biosynthesis in cyanobacteria inhabiting halites at Salar Grande Atacama desert. Microorganisms 8, 1690 (2020).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Hoiczyk, E. & Hansel, A. Cyanobacterial cell walls: news from an unusual prokaryotic envelope. J. Bacteriol. 182, 1191–1199 (2000).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Snyder, D. S., Brahamsha, B., Azadi, P. & Palenik, B. Structure of compositionally simple lipopolysaccharide from marine synechococcus. J. Bacteriol. 191, 5499–5509 (2009).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
McCarren, J. et al. Inactivation of swmA results in the loss of an outer cell layer in a swimming synechococcus strain. J. Bacteriol. 187, 224–230 (2005).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Anwar, M. A. & Choi, S. Gram-negative marine bacteria: Structural features of lipopolysaccharides and their relevance for economically important diseases. Mar. Drugs. 12, 2485–2514 (2014).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
DeMarco, M. L. Three-dimensional structure of glycolipids in biological membranes. Biochemistry 51, 5725–5732 (2012).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Kirschbaum, C. et al. Unravelling the structural complexity of glycolipids with cryogenic infrared spectroscopy. Nat. Commun. 12, 1201 (2021).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Azimzadeh Irani, M. Correlation between experimentally indicated and atomistically simulated roles of EGFR N-glycosylation. Mol. Simul. 44, 743–748 (2018).ArticleÂ
CASÂ
Google ScholarÂ
Lee, J. et al. CHARMM-GUI membrane builder for complex biological membrane simulations with glycolipids and lipoglycans. J. Chem. Theory Comput. 15, 775–786 (2019).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Mikheyskaya, L. V., Ovodova, R. G. & Ovodov, Y. S. Isolation and characterization of lipopolysaccharides from cell walls of blue-green algae of the genus. Phormidium J. Bacteriol. 130, 1–3 (1977).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Buttke, T. M. & Ingram, L. O. Comparison of lipopolysaccharides from Agmenellum quadruplicatum to Escherichia coli and Salmonella typhimurium by using thin-layer chromatography. J. Bacteriol. 124, 1566–1573 (1975).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Weise, G., Drews, G., Jann, B. & Jann, K. Identification and analysis of a lipopolysaccharide in cell walls of the blue-green alga Anacystis nidulans. Arch. Microbiol. 71, 89–98 (1970).CASÂ
Google ScholarÂ
Keleti, G. & Sykora, J. L. Production and properties of cyanobacterial endotoxins. Appl. Environ. Microbiol. 43, 104–109 (1982).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Keleti, G., Sykora, J. L., Lippy, E. C. & Shapiro, M. A. Composition and biological properties of lipopolysaccharides isolated from Schizothrix calcicola (Ag) Gomont (Cyanobacteria). Appl. Environ. Microbiol. 38, 471–477 (1979).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Weckesser, J., Katz, A., Drews, G., Mayer, H. & Fromme, I. Lipopolysaccharide containing L-acofriose in the filamentous blue-green alga Anabaena variabilis. J. Bacteriol. 120, 672–678 (1974).ArticleÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Gemma, S., Molteni, M. & Rossetti, C. Lipopolysaccharides in cyanobacteria: A brief overview. Adv. Microbiol. 6, 391–397 (2016).ArticleÂ
CASÂ
Google ScholarÂ
Paracini, N., Schneck, E., Imberty, A. & Micciulla, S. Lipopolysaccharides at solid and liquid interfaces: Models for biophysical studies of the gram-negative bacterial outer membrane. Adv. Colloid Interface Sci. 301, 102603 (2022).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Wang, B. et al. The combined effects of UV-C radiation and H2O2 on Microcystis aeruginosa, a bloom-forming cyanobacterium. Chemosphere 141, 34–43 (2015).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
Google ScholarÂ
Phukan, T., Rai, A. N. & Syiem, M. B. Dose dependent variance in UV-C radiation induced effects on carbon and nitrogen metabolism in the cyanobacterium Nostoc muscorum Meg1. Ecotoxicol. Environ. Saf. 155, 171–179 (2018).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Hakkila, K. et al. Oxidative stress and photoinhibition can be separated in the cyanobacterium Synechocystis sp. PCC 6803. Biochimica et Biophysica Acta BBA Bioenerget. 137, 217–225 (2014).ArticleÂ
Google ScholarÂ
LupÃnková, L. & Komenda, J. Oxidative modifications of the Photosystem II D1 protein by reactive oxygen species: From isolated protein to cyanobacterial cells. Photochem. Photobiol. 79, 152–162 (2004).ArticleÂ
PubMedÂ
Google ScholarÂ
Ye, T. et al. Exposure of cyanobacterium Nostoc sp. to the Mars-like stratosphere environment. J. Photochem. Photobiol. B. 224, 112307 (2021).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Apel, K. & Hirt, H. Reactive oxygen species: Metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55, 373–399 (2004).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ
Rath, J. & Adhikary, S. Response of the estuarine cyanobacterium Lyngbya aestuarii to UV-B radiation. J. Appl. Phycol. 19, 529–536 (2007).ArticleÂ
CASÂ
Google ScholarÂ
Shen, S. G. et al. The physiological responses of terrestrial cyanobacterium Nostoc flagelliforme to different intensities of ultraviolet-B radiation. RSC Adv. 8, 21065–21074 (2018).ArticleÂ
ADSÂ
CASÂ
PubMedÂ
PubMed CentralÂ
Google ScholarÂ
Wang, G. et al. The involvement of the antioxidant system in protection of desert cyanobacterium Nostoc sp. against UV-B radiation and the effects of exogenous antioxidants. Ecotoxicol. Environ. Saf. 69, 150–157 (2008).ArticleÂ
CASÂ
PubMedÂ
Google ScholarÂ