Cyanobacteria: a precious bio-resource in agriculture, ecosystem, and environmental sustainability
Open accessAbstract
Keeping in view, the challenges concerning agro-ecosystem and environment, the recent developments in biotechnology offers a more reliable approach to address the food security for future generations and also resolve the complex environmental problems. Several unique features of cyanobacteria such as oxygenic photosynthesis, high biomass yield, growth on non-arable lands and a wide variety of water sources (contaminated and polluted waters), generation of useful by-products and bio-fuels, enhancing the soil fertility and reducing green house gas emissions, have collectively offered these bio-agents as the precious bio-resource for sustainable development. Cyanobacterial biomass is the effective bio-fertilizer source to improve soil physico-chemical characteristics such as water-holding capacity and mineral nutrient status of the degraded lands. The unique characteristics of cyanobacteria include their ubiquity presence, short generation time and capability to fix the atmospheric N2. Similar to other prokaryotic bacteria, the cyanobacteria are increasingly applied as bio-inoculants for improving soil fertility and environmental quality. Genetically engineered cyanobacteria have been devised with the novel genes for the production of a number of bio-fuels such as bio-diesel, bio-hydrogen, bio-methane, synga, and therefore, open new avenues for the generation of bio-fuels in the economically sustainable manner. This review is an effort to enlist the valuable information about the qualities of cyanobacteria and their potential role in solving the agricultural and environmental problems for the future welfare of the planet.
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Microcoleaceae have been shown to improve soil fertility and support healthy plant growth.
“Microcoleaceae have been shown to improve soil fertility and support healthy plant growth (Singh et al., 2016;Shariatmadari et al., 2013;Rai et al., 2019).”
From Spirulina supported plant growth in regolith simulants and elevated levels of CO2 (2025) · cites this paper as Singh et al., 2016
The ‘Cyanobacteria in Sustainable Management’ section says cyanobacteria can restore soil fertility and stimulate plant growth; the ‘Plant Growth Promoters’ section describes reported growth benefits. The paper lists Microcoleus chthonoplastes among cyanobacteria, but the cited passages do not establish these benefits specifically for Microcoleaceae. Page numbers are unavailable in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measuredMicrocoleaceae increase water-holding capacity and nutrient content of degraded soils.
“In terrestrial soils, they contribute to soil aggregation and stability (Rashid et al., 2016), increase the water-holding capacity and nutrient content of degraded soils (Singh et al., 2016), and enhance salt tolerance, disease resistance, and polysaccharide production (Singh, 2014).”
From Spirulina supported plant growth in regolith simulants and elevated levels of CO2 (2025) · cites this paper as Singh et al., 2016
The sections on cyanobacteria under extreme environments and reclamation of salt-affected soils say cyanobacteria can improve soil water-holding capacity and raise carbon and nitrogen levels in poor soils. The paper identifies Microcoleus chthonoplastes as a cyanobacterium in Table 1, but does not establish these effects specifically for Microcoleaceae. (LLM, conf=0.86)
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Cites
Chisti, Y. (2007) · Biotechnology Advances · doi:10.1016/j.biotechadv.2007.02.001 · Cited by 9,524 · see citing works
Woese, C. R. (1987) · Microbiological Reviews · doi:10.1128/mr.51.2.221-271.1987 · Cited by 5,042 · cited 1× · see citing works
“Cyanobacteria are the group of photosynthetic organisms which can easily survive on bare minimum requirement of light, carbon dioxide (CO 2 ) and water (Woese, 1987; Castenholz, 2001).”
Direct photosynthetic recycling of carbon dioxide to isobutyraldehyde
Atsumi, S., Higashide, W., & Liao, J. C. (2009) · Nature Biotechnology · doi:10.1038/nbt.1586 · Cited by 870 · see citing works
Microalgae in Human and Animal Nutrition
Becker, W. (2003) · Handbook of Microalgal Culture · doi:10.1002/9780470995280.ch18 · Cited by 613 · see citing works
Lindberg, P., Park, S., & Melis, A. (2010) · Metabolic Engineering · doi:10.1016/j.ymben.2009.10.001 · Cited by 596 · see citing works
Yamaguchi, K. (1996) · Journal of Applied Phycology · doi:10.1007/bf02186327 · Cited by 263 · see citing works
Cyanobacteria as a Platform for Biofuel Production.
Nozzi, N. E., Oliver, J. W. K., & Atsumi, S. (2013) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2013.00007 · Cited by 227 · see citing works
Kulik, M. M. (1995) · European Journal of Plant Pathology · doi:10.1007/bf01874863 · Cited by 224 · see citing works
Biogas production and valorization by means of a two-step biological process
Converti, A., Oliveira, R. P. S., Torres, B. R., Lodi, A., & Zilli, M. (2009) · Bioresource Technology · doi:10.1016/j.biortech.2009.05.072 · Cited by 142 · see citing works
Carbon Dioxide Mitigation using Thermophilic Cyanobacteria
Ono, E., & Cuello, J. L. (2007) · Biosystems Engineering · doi:10.1016/j.biosystemseng.2006.09.010 · Cited by 140 · see citing works
Current microalgal health food R & D activities in China
Liang, S., Liu, X., Chen, F., & Chen, Z. (2004) · Hydrobiologia · doi:10.1023/b:hydr.0000020366.65760.98 · Cited by 93 · see citing works
Flagged first, then by citations
Research works printed but not linked: 166
- Abarzua S. Jakubowski S. Eckert S. Fuchs P. (1999). Biotechnological investigation for the prevention of marine biofouling II. Blue-green algae as potential producers of biogenic agents for the growth inhibition of microfouling organisms. Botanica Mar. 42 459– 465. 10.1515/BOT.1999.053 · DOI
- Ahmad M. R. Winter A. (1968). Studies on the hormonal relationships of algae in pure culture. I. The effect of indole-3-acetic acid on the growth of blue-green and green algae. Planta 78 277– 286. 10.1007/BF00386428 24522736 · DOI
- Al-Hasan R. H. Al-Bader D. A. Sorkhoh N. A. Radwan S. S. (1998). Evidence for n-alkane consumption and oxidation by filamentous cyanobacteria from oil-contaminated coasts of the Arabian Gulf. Mar. Biol. 130 521– 527. 10.1007/s002270050272 · DOI
- Al-Hasan R. H. Khanafer M. Eliyas M. Radwan S. S. (2001). Hydrocarbon accumulation by picocyanobacteria from the Arabian Gulf. J. Appl. Microbiol. 91 533– 540. 10.1046/j.1365-2672.2001.01414.x 11556921 · DOI
- Ali I. Basit M. A. (1993). Significance of hydrogen content in fuel combustion. Inter. J. Hydrogen Energ. 18 1009– 1011. 10.1016/0360-3199(93)90083-M · DOI
- Anjana K. Kaushik A. Kiran B. Nisha R. (2007). Biosorption of Cr (VI) by immobilized biomass of two indigenous strains of cyanobacteria isolated from metal contaminated soil. J. Hazard. Mater. 148 383– 386. 10.1016/j.jhazmat.2007.02.051 17403568 · DOI
- Apt K. E. Behrens P. W. (1999). Commercial developments in microalgal biotechnology. J. Phycol. 35 215– 226. 10.1046/j.1529-8817.1999.3520215.x · DOI
- Apte S. K. Reddy B. R. Thomas J. (1987). Relationship between sodium influx and salt tolerance of nitrogen-fixing cyanobacteria. Appl. Environ. Microbiol. 53 1934– 1939. 16347419 PMC204028
- Badger M. R. Price G. D. (2003). CO2 concentrating mechanisms in cyanobacteria: molecular components, their diversity and evolution. J. Exp. Bot. 54 609– 622. 10.1093/jxb/erg076 12554704 · DOI · Paper page
- Bandaranayake W. M. (1998). Mycosporines: are they nature’s sunscreens? Nat. Prod. Rep. 15 159– 172. 10.1039/a815159y 9586224 · DOI
- Benedetti S. Benvenuti F. Pagliarani S. Francogli S. Scoglio S. Canestrari F. (2004). Antioxidant properties of a novel phycocyanin extract from the blue green alga Aphanizomenon flos-aquae. Life Sci. 75 2353– 2362. 10.1016/j.lfs.2004.06.004 15350832 · DOI
- Benson D. Kerry K. Malin G. (2014). Algal biofuels: impact significance and implications for EU multi-level governance. J. Clean. Prod. 72 4– 13. 10.1016/j.jclepro.2014.02.060 · DOI
- Benson S. M. Orr J. F. M. (2008). Carbon dioxide capture and storage. MRS Bull. 33 303– 305. 10.1557/mrs2008.63 · DOI
- Bhaskar S. U. Gopalswamy G. Raghu R. (2005). A simple method for efficient extraction and purification of C-phycocyanin from Spirulina platensis Geitler. Indian J. Exp. Biol. 43 277– 279. 15816417
- Biondi N. Piccardi R. Margheri M. C. Rodolfi L. Smith G. D. Tredici M. R. (2004). Evaluation of Nostoc strain ATCC 53789 as a potential source of natural pesticides. Appl. Environ. Microbiol. 70 3313– 3320. 10.1128/AEM.70.6.3313-3320.2004 15184126 PMC427721 · DOI
- Bohm G. A. Pfleiderer W. Boger P. Scherer S. (1995). Structure of a novel oligosaccharide-mycosporine-aminoacid ultraviolet A/B sunscreen pigment from the terrestrial scyanobacterium Nostoc commune. J. Biol. Chem. 270 8536– 8539. 10.1074/jbc.270.15.8536 7721752 · DOI
- Borowitzka M. A. (1999). Commercial production of microalgae: ponds, tanks, tubes and fermenters. J. Biotechnol. 70 313– 321. 10.1016/S0168-1656(99)00083-8 · DOI · Paper page
- Brown M. R. Jeffrey S. W. Volkman J. K. Dunstan G. A. (1997). Nutritional properties of microalgae for mariculture. Aquaculture 151 315– 331. 10.1016/S0044-8486(96)01501-3 · DOI
- Burja A. M. Banaigs B. Abou-Mansour E. Burgess J. G. Wright P. C. (2001). Marine cyanobacteria – a prolific source of natural products. Tetrahedron 57 9347– 9377. 10.1016/S0040-4020(01)00931-0 · DOI · Paper page
- Cain A. Vannela R. Woo L. K. (2008). Cyanobacteria as a biosorbent for mercuric ion. Bioresour. Technol. 99 6578– 6586. 10.1016/j.biortech.2007.11.034 18158240 · DOI
- Cameron H. J. Julian G. R. (1988). Utilisation of hydroxyapatite by cyanobacteria as their sole source of phosphate and calcium. Plant Soil 109 123– 124. 10.1007/BF02197589 · DOI
- Castenholz R. W. (2001). “ Phylum BX. Cyanobacteria,” in Bergey’s Manual of Systematic Bacteriology, 2nd Edn, eds Boone D. R. Castenholz R. W. (New York, NY: Springer), 473– 599.
- Cerniglia C. E. Baalen C. V. Gibson D. T. (1980a). Oxidation of biphenyl by the cyanobacterium, Oscillatoria sp. strain JCM. Arch. Microbiol. 125 203– 207. 10.1007/BF00446877 6769418 · DOI
- Cerniglia C. E. Gibson D. T. Baalen C. V. (1979). Algal oxidation of aromatic hydrocarbons: formation of 1-naphthol from naphthalene by Agmenellum quadruplicatum, strain PR-6. Biochem. Biophys. Res. Commun. 88 50– 58. 10.1016/0006-291X(79)91695-4 110329 · DOI
- Cohen R. R. H. (2006). Use of microbes for cost reduction of metal removal from metals and mining industry waste streams. J. Clean. Prod. 14 1146– 1157. 10.1016/j.jclepro.2004.10.009 · DOI
- Cohen Y. (2002). Bioremediation of oil by marine microbial mats. Inter. Microbiol. 5 189– 193. 10.1007/s10123-002-0089-5 12497184 · DOI
- Coutinho R. Seeliger U. (1984). The horizontal distribution of benthic algal flora in the Patos Lagoon estuary, Brazil, in relation to salinity, substratum and wave. J. Exp. Marine Biol. Ecol. 80 247– 257. 10.1016/0022-0981(84)90153-9 · DOI
- Dahms H. U. Xu Y. Pfeiffer C. (2006). Antifouling potential of cyanobacteria: a mini-review. Biofouling 22 317– 327. 10.1080/08927010600967261 17110355 · DOI
- Desmorieux H. Decaen N. (2005). Convective drying of Spirulina in thin layer. J. Food Eng. 66 497– 503. 10.1016/j.jfoodeng.2004.04.021 · DOI
- Dhar N. R. Mukherji S. K. (1936). Alkali soils and their reclamation. Proc. Natl. Acad. Sci. Ind. 6 136– 148.
- Dorich R. A. Nelson D. W. Sommers L. E. (1985). Estimating algal available phosphorus in suspended sediments by chemical extraction. J. Environ. Qual. 14 400– 405. 10.2134/jeq1985.143400x · DOI
- Dutta D. De D. Chaudhuri S. Bhattacharya S. K. (2005). Hydrogen production by Cyanobacteria. Microb. Cell Fact. 4 36– 47. 10.1186/1475-2859-4-36 16371161 PMC1343573 · DOI
- El-Bestawy E. A. Abd El-Salam A. Z. Mansy A. E. R. H. (2007). Potential use of environmental cyanobacterial species in bioremediation on lindane-contaminated effluents. Inter. Biodeterior. Biodegrad. 59 180– 192. 10.1016/j.ibiod.2006.12.005 · DOI
- El-Enany A. E. Issa A. A. (2000). Cyanobacteria as a biosorbent of heavy metals in sewage water. Environ. Toxicol. Pharmacol. 8 95– 101. 10.1016/S1382-6689(99)00037-X 10867368 · DOI
- El-Sheekh M. M. El-Shouny W. A. Osman M. E. H. El-Gammal E. W. E. (2005). Growth and heavy metals removal efficiency of Nostoc muscorum and Anabaena subcylindrica in sewage and industrial wastewater effluents. Environ. Toxicol. Pharmacol. 19 357– 365. 10.1016/j.etap.2004.09.005 21783496 · DOI
- Flaibani A. Olsen Y. Painter T. J. (1989). Polysaccharides in desert reclamation: compositions of exocellular proteoglycan complexes produced by filamentous blue-green and unicellular green edaphic algae. Carbohydr. Res. 190 235– 248. 10.1016/0008-6215(89)84128-X · DOI
- Fogg G. E. (1956). The comparative physiology and biochemistry of the blue-green algae. Bacteriol. Rev. 20 148– 165. 13363770 PMC180857
- Forlani G. Pavan M. Gramek M. Kafarski P. Lipok J. (2008). Biochemical basis for a wide spread tolerance of cyanobacteria to the phosphonate herbicide glyphosate. Plant Cell Physiol. 49 443– 456. 10.1093/pcp/pcn021 18263622 · DOI
- Fritsch F. E. (1945). The Structure and Reproduction of Algae—II. London: Cambridge University Press.
- Fuhrman J. (2003). Genome sequences from the sea. Nature 424 1001– 1002. 10.1038/4241001a 12944945 · DOI
- Fuller W. H. Roger R. N. (1952). Utilisation of the phosphorus of algal cells as measured by the Neubauer technique. Soil Sci. 74 417– 429. 10.1097/00010694-195212000-00002 · DOI
- Gantar M. Kerby N. W. Rowell P. Obreht Z. (1991). Colonization of wheat (Triticum vulgare L.) by N2-fixing cyanobacteria: a survey of soil cyanobacterial isolates forming associations with roots. New Phytol. 118 477– 483. 10.1111/j.1469-8137.1991.tb00030.x · DOI
- Gantar M. Kerby N. W. Rowell P. Obreht Z. Scrimgeour R. (1995a). Colonization of wheat (Triticum vulgare L.) by N2-fixing cyanobacteria. IV. Dark nitrogenase activity and effects of cyanobacteria on natural 15N abundance on plants. New Phytol. 129 337– 343. 10.1111/j.1469-8137.1995.tb04304.x 33874558 · DOI
- Gantar M. Rowell P. Kerby N. W. Sutherland I. W. (1995b). Role of extracellular polysaccharide in the colonization of wheat (Triticum vulgare L.) roots by N2- fixing cyanobacteria. Biol. Fertil. Soils 19 41– 48. 10.1007/BF00336345 · DOI
- Gantar M. Svircev Z. (2008). Microalgae and cyanobacteria: food for thought. J. Phycol. 44 260– 268. 10.1111/j.1529-8817.2008.00469.x 27041182 · DOI
- Garcia-Pichel F. Wingard C. E. Castenholz R. W. (1993). Evidence regarding the UV sunscreen role of a mycosprine-like compound in the cyanobacterium Gloecapsa sp. Appl. Environ. Microbiol. 59 170– 176. 16348840 PMC202073
- Golden S. S. Brusslan J. Haselkorn R. (1987). Genetic engineering of the cyanobacterial chromosome. Methods Enzymol. 153 215– 231. 10.1016/0076-6879(87)53055-5 3123881 · DOI
- Grieco E. Desrochers R. (1978). Production de vitamine B12 par une algae blue. Can. J. Microbiol. 24 1562– 1566. 10.1139/m78-250 106945 · DOI
- Hagmann L. Juttner F. (1996). Fischerellin A, a novel photosystem-II-inhibiting allelochemical of the cyanobacterium Fischerella muscicola with antifungal and herbicidal activity. Tetrahedron Lett. 37 6539– 6542. 10.1016/0040-4039(96)01445-1 · DOI
- Hanagata N. Takeuchi T. Fukuju Y. Barnes D. J. Karube I. (1992). Tolerance of microalgae to high CO2 and high temperature. Photochemistry 31 3345– 3348. 10.1016/0031-9422(92)83682-O · DOI
- Hankamer B. Lehr F. Rupprecht J. Mssgnug J. H. Posten C. Kruse O. (2007). Photosynthetic biomass and H2 production by green algae: from bioengineering to bioreactor scale-up. Physiol. Plant. 131 10– 21. 10.1111/j.1399-3054.2007.00924.x 18251920 · DOI
- Heidorn T. Camsund D. Huang H. H. Lindberg P. Oliveira P. Stensjo K. (2011). Synthetic biology in cyanobacteria engineering and analyzing novel functions. Methods Enzymol. 497 539– 579. 10.1016/B978-0-12-385075-1.00024-X 21601103 · DOI
- Higa T. (1991). “ Effective microorganisms: a biotechnology for mankind,” in Proceedings of the First International Conference on Kyusei Nature Farming, eds Parr J. F. Hornick S. B. Simpson M. E. (Washington, DC: U.S. Department of Agriculture), 8– 14.
- Higa T. Wididana G. N. (1991). “ Changes in the soil microflora induced by Effective Microorganisms,” in Proceedings of the First International Conference on Kyusei Nature Farming, eds Parr J. F. Hornick S. B. Whitman C. E. (Washington, DC: U.S. Department of Agriculture), 153– 162.
- Hirata S. Hayashitani M. Taya M. Tone S. (1996a). Carbon dioxide fixation in batch culture of Chlorella sp. using a photobioreactior with a sunlight-collection device. J. Ferment. Bioeng. 81 470– 472. 10.1016/0922-338X(96)85151-8 · DOI
- Hirata S. Taya M. Tone S. (1996b). Characterisation of Chlorella cell cultures in batch and continuous operations under a photoautotrophic condition. J. Chem. Eng. Jpn 29 953– 959. 10.1252/jcej.29.953 · DOI
- Huang H. H. Camsund D. Lindblad P. Heidorn T. (2010). Design and characterization of molecular tools for a synthetic biology approach towards developing cyanobacterial biotechnology. Nucleic Acids Res. 38 2577– 2593. 10.1093/nar/gkq164 20236988 PMC2860132 · DOI
- Inglesby A. E. Fisher A. C. (2012). Enhanced methane yields from anaerobic digestion of Arthrospira maxima biomass in an advanced flow-through reactor with an integrated recirculation loop microbial fuel cell. Energy Environ. Sci. 5 7996– 8006. 10.1039/c2ee21659k · DOI
- Inthorn D. Nagase H. Isaji Y. Hirata K. Miyamoto K. (1996). Removal of Cadmium from aqueous solution by the filamentous cyanobacterium Tolypothrix Tenuis. J. Ferment. Bioeng. 8 580– 584. 10.1016/S0922-338X(97)81256-1 · DOI
- Jacob-Lopes E. Scoparo C. H. G. Franco T. T. (2008). Rates of CO2 removal by Aphanothece microscopica Nageli in tubular photobioreactors. Chem. Engin. Process. 47 1371– 1379. 10.1016/j.cep.2007.06.004 · DOI
- Jansson C. Northen T. (2010). Calcifying cyanobacteria—the potential of biomineralization for carbon capture and storage. Curr. Opin. Biotechnol. 21 365– 371. 10.1016/j.copbio.2010.03.017 20456936 · DOI
- Jansson C. Wullschleger S. D. Udaya C. K. Tuskan G. A. (2010). Phytosequestration: carbon biosequestration by plants and the prospects of genetic engineering. BioSci 60 685– 696. 10.1525/bio.2010.60.9.6 · DOI
- Karthikeyan N. Prasanna R. Lata D. P. Kaushik B. D. (2007). Evaluating the potential of plant growth promoting cyanobacteria as inoculants for wheat. Eur. J. Soil Biol. 43 23– 30. 10.1016/j.ejsobi.2006.11.001 · DOI
- Karthikeyan N. Prasanna R. Sood A. Jaiswal P. Nayak S. Kaushik B. D. (2009). Physiological characterization and electron microscopic investigations of cyanobacteria associated with wheat rhizosphere. Folia Microbiol. 54 43– 51. 10.1007/s12223-009-0007-8 19330544 · DOI
- Kaushik B. D. (2012). Developments in cyanobacterial biofertilizer. Proc. Indian Natn. Acad. 80 379– 388. 10.16943/ptinsa/2014/v80i2/55115 · DOI
- Kaushik B. D. Subhashini D. (1985). Amelioration of salt affected soils with blue-green algae: improvements in soil properties. Proc. Ind. Natl. Sci. Acad. 51 380– 389.
- Kedar L. Kashman Y. Oren A. (2002). Mycosprine-2- glycine is the major mycosprine-like amino acid in a unicellular cyanobacterium (Euhalothece sp.) isolated from a gypsum crust in a hypersaline saltern pond. FEMS Microbiol. Lett. 208 233– 237. 10.1111/j.1574-6968.2002.tb11087.x 11959442 · DOI
- Koksharova O. A. Wolk C. P. (2002). Genetic tools for cyanobacteria. Appl. Microbiol. Biotechnol. 58 123– 137. 10.1007/s00253-001-0864-9 11876404 · DOI
- Koller M. Salernoa A. Tuffnerb P. Koiniggb M. Bochzeltb H. Schoberd S. (2012). Characteristics and potential of micro algal cultivation strategies: a review. J. Clean. Prod. 37 377– 388. 10.1016/j.jclepro.2012.07.044 · DOI
- Kulshreshtha A. Zacharia J. Jarouliya U. Bhadauriya P. Prasad G. B. K. S. Bisen P. S. (2008). Spirulina in healthcare management. Curr. Pharm. Biotechnol. 9 400– 405. 10.2174/138920108785915111 18855693 · DOI
- Kumar A. Singh J. S. (2016). “ Microalgae and cyanobacteria biofuels: a sustainable alternate to crop-based fuels,” in Microbes and Environmental Management, eds Singh J. S. Singh D. P. (New Delhi: Studium Press Pvt. Ltd.), 1– 20.
- Kumar K. Dasgupta C. N. Nayak B. Lindblad P. Das D. (2011). Development of suitable photobioreactors for CO2 sequestration addressing global warming using green algae and cyanobacteria. Bioresour. Technol. 102 4945– 4953. 10.1016/j.biortech.2011.01.054 21334885 · DOI · Paper page
- Kumar M. Bauddh K. Sainger M. Sainger P. A. Singh J. S. Singh R. P. (2012). Increase in growth, productivity and nutritional status of rice (Oryza sativa L. cv. Basmati) and enrichment in soil fertility applied with an organic matrix entrapped urea. J. Crop Sci. Biotechnol. 15 137– 144. 10.1007/s12892-012-0024-z · DOI
- Kuritz T. Wolk C. P. (1995). Use of filamentous cyanobacteria for biodegradation of organic pollutants. Appl. Environ. Microbiol. 61 234– 238. 7534052 PMC167278
- Lan E. I. Liao J. C. (2011). Metabolic engineering of cyanobacteria for 1-butanol production from carbon dioxide. Metab. Eng. 13 353– 363. 10.1016/j.ymben.2011.04.004 21569861 · DOI
- Lawson P. A. Allen T. D. Caldwell M. E. Tanner R. S. (2011). Anerobes: a piece in the puzzle for alternative bio-fuels. Anaerobe 17 206– 210. 10.1016/j.anaerobe.2011.05.011 21699990 · DOI
- Lee B. D. Apel W. A. Walton M. R. (2004). Screening of cyanobacterial species for calcification. Biotechnol. Prog. 20 1345– 1351. 10.1021/bp0343561 15458316 · DOI
- Lipok J. Owsiak T. Młynarz P. Forlani G. Kafarski P. (2007). Phosphorus NMR as a tool to study mineralization of organophosphonates-The ability of Spirulina spp. to degrade glyphosate. Enzyme Microb. Technol. 41 286– 291. 10.1016/j.enzmictec.2007.02.004 · DOI
- Lipok J. Wieczorek D. Jewginski M. Kafarski P. (2009). Prospects of in vivo 31P NMR method in glyphosate degradation studies in whole cell system. Enzyme Microb. Technol. 44 11– 16. 10.1016/j.enzmictec.2008.09.011 · DOI
- Liu X. Sheng J. Curtiss R. (2011). Fatty acid production in genetically modified cyanobacteria. Proc. Natl. Acad. Sci. U.S.A. 108 6899– 6904. 10.1073/pnas.1103014108 21482809 PMC3084101 · DOI · Paper page
- Lumpkin T. A. Plucknett D. L. (1982). Azolla as a Green Manure: Use and Management in Crop Production: Westview Tropical Agriculture Series No. 5. Boulder, Colo: Westview Press, 230.
- Machado I. M. P. Atsumi S. (2012). Cyanobacterial biofuel production. J. Biotechnol. 162 50– 56. 10.1016/j.jbiotec.2012.03.005 22446641 · DOI
- Maeda K. Owada M. Kimura N. Omata K. Karub I. (1995). CO2 fixation from the flue gas on coal-fired thermal power plant by microalgae. Energ. Convers. Manage. 36 717– 720. 10.1016/0196-8904(95)00105-M · DOI
- Mandal B. Das S. C. Mandal L. N. (1992). Effect of growth and subsequent decomposition of blue-green algae in the transformation of phosphorus in submerged soils. Plant Soil 143 289– 297. 10.1007/BF00007885 · DOI
- Mandal B. Vlek P. L. G. Mandal L. N. (1999). Beneficial effects of blue-green algae and Azolla, excluding supplying nitrogen, on wetland rice fields: a review. Biol. Fertil. Soils 28 329– 342. 10.1007/s003740050501 · DOI
- Mansy A. E. El-Bestway E. (2002). Toxicity and biodegradation of fluometuron by selected cyanobacterial species. World J. Microbiol. Biotechnol. 18 125– 131. 10.1023/A:1014490811121 · DOI
- Marsalek B. Zahradnickova H. Hronkova M. (1992). Extracellular abscisic acid produced by cyanobacteria under salt stress. J. Plant Physiol. 139 506– 508. 10.1016/S0176-1617(11)80503-1 · DOI
- Mason J. (2003). Sustainable Agriculture, 2nd Edn. Collingwood, VIC: Landlinks Press.
- Masukawa H. Nakamura K. Mochimaru M. Sakurai H. (2001). “ Photobiological hydrogen production and nitrogenase activity in some heterocystous cyanobacteria,” in Biohydrogen II, eds Miyake J. Matsunaga T. San Pietro A. (Oxford: Elsevier Science Ltd), 63– 66.
- Mazor G. Kidron G. J. Vanshak A. Abeliovich A. (1996). The role of cyanobacterial exopolysaccharides in structuring desert microbial crusts. FEMS Microbiol. Ecol. 21 121– 130. 10.3390/life5021218 · DOI
- Megharaj M. Madhavi D. R. Sreenivasulu C. Umamaheswari A. Venkateswarlu K. (1994). Biodegradation of methyl parathion by soil isolates of microalgae and cyanobacteria. Bull. Environ. Contam. Toxicol. 53 292– 297. 10.1007/BF00192047 8086714 · DOI
- Megharaj M. Venkateswarlu K. Rao A. S. (1987). Metabolism of monocrotophos and quinalphos by algae isolated from soil. Bull. Environ. Contam. Toxicol. 39 251– 256. 10.1007/BF01689414 3663978 · DOI
- Miller S. R. Castenholz R. W. Pedersen D. (2007). Phylogeography of the Thermophilic Cyanobacterium Mastigocladus laminosus. Appl. Environ. Microbiol. 73 4751– 4759. 10.1128/AEM.02945-06 17557856 PMC1951016 · DOI
- Misra S. Kaushik B. D. (1989a). Growth promoting substances of cyanobacteria. I. Vitamins and their influence on rice plant. Proc. Indian Sci. Acad. 55 295– 300.
- Misra S. Kaushik B. D. (1989b). Growth promoting substances of cyanobacteria II: detection of amino acids, sugars and auxins. Proc. Ind. Natl. Sci. Acad. 6 499– 504.
- Moisander P. H. McClinton E. III Paerl H. W. (2002). Salinity effects on growth, photosynthetic parameters, and nitrogenase activity in estuarine planktonic cyanobacteria. Microbial. Ecol. 43 432– 442. 10.1007/s00248-001-1044-2 12043002 · DOI
- Muhs J. (2000). Design and analysis of hybrid solar lighting and full-spectrum solar energy systems. Proc. Inter Solar Energ, Confer. (ISEC) 229– 237.
- Muller-Feuga A. (2000). The role of microalgae in aquaculture: situation and trends. J. Appl. Phycol. 12 527– 534. 10.1023/A:1008106304417 · DOI · Paper page
- Mussgnug J. H. Klassen V. Schluter A. Kruse O. (2010). Microalgae as substrates for fermentative biogas production in a combined biorefinery concept. J. Biotechnol. 150 51– 56. 10.1016/j.jbiotec.2010.07.030 20691224 · DOI
- Nakamura H. Kobayashi J. Hirata Y. (1982). Separation of mycosporine- like amino acids in marine organisms using reversed phase high performance liquid chromatography. J. Chromatogr. 250 113– 118. 10.1016/S0021-9673(00)95219-1 · DOI
- Narro M. L. (1985). Oxidation of Aromatic Hydrocarbons by Marine Cyanobacteria. Ph.D. Thesis, The University of Texas, Austin, TX.
- Narro M. L. Cerniglia C. E. Van B. C. Gibson D. T. (1992). Metabolism of phenanthrene by the marine cyanobacterium Agmenellum quadruplicate PR-6. Appl. Environ. Microbiol. 58 1351– 1359. 1599252 PMC195597
- Nelis H. J. DeLeenheer A. P. (1991). Microbial sources of carotenoid pigments used in foods and feeds. J. Appl. Bacteriol. 70 181– 191. 10.1111/j.1365-2672.1991.tb02922.x · DOI
- Nisha R. Kaushik A. Kaushik C. P. (2007). Effect of indigenous cyanobacterial application on structural stability and productivity of an organically poor semiarid soil. Geoderma 138 49– 56. 10.1016/j.geoderma.2006.10.007 · DOI
- Obreht Z. Kerby N. W. Gantar M. Rowell P. (1993). Effects of root associated N2-fixing cyanobacteria on the growth and nitrogen content of wheat (Triticum vulgare L.) seedlings. Biol. Fertil. Soils 15 68– 72. 10.1007/BF00336292 · DOI
- Ono E. Cuello J. L. (2004). Design parameters of solar concentrating systems for CO2 mitigating algal photo-bioreactors. Energy 29 1651– 1657. 10.1016/j.energy.2004.03.067 · DOI
- Pandey K. D. Shukla S. P. Skukla P. N. Giri D. D. Singh J. S. Singh P. (2004). Cyanobacteria in Antarctica: ecology, physiology and cold adaptation. Cell. Mol. Biol. 50 574– 584. 15559974
- Pandey V. C. Singh J. S. Singh D. P. Singh R. P. (2014). Methanotrophs: promising bacteria for environmental remediation. Int. J. Environ. Sci. Technol. 11 241– 250. 10.2134/jeq2011.0179 · DOI
- Papke U. Gross E. M. Francke W. (1997). Isolation, identification and determination of the absolute configuration of Fischerellin B. A new algicide from the freshwater cyanobacterium Fischerellin muscicola (Thuret). Tetrahedron Lett. 38 379– 382. 10.1016/S0040-4039(96)02284-8 · DOI
- Parmar A. Singh N. K. Pandey A. Gnansounou E. Madamwar D. (2011). Cyanobacteria and microalgae: a positive prospect for biofuels. Bioresour. Technol. 102 10163– 10172. 10.1016/j.biortech.2011.08.030 21924898 · DOI · Paper page
- Peters G. A. Toia R. E. J. Lough S. M. (1977). The Azolla-Anabaena Azollae relationship. V.15 N2 fixation, acetylene reduction and H2 production. Plant Physiol. 59 1021– 1025. 10.1104/pp.59.6.1021 16659984 PMC542497 · DOI
- Pfennig N. (1969). Rhodopseudomonas acidophila, sp. n., a new species of the budding purple nonsulfur bacteria. J. Bacteriol. 99 597– 602. 5821103 PMC250060
- Pfennig N. (1974). Rhodopseudomonas globformis, sp. n., a new species of the Rhodospirillaceae. Arch. Microbiol. 100 197– 206. 10.1007/BF00446317 · DOI
- Pinzon-Gamez N. M. Sundaram S. Ju L. K. (2005). “ Heterocyst differentiation and H2 production in N2-fixing cyanobacteria,” in Proceedings of the AIChE Annual Meeting, Cincinnati, OH.
- Plavsic M. Terzic S. Ahel M. Van Den Berg C. M. G. (2004). Folic acid in coastal waters of the Adriatic Sea. Mar. Freshw. Res. 53 1245– 1252. 10.1071/MF02044 · DOI
- Prasanna R. Kumar V. Kumar S. Yadav A. K. Tripathi U. Singh A. K. (2002). Methane production in rice soils is inhibited by cyanobacteria. Microbiol. Res. 157 1– 6. 10.1078/0944-5013-00124 11911608 · DOI
- Prasanna R. Sood A. Jaiswal P. Nayak S. Gupta V. Chaudhary V. (2010). Rediscovering Cyanobacteria as valuable sources of bioactive compounds (Review). Appl. Biochem. Microbiol. 46 119– 134. 10.1134/S0003683810020018 20391755 · DOI
- Priyadarshani I. Rath B. (2012). Commercial and industrial applications of microalgae- a review. J. Algal Biomass Utln. 3 89– 100.
- Radmer R. J. (1996). Algal diversity and commercial algal products. Bioscience 46 263– 270. 10.2307/1312833 · DOI
- Raghukumar C. Vipparty V. David J. J. Chandramohan D. (2001). Degradation of crude oil by marine cyanobacteria. Appl. Microbiol. Biotechnol. 57 433– 436. 10.1007/s002530100784 11759698 · DOI
- Rajeev K. J. Xu Z. (2004). Biomedical compounds from marine organisms. Mar. Drugs 2 123– 146. 10.3390/md203123 · DOI
- Rangel-Yagui C. O. Godoy Danesi E. D. Carvalho J. C. M. Sato S. (2004). Chlorophyll production from Spirulina platensis: cultivation with urea addition by fed-batch process. Bioresour. Technol. 92 133– 141. 10.1016/j.biortech.2003.09.002 14693445 · DOI · Paper page
- Rau G. H. Knauss K. G. Langer W. H. Caldeira K. (2007). Reducing energy related CO2 emissions using accelerated weathering of limestone. Energy 32 1471– 1477. 10.1016/j.energy.2006.10.011 · DOI
- Raungsomboon S. Chidthaisonga A. Bunnagb B. Inthornc D. Harveya N. W. (2006). Production, composition and Pb2+ adsorption characteristics of capsular polysaccharides extracted from a cyanobacterium Gloeocapsa gelatinosa. Water Res. 40 3759– 3766. 10.1016/j.watres.2006.08.013 17052742 · DOI
- Rimbau V. Camins A. Pubill D. Sureda F. X. Romay C. Gonzalez R. (2001). C-phycocyanin protects cerebellar granule cells from low potassium/ serum deprivation-induced apoptsis. Arch. Pharmacol. 364 96– 104. 10.1007/s002100100437 11534860 · DOI
- Rissanen T. Voutilainen S. Nyyssonen K. Salonen J. T. (2002). Lycopene atherosclerosis, and coronary heart disease. Exp. Biol. Med. 227 900– 907. 12424332
- Rodgers G. A. Bergman B. Henriksson E. Udris M. (1979). Utilization of blue-green algae as bio-fertilizers. Plant Soil 52 99– 107. 10.1007/BF02197736 · DOI
- Rogers S. L. Burns R. G. (1994). Changes in aggregate stability, nutrient status, indigenous microbial populations and seedling emergence following inoculation of soil with Nostoc muscorum. Biol. Fertil. Soils 18 209– 215. 10.1007/BF00647668 · DOI
- Rohwer F. Thurber R. V. (2009). Viruses manipulate the marine environment. Nature 459 207– 212. 10.1038/nature08060 19444207 · DOI
- Romay C. P. Gonazelz R. Ledon N. Ramirez D. Vimbare V. (2003). C-phycocyanin: a biliprotein with antioxidant, anti-inflammetry and neuroprotective effects. Curr. Protein Peptide Sci. 4 207– 216. 10.2174/1389203033487216 12769719 · DOI
- Rosgaard L. de Porcellinis A. J. Jacobsenc J. H. Frigaardc N. U. Sakuragia Y. (2012). Bioengineering of carbon fixation, biofuels, and biochemicals in cyanobacteria and plants. J. Biotechnol. 162 134– 147. 10.1016/j.jbiotec.2012.05.006 22677697 · DOI
- Ruffing A. M. (2011). Engineered cyanobacteria: teaching an old bug new tricks. Bioeng. Bugs 2 136– 149. 10.4161/bbug.2.3.15285 21637004 · DOI · Paper page
- Samson R. Leduy A. (1986). Detailed study of anaerobic-digestion of Spirulina maxima algal biomass. Biotechnol. Bioeng. 28 1014– 1023. 10.1002/bit.260280712 18555423 · DOI
- Sergeeva E. Liaimer A. Bergman B. (2002). Evidence for production of the phytohormone indole-3-acetic acid by cyanobacteria. Planta 215 229– 238. 10.1007/s00425-002-0749-x 12029472 · DOI
- Shashirekha S. Uma L. Subramanian G. (1997). Phenol degradation by the marine cyanobacterium Phormidium valderianum BDU-30501. J. Ind. Microbiol. Biotechnol. 19 130– 133. 10.1038/sj.jim.2900438 · DOI
- Sialve B. Bernet N. Bernard O. (2009). Anaerobic digestion of microalgae as a necessary step to make microalgal biodiesel sustainable. Biotech. Adv. 4 409– 416. 10.1016/j.biotechadv.2009.03.001 19289163 · DOI · Paper page
- Singh J. S. (2013a). Anticipated effects of climate change on methanotrophic methane oxidation. Climate Change Environ. Sustain. 1 20– 24. 10.5958/j.2320-6411.1.1.003 · DOI
- Singh J. S. (2013b). Plant growth promoting rhizobacteria. Resonance 18 275– 281. 10.1007/s12045-013-0038-y · DOI
- Singh J. S. (2015a). Microbes: the chief ecological engineers in reinstating equilibrium in degraded ecosystems. Agric. Ecosyst. Environ. 203 80– 82. 10.1016/j.agee.2015.01.026 · DOI
- Singh J. S. (2015b). Plant-microbe interactions: a viable tool for agricultural sustainability. Appl. Soil Ecol. 92 45– 46. 10.1016/j.apsoil.2015.03.004 · DOI
- Singh J. S. Pandey V. C. (2013). Fly ash application in nutrient poor agriculture soils: impact on methanotrophs density dynamics and paddy yields. Ecotoxicol. Environ. Safe. 89 43– 51. 10.1016/j.ecoenv.2012.11.011 23260239 · DOI
- Singh J. S. Pandey V. C. Singh D. P. (2011a). Efficient soil microorganisms: a new dimension for sustainable agriculture and environmental development. Agric. Ecosyst. Environ. 140 339– 353. 10.1016/j.agee.2011.01.017 · DOI
- Singh J. S. Pandey V. C. Singh D. P. Singh R. P. (2010). Influence of pyrite and farmyard manure on population dynamics of soil methanotroph and rice yield in saline rain-fed paddy field. Agric. Ecosyst. Environ. 139 74– 79. 10.1016/j.agee.2010.07.003 · DOI
- Singh J. S. Singh D. P. (2012). Reforestation: a potential approach to mitigate the excess CH4 build-up. Ecol. Manage. Restor. 13 245– 248. 10.1111/emr.12004 · DOI
- Singh J. S. Singh D. P. (2013b). “ Plant growth promoting rhizobacteria (PGPR): microbes in sustainable agriculture,” in Management of Microbial Resources in the Environment, eds Malik A. Grohmann E. Alves M. (Berlin: Springer), 307– 319.
- Singh J. S. Strong P. J. (2016). Biologically derived fertilizer: a multifaceted bio-tool in methane mitigation. Ecotoxicol. Environ. Saf. 124 267– 276. 10.1016/j.ecoenv.2015.10.018 26547397 · DOI · Paper page
- Singh V. P. Trehan T. (1973). Effects of extracellular products of Aulosira fertilissuna on the growth of rice seedlings. Plant Soil 38 457– 464. 10.1007/BF00779027 · DOI
- Sinha R. P. Häder D. P. (1996). Photobiology and ecophysiology of rice field cyanobacteria. Photochem. Photobiol. 64 887– 896. 10.1111/j.1751-1097.1996.tb01852.x · DOI
- Sinha R. P. Klisch M. Groniger A. Hader D. P. (1998). Ultraviolet-absorbing/ screening substances in cyanobacteria, phytoplankton and macroalgae. J. Photochem. Photobiol. 47 83– 94. 10.1016/S1010-6030(98)00332-3 11233638 · DOI
- Sinha R. P. Klisch M. Helbling E. W. Hader D. P. (2001). Induction of mycosprine-like amino acids (MAA’s) in cyanobacteria by ultraviolet B radiation. J. Photochem. Photobiol. 60 129– 135. 10.1016/S1011-1344(01)00137-3 11470569 · DOI
- Sokhoh N. A. Al-Hasan R. H. Radwan S. S. Hopner T. (1992). Self-cleaning of the Gulf. Nature 359: 109 10.1038/359109a0 · DOI
- Soletto D. Binaghi L. Lodi A. Carvalho J. C. M. Converti A. (2005). Batch and fed-batch cultivations of Spirulina platensis using ammonium sulphate and urea as nitrogen sources. Aquaculture 243 217– 224. 10.1016/j.aquaculture.2004.10.005 · DOI · Paper page
- Sorkhoh N. A. Al-Hasan R. H. Khanafer M. Radwan S. S. (1995). Establishment of oil-degrading bacteria associated with cyanobacteria in oil-polluted soil. J. Appl. Bacteriol. 78 194– 199. 10.1111/j.1365-2672.1995.tb02842.x 7698954 · DOI
- Stewart W. D. P. Fitzgerald G. P. Burns R. H. (1968). Acetylene reduction by nitrogen-fixing blue-green algae. Arch. Microbiol. 62 336– 348. 5709637
- Subhashini J. Mahipal S. V. Reddy M. C. Mallikarjuna Reddy M. Rachamallu A. Reddanna P. (2004). Molecular mechanisms in C-phycocyanin induced apoptsis in human chronic myeloid leukemia cell line-K 562. Biochem. Pharmacol. 68 453– 462. 10.1016/j.bcp.2004.02.025 15242812 · DOI
- Subramanian G. Sundaram S. S. (1986). Induced ammonia release by the nitrogen fixing cyanobacterium Anabaena. FEMS Microbiol. Lett. 37 151– 154. 10.1111/j.1574-6968.1986.tb01784.x · DOI
- Tiwari A. Pandey A. (2012). Cyanobacterial hydrogen- a step towards clean environment. Inter. J. Hydrogen Energ. 37 139– 150. 10.1016/j.ijhydene.2011.09.100 · DOI
- Tiwari S. Singh J. S. Singh D. P. (2015). Methanotrophs and CH4 sink: effect of human activity and ecological perturbations. Climate Change Environ. Sustain. 3 35– 50. 10.5958/2320-642X.2015.00004.6 · DOI
- Vijayakumar S. (2012). Potential applications of cyanobacteria in industrial effluents- a review. J. Bioremed. Biodeg. 3 1– 6. 10.4172/2155-6199.1000154 · DOI
- Vílchez C. Garbayo I. Lobato M. V. Vega J. M. (1997). Microalgae-mediated chemicals production and wastes removal. Enzyme Microb. Technol. 20 562– 572. 10.1016/j.biortech.2015.03.112 · DOI
- Volkmann M. Gorbushina A. A. (2006). A broadly applicable method for extraction and characterization of mycosporines and mycosprine-like amino acids of terrestrial, marine and freashwater origin. FEMS Microbiol. Lett. 255 286– 295. 10.1111/j.1574-6968.2006.00088.x 16448508 · DOI
- Volkmann M. Gorbushina A. A. Kedar L. Oren A. (2006). Structure of euhalothece-362 a novel red-shifted mycosprine-like amino acid; from a halophilic cyanobacterium (Euhalothece sp.). FEMS Microbiol. Lett. 258 50– 54. 10.1111/j.1574-6968.2006.00203.x 16630254 · DOI
- Wolf A. M. Baker D. E. Pionke H. B. Kunichi H. M. (1985). Soil test for estimating labile, soluble and algal available phosphorus in agricultural soils. J. Environ. Qual. 14 341– 348. 10.2134/jeq1985.00472425001400030008x · DOI
- Zeng S. J. Yuan X. Z. Shi X. S. Qiu Y. L. (2010). Effect of inoculum/substrate ratio on methane yield and orthophosphate release from anaerobic digestion of Microcystis sp. J. Hazard. Mater. 178 89– 93. 10.1016/j.jhazmat.2010.01.047 20138427 · DOI
- Zhong W. Zhang Z. Luo Y. Qiao W. Xiao M. Zhang M. (2012). Biogas productivity by co-digesting Taihu blue algae with corn straw as an external carbon source. Bioresour. Technol. 114 281– 286. 10.1016/j.biortech.2012.02.111 22459954 · DOI
- Zulpa G. Zaccaro M. C. Boccazzi F. Parada J. L. Storni M. (2003). Bioactivity of intra and extracellular substances from cyanobacteria and lactic acid bacteria on “wood blue stain” fungi. Biol. Control 27 345– 348. 10.1016/S1049-9644(03)00015-X · DOI
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- Authors
- Singh, J. S., Kumar, A., Rai, A. N., & Singh, D. P.
- Affiliations
- Babasaheb Bhimrao Ambedkar University (IN)
- North Eastern Hill University (IN)
- Corresponding author
- Singh, Jay Shankar
- Venue
- Frontiers in Microbiology
- Publisher
- Frontiers Media SA
- Published
- 2016-04-21
- Volume
- 7
- Pages
- 529-529
- ISSN
- 1664-302X (ISSN-L)
- PMC
- PMC4838734
- OpenAlex
- W2340027296
- Cited by
- 758
- References
- 11
- Citations by year
- 2026: 75 · 2025: 84 · 2024: 111 · 2023: 90 · 2022: 105 · 2021: 102 · 2020: 77 · 2019: 48 · 2018: 36 · 2017: 24 · 2016: 6
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Microbiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Banaras Hindu University
- Topics
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Biocrusts and Microbial Ecology
- Physical Sciences › Environmental Science › Environmental Chemistry › Aquatic Ecosystems and Phytoplankton Dynamics
- Keywords
- cyanobacteria, biofertilizers, microbial inoculants, nitrogen fixation, soil fertility, biofuels, biohydrogen, biodiesel, biomethane, syngas, oxygenic photosynthesis, greenhouse gas emissions reduction, water holding capacity, degraded land, food security, genetically engineered cyanobacteria, environmental sustainability
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