Co-production of bioethanol and commercially important exopolysaccharides from the marine cyanobacterium Synechococcus elongatus BDU 10144 in a novel low-cost seawater-fertilizer-based medium
Neha Chandra
Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India
Search for more papers by this authorCorresponding Author
Nirupama Mallick
Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India
Correspondence
Nirupama Mallick, Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India.
Email: [email protected] and [email protected]
Search for more papers by this authorNeha Chandra
Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India
Search for more papers by this authorCorresponding Author
Nirupama Mallick
Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India
Correspondence
Nirupama Mallick, Agricultural and Food Engineering Department, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India.
Email: [email protected] and [email protected]
Search for more papers by this authorFunding information: Indian Institute of Technology (IIT) Kharagpur
Summary
The production of bioethanol by cyanobacteria can become economically sustainable if other valuable commercial products, such as exopolysaccharides (EPS), are produced simultaneously. This study investigates the feasibility of producing bioethanol and the commercially important EPS from a non-nitrogen fixing marine cyanobacterium, Synechococcus elongatus BDU 10144 in a novel low-cost seawater-fertilizer medium for the development of a biorefinery strategy. Herein, agricultural fertilizer diammonium phosphate (DAP) (nitrogen source), magnesium sulfate (MgSO4) and potassium were optimized by the central composite design to produce maximum biomass and carbohydrate accretion. The optimal physical conditions for attaining maximum growth and carbohydrate accumulation were determined to be pH 10, 50 μmol m−2 s−1 (light intensity) and 25°C. Further, different concentrations of seawater were mixed with the optimized fertilizer-salts, and it was observed that 70% of seawater mixed with the optimized fertilizer-salts (hereafter FSW medium) was an optimum condition for growing the test cyanobacterium, which ultimately reduced the cost of the medium by >40 times compared to the standard artificial seawater nutrient (ASN-III) medium. Under the optimal conditions, the maximum biomass (1.79 g/L) and carbohydrate (702.4 mg/L) yield obtained were ~1.7 and 2.2 times higher than the ASN-III. The yield of bioethanol was noted to be 318.1 mg/L, which was ~2.3 times greater than ASN-III. The commercially important EPS was obtained from the discarded supernatant (0.28 g/L), which was ~1.6 times higher in the FSW medium. Thus, the present investigation paves a way forward for mass cultivation of the S. elongatus BDU 1044 in the novel FSW medium for the cost-efficient and sustainable development of a biorefinery concept.
CONFLICT OF INTEREST
The authors declare that they have no conflicts of interest.
Open Research
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Supporting Information
Filename | Description |
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er8069-sup-0001-Tables.docxWord 2007 document , 28.5 KB | Supplementary Table S1 Comparison of composition of the newly formulated different fertilizer-based media (1× concentration) with standard ASN-III Supplementary Table S2 Central composite design matrix with actual and predicted response for growth and carbohydrate accumulation in Synechococcus elongatus BDU 10144 Supplementary Table S3 ANOVA summary of the response surface quadratic model for biomass yield Supplementary Table S4 ANOVA summary of the response surface quadratic model for total carbohydrate yield Supplementary Table S5 Cost comparison of standard ASN-III, U 1X, NPK 1X and DAP 1X media for 1000 L (in US$) Supplementary Table S6 Cost comparison of optimized FSW with standard ASN-III for preparation of 1000 L medium |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
REFERENCES
- 1Razack A, Surendhiran D. Algae—a quintessential and positive resource of bioethanol. Renew Sustain Energy Rev. 2016; 66: 248-267.
- 2Anto S, Sankha S, Muthappa R, et al. Algae as green energy reserve: technological outlook on biofuel production. Chemosphere. 2020; 242:125079.
- 3Kumar M, Sun Y, Rathour R, Pandey A, Shekhar I, Tsang DCW. Algae as potential feedstock for the production of biofuels and value-added products: opportunities and challenges. Sci Total Environ. 2020; 716:137116.
- 4Jaiswal KK, Dutta S, Banerjee I, Pohrmen CB, Kumar V. Photosynthetic microalgae-based carbon sequestration and generation of biomass in biorefinery approach for renewable biofuels for a cleaner environment. Biomass Convers Biorefin. 2021; 1-19.
- 5Meinita MDN, Marhaeni B, Oktaviani DF, Jeong G-T, Hong Y-K. Comparison of bioethanol production from cultivated versus wild Gracilaria verrucosa and Gracilaria gigas. J Appl Phycol. 2018; 30: 143-147.
- 6Jambo SA, Abdulla R, Mohd Azhar SH, Marbawi H, Gansau JA, Ravindra P. A review on third generation bioethanol feedstock. Renew Sustain Energy Rev. 2016; 65: 756-769.
- 7Lee OK, Lee EY. Sustainable production of bioethanol from renewable brown algae biomass. Biomass Bioenergy. 2016; 92: 70-75.
- 8Sharma NK, Tiwari SP, Tripathi K, Rai AK. Sustainability and cyanobacteria (blue-green algae): facts and challenges. J Appl Phycol. 2011; 23: 1059-1081.
- 9Mota R, Flores C, Tamagnini P. Cyanobacterial extracellular polymeric substances (EPS). In: JM Oliveira, H Radhouani, RL Reis, eds. Polysaccharides of Microbial Origin. Cham: Springer; 2021: 1-28.
10.1007/978-3-030-35734-4_11-1 Google Scholar
- 10Kim EJ, Kim S, Choi HG, Han SJ. Co-production of biodiesel and bioethanol using psychrophilic microalga Chlamydomonas sp. KNM0029C isolated from Arctic Sea ice. Biotechnol Biofuels. 2020; 13: 1-13.
- 11Prabha S, Vijay AK, Rajan R, George B. Cyanobacterial biorefinery: towards economic feasibility through the maximum valorization of biomass. Sci Total Environ. 2022; 814:152795.
- 12Costa JAV, Lucas BF, Alvarenga AGP, Moreira JB, de Morais MG. Microalgae polysaccharides: an overview of production, characterization, and potential applications. Polysaccharides. 2021; 2(4): 759-772.
- 13Sutherland IW. Microbial polysaccharides from gram-negative bacteria. Int Dairy J. 2001; 11: 663-674.
- 14Rossi F, De Philippis R, Haselkorn R. Role of cyanobacterial exopolysaccharides in phototrophic biofilms and in complex microbial mats. Life (Basel). 2015; 5: 1218-1238.
- 15Delattre C, Pierre G, Laroche C, Michaud P. Production, extraction and characterization of microalgal and cyanobacterial exopolysaccharides. Biotechnol Adv. 2016; 34: 1159-1179.
- 16Ameen F, Alnadhari S, Al-homaidan AA. Marine microorganisms as an untapped source of bioactive compounds, Saudi. Aust J Biol Sci. 2021; 28: 224-231.
- 17Maity S, Mallick N. Trends and advances in sustainable bioethanol production by marine microalgae: a critical review. J Clean Prod. 2022; 345:131153.
- 18Taikhao S, Incharoensakdi A. Dark fermentative hydrogen production by the unicellular halotolerant cyanobacterium Aphanothece halophytica grown in seawater. J Appl Phycol. 2015; 27: 187-196.
- 19Maeda Y, Yoshino T, Matsunaga T, Matsumoto M, Tanaka T. Marine microalgae for production of biofuels and chemicals. Curr Opin Biotechnol. 2018; 50: 111-120.
- 20Shukla SP, Lekshmi M, Alagarsamy V. Cultivation of Spirulina (Arthrospira) platensis in low cost seawater based medium for extraction of value added pigments. Indian J Geo Mar Sci. 2015; 44: 384-393.
- 21Tran D, Doan N, Louime C, Giordano M, Portilla S. Growth, antioxidant capacity and total carotene of Dunaliella salina DCCBC15 in a low cost enriched natural seawater medium. World J Microbiol Biotechnol. 2014; 30: 317-322.
- 22Ishika T, Bahri PA, Laird DW, Moheimani NR. The effect of gradual increase in salinity on the biomass productivity and biochemical composition of several marine, halotolerant, and halophilic microalgae. J Appl Phycol. 2018; 30: 1453-1464.
- 23Wang X, Huang L, Ji P, Chen C, Li X, Gao Y. Using a mixture of wastewater and seawater as the growth medium for wastewater treatment and lipid production by the marine diatom Phaeodactylum tricornutum. Bioresour Technol. 2019; 289:121681.
- 24Debnath C, Kanti T, Bhunia B, Mishra U. Microalgae: sustainable resource of carbohydrates in third-generation biofuel production. Renew Sustain Energy Rev. 2021; 150:111464.
- 25Tsolcha ON, Patrinou V, Economou CN, Dourou M, Aggelis G, Tekerlekopoulou AG. Utilization of biomass derived from cyanobacteria-based agro-industrial wastewater treatment and raisin residue extract for bioethanol production. Water. 2021; 13:486.
- 26Ahmad AL, Yasin NHM, Derek CJC, Lim JK. Microalgae as a sustainable energy source for biodiesel production: a review. Renew Sustain Energy Rev. 2011; 15: 584-593.
- 27Rodolfi L, Zittelli GC, Bassi N, et al. Microalgae for oil: strain selection, induction of lipid synthesis and outdoor mass cultivation in a low-cost photobioreactor. Biotechnol Bioeng. 2009; 102: 100-112.
- 28Guzmán-Murillo MA, López-Bolaños CC, Ledesma-Verdejo T, Roldan-Libenson G, Cadena-Roa MA, Ascencio F. Effects of fertilizer-based culture media on the production of exocellular polysaccharides and cellular superoxide dismutase by Phaeodactylum tricornutum (Bohlin). J Appl Phycol. 2007; 19: 33-41.
- 29Koley S, Mathimani T, Bagchi SK, Sonkar S, Mallick N. Microalgal biodiesel production at outdoor open and polyhouse raceway pond cultivations: a case study with Scenedesmus accuminatus using low-cost farm fertilizer medium. Biomass Bioenergy. 2019; 120: 156-165.
- 30Rippka R, Deruelles J, Waterbury JB, Herdman M, Stanier RY. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. Microbiology. 1979; 111: 1-61.
- 31Rai LC, Mallick N, Singh JB, Kumar HD. Physiological and biochemical characteristics of a copper tolerant and a wild type strain of Anabaena doliolum under copper stress. J Plant Physiol. 1991; 138: 68-74.
- 32Sukumaran P, Nulit R, Halimoon N, Simoh S, Omar H, Ismail A. Formulation of cost-effective medium using urea as a nitrogen source for Arthrospira platensis cultivation under real environment. Ann Res Rev Biol. 2018; 22: 1-12.
10.9734/ARRB/2018/38182 Google Scholar
- 33Yarish C, Redmond S, Kim JK. General seaweed culture system components. Gracilaria Culture Handbook for New England; Connecticut: Wrack lines; 2017.
- 34Herbert D, Phipps PJ, Strange RE. Chemical analysis of microbial cells. In: JR Norris, DW Ribbons, eds. Methods in Microbiology. London: Academic Press Inc. Ltd. Published by Elsevier Ltd. 1971; 5: 209-344.
10.1016/S0580-9517(08)70641-X Google Scholar
- 35Donald Nicholas DJ, Nason A. Determination of nitrate and nitrite. Methods Enzymol. 1957; 3: 981-984.
- 36DuBois M, Gilles KA, Hamilton JK, Rebers PA, Smith F. Colorimetric method for determination of sugars and related substances. Anal Chem. 1956; 28: 350-356.
- 37Chandra N, Shukla P, Mallick N. Role of cultural variables in augmenting carbohydrate accumulation in the green microalga Scenedesmus acuminatus for bioethanol production. Biocatal Agric Biotechnol. 2020; 26:101632.
- 38Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193: 265-275.
- 39Bligh EG, Dyer WJ. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959; 37: 911-917.
- 40Koley S, Khadase MS, Mathimani T, Raheman H, Mallick N. Catalytic and non-catalytic hydrothermal processing of Scenedesmus obliquus biomass for bio-crude production—a sustainable energy perspective. Energ Conver Manage. 2018; 163: 111-121.
- 41Miller GL. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem. 1959; 31: 426-428.
- 42Updegraff DM. Semimicro determination of cellulose inbiological materials. Anal Biochem. 1969; 32: 420-424.
- 43Ververis C, Georghiou K, Danielidis D, et al. Cellulose, hemicelluloses, lignin and ash content of some organic materials and their suitability for use as paper pulp supplements. Bioresour Technol. 2007; 98: 296-301.
- 44Hodge BT, Hofreiter JE. Determination of reducing sugars and carbohydrates. In: RL Whistler, ML Wolfrom, eds. Methods in Carbohydrate Chemistry. New York: Academic Press. 1962; 1: 380-394.
- 45Seifter S, Dayton S. The estimation of glycogen with the anthrone reagent. Arch Biochem. 1950; 25: 191-200.
- 46Deb D, Mallick N, Bhadoria PBS. Analytical studies on carbohydrates of two cyanobacterial species for enhanced bioethanol production along with poly-β-hydroxybutyrate, C-phycocyanin, sodium copper chlorophyllin, and exopolysaccharides as co-products. J Clean Prod. 2019; 221: 695-709.
- 47Seo HB, Kim HJ, Lee OK, Ha JH, Lee HY, Jung KH. Measurement of ethanol concentration using solvent extraction and dichromate oxidation and its application to bioethanol production process. J Ind Microbiol Biotechnol. 2009; 36: 285-292.
- 48Nagle VL, Mhalsekar M, Jagtap TG. Isolation, optimization and characterization of selected cyanophycean members. Ind J Geo Mar Sci. 2010; 39: 212-218.
- 49Aouir A, Amiali M, Bitam A, Benchabane A. Comparison of the biochemical composition of different Arthrospira platensis strains from Algeria, Chad and the USA. J Food Meas Charact. 2017; 11: 913-923.
- 50Nayak M, Thirunavoukkarasu M, Mohanty RC. Cultivation of freshwater microalga Scenedesmus sp. using a low-cost inorganic fertilizer for enhanced biomass and lipid yield. J Gen Appl Microbiol. 2016; 62: 7-13.
- 51Madkour FF, Kamil AE, Nasr HS. Production and nutritive value of Spirulina platensis in reduced cost media. Egypt J Aquat Res. 2012; 38: 51-57.
10.1016/j.ejar.2012.09.003 Google Scholar
- 52Mostert ES, Grobbelaar JU. The influence of nitrogen and phosphorus on algal growth and quality in outdoor mass algal cultures. Biomass. 1987; 13: 219-233.
- 53Giraldo ND, Correa SM, Arbeláez A, Figueroa FL. Reducing self-shading effects in Botryococcus braunii cultures: effect of Mg2+ deficiency on optical and biochemical properties, photosynthesis and lipidomic profile. Bioresour Bioprocess. 2021; 8: 33.
- 54Cakmak I, Yazici A. Magnesium: a forgotten element in crop production. Better Crops. 2010; 94: 23-25.
- 55Hanifzadeh M, Cerdan E, Viamajala S. Production of lipid and carbohydrate from microalgae without compromising biomass productivities: role of Ca and Mg. Renew Energy. 2018; 127: 989-997.
- 56Kumari A, Pathak AK, Guria C. Effect of light emitting diodes on the cultivation of Spirulina platensis using NPK-10:26:26 complex fertilizer. Phycol Res. 2015; 63: 274-283.
- 57Koley S, Prasad S, Bagchi SK, Mallick N. Development of a harvesting technique for large-scale microalgal harvesting for biodiesel. RSC Adv. 2017; 7: 7227-7237.
- 58Bagchi SK, Rao PS, Mallick N. Development of an oven drying protocol to improve biodiesel production for an indigenous chlorophycean microalga Scenedesmus sp. Bioresour Technol. 2015; 180: 207-213.
- 59Deb D, Mallick N, Bhadoria PBS. Engineering culture medium for enhanced carbohydrate accumulation in Anabaena variabilis to stimulate production of bioethanol and other high-value co-products under cyanobacterial refinery approach. Renew Energy. 2021; 163: 1786-1801.
- 60Kothari R, Pandey A, Ahmad S, Kumar A, Pathak VV, Tyagi VV. Microalgal cultivation for value-added products: a critical enviro-economical assessment. 3 Biotech. 2017; 7: 243.
- 61Juneja A, Ceballos RM, Murthy GS. Effects of environmental factors and nutrient availability on the biochemical composition of algae for biofuels production: a review. Energies. 2013; 6: 4607-4638.
- 62Eduardo de Farias Silva C, Sforza E, Bertucco A. Enhancing carbohydrate productivity in photosynthetic microorganism production: A comparison between cyanobacteria and microalgae and the effect of cultivation systems. In: M, ed. Hosseini Advances in Feedstock Conversion Technologies for Alternative Fuels and Bioproducts. UK: Woodhead publishing, Elsevier Inc. 2019: 37-67. Woodhead Publishing Series in Energy.
10.1016/B978-0-12-817937-6.00003-5 Google Scholar
- 63Muhetaer G, Asaeda T, Jayasanka SMDH, et al. Effects of light intensity and exposure period on the growth and stress responses of two cyanobacteria species: Pseudanabaena and Microcystis aeruginosa. Water. 2020; 12: 407.
- 64Samiotis G, Stamatakis K, Amanatidou E. Assessment of Synechococcus elongatus PCC 7942 as an option for sustainable wastewater treatment. Water Sci Technol. 2021; 84: 1438-1451.
- 65Bochenski T, Chaturvedi T, Thomsen MH. Evaluation of marine Synechococcus for an algal biorefinery in arid regions. Energies. 2019; 12: 2233.
- 66Converti A, Casazza AA, Ortiz EY, Perego P, Del Borghi M. Effect of temperature and nitrogen concentration on the growth and lipid content of Nannochloropsis oculata and Chlorella vulgaris for biodiesel production. Chem Eng Process Process Intensif. 2009; 48: 1146-1151.
- 67Atkinson D, Ciotti BJ, Montagnes DJS. Protists decrease in size linearly with temperature: ca. 2.5% degrees C(−1). Proc R Soc Lond B. 2003; 270: 2605-2611.
- 68Salvucci ME, Crafts-brandner SJ. Relationship between the heat tolerance of photosynthesis and the thermal stability of rubisco activase in plants from contrasting thermal environments. Plant Physiol. 2004; 134: 1460-1470.
- 69Mathur S, Agrawal D, Jajoo A. Photosynthesis: response to high temperature stress. J Photochem Photobiol B Biol. 2014; 137: 116-126.
- 70Vonshak G, Torzillo A. Environmental stress physiology. In: A Richmond, ed. Handbook of Microalgal Culture. Oxford, UK: Blackwell; 2004: 57-82.
- 71Touloupakis E, Cicchi B, Benavides AMS, Torzillo G. Effect of high pH on growth of Synechocystis sp. PCC 6803 cultures and their contamination by golden algae (Poterioochromonas sp.). Appl Microbiol Biotechnol. 2016; 100: 1333-1341.
- 72Mathimani T, Uma L, Prabaharan D. Formulation of low-cost seawater medium for high cell density and high lipid content of Chlorella vulgaris BDUG 91771 using central composite design in biodiesel perspective. J Clean Prod. 2018; 198: 575-586.
- 73Ogbonda KH, Aminigo RE, Abu GO. Infuence of temperature and pH on biomass production and protein biosynthesis in a putative Spirulina sp. Bioresour Technol. 2007; 98: 2207-2211.
- 74Piiparinen J, Barth D, Eriksen NT, Teir S, Spilling K, Wiebe MG. Microalgal CO2 capture at extreme pH values. Algal Res. 2018; 32: 321-328.
10.1016/j.algal.2018.04.021 Google Scholar
- 75De Farias Silva CE, Sforza E, Bertucco A. Effects of pH and carbon source on Synechococcus PCC 7002 cultivation: biomass and carbohydrate production with different strategies for pH control. Appl Biochem Biotechnol. 2017; 181: 682-698.
- 76Greetham D, Zaky A, Makanjuola O, Du C. A brief review on bioethanol production using marine biomass, marine microorganism and seawater. Curr Opin Green Sustain Chem. 2018; 14: 53-59.
- 77Möllers K, Cannella D, Jørgensen H, Frigaard N-U. Cyanobacterial biomass as carbohydrate and nutrient feedstock for bioethanol production by yeast fermentation. Biotechnol Biofuels. 2014; 7: 64.
- 78Markou G, Angelidaki I, Nerantzis E, Georgakakis D. Bioethanol production by carbohydrate-enriched biomass of Arthrospira (Spirulina) platensis. Energies. 2013; 6: 3937-3950.
- 79Pyo D, Kim T, Yoo J. Efficient extraction of bioethanol from freshwater cyanobacteria using supercritical fluid pretreatment. Bull Korean Chem Soc. 2013; 34: 379-383.
- 80Guo H, Daroch M, Liu L, Qiu G, Geng S, Wang G. Biochemical features and bioethanol production of microalgae from coastal waters of Pearl River Delta. Bioresour Technol. 2013; 127: 422-428.
- 81Chow TJ, Su HY, Tsai TY, Chou HH, Lee TM. Using recombinant cyanobacterium (Synechococcus elongatus) with increased carbohydrate productivity as feedstock for bioethanol production via separate hydrolysis and fermentation process. Bioresour Technol. 2015; 184: 33-41.
- 82Ben N, Amine M, Ben M, Bouallagui H, Marzouki MN, Smaali I. A biorefinery concept using the green macroalgae Chaetomorpha linum for the coproduction of bioethanol and biogas. Energ Conver Manage. 2016; 119: 257-265.
- 83Singh S, Verma E, Balkrishna N, Arun T, Mishra K. Exopolysaccharide production in Anabaena sp. PCC 7120 under different CaCl2 regimes. Physiol Mol Biol Plants. 2016; 22: 557-566.
- 84Casillo A, Lanzetta R, Parrilli M, Corsaro MM. Exopolysaccharides from marine and marine extremophilic bacteria: structures, properties, ecological roles and applications. Mar Drugs. 2018; 16: 69.
- 85Nouha K, Kumar RS, Balasubramanian S, Tyagi RD, Gk Q. Critical review of EPS production, synthesis and composition for sludge flocculation. J Environ Sci. 2017; 66: 225-245.
- 86Wingender J, Thomas RN, Flemming H-C. What are bacterial extracellular polymeric substances? Microbial Extracellular Polymeric Substances. Berlin, Heidelberg: Springer; 1999: 1-19.
- 87Silva MBF, Azero EG, Teixeira CMLL, Andrade CT. Influence of culture conditions on the production of extracellular polymeric substances (EPS) by Arthrospira platensis. Bioresour Bioprocess. 2020; 47: 1-11.
- 88Vicente-garcı V, Rı E, Caldero G. Detection, isolation, and characterization of exopolysaccharide produced by a strain of Phormidium 94a isolated from an arid zone of Mexico. Biotechnol Bioeng. 2004; 85: 306-310.
- 89Kavita K, Mishra A, Jha B. Isolation and physico-chemical characterisation of extracellular polymeric substances produced by the marine bacterium Vibrio parahaemolyticus. Biofouling. 2011; 3: 309-317.
- 90Freitas F, Alves VD, Pais J, et al. Characterization of an extracellular polysaccharide produced by a Pseudomonas strain grown on glycerol. Bioresour Technol. 2009; 100: 859-865.
- 91Baldev E, MubarakAli D, Shriraman R, Pandiaraj D, Alharbi NS. Thajuddin extraction and partial characterization of exopolysaccharides from marine cyanobacteria and their flocculation property. Res J Environ Sci. 2015; 9: 28-38.
10.3923/rjes.2015.28.38 Google Scholar
- 92Cesàro A, Liut G, Bertocchi C, Navarini L, Urbani R. Physicochemical properties of the exocellular polysaccharide from Cyanospira capsulata. Int J Biol Macromol. 1990; 12: 79-84.
- 93Chen L, Li D, Song L, Hu C, Wang G, Liu Y. Effects of salt stress on carbohydrate metabolism in desert soil alga Microcoleus vaginatus Gom. J Integrat Plant Biol. 2006; 48: 914-919.
- 94Samiotis G, Stamatakis K, Amanatidou E. Dimensioning of Synechococcus elongatus PCC 7492 cultivation photobioreactor for valorization of wastewater resources. Chem Eng J. 2022; 435:134895.
- 95Cruz D, Vasconcelos V, Pierre G, Michaud P, Delattre C. Exopolysaccharides from cyanobacteria: strategies for bioprocess development. Appl Sci. 2020; 10: 3763.
- 96Nicolaus B, Panico A, Lama L, et al. Chemical composition and production of exopolysaccharides from representative members of heterocystous and non-heterocystous cyanobacteria. Phytochemistry. 1999; 52: 639-647.
- 97Tan N, Jia SR, Han PP, Guo W, Dai YJ. The open culture of Nostoc flagelliforme with a 25 L open pond. Adv Mater Res. 2012: 554-556: 1009-1012.
- 98Han P, Shen S, Wang H, Yao S, Tan Z. Applying the strategy of light environment control to improve the biomass and polysaccharide production of Nostoc flagelliforme. J Appl Phycol. 2017; 29: 55-65.
- 99Kvíderová J, Kumar D, Lukavský J, Kaštánek P, Adhikary SP. Estimation of growth and exopolysaccharide production by two soil cyanobacteria, Scytonema tolypothrichoides and Tolypothrix bouteillei as determined by cultivation in irradiance and temperature crossed gradients. Eng Life Sci. 2019; 19: 184-195.
- 100Ge H, Zhang J, Zhou X, Xia L, Hu C. Effects of light intensity on components and topographical structures of extracellular polymeric substances from Microcoleus vaginatus (Cyanophyceae). Phycologia. 2019; 8884: 167-173.
- 101Zhang J, Liu L, Chen F. Production and characterization of exopolysaccharides from Chlorella zofingiensis and Chlorella vulgaris with anti-colorectal cancer activity. Int J Biol Macromol. 2019; 134: 976-983.
- 102Kumar A, Akash P, Vadrale P, et al. Algal polysaccharides: current status and future prospects. Phytochem Rev. 2022; 5: 1-31.
- 103Salama ES, Kurade MB, Abou-Shanab RAI, et al. Recent progress in microalgal biomass production coupled with wastewater treatment for biofuel generation renew. Sustain Energy Rev. 2017; 79: 1189-1211.
- 104Velazquez-Lucio J, Rodríguez-Jasso RM, Colla LM, et al. Microalgal biomass pretreatment for bioethanol production: a review. Biofuel Res J. 2018; 5: 780-791.
- 105 CredenceResearch Algae products market by type (Spirulina, Chlorella, Astaxanthin, Beta Carotene, Hydrocolloids), by Source (Brown, Blue-Green, Green, Red, Others), by application (nutraceuticals, food & feed supplements, pharmaceuticals, colorants, chemicals, fuels, others)-growth, share, opportunities & competitive analysis, (2019–2027); 2020: 120. https://www.credenceresearchcom/report/algae-products-market. Accessed 3 April 2022.
- 106Kraan S. Algal polysaccharides, novel applications and outlook. In: CF, ed. Chang, Carbohydrates; Comprehensive Studies on Glycobiology and Glycotechnology; London: IntechOpen. 2014: 489-528.
- 107Barsanti L, Gualtieri P. Is exploitation of microalgae economically and energetically sustainable? Algal Res. 2018; 31: 107-115.
10.1016/j.algal.2018.02.001 Google Scholar