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dc.contributor.authorSuárez Quintana, William H.
dc.contributor.authorGarcía Rico, Ramón O.
dc.contributor.authorGarcía Martínez, Janet B.
dc.contributor.authorUrbina Suarez, Néstor A.
dc.contributor.authorLópez-Barrera, Germán L.
dc.contributor.authorBarajas Solano, Andrés F.
dc.contributor.authorZuorro, Antonio
dc.date.accessioned2022-11-18T00:41:15Z
dc.date.available2022-11-18T00:41:15Z
dc.date.issued2022-07-04
dc.identifier.urihttps://repositorio.ufps.edu.co/handle/ufps/6532
dc.description.abstract: This study evaluated the role of C/N/P in the increase in the synthesis of carbohydrates, proteins, and lipids in two high-mountain strains of algae (Chlorella sp. UFPS019 and Desmodesmus sp. UFPS021). Three carbon sources (sodium acetate, sodium carbonate, and sodium bicarbonate), and the sources of nitrogen (NaNO3 ) and phosphate (KH2PO4 and K2HPO4 ) were analyzed using a surface response (3 factors, 2 levels). In Chlorella sp. UFPS019, the optimal conditions to enhance the synthesis of carbohydrates were high sodium carbonate content (3.53 g/L), high KH2PO4 and K2HPO4 content (0.06 and 0.14 g/L, respectively), and medium-high NaNO3 (0.1875 g/L). In the case of lipids, a high concentration of sodium acetate (1.19 g/L) coupled with high KH2PO4 and K2HPO4 content (0.056 and 0.131 g/L, respectively) and a low concentration of NaNO3 (0.075 g/L) drastically induced the synthesis of lipids. In the case of Desmodesmus sp. UFPS021, the protein content was increased using high sodium acetate (2 g/L), high KH2PO4 and K2HPO4 content (0.056 and 0.131 g/L, respectively), and high NaNO3 concentration (0.25 g/L). These results demonstrate that the correct adjustment of the C/N/P ratio can enhance the capacity of high-mountain strains of algae to produce high concentrations of carbohydrates, proteins, and lipids.eng
dc.format.extent19spa
dc.format.mimetypeapplication/pdfspa
dc.publisherApplied Sciencesspa
dc.relation.ispartofApplied Sciences Vol 12 No°13[2022]
dc.rights© 2022 by the authorseng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/spa
dc.sourcehttps://www.mdpi.com/2076-3417/12/13/6779spa
dc.titleEnhancement of Metabolite Production in High-Altitude Microalgal Strains by Optimized C/N/P Ratioeng
dc.typeArtículo de revistaspa
dcterms.referencesMatos, Â.P. The Impact of Microalgae in Food Science and Technology. JAOCS J. Am. Oil Chem. Soc. 2017, 94, 1333–1350.spa
dcterms.referencesAmini, Z.; Ilham, Z.; Ong, H.C.; Mazaheri, H.; Chen, W.-H. State of the Art and Prospective of Lipase-Catalyzed Transesterification Reaction for Biodiesel Production. Energy Convers. Manag. 2017, 141, 339–353. [spa
dcterms.referencesTekin, K.; Karagöz, S.; Bekta¸s, S. A Review of Hydrothermal Biomass Processing. Renew. Sustain. Energy Rev. 2014, 40, 673–687spa
dcterms.referencesBaykara, S.Z. Hydrogen: A Brief Overview on Its Sources, Production and Environmental Impact. Int. J. Hydrgen Energy 2018, 43, 10605–10614.spa
dcterms.referencesKosourov, S.; Murukesan, G.; Seibert, M.; Allahverdiyeva, Y. Evaluation of Light Energy to H2 Energy Conversion Efficiency in Thin Films of Cyanobacteria and Green Alga under Photoautotrophic Conditions. Algal Res. 2017, 28, 253–263.spa
dcterms.referencesAbbas, J.; Sa ˘gsan, M. Impact of Knowledge Management Practices on Green Innovation and Corporate Sustainable Development: A Structural Analysis. J. Clean. Prod. 2019, 229, 611–620.spa
dcterms.referencesNagarajan, D.; Lee, D.-J.; Kondo, A.; Chang, J.-S. Recent Insights into Biohydrogen Production by Microalgae—From Biophotolysis to Dark Fermentation. Bioresour. Technol. 2017, 227, 373–387.spa
dcterms.referencesShow, P.L.; Tang, M.S.Y.; Nagarajan, D.; Ling, T.C.; Ooi, C.-W.; Chang, J.-S. A Holistic Approach to Managing Microalgae for Biofuel Applications. Int. J. Mol. Sci. 2017, 18, 215.spa
dcterms.referencesBleakley, S.; Hayes, M. Algal Proteins: Extraction, Application, and Challenges Concerning Production. Foods 2017, 6, 33.spa
dcterms.referencesKoyande, A.K.; Chew, K.W.; Rambabu, K.; Tao, Y.; Chu, D.-T.; Show, P.-L. Microalgae: A Potential Alternative to Health Supplementation for Humans. Food Sci. Hum. Wellness 2019, 8, 16–24.spa
dcterms.referencesKusmayadi, A.; Leong, Y.K.; Yen, H.-W.; Huang, C.-Y.; Chang, J.-S. Microalgae as Sustainable Food and Feed Sources for Animals and Humans—Biotechnological and Environmental Aspects. Chemosphere 2021, 271, 129800.spa
dcterms.referencesDel Mondo, A.; Smerilli, A.; Sané, E.; Sansone, C.; Brunet, C. Challenging Microalgal Vitamins for Human Health. Microb. Cell Fact. 2020, 19, 201.spa
dcterms.referencesFu, Y.; Chen, T.; Chen, S.H.Y.; Liu, B.; Sun, P.; Sun, H.; Chen, F. The Potentials and Challenges of Using Microalgae as an Ingredient to Produce Meat Analogues. Trends Food Sci. Technol. 2021, 112, 188–200.spa
dcterms.referencesKent, M.; Welladsen, H.M.; Mangott, A.; Li, Y. Nutritional Evaluation of Australian Microalgae as Potential Human Health Supplements. PLoS ONE 2015, 10, e0118985.spa
dcterms.referencesQuintero-Dallos, V.; García-Martínez, J.B.; Contreras-Ropero, J.E.; Barajas-Solano, A.F.; Barajas-Ferrerira, C.; Lavecchia, R.; Zuorro, A. Vinasse as a Sustainable Medium for the Production of Chlorella Vulgaris UTEX 1803. Water 2019, 11, 1526.spa
dcterms.referencesda Silva, M.E.T.; Correa, K.d.P.; Martins, M.A.; da Matta, S.L.P.; Martino, H.S.D.; Coimbra, J.S. dos R. Food Safety, Hypolipidemic and Hypoglycemic Activities, and in Vivo Protein Quality of Microalga Scenedesmus Obliquus in Wistar Rats. J. Funct. Foods 2020, 65, 103711.spa
dcterms.referencesAmorim, M.L.; Soares, J.; Vieira, B.B.; Batista-Silva, W.; Martins, M.A. Extraction of Proteins from the Microalga Scenedesmus Obliquus BR003 Followed by Lipid Extraction of the Wet Deproteinized Biomass Using Hexane and Ethyl Acetate. Bioresour. Technol. 2020, 307, 123190.spa
dcterms.referencesGateau, H.; Blanckaert, V.; Veidl, B.; Burlet-Schiltz, O.; Pichereaux, C.; Gargaros, A.; Marchand, J.; Schoefs, B. Application of Pulsed Electric Fields for the Biocompatible Extraction of Proteins from the Microalga Haematococcus Pluvialis. Bioelectrochemistry 2021, 137, 107588.spa
dcterms.referencesGrossmann, L.; Wörner, V.; Hinrichs, J.; Weiss, J. Mechanism of the Formation of Insoluble Structures in a Protein Extract of the Microalga Chlorella Protothecoides at PH 3. Food Biosci. 2019, 28, 140–142.spa
dcterms.referencesCheng, D.; Li, D.; Yuan, Y.; Zhou, L.; Li, X.; Wu, T.; Wang, L.; Zhao, Q.; Wei, W.; Sun, Y. Improving Carbohydrate and Starch Accumulation in Chlorella sp. AE10 by a Novel Two-Stage Process with Cell Dilution. Biotechnol. Biofuels 2017, 10, 75.spa
dcterms.referencesMathimani, T.; Baldinelli, A.; Rajendran, K.; Prabakar, D.; Matheswaran, M.; Pieter van Leeuwen, R.; Pugazhendhi, A. Review on Cultivation and Thermochemical Conversion of Microalgae to Fuels and Chemicals: Process Evaluation and Knowledge Gaps. J. Clean. Prod. 2019, 208, 1053–1064.spa
dcterms.referencesBarajas-Solano, A.F.; Gonzalez-Delgado, A.D.; Kafarov, V. Effect of Thermal Pre-Treatment On Fermentable Sugar Production of Chlorella Vulgaris. Chem. Eng. Trans. 2014, 37, 655–660.spa
dcterms.referencesCuellar García, D.J.; Rangel-Basto, Y.A.; Barajas-Solano, A.F.; Muñoz-Peñalosa, Y.A.; Urbina-Suarez, N.A. Towards the Production of Microalgae Biofuels: The Effect of the Culture Medium on Lipid Deposition. Biotechnologia 2019, 100, 273–278.spa
dcterms.referencesBarajas-Solano, A.F.; Guzmán-Monsalve, A.; Kafarov, V. Effect of Carbon-Nitrogen Ratio for the Biomass Production, Hydrocarbons and Lipids on Botryoccus Braunii UIS 003. Chem. Eng. Trans. 2016, 49, 247–252spa
dcterms.referencesZuorro, A.; Malavasi, V.; Cao, G.; Lavecchia, R. Use of Cell Wall Degrading Enzymes to Improve the Recovery of Lipids from Chlorella Sorokiniana. Chem. Eng. J. 2019, 377, 120325.spa
dcterms.referencesZuorro, A.; Lavecchia, R.; Maffei, G.; Marra, F.; Miglietta, S.; Petrangeli, A.; Familiari, G.; Valente, T. Enhanced lipid extraction from unbroken microalgal cells using enzymes. Chem. Eng. Trans. 2015, 43, 211–216.spa
dcterms.referencesChew, K.W.; Yap, J.Y.; Show, P.L.; Suan, N.H.; Juan, J.C.; Ling, T.C.; Lee, D.-J.; Chang, J.-S. Microalgae Biorefinery: High Value Products Perspectives. Bioresour. Technol. 2017, 229, 53–62.spa
dcterms.references. Kumar, G.; Shobana, S.; Chen, W.-H.; Bach, Q.-V.; Kim, S.-H.; Atabani, A.E.; Chang, J.-S. A Review of Thermochemical Conversion of Microalgal Biomass for Biofuels: Chemistry and Processes. Green Chem. 2017, 19, 44–67.spa
dcterms.referencesBrigljevi´c, B.; Liu, J.; Lim, H. Green Energy from Brown Seaweed: Sustainable Polygeneration Industrial Process via Fast Pyrolysis of S. Japonica Combined with the Brayton Cycle. Energy Convers. Manag. 2019, 195, 1244–1254spa
dcterms.referencesXu, X.; Gu, X.; Wang, Z.; Shatner, W.; Wang, Z. Progress, Challenges and Solutions of Research on Photosynthetic Carbon Sequestration Efficiency of Microalgae. Renew. Sustain. Energy Rev. 2019, 110, 65–82.spa
dcterms.referencesYu, K.L.; Show, P.L.; Ong, H.C.; Ling, T.C.; Chen, W.-H.; Salleh, M.A.M. Biochar Production from Microalgae Cultivation through Pyrolysis as a Sustainable Carbon Sequestration and Biorefinery Approach. Clean Technol. Environ. Policy 2018, 20, 2047–2055.spa
dcterms.referencesZuorro, A.; García-Martínez, J.B.; Barajas-Solano, A.F. The Application of Catalytic Processes on the Production of Algae-Based Biofuels: A Review. Catalysts 2021, 11, 22.spa
dcterms.referencesMohamed, A.G.; Abo-El-Khair, B.E.; Shalaby, S.M. Quality of novel healthy processed cheese analogue enhanced with marine microalgae Chlorella vulgaris biomass. World Appl. Sci. J. 2013, 23, 914–925spa
dcterms.references4. Furbeyre, H.; van Milgen, J.; Mener, T.; Gloaguen, M.; Labussière, E. Effects of Dietary Supplementation with Freshwater Microalgae on Growth Performance, Nutrient Digestibility and Gut Health in Weaned Piglets. Animal 2017, 11, 183–192.spa
dcterms.referencesOh, S.T.; Zheng, L.; Kwon, H.J.; Choo, Y.K.; Lee, K.W.; Kang, C.W.; An, B.K. Effects of Dietary Fermented Chlorella Vulgaris (CBT®) on Growth Performance, Relative Organ Weights, Cecal Microflora, Tibia Bone Characteristics, and Meat Qualities in Pekin Ducks. Asian-Australas. J. Anim. Sci. 2015, 28, 95–101.spa
dcterms.referencesKang, H.K.; Salim, H.M.; Akter, N.; Kim, D.W.; Kim, J.H.; Bang, H.T.; Kim, M.J.; Na, J.C.; Hwangbo, J.; Choi, H.C.; et al. Effect of Various Forms of Dietary Chlorella Supplementation on Growth Performance, Immune Characteristics, and Intestinal Microflora Population of Broiler Chickens. J. Appl. Poult. Res. 2013, 22, 100–108.spa
dcterms.referencesEl-Baz, F.K.; Abdo, S.M.; Hussein, A.M.S. Microalgae Dunaliella salina for use as food supplement to improve pasta quality. Int. J. Pharm. Sci. Rev. Res. 2017, 46, 45–51.spa
dcterms.referencesXu, Y.; Ibrahim, I.M.; Wosu, C.I.; Ben-Amotz, A.; Harvey, P.J. Potential of New Isolates of Dunaliella Salina for Natural β-Carotene Production. Biology 2018, 7, 14.spa
dcterms.referencesSui, Y.; Mazzucchi, L.; Acharya, P.; Xu, Y.; Morgan, G.; Harvey, P.J. A Comparison of β-Carotene, Phytoene and Amino Acids Production in Dunaliella salina DF 15 (CCAP 19/41) and Dunaliella salina CCAP 19/30 Using Different Light Wavelengths. Foods 2021, 10, 2824.spa
dcterms.referencesChan, K.; Chen, S.; Chen, P. Astaxanthin Attenuated Thrombotic Risk Factors in Type 2 Diabetic Patients. J. Funct. Foods 2019, 53, 22–27.spa
dcterms.referencesSheikhzadeh, N.; Tayefi-Nasrabadi, H.; Khani Oushani, A.; Najafi Enferadi, M.H. Effects of Haematococcus Pluvialis Supplementation on Antioxidant System and Metabolism in Rainbow Trout (Oncorhynchus Mykiss). Fish Physiol. Biochem. 2012, 38, 413–419.spa
dcterms.referencesDo, T.-T.; Ong, B.-N.; Le, T.-L.; Nguyen, T.-C.; Tran-Thi, B.-H.; Thu Hien, B.T.; Melkonian, M.; Tran, H.-D. Growth of Haematococcus pluvialis on a Small-Scale Angled Porous Substrate Photobioreactor for Green Stage Biomass. Appl. Sci. 2021, 11, 1788.spa
dcterms.referencesRizzo, A.; Ross, M.E.; Norici, A.; Jesus, B. A Two-Step Process for Improved Biomass Production and Non-Destructive Astaxanthin and Carotenoids Accumulation in Haematococcus pluvialis. Appl. Sci. 2022, 12, 1261.spa
dcterms.referencesNeves, M.; Ferreira, A.; Antunes, M.; Laranjeira Silva, J.; Mendes, S.; Gil, M.M.; Tecelão, C. Nannochloropsis oceanica as a Sustainable Source of n-3 Polyunsaturated Fatty Acids for Enrichment of Hen Eggs. Appl. Sci. 2021, 11, 8747.spa
dcterms.referencesdu Preez, R.; Majzoub, M.E.; Thomas, T.; Panchal, S.K.; Brown, L. Nannochloropsis oceanica as a Microalgal Food Intervention in Diet-Induced Metabolic Syndrome in Rats. Nutrients 2021, 13, 3991.spa
dcterms.referencesSaito, T.; Ichihara, T.; Inoue, H.; Uematsu, T.; Hamada, S.; Watanabe, T.; Takimura, Y.; Webb, J. Comparison of Areal Productivity of Nannochloropsis Oceanica Between Lab-Scale and Industrial-Scale Raceway Pond. Mar. Biotechnol. 2020, 22, 836–841.spa
dcterms.referencesZhang, R.; Parniakov, O.; Grimi, N.; Lebovka, N.; Marchal, L.; Vorobiev, E. Emerging Techniques for Cell Disruption and Extraction of Valuable Bio-Molecules of Microalgae Nannochloropsis sp. Bioprocess Biosyst. Eng. 2019, 42, 173–186.spa
dcterms.referencesMitra, M.; Mishra, S. A Biorefinery from Nannochloropsis spp. Utilizing Wastewater Resources BT—Application of Microalgae in Wastewater Treatment: Volume 2: Biorefinery Approaches of Wastewater Treatment; Gupta, S.K., Bux, F., Eds.; Springer International Publishing: Cham, Switzerland, 2019; pp. 123–145.spa
dcterms.referencesBranco-Vieira, M.; San Martin, S.; Agurto, C.; Santos, M.A.d.; Freitas, M.A.V.; Mata, T.M.; Martins, A.A.; Caetano, N.S. Potential of Phaeodactylum tricornutum for Biodiesel Production under Natural Conditions in Chile. Energies 2018, 11, 54.spa
dcterms.referencesAfonso, C.; Bragança, A.R.; Rebelo, B.A.; Serra, T.S.; Abranches, R. Optimal Nitrate Supplementation in Phaeodactylum tricornutum Culture Medium Increases Biomass and Fucoxanthin Production. Foods 2022, 11, 568.spa
dcterms.referencesNeumann, U.; Derwenskus, F.; Flaiz Flister, V.; Schmid-Staiger, U.; Hirth, T.; Bischoff, S.C. Fucoxanthin, A Carotenoid Derived from Phaeodactylum tricornutum Exerts Antiproliferative and Antioxidant Activities In Vitro. Antioxidants 2019, 8, 183.spa
dcterms.referencesEilers, U.; Bikoulis, A.; Breitenbach, J.; Büchel, C.; Sandmann, G. Limitations in the Biosynthesis of Fucoxanthin as Targets for Genetic Engineering in Phaeodactylum Tricornutum. J. Appl. Phycol. 2016, 28, 123–129.spa
dcterms.referencesKwon, D.Y.; Vuong, T.T.; Choi, J.; Lee, T.S.; Um, J.-I.; Koo, S.Y.; Hwang, K.T.; Kim, S.M. Fucoxanthin Biosynthesis Has a Positive Correlation with the Specific Growth Rate in the Culture of Microalga Phaeodactylum Tricornutum. J. Appl. Phycol. 2021, 33, 1473–1485.spa
dcterms.referencesLi, Y.; Ma, Q.; Pan, Y.; Chen, Q.; Sun, Z.; Hu, P. Development of an Effective Flocculation Method by Utilizing the Auto-Flocculation Capability of Phaeodactylum Tricornutum. Algal Res. 2021, 58, 102413.spa
dcterms.referencesPereira, H.; Sá, M.; Maia, I.; Rodrigues, A.; Teles, I.; Wijffels, R.H.; Navalho, J.; Barbosa, M. Fucoxanthin Production from Tisochrysis Lutea and Phaeodactylum Tricornutum at Industrial Scale. Algal Res. 2021, 56, 102322.spa
dcterms.referencesKadalag, N.L.; Pawar, P.R.; Prakash, G. Co-Cultivation of Phaeodactylum Tricornutum and Aurantiochytrium Limacinum for Polyunsaturated Omega-3 Fatty Acids Production. Bioresour. Technol. 2022, 346, 126544.spa
dcterms.referencesHan, S.-I.; Jeon, M.S.; Park, Y.H.; Kim, S.; Choi, Y.-E. Semi-Continuous Immobilized Cultivation of Porphyridium Cruentum for Sulfated Polysaccharides Production. Bioresour. Technol. 2021, 341, 125816.spa
dcterms.referencesMedina-Cabrera, E.V.; Gansbiller, M.; Rühmann, B.; Schmid, J.; Sieber, V. Rheological Characterization of Porphyridium Sordidum and Porphyridium Purpureum Exopolysaccharides. Carbohydr. Polym. 2021, 253, 117237.spa
dcterms.referencesSeemashree, M.H.; Chauhan, V.S.; Sarada, R. Phytohormone Supplementation Mediated Enhanced Biomass Production, Lipid Accumulation, and Modulation of Fatty Acid Profile in Porphyridium Purpureum and Dunaliella Salina Cultures. Biocatal. Agric. Biotechnol. 2022, 39, 102253.spa
dcterms.referencesda Silva, M.E.T.; Leal, M.A.; Resende, M.d.O.; Martins, M.A.; Coimbra, J.S.d.R. Scenedesmus Obliquus Protein Concentrate: A Sustainable Alternative Emulsifier for the Food Industry. Algal Res. 2021, 59, 102468.spa
dcterms.referencesTao, R.; Lakaniemi, A.-M.; Rintala, J.A. Cultivation of Scenedesmus Acuminatus in Different Liquid Digestates from Anaerobic Digestion of Pulp and Paper Industry Biosludge. Bioresour. Technol. 2017, 245, 706–713.spa
dcterms.referencesSingh, D.V.; Upadhyay, A.K.; Singh, R.; Singh, D.P. Implication of Municipal Wastewater on Growth Kinetics, Biochemical Profile, and Defense System of Chlorella Vulgaris and Scenedesmus Vacuolatus. Environ. Technol. Innov. 2022, 26, 102334.spa
dcterms.referencesTavanandi, H.A.; Raghavarao, K.S.M.S. Ultrasound-Assisted Enzymatic Extraction of Natural Food Colorant C-Phycocyanin from Dry Biomass of Arthrospira Platensis. LWT 2020, 118, 108802.spa
dcterms.references. ˙Ilter, I.; Akyıl, S.; Demirel, Z.; Koç, M.; Conk-Dalay, M.; Kaymak-Ertekin, F. Optimization of Phycocyanin Extraction from Spirulina Platensis Using Different Techniques. J. Food Compos. Anal. 2018, 70, 78–88.spa
dcterms.referencesAyekpam, C.; Hamsavi, G.K.; Raghavarao, K.S.M.S. Efficient Extraction of Food Grade Natural Blue Colorant from Dry Biomass of Spirulina Platensis Using Eco-Friendly Methods. Food Bioprod. Process. 2021, 129, 84–93.spa
dcterms.referencesFerreira-Santos, P.; Nunes, R.; De Biasio, F.; Spigno, G.; Gorgoglione, D.; Teixeira, J.A.; Rocha, C.M.R. Influence of Thermal and Electrical Effects of Ohmic Heating on C-Phycocyanin Properties and Biocompounds Recovery from Spirulina Platensis. LWT 2020, 128, 109491.spa
dcterms.referencesTavanandi, H.A.; Mittal, R.; Chandrasekhar, J.; Raghavarao, K.S.M.S. Simple and Efficient Method for Extraction of C-Phycocyanin from Dry Biomass of Arthospira Platensis. Algal Res. 2018, 31, 239–251.spa
dcterms.referencesDevi, A.C.; Tavanandi, H.A.; Govindaraju, K.; Raghavarao, K.S.M.S. An Effective Method for Extraction of High Purity Phycocyanins (C-PC and A-PC) from Dry Biomass of Arthrospira Maxima. J. Appl. Phycol. 2020, 32, 1141–1151.spa
dcterms.referencesCarullo, D.; Pataro, G.; Donsì, F.; Ferrari, G. Pulsed Electric Fields-Assisted Extraction of Valuable Compounds from Arthrospira Platensis: Effect of Pulse Polarity and Mild Heating. Front. Bioeng. Biotechnol. 2020, 8, 1–15.spa
dcterms.referencesKhandual, S.; Sanchez, E.O.L.; Andrews, H.E.; de la Rosa, J.D.P. Phycocyanin Content and Nutritional Profile of Arthrospira Platensis from Mexico: Efficient Extraction Process and Stability Evaluation of Phycocyanin. BMC Chem. 2021, 15, 1–13.spa
dcterms.referencesdel Pilar Sánchez-Saavedra, M.; Maeda-Martínez, A.N.; Acosta-Galindo, S. Effect of Different Light Spectra on the Growth and Biochemical Composition of Tisochrysis Lutea. J. Appl. Phycol. 2016, 28, 839–847.spa
dcterms.referencesMatsui, H.; Intoy, M.M.B.; Waqalevu, V.; Ishikawa, M.; Kotani, T. Suitability of Tisochrysis Lutea at Different Growth Phases as an Enrichment Diet for Brachionus Plicatilis sp. Complex Rotifers. J. Appl. Phycol. 2020, 32, 3933–3947.spa
dcterms.referencesMarchetti, J.; da Costa, F.; Bougaran, G.; Quéré, C.; Soudant, P.; Robert, R. The Combined Effects of Blue Light and Dilution Rate on Lipid Class and Fatty Acid Composition of Tisochrysis Lutea. J. Appl. Phycol. 2018, 30, 1483–1494.spa
dcterms.referencesGao, F.; Cabanelas, I.T.D.; Wijffels, R.H.; Barbosa, M.J. Fucoxanthin and Docosahexaenoic Acid Production by Cold-Adapted Tisochrysis Lutea. New Biotechnol. 2022, 66, 16–24.spa
dcterms.referencesMohamadnia, S.; Tavakoli, O.; Faramarzi, M.A. Production of Fucoxanthin from the Microalga Tisochrysis Lutea in the Bubble Column Photobioreactor Applying Mass Transfer Coefficient. J. Biotechnol. 2022, 348, 47–54.spa
dcterms.referencesHernández-López, I.; Benavente Valdés, J.R.; Castellari, M.; Aguiló-Aguayo, I.; Morillas-España, A.; Sánchez-Zurano, A.; Acién-Fernández, F.G.; Lafarga, T. Utilisation of the Marine Microalgae Nannochloropsis sp. and Tetraselmis sp. as Innovative Ingredients in the Formulation of Wheat Tortillas. Algal Res. 2021, 58, 102361.spa
dcterms.referencesMagpusao, J.; Giteru, S.; Oey, I.; Kebede, B. Effect of High Pressure Homogenization on Microstructural and Rheological Properties of A. Platensis, Isochrysis, Nannochloropsis and Tetraselmis Species. Algal Res. 2021, 56, 102327.spa
dcterms.referencesKhatoon, H.; Penz, K.R.; Banerjee, S.; Rahman, M.R.; Minhaz, T.M.; Islam, Z.; Mukta, F.A.; Nayma, Z.; Sultana, R.; Amira, K.I. Immobilized Tetraselmis sp. for Reducing Nitrogenous and Phosphorous Compounds from Aquaculture Wastewater. Bioresour. Technol. 2021, 338, 125529.spa
dcterms.referencesFarahin, A.W.; Natrah, I.; Nagao, N.; Katayama, T.; Imaizumi, Y.; Mamat, N.Z.; Yusoff, F.M.; Shariff, M. High Intensity of Light: A Potential Stimulus for Maximizing Biomass by Inducing Photosynthetic Activity in Marine Microalga, Tetraselmis Tetrathele. Algal Res. 2021, 60, 102523.spa
dcterms.referencesSouto, M.; Saavedra, M.; Pousão-Ferreira, P.; Herrero, C. Riboflavin Enrichment throughout the Food Chain from the Marine Microalga Tetraselmis Suecica to the Rotifer Brachionus Plicatilis and to White Sea Bream (Diplodus Sargus) and Gilthead Sea Bream (Sparus Aurata) Larvae. Aquaculture 2008, 283, 128–133.spa
dcterms.referencesAraújo, R.; Vázquez Calderón, F.; Sánchez López, J.; Azevedo, I.C.; Bruhn, A.; Fluch, S.; Garcia Tasende, M.; Ghaderiardakani, F.; Ilmjärv, T.; Laurans, M.; et al. Current Status of the Algae Production Industry in Europe: An Emerging Sector of the Blue Bioeconomy. Front. Mar. Sci. 2021, 7, 626389.spa
dcterms.referencesNascimento, I.A.; Marques, S.S.I.; Cabanelas, I.T.D.; de Carvalho, G.C.; Nascimento, M.A.; de Souza, C.O.; Druzian, J.I.; Hussain, J.; Liao, W. Microalgae Versus Land Crops as Feedstock for Biodiesel: Productivity, Quality, and Standard Compliance. BioEnergy Res. 2014, 7, 1002–1013.spa
dcterms.referencesNeofotis, P.; Huang, A.; Sury, K.; Chang, W.; Joseph, F.; Gabr, A.; Twary, S.; Qiu, W.; Holguin, O.; Polle, J.E.W. Characterization and Classification of Highly Productive Microalgae Strains Discovered for Biofuel and Bioproduct Generation. Algal Res. 2016, 15, 164–178.spa
dcterms.referencesHobbs, W.O.; Telford, R.J.; Birks, H.J.B.; Saros, J.E.; Hazewinkel, R.R.O.; Perren, B.B.; Saulnier-Talbot, É.; Wolfe, A.P. Quantifying Recent Ecological Changes in Remote Lakes of North America and Greenland Using Sediment Diatom Assemblages. PLoS ONE 2010, 5, e10026.spa
dcterms.referencesDunck, B.; Felisberto, S.A.; de Souza Nogueira, I. Effects of Freshwater Eutrophication on Species and Functional Beta Diversity of Periphytic Algae. Hydrobiologia 2019, 837, 195–204.spa
dcterms.referencesSchuster, K.F.; Tremarin, P.I.; de Souza-Franco, G.M. Alpha and beta diversity of phytoplankton in two subtropical eutrophic streams in southern Brazil. Acta Bot. Bras. 2015, 29, 597–607.spa
dcterms.referencesGunkel, G.; Casallas, J. Limnology of an Equatorial High Mountain Lake—Lago San Pablo, Ecuador: The Significance of Deep Diurnal Mixing for Lake Productivity. Limnologica 2002, 32, 33–43.spa
dcterms.referencesZuorro, A.; Leal-Jerez, A.G.; Morales-Rivas, L.K.; Mogollón-Londoño, S.O.; Sanchez-Galvis, E.M.; García-Martínez, J.B.; Barajas-Solano, A.F. Enhancement of Phycobiliprotein Accumulation in Thermotolerant Oscillatoria sp. through Media Optimization. ACS Omega 2021, 6, 10527–10536.spa
dcterms.referencesSánchez-Zurano, A.; Morillas-España, A.; Gómez-Serrano, C.; Ciardi, M.; Acién, G.; Lafarga, T. Annual Assessment of the Wastewater Treatment Capacity of the Microalga Scenedesmus Almeriensis and Optimisation of Operational Conditions. Sci. Rep. 2021, 11, 21651spa
dcterms.referencesLv, J.-M.; Cheng, L.-H.; Xu, X.-H.; Zhang, L.; Chen, H.-L. Enhanced Lipid Production of Chlorella Vulgaris by Adjustment of Cultivation Conditions. Bioresour. Technol. 2010, 101, 6797–6804.spa
dcterms.referencesMandik, Y.I.; Cheirsilp, B.; Boonsawang, P.; Prasertsan, P. Optimization of Flocculation Efficiency of Lipid-Rich Marine Chlorella sp. Biomass and Evaluation of Its Composition in Different Cultivation Modes. Bioresour. Technol. 2015, 182, 89–97.spa
dcterms.referencesCuéllar-García, D.J.; Rangel-Basto, Y.A.; Urbina-Suarez, N.A.; Barajas-Solano, A.F.; Muñoz-Peñaloza, Y.A. Lipids production from Scenedesmus obliquus through carbon/nitrogen ratio optimization. J. Phys. Conf. Ser. 2019, 1388, 012043.spa
dcterms.referencesBarajas-Solano, A.F. Optimization of Phycobiliprotein Solubilization from a Thermotolerant Oscillatoria sp. Processes 2022, 10, 836.spa
dcterms.referencesGonzález-Delgado, A.D.; Barajas-Solano, A.F.; Ardila-Álvarez, A.M. Biomass and Protein Production of Chlorella vulgaris Beyerinck (Chlorellales: Chlorellaceae) via the Design of Selective Culture Media. Corpoica Cienc. Tecnol. Agropecu. 2017, 18, 451–461.spa
dcterms.referencesWang, S.; Cao, M.; Wang, B.; Deng, R.; Gao, Y.; Liu, P. Optimization of growth requirements and scale-up cultivation of freshwater algae Desmodesmus armatus using response surface methodology. Aquacult. Res. 2019, 50, 3313–3325.spa
dcterms.referencesPauline, J.M.N.; Achary, A. Novel media for lipid production of Chlorococcum oleofaciens: A RSM approach. Acta Protozool. 2019, 58, 31–41.spa
dcterms.referencesMubarak, M.; Shaija, A.; Suchithra, T.V. Cost effective approach for production of Chlorella pyrenoidosa: A RSM based study. Waste Biomass Valorization 2019, 10, 3307–3319.spa
dcterms.referencesFawley, M.W.; Fawley, K.P. A Simple and Rapid Technique for The Isolation Of DNA From Microalgae. J. Phycol. 2004, 40, 223–225.spa
dcterms.referencesWhite, T.J.; Bruns, T.D.; Lee, S.B.; Taylor, J.W. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In PCR Proto- Cols: A Guide to Methods and Applications; Innis, M.A., Gelfand, D.H., Sninsky, J.J., Whire, T.J., Eds.; Academic Press: London, UK, 1990; pp. 315–322.spa
dcterms.referencesFei, C.; Zou, S.; Wang, T.; Wang, C.; Kemuma, N.D.; He, M.; Amin, S.A.; Wang, C. A Quick Method for Obtaining High-Quality DNA Barcodes without DNA Extraction in Microalgae. J. Appl. Phycol. 2020, 32, 1165–1175.spa
dcterms.referencesAndersen, R.A.; Berges, J.A.; Harrison, P.J.; Watanabe, M.M. Appendix A—Recipes for Freshwater and Seawater Media. In Algal Culturing Techniques; Andersen, R.A., Ed.; Elsevier Academic Press: Burlington, MA, USA, 2005; pp. 429–538.spa
dcterms.referencesSanchez-Galvis, E.M.; Cardenas-Gutierrez, I.Y.; Contreras-Ropero, J.E.; García-Martínez, J.B.; Barajas-Solano, A.F.; Zuorro, A. An Innovative Low-Cost Equipment for Electro-Concentration of Microalgal Biomass. Appl. Sci. 2020, 10, 4841.spa
dcterms.referencesMishra, S.K.; Suh, W.I.; Farooq, W.; Moon, M.; Shrivastav, A.; Park, M.S.; Yang, J.W. Rapid Quantification of Microalgal Lipids in Aqueous Medium by a Simple Colorimetric Method. Bioresour. Technol. 2014, 155, 330–333.spa
dcterms.referencesGarcía-Martínez, J.B.; Ayala-Torres, E.; Reyes-Gómez, O.; Zuorro, A.; Barajas-Solano, A.F.; Barajas-Ferreira, C. Evaluation of a Two-Phase Extraction System of Carbohydrates and Proteins from Chlorella Vulgaris Utex 1803. Chem. Eng. Trans. 2016, 49, 355–360.spa
dcterms.referencesMota, M.F.S.; Souza, M.F.; Bon, E.P.S.; Rodrigues, M.A.; Freitas, S.P. Colorimetric Protein Determination in Microalgae (Chlorophyta): Association of Milling and SDS Treatment for Total Protein Extraction. J. Phycol. 2018, 54, 577–580.spa
dcterms.referencesHynstova, V.; Sterbova, D.; Klejdus, B.; Hedbavny, J.; Huska, D.; Adam, V. Separation, Identification and Quantification of Carotenoids and Chlorophylls in Dietary Supplements Containing Chlorella Vulgaris and Spirulina Platensis Using HighPerformance Thin Layer Chromatography. J. Pharm. Biomed. Anal. 2018, 148, 108–118.spa
dcterms.referencesChen, C.-Y.; Zhao, X.-Q.; Yen, H.-W.; Ho, S.-H.; Cheng, C.-L.; Lee, D.-J.; Bai, F.-W.; Chang, J.-S. Microalgae-Based Carbohydrates for Biofuel Production. Biochem. Eng. J. 2013, 78, 1–10.spa
dcterms.referencesRuangsomboon, S. Effects of Different Media and Nitrogen Sources and Levels on Growth and Lipid of Green Microalga Botryococcus Braunii KMITL and Its Biodiesel Properties Based on Fatty Acid Composition. Bioresour. Technol. 2015, 191, 377–384.spa
dcterms.referencesWhangchai, K.; Mathimani, T.; Sekar, M.; Shanmugam, S.; Brindhadevi, K.; Van Hung, T.; Chinnathambi, A.; Alharbi, S.A.; Pugazhendhi, A. Synergistic Supplementation of Organic Carbon Substrates for Upgrading Neutral Lipids and Fatty Acids Contents in Microalga. J. Environ. Chem. Eng. 2021, 9, 105482.spa
dcterms.referencesRehman, Z.U.; Anal, A.K. Enhanced Lipid and Starch Productivity of Microalga (Chlorococcum sp. TISTR 8583) with Nitrogen Limitation Following Effective Pretreatments for Biofuel Production. Biotechnol. Rep. 2019, 21, e00298.spa
dcterms.referencesXu, J.; Li, T.; Li, C.-L.; Zhu, S.-N.; Wang, Z.-M.; Zeng, E.Y. Lipid Accumulation and Eicosapentaenoic Acid Distribution in Response to Nitrogen Limitation in Microalga Eustigmatos Vischeri JHsu-01 (Eustigmatophyceae). Algal Res. 2020, 48, 101910.spa
dcterms.referencesZarrinmehr, M.J.; Farhadian, O.; Heyrati, F.P.; Keramat, J.; Koutra, E.; Kornaros, M.; Daneshvar, E. Effect of Nitrogen Concentration on the Growth Rate and Biochemical Composition of the Microalga, Isochrysis Galbana. Egypt. J. Aquat. Res. 2020, 46, 153–158.spa
dcterms.referencesKokabi, K.; Gorelova, O.; Ismagulova, T.; Itkin, M.; Malitsky, S.; Boussiba, S.; Solovchenko, A.; Khozin-Goldberg, I. Metabolomic Foundation for Differential Responses of Lipid Metabolism to Nitrogen and Phosphorus Deprivation in an Arachidonic AcidProducing Green Microalga. Plant Sci. 2019, 283, 95–115.spa
dcterms.referencesChakravarty, S.; Mallick, N. Engineering a Cultivation Strategy for Higher Lipid Accretion and Biodiesel Production by the Marine Microalga Picochlorum Soloecismus. Sustain. Chem. Pharm. 2022, 26, 100635.spa
dcterms.referencesZuorro, A. Enhanced Lycopene Extraction from Tomato Peels by Optimized Mixed-Polarity Solvent Mixtures. Molecules 2020, 25, 2038.spa
dcterms.referencesZuorro, A.; Lavecchia, R. Polyphenols and Energy Recovery from Spent Coffee Grounds. Chem. Eng. Trans. 2011, 25, 285–290.spa
dcterms.referencesZuorro, A.; Iannone, A.; Natali, S.; Lavecchia, R. Green Synthesis of Silver Nanoparticles Using Bilberry and Red Currant Waste Extracts. Processes 2019, 7, 193.spa
dcterms.referencesMontanaro, D.; Lavecchia, R.; Petrucci, E.; Zuorro, A. UV-Assisted Electrochemical Degradation of Coumarin on Boron-Doped Diamond Electrodes. Chem. Eng. J. 2017, 323, 512–519.spa
dcterms.referencesZuorro, A.; Maffei, G.; Lavecchia, R. Kinetic Modeling of Azo Dye Adsorption on Non-Living Cells of Nannochloropsis Oceanica. J. Environ. Chem. Eng. 2017, 5, 4121–4127.spa
dcterms.referencesSingh, P.; Guldhe, A.; Kumari, S.; Rawat, I.; Bux, F. Investigation of Combined Effect of Nitrogen, Phosphorus and Iron on Lipid Productivity of Microalgae Ankistrodesmus Falcatus KJ671624 Using Response Surface Methodology. Biochem. Eng. J. 2015, 94, 22–29.spa
dcterms.referencesPolat, E.; Yüksel, E.; Altınba¸s, M. Mutual Effect of Sodium and Magnesium on the Cultivation of Microalgae Auxenochlorella Protothecoides. Biomass Bioenergy 2020, 132, 105441.spa
dcterms.referencesVishwakarma, R.; Dhar, D.W.; Pabbi, S. Formulation of a Minimal Nutritional Medium for Enhanced Lipid Productivity in Chlorella sp. and Botryococcus sp. Using Response Surface Methodology. Water Sci. Technol. 2018, 77, 1660–1672.spa
dcterms.referencesTran, H.-L.; Kwon, J.-S.; Kim, Z.-H.; Oh, Y.; Lee, C.-G. Statistical Optimization of Culture Media for Growth and Lipid Production of Botryococcus Braunii LB572. Biotechnol. Bioprocess Eng. 2010, 15, 277–284.spa
dcterms.referencesCheng, K.C.; Ren, M.; Ogden, K.L. Statistical Optimization of Culture Media for Growth and Lipid Production of Chlorella protothecoides UTEX 250. Bioresour. Technol. 2013, 128, 44–48.spa
dcterms.referencesLeón-Vaz, A.; León, R.; Díaz-Santos, E.; Vigara, J.; Raposo, S. Using Agro-Industrial Wastes for Mixotrophic Growth and Lipids Production by the Green Microalga Chlorella Sorokiniana. New Biotechnol. 2019, 51, 31–38.spa
dcterms.referencesLi, T.; Zheng, Y.; Yu, L.; Chen, S. Mixotrophic Cultivation of a Chlorella Sorokiniana Strain for Enhanced Biomass and Lipid Production. Biomass Bioenergy 2014, 66, 204–213.spa
dcterms.referencesRa, C.H.; Kang, C.-H.; Kim, N.K.; Lee, C.-G.; Kim, S.-K. Cultivation of Four Microalgae for Biomass and Oil Production Using a Two-Stage Culture Strategy with Salt Stress. Renew. Energy 2015, 80, 117–122.spa
dcterms.referencesFawzy, M.A.; Alharthi, S. Use of Response Surface Methodology in Optimization of Biomass, Lipid Productivity and Fatty Acid Profiles of Marine Microalga Dunaliella Parva for Biodiesel Production. Environ. Technol. Innov. 2021, 22, 101485.spa
dcterms.referencesPandey, A.; Gupta, A.; Sunny, A.; Kumar, S.; Srivastava, S. Multi-Objective Optimization of Media Components for Improved Algae Biomass, Fatty Acid and Starch Biosynthesis from Scenedesmus sp. ASK22 Using Desirability Function Approach. Renew. Energy 2020, 150, 476–486.spa
dcterms.referencesChoix, F.J.; De-Bashan, L.E.; Bashan, Y. Enhanced Accumulation of Starch and Total Carbohydrates in Alginate-Immobilized Chlorella Spp. Induced by Azospirillum Brasilense: I. Autotrophic Conditions. Enzyme Microb. Technol. 2012, 51, 294–299.spa
dcterms.referencesHo, S.-H.; Chen, C.-Y.; Yeh, K.-L.; Chen, W.-M.; Lin, C.-Y.; Chang, J.-S. Characterization of Photosynthetic Carbon Dioxide Fixation Ability of Indigenous Scenedesmus Obliquus Isolates. Biochem. Eng. J. 2010, 53, 57–62.spa
dcterms.referencesde Farias Silva, C.E.; Sforza, E.; Bertucco, A. Stability of Carbohydrate Production in Continuous Microalgal Cultivation under Nitrogen Limitation: Effect of Irradiation Regime and Intensity on Tetradesmus Obliquus. J. Appl. Phycol. 2018, 30, 261–270spa
dcterms.referencesMcClain, A.M.; Sharkey, T.D. Triose Phosphate Utilization and beyond: From Photosynthesis to End Product Synthesis. J. Exp. Bot. 2019, 70, 1755–1766.spa
dcterms.referencesGhosh, A.; Samadhiya, K.; Kashyap, M.; Anand, V.; Sangwan, P.; Bala, K. The Use of Response Surface Methodology for Improving Fatty Acid Methyl Ester Profile of Scenedesmus Vacuolatus. Environ. Sci. Pollut. Res. 2020, 27, 27457–27469.spa
dcterms.referencesGonzález-Fernández, C.; Ballesteros, M. Linking Microalgae and Cyanobacteria Culture Conditions and Key-Enzymes for Carbohydrate Accumulation. Biotechnol. Adv. 2012, 30, 1655–1661.spa
dcterms.referencesDragone, G.; Fernandes, B.D.; Abreu, A.P.; Vicente, A.A.; Teixeira, J.A. Nutrient Limitation as a Strategy for Increasing Starch Accumulation in Microalgae. Appl. Energy 2011, 88, 3331–3335.spa
dcterms.referencesMuthuraj, M.; Kumar, V.; Palabhanvi, B.; Das, D. Evaluation of Indigenous Microalgal Isolate Chlorella sp. FC2 IITG as a Cell Factory for Biodiesel Production and Scale up in Outdoor Conditions. J. Ind. Microbiol. Biotechnol. 2014, 41, 499–511.spa
dcterms.referencesTourang, M.; Baghdadi, M.; Torang, A.; Sarkhosh, S. Optimization of Carbohydrate Productivity of Spirulina Microalgae as a Potential Feedstock for Bioethanol Production. Int. J. Environ. Sci. Technol. 2019, 16, 1303–1318.spa
dcterms.referencesLi-Beisson, Y.; Beisson, F.; Riekhof, W. Metabolism of Acyl-Lipids in Chlamydomonas Reinhardtii. Plant J. 2015, 82, 504–522.spa
dcterms.referencesChakravarty, S.; Mallick, N. Optimization of Lipid Accumulation in an Aboriginal Green Microalga Selenastrum sp. GA66 for Biodiesel Production. Biomass Bioenergy 2019, 126, 1–13.spa
dcterms.referencesSchüler, L.M.; Santos, T.; Pereira, H.; Duarte, P.; Katkam, N.G.; Florindo, C.; Schulze, P.S.C.; Barreira, L.; Varela, J.C.S. Improved Production of Lutein and β-Carotene by Thermal and Light Intensity Upshifts in the Marine Microalga Tetraselmis sp. CTP4. Algal Res. 2020, 45, 101732.spa
dcterms.referencesAburai, N.; Sumida, D.; Abe, K. Effect of Light Level and Salinity on the Composition and Accumulation of Free and Ester-Type Carotenoids in the Aerial Microalga Scenedesmus sp. (Chlorophyceae). Algal Res. 2015, 8, 30–36.spa
dcterms.referencesde Souza da Silva, S.P.; Perrone, D.; do Valle, A.F. Optimization of Arthrospira Maxima Cultivation for Biomass and Protein Production and Biomass Technological Treatment to Color, Flavor, and Aroma Masking for Addition to Food Products. J. Appl. Phycol. 2022, 34, 65–80.spa
dcterms.referencesKumaran, J.; Poulose, S.; Joseph, V.; Bright Singh, I.S. Enhanced Biomass Production and Proximate Composition of Marine Microalga Nannochloropsis Oceanica by Optimization of Medium Composition and Culture Conditions Using Response Surface Methodology. Anim. Feed Sci. Technol. 2021, 271, 114761.spa
dc.contributor.corporatenameApplied Sciencesspa
dc.identifier.doihttps://doi.org/10.3390/app12136779
dc.publisher.placeSuizaspa
dc.relation.citationeditionVol. 12 No° 13 [2022]spa
dc.relation.citationendpage19spa
dc.relation.citationissue13 [2022]spa
dc.relation.citationstartpage1spa
dc.relation.citationvolume12spa
dc.relation.citesSuárez Quintana, W.H.; García-Rico, R.O.; García-Martínez, J.B.; Urbina-Suarez, N.A.; López-Barrera, G.L.; Barajas-Solano, A.F.; Zuorro, A. Enhancement of Metabolite Production in High-Altitude Microalgal Strains by Optimized C/N/P Ratio. Appl. Sci. 2022, 12, 6779. https://doi.org/ 10.3390/app12136779
dc.relation.ispartofjournalApplied Sciencesspa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.rights.creativecommonsAtribución 4.0 Internacional (CC BY 4.0)spa
dc.subject.proposalsodium carbonateeng
dc.subject.proposalsodium acetateeng
dc.subject.proposalsodium nitrateeng
dc.subject.proposalcarbon-nitrogen-phosphate ratioeng
dc.subject.proposallipidseng
dc.subject.proposalcarbohydrateseng
dc.type.coarhttp://purl.org/coar/resource_type/c_6501spa
dc.type.contentTextspa
dc.type.driverinfo:eu-repo/semantics/articlespa
dc.type.redcolhttp://purl.org/redcol/resource_type/ARTspa
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oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.type.versioninfo:eu-repo/semantics/publishedVersionspa


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