Comparative study of the production of biomass and omega 3 and 6 in Thraustochytrium kinney
DOI:
https://doi.org/10.18633/biotecnia.v23i2.1405Keywords:
Polyunsaturated fatty acids, crude glycerol, microbial oils, docosahexaenoic acid.Abstract
Thraustochytrids are characterized by producing omega 3 and 6 type microbial oils. VAL-B1 and EMA-T5 are strains of the same genus and take advantage of pure sources of carbon and residual to produce polyunsaturated fatty acids. Pure (GP) and crude (GC) glycerol were used to compare biomass production and omega 3 and 6 yield and production, using 3 different substrate concentrations. Using 100 mL of culture at 25 ° C and 180 rpm, the strains were grown for 7 days, then the biomass was centrifuged and the fatty acid profile was quantified by gas chromatography. The results show that EMA-T5 generates a greater amount of biomass at day 5 using 20 g/L of GC with 6.984±0.66 g/L. Regarding the yield and production of omega 3 and 6, VAL-B1 obtained the best results with 91.80±8.78 mg/g and 1167.71±70.88 mg/L, being the most abundant omega 3, especially DHA which presented the highest abundance with 52.72±4.94 % total fatty acids (TFA). It is concluded that EMA-T5 generates higher biomass production using GC and VAL-B1 presents the best performance and omega production results using GP, which indicates that both strains make good use of both the pure and raw sources of glycerol.
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Abad, S., Turon X. (2012). Valorization of biodiesel derived glicerol as a carbon source to obtain added-value metabolites: focus on polyunsaturated fatty acids. Biotechnol. Adv. 30:733-741.
Adarme-Vega, T.C., Thomas-Hall, S R., and Peer M Schenk, P.M. (2014). Towards sustainable sources for omega-3 fatty acids production. Current Opinion in Biotechnology26:14-18.
Armenta, R.E., Burja A., Radianingtyas H. and Barrow C.J. (2006). Critical assessment of various techniques for the extraction of carotenoids and co-enzyme Q10 from the thraustochytrid strain ONC-T18. J. Agric. Food Chem. 54: 9752-9758.
Armenta, R.E. and Valentine M. (2013). Single-Cell oils as a source of omega-3 fatty acids: an overview of recent advances. Journal of the American Oil Chemists’ Society. 90(2):167-82.
Beligon V., Christopher G., Fontanille P. and Larroche C. (2016). Microbial lipids as potential source to food supplements. Current Opinion in Food Science. 7:35-42.
Beopoulos, A., Cescut J., Haddouche R., Uribelarrea J-L., Molma-Jouve C. and Nicaud J-M. (2009). Yarrowia lipolytica as a model for bio-oil production. Prog. Lipid Res. 48:375-387.
Bongiorni, L., Pusceddu A. and Danovaro R. (2005). Enzymatic activities of epiphytic and benthic thraustochytrids involved in organic matter degradation. Aquat. Microb. Ecol. 41:299-305.
Bremer, G. (2000). Isolation and culture of thraustochytrids. Marine Mycology – A Practical Approach. p. 49-61. In Hyde KD & Pointing SB (ed.) Fungal Diversity Press, Hong Kong.
Burja, A.M., Radianingtyas H., Windust A., and Barrow C.J. (2006). Isolation and characterization of polyunsaturated fatty acid producing Thraustochytrium species: screening of strains and optimization of omega-3 production. Appl. Microbiol. Biotechnol. 72:1161-1169.
Caamano, E., Loperena L., Hinzpeter I., Pradel P., Gordillo F., Corsini G., Tello M., Lavin P., Gonzalez A. (2017). Isolation and molecular characterization of Thraustochytrium strain isolated from Antarctic Peninsula and its biotechnological potential in the production of fatty acids. Brazilian Journal of Microbiology. 48:671-79.
Chang, W., Gao N., Tian G., Wu Q., Chang M., Wang X. (2013). Improvement of docosahexaenoic acid production on glycerol by Schizochytrium sp. S31 with constantly high oxygen transfer coefficient. Bioresource Technology. 142:400-406.
Chang K., Paul H., Nichols P.D., Koutoulis A. and Blackburn S.I. (2015). Australian thraustochytrids: Potential production of dietary long-chain omega-3 oils using crude glycerol. Journal of Functional Foods I9:810-20.
Chi, Z., Pyle D., Wen Z., Frear C. and Chen S. (2007). A laboratory study of producing docosahexaenoic acid from biodieselwaste glycerol by microalgal fermentation. Process Biochem. 42:1537-1545.
Ethier, S., Woisard K., Vaughan D. and Wen Z. (2011). Continuous culture of the microalgae Schizochytrium limacinum on biodiesel derived crude glycerol for producing docosahexaenoic acid. Bioresour. Technol. 102:88-93.
Gaertner A. (1968). Eine Methode des quantitativen Nachweises niederer mit Pollen koderbarer Pilze im Meerwasser und im Sediment. Veroff Inst Meeresforsch Bremerh Suppl. 3:75-92.
Gaffney M., O’Rourke R. and Murphy R. (2014). Manipulation of fatty acid and antioxidant profiles on the microalgae Schizochytrium sp. through flaxseed oil supplementation. Algal Research 6:195-200.
Gupta, A., Barrow C.J. and Puri M. (2012). Omega-3 biotechnology: thraustochytrids as a novel source of omega-3 oils. Biotechnol. Adv. 30:1733-1745.
Gupta, A., Reinu A., Barrow C. and Puri M. (2015). Omega-3 fatty acid production from enzyme saccharified hemp hydrolysate using a novel marine thraustochytrid strain. Bioresource Technology 183:373-78.
Hong, K., Rairakhwada, K. and Kondo H. (2012). Growth of the oleaginous microalgae Aurantochytrium sp. KRS101 on cellulosic biomass and the production of lipids containing high levels of docosahexaenoic acid. Bioprocess Biosys. Eng. 35:129-133.
Huang, T.Y., Lu W.C. and Chu I.M. (2012). A fermentation strategy for producing docosahexaenoic acid in Aurantiochytrium limacinum SR21 and increasing C22:6 proportions in total fatty acid. Bioresource Technology 123:8-14.
Loperena L., Soria V., Varela H., Lupo S., Bergalli A., Guigou M., Pellegrino A., Bernardo A., Calvino A., Rivas F. and Batista S. (2012). Extracellular enzymes produced by microorganisms isolated from maritime Antarctica. World J. Microbiol Technol. 28:2249-2256.
Nagano N, Taoka Y., Honda D. and Hayashi M. (2013). Effect of trace elements on growth of marine eukaryotes, thraustochytrids. J Biosci Bioeng. 116(3):337–9.
Pérez-García, O., Escalante F.M., Bashan L.E. and Bashan Y. (2011). Heterotrophic cultures of microalgae: Metabolism and potential products. Water Research. 45:11-36.
Pyle D.J., Garcia R.A., Wen Z. (2008). Producing docosahexaenoic acid (DHA)-rich algae from biodiesel-derived crude glycerol: effects of impurities on DHA production and algal biomass composition. J Agric Food Chem. 56:3933-3939.
Pino, N., Socias C. and Gonzalez R. (2015). Marine fungoids producers of DHA, EPA and carotenoids from central and southern Chilean marine ecosystems. Revista de Biologia Marina y Oceanografia. 50(3):507-20.
Quilodran B., Hinzpeter I., Quiroz A. and Shene C. (2009). Evaluation of liquid residues from beer and potato processing to produce docosahexaenoic acid (C22:6n−3, DHA) by native thraustochytrid strains. World J. Microbiol Biotechnol. 25:2121-2128.
Raghukumar, S. (2008). Thraustochytrid Marine Protists: Production of PUFAs and Other Emerging Technologies. Mar Biotechnol. 10:631-640.
Rosa, S.M., Galvagno M.A. and Velez C.G. (2011). Adjusting cultura conditions to isolate thraustochytrids from temperate and cold environments in southern Argentina. Mycoscience. 52:242-52.
Scott S.D., Armenta R., Berryman K.T and Norman A.W. (2011). Use of raw glycerol to produce oil rich in polyunsaturated fatty acids by a thraustochytrid. Enzyme and Microbial Technol. 48:267 272.
Shene C., Leyton A., Esparza Y., Flores L., Quilodran B., Hinzpeter I. and Rubilar M. (2010). Microbial oils and fatty acids: Effect of carbon source on docosahexaenoic acid (C22:3 n-3, DHA) production by Thraustochytrid strains. J. Soil Sci. Plant. Nutr. 10:207-216.
Shene, C., Garces M., Vergara D., Pena J., Claverol S., Rubilar M. and Leyton A. (2018). Production of lipids and proteome variation in a Chilean Thraustochytrium stratium strain cultured under different grown conditions. Marine Biotechnol. 21(1):99-110.
Silva D., Roa A., Quevedo R. and Quilodran B. (2015). Production of biodiesel from soybean frying oil using native strains of Thraustochytrids. Chilean J Agric Anim Sci; 31(1):29-41.
Singh, A., Mathur A., Tuli D., Puri M. and Barrow C. (2015). Propyl gallate and butylated hidroxytoluene influence accumulation of saturated fatty acids, omega-3 fatty acid and carotenoids in thraustochytrids. Journal of functional foods 15:186-92.
Thyagarajan, T., Puri M., Vongsvivut J. and Barrow C.J. (2014). Evaluation of Bread Crumbs as a Potential Carbon Source for the Growth of Thraustochytrid Species for Oil and Omega-3 Production. Nutrients. 6:2104-2114.
Wang, Q., Ye H., Xie Y., He Y., Sen B. and Wang G. (2019). Culturable Diversity and Lipid Production Profile of Labyrinthulomycete Protists Isolated from Coastal Mangrove Habitats of China. Mar. Drugs. 17, 268; doi:10.3390/md17050268.
Zhu, L., Zhang X., Ren X. and Zhu Q. (2008). Effects of cultura conditions on growth and docosahexaenoic acid production from Schizochytrium limacinum. J. Ocean Univ. China. 7:83-88.
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