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http://dx.doi.org/10.4014/mbl.1808.08003

Optimization of Phototrophic Growth and Lipid Production of a Newly Isolated Microalga, Desmodesmus sp. KAERI-NJ5  

Joe, Min-Ho (Department of Biotechnology, Korea Atomic Energy Research Institute)
Kim, Dong-Ho (Department of Biotechnology, Korea Atomic Energy Research Institute)
Choi, Dae Seong (Department of Biotechnology, Korea Atomic Energy Research Institute)
Bai, Suk (Department of Biological Sciences, College of Natural Sciences, Chonnam National University)
Publication Information
Microbiology and Biotechnology Letters / v.46, no.4, 2018 , pp. 377-389 More about this Journal
Abstract
In this study, a novel microalgal strain, Desmodesmus sp. KAERI-NJ5, was isolated, identified, and evaluated as a candidate for biodiesel feedstock. In a preliminary study, the effects of four general microalgal growth factors, including temperature, pH, light intensity, and concentration of nitrogen source ($KNO_3$), on the microalgal photoautotrophic growth were evaluated. With the exception of light intensity, the growth factors needed to be optimized for the microalgal biomass production. Optimization was done using response surface methodology. The optimal conditions for biomass production were pH 6.54, $27.66^{\circ}C$, and 0.52 g/l $KNO_3$. The biomass production at the optimal conditions was 1.55 g/l, which correlated well with the predicted value of 1.5 g/l. The total lipid and fatty acid methyl ester contents of the cells grown at the optimal conditions were 49% and 21.2% of cell dry weight, respectively. To increase the lipid content of the biomass, microalgae were challenged by nitrogen starvation. Enhancement of total lipid and fatty acid content up to 52.02% and 49%, respectively, were observed. Lipid analysis of the nitrogen-starved cells revealed that C16 and C18 species accounted for 95.9% of the total fatty acids. Among them, palmitic acid (46.17%) and oleic acid (39.43%) dominantly constituted the algal fatty acids. These results suggest Desmodesmus sp. KAERI-NJ5 as a promising feedstock for biodiesel production.
Keywords
Microalgae; Desmodesmus sp. KAERI-NJ5; biomass production; response surface methodology; biodiesel feedstock;
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1 Lang X, Dalai AK, Bakhshi NN, Reaney MJ, Hertz PB. 2001. Preparation and characterization of bio-diesels from various bio-oils. Bioresour. Technol. 80: 53-62.   DOI
2 Greenwell HC, Laurens LML, Shields RJ, Lovitt RW, Flynn KJ. 2010. Placing microalgae on the biofuels priority list: a review of the technological challenges. J. R. Soc. Interface 7: 703-726.   DOI
3 Scott SA, Davey MP, Dennis JS, Horst I, Howe CJ, Lea-Smith DJ, et al. 2010. Biodiesel from algae: challenges and prospects. Curr. Opin. Biotechnol. 21: 277-286.   DOI
4 Chisti Y. 2008. Biodiesel from microalgae beats bioethanol. Trends Biotechnol. 26: 126-131.   DOI
5 Li YG, Xu L, Huang YM, Wang F, Guo C, Liu CZ. 2011. Microalgal biodiesel in China: Opportunities and challenges. Appl. Energy 88: 3432-3437.   DOI
6 Chaichalerm S, Pokethitiyook P, Yuan W, Meetam M, Sritong K, Pugkaew W, et al. 2012. Culture of microalgal strains isolated from natural habitats in Thailand in various enriched media. Appl. Energy 89: 296-302.   DOI
7 Sharma YC, Singh V. 2017. Microalgal biodiesel: A possible solution for India's energy security. Renew. Sustain. Energy Rev. 67: 72-78.   DOI
8 Sharma YC, Singh B, Upadhyay SN. 2008. Advancements in development and characterization of biodiesel: A review. Fuel 12: 2355-2373.
9 Chung WS, Kim SS, Moon KH, Lim CY, Yun SW. 2017. A conceptual framework for energy security evaluation of power sources in South Korea. Energy 137: 1066-1074.   DOI
10 Rios LF, Klein BC, Luz LF, Maciel Filho R, Wolf Maciel MR. 2015. Nitrogen Starvation for Lipid Accumulation in the Microalga Species Desmodesmus sp. Appl. Biochem. Biotechnol. 175: 469-476.   DOI
11 Courchesne NMD, Parisien A, Wang B, Lan CQ. 2009. Enhancement of lipid production using biochemical, genetic and transcription factor engineering approaches. J. Biotechnol. 141: 31-41.   DOI
12 Hempel N, Petrick I, Behrendt F. 2012. Biomass productivity and productivity of fatty acids and amino acids of microalgae strains as key characteristics of suitability for biodiesel production. J. Appl. Phycol. 24: 1407-1418.   DOI
13 Wu H, Miao X. 2014. Biodiesel quality and biochemical changes of microalgae Chlorella pyrenoidosa and Scenedesmus obliquus in response to nitrate levels. Bioresour. Technol. 170: 421-427.   DOI
14 Hall TA. 1999. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 41: 95-98.
15 Hong JW, Jo SW, Yoon HS. 2015. Research and development for algae-based technologies in Korea: a review of algae biofuel production. Photosynth. Res. 123: 297-303.   DOI
16 Nichols HW, Bold HC. 2007. Trichosarcina polymorpha Gen. et Sp. Nov. J. Phycol. 1: 34-38.
17 Ren HY, Liu BF, Ma C, Zhao L, Ren NQ. 2013. A new lipid-rich microalga Scenedesmus sp. strain R-16 isolated using Nile red staining: effects of carbon and nitrogen sources and initial pH on the biomass and lipid production. Biotechnol. Biofuels 6: 143.   DOI
18 Saitou N, Nei M. 1987. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 4: 406-425.
19 Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. 2013. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evol. 30: 2725-2729.   DOI
20 Kimura M. 1980. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J. Mol. Evol. 16: 111-120.   DOI
21 Vonshak A, Richmond A. 1986. Handbook of microalgal mass culture. pp. 117-145. CRC Press, Boca Raton Florida.
22 Felsenstein J. 1985. Confidence limits on phylogenies: An approach using the bootstrap. Evolution 39: 783-791.   DOI
23 Prescott DM. 1964. Methods in cell physiology. pp. 159-187. In Kuhl A, Lorenzen H (eds), Handling and culturing of Chlorella, 1st Ed. Academic Press, New York and London.
24 Rippka R, Herdman H. 1992. Pasteur Culture Collection of Cyanobacteria. pp. 103. Catalogue & Taxonomic Handbook. Institut Pasteur, Paris.
25 Khozin-Goldberg I, Cohen Z. 2006. The effect of phosphate starvation on the lipid and fatty acid composition of the fresh water eustigmatophyte Monodus subterraneus. Phytochemistry 67: 696-701.   DOI
26 Butterwick C, Heaney SI, Talling JF. 2005. Diversity in the influence of temperature on the growth rates of freshwater algae, and its ecological relevance. Freshw. Biol. 50: 291-300.
27 Pan YY, Wang ST, Chuang LT, Chang YW, Chen CNN. 2011. Isolation of thermo-tolerant and high lipid content green microalgae: Oil accumulation is predominantly controlled by photosystem efficiency during stress treatments in Desmodesmus. Bioresour. Technol. 102: 10510-10517.   DOI
28 Chiu PH, Soong K, Chen CNN. 2016. Cultivation of two thermotolerant microalgae under tropical conditions: Influences of carbon sources and light duration on biomass and lutein productivity in four seasons. Bioresour. Technol. 212: 190-198.   DOI
29 Rios LF, Martinez A, Klein BC, Wolf Maciel MR, Maciel Filho R. 2018. Comparison of growth and lipid accumulation at three different growth regimes with Desmodesmus sp. Waste and Biomass Valorization 9: 421-427.   DOI
30 Ji F, Hao R, Liu Y, Li G, Zhou Y, Dong R. 2013. Isolation of a novel microalgae strain Desmodesmus sp. and optimization of environmental factors for its biomass production. Bioresour. Technol. 148: 249-254.   DOI
31 Ho SH, Chang JS, Lai YY, Chen CNN. 2014. Achieving high lipid productivity of a thermotolerant microalga Desmodesmus sp. F2 by optimizing environmental factors and nutrient conditions. Bioresour. Technol. 156: 108-116.   DOI
32 Zhu J, Rong J, Zong B. 2013. Factors in mass cultivation of microalgae for biodiesel. Chinese J. Catal. 34: 80-100.   DOI