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Effects of carbon source and light intensity on the growth and total lipid production of three microalgae under different culture conditions

  • Bioenergy/Biofuels/Biochemicals
  • Published:
Journal of Industrial Microbiology & Biotechnology

Abstract

We attempted to enhance the growth and total lipid production of three microalgal species, Isochrysis galbana LB987, Nannochloropsis oculata CCAP849/1, and Dunaliella salina, which are capable of accumulating high content of lipid in cells. Low nitrogen concentration under photoautotrophic conditions stimulated total lipid production, but a decreasing total lipid content and an increasing biomass were observed with increasing nitrogen concentration. Among the different carbon sources tested for heterotrophic cultivation, glucose improved the growth of all three strains. The optimal glucose concentration for growth of I. galbana LB987 and N. oculata CCAP849/1 was 0.02 M, and that of D. salina was 0.05 M. Enhanced growth occurred when they were cultivated under heterotrophic or mixotrophic conditions compared with photoautotrophic conditions. Meanwhile, high total lipid accumulation in cells occurred when they were cultivated under photoautotrophic or mixotrophic conditions. During mixotrophic cultivation, biomass production was not affected significantly by light intensity; however, both chlorophyll concentration and total lipid content increased dramatically with increasing light intensity up to 150 µmol/m2/s. The amount and composition ratio of saturated and unsaturated fatty acids in cells were different from each other depending on both species and light intensity. The highest accumulation of total fatty acid (C16–C18) among the three strains was found from cells of N. oculata CCAP849/1, which indicates that this species can be used as a source for production of biodiesel.

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References

  1. Arroyo J, Hutzler J, Bermejo C, Ragni E, GarcÃ-a-Cantalejo J, BotÃ-as P, Piberger H, Schott A, Sanz BS, Strahl S (2011) Functional and genomic analyzes of blocked protein O-mannosylation in baker’s yeast. Mol Microbiol 79:1529–1546

    Article  CAS  PubMed  Google Scholar 

  2. Becker EW (1994) Microalgae: biotechnology and microbiology. Cambridge University, New York

    Google Scholar 

  3. Brown MR, Dunstan GA, Norwood SJ, Miller KA (1996) Effects of harvest stage and light on the biochemical composition of the diatom Thalassiosira pseudinana. J Phycol 32:64–73

    Article  CAS  Google Scholar 

  4. Castenholz RW (1969) Thermophilic blue-green algae and the thermal environment. Bact Rev 33:476–504

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Cerón-García MC, Fernández-Sevilla JM, Sánchez-Mirón A, García-Camacho F, Contreras-Gómez A, Molina-Grima E (2013) Mixotrophic growth of Phaeodactylum tricornutum on fructose and glycerol in fed-batch and semi-continuous modes. Bioresour Technol 147:569–576

    Article  PubMed  Google Scholar 

  6. Cheirsilp B, Torpee S (2012) Enhanced growth and lipid production of microalgae under mixotrophic culture condition: effect of light intensity, glucose concentration and fed-batch cultivation. Bioresour Technol 110:510–516

    Article  CAS  PubMed  Google Scholar 

  7. Converti A, Casazza AA, Ortiz EY, Perego P, Del Borghi M (2009) Effect of temperature and nitrogen concentration on the growth and lipid content of Nannochloropsis oculata and Chlorella vulgaris for biodiesel production. Chem Eng Process 48:1146–1151

    Article  CAS  Google Scholar 

  8. Das P, Lei W, Aziz SS, Obbard JP (2011) Enhanced algal growth in both phototrophic and mixotrophic culture under blue light. Bioresour Technol 102:3883–3887

    Article  CAS  PubMed  Google Scholar 

  9. Feuillade M, Feuillade J (1989) Heterotrophic capabilities of blue–green alga Oscillatoria rubescens. Arch Hydrobiol 117:61–76

    Google Scholar 

  10. Folch J, Lees M, Sloane Stanley GH (1957) A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226:497–509

    CAS  PubMed  Google Scholar 

  11. Gim GH, Kim JK, Kim HS, Kathiravan MN, Yang H, Jeong SH, Kim SW (2014) Comparison of biomass production and total lipid content of freshwater green microalgae cultivated under various culture conditions. Bioprocess Biosyst Eng 37:99–106

    Article  CAS  PubMed  Google Scholar 

  12. Gouveia L, Oliveira AC (2009) Microalgae as raw material for biofuels production. J Ind Microbiol Biotechnol 36:269–274

    Article  CAS  PubMed  Google Scholar 

  13. Griffiths DJ, Thresher CL, Street HE (1960) The heterotrophic nutrition of Chlorella vulgaris. Ann Bot 24:1–11

    CAS  Google Scholar 

  14. Guillard RRL, Ryther JH (1962) Studies of marine planktonic diatoms I. Cyclotella nana hustedt and Detonula confervaceae (Cleve) gran. Can J Microbiol 8:229–239

    Article  CAS  PubMed  Google Scholar 

  15. Haass D, Tanner W (1973) Regulation of hexose transport in Chlorella vulgaris. Plant Physiol 53:14–20

    Article  Google Scholar 

  16. Imamoglu E, Sukan FV, Dalay MC (2007) Effect of different culture media and light intensities on growth of Haematococcus pluvialis. Int J Natural Eng Sci 1:5–9

    Google Scholar 

  17. Kong WB, Yang H, Cao YT, Song H, Hua SF, Xia CG (2013) Effect of glycerol and glucose on the enhancement of biomass, lipid and soluble carbohydrate production by Chlorella vulgaris in mixotrophic culture. Food Technol Biotechnol 51:62–69

    CAS  Google Scholar 

  18. Sj Lee, Go S, Jeong GT, Kim SK (2011) Oil production from five marine microalgae for the production of biodiesel. Biotechnol Bioprocess Eng 16:561–566

    Article  Google Scholar 

  19. Li Y, Wang B, Wu N, Lan CQ (2008) Effects of nitrogen sources on cell growth and lipid production of Neochloris oleoabundans. Appl Microbiol Biotechnol 81:629–636

    Article  CAS  PubMed  Google Scholar 

  20. Liang Y, Sarkany N, Cui Y (2009) Biomass and lipid productivities of Chlorella vulgaris under autotrophic, heterotrophic and mixotrophic growth conditions. Biotechnol Lett 31:1043–1049

    Article  CAS  PubMed  Google Scholar 

  21. Liu J, Hung J, Fan KW, Jiang Y, Zhong Y, Sun Z, Chen F (2010) Production potential of Chlorella zofingienesis as a feedstock for biodiesel. Bioresour Technol 101:8658–8663

    Article  CAS  PubMed  Google Scholar 

  22. Liu ZY, Wang GC, Zhou BC (2008) Effect of iron on growth and lipid accumulation in Chlorella vulgaris. Bioresour Technol 99:4717–4722

    Article  CAS  PubMed  Google Scholar 

  23. Liu J, Yuan C, Hu G, Li F (2012) Effects of light intensity on the growth and lipid accumulation of microalga Scenedesmus sp. 11-1 under nitrogen limitation. Appl Biochem Biotechnol 166:2127–2137

    Article  CAS  PubMed  Google Scholar 

  24. Mata TM, Martins AA, Caetano NS (2010) Microalgae for biodiesel production and other applications: a review. Renew Sustain Energy Rev 14:217–232

    Article  CAS  Google Scholar 

  25. Merzlyak MN, Chivkunova OB, Gorelova OA, Reshetnikova IV, Solovchenko AE, Khozin-Goldberg I, Cohen Z (2007) Effect of nitrogen starvation on optical properties, pigments, and arachidonic acid content of the unicellular green alga Parieto-chloris incise rebouxiophyceae, Chlorophyta). J Phycol 43:833–843

    Article  CAS  Google Scholar 

  26. Metcalfe LD, Schmitz AA, Pelka JR (1966) Rapid preparation of fatty acid esters from lipids for gas chromatographic analysis. Anal Chem 38:514–515

    Article  CAS  Google Scholar 

  27. Miller GL (1959) Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem 31:426–428

    Article  CAS  Google Scholar 

  28. Ra CH, Kang CH, Kim NK, Lee CG, Kim SK (2015) Cultivation of four microalgae for biomass and oil production using a two-stage culture strategy with salt stress. Renew Energy 80:117–122

    Article  CAS  Google Scholar 

  29. 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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Romieu I, Tellez-Rojo MM, Lazo M, Manzano-Patino A, Cortez-Lugo M, Julien P, Belanger MC, Hernandez-Avila M, Holguin F (2005) Omega-3 fatty acid prevents heart rate variability reductions associated with particulate matter. Am J Respir Crit Care Med 12:1534–1540

    Article  Google Scholar 

  31. Scott SA, Davey MP, Dennis JS, Horst I, Howe CJ, Lea-Smith DJ, Smith AG (2010) Biodiesel from algae: challenges and prospects. Curr Opinion Biotechnol 21:277–286

    Article  CAS  Google Scholar 

  32. Solovchenko AE, Chivkunova OB, Semenova LR, Selyakh IO, Shcherbakov PN, Karpova EA, Lobakova ES (2013) Stress-induced changes in pigment and fatty acid content in the microalga Desmodesmus sp. isolated from a white sea hydroid. Russ J Plant Physiol 60:313–321

    Article  CAS  Google Scholar 

  33. Spolaore P, Joannis-Cassan C, Duran E, Isambert A (2006) Commercial applications of microalgae. J Biosci Bioeng 101:87–96

    Article  CAS  PubMed  Google Scholar 

  34. Sugimoto K, Midorikawa T, Tsuzuki M, Sato N (2008) Upregulation of PG synthesis on sulfur-starvation for PS I in Chlamydomonas. Biochem Biophys Res Commun 369:660–665

    Article  CAS  PubMed  Google Scholar 

  35. Tanner W (1969) Light-driven active uptake of 3-O-methylglucose via an inducible hexose uptake system of Chlorella. Biochem Biophys Res Commun 36:278–283

    Article  CAS  PubMed  Google Scholar 

  36. Thompson GA Jr (1996) Lipids and membrane function in green algae. Biochim Biophys Acta 1302:17–45

    Article  PubMed  Google Scholar 

  37. Tian-Yuan Z, Yin-Hu Wu, Shu-feng Z, Feng-Min L, Hong-Ying H (2013) Isolation and heterotrophic cultivation of mixotrophic microalgae strains for domestic wastewater treatment and lipid production under dark condition. Biresour Technol 149:586–589

    Article  Google Scholar 

  38. Ukeles R, Rose WE (1976) Observations on organic carbon utilisation by photosynthetic marine microalgae. Marine Biol 7:11–28

    Article  Google Scholar 

  39. Vazhappilly R, Chen F (1998) Eicosapentaenoic acid and docosahexaenoic acid production potential of microalgae and their heterotrophic growth. J Am Oil Chem Soc 75:393–397

    Article  CAS  Google Scholar 

  40. Wan M, Liu P, Xia J, Rosenberg JN, Oyler GA, Betenbaugh MJ, Nie Z, Qui G (2011) The effect of mixotrophy on microalgal growth, lipid content, and expression levels of three pathway genes in Chlorella sorokiniana. Appl Microbiol Bitechnol 91:825–844

    Google Scholar 

  41. Widjaja A, Chien CC, Ju YH (2009) Study of increasing lipid production from fresh water Microalgae Chlorella vulgaris. J Taiwan Institute of Chem Eng 40:13–20

    Article  CAS  Google Scholar 

  42. Xia L, Ge H, Zhou X, Zhang D, Hu C (2013) Photoautotrophic outdoor two-stage cultivation for oleaginous microalgae Scenedesmus obtusus XJ-15. Bioresour Technol 144:261–267

    Article  CAS  PubMed  Google Scholar 

  43. Xin L, Hong-ying H, Ke G, Ying-xue S (2010) Effects of different nitrogen and phosphorus concentrations on the growth, nutrient uptake, and lipid accumulation of a freshwater microalga Scenedesmus sp. Bioresour Technol 101:5494–5500

    Article  CAS  PubMed  Google Scholar 

  44. Yang C, Hua Q, Shimizu K (2000) Energetics and carbon metabolism during growth of microalgal cells under photoautotrophic, mixotrophic and cyclic light-autotrophic/dark-heterotrophic conditions. Biochem Eng J 6:87–102

    Article  CAS  PubMed  Google Scholar 

  45. Yeesang C, Cheirsilp B (2011) Effect of nitrogen, salt, and iron content in the growth medium and light intensity on lipid production by microalgae isolated from freshwater sources in Thailand. Bioresour Technol 102(3):3034–3040

    Article  CAS  PubMed  Google Scholar 

  46. Yeh KL, Chang JS, Chen WM (2010) Effect of light supply and carbon source on cell growth and cellular composition of a newly isolated microalga Chlorella vulgaris ESP-31. Eng Life Sci 10:201–208

    Article  CAS  Google Scholar 

  47. Zhukova NV, Titlyanov EA (2006) Effect of light intensity on the fatty acid composition of dinoflagellates symbiotic with hermatypic corals. Bot Mar 49:339–346

    Article  CAS  Google Scholar 

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Acknowledgments

This work was supported by the Ministry of Science, ICT, and Future Planning Research Grant (NRF-2015R1D1A3A01020290) and in part by the Human Resources Development program (20114010100090) of the KETEP grant funded by the Ministry of Trade, Industry and Energy, Republic of Korea.

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Correspondence to Si Wouk Kim.

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Gim, G.H., Ryu, J., Kim, M.J. et al. Effects of carbon source and light intensity on the growth and total lipid production of three microalgae under different culture conditions. J Ind Microbiol Biotechnol 43, 605–616 (2016). https://doi.org/10.1007/s10295-016-1741-y

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  • DOI: https://doi.org/10.1007/s10295-016-1741-y

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