Skip to main content
Log in

The Use of Light Spectra to Improve the Growth and Lipid Content of Chlorella vulgaris for Biofuels Production

  • Published:
BioEnergy Research Aims and scope Submit manuscript

Abstract

The effects of light spectra on cell concentration, cell size, biomass production, proximate composition, pigment content, and fatty acid content in Chlorella vulgaris during two growth phases were measured. Growth rates were higher with white (0.70 division day−1) and blue light (0.67 divisions day−1). Cell size was greater in the exponential growth with yellow light (16.29 μm) versus blue light (14.26 μm). Higher organic dry weight (ODW) values were observed during exponential growth under green light (70.58 pg cell−1) compared with white light (36.56 pg cell−1). Proximate composition differed significantly by effect of light spectra and growth phases. Protein content was significantly higher in the exponential growth with white light (34.42%) and green (31.64%) light. Carbohydrate levels were significantly higher during stationary growth under yellow light (27.05%). In the exponential growth, lipid content was significantly higher with blue light (18.74%). Biomass productivity was highest in exponential growth phase with blue light (0.064 gL-1 day-1), meanwhile, in stationary growth phase yellow light (0.031 gL-1 day-1). Chlorophyll a and carotenoid levels were significantly greater during exponential growth with green and yellow lights. Fatty acid content was significantly modified by the light spectra and growth phase. The predominant saturated fatty acid was C:16:0 (palmitic acid), ranging between 10.26 (green light and exponential growth) and 20.01% (white light and stationary growth). The content of C18:1n-9 was higher (28.34 %) with the white light in the stationary growth, and C18:3n-3 content was greater with white (41.41%) and blue light (40.82%) in the exponential growth. It was concluded that blue light is the most suitable condition to induce biomass productivity and lipid content on both growth phases. Blue light during the stationary growth phase induces the production of lipids and saturated fatty acids (SFAs) which are suitable for biodiesel production.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Abbreviations

μ:

Growth rate (divisions day-1)

Log2 :

Logarithm base 2

TDW:

Total dry weight (pg cell-1)

ODW:

Organic dry weight (pg cell-1)

BPD:

Biomass productivity by day (g L-1 day-1)

BPT:

Biomass productivity total (g L-1 8 day-1)

E:

Exponential growth

S:

Stationary growth

SFA:

Saturated fatty acid

MUFA:

Monounsaturated fatty acid

PUFA:

Polyunsaturated fatty acid

FAMEs:

Fatty acid methyl esters

RU:

Relation of total unsaturated fatty acids. RU = ∑MUFA+∑PUFA

RSU:

Relation RSU of total saturated fatty acids (SFAs) to total unsaturated fatty acids (UFAs). RSU = ∑SFAs/∑MUFA+∑PUFA

CN:

Cetane number

ρ:

Density (g cm-3)

MW:

Molecular weight (g mol-1)

Mp:

Melting point (°C)

Bp:

Boiling point (°C)

CAS:

Register number of chemicals

References

  1. Christi T (2007) Biodiesel from microalgae. Biotechnol Adv 25:294–306

    Article  CAS  Google Scholar 

  2. Wang L, Min M, Li Y, Chen P, Chen Y, Liu Y, Ruan R (2010) Cultivation of green algae Chlorella sp. in different wastewaters from municipal wastewater treatment plant. Appl Biochem Biotechnol 162(4):1174–1186

    Article  CAS  PubMed  Google Scholar 

  3. Phukan MM, Chutia KS, Konwar BK, Kataki R (2011) Microalgae Chlorella as a potential bio-energy feedstock. Appl Energy 88(10):3307–3312

    Article  CAS  Google Scholar 

  4. Voskresenskaya NP (1972) Blue-light and carbon metabolism. Annu Rev Plant Physiol 23(1):219–234

    Article  CAS  Google Scholar 

  5. Rosenberg JN, Oyler GA, Wilkinson L, Betenbaugh MJ (2008) A green light for engineered algae: redirecting metabolism to fuel a biotechnology revolution. Curr Opin Biotechnol 19(5):430–436

    Article  CAS  PubMed  Google Scholar 

  6. Blair MF, Kokabian B, Gude VG (2014) Light and growth medium effect on Chlorella vulgaris biomass production. J Environ Chem Eng 2:665–674

    Article  CAS  Google Scholar 

  7. Sánchez-Saavedra MP, Jiménez C, Figueroa FL (1996) Far-red light inhibit growth but promotes carotenoid accumulation in the green microalgae Dunaliella bardawil. Physiol Plant 95:419–423

    Google Scholar 

  8. Shu CH, Tsai CC, Liao WH, Chen KY, Huang HC (2012) Effects of light quality on the accumulation of oil in a mixed culture of Chlorella sp. and Saccharomyces cerevisiae. J Chem Technol Biotechnol 87(5):601–607

    Article  CAS  Google Scholar 

  9. Romero-Romero CC, Sánchez-Saavedra MP (2016) Effect of light quality on the growth and proximal composition of Amphora sp. J Appol Phycol 29:1203–1211. https://doi.org/10.1007/s10811-016-1029-7

    Article  CAS  Google Scholar 

  10. Kim DG, Lee C, Park S-E, Choi Y-E (2014) Manipulation of light wavelength at appropriate growth stage to enhance biomass productivity and fatty acid methyl ester yield using Chlorella vulgaris. Bioresour Technol 159:240–248

    Article  CAS  PubMed  Google Scholar 

  11. Chaundhary R, Khattar JIS, Singh DP (2014) Microalgae as feedstock for biofuel: biomass yield, lipid content and fatty acid composition as selection criteria. Intern J Power Renew Energy Syst:62–71

  12. Breuer G, Lamers PP, Martens DE, Draaisma RB, Wijffels RH (2012) The impact of nitrogen starvation on the dynamics of triacylglycerol accumulation in nine microalgae strains. Bioresour Technol 124:217–226

    Article  CAS  PubMed  Google Scholar 

  13. Ho SH, Chen CY, Chang JS (2012) Effect of light intensity and nitrogen starvation on CO2 fixation and lipid/carbohydrate production of an indigenous microalga Scenedesmus obliquus CNW-N. Bioresour Technol 113:244–252

    Article  CAS  PubMed  Google Scholar 

  14. Chen CY, Yeh KL, Aisyah R, Lee DJ, Chang JS (2011) Cultivation, photobioreactor design and harvesting of microalgae for biodiesel production: a critical review. Bioresour Technol 102(1):71–81

    Article  CAS  PubMed  Google Scholar 

  15. Guillard RRL, Rhyter JH (1962) Studies on marine planktonic diatoms I. Cyclotella nana Hustedt and Detonula confervacea (Cleve) Gran. Can J Microbiol 8:229–239

    Article  CAS  PubMed  Google Scholar 

  16. Fogg GE, Thake BJ (1987) Algal cultures and phytoplankton ecology. University of Wisconsin Press, London, p 269

    Google Scholar 

  17. Whyte JNC (1987) Biochemical composition and energy content of six species of phytoplankton used in mariculture of bivalves. Aquaculture 60:231–241

    Article  CAS  Google Scholar 

  18. Lowry OH, Rosebrugh HJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin-phenol reagent. J Biol Chem 193:265–275

    CAS  PubMed  Google Scholar 

  19. Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356

    Article  CAS  Google Scholar 

  20. Bligh EG, Dyer WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37:911–917

    Article  CAS  PubMed  Google Scholar 

  21. Pande SV, Khan RP, Venkitasubramanian TA (1963) Microdetermination of lipids and serum total acids. Anal Biochem 6:415–423

    Article  CAS  PubMed  Google Scholar 

  22. Parsons TR, Maita Y, Lalli CM (1984) A manual of chemical and biological methods for seawater analysis. Pergamon Press, Oxford, p 173

    Google Scholar 

  23. Woodworth BD, Mead RL, Nichols CN, Kolling DRJ (2015) Photosynthetic light reactions increase total lipid accumulation in carbon-supplemented batch cultures of Chlorella vulgaris. Bioresour Technol 179:159–164

    Article  CAS  PubMed  Google Scholar 

  24. Folch J, Lee M, Sloane-Stanley GH (1957) A simple method for the isolation and purification of total lipids from animal tissue. J Biol Chem 22:477–509

    Google Scholar 

  25. Metcalfe LD, Schmitz AA, Pelka JR (1966) Rapid preparation of fatty acid esters from lipids for gas chromatographic analysis. Anal Chem 574(38):514–515

    Article  Google Scholar 

  26. Kim TH, Lee Y, Han SH, Hwang SJ (2013) The effects of wavelength and wavelength mixing ratios on microalgae growth and nitrogen, phosphorus removal using Scenedesmus sp. for wastewater treatment. Bioresour Technol 130:75–80

    Article  CAS  PubMed  Google Scholar 

  27. Chia MA, Lombardi AT, Melão MD (2013) Growth and biochemical composition of Chlorella vulgaris in different growth media. Ana Acad Bras Ciênc 85(4):1427–1438

    Article  CAS  Google Scholar 

  28. Ong SC, Kao CY, Chiu SY, Tsai MT, Lin CS (2010) Characterization of the thermal-tolerant mutants of Chlorella sp. with high growth rate and application in outdoor photobioreactor cultivation. Bioresour Technol 101(8):2880–2883

    Article  CAS  PubMed  Google Scholar 

  29. Beare-Rogers J, Dieffenbacher A, Holm JV (2001) Lexicon of lipid nutrition (IUPAC Technical Report). Pure Appl Chem 73(4):685–744

    Article  CAS  Google Scholar 

  30. Mao A-J, Wang J, Lin X-Z, Ming J-W (2008) Effect of spectra on growth of Chlorella and Isochrysis. Spectrosc Spectr Anal 28:991–994

    CAS  Google Scholar 

  31. Lee CG, Palsson BØ (1996) Photoacclimation of Chlorella vulgaris to red light from light-emitting diodes leads to autospore release following each cellular division. Biotechnol Prog 12(2):249–256

    Article  CAS  Google Scholar 

  32. Koc C, Anderson GA, Kommareddy A (2013) Use of red and blue light-emitting diodes (LED) and fluorescent lamps to grow microalgae in a photobioreactor. Isr J Aquacult Bamidgeh 65(797):8

    Google Scholar 

  33. Muller-Feuga A, Moaly J, Kaas R (2007) The microalgae of aquaculture. In: Stϕttrup JG, McEvoy LA (eds) Live feeds in marine aquaculture. Blackweel Science, Oxford, pp 207–225

    Google Scholar 

  34. Kowallik W (1987) Blue light effect on carbohydrate and protein metabolism. In: Senger H (ed) Blue Light Responses: Phenomena and Occurrence in Plants and Microorganisms, vol II. CRC Press, Boca Raton, pp 7–16

    Google Scholar 

  35. Azuara MP, Aparicio PJ (1983) In vivo blue-light activation of Chlamydomonas reinhardtii nitrate reductase. Plant Physiol 71(2):286–290

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Seyfabadi J, Ramezanpour Z, Khoeyi ZA (2011) Protein, fatty acid, and pigment content of Chlorella vulgaris under different light regimes. J Appl Phycol 23(4):721–726

    Article  CAS  Google Scholar 

  37. Wang CY, Fu CC, Liu C (2007) Effects of using light-emitting diodes on the cultivation of Spirulina platensis. Biochem Eng 37:21–25

    Article  CAS  Google Scholar 

  38. Mãnsson S (2012) Cultivation of Chlorella vulgaris in nutrient solution from greenhouse tomato production. Masther`s Thesis. Swedish University of Agricultural Science. Department of Horticulture. Alnarp, Suecia. p 40

  39. Yan C, Luo X, Zhao Y, Zheng Z (2013) Effects of various LED light wavelengths and light intensity supply strategies on synthetic high-strength wastewater purification by Chlorella vulgaris. Biodegradation 24:721–732

    Article  CAS  PubMed  Google Scholar 

  40. Sorigué D, Léger B, Cuiné S, Morales P, Mirabella B, Guédeney G, Li-Beisson Y, Jetter R, Peltier G, Beisson F (2016) Microalgae synthesize hydrocarbons from long chain fatty acids via a light-dependent pathway. Plant Physiol 171:2393–2405

    PubMed  PubMed Central  Google Scholar 

  41. Gustone F (1996) Fatty acid and lipid chemistry. Blackie Academic & Professional, Chapman & Hall, London, p 252

    Book  Google Scholar 

  42. Ra CH, Kang CH, Jung JH, Jeong GT, Kim SK (2016) Effects of light-emitting diodes (LEDs) on the accumulation of lipid content using a two-phase culture process with three microalgae. Bioresour Technol 212:254–261

    Article  CAS  PubMed  Google Scholar 

  43. Wang F, Gao B, Huang L, Su M, Dai C, Zhang C (2018) Evaluation of oleaginous eustigmatophycean microalgae as potential biorefinery feedstock for the production of palmitoleic acid and biodiesel. Bioresour Technol 270:30–37

    Article  CAS  PubMed  Google Scholar 

  44. Nalley JO, O'Donnell DR, Litchman E (2018) Temperature effects on growth rates and fatty acid content in freshwater algae and cyanobacteria. Algal Res 35:500–507

    Article  Google Scholar 

  45. Meng X, Yang J, Xu X, Zhang L, Ni Q, Xian M (2009) Biodiesel production from oleaginous microorganisms. Renew Energy 34(1):1–5

    Article  CAS  Google Scholar 

  46. Scarsella M, Parisi MP, D’Urso A, De Filippis P, Opoka J, Bravi M (2009) Achievements and perspectives in hetero- and mixotrophic culturing of microalgae. Chem Eng Trans 17:1065–1070

    Google Scholar 

  47. Knothe G (2015) Dependence of biodiesel fuel properties on the structure of fatty acid alkyl esters. Fuel Process Technol 86(10):1059–1070

    Article  CAS  Google Scholar 

  48. Knothe G, Matheaus AC, Ryan TW (2003) Cetane numbers of branched and straight-chain fatty esters determined in an ignition quality tester. Fuel 82(8):971–975

    Article  CAS  Google Scholar 

  49. Tong D, Hu C, Jiang K, Li Y (2011) Cetane number prediction of biodiesel from the composition of the fatty acid methyl esters. J Am Oil Chem Soc 88(3):415–423

    Article  CAS  Google Scholar 

  50. Biresaw G, Mittal KL (2014) Surfactants in tribology, volume 4. CRC Press, Taylor & Francis Group, Boca Raton, London, p 485

    Book  Google Scholar 

  51. Fakhry EM, El Maghraby DM (2013) Fatty acids composition and biodiesel characterization of Dunaliella salina. J Water Res Prot 5:894–899

    Article  CAS  Google Scholar 

  52. Barabás I, Todoruţ IA (2011) Biodiesel quality, standards and properties. In: Montero G, Stoytcheva M (eds) Biodiesel-Quality, Emissions and By-Products. InTech, Rijeka, Croacia, pp 3–28

    Google Scholar 

  53. Schenk PM, Thomas-Hall SR, Stephens E, Marx UC, Mussgnug JH, Posten C, Kruse O, Hankamer B (2008) Second generation biofuels: high-efficiency microalgae for biodiesel production. Bioenergy Res 1(1):20–43

    Article  Google Scholar 

  54. Ramírez-Verduzco LF, García-Flores BE, Rodríguez-Rodríguez JE, del Rayo J-JA (2011) Prediction of the density and viscosity in biodiesel blends at various temperatures. Fuel 90(5):751–176

    Article  CAS  Google Scholar 

  55. Knothe G, Dunn RO, Bagby MO (1997) Biodiesel: the use of vegetable oils and their derivatives as alternative diesel fuels. National Center for Agricultural Utilization Research, USD/ARS. ACS Symp Ser 666:172–208

    Article  CAS  Google Scholar 

Download references

Funding

This work was funded by “Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE),” the Fund for Scientific Research and Technological Development of CICESE Call 2015 (Project: 623801).

Author information

Authors and Affiliations

Authors

Contributions

M.P.S.S. wrote and organized the project, designed and supervised the research, and wrote the manuscript. D.S.C. wrote the project and revised the manuscript. F.Y.C.O. performed the experiments, obtained the data for all the experiments, and analyzed the data. C.A.M.C. helped to obtain data of cell counts and lipids profiles.

Corresponding author

Correspondence to M. del Pilar Sánchez-Saavedra.

Ethics declarations

Conflict of Interest

The authors declare that they have no conflict of interest.

Ethics Approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Authorship Consent

All authors read, approved the final manuscript, and agreed for this submission.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

ESM 1

(DOCX 57 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sánchez-Saavedra, M., Sauceda-Carvajal, D., Castro-Ochoa, F.Y. et al. The Use of Light Spectra to Improve the Growth and Lipid Content of Chlorella vulgaris for Biofuels Production. Bioenerg. Res. 13, 487–498 (2020). https://doi.org/10.1007/s12155-019-10070-1

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12155-019-10070-1

Keywords

Navigation