Skip to main content
Log in

Effects of spectral light quality and carbon dioxide on the physiology of Micractinium inermum: growth, photosynthesis, and biochemical composition

  • Published:
Journal of Applied Phycology Aims and scope Submit manuscript

Abstract

Growth, photosynthetic parameters, and biochemical composition of the chlorophyte Micractinium inermum were determined under conditions of different light-emitting diode (LED) wavelength distributions and carbon dioxide (CO2) levels of 1, 5, and 10% v/v. Increasing the inflowing CO2 concentration from 1 to 5 to 10% had negative effects on maximum growth rate (μmax), relative growth rate (RGR), biomass production, and CO2 fixation rate. Cultures subjected to a spectral distribution containing a blue wavelength peak were less negatively affected than red as CO2 stress increased, and evidently there was a quantitative effect depending on the peak area percentage. Under non-stressful conditions (1% CO2), there were no significant differences in μmax or RGR among light treatments; however, blue light resulted in decreased lag phases (0.75 less days than red). Biomass production was significantly higher in red wavelength peak treatments at 1% CO2 (i.e., monochromatic red treatment = 0.772 ± 0.07 g L−1) which demonstrates that although blue light allows for an early growth advantage, cultures grown with red light are able to catch up and result in more biomass. At a 10% CO2 level, RGR was higher in treatments with blue peaks; red peak treatments were no longer able to overcome the stress and demonstrated lag phases 4.87 days longer than blue peak treatments. Inhibition of photosystem II function was evident as CO2 concentrations increased. Evaluation of biochemical composition revealed that protein content was significantly greater in blue peak treatments at 10% CO2, pigment content was up to 2× greater than red at all CO2 levels, and total FAME and fatty acid profiles did not exhibit major changes.

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
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Abiusi F, Sampietro G, Marturano G, Biondi N, Rodolfi L, D’Ottavio M, Tredici MR (2014) Growth, photosynthetic efficiency, and biochemical composition of Tetraselmis suecica F&M-M33 grown with LEDs of different colors. Biotechnol Bioeng 111:956–964

    CAS  PubMed  Google Scholar 

  • Baer S, Heining M, Schwerna P, Buchholz R, Hübner H (2016) Optimization of spectral light quality for growth and product formation in different microalgae using a continuous photobioreactor. Algal Res 14:109–115

    Google Scholar 

  • Beardall J, Johnston A, Raven J (1998) Environmental regulation of CO2-concentrating mechanisms in microalgae. Can J Bot 76:1010–1017

    CAS  Google Scholar 

  • Borodin V, Gardeström P, Samuelsson G (1994) The effect of light quality on the induction of efficient photosynthesis under low CO2 conditions in Chlamydomonas reinhardtii and Chlorella pyrenoidosa. Physiol Plant 92:254–260

    CAS  Google Scholar 

  • Campbell D, Hurry V, Clarke AK, Gustafsson P, Öquist G (1998) Chlorophyll fluorescence analysis of cyanobacterial photosynthesis and acclimation. Microbiol Mol Biol Rev 62:667–668 3

    CAS  PubMed  PubMed Central  Google Scholar 

  • Carvalho AP, Silva SO, Baptista JM, Malcata FX (2011) Light requirements in microalgal photobioreactors: an overview of biophotonic aspects. Appl Microbiol Biotechnol 89:1275–1288

    CAS  PubMed  Google Scholar 

  • Chaloub RM, Reinert F, Nassar CG, Fleury BG, Mantuano DG, Larkum AWD (2010) Photosynthetic properties of three Brazilian seaweeds. Rev Bras Bot 33:371–374

    Google Scholar 

  • Chiu SY, Kao CY, Tsai MT, Ong SC, Chen CH, Lin CS (2009) Lipid accumulation and CO2 utilization of Nannochloropsis oculata in response to CO2 aeration. Bioresour Technol 100:833–838

    CAS  PubMed  Google Scholar 

  • Cuellar-Bermudez SP, Garcia-Perez JS, Rittman BE (2015) Photosynthetic bioenergy utilizing CO2: an approach on flue gases utilization for third generation biofuels. J Clean Prod 98:53–65

    CAS  Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Dickinson KE, Whitney CG, McGinn PJ (2013) Nutrient remediation rates in municipal wastewater and their effect on biochemical composition of the microalga Scenedesmus sp. AMDD. Algal Res 2:127–134

    Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Hess JL, Tolbert NE (1967) Changes in chlorophyll a/b ratio and products of 14CO2 fixation by algae grown in blue or red light. Plant Physiol 42:1123–1130

    CAS  PubMed  PubMed Central  Google Scholar 

  • Hogewoning SW, Trouwborst G, Maljaars H, Poorter H, van Ieperen W, Harbinson J (2010) Blue light dose-responses of leaf photosynthesis, morphology, and chemical composition of Cucumis sativus grown under different combinations of red and blue light. J Exp Bot 61:3107–3117

    CAS  PubMed  PubMed Central  Google Scholar 

  • Janssen M, Tramper J, Mur LR, Wijffels RH (2002) Enclosed outdoor photobioreactors: light regime, photosynthetic efficiency, scale-up, and future prospects. Biotechnol Bioeng 81:193–210

    Google Scholar 

  • Jeffrey SW, Humphrey GF (1975) New spectrophotometric equations for determining chlorophylls a, b and c 1 and c 2 in higher plants, algae and natural phytoplankton. Biochem Physiol Pflanz 167:191–194

    CAS  Google Scholar 

  • Katsuda T, Lababpour A, Shimahara K, Katoh S (2004) Astaxanthin production by Haematococcus pluvialis under illumination with LEDs. Enzym Microb Technol 35:81–86

    CAS  Google Scholar 

  • Kumar K, Banerjee D, Das D (2014a) Carbon dioxide sequestration from industrial flue gas by Chlorella sorokiniana. Bioresour Technol 152:225–233

    CAS  PubMed  Google Scholar 

  • Kumar MS, Hwang J, Abou-Shanab RAI, Kabra AN, Ji M, Jeon B (2014b) Influence of CO2 and light spectra on the enhancement of microalgal growth and lipid content. J Renew Sustain Energy 6:063107

    Google Scholar 

  • Laurens LML, Dempster TA, Jones HDT, Wolfrum EJ, Van Wychen S, McAllister JSP, Rencenberger M, Parchert KJ, Gloe LM (2012) Algal biomass constituent analysis: method uncertainties and investigation of the underlying measuring chemistries. Anal Chem 84:1879–1887

    CAS  PubMed  Google Scholar 

  • Lourenço SO, Barbarino E, Lavíín PL, Marquez UML, Aidar E (2004) Distribution of intracellular nitrogen in marine microalgae: calculation of new nitrogen-to-protein conversion factors. Eur J Phycol 39:17–32

    Google Scholar 

  • Mallick N, Mohn FH (2000) Reactive oxygen species: response of algal cells. J Plant Physiol 157:183–193

    CAS  Google Scholar 

  • Mattos ER, Singh M, Cabrera ML, Das KC (2015) Enhancement of biomass production in Scenedesmus bijuga high-density culture using weakly absorbed green light. Biomass Bioenergy 81:473–478

    CAS  Google Scholar 

  • Packer M (2009) Algal capture of carbon dioxide; biomass generation as a tool for greenhouse gas mitigation with reference to New Zealand energy strategy and policy. Energy Policy 3428:3437

    Google Scholar 

  • Pienkos PT, Darzins A (2009) The promise and challenges of microalgal-derived biofuels. Biofuels Bioprod Biorsour 3:431–440

    CAS  Google Scholar 

  • Pires JCM, Alvim-Ferraz MCM, Martins FG, Simões M (2012) Carbon dioxide capture from flue gases using microalgae: engineering aspects and biorefinery concept. Renew Sustain Energy Rev 16:3043–3053

    CAS  Google Scholar 

  • Rossa MM, de Oliveira MC, Okamoto OK, Lopes PF, Colepicolo P (2002) Effect of visible light on superoxide dismutase (SOD) activity in the red alga Gracilariopsis tenuifrons (Gracilariales, Rhodophyta). J Appl Phycol 14:151–157

    CAS  Google Scholar 

  • Rivkin RB (1989) Influence of irradiance and spectral quality on the carbon metabolism of phytoplankton I. Photosynthesis, chemical composition and growth. Mar Ecol Prog Ser 55:291–304

    CAS  Google Scholar 

  • Round FE (1984) The ecology of algae. Cambridge University Press, Cambridge, pp 353–355

    Google Scholar 

  • Ruiz J, Oliveira G, de Vree J, Bosma R, Willems P, Reith JH, Eppink MHM, Kleinegris DMM, Wijffels RH, Barbosa MJ (2016) Towards industrial products from microalgae. Energy Environ Sci 9:3036–3043

    Google Scholar 

  • Ruyters G (1984) Effects of blue light on enzymes. In: Senger H (ed) Blue light effects in biological systems. Springer, Berlin, pp 283–301

    Google Scholar 

  • Sanchez-Saavedra MD, Maeda-Martinez AN, Acosta-Galindo S (2016) Effect of different light spectra on the growth and biochemical composition of Tisochrysis lutea. J Appl Phycol 28:839–847

    Google Scholar 

  • Shultze PSC, Barreira LA, Pereira HGC, Perales JA, Varela JCS (2014) Light emitting diodes (LEDs) applied to microalgal production. Trends Biotechnol 32:422–430

    Google Scholar 

  • Strickland JDH, Parsons TR (1968) A practical handbook of seawater analysis. Bull Fish Res Bd Can 167:1–310

    Google Scholar 

  • Tang D, Han W, Li P, Miao X, Zhong J (2011) CO2 biofixation and fatty acid composition of Scenedesmus obliquus and Chlorella pyrenoidosa in response to different CO2 levels. Bioresour Technol 102:3071–3076

    CAS  PubMed  Google Scholar 

  • Tibbetts SM, Milley JE, Lall SP (2015a) Chemical composition and nutritional properties of freshwater and marine microalgal biomass cultured in photobioreactors. J Appl Phycol 27:1109–1119

    CAS  Google Scholar 

  • Tibbetts SM, Whitney CG, MacPherson MJ, Bhatti S, Banskota AH, Stefanova R, McGinn PJ (2015b) Biochemical characterization of microalgal biomass from freshwater species isolated in Alberta, Canada for animal feed applications. Algal Res 11:435–447

    Google Scholar 

  • Umino Y, Satoh A, Shiraiwa Y (1991) Factors controlling induction of external carbonic anhydrase and change in K1/2(CO2) of photosynthesis in Chlorella regularis. Plant Cell Physiol 32:379–384

    CAS  Google Scholar 

  • Wallen DG, Geen GH (1971) Light quality in relation to growth, photosynthetic rates and carbon metabolism in two species of marine plankton algae. Mar Biol 10:34–43

    CAS  Google Scholar 

  • Wijffels RH, Barbosa MJ (2010) An outlook on microalgal biofuels. Science 329:796–799

    CAS  PubMed  Google Scholar 

  • Wu H (2016) Effect of different light qualities on growth, pigment content, chlorophyll fluorescence, and antioxidant enzyme activity in the red alga Pyropia haitanensis (Bangiales, Rhodophyta). Biomed Res Int 2016:8

    Google Scholar 

  • Yan C, Zhang L, Luo X, Zheng Z (2013) Effects of various LED light wavelengths and intensities on the performance of purifying synthetic domestic sewage by microalgae at different influent C/N ratios. Ecol Eng 51:24–32

    Google Scholar 

  • Yoo C, Jun S, Lee J, Ahn C, Oh H (2010) Selection of microalgae for lipid production under high levels of carbon dioxide. Bioresour Technol 101:71–74

    Google Scholar 

  • Yun Y, Lee SB, Park JM, Lee C, Yang J (1997) Carbon dioxide fixation by algal cultivation using wastewater nutrients. J Chem Technol Biotechnol 69:451–455

    CAS  Google Scholar 

  • Zhao Y, Wang J, Zhang H, Yan C, Zhang Y (2013) Effects of various LED light wavelengths and intensities on microalgae-based simultaneous biogas upgrading and digestate nutrient reduction process. Bioresour Technol 136:461–468

    CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors wish to thank Laura Garrison and Cheryl Wall for their technical support during this study. We gratefully acknowledge Sean Tibbetts and Shane Patelakis for reviewing a draft of this manuscript.

Funding

Funding for this work was provided by NRC’s Algal Carbon Conversion Program. This is NRC publication no. 56441.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kathryn E. Dickinson.

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 15 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dickinson, K.E., Lalonde, C.G. & McGinn, P.J. Effects of spectral light quality and carbon dioxide on the physiology of Micractinium inermum: growth, photosynthesis, and biochemical composition. J Appl Phycol 31, 3385–3396 (2019). https://doi.org/10.1007/s10811-019-01880-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10811-019-01880-z

Keywords

Navigation