Skip to main content

Advertisement

Log in

Stoichiometrically balanced nutrient management using a newly designed nutrient medium for large scale cultivation of Cyanobacterium aponinum

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

Abstract

Cyanobacteria have tremendous potential to produce bioactive molecules, which makes them a highly lucrative organism for use in industrial applications. In the present study, the first commercial nutrient medium for Cyanobacterium aponinum is developed and a process for large scale cultivation of cyanobacteria is established by combining economical medium, pre-emptive nutrient feeding strategy, and semi-continuous mode (SCM) of cultivation. The parameters measured were growth in terms of OD750 biomass, total nitrogen, nitrate, and phosphorous. Results indicated 13% more biomass yield in urea-phosphoric acid medium (UPA), in comparison to blue-green medium (BG-11). Biomass concentration was 5.3 and 4.7 g L−1 with UPA and BG-11 media, respectively. Urea was found to be a preferred nitrogen source for C. aponinum. Nutrient-dosing studies with UPA medium in SCM of operation resulted in an average daily biomass productivity of ~ 0.44 g L−1 day−1, which is significantly higher than those reported in previous studies. Here, the stoichiometric requirement of nitrogen and phosphorous was found to be 31 mg L−1 and 4.5 mg L−1, respectively. Stoichiometric nutrient addition in SCM resulted in a reduction in nutrient loss in blow down. In addition, the outdoor scale-up studies in flat panel photobioreactors further established the efficacy of UPA medium. Cost analysis of media revealed that UPA medium is 4.4 times less expensive than BG-11 and hence is a suitable and economical medium for large scale cultivation of C. aponinum. Further, this nutrient feeding strategy has wider applications which can be extended to other algal strains and cultivation systems.

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

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

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

  • Andersen RA, Berges JA, Harrison PJ, Watanabe MM (2005) Appendix A – Recipes for freshwater and seawater media. In: Andersen RA (ed) Algal culturing techniques. Elsevier, Academic Press, Amsterdam, pp 429–538

    Google Scholar 

  • Belisle BS, Steffen MM, Pound HL, Watson SB, DeBruyn JM, Bourbonniere RA, Boyer GL, Wilhelm SW (2016) Urea in Lake Erie: organic nutrient sources as potentially important drivers of phytoplankton biomass. J Great Lakes Res 42:599–607

    CAS  Google Scholar 

  • Bellaloui N, Mengistu A (2015) Effects of boron nutrition and water stress on nitrogen fixation, seed δ15N and δ13C dynamics, and seed composition in soybean cultivars differing in maturities. Sci World J 2015:407872

    Google Scholar 

  • Bezerra RP, Montoya EYO, Sato S, Perego P, de Carvalho JCM, Converti A (2011) Effects of light intensity and dilution rate on the semicontinuous cultivation of Arthrospira (Spirulina) platensis. A kinetic Monod-type approach. Bioresour Technol 102:3215–3219

    CAS  PubMed  Google Scholar 

  • Bolch CJS, Blackburn SI (1996) Isolation and purification of Australian isolates of the toxic cyanobacterium Microcystis aeruginosa Kütz. J Appl Phycol 8:5–13

    Google Scholar 

  • Borowitzka MA (1988) Appendix: Algal growth media and sources of algal cultures. In: Borowitzka MA, Borowitzka LJ (eds) Micro-algal biotechnology. Cambridge University Press, Cambridge, pp 456–465

    Google Scholar 

  • Chaiklahan R, Nattayaporn C, Wipawan S, Kalyanee P, Boosya B (2010) Cultivation of Spirulina platensis using pig wastewater in a semi-continuous process. J Microbiol Biotechnol 20:609–614

    CAS  PubMed  Google Scholar 

  • Chisti Y (2008) Biodiesel from microalgae beats bioethanol. Trends Biotechnol 26:126–131

    CAS  PubMed  Google Scholar 

  • Collos Y, Mornet F, Sciandra A, Waser N, Larson A, Harrison PJ (1999) An optical method for the rapid measurement of micromolar concentrations of nitrate in marine phytoplankton cultures. J Appl Phycol 11:179–184

    Google Scholar 

  • Danesi EDG, de O. Rangel-Yagui C, de Carvalho JCM, Sato S (2002) An investigation of effect of replacing nitrate by urea in the growth and production of chlorophyll by Spirulina platensis. Biomass Bioenergy 23:261–269

    CAS  Google Scholar 

  • De Philippis R, Vincenzini M (1998) Exocellular polysaccharides from cyanobacteria and their possible applications. FEMS Microbiol Rev 22:151–175

    Google Scholar 

  • De Philippis R, Sili C, Paperi R, Vincenzini M (2001) Exopolysaccharide-producing cyanobacteria and their possible exploitation: a review. J Appl Phycol 13:293–299

    Google Scholar 

  • Donald DB, Bogard MJ, Finlay K, Leavitt PR (2011) Comparative effects of urea, ammonium, and nitrate on phytoplankton abundance, community composition, and toxicity in hypereutrophic freshwaters. Limnol Oceanogr 56:2161–2175

    CAS  Google Scholar 

  • Erratt KJ (2017) Urea as an effective nitrogen source for Cyanobacteria. MSc Thesis, The University of Western Ontario, Canada 89 pp

  • Erratt KJ, Creed IF, Trick CG (2018) Comparative effects of ammonium, nitrate and urea on growth and photosynthetic efficiency of three bloom-forming cyanobacteria. Freshw Biol 63:626–638

    CAS  Google Scholar 

  • Flores E, Herrero A (2005) Nitrogen assimilation and nitrogen control in cyanobacteria. Biochem Soc Trans 33:164–167

    CAS  PubMed  Google Scholar 

  • Garcia-Pichel F, López-Cortés A, Nübel U (2001) Phylogenetic and morphological diversity of cyanobacteria in soil desert crusts from the Colorado plateau. Appl Environ Microbiol 67:1902–1910

    CAS  PubMed  PubMed Central  Google Scholar 

  • Glibert PM, Heil CA (2006) Escalating worldwide use of urea – a global change contributing to coastal eutrophication. Biogeochem 77:441–463

    CAS  Google Scholar 

  • Gris B, Sforza E, Morosinotto T, Bertucco A, La Rocca N (2017) Influence of light and temperature on growth and high-value molecules productivity from Cyanobacterium aponinum. J Appl Phycol 29:1781–1790

    CAS  Google Scholar 

  • Grobbelaar JU (2012) Microalgae mass culture: the constraints of scaling-up. J Appl Phycol 24:315–318

    CAS  Google Scholar 

  • Gudmundsdottir AB, Omarsdottir S, Brynjolfsdottir A, Paulsen BS, Olafsdottir ES, Freysdottir J (2015) Exopolysaccharides from Cyanobacterium aponinum from the Blue Lagoon in Iceland increase IL-10 secretion by human dendritic cells and their ability to reduce the IL-17+RORγt+/IL-10+FoxP3+ ratio in CD4+ T cells. Immunol Lett 163:157–162

    CAS  PubMed  Google Scholar 

  • Herrero A, Muro-Pastor AM, Flores E (2001) Nitrogen control in cyanobacteria. J Bacteriol 183:411–425

    CAS  PubMed  PubMed Central  Google Scholar 

  • Johnson TJ, Jahandideh A, Isaac IC, Baldwin EL, Muthukumarappan K, Zhou R, Gibbons WR (2017) Determining the optimal nitrogen source for large-scale cultivation of filamentous cyanobacteria. J Appl Phycol 29:1–13

    CAS  Google Scholar 

  • Lau N-S, Matsui M, Abdullah AA-A (2015) Cyanobacteria: photoautotrophic microbial factories for the sustainable synthesis of industrial products. Biomed Res Int 2015:1–9

    Google Scholar 

  • Li J, Zhang J, Huang W, Kong F, Li Y, Xi M, Zheng Z (2016) Comparative bioavailability of ammonium, nitrate, nitrite and urea to typically harmful cyanobacterium Microcystis aeruginosa. Mar Pollut Bull 110:93–98

    CAS  PubMed  Google Scholar 

  • María A, Guzmán-Murillo MA, López-Bolaños CC, Ledesma-Verdejo T, Roldan-Libenson G, Cadena-Roa MA, Ascencio F (2007) Effects of fertilizer-based culture media on the production of exocellular polysaccharides and cellular superoxide dismutase by Phaeodactylum tricornutum (Bohlin). J Appl Phycol 19:33–41

    Google Scholar 

  • Melis A (2009) Solar energy conversion efficiencies in photosynthesis: minimizing the chlorophyll antennae to maximize efficiency. Plant Sci 177:272–280

    CAS  Google Scholar 

  • Meng F, Cui H, Wang Y, Li X (2018) Responses of a new isolated Cyanobacterium aponinum strain to temperature, pH, CO2 and light quality. J Appl Phycol 30:1525–1532

    CAS  Google Scholar 

  • Modiri S, Sharafi H, Alidoust L, Hajfarajollah H, Haghighi O, Azarivand A, Zamanzadeh Z, Zahiri HS, Vali H, Noghabi KA (2015) Lipid production and mixotrophic growth features of cyanobacterial strains isolated from various aquatic sites. Microbiol 161:662–673

    CAS  Google Scholar 

  • Moreno J, Vargas MÁ, Rodrix g H, Rivas J, Guerrero MG (2003) Outdoor cultivation of a nitrogen-fixing marine cyanobacterium, Anabaena sp. ATCC 33047. Biomol Eng 20:191–197

    CAS  PubMed  Google Scholar 

  • Mourelle M, Gómez C, Legido J (2017) The potential use of marine microalgae and cyanobacteria in cosmetics and thalassotherapy. Cosmetics 4:46–59

    Google Scholar 

  • Probir D, Abdul QM, Kiran CA, Ibrahim TM, Shoyeb K, Ghamza A, Hareb A-J (2018) Outdoor continuous cultivation of self-settling marine cyanobacterium Chroococcidiopsis sp. Ind Biotechnol 14:45–53

    Google Scholar 

  • Reichert CC, Reinehr CO, Costa JAV (2006) Semicontinuous cultivation of the cyanobacterium Spirulina platensis in a closed photobioreactor. Braz J Chem Eng 23:23–28

    Google Scholar 

  • Rippka R, Deruelles J, Waterbury JB, Herdman M, Stanier RY (1979) Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol 111:1–61

    Google Scholar 

  • Sakamoto T, Inoue-Sakamoto K, Bryant DA (1999) A novel nitrate/nitrite permease in the marine cyanobacterium Synechococcus sp strain PCC 7002. J Bacteriol 181:7363–7372

    CAS  PubMed  PubMed Central  Google Scholar 

  • Sayre R (2010) Microalgae: the potential for carbon capture. Bioscience 60:722–727

    Google Scholar 

  • Scherholz ML, Curtis WR (2013) Achieving pH control in microalgal cultures through fed-batch addition of stoichiometrically-balanced growth media. BMC Biotechnol 13:39–54

    CAS  PubMed  PubMed Central  Google Scholar 

  • Schuurmans RM, Schuurmans JM, Bekker M, Kromkamp JC, Matthijs HCP, Hellingwerf KJ (2014) The redox potential of the plastoquinone pool of the cyanobacterium Synechocystis species strain PCC6803 is under strict homeostatic control. Plant Physiol 165:463–475

    CAS  PubMed  PubMed Central  Google Scholar 

  • Setyoningrum Tutik M, Nur MMA (2015) Optimization of C-phycocyanin production from S. platensis cultivated on mixotrophic condition by using response surface methodology. Biocatal Agric Biotechnol 4:603–607

    Google Scholar 

  • Sheehan J, Dunahay T, Benemann J, Roessler P (1998) Look back at the U.S. Department of Energy’s aquatic species program: biodiesel from algae – laboratory NRE, Golden, Colorado. NREL/TP-580-24190 pp 1-328

  • Singh S, Kate BN, Banerjee UC (2005) Bioactive compounds from cyanobacteria and microalgae: an overview. Crit Rev Biotechnol 25:73–95

    CAS  PubMed  Google Scholar 

  • Singh JS, Kumar A, Rai AN, Singh DP (2016) Cyanobacteria: a precious bio-resource in agriculture, ecosystem, and environmental sustainability. Front Microbiol 7:1–19

    CAS  Google Scholar 

  • Velu C, Cirés S, Alvarez-Roa C, Heimann K (2015) First outdoor cultivation of the N2-fixing cyanobacterium Tolypothrix sp. in low-cost suspension and biofilm systems in tropical Australia. J Appl Phycol 27:1743–1753

    CAS  Google Scholar 

  • Walker DA (2009) Biofuels, facts, fantasy, and feasibility. J Appl Phycol 21:509–517

    Google Scholar 

  • Wang Q-l, Liu Y-d, Shen Y-w, Jin C-y, Lu J-s, Zhu J-m, Li S-h (1991) Studies on mixed mass cultivation of Anabaena spp. (nitrogen-fixing blue-green algae, cyanobacteria) on a large scale. Bioresour Technol 38:221–228

    CAS  Google Scholar 

  • Wang Q, Li H, Post AF (2000) Nitrate assimilation genes of the marine diazotrophic, filamentous cyanobacterium Trichodesmium sp. strain WH9601. J Bacteriol 182:1764–1767

    CAS  PubMed  PubMed Central  Google Scholar 

  • Weyer KM, Bush DR, Darzins A, Willson BD (2010) Theoretical maximum algal oil production. Bioenergy Res 3:204–213

    CAS  Google Scholar 

  • Winckelmann D, Bleeke F, Bergmann P, Klöck G (2015) Growth of Cyanobacterium aponinum influenced by increasing salt concentrations and temperature. Biotech 5:253–260

    Google Scholar 

Download references

Acknowledgments

We sincerely acknowledge Reliance Industries Limited for providing the laboratory resources. We also appreciate Ajit Sapre (Group President, Research & Technology, Reliance Industries Limited) for his support; Saranya Karuppasamy for strain isolation and purification; Vinod Nagle and Akshay Chawande for maintaining Cyanobacterium aponinum; Badrish Soni for providing strain information; Chaitanya Joshi, Rakhi Dixit, and Ashish Waghmare for technical assistance; Debanjan Sanyal and Nishant Saxena for providing sea water analysis data and Uma Shankar Sagaram, G Venkata Subhash, and Tomal Dattaroy for their critical inputs in refining the manuscript.

Funding

This study received funding from Reliance Industries Limited.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Santanu Dasgupta.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts.

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 16 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Rajvanshi, M., Gautam, K., Manjre, S. et al. Stoichiometrically balanced nutrient management using a newly designed nutrient medium for large scale cultivation of Cyanobacterium aponinum. J Appl Phycol 31, 2779–2789 (2019). https://doi.org/10.1007/s10811-019-01851-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10811-019-01851-4

Keywords