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High-Throughput In Vitro Screening of Changed Algal Community Structure Using the PhotoBiobox

  • Cho, Dae-Hyun (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Cho, Kichul (Department of Genetic Resources Research, National Marine Biodiversity Institute of Korea) ;
  • Heo, Jina (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Kim, Urim (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Lee, Yong Jae (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Choi, Dong-Yun (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Yoo, Chan (Department of Chemical and Biomolecular Engineering, KAIST) ;
  • Kim, Hee-Sik (Cell Factory Research Center, Korea Research Institute of Bioscience & Biotechnology (KRIBB)) ;
  • Bae, Seunghee (Research Institute for Molecular-Targeted Drugs, Department of Cosmetics Engineering, Konkuk University)
  • Received : 2020.06.18
  • Accepted : 2020.08.19
  • Published : 2020.11.28

Abstract

In a previous study, the sequential optimization and regulation of environmental parameters using the PhotoBiobox were demonstrated with high-throughput screening tests. In this study, we estimated changes in the biovolume-based composition of a polyculture built in vitro and composed of three algal strains: Chlorella sp., Scenedesmus sp., and Parachlorella sp. We performed this work using the PhotoBiobox under different temperatures (10-36℃) and light intensities (50-700 μmol m-2 s-1) in air and in 5% CO2. In 5% CO2, Chlorella sp. exhibited better adaptation to high temperatures than in air conditions. Pearson's correlation analysis showed that the composition of Parachlorella sp. was highly related to temperature whereas Chlorella sp. and Scenedesmus sp. showed negative correlations in both air and 5% CO2. Furthermore, light intensity slightly affected the composition of Scenedesmus sp., whereas no significant effect was observed in other species. Based on these results, it is speculated that temperature is an important factor in influencing changes in algal polyculture community structure (PCS). These results further confirm that the PhotoBiobox is a convenient and available tool for performance of lab-scale experiments on PCS changes. The application of the PhotoBiobox in PCS studies will provide new insight into polyculture-based ecology.

Keywords

References

  1. Bilal M, Rasheed T, Ahmed I, Iqbal HMN. 2017. High-value compounds from microalgae with industrial exploitability - a review. Front. Biosci. (Schol Ed) 9: 319-342. https://doi.org/10.2741/s490
  2. Ramanan R, Kim BH, Cho DH, Oh HM, Kim HS. 2016. Algae-bacteria interactions: Evolution, ecology and emerging applications. Biotechnol. Adv. 34: 14-29. https://doi.org/10.1016/j.biotechadv.2015.12.003
  3. Chisti Y. 2007. Biodiesel from microalgae. Biotechnol. Adv. 25: 294-306. https://doi.org/10.1016/j.biotechadv.2007.02.001
  4. Yun JH, Cho DH, Lee S, Heo J, Tran QG, Chang YK, et al. 2018. Hybrid operation of photobioreactor and wastewater-fed open raceway ponds enhances the dominance of target algal species and algal biomass production. Algal. Res. 29: 319-329. https://doi.org/10.1016/j.algal.2017.11.037
  5. Radakovits R, Jinkerson RE, Darzins A, Posewitz MC. 2010. Genetic engineering of algae for enhanced biofuel production. Eukaryot. Cell 9: 486-501. https://doi.org/10.1128/EC.00364-09
  6. Markou G, Nerantzis E. 2013. Microalgae for high-value compounds and biofuels production: a review with focus on cultivation under stress conditions. Biotechnol. Adv. 31: 1532-1542. https://doi.org/10.1016/j.biotechadv.2013.07.011
  7. Novoveska L, Franks DT, Wulfers TA, Henley WJ. 2016. Stabilizing continuous mixed cultures of microalgae. Algal Res. 13: 126-133. https://doi.org/10.1016/j.algal.2015.11.021
  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: 601-607. https://doi.org/10.1002/jctb.2750
  9. Heo J, Cho DH, Ramanan R, Oh HM, Kim HS. 2015. PhotoBiobox: a tablet sized, low-cost, high throughput photobioreactor for microalgal screening and culture optimization for growth, lipid content and CO2 sequestration. Biochem. Eng. J. 103: 193-197. https://doi.org/10.1016/j.bej.2015.07.013
  10. Cho DH, Choi JW, Kang Z, Kim BH, Oh HM, Kim HS, et al. 2017. Microalgal diversity fosters stable biomass productivity in open ponds treating wastewater. Sci. Rep. 7: 1-11. https://doi.org/10.1038/s41598-016-0028-x
  11. Cho DH, Ramanan R, Kim BH, Lee J, Kim S, Yoo C, et al. 2013. Novel approach for the development of axenic microalgal cultures from environmental samples. J. Phycol. 49: 802-810. https://doi.org/10.1111/jpy.12091
  12. Stanier RY, Kunisawa R, Mandel M, Cohen-Bazire G. 1971. Purification and properties of unicellular blue-green algae (order Chroococcales). Bacteriol. Rev. 35: 171-205. https://doi.org/10.1128/br.35.2.171-205.1971
  13. Hillebrand H, Durselen CD, Kirschtel D, Pollingher U, Zohary T. 1999. Biovolume calculation for pelagic and benthic microalgae. J. Phycol. 35: 403-424. https://doi.org/10.1046/j.1529-8817.1999.3520403.x
  14. Cho DH, Ramanan R, Heo J, Kang Z, Kim BH, Ahn CY, et al. 2015. Organic carbon, influent microbial diversity and temperature strongly influence algal diversity and biomass in raceway ponds treating raw municipal wastewater. Bioresour. Technol. 191: 481-487. https://doi.org/10.1016/j.biortech.2015.02.013
  15. Olofsson M, Karlberg M, Lage S, Ploug H. 2017. Phytoplankton community composition and primary production in the tropical tidal ecosystem, Maputo Bay (the Indian Ocean). J. Sea Res. 125: 18-25. https://doi.org/10.1016/j.seares.2017.05.007
  16. Park JBK, Craggs RJ, Shilton AN. 2011. Recycling algae to improve species control and harvest efficiency from a high rate algal pond. Water Res. 45: 6637-6649. https://doi.org/10.1016/j.watres.2011.09.042
  17. Olenina I, Hajdu S, Edler L, Andersson A. 2006. Biovolumes and sizeclasses of phytoplankton in the Baltic Sea. HELCOM Baltic Sea Environ. Proc. 106: 1-144.
  18. Chinnasamy S, Ramakrishnan B, Bhatnagar A, Das KC. 2009. Biomass production potential of a wastewater alga Chlorella vulgaris ARC 1 under elevated levels of CO2 and temperature. Int. J. Mol. Sci. 10: 518-532. https://doi.org/10.3390/ijms10020518
  19. Beardall J, Raven JA. 2004. The potential effects of global climate change on microalgal photosynthesis, growth and ecology. Phycologia 43: 26-40. https://doi.org/10.2216/i0031-8884-43-1-26.1
  20. Beardall J, Quigg A, Raven JA. 2003. Oxygen Consumption: Photorespiration and Chlororespiration, pp. 157-181. In Larkum AWD, Douglas SE, Raven JA (eds.), Photosynthesis in Algae, Springer
  21. Raven JA, Kubler JE, Beardall J. 2000. Put out the light, and then put out the light. J. Mar. Biol. Assoc. UK 80: 1-25. https://doi.org/10.1017/S0025315499001526
  22. Tortell PD. 2000. Evolutionary and ecological perspectives on carbon acquisition in phytoplankton. Limnol. Oceanogr. 45: 744-750. https://doi.org/10.4319/lo.2000.45.3.0744
  23. Hare CE, Leblanc K, DiTullio GR, Kudela RM, Zhang Y, Lee PA, et al. 2007. Consequences of increased temperature and CO2 for phytoplankton community structure in the Bering Sea. Mar. Ecol. Prog. Ser. 352: 9-16. https://doi.org/10.3354/meps07182
  24. Murata N, Takahashi S, Nishiyama Y, Allakhverdiev SI. 2007. Photoinhibition of photosystem II under environmental stress. BbaBioenergetics 1767: 414-421. https://doi.org/10.1016/j.bbabio.2006.11.019
  25. Yanguez K, Lovazzano C, Contreras-Porcia L, Ehrenfeld N. 2015. Response to oxidative stress induced by high light and carbon dioxide (CO2) in the biodiesel producer model Nannochloropsis salina (Ochrophyta, Eustigmatales). Rev. Biol. Mar. Oceanog. 50: 163-175. https://doi.org/10.4067/S0718-19572015000200003
  26. Sukenik A, Tchernov D, Kaplan A, Huertas E, Lubian LM, Livne A. 1997. Uptake, efflux, and photosynthetic utilization of inorganic carbon by the marine eustigmatophyte Nannochloropsis sp. J. Phycol. 33: 969-974. https://doi.org/10.1111/j.0022-3646.1997.00969.x
  27. Gentile MP, Blanch HW. 2001. Physiology and xanthophyll cycle activity of Nannochloropsis gaditana. Biotechnol. Bioeng. 75: 1-12. https://doi.org/10.1002/bit.1158