Improved Production of Astaxanthin from Haematococcus pluvialis Using a Hybrid Open–Closed Cultivation System
Source abstract
Abstract
Haematococcus species are rich sources of the antioxidant astaxanthin and have good potential for carbon dioxide reduction. A variety of culture systems for these microalgae are currently in development, but clearly profitable approaches have yet to be reported. Open outdoor culture is currently the only feasible culture system for producing large amounts of biomass. In this study, based on laboratory results, the cultivation of Haematococcus was divided into two stages: a green stage characterised by cell growth, and a red stage characterised by astaxanthin accumulation. For mass culture, we adopted a hybrid open–closed pond system for astaxanthin production. The open culture system was shown to produce approximately 50 kg (dry weight) of biomass per culture at an average rate of 0.51 g L−1, with 0.52 μg mL−1 of astaxanthin content in a 12 -m3 water tank. As large amounts of microalgal bioproducts are in high demand, inexpensive open outdoor culture methods should be adopted as an alternative to costly closed photobioreactors. Although the levels of biomass and astaxanthin production were found to be 30% lower in the field than in the laboratory in this study, the basic data obtained in this research may be useful for lowering astaxanthin production costs.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Algal biology and biofuel production · Aquatic Ecosystems and Phytoplankton Dynamics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Biology, Soonchunhyang University, Asan 336-745, Chungcheongnam-do, Republic of Korea
Korea Fisheries Resources Agency East Sea Branch, 457, Samho-ro, Buk-gu, Pohang 37601, Gyungsangbuk-do, Republic of Korea
Research Institute for Basic Science, Soonchunhyang University, Asan 336-745, Chungcheongnam-do, Republic of Korea
AlgaeBio, Inc., Asan 31459, Chungcheongnam-do, Republic of Korea
Funding
Ministry of Science and ICT · Basic Science Research Program · Ministry of Oceans and Fisheries · Soonchunhyang University
References (58)
Show source-provided references
1. Udayan, A., Sirohi, R., Sreekumar, N., Sang, B.I., and Sim, S.J. (2022). Mass cultivation and harvesting of microalgal biomass: Current trends and future perspectives. Bioresour. Technol., 344 Pt B.10.1016/j.biortech.2021.126406 ↗
2. Mass cultivation of microalgae in open raceway pond for biomass and biochemicals production
3. The promising future of microalgae: Current status, challenges, and optimization of a sustainable and renewable industry for biofuels, feed, and other products10.1186/s12934-018-0879-x ↗
4. Research and development for algae-based technologies in Korea: A review of algae biofuel production10.1007/s11120-014-9974-y ↗
5. Mixotrophic and photoautotrophic cultivation of 14 microalgae isolates from Saskatchewan, Canada: Potential applications for wastewater remediation for biofuel production10.1007/s10811-011-9772-2 ↗
6. Wegeberg, S. (2010). Algae Biomass for Bioenergy in Denmark Biological/Technical Challenges and Opportunities, DONG Energy.
7. From genetic improvement to commercial-scale mass culture of a Chilean strain of the green microalga Haematococcus pluvialis with enhanced productivity of the red ketocarotenoid astaxanthin
8. Commercial applications of microalgae10.1263/jbb.101.87 ↗
9. Mass Cultivation from a Korean Raceway Pond System of Indigenous Microalgae as Potential Biofuel Feedstock
10. Nishida, Y., Berg, P.C., Shakersain, B., Hecht, K., Takikawa, A., Tao, R., Kakuta, Y., Uragami, C., Hashimoto, H., and Misawa, N. (2023). Astaxanthin: Past, Present, and Future. Mar. Drugs, 21.10.3390/md21100514 ↗
11. Stachowiak, B., and Szulc, P. (2021). Astaxanthin for the Food Industry. Molecules, 26.10.3390/molecules26092666 ↗
12. Jannel, S., Caro, Y., Bermudes, M., and Petit, T. (2020). Novel Insights into the Biotechnological Production of Haematococcus pluvial-is-Derived Astaxanthin: Advances and Key Challenges to Allow Its Industrial Use as Novel Food Ingredient. J. Mar. Sci. Eng., 8.10.3390/jmse8100789 ↗
13. Rizzo, A., Ross, M.E., Norici, A., and Jesus, B. (2022). A Two-Step Process for Improved Biomass Production and Non-Destructive Astaxanthin and Carotenoids Accumulation in Haematococcus pluvialis. Appl. Sci., 12.10.3390/app12031261 ↗
14. Assessing contamination of microalgal astaxanthin producer Haematococcus cultures with high-resolution melting curve analysis10.1007/s13353-016-0378-x ↗
15. Combined effect of initial biomass density and nitrogen concentration on growth and astaxanthin production of Haematococcus pluvialis (Chlorophyta) in outdoor cultivation10.4490/algae.2013.28.2.193 ↗
16. Production of astaxanthin from Haematococcus in open pond by two-stage growth one-step process10.1016/j.aquaculture.2009.06.043 ↗
17. Oslan, S.N.H., Shoparwe, N.F., Yusoff, A.H., Rahim, A.A., Chang, C.S., Tan, J.S., Oslan, S.N., Arumugam, K., Ariff, A.B., and Sulaiman, A.Z. (2021). A Review on Haematococcus pluvialis Bioprocess Optimization of Green and Red Stage Culture Conditions for the Production of Natural Astaxanthin. Biomolecules, 11.10.3390/biom11020256 ↗
18. Mixotrophic Growth of Astaxanthin-Rich Alga Haematococcus pluvialis using Refined Crude Glycerol as Carbon Substrate: Batch and Fed-Batch Cultivations10.48048/wjst.2021.7354 ↗
19. Recent breakthroughs in the biology of astaxanthin accumulation by microalgal cell10.1007/s11120-015-0156-3 ↗
20. Johnsen, M.N. (2012). Microalgae: Biotechnology, Microbiology and Energy, Nova Science Publishers.
21. Recent trends in the mass cultivation of algae in raceway ponds10.1016/j.rser.2015.06.033 ↗
22. Yadala, S., and Cremaschi, S. (2016). A Dynamic Optimization Model for Designing Open-Channel Raceway Ponds for Batch Production of Algal Biomass. Processes, 4.10.3390/pr4020010 ↗
23. Carotenoids of Microalgae Used in Food Industry and Medicine10.2174/1389557516666160808123841 ↗
24. Li, Y., Gong, F., Guo, S., Yu, W., and Liu, J. (2021). Adonis amurensis Is a Promising Alternative to Haematococcus as a Resource for Natural Esterified (3S,3′S)-Astaxanthin Production. Plants, 10.10.3390/plants10061059 ↗
25. Microalgae as a source for secondary carotenoid production: A screening study
26. Astaxanthin accumulation in Haematococcus requires a cytochrome P450 hydroxylase and an active synthesis of fatty acids10.1016/S0014-5793(01)02596-0 ↗
27. Borowiak, D., Pstrowska, K., Wiśniewski, M., and Grzebyk, M. (2020). Propagation of Inoculum for Haematococcus pluvialis Microalgae Scale-Up Photobioreactor Cultivation System. Appl. Sci., 10.10.3390/app10186283 ↗
28. Borowitzka, M.A., and Navid, R.M. (2013). Algae Biofuels Energy, Springer.10.1007/978-94-007-5479-9 ↗
29. Qin, S., Wang, K., Gao, F., Ge, B., Cui, H., and Li, W. (2023). Biotechnologies for bulk production of microalgal biomass: From mass cultivation to dried biomass acquisition. Biotechnol. Biofuels, 16.10.1186/s13068-023-02382-4 ↗
30. Comparison of Microalgae Cultivation in Photobioreactor, Open Raceway Pond, and a Two-Stage Hybrid System10.3389/fenrg.2016.00029 ↗
31. Large Scale Cultivation of Microalgae: Open and Closed Systems
32. Maltsev, Y., Maltseva, K., Kulikovskiy, M., and Maltseva, S. (2021). Influence of Light Conditions on Microalgae Growth and Content of Lipids, Carotenoids, and Fatty Acid Composition. Biology, 10.10.3390/biology10101060 ↗
33. Effects of Nitrogen and Light Intensity on the Astaxanthin Accumulation in Motile Cells of Haematococcus pluvialis10.3389/fmars.2022.909237 ↗
34. Astaxanthin in microalgae: Pathways, functions and biotechnological implications10.4490/algae.2013.28.2.131 ↗
35. An economic assessment of astaxanthin production by large scale cultivation of Haematococcus pluvialis10.1016/j.biotechadv.2011.04.001 ↗
36. A novel strategy for the hyper-production of astaxanthin from the newly isolated microalga Haematococcus pluvialis JNU3510.1016/j.algal.2019.101466 ↗
37. Simultaneous promotion of photosynthesis and astaxanthin accumulation during two stages of Haematococcus pluvialis with ammonium ferric citrate10.1016/j.scitotenv.2020.141689 ↗
38. The effect of culture medium on the oil yield and fatty acid methyl ester of freshwater microalgae Chlorella vulgaris10.1080/00986445.2020.1864622 ↗
39. Byeon, H., An, Y., Kim, T., Rayamajhi, V., Lee, J., Shin, H., and Jung, S. (2024). Effects of Four Organic Carbon Sources on the Growth and Astaxanthin Accumulation of Haematococcus lacustris. Life, 14.10.3390/life14010029 ↗
40. The Spectral Determination of Chlorophylls a and b, as well as Total Carotenoids, Using Various Solvents with Spectrophotometers of Different Resolution10.1016/S0176-1617(11)81192-2 ↗
41. Enhancing the growth rate and astaxanthin yield of Haematococcus pluvialis by nuclear irradiation and high concentration of carbon dioxide stress10.1016/j.biortech.2015.12.076 ↗
42. An alternative approach to the traditional mixotrophic cultures of Haematococcus pluvialis Flotow (Chlorophyceae)10.4014/jmb.0909.09005 ↗
43. Liu, L., Ying, K., Wu, K., Tang, S., Zhou, J., and Cai, Z. (2022). Promoting the Growth of Haematococcus lacustris under High Light In-tensity through the Combination of Light/Dark Cycle and Light Color. J. Mar. Sci. Eng., 10.10.3390/jmse10070839 ↗
44. Effects of red and blue light emitting diodes on biomass and astaxanthin of Haematococcus pluvialis in pilot scale angled twin-layer porous substrate photobioreactors
45. Li, K., Ye, Q., Li, Q., Xia, R., Guo, W., and Cheng, J. (2020). Effects of the spatial and spectral distribution of red and blue light on Haematococcus pluvialis growth. Algal Res.-Biomass Biofuels Bioprod., 51.10.1016/j.algal.2020.102045 ↗
46. Enhanced production of astaxanthin and co-bioproducts from microalga Haematococcus sp. integrated with valorization of industrial wastewater under two-stage LED light illumination strategy10.1016/j.eti.2022.102620 ↗
47. Blue Light Enhances Astaxanthin Biosynthesis Metabolism and Extraction Efficiency in Haematococcus Pluvialis by Inducing Haematocyst Ger-mination10.1016/j.algal.2018.08.023 ↗
48. Photoautotrophic High-Density Cultivation of Vegetative Cells of Haematococcus Pluvialis in Airlift Bioreactor10.1016/j.biortech.2006.01.011 ↗
49. A new paradigm for producing astaxanthin from the unicellular green alga Haematococcus pluvialis10.1002/bit.25976 ↗
50. Comparison of different cultivation modes and light intensities using mono-cultures and co-cultures of Haematococcus pluvialis and Chlorella zofingiensis10.1002/jctb.2532 ↗
51. Enhancing the production of astaxanthin by mixotrophic cultivation of Haematococcus pluvialis in open raceway ponds10.1007/s10499-019-00483-2 ↗
52. Strategies to control biological contaminants during microalgal cultivation in open ponds10.1016/j.biortech.2017.12.088 ↗
53. Heterotrophic cultivation of microalgae for pigment production: A review10.1016/j.biotechadv.2017.09.009 ↗
54. Nitrogen uptake by heterotrophic bacteria and phytoplankton in the nitrate-rich Thames estuary10.3354/meps203013 ↗
55. Mixotrophic production of microalgae in pilot-scale photobioreactors: Practicability and process considerations10.1016/j.algal.2015.04.015 ↗
56. Zhao, K., Li, Y., Yan, H., Hu, Q., and Han, D. (2022). Regulation of Light Spectra on Cell Division of the Unicellular Green Al-ga Haematococcus pluvialis: Insights from Physiological and Lipidomic Analysis. Cells, 11.10.3390/cells11121956 ↗
57. Effects of temperature on the astaxanthin productivity and light harvesting characteristics of the green alga Haematococcus pluvialis10.1016/j.jbiosc.2014.09.002 ↗
58. Diaz-MacAdoo, D., Mata, M.T., and Riquelme, C. (2022). Influence of Irradiance and Wavelength on the Antioxidant Activity and Carotenoids Accumulation in Muriellopsis sp. Isolated from the Antofagasta Coastal Desert. Molecules, 27.10.3390/molecules27082412 ↗