Comparative analysis of two Porphyridium species for phycobiliprotein and polysaccharide production under different photoperiods

Liang Ji , Luxuan Xu , Zhangzhen Chen , Yulong He , Artem Yurevich Manyakhin , Pengfei Cheng , Liyun Sun , Jianhua Fan

Bioresources and Bioprocessing ›› 2025, Vol. 12 ›› Issue (1) : 154

PDF
Bioresources and Bioprocessing ›› 2025, Vol. 12 ›› Issue (1) :154 DOI: 10.1186/s40643-025-00996-0
Research
research-article

Comparative analysis of two Porphyridium species for phycobiliprotein and polysaccharide production under different photoperiods

Author information +
History +
PDF

Abstract

Phycobiliproteins and microalgal exopolysaccharides serve as natural pigments and functional additives in food applications. Current production primarily relies on multicellular algae, where yields are constrained by challenges in achieving high-density cultivation. This study investigated photoperiod effects on growth and production of phycobiliproteins and polysaccharides in two unicellular red algae (Porphyridium purpureum and Porphyridium aerugineum). Results demonstrated that short photoperiods enhanced the accumulation of core phycobiliproteins, specifically by increasing phycoerythrin in P. purpureum to a maximum of 30.5 ± 0.8 mg/g DW and phycocyanin in P. aerugineum to 41.9 ± 0.2 mg/g DW. Conversely, long photoperiods promoted biomass accumulation, yielding peak phycoerythrin production (140.6 ± 0.9 mg/L) in P. purpureum and phycocyanin (137.7 ± 1.2 mg/L) in P. aerugineum at day 12. Both species exhibited superior exopolysaccharide production under long photoperiods, though P. purpureum showed significantly higher productivity (898.7 ± 41.0 mg/L at day 20). These findings offer strategic solutions for sustainable production of food-grade pigments and polysaccharides through optimized unicellular algal cultivation.

Graphical abstract

Keywords

Porphyridium purpureum / Porphyridium aerugineum / Phycoerythrin / Phycocyanin / Polysaccharide

Cite this article

Download citation ▾
Liang Ji, Luxuan Xu, Zhangzhen Chen, Yulong He, Artem Yurevich Manyakhin, Pengfei Cheng, Liyun Sun, Jianhua Fan. Comparative analysis of two Porphyridium species for phycobiliprotein and polysaccharide production under different photoperiods. Bioresources and Bioprocessing, 2025, 12(1): 154 DOI:10.1186/s40643-025-00996-0

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Abebaw SE. A global review of the impacts of climate change and variability on agricultural productivity and farmers' adaptation strategies. Food Sci Nutr, 2025, 13(5e70260

[2]

Ahmad A, W. Hassan S, Banat F. An overview of microalgae biomass as a sustainable aquaculture feed ingredient: food security and circular economy. Bioengineered, 2022, 13(4): 9521-9547.

[3]

Ahmadi A, Anvar SAA, Nowruzi B, Golestan L. Effect of phycocyanin and phycoerythrin on antioxidant and antimicrobial activity of refrigerated low-fat yogurt and cream cheese. Sci Rep, 2024, 14(1): 27661

[4]

Bennett A, Bogorad L. Complementary chromatic adaptation in a filamentous blue-green alga. J Cell Biol, 1973, 582): 419-435.

[5]

Capek P, Matulova M, Sutovska M, et al. . Chlorella vulgaris alpha-L-arabino-alpha-L-rhamno-alpha,beta-D-galactan structure and mechanisms of its anti-inflammatory and anti-remodelling effects. Int J Biol Macromol, 2020, 162: 188-198.

[6]

Chen W, Zhang C, Song L, et al. . A high throughput Nile red method for quantitative measurement of neutral lipids in microalgae. J Microbiol Methods, 2009, 77(1): 41-47.

[7]

Chen C, Tang T, Shi Q, et al. . The potential and challenge of microalgae as promising future food sources. Trends Food Sci Technol, 2022, 126: 99-112.

[8]

Chen W, Liu J, Chu G, et al. . Comparative evaluation of four Chlorella species treating mariculture wastewater under different photoperiods: Nitrogen removal performance, enzyme activity, and antioxidant response. Bioresour Technol, 2023

[9]

Chu G, Wang Q, Song C, et al. . Platymonas helgolandica-driven nitrogen removal from mariculture wastewater under different photoperiods: performance evaluation, enzyme activity and transcriptional response. Bioresour Technol, 2023, 372128700

[10]

Dai J, Yang Z, Liu L, Lv L. Acomprehensive review on microalgae protein as an emerging protein resource. Food Res Int, 2025, 212116511

[11]

Dubois M, Gilles KA, Hamilton JK, et al. . Colorimetric method for determination of sugars and related substances. Anal Chem, 1956, 28(3): 350-356.

[12]

Fu HY, Wang MW. Ascorbate peroxidase plays an important role in photoacclimation in the extremophilic red alga Cyanidiococcus yangmingshanensis. Front Plant Sci, 2023, 14: 1176985

[13]

Galetovic A, Seura F, Gallardo V, et al. . Use of phycobiliproteins from Atacama cyanobacteria as food colorants in a dairy beverage prototype. Foods, 2020, 9(2): 244

[14]

George B, Pancha I, Desai C, et al. . Effects of different media composition, light intensity and photoperiod on morphology and physiology of freshwater microalgae Ankistrodesmus falcatus: a potential strain for bio-fuel production. Bioresour Technol, 2014, 171: 367-374.

[15]

Grintzalis K, Georgiou CD, Schneider Y-J. An accurate and sensitive Coomassie Brilliant Blue G-250-based assay for protein determination. Anal Biochem, 2015, 480: 28-30.

[16]

Grossman AR, Schaefer MR, Chiang GG, Collier JL. The phycobilisome, a light-harvesting complex responsive to environmental conditions. Microbiol Rev, 1993, 57(3): 725-749.

[17]

Guérin S, Bruyant F, Gosselin M, et al. . Photoperiodic dependent regulation of photosynthesis in the polar diatom Fragilariopsis cylindrus. Front Photobiol, 2024, 2: 1387119.

[18]

He Q, Yang H, Wu L, Hu C. Effect of light intensity on physiological changes, carbon allocation and neutral lipid accumulation in oleaginous microalgae. Bioresour Technol, 2015, 191: 219-228.

[19]

He Y, Ji L, Yuan Y, et al. . Recent advances in polysaccharide-dominated extracellular polymeric substances from microalgae: a review. Int J Biol Macromol, 2025, 302140572

[20]

Hsieh-Lo M, Castillo G, Ochoa-Becerra MA, Mojica L. Phycocyanin and phycoerythrin: strategies to improve production yield and chemical stability. Algal Res, 2019, 42101600

[21]

Ji L, Li S, Chen C, et al. . Physiological and transcriptome analysis elucidates the metabolic mechanism of versatile Porphyridium purpureum under nitrogen deprivation for exopolysaccharides accumulation. Bioresour Bioprocess, 2021, 8(1): 73.

[22]

Ji L, Liu Y, Luo J, Fan J. Freeze-thaw-assisted aqueous two-phase system as a green and low-cost option for analytical grade B-phycoerythrin production from unicellular microalgae Porphyridium purpureum. Algal Res, 2022, 67102831

[23]

Ji L, Qiu S, Wang Z, et al. . Phycobiliproteins from algae: current updates in sustainable production and applications in food and health. Food Res Int, 2023

[24]

Ji L, Zhao C, He Y, et al. . Exploring Porphyridium purpureum and Porphyridium aerugineum as alternative resources for phycobiliprotein production. Bioresour Technol, 2024

[25]

Klepacz-Smolka A, Pietrzyk D, Szelag R, et al. . Effect of light colour and photoperiod on biomass growth and phycocyanin production by Synechococcus PCC 6715. Bioresour Technol, 2020, 313123700

[26]

Kumar S, Gaber SM, Knezevic D, et al. . Application of R-phycoerythrin of different purities from Furcellaria lumbricalis in extruded food products. Food Res Int, 2025, 204115971

[27]

Lee M-C, Yeh H-Y, Jhang F-J, et al. . Enhancing growth, phycoerythrin production, and pigment composition in the red alga Colaconema sp. through optimal environmental conditions in an indoor system. Bioresour Technol, 2021, 333125199

[28]

Li S, Ji L, Shi Q, et al. . Advances in the production of bioactive substances from marine unicellular microalgae Porphyridium spp. Bioresour Technol, 2019, 292122048

[29]

Li S, Ji L, Chen C, et al. . Efficient accumulation of high-value bioactive substances by carbon to nitrogen ratio regulation in marine microalgae Porphyridium purpureum. Bioresour Technol, 2020, 309123362

[30]

Li S, Huang J, Ji L, et al. . Assessment of light distribution model for marine red microalga Porphyridium purpureum for sustainable production in photobioreactor. Algal Res, 2021, 58102390

[31]

Li Q, Chen Y, Liu X, et al. . Effect of salinity on the biochemical characteristics and antioxidant activity of exopolysaccharide of Porphyridium purpureum FACHB 806. Front Mar Sci, 2023, 9: 1097200.

[32]

Li S, Guo W, Zhang M, et al. . Microalgae polysaccharides exert antioxidant and anti-inflammatory protective effects on human intestinal epithelial cells in vitro and dextran sodium sulfate-induced mouse colitis in vivo. Int J Biol Macromol, 2024, 254(Pt 1127811

[33]

Marsac NTd, Houmard J. Complementary chromatic adaptation: physiological conditions and action spectra. Methods Enzymol, 1988, 167: 318-328.

[34]

Mysliwa-Kurdziel B, Solymosi K. Phycobilins and phycobiliproteins used in food industry and medicine. Mini-Rev Med Chem, 2017, 17(13): 1173-1193.

[35]

Patel A, Mishra S, Pawar R, Ghosh PK. Purification and characterization of C-Phycocyanin from cyanobacterial species of marine and freshwater habitat. Protein Expr Purif, 2005, 40(2): 248-255.

[36]

Pekárková B, Šmarda J, Hindák F. Cell morphology and growth characteristics of Porphyridium aerugineum (Rhodophyta)*. Plant Syst Evol, 1989, 164: 263-272.

[37]

Sarıtaş S, Kalkan AE, Yılmaz K, et al. . Biological and nutritional applications of microalgae. Nutrients, 2024, 17(1): 93

[38]

Tian X, Lin X, Xie Q, et al. . Effects of temperature and light on microalgal growth and nutrient removal in turtle aquaculture wastewater. Biology (Basel), 2024, 1311901

[39]

Vieira MV, Noore S, Tiwari B, et al. . Enhancing the stability and functionality of phycobiliproteins as natural food colourants through microparticle formulation. Food Chem, 2025, 465Pt 2142077

[40]

Voerman SE, Ruseckas A, Turnbull GA, et al. . Red algae acclimate to low light by modifying phycobilisome composition to maintain efficient light harvesting. BMC Biol, 2022, 201): 291

[41]

Xiao R, Zheng Y. Overview of microalgal extracellular polymeric substances (EPS) and their applications. Biotechnol Adv, 2016, 34(7): 1225-1244.

[42]

Xu Y, Jiao K, Zhong H, et al. . Induced cultivation pattern enhanced the phycoerythrin production in red alga Porphyridium purpureum. Bioprocess Biosyst Eng, 2019, 43(2): 347-355.

[43]

Yao D, Jiang Y, Daroch M, Tang J. Effect of light conditions on phycoerythrin accumulation by thermophilic cyanobacterium Leptothermofonsia sichuanensis and characterization of pigment stability. Bioresour Technol, 2024, 413131542

[44]

Yeh H-Y, Wang W-L, Nan F-H, Lee M-C. Enhanced Colaconema formosanum biomass and phycoerythrin yield after manipulating inorganic carbon, irradiance, and photoperiod. Bioresour Technol, 2022

Funding

National Key Research and Development Project of China (2025YFA0921100)

Natural Science Foundation of Shanghai(24ZR1490800)

Ningbo “Innovation Yongjiang 2035” Key R&D Programme - International Sci-tech Cooperation Projects(2024H002)

RIGHTS & PERMISSIONS

The Author(s)

AI Summary AI Mindmap
PDF

8

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/