Chemical, rheological, and volatile profiling of microalgae Arthrospira, Isochrysis, Nannochloropsis, and Tetraselmis species
Johannes Magpusao, Indrawati Oey, Biniam Kebede
Chemical, rheological, and volatile profiling of microalgae Arthrospira, Isochrysis, Nannochloropsis, and Tetraselmis species
Microalgae are increasingly regarded as a sustainable source of novel food and functional products due to their nutritional composition. This study aimed to conduct an in-depth analysis of the chemical, microstructural and rheological, and volatile-flavour related properties of Arthrospira, Isochrysis, Nannochloropsis, and Tetraselmis species. Chemometric data analysis was employed to integrate the multivariate data, investigate the classification among the four species, and identify discriminating and distinct features. Arthrospira is high in protein content, and Nannochloropsis is lipid-rich with dominantly polyunsaturated fatty acids. Isochrysis is rich in carotenoids and total phenolics, while Tetraselmis is high in carbohydrates. Key discriminant volatile markers encompass aldehydes, terpenes, and hydrocarbons for Arthrospira; ketones and alcohols for Nannochloropsis; aldehydes, ketones, and sulfur-containing compounds for Tetraselmis; and furans and aldehydes for Isochrysis. Moreover, Arthrospira and Isochrysis demonstrate elevated viscosity and notable thickening potential. In summary, the different microalgal biomass studied in this study showcase unique compositional, rheological, and volatile properties, highlighting their potential as functional ingredients for diverse applications in the food and pharmaceutical industries.
Microalgae / Chemical composition / Rheology / Volatile / Fatty acid / Chemometrics
[1] |
De Morais MG, Vaz BDS, De Morais EG, Costa JAV. Biologically Active Metabolites Synthesized by Microalgae Biomed Research International. 2015, 2015, 835761
CrossRef
Google scholar
|
[2] |
Draaisma RB, Wijffels RH, Slegers PME, Brentner LB, Roy A, et al. Food commodities from microalgae Current Opinion in Biotechnology. 2013, 24 2 169-77
CrossRef
Google scholar
|
[3] |
Matos J, Cardoso C, Bandarra NM, Afonso C. Microalgae as healthy ingredients for functional food: A review Food & Function. 2017, 8 8 2672-85
CrossRef
Google scholar
|
[4] |
Vigani M, Parisi C, Rodríguez-Cerezo E, Barbosa MJ, Sijtsma L, et al. Food and feed products from micro-algae: Market opportunities and challenges for the EU Trends in Food Science & Technology. 2015, 42 1 81-92
CrossRef
Google scholar
|
[5] |
Laurens LML, Van Wychen S, McAllister JP, Arrowsmith S, Dempster TA, et al. Strain, biochemistry, and cultivation-dependent measurement variability of algal biomass composition Analytical Biochemistry. 2014, 452 1 86-95
CrossRef
Google scholar
|
[6] |
Batista AP, Gouveia L, Bandarra NM, Franco JM, Raymundo A. Comparison of microalgal biomass profiles as novel functional ingredient for food products Algal Research. 2013, 2 2 164-73
CrossRef
Google scholar
|
[7] |
Caporgno MP, Mathys A. Trends in microalgae incorporation into innovative food products with potential health benefits Frontiers in Nutrition. 2018, 5, 58
CrossRef
Google scholar
|
[8] |
Bernaerts TMM, Gheysen L, Foubert I, Hendrickx ME, Van Loey AM. The potential of microalgae and their biopolymers as structuring ingredients in food: a review Biotechnology Advances. 2019, 37, 107419
CrossRef
Google scholar
|
[9] |
Van Durme J, Goiris K, De Winne A, De Cooman L, Muylaert K. Evaluation of the volatile composition and sensory properties of five species of microalgae Journal of Agricultural and Food Chemistry. 2013, 61 46 10881-90
CrossRef
Google scholar
|
[10] |
Spolaore P, Joannis-Cassan C, Duran E, Isambert A. Commercial applications of microalgae Journal of Bioscience and Bioengineering. 2006, 101 2 87-96
CrossRef
Google scholar
|
[11] |
Ferdous UT, Yusof ZNB. Medicinal prospects of antioxidants from algal sources in cancer therapy Frontiers in Pharmacology. 2021, 12, 593116
CrossRef
Google scholar
|
[12] |
García-Segovia P, Pagán-Moreno MJ, Lara IF, Martínez-Monzó J. Effect of microalgae incorporation on physicochemical and textural properties in wheat bread formulation Food Science and Technology International. 2017, 23 5 437-47
CrossRef
Google scholar
|
[13] |
Rao A, Briskey D, Nalley JO, Ganuza E. Omega-3 eicosapentaenoic acid (EPA) rich extract from the microalga Nannochloropsis decreases cholesterol in healthy individuals: A double-blind, randomized, placebo-controlled, three-month supplementation study Nutrients. 2020, 12 6 1869
CrossRef
Google scholar
|
[14] |
Schwenzfeier A, Helbig A, Wierenga PA, Gruppen H. Emulsion properties of algae soluble protein isolate from Tetraselmis sp Food Hydrocolloids. 2013, 30 1 258-63
CrossRef
Google scholar
|
[15] |
Magpusao J, Giteru S, Oey I, Kebede B. Effect of high pressure homogenization on microstructural and rheological properties of A. platensis, Isochrysis, Nannochloropsisand Tetraselmisspecies Algal Research. 2021, 56, 102327
CrossRef
Google scholar
|
[16] |
[17] |
Burja AM, Armenta RE, Radianingtyas H, Barrow CJ. Evaluation of fatty acid extraction methods for Thraustochytrium sp. ONC-T18 Journal of Agricultural and Food Chemistry. 2007, 55 12 4795-801
CrossRef
Google scholar
|
[18] |
[19] |
González López CV, García MdCC, Fernández FGA, Bustus CS, Chisti Y, et al. Protein measurements of microalgal and cyanobacterial biomass Bioresource Technology. 2010, 101, 7587-91
CrossRef
Google scholar
|
[20] |
Lourenço SO, Barbarino E, Lavín PL, Lanfer Marquez UM, Aidar E. Distribution of intracellular nitrogen in marine microalgae: Calculation of new nitrogen-to-protein conversion factors European Journal of Phycology. 2004, 39 1 17-32
CrossRef
Google scholar
|
[21] |
Kulkarni S, Nikolov Z. Process for selective extraction of pigments and functional proteins from Chlorella vulgaris Algal Research. 2018, 35, 185-93
CrossRef
Google scholar
|
[22] |
Wellburn AR. The Spectral Determination of Chlorophylls a and b, as well as Total Carotenoids, Using Various Solvents with Spectrophotometers of Different Resolution Journal of Plant Physiology. 1994, 144 3 307-13
CrossRef
Google scholar
|
[23] |
Li HB, Cheng KW, Wong CC, Fan KW, Chen F, et al. Evaluation of antioxidant capacity and total phenolic content of different fractions of selected microalgae Food Chemistry. 2007, 102 3 771-76
CrossRef
Google scholar
|
[24] |
Bernaerts TMM, Panozzo A, Doumen V, Foubert I, Gheysen L, et al. Microalgal biomass as a (multi)functional ingredient in food products: Rheological properties of microalgal suspensions as affected by mechanical and thermal processing Algal Research. 2017, 25, 452-63
CrossRef
Google scholar
|
[25] |
Khrisanapant P, Kebede B, Leong SY, Oey I. A comprehensive characterisation of volatile and fatty acid profiles of legume seeds Foods. 2019, 8 12 651
CrossRef
Google scholar
|
[26] |
Kebede BT, Grauwet T, Magpusao J, Palmers S, Michiels C, Hendrickx M, et al. An integrated fingerprinting and kinetic approach to accelerated shelf-life testing of chemical changes in thermally treated carrot puree Food Chemistry. 2015, 179, 94-102
CrossRef
Google scholar
|
[27] |
Ryckebosch E, Bruneel C, Muylaert K, Foubert I. Microalgae as an alternative source of omega-3 long chain polyunsaturated fatty acids Lipid Technology. 2012, 24 6 128-30
CrossRef
Google scholar
|
[28] |
Tokuşoglu Ö, Ünal MK. Biomass nutrient profiles of three microalgae: Spirulina platensis, Chlorella vulgaris, and Isochrisis galbana Journal of Food Science. 2003, 68 4 1144-48
CrossRef
Google scholar
|
[29] |
Graziani G, Schiavo S, Nicolai MA, Buono S, Fogliano V, et al. Microalgae as human food: Chemical and nutritional characteristics of the thermo-acidophilic microalga Galdieria sulphuraria Food & Function. 2013, 4 1 144-52
CrossRef
Google scholar
|
[30] |
Rebolloso-Fuentes MM, Navarro-Pérez A, García-Camacho F, Ramos-Miras JJ, Guil-Guerrero JL. Biomass Nutrient Profiles of the Microalga Nannochloropsis Journal of Agricultural and Food Chemistry. 2001, 49 6 2966-72
CrossRef
Google scholar
|
[31] |
Bernaerts TMM, Gheysen L, Kyomugasho C, Jamsazzadeh Kermani Z, Vandionant S, et al. Comparison of microalgal biomasses as functional food ingredients: Focus on the composition of cell wall related polysaccharides Algal Research. 2018, 32, 150-61
CrossRef
Google scholar
|
[32] |
Grossmann L, Ebert S, Hinrichs J, Weiss J. Production of protein-rich extracts from disrupted microalgae cells: Impact of solvent treatment and lyophilization Algal Research. 2018, 36, 67-76
CrossRef
Google scholar
|
[33] |
[34] |
Saoudi-Helis L, Dubacq JP, Marty Y, Samain JF, Gudin C. Influence of growth rate on pigment and lipid composition of the microalga Isochrysis aff galbana clone T. iso. Journal of Applied Phycology. 1994, 6 3 315-22
CrossRef
Google scholar
|
[35] |
Gheysen L, Bernaerts T, Bruneel C, Goiris K, Durme J Van. Impact of processing on n-3 LC-PUFA in model systems enriched with microalgae Food Chemistry. 2018, 268 June 441-50
CrossRef
Google scholar
|
[36] |
Guo W, Zhu S, Feng G, Wu L, Feng Y, et al. Microalgae aqueous extracts exert intestinal protective effects in Caco-2 cells and dextran sodium sulphate-induced mouse colitis Food & Function. 2020, 11 1 1098-109
CrossRef
Google scholar
|
[37] |
Abd El Baky HH, El Baroty GS, Ibrahem EA. Functional characters evaluation of biscuits sublimated with pure phycocyanin isolated from Spirulina and Spirulina biomass Nutricion Hospitalaria. 2015, 32 1 231-41
CrossRef
Google scholar
|
[38] |
Di Lena G, Casini I, Lucarini M, Lombardi-Boccia G. Carotenoid profiling of five microalgae species from large-scale production Food Research International. 2019, 120, 810-18
CrossRef
Google scholar
|
[39] |
Parniakov O, Apicella E, Koubaa M, Barba FJ, Grimi N, et al. Ultrasound-assisted green solvent extraction of high-added value compounds from microalgae Nannochloropsis spp Bioresource Technology. 2015, 198, 262-67
CrossRef
Google scholar
|
[40] |
Matos J, Cardoso CL, Falé P, Afonso CM, Bandarra NM. Investigation of nutraceutical potential of the microalgae Chlorella vulgaris and Arthrospira platensis International Journal of Food Science & Technology. 2020, 55 1 303-12
CrossRef
Google scholar
|
[41] |
Custódio L, Soares F, Pereira H, Barreira L, Vizetto-Duarte C, et al. Fatty acid composition and biological activities of Isochrysis galbana T-ISO, Tetraselmis sp. and Scenedesmus sp.: Possible application in the pharmaceutical and functional food industries Journal of Applied Phycology. 2014, 26 1 151-61
CrossRef
Google scholar
|
[42] |
Günerken E, D'Hondt E, Eppink MHM, Garcia-Gonzalez L, Elst K, et al. Cell disruption for microalgae biorefineries Biotechnology Advances. 2015, 33 2 243-60
CrossRef
Google scholar
|
[43] |
[44] |
Liu C, Lin L. Ultrastructural study and lipid formation of Isochrysis sp Botanical Bulletin of Academia Sinica. 2001, 42, 207-14
|
[45] |
Scholz MJ, Weiss TL, Jinkerson RE, Jing J, Roth R, et al. Ultrastructure and composition of the Nannochloropsis gaditana cell wall Eukaryotic Cell. 2014, 13 11 1450-64
CrossRef
Google scholar
|
[46] |
Halim R, Rupasinghe TWT, Tull DL, Webley PA. Mechanical cell disruption for lipid extraction from microalgal biomass Bioresource Technology. 2013, 140, 53-63
CrossRef
Google scholar
|
[47] |
[48] |
Shekarabi SPH, Mehrgan MS, Razi N, Sabzi S. Biochemical composition and fatty acid profile of the marine microalga Isochrysis galbana dried with different methods Journal of Microbiology, Biotechnology and Food Sciences. 2019, 9 3 521-24
CrossRef
Google scholar
|
[49] |
Gu N, Lin Q, Li G, Tan Y, Huang L, et al. Effect of salinity on growth, biochemical composition, and lipid productivity of Nannochloropsis oculata CS 179 Engineering in Life Sciences. 2012, 12 6 631-37
CrossRef
Google scholar
|
[50] |
Milovanović I, Mišan A, Simeunović J, Kovač D, Jambrec D, et al. Determination of volatile organic compounds in selected strains of cyanobacteria Journal of Chemistry. 2015, 2015, 969542
CrossRef
Google scholar
|
[51] |
[52] |
Achyuthan KE, Harper JC, Manginell RP, Moorman MW. Volatile metabolites emission by in vivo microalgae—an overlooked opportunity? Metabolites. 2017, 7 3 39
CrossRef
Google scholar
|
[53] |
Isleten Hosoglu M. Aroma characterization of five microalgae species using solid-phase microextraction and gas chromatography – mass spectrometry/olfactometry Food Chemistry. 2018, 240, 1210-18
CrossRef
Google scholar
|
[54] |
Kettlitz B, Scholz G, Theurillat V, Cselovszky J, Buck NR, et al. Furan and methylfurans in foods: an update on occurrence, mitigation, and risk assessment Comprehensive Reviews in Food Science and Food Safety. 2019, 18 3 738-52
CrossRef
Google scholar
|
[55] |
Zhou L, Chen J, Xu J, Li Y, Zhou C, et al. Change of volatile components in six microalgae with different growth phases Journal of the Science of Food and Agriculture. 2017, 97 3 761-69
CrossRef
Google scholar
|
[56] |
Bernaerts TMM, Verstreken H, Dejonghe C, Gheysen L, Foubert I, et a. Cell disruption of Nannochloropsis sp. improves in vitro bioaccessibility of carotenoids and ω3-LC-PUFA Journal of Functional Foods. 2020, 65, 103770
CrossRef
Google scholar
|
[57] |
Di Lena G, Casini I, Lucarini M, Sanchez del Pulgar J, Aguzzi A, et al. Chemical characterization and nutritional evaluation of microalgal biomass from large-scale production: a comparative study of five species European Food Research and Technology. 2020, 246 2 323-32
CrossRef
Google scholar
|
[58] |
Buono S, Langellotti AL, Martello A, Rinna F, Fogliano V. Functional ingredients from microalgae Food & Function. 2014, 5, 1669-85
CrossRef
Google scholar
|
[59] |
Yamamoto M, Baldermann S, Yoshikawa K, Fujita A, Mase N, et al. Determination of volatile compounds in four commercial samples of Japanese Green Algae using solid phase microextraction gas chromatography mass spectrometry The Scientific World Journal. 2014, 2014, 289780
CrossRef
Google scholar
|
[60] |
/
〈 | 〉 |