Next Article in Journal
Ideas Generation for New Aquaculture Products (Sea Bream and Prawns) Developing Using Focus Group by Different Participants Profiles
Previous Article in Journal
Comparative Cytotoxic Assessment of Hydro-Methanolic Extracts Derived from Ripe Morinda citrifolia L. Fruit (Fresh, Dried, Pasteurized Juice) and Dried Seeds on Eukaryotic Normal and Carcinogenic Cellular Models
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Proceeding Paper

Assessment of Nutritional Profile of Sargassum muticum Alga from the Spanish Coastline †

1
REQUIMTE/LAQV, Instituto Superior de Engenharia do Porto, Instituto Politécnico do Porto, Rua Dr. António Bernardino de Almeida 431, 4200-072 Porto, Portugal
2
Nutrition and Bromatology Group, Department of Analytical Chemistry and Food Science, Instituto de Agroecoloxía e Alimentación (IAA)—CITEXVI, Universidade de Vigo, 36310 Vigo, Spain
*
Authors to whom correspondence should be addressed.
Presented at the 4th International Electronic Conference on Foods, 15–30 October 2023; Available online: https://foods2023.sciforum.net/.
Biol. Life Sci. Forum 2023, 26(1), 94; https://doi.org/10.3390/Foods2023-15028
Published: 14 October 2023
(This article belongs to the Proceedings of The 4th International Electronic Conference on Foods)

Abstract

:
Macroalgae, or seaweed, has a long history of use in human diets, especially in Eastern nations. However, the present interest in these species is driven by their remarkable bioactive and nutritional qualities and their significant availability and underutilization, making them incredibly alluring to people following alternative dietary patterns like vegetarianism and veganism. Sargassum muticum, also known as Japanese wireweed or Asian seaweed, is considered edible and has been consumed in some cultures, popular as a soup ingredient in Korea. This brown macroalgae found in marine environments has been introduced in various regions outside its native range, including Europe and North America. Moreover, this species could be helpful in feeding animals or as soil fertilizer. In this study, the nutritional properties of this marine macroalga were investigated. Nutritional parameters such as protein, sugar, and fiber content were analyzed using classical techniques. In addition, its proximate composition was also determined in terms of moisture, fixed and volatile carbon, and ash content using thermogravimetry, and their major minerals, including calcium, potassium, and magnesium, was determined using the ICP-OS technique. In terms of its mineral content, it was found to have a high mineral content (21% of ash), which consisted mainly of calcium (9 g/kg dw), potassium (77 g/kg dw), and magnesium (12 g/kg dw). In addition, this study determined the presence of iodine using ICP-MS, and 106 mg/kg dw of this essential element was quantified in these algae. The results of this study highlighted the potential nutritional benefits of the tested marine algae. Their composition revealed significant concentrations of vital elements, making them highly advantageous for human/animal dietary requirements with possible health benefits.

1. Introduction

Sargassum muticum (Yendo) Fensholt is a brown alga belonging to the class Ochrophyta and the order Fucales. It originated in Japan and, as an aggressive invasive species, is now one of the most common macroalgae species on European coasts [1]. Various bioactive properties are attributed to this marine species, including antioxidant, cell protection, and antimicrobial capacity [2,3]. Nevertheless, S. muticum’s primary use in Europe is to fertilize soil and as animal feed [4], and the alga is considered simultaneously an environmental threat and an unexploited resource [2].
Yet, in some Asian cultures, S. muticum, also known as Japanese wire algae or Asian seaweed, is considered edible, and seaweeds have a long history in nutrition and cuisine. In Korea, it is popular as a soup ingredient [5]. Although it is very abundant, being present along the European shoreline and Mediterranean Sea [6,7], the use of this alga as food/feedstock is not very widespread. It is a species that compares well with others in terms of protein and fat content, and it is also rich in polysaccharides such as fucoidan and alginates [6].
The current interest in these species is driven by their remarkable bioactive and antioxidant properties [2] and their abundant availability and underutilization. This makes this species particularly appealing as a source of potential nourishment during periods of food insecurity caused by environmental changes. Also, there is an urgent need to promote food diversification so that more diversified forms of food with higher nutritional content can be integrated into dietary patterns. This becomes especially relevant when local alternative food sources can contribute to food security and reduce the ecological footprint of food consumption [8].
Furthermore, these environmental and nutritional properties are particularly appealing to individuals who follow alternative diets, such as vegetarians and vegans.
In this framework, the nutritional profile of S. muticum harvested on the coastline of Galicia (NW Spain) was analyzed for macronutrients including total fat, protein, sugars, and fibers. Its mineral content was also assessed to evaluate the potential nutritional value of this species, whether as food, food ingredient, or supplement.

2. Materials and Methods

2.1. Alga Material

S. muticum was collected (15 specimens) from the coast of Galicia in the winter of 2019. The algal material was sorted, identified by our expert biologists against the available literature [9,10], and thoroughly washed to remove sand and other impurities. Finally, the algae were freeze-dried, finely ground, mixed to form a representative sample, and stored at −80 °C until use.

2.2. Proximate Analysis

Proximate analyses were performed thermogravimetrically using a Netzsch STA 449 F3 (Netzsch Gruppe—Wittelsbacherstrasse, Selb, Germany). Residual moisture content was determined by the change in weight when samples (5–15 mg) were heated from 40 to 105 °C 10 °C/min under an inert atmosphere. The mass change between 105 and 600 °C (10 °C/min) was used to determine the volatile fraction under a nitrogen flow of 40 mL/min. Finally, the ash content was determined until constant weight after complete combustion of the sample at 900 °C in the presence of oxygen (airflow of 40 mL/min). The fixed carbon content was estimated by subtracting the combined percentages of moisture, volatiles, and ash from 100% [11,12].

2.3. Proteins and Carbohydrates

Nitrogen content was measured using the Kjeldahl method and multiplied by a factor of 5 to estimate the total protein content [13].
To determine the carbohydrate content, the phenol-sulfuric acid method was applied. For that, 1 g of macroalga was stirred in 20 mL of an ethanol/water solution (80:20) for 15 min at 80 °C. Subsequently, 100 µL of the sample was placed on a 96-well microplate. An equal volume of 20% phenol solution and 500 µL concentrated sulfuric acid were added. Absorbance was read at 490 nm and the results are expressed as mg of glucose equivalent/g dw [14].

2.4. Lipids

The lipidic content of the alga was determined using the Soxhlet method. The extraction was carried out with hexane for two hours, and the lipids were determined gravimetrically.

2.5. Fibers

The fiber content was determined following a method described in previous works [15]. Briefly, 0.5 g of sample was added to 25 mL of CTAB reagent and boiled for one hour. Afterward, the residue was filtered, washed with hot water and acetone, and dried to constant weight. The results are presented as g/100 g dw [15].

2.6. Macro- and Micro-Nutrients and Other Elements

Quantifications of the macro- (Na, Mg, Ca, K) and micro-nutrients (Cu, Fe, Zn) and toxic elements (Hg, Pb, As) were carried out using the methodology developed by Millos et al. [16], and already described thoroughly in a previous work [12] using a Perkin–Elmer Optima 4300 DV spectrometer (Shelton, CT, USA).
Mercury (Hg) was determined using cold vapor atomic absorption spectrometry (CVAAS) (Fims 400 Perkin Elmer Massachusetts, EUA). Iodine (I), arsenic (As), and lead (Pb) were quantified using ICP-MS (Thermo Elemental X7 Series). Isotope 115In was used as an internal standard for quantification of these elements. All determinations were performed at least in triplicate to achieve a coefficient of variation below 5%. The results are expressed as mg/kg dw. These studies were conducted in the Food Security and Sustainable Development Laboratory, Scientific and Technological Support Centre for Research (SSADS-CACTI, University of Vigo, Vigo, Spain). The quantification limits (LOQ) are present in Table 1.

3. Results and Discussion

The alga was tested to determine the proximate composition, nutrient profile, and elements present. The results are shown in Figure 1.
The proximate composition indicated that some residual water remained after lyophilization. Volatile compounds are the most critical group, accounting for 50.99 ± 1.31% of the algal material. However, the experiment revealed a high percentage of ashes, 20.97 ± 1.37, corresponding to significant mineral content. These results align with previous findings [6] and the reported seasonal variations in the ash content, ranging from 13.2% to 40.54%, for this alga species [17,18].
The nutritional profile is shown in Figure 1B. The determined protein content was 8.29 ± 0.67 and the lipid content was 0.94 ± 0.06%, in agreement with the values reported by Balboa et al. [17]. These values fall within the expected range for brown algae, which is 0.3–4.5% for protein and 1–24% for lipids [19], but are lower than those reported for the same species collected on the coast of Portugal [6]. The total carbohydrates, quantified as 27.32 ± 7.25 mg glucose eq/g dw, and fiber, quantified as 32.15 ± 6.3%, were also measured. The fiber’s values are higher than those described (around 20%) for other sargassum species [20]. Nevertheless, these values are within the expected range of this biomaterial [21].
Brown algae carbohydrates, like fucoidan, laminarans, and alginates, have been found to have several bioactive abilities [19]. For instance, alginates not only reduce cholesterol levels but also have antihypertensive effects. Unlike terrestrial plants, these beneficial dietary polysaccharides are uniquely present in marine algae. Furthermore, fibers from these algae play a vital role in cleansing the digestive tract and safeguarding the surface of the stomach and intestines [22].
The results also showed a considerable amount of macrominerals in the algal constitution. Ca and Mg were determined at 9.56 g/kg dw and 11.96 g/kg dw, respectively, deviating from the 2:1 ratio described as optimal for osteoporosis prevention [23]. Ca values are reported to be as high as 69.6 g/kg, and magnesium reaches 15.5 g/kg in this alga [17], highlighting the potential of this species as a source of these nutrients. Emerging research indicates magnesium’s role in many physiological processes, suggesting that adequate magnesium intake is crucial for cardiovascular health, muscle function, sleep, and mood, among other things [24,25]. Sodium was determined at a concentration of 26.5 g/kg dw, while potassium was determined at 77.8 g/kg dw; the Na content agrees with previous work (20.1 mg/g), while K values are slightly higher than the 38.8 mg/g reported [17]. The determined concentrations correspond to a Na: K molar ratio of <1, associated with a decrease in cardiovascular disease risk. The recommended daily dietary intake of these macrominerals is 375 mg for Mg, 800 mg for Ca, and 2000 mg each for K and Na [26].
The concentrations of other microelements were also assessed. Of these, copper, iron, and zinc were determined at 0.67, 57.6, and 10.9 mg/kg dw, respectively. The toxic metals Hg and Pb were not detected in the seaweed sample.
With iodine deficiency reemerging in Europe, it is crucial to ensure adequate intake either through diet or supplements. For S. muticum, a value of 101.6 mg/kg dw was identified, consistent with levels reported for other brown algae [12] but much higher than those reported in S. muticum [17]. This difference could be related to different extraction techniques.
The arsenic concentration was also high at 117 mg/kg dw, similar to the levels reported in other studies on Sargassum sp. [27]. While algae generally contain higher amounts of arsenic compared to other vegetables and grains, most of the arsenic detected is metabolized and is present in the non-toxic form known as arsenosugars [28].
In conclusion, a comprehensive nutritional evaluation of S. muticum revealed its potential as a dietary source. The alga boasts a low fat content and moderate protein levels while also notably being rich in carbohydrates and fiber. Its mineral composition is particularly striking because it not only meets but also aligns with the recommended dietary ratios of Na: K. The high iodine content offers potential nutritional benefits, especially given the resurgent iodine deficiency in some regions. While the considerable presence of arsenic, a metalloid commonly found in algae, is noteworthy, it is crucial to underscore the need for detailed speciation. Such analysis will determine the safety and appropriateness of integrating this marine resource into regular human consumption or animal feed.
Seaweeds, particularly the species studied, present numerous opportunities for commercial exploitation due to their rich bioactive compounds and sustainable growth characteristics. To this end, this seaweed shows potential in the food industry as a source of natural food additives or as primary ingredients in plant-based dishes, given their rich nutritional profile; in cosmetics and pharmaceuticals by leveraging their bioactive compounds for skincare products or nutraceutical supplements; and in the bioenergy industry by exploring their biomass as a potential renewable energy source.
Furthermore, future research could focus on the scalability of seaweed cultivation, post-harvest processing techniques, and in-depth exploration of the bioactive compounds’ potential therapeutic effects. However, for a detailed discussion on industrial applications, a comprehensive up-scaled laboratory and pilot testing would be a prerequisite to validate real-world feasibility and ensure the sustainable and efficient use of these seaweed resources.

Author Contributions

Conceptualization, M.A.P. and M.F.B.; methodology, C.S., A.S., F.C. and J.E.; validation, S.S.M. and P.D.; formal analysis, A.S. and P.G.O.; investigation, A.S. and C.S.; resources, M.F.B. and M.A.P.; data curation, C.S.; writing—original draft preparation, A.S.; writing—review and editing, M.C. and C.S.; project administration, M.A.P. and M.F.B.; funding acquisition, M.A.P., P.G.O., F.C., J.E., M.C. and M.F.B. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by an MICINN Ramón y Cajal grant for M.A.P. (RYC-2017-22891) and P.G.O., by Xunta de Galicia for the programs EXCELENCIA-ED431F 2020/12 (for F.C.) and EXCELENCIA-ED431F 2022/01 (for J.E.), and by the pre-doctoral grant of M.C. (ED481A 2021/313). The authors are grateful to the Bio-Based Industries Joint Undertaking (JU) under grant agreement no. 888003 UP4HEALTH Project (H2020-BBI-JTI-2019). The authors thank the Ibero-American Program on Science and Technology (CYTED—GENOPSYSEN, P222RT0117) and the support from the European Union’s Horizon 2020. The project SYSTEMIC Knowledge hub on Nutrition and Food Security has received funding from national research funding parties in Belgium (FWO), France (INRA), Germany (BLE), Italy (MIPAAF), Latvia (IZM), Norway (RCN), Portugal (FCT), and Spain (AEI) in a joint action of JPI HDHL, JPI-OCEANS, and FACCE-JPI launched in 2019 under the ERA-NET ERA-HDHL (n° 696295). Also, the authors would like to thank the EU and FCT for funding through the programs UIDB/50006/2020, UIDP/50006/2020, and LA/P/0008/2020. M.F.B. (2020.03107.CEECIND) thanks the FCT for the FCT Investigator grant.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Tanniou, A.; Vandanjon, L.; Incera, M.; Serrano Leon, E.; Husa, V.; Le Grand, J.; Nicolas, J.L.; Poupart, N.; Kervarec, N.; Engelen, A.; et al. Assessment of the Spatial Variability of Phenolic Contents and Associated Bioactivities in the Invasive Alga Sargassum muticum Sampled along Its European Range from Norway to Portugal. J. Appl. Phycol. 2014, 26, 1215–1230. [Google Scholar] [CrossRef]
  2. Pinteus, S.; Lemos, M.F.L.; Alves, C.; Neugebauer, A.; Silva, J.; Thomas, O.P.; Botana, L.M.; Gaspar, H.; Pedrosa, R. Marine Invasive Macroalgae: Turning a Real Threat into a Major Opportunity—The Biotechnological Potential of Sargassum muticum and Asparagopsis armata. Algal Res. 2018, 34, 217–234. [Google Scholar] [CrossRef]
  3. Silva, A.; Cassani, L.; Grosso, C.; Garcia-Oliveira, P.; Morais, S.L.; Echave, J.; Carpena, M.; Xiao, J.; Barroso, M.F.; Simal-Gandara, J.; et al. Recent Advances in Biological Properties of Brown Algae-Derived Compounds for Nutraceutical Applications. Crit. Rev. Food Sci. Nutr. 2022, 1–29. [Google Scholar] [CrossRef] [PubMed]
  4. Silva, L.D.; Bahcevandziev, K.; Pereira, L. Production of Bio-Fertilizer from Ascophyllum nodosum and Sargassum muticum (Phaeophyceae). J. Oceanol. Limnol. 2019, 37, 918–927. [Google Scholar] [CrossRef]
  5. Young Park, S.; Su Seo, I.; Joo Lee, S.; Pyung Lee, S. Study on the Health Benefits of Brown Algae (Sargassum muticum) in Volunteers. J. Food Nutr. Res. 2015, 3, 126–130. [Google Scholar] [CrossRef]
  6. Rodrigues, D.; Freitas, A.C.; Pereira, L.; Rocha-Santos, T.A.P.; Vasconcelos, M.W.; Roriz, M.; Rodríguez-Alcalá, L.M.; Gomes, A.M.P.; Duarte, A.C. Chemical Composition of Red, Brown and Green Macroalgae from Buarcos Bay in Central West Coast of Portugal. Food Chem. 2015, 183, 197–207. [Google Scholar] [CrossRef]
  7. Pacheco, D.; Araújo, G.S.; Cotas, J.; Gaspar, R.; Neto, J.M.; Pereira, L. Invasive Seaweeds in the Iberian Peninsula: A Contribution for Food Supply. Mar. Drugs 2020, 18, 560. [Google Scholar] [CrossRef]
  8. Amanto, B.S.; Umanailo, M.C.B.; Wulandari, R.S.; Taufik, T.; Susiati, S. Local Consumption Diversification. Int. J. Sci. Technol. Res. 2019, 8, 1865–1869. [Google Scholar]
  9. Lourenço-Lopes, C.; Silva, A.; Garcia-Oliveira, P.; Soria-Lopez, A.; Echave, J.; Grosso, C.; Cassani, L.; Barroso, M.F.; Simal-Gandara, J.; Fraga-Corral, M.; et al. Kinetic Extraction of Fucoxanthin from Undaria pinnatifida Using Ethanol as a Solvent. Mar. Drugs 2023, 21, 414. [Google Scholar] [CrossRef]
  10. Guiry, M.D.; Guiry, G.M. AlgaeBase. World-Wide Electronic Publication; National University of Ireland: Galway, Ireland, 2023. [Google Scholar]
  11. García, R.; Pizarro, C.; Lavín, A.G.; Bueno, J.L. Biomass Proximate Analysis Using Thermogravimetry. Bioresour. Technol. 2013, 139, 1–4. [Google Scholar] [CrossRef]
  12. Cassani, L.; Lourenço-Lopes, C.; Barral-Martinez, M.; Chamorro, F.; Garcia-Perez, P.; Simal-Gandara, J.; Prieto, M.A. Thermochemical Characterization of Eight Seaweed Species and Evaluation of Their Potential Use as an Alternative for Biofuel Production and Source of Bioactive Compounds. Int. J. Mol. Sci. 2022, 23, 2355. [Google Scholar] [CrossRef] [PubMed]
  13. Angell, A.R.; Mata, L.; de Nys, R.; Paul, N.A. The Protein Content of Seaweeds: A Universal Nitrogen-to-Protein Conversion Factor of Five. J. Appl. Phycol. 2016, 28, 511–524. [Google Scholar] [CrossRef]
  14. Soares, C.; Tenreiro Machado, J.A.; Lopes, A.M.; Vieira, E.; Delerue-Matos, C. Electrochemical Impedance Spectroscopy Characterization of Beverages. Food Chem. 2020, 302, 125345. [Google Scholar] [CrossRef] [PubMed]
  15. Rowland, A.P.; Roberts, J.D. Lignin and Cellulose Fractionation in Decomposition Studies Using Acid-Detergent Fibre Methods. Commun. Soil Sci. Plant Anal. 1994, 25, 269–277. [Google Scholar] [CrossRef]
  16. Millos, J.; Costas Rodriguez, M.; Lavilla, I.; Bendicho, C. Multiple Small Volume Microwave-Assisted Digestions Using Conventional Equipment for Multielemental Analysis of Human Breast Biopsies by Inductively Coupled Plasma Optical Emission Spectrometry. Talanta 2009, 77, 1490–1496. [Google Scholar] [CrossRef] [PubMed]
  17. Balboa, E.M.; Gallego-Fábrega, C.; Moure, A.; Domínguez, H. Study of the Seasonal Variation on Proximate Composition of Oven-Dried Sargassum muticum Biomass Collected in Vigo Ria, Spain. J. Appl. Phycol. 2016, 28, 1943–1953. [Google Scholar] [CrossRef]
  18. VANDANJON, L.; Maureen, D.; Maya, P.; Philippe, D.; Valarie, S.-P.; Gilles, B.; Nathalie, B. Seasonal Variation of Sargassum muticum Biochemical Composition Determined by Fourier Transform Infra-Red Spectroscopy. J. Anal. Bioanal. Sep. Tech. 2017, 2, 75–84. [Google Scholar] [CrossRef]
  19. Quitério, E.; Soares, C.; Ferraz, R.; Delerue-Matos, C.; Grosso, C. Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications. Foods 2021, 10, 3100. [Google Scholar] [CrossRef]
  20. Dewinta, A.F.; Susetya, I.E.; Suriani, M. Nutritional Profile of Sargassum sp. from Pane Island, Tapanuli Tengah as a Component of Functional Food. J. Phys. Conf. Ser. 2020, 1542, 012040. [Google Scholar] [CrossRef]
  21. Jiménez-Escrig, A.; Sánchez-Muniz, F.J. Dietary Fibre from Edible Seaweeds: Chemical Structure, Physicochemical Properties and Effects on Cholesterol Metabolism. Nutr. Res. 2000, 20, 585–598. [Google Scholar] [CrossRef]
  22. Holdt, S.L.; Kraan, S. Bioactive Compounds in Seaweed: Functional Food Applications and Legislation. J. Appl. Phycol. 2011, 23, 543–597. [Google Scholar] [CrossRef]
  23. DeLuccia, R.; Cheung, M.; Ng, T.; Ramadoss, R.; Altasan, A.; Sukumar, D. Calcium to Magnesium Ratio Higher Than Optimal Across Age Groups (P10-100-19). Curr. Dev. Nutr. 2019, 3, nzz034.P10-100-19. [Google Scholar] [CrossRef]
  24. Al Alawi, A.M.; Majoni, S.W.; Falhammar, H. Magnesium and Human Health: Perspectives and Research Directions. Int. J. Endocrinol. 2018, 2018, 9041694. [Google Scholar] [CrossRef] [PubMed]
  25. Morrissey, E.; Giltinan, M.; Kehoe, L.; Nugent, A.P.; McNulty, B.A.; Flynn, A.; Walton, J. Sodium and Potassium Intakes and Their Ratio in Adults (18–90 y): Findings from the Irish National Adult Nutrition Survey. Nutrients 2020, 12, 938. [Google Scholar] [CrossRef]
  26. World Health Organization. Guideline: Sodium Intake for Adults and Children; World Health Organization: Geneva, Switzerland, 2012. [Google Scholar]
  27. Cipolloni, O.-A.; Gigault, J.; Dassié, É.P.; Baudrimont, M.; Gourves, P.-Y.; Amaral-Zettler, L.; Pascal, P.-Y. Metals and Metalloids Concentrations in Three Genotypes of Pelagic Sargassum from the Atlantic Ocean Basin-Scale. Mar. Pollut. Bull. 2022, 178, 113564. [Google Scholar] [CrossRef]
  28. Park, G.; Kang, D.; Davaatseren, M.; Shin, C.; Kang, G.-J.; Chung, M.-S. Reduction of Total, Organic, and Inorganic Arsenic Content in Hizikia fusiforme (Hijiki). Food Sci. Biotechnol. 2019, 28, 615–622. [Google Scholar] [CrossRef]
Figure 1. Characterization of S. muticum algae: (A) proximate composition; (B) nutritional profile; (C) mineral composition. Bars represent the standard deviation, n = 3, and * carbohydrates are given in mg glucose equivalents/g dw.
Figure 1. Characterization of S. muticum algae: (A) proximate composition; (B) nutritional profile; (C) mineral composition. Bars represent the standard deviation, n = 3, and * carbohydrates are given in mg glucose equivalents/g dw.
Blsf 26 00094 g001
Table 1. Detection limits of the elements analyzed.
Table 1. Detection limits of the elements analyzed.
CaCuFeKMgNaZnHgAsIPb
Analytical techniqueICP-OESICP-OESICP-OESICP-OESICP-OESICP-OESICP-OESCVAASICP-MSICP-MSICP-MS
LOQ mg/kg10.000.601.0020.0010.0020.000.200.0402.505.001.25
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Silva, A.; Soares, C.; Carpena, M.; Oliveira, P.G.; Echave, J.; Chamorro, F.; Donn, P.; Mansour, S.S.; Barroso, M.F.; Prieto, M.A. Assessment of Nutritional Profile of Sargassum muticum Alga from the Spanish Coastline. Biol. Life Sci. Forum 2023, 26, 94. https://doi.org/10.3390/Foods2023-15028

AMA Style

Silva A, Soares C, Carpena M, Oliveira PG, Echave J, Chamorro F, Donn P, Mansour SS, Barroso MF, Prieto MA. Assessment of Nutritional Profile of Sargassum muticum Alga from the Spanish Coastline. Biology and Life Sciences Forum. 2023; 26(1):94. https://doi.org/10.3390/Foods2023-15028

Chicago/Turabian Style

Silva, Aurora, Cristina Soares, Maria Carpena, Paula Garcia Oliveira, Javier Echave, Franklin Chamorro, Pauline Donn, Sepidar S. Mansour, Maria Fátima Barroso, and Miguel A. Prieto. 2023. "Assessment of Nutritional Profile of Sargassum muticum Alga from the Spanish Coastline" Biology and Life Sciences Forum 26, no. 1: 94. https://doi.org/10.3390/Foods2023-15028

Article Metrics

Back to TopTop