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Global seaweed farming and processing in the past 20 years
Food Production, Processing and Nutrition volume 4, Article number: 23 (2022)
Abstract
Seaweed has emerged as one of the most promising resources due to its remarkable adaptability, short development period, and resource sustainability. It is an effective breakthrough to alleviate future resource crises. Algal resources have reached a high stage of growth in the past years due to the increased output and demand for seaweed worldwide. Several aspects global seaweed farming production and processing over the last 20 years are reviewed, such as the latest situation and approaches of seaweed farming. Research progress and production trend of various seaweed application are discussed. Besides, the challenges faced by seaweed farming and processing are also analyzed, and the related countermeasures are proposed, which can provide advice for seaweed farming and processing. The primary products, extraction and application, or waste utilization of seaweed would bring greater benefits with the continuous development and improvement of applications in various fields.
Graphical Abstract
Introduction
In the past 20 years, the seaweed farming and production process have increased significantly, and play the important role in the fishing industry by country (Cai et al. 2021). According to the Food and Agriculture Organization (FAO) data, the global seaweed output (both aquaculture and wild) has increased nearly three-fold from 118,000 tons to 358,200 tons from 2000 to 2019 (FAO 2021) (Fig. 1). In 2019, 97% of the global aquaculture output came from artificial farming. The world’s seaweed production mostly comes from the five major continents with Asia accounting for 97.38%. In Asia, 99% of seaweed is cultured artificially. In particular, China ranks first in the world in terms of aquaculture production, accounting for 56.82% of the global aquaculture. The main algae are Japanese kelp (Laminaria japonica), Gracilaria seaweeds (Gracilaria spp.) and nori Nei (Porphyra spp.). The second is Indonesia, another major seaweed farming country, which accounts for 28.6% of the global breeding. Eucheuma seaweeds nei (Eucheuma spp.) and Gracilaria seaweeds (Gracilaria spp.) are the main species. South Korea has a developed seaweed culture industry and many seaweed species, accounting for 5.09% of the world, including brown, red, and green seaweeds (excluding microalgae). Among them, Japanese kelp (Laminaria japonica) is the most cultured, followed by laver (Porphyra tenera) and wakame (Undaria pinnatifida). The aquaculture in the Philippines accounts for 4.19% of the global market, mainly planting Elkhorn Sea moss (Kappaphycus alvarezii), accounting for more than 90% of the country. North Korea accounts for 1.6% of the global aquaculture and mainly grows Japanese kelp (Laminaria japonica). Japan accounts for 1.15% of the global seaweed production, mainly planting laver (nori, Porphyra tenera), wakame (Undaria pinnatifida), and Japanese kelp (Laminaria japonica). Malaysia accounts for 0.53% of the global aquaculture, mainly planting Elkhorn Sea moss (Kappaphycus alvarezii). North America accounts for 1.36% of the world's seaweed, and 95% of the seaweed in North America is obtained from natural resources. In terms of seaweed cultivation, Chile is the main producer, accounting for 0.3% of the global production, and it mainly grows Gracilaria seaweeds and Spirulina maxima, but 99% of them comes from natural riverbeds. Mexico accounts for 0.02% of the global output of raw seaweed. Brown seaweeds has been planted in recent years, but currently, 99% of brown seaweeds (Phaeophyceae) and red seaweeds Nei (Rhodophyceae) come from natural riverbeds. Algae are largely obtained from natural resources in the United States, Peru, and Canada. Europe accounts for 0.8% of global seaweed production. In Europe, 96% of the seaweed is obtained from natural resources. Only since 2010, artificial cultivation has been experimenting in Europe. Africa accounts for 0.41% of the world's seaweed. By 2019, the percentage of 81% of seaweed came from seaweed farming. Zanzibar accounts for 0.5% of the global aquaculture, mainly spiny Eucheuma (Eucheuma denticulatum). Oceania accounts for 0.05% of the world. 99% come from cultured seaweed. It mainly produces miscellaneous brown seaweeds (Fig. 2).
In general, the following five kinds of seaweeds accounted for more than 95% of world’s seaweed culture production in 2019. Laminaria and Saccharina account for 34.65% of the global cultivation for human consumption, mainly as salads, condiments, and sauces. Carageen from tropical algae Kappaphycus and Eucheuma accounted for 32.62% and was mostly used for carrageenan extraction. Gracilaria, Porphyra, and Undaria accounted for 10.32%, 8.33%, and 7.16%, respectively. In Asia and South Africa countries, seaweeds (such as brown algae, leafy algae, and kelp) are often used as fish feed like Laminaria and Sargassum in China, Kappaphycus are used as seaweed fertilizer in India, and made into livestock feed in most European countries (Fig. 3).
Excepted for commercially important brown algae species, research on green algae have so far focused on Ulva lactuca, Enteromorpha prolifera, Monostroma nitidum, Chlorella pyrenoidosa, and Ulva conglobata, with the bioeffects of regulating intestinal flora and improving immune function (Lee et al. 2013; Zheng et al. 2020a, 2020b). In contrast, the development of edible green algae resources is not enough. More nutrients in seaweed are discovered now, and the potential demand for algal compounds and other chemicals generated by biotechnology is growing In the future, it is expected that research and utilization of edible green algae will attract increasing attention.
Seaweed contains a wide range of bioactive compounds as well as nutritional benefits. Furthermore, algae can produce far more biomass than terrestrial plants and may be cultured successfully in fresh or seawater without the use of antibiotics or pesticides, which lead to an increase in consumer demand and economic interest over the last two decades. In this review, the development of global seaweed cultivation production and processing in the past 20 years was reviewed, and the latest situation and technology of seaweed farming were introduced (Fig. 4). The present situation of seaweed processing and extraction technologies were also reviewed. Moreover, the new applications of seaweed products in food, agriculture, medicine, and cosmetics were introduced. Finally, the challenges of seaweed farming and processing were discussed.
Global seaweed farming and processing
Current research progress of active substances
Diseases such as cancer, diabetes, inflammation, and chronic cardiovascular diseases are major global health problems (Pradhan et al. 2020a). Currently, the chemotherapy and synthetic drugs are widely used in the medical field. However, some drugs are often associated with side effects such as toxicity, drug tolerance, and metabolic disorders (Pradhan et al. 2020b). Therefore, the natural bioactive ingredients have become interesting substitutes to prevent diseases. Seaweed is one of the most abundant and promising sources of biologically active metabolites. These bioactive components of seaweed include polysaccharides, unsaturated fatty acids, phenols, peptides, terpenoids, and other compounds with unique structures and properties, which have the antioxidant, antiviral, anticoagulant, antibacterial and antitumor effects. Many active substances are found in the brown, red, and green seaweeds, which have the great potential in agricultural, edible, and medical fields.
Brown seaweeds
Brown seaweeds are multicellular algae with a high degree of evolution that are found in cold water of continental coastal waters and are uncommon in fresh water. The main species of brown seaweeds include Laminaria digitata, Sargassum, Ascophyllum, Undaria and Laminaria (Li et al. 2021a, 2021b). Take Sargassum for example, because it contains polysaccharides, proteins, polyphenols, lipids, sterols, carotenoids, and other active compounds, showing a variety of pharmacological properties, so it is called the twenty-first century medicinal food (Yende & Chaugule 2014). Some bioactive compounds of brown seaweed and their important bioactivities are summarized in Table 1.
Polysaccharides are the main components of brown algae. The concentration of total polysaccharides in common seaweed species ranges from 4–70% of dry weight, and the main bioactive polysaccharides include alginate, fucoidan, mannitol and laminarin (Mohd et al. 2021; Holdt & Kraan 2011; Shen et al. 2017). Alginates, the only polysaccharide with carboxyl groups in monomers, provide several health advantages, including anti-inflammatory, antioxidant, anti-obesity, antiallergic and immunomodulatory (Feng et al. 2020; Horibe et al. 2016; Wang et al. 2018, 2021; Yu et al. 2020). Fucoidan is a sulfated polysaccharide found in large quantities in the cell wall. It has the potential to be employed as an antioxidant, anticancer, anti-angiogenic, antiphotoaging and antitumor drug, according to several in vitro investigations (Cong et al. 2016; Jing et al. 2021; Palanisamy et al. 2018; Park et al. 2011; Shannon et al. 2021; Shen et al. 2017). Mannitol is a monosaccharide found in the cytoplasm of brown seaweeds. It has a high permeability and shows promise as a free radical scavenger, lowers stroke-related edema and tissue damage, and is frequently employed in the production of chewing gum, diabetic foods, and various tablets (Bereczki et al. 2007; Cavone et al. 2012; Dai et al. 2017; Ruiz et al. 2017; Holdt et al. 2011; Karthikeyan et al. 2010). Laminarin is a storage β-glucan containing up to 35% laminarin (on a dry weight basis) and is increasingly recognized for its biofunctional activities (Kadam et al. 2015). Laminarin has been reported to have biological functional activities, including anticancer, antioxidant, anti-bacterial and immune stimulation (Bae et al. 2020; Hu et al. 2012; Ji et al. 2020; Lee et al. 2012; Liu et al. 2017).
Brown seaweeds usually have a small protein content ranges from 5 to 15% of its dry weight. It has been reported that peptides isolated from Undaria pinnatifida have hypotensive effects on blood pressure in spontaneously hypertensive rats (Sato et al. 2002; Suetsuna et al. 2004). Furthermore, lectins, a functional active protein isolated from the brown seaweed Hizikia fusiformis, have been demonstrated to have high antioxidant capacity and robust free radical scavenging activity (Wu et al. 2016a, 2016b).
Various bioactive substances, including omega-3 PUFAs, omega-6 arachidonic acid (ARA), and fucoxanthin, can be found in brown seaweed lipids (Miyashita & Hosokawa 2013). The active forms of omega-3 PUFA include eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which lower the risk of cardiovascular disease (Lavie et al. 2009; Ruxton et al. 2007; Yanai et al. 2018). Additionally, ARA is crucial for the functioning of the immune system, thrombosis, and the brain (Miyashita & Hosokawa 2013).
Fucoxanthin is the most abundant pigment of all carotenoids in brown seaweed and has been shown to have anti-inflammatory, anti-obesity, antioxidant, and anti-diabetic properties (Jung et al. 2016, 2014a, 2014b; Lee et al. 2003; Yoo et al. 2012). Furthermore, sterols have been found in brown seaweed and have been associated with antidepressant and lipid-lowering properties (Ruqqia et al. 2020; Zhao et al. 2016). In particular, fucosterol, which is the characteristic sterol of all brown seaweed phylum, has antioxidant, anti-diabetic anti-inflammatory and other biological activities (Abdul et al. 2016; Jung et al. 2016, 2014a, 2014b; Lee et al. 2003; Sun et al. 2015; Yoo et al. 2012).
Most brown seaweeds contain fucoxanthin pigments and brown tannins, which give their distinctive greenish-brown hue. Among these, phenolotannins are the most abundant phenolic chemicals in brown seaweed, accounting for 25% of dry weight (Qin 2018). Phlorotannins are found only in brown seaweed and have the 2–tenfold antioxidant activity of ascorbic acid and tocopherol (Bogolitsyn et al. 2019). In addition to the anti-oxidative properties of phlorotannins from brown seaweed, phlorotannins also can prevent obesity by inhibiting the adipocyte differentiation of stem cells (Suzuki et al. 2016). In particular, tannins can improve memory by modulating the ERK-CREB-BDNF pathway (Um et al. 2018).
At present, many active ingredients in brown seaweed have been proved to have functional activities such as antioxidant, anti-inflammatory, anti-tumor, and anti-diabetic. For example, mannitol has been used medicinally as a good diuretic and hyperosmolar antihypertensive agent, but verification of these functional activities with mannitol extracted from brown seaweed is rare. In addition, studies on functional components in brown seaweed mainly focus on macromolecules, such as polysaccharides, sulfated polysaccharides. There are few reports on the mechanism of action of alginate and fucoidan contained in polysaccharides in brown seaweed.
Red seaweeds
The majority of red seaweeds grows in the deep sea, which is the largest group of marine macroalgae. The bioactive compounds of red seaweed and their important bioactivities are summarized in Table 2.
Red seaweed contains comprises polysaccharides (carrageenan or agar), proteins, amino acids, sterols, carotenoids, bromophenols, and other natural bioactive compounds. Polysaccharide is the most developed molecule in the cell wall of seaweed, accounting for 40–50 percent of its dry matter. It is worth noting that carrageenan and agar are the most relevant and developed compounds in red seaweed (Carpena et al. 2022). Carrageenan, the primary algal group of red seaweed, has been extensively studied for its wide range of biological activities, including its antitumor, antiproliferation, antiviral and anticoagulant activities (Guo et al. 2019; Cotas et al. 2020a, 2020b, 2020c; Jazzara et al. 2016; Gomaa & Elshoubaky et al. 2016; Carlucci et al. 1997). Agar is a mixture of polysaccharides with similar functional properties to carrageenan, exhibiting antiviral, anti-diabetic, anti-colon cancer and anti-inflammatory properties (Ślusarczyk & Czerwik-Marcinkowska 2021; Geetha & Tuvikene 2021; Hardoko et al. 2015; Yun et al. 2021; Lee et al. 2018).
The amount of protein in red seaweed varies depending on the species and other conditions such as season, temperature, and light (Cotas et al. 2020b). Protein content ranges from 35 to 47%, which is comparable to or higher than that of legumes and soybeans (Murata & Nakazoe 2001). Most total proteins found in red seaweeds are phycobiliproteins, which also give these species their characteristic red color and are widely used as natural colorants in food and cosmetics (Francavilla et al. 2013). This compound has medicinal potential due to its antioxidant and anti-inflammatory activities (Kim et al. 2018; Lee et al. 2012, 2017). Recently, bioactive peptides with therapeutic and anti-inflammatory effects have attracted particular attention (Lee et al. 2015). In addition, it has shown great therapeutic potential in the lectin of red seaweed, which has anti-inflammatory, hypoglycemic and antioxidant effects (Alves et al. 2020; Mesquita et al. 2021). Furthermore, red seaweed contains numerous glycine, arginine, alanine, and glutamic acids, including mycosporine-like amino acids, which have been demonstrated to provide UV protection and antioxidant characteristics (De et al. 2009; Karsten et al. 1998; Sun et al. 2020).
Palmitic acid, EPA, arachidonic acid, oleic acid, linoleic acid (LA), and alpha-linolenic acid (ALA) are the main fatty acids in the red and brown seaweeds. Red seaweed in Japan and South Korea mainly contains docenoic acid, and Undaria pinnatifida and kelp mainly contain arachidonic acid (Dawczynski et al. 2007; Tamama 2021). Despite the low lipid content of their constituents, they include vital fatty acids for human health (Amador-Castro et al. 2021). Most sterols present in red seaweed are cholesterol and its derivatives, such as 24-propylidene cholest-5-en-3β-ol, a compound that could be used as a potential lead molecule in the development of anti-broad-spectrum drugs (Kavita et al. 2014).
Red seaweeds are mostly represented by phenolic acids and flavonoids among phenolic compounds. Additionally, In addition, phenolic compounds (phlorotannins and bromphenol) unique to Marine sources, although in small quantities, have strong antioxidant activity (Cotas et al. 2020a; Dong et al. 2021; Olsen et al. 2013). It possesses anti-AIDS and anti-inflammatory properties in addition to its antioxidant action (Choi et al. 2018; Paudel et al. 2019). Carotenoids are thought to be one of the major terpenoids found in red seaweed and also contribute to their special pigmentation, mainly represented by α-carotenes and β-carotenes, lutein and zeaxanthin. This carotenoid has antioxidant, anti-inflammatory and anticancer properties, which may reduce the risk of eye disease in humans (Ávila-Román et al. 2021; Cotas et al. 2020b; Holdt & Kraan 2011; Kavalappa et al. 2019; Zubia et al. 2014). Red seaweeds of the Gracilaria genus have been identified as excellent sources of these Marine alkaloids, and their anti-inflammatory and antimicrobial mechanisms of action have been extensively characterized (Kasanah et al. 2019; Souza et al. 2020).
At present, polysaccharide is still the most studied functional component, but the research on red seaweed polysaccharide mainly focuses on monosaccharide composition, molecular weight, etc., but there are still few reports on its advanced structure. In addition, although there are many research on the active ingredients of red seaweed, there is a lack of in-depth pharmacological research and clinical trial research. In conclusion, to realize the further development and application of red seaweed active ingredients, these problems and challenges must be solved first. It is believed that soon, the application of red seaweed functional activity in the medical field will no longer be a limitation.
Green seaweeds
There are over 6700 species of green seaweed in the world, the majority of which live in fresh water. Despite their microscopic size, they are bursting with life and contain nearly all of the nutrients required for human survival. It is regarded as the most ideal diet of the twenty-first century by the United Nations FAO due to its high protein, low fat, low sugar, and low cholesterol content. The bioactive compounds of green seaweed and their important bioactivities are summarized in Table 3.
Enteromorpha, Ulva, and Chlorella are the most prevalent green seaweed. Ulva and Enteromorpha are rich sources of polysaccharides from green seaweed, especially Ulva (total polysaccharide content up to 65% of dry weight). Green seaweed polysaccharide is a kind of acidic polysaccharide (such as sulfated polysaccharides, sulfated galactans and xylans) located on the cell wall of green seaweed. It has special molecular structure and can play a variety of biological functions by regulating cell signal transduction function, such as anti-hyperuricemia, anti-oxidation, anti-coagulation, anti-virus, and blood glucose regulation (Cao et al. 2022; Chen et al. 2022; Li et al. 2017, 2021a, 2021b; Lin et al. 2020; Wang et al. 2020a, 2020b, 2013a, 2013b; Wassie et al. 2021; Wu et al. 2020). Chlorella is a type of single-celled green seaweed. It grows quickly and is the only plant that may double in size in 20 h. Proteinucleococcus has high protein content and can be used as high nutritional value food. It contains bioactive glycoproteins, polysaccharides and up to 13% nucleic acid and has antioxidant, immunomodulatory, anti-aging, and anti-tumor properties (Chen et al. 2018a, 2018b; Tanaka et al. 1998; Wan et al. 2021; Yang et al. 2006). Lectins are one of the protein types binding to carbohydrates or substances in a reversible manner. It has been reported that green seaweed lectins can show potent anti-influenza virus activity with the help of high affinity binding to viral hemagglutinin (Mu et al. 2017).
Because green seaweed contains just 5% fat and very little cholesterol (mostly in the form of sitosterol), there is no risk of elevated cholesterol from animal protein. The fats in green seaweed are mainly unsaturated fatty acids, of which EPA and DHA are important unsaturated fatty acids in marine lipids, which are mainly produced by Eustigmatophyte species. They have potential therapeutic effects in cardiovascular disease, Alzheimer's disease, hypertension, coronary artery disease, arthritis, and cancer (Leone et al. 2019; Peltomaa & Taipale 2017; Van et al. 2011).
The antioxidant qualities of β-carotene produced by the microalgal Dunaliella salina help to regulate the detrimental effects of free radicals, which have been related to a variety of life-threatening disorders, including cancer, coronary heart disease, premature aging, and arthritis. It may also aid the body in combating the effects of ultraviolet light-induced accelerated aging (Dembitsky & Maoka 2007; Miyashita 2009). Haematococcus pluvialis is known to produce astaxanthin, a blood-red carotenoid whose antioxidant properties give astaxanthin an interesting therapeutic potential as an anti-cancer, anti-diabetic, and anti-inflammatory agent (Ambati et al. 2014; El-Baz et al. 2018). Compared with brown seaweed, green seaweed contains relatively few polyphenols. Preliminary studies have shown that Enteromorpha prolifera can demonstrate anti-inflammatory and hypoglycemic effects by regulating signaling pathways (Huang et al. 2022; Yan et al. 2019).
Although there has been some advancement in recent years in the study of structure and activity, particularly in the study of the polysaccharide activity of green seaweeds, other green seaweeds active components have not yet been fully developed and utilized, and the specific biological active components have not been fully explored. Research on the mechanism of action is also necessary.
Although the application of seaweed active substances has developed rapidly in recent years, the following problems still need to be solved: most studies on anti-tumor peptides from seaweed currently ignore peptide preservation, which is very unfavorable for peptides with unstable chemical properties. It is useful to improve the stability of anti-tumor active peptides from seaweed by developing existing active peptide preservation and delivery technologies, such as encapsulation of chitosan nanoparticles and administration of multi-encapsulated liposomes. Furthermore, the active substance of seaweed extract must be produced in a more efficient manner. The method of trehalose synthase catalytic synthesis is simple and low-cost. However, it has some advantages of high energy consumption material, but the enzyme also has some disadvantages, such as resistance to high temperature and pH. To tackle this challenge, trehalose synthase's structure and function need to be learned more. In addition, seaweed extracts are limited to purify the active substance. If the purification enhanced, it will be helpful to further study its function and excitation, which is also the future research direction of seaweed extract. It is worth emphasizing that most of the bioactive studies currently being conducted are non-human including in vitro and in vivo animal models. However, due to the different enzyme catalytic centers and the complexity of organisms, the applicability and safety of algal bioactive substances as drugs for further research remain to be solved. Therefore, the stability, spatial structure, and physiological function of these bioactive substances still need to be further studied.
Seaweed farming technologies
Early algae were mainly from natural growth, and people mainly collected wild algae (Tseng et al. 2001). With the growing market for food industrial and medical use of seaweed products, the wild seaweed resources are limited, which has promoted the seaweed farming. Seaweed culture can be cultivated on land, sea, desert and even in integrated aquaculture system. Even the seaweed farming technology is not different in essence, there are obvious differences in culture methods due to the different environment.
Land farming
The cultivation of algae on land is mainly in closed systems such as water tanks, ponds, lagoons, and pipelines (Sara et al. 2020). The culture method is suitable for a wide range of seaweed genera. It has simple and easily accessible equipment that allows real-time monitoring and effective regulation of seaweed culture conditions (nutrients, light, pH value, CO2 and salinity) to produce more target products. However, land-based aquaculture occupies scarce cultivated land and water resources, which requires high maintenance cost and cannot achieve mass production. In recent decades, there has also been a way to use saline alkali groundwater for algal culture (Sara et al. 2020), using the existing salt water resources at low cost and high economic efficiency. A circular culture system was developed to reduce the cost by reducing the required medium (Sebök et al. 2017).
Mariculture
Inshore shallow water aquaculture is carried out in the sea area close to the land and is the main method of algae culture, at sea depth of 5–50 m, using fixed piles off the bottom. It has sufficient land nutrients and benefits from moderate seawater velocity and wind wave degree. To meet the growing demand for seaweed products, the field of seaweed culture has extended outward, and there is a way of offshore deep-water culture that relies on floating rafts or long ropes to make culture rafts (Fig. 5). Mariculture does not occupy scarce land resources. Compared with shallow sea culture, offshore deep-water culture is greatly affected by uncertainties such as wind and waves, and alien species, and is difficult to manage and costly to maintain. It has high requirements for breeding equipment, seaweed varieties and technology, which has not been popularized. Semi floating rafts and supporting rafts are mostly used in intertidal aquaculture, with high requirements for the selection of sea areas. Due to the increasing breeding density, pest and disease problems occur frequently, inshore aquaculture appeared, which does not occupy scarce land resources and is free from the impact of marine turbulence. Desert farming technology through water and nutrient recycling effectively exploits the rich desert resources and alleviates the shortage of land resources (Buschmann et al. 2017).
Integrated aquaculture system
In the integrated aquaculture recycling system, the algae can absorb nitrogen and phosphorus from the waste produced by aquatic products and serve as feed when algae and aquatic products are mixed. The cultivation of seaweed in this cycle system can reduce marine eutrophication and repair the damaged marine ecological environment system better (Sun et al. 2016). Sashimi seaweed quantitative ecological breeding model was developed. The advantages of high yield and benefit by using kelp culture raft for large-scale economic algae and sea cucumber multi variety rotation culture was proved. Algae-bacteria symbiotic system is used for algae culture to treat organic wastewater and human and livestock waste. The integrated high-rate algal ponds (HRAP) system is applied for wastewater treatment and algae production. However, the system has too many links and is inefficient. It is only suitable for large-scale aquaculture in ponds and lakes, but not for industrial aquaculture. Moreover, the seaweed seedling raising technology in China is weak and the supply of seedlings is insufficient to meet the demand for year-round supply of seedlings for this system.
Seaweed processing and applications
Current status of development
The Financial Times has reported that the global population will rise to 10 billion by 2050. And algae could supply the protein needed for people while conserving natural resources (Koyande et al. 2021). Because algae grow 10 times faster than terrestrial plants, less than one-tenth of the land is needed to produce the same amount of biomass. The growth of algae does not compete with other crops for land and does not require fresh water. It fertilizes more efficiently than land crops, and avoids the intensive water use, fertilizer wasting, and downstream eutrophication associated with modern agriculture (Tzachor 2019). Therefore, seaweed has aroused great interest as for these advantages around the world, especially in Asia, Europe, and South America, as well as in North America and Australia. Particular attention has been paid to seaweed resource processing and utilization (García-Poza et al. 2020). Forbes reported that the market for algal products was expected to be approximately $4 billion in 2018, growing to $5.2 billion by 2023 (Kite-Powell 2018). In the past twenty years, algae contain high levels of minerals, dietary fiber, and low fat levels, which has regarded as an attractive raw material in food, medicine, chemical industries, and even as the natural source of CO2 and biomass energy.
Current extraction techniques
In recent decades, research on extracting bioactive ingredients from natural resources have attracted special attention. Studies have shown that many ingredients have a variety of biological characteristics and potential industrial application prospects. Therefore, it is necessary to find new technologies for improving the production of algae extracts, instead of choosing extraction conditions which are time consuming, low selectivity, low efficiency and harmful for human health. In this paper, the extraction methods of algae oil and the extraction techniques of volatile substances from algae in recent years are summarized, and the new extraction techniques such as microwave-assisted extraction (MAE), ultrasound-assisted extraction (UAE), supercritical fluid extraction (SFE), pressurized solvent extraction (PSE), and enzyme-assisted extraction (EAE) are introduced. Additionally, the traditional extraction technology is compared with the new extraction technology in order to better develop and utilize algae resources (Table 4).
MAE is a relatively new extraction technique that combines microwave and traditional solvent extraction. The use of microwave radiation, which generates heat directly in the matrix through the friction and collision between molecules, has been used to extract seaweed hydrocolloids and other derivatives from red and brown seaweeds to obtain high quality seaweed hydrocolloids with less extraction time and solvent consumption. Compared to the traditional methods of extracting compounds from natural products, MAE has shorter extraction time, less solvent, higher extraction rate, and lower cost (Delazar et al. 2012).
UAE can be carried out at low temperatures by taking advantage of the vibration cavitation effect of ultrasonic waves, which reduces heat loss from high temperatures and prevents bioactive substances. It is suitable for the extraction of heat-resistant compounds and is simpler and faster than microwave-assisted extraction and has great potential for large-scale production (Chandrapala et al. 2013). However, the process is also affected by many factors such as extraction time, microwave power, and solid–liquid ratio. Currently, this technique has been used in the extraction of many plant materials by significantly reducing extraction time and increasing the maximum extraction rate (Ma et al. 2010; Surin et al. 2020).
SFE is a process of extracting valuable substances by using solvents at pressures and temperatures above critical points, which is environmentally friendly, inexpensive, widely available, non-flammable, and timesaving. Carbon dioxide and water are the most common uses of supercritical fluids. Hydrocolloid from marine algae contains many bioactive substances that are susceptible to degrade at high temperatures. SFE-CO2 provides a non-oxidizing atmosphere during the extraction, thus preventing the degradation of the extract. Kumar extracted total phenols with antioxidant activity from brown seaweed (Sargassum wightii and Turbinaria), and this activity was greatly improved compared to the traditional organic solvent extraction method (Kumar et al. 2020). Although extracting algal flavor compounds usually takes several hours, it is expensive and difficult for machines to clean (Dmytryk et al. 2015).
PSE is a relatively new automated technique that extracts target compounds at 200℃ and 3000 psi, using solvents or mixtures of solvents with low boiling points. The solubility, solvent diffusivity and mass transfer rate increased significantly by PSE method, while solvent viscosity and surface tension decreased significantly. Compared with SFE, PSE extraction can use a wider range of solvents. However, PSE is not suitable for heat-resistant compounds that are sensitive to high temperature and high pressure and is not selective for SFE. It has been shown that the extraction of carotenoids from Dunaliella halogensis, as well as kavanolides from pepper, can yield higher yields with less solvents in a shorter time while maintaining chemical integrity (Hossain et al. 2011).
EAE uses specific enzymes to break down unwanted components of the cell wall, thereby releasing the desired components. Compared with the traditional water extraction method, this method has the advantage of high catalytic efficiency, and retains the original effect of the compound to a large extent. Billakanti et al. (2012) extracted haloxanthine from wakame by alga lyase hydrolysis with the optimum temperature at 37℃ and pH at 6.2 to yield well performing bioactive compounds.
It is necessary to select appropriate extraction technologies for different active substances. In particular, the combination technology has great potential to minimize the degradation of bioactive compounds caused by different extraction steps. Many bioactive substances from seaweed play an important role and have promising applications in functional foods, health care products, cosmetics, and medicine. However, more researches are needed to improve modern extraction technologies to enlarge industrial scale.
New applications
Food industry
Today, seaweed is as widely used as a vegetable. In many Asian countries, seaweed is an important part of human diet in its fresh, dried, flaky, and flour form. Commercial production of seaweed has been the focus of seaweed research in the past, but recently the researches has been a shift towards high-value products with health benefits. Studies have shown that adding Chlorella to foods (such as pasta and biscuits) can improve the nutritional quality of the diet. Chlorella and Spirulina are mostly applied in tablet, capsule, and liquid form for nutritional supplements because of their high nutritional value and ease of growth. Moreover, an edible cyanobacterium Spirulina platensis has gained worldwide attention as a food additive due to its high nutritional value as a human food (Andrade et al. 2018; Batista et al. 2017; Martelli et al. 2020). It has proven to be a rich source of protein, polyunsaturated fatty acids, and pigment. Clearly, the food industry is beginning to focus on developing high-value non-commercial products for human health. In the future, many seaweeds are likely to become important components of functional products.
Agriculture
Farmland natural ecology is currently deteriorating due to excessive usage of artificial fertilizers and pesticides. Seaweed is abundant in unique mineral elements, nutrients, and biologically active chemicals. In recent years, agricultural output has played an increasingly vital role. Seaweed can be utilized as a protectant for diseases and as a stimulant in horticulture, promoting and enhancing all aspects of plant growth and development (Battacharyya et al. 2015). Green seaweed Ulva crude extracts and sulfated polysaccharides have antibacterial activity against common bean (Phaseolus vulgaris L.) anthracnose, as well as considerably promoting soybean growth (Paulert et al. 2009). Furthermore, seaweed can boost the ability of plants to absorb nutrients, hence improving plant quality. A new study showed that leaf spraying and seed soaking can significantly improve the yield and nutritional quality of carrots treated with seaweed (Sargassum vulgare) extract (Mahmoud et al. 2019). Seaweed is a valuable animal feeding as well as a source of agricultural chemicals. A variety of algal diets have been utilized to grow a range of fish, shrimp, crabs, and shellfish throughout the last two decades. The most commonly alga are Chlorella, Spirulina, and other microalgae (Kim et al. 2006). Many minerals remain in the waste biomass after cyanobacteria recovering oil and carbohydrate, which can be used as fertilizers to improve various physical and chemical properties of soil while boosting yield and conserving fertilizer nitrogen. The Asia–Pacific region accounted for more than 15% of global seaweed fertilizer market revenue in 2017. By 2025, the global market for seaweed fertilizer is estimated to reach 17.1 million US dollars. Organic agriculture is gaining traction, and the usage of seaweed fertilizer is on the rise. As a result, seaweed processing is predicted to become a key resource guarantee in green and modern agriculture.
Biological medicine
In medicine, seaweed has attracted a lot of attention as a potential source of various drug properties. In the last two decades, seaweed polysaccharides have been shown to have a variety of promising biological activities, such as anti-tumor (Zhao et al. 2020), immunomodulatory (Huang et al. 2015), antioxidant (Maheswari et al. 2021), anti-hyperglycemic (Pantidos et al. 2014), anti-cancer (Lee et al. 2013), antiviral, anti-fungal (Pallela & Kim, 2011), anti-diabetic (Lin et al. 2018; Zhao et al. 2018), anti-hypertensive (Seca & Pinto 2018), anti-inflammatory, uv-protective, and neuroprotection effects (Schepers et al. 2020). Meanwhile, algal hydrogels and hydrocolloids are valuable components in the medical field, which are widely used in wound healing, drug delivery, in vitro cell culture and tissue engineering (Senthilkuma et al. 2017). These gels maintain structural similarity to the extracellular matrix in tissues and can be manipulated to perform several key roles. Although some specific drug-specific gels have been clinically used for wound healing, they play a rather passive role. In wound healing and drug delivery applications, there is a great need for precise control of single drug delivery versus multiple drug delivery, or continuous and sequential release in response to changes in the external environment, which is useful for future development of products (Lee & Mooney 2012).
Chemical industry
For nearly 20 years, the bioactive substances from macro- and micro-algae are popular in the cosmetic industry. Compared with terrestrial plants, algae contain many unique and novel bioactive ingredients such as polyphenol compounds, halogen, terpenoids, sterol compounds, unsaturated fatty acids, and polysaccharides in addition to vitamin, protein, minerals and trace elements (López-Hortas et al. 2021). Various algal composition as a thickener, water binder, antioxidant, and UV blockers, are present in a variety of facial and skin care products (such as masks, eye creams, and sunscreens) to improve moisture balance, reduce wrinkles, and improve skin tone (Priyan Shanura Fernando et al. 2018; Wijesinghe & Wedamulla 2019). Thus, seaweed could be a sustainable and profitable source of bioactive substances with the growing demand for cosmetics and cosmetic ingredients.
Other applications
Algae is a decent candidate because of its renewable and sustainable features, as well as its economic viability meeting the world's demand of fuels for transportation. Algae can be used to produce biodiesel, bioethanol, biohydrogen, and biomethane. And it is particularly popular in energy applications due to its high safety, lack of competition from food crops, high reproductive capacity, and short cycle (Adeniyi et al. 2018). In addition, algae has been used in the construction industry. Vijayaraghavan and Joshi (2015) developed a new alga-based green roof growth matrix, which found that the green roof's runoff quality improved after adding brown seaweed (Turbinaria conoides) to the growth matrix. It can improve building insulation, rainfall attenuation, sound insulation, and lessen the heat island effect and extend the life of the roof. Besides, algae can also help to tackle the problem of eutrophication in water bodies. Green algae were utilized to treat municipal wastewater in ponds (Woertz et al. 2009). They may remove up to 99% of ammonium and phosphate under cultivation conditions, and then offer valuable wastewater treatment services and supply raw materials for liquid biofuel synthesis. Seaweed would encapsulate its value in a variety of industries due to its unique composition.
Challenges and solutions
Over the past 20 years, the situations of algal breeding and processing industry have risen steadily, which playing the active role in economic, social, and ecological aspects. Especially, the marine ecological problems have been alleviated due to the positive ecological benefits of breeding algae. However, this field still faces some challenges including the lack of improved varieties, poor growth environment, immature breeding and processing technology, shortage of cultivated land resources, and restrictions of relevant policies. Due to the continuous expansion of seaweed market and the increased demand for seaweed products, it is urgent to overcome their own and external constraints.
External challenges
The external challenges are mainly in the following aspects: global warming and sea-level rise lead to the declined seaweed biomass and quality. In order to deal with the harsh environment, the cost of breeding management including equipment maintenance, renewal and growth environment management has been increased. However, it is a burden for many low-income areas for the increase of technical investment in the development of high-quality seaweed species and processing products. Seawater eutrophication and the emergence of harmful algal blooms are happened due to rapidly expanding human activities (Yu et al. 2016). Harmful algal blooms usually contain the toxic substances. Accidental poisoning may occur by eating contaminated food (Lewitus et al. 2012). The environmental problems caused by the development of algae breeding and processing will eventually become factors affecting themselves. For example, halogenated hydrocarbons produced by many algae will affect the flux of ozone and ultraviolet rays. The density on growing environment is easy to bring about the invasion of alien species. The breeding equipment is the attachment base of the green algae. And the water body in the breeding area is relatively stable because a large number of rafts hinder the flow of sea water. With the increase of temperature, these large amounts of green algae reproduce and eventually enter the ocean to form a “green tide” (Yu et al. 2016). Microplastics in the ocean will be captured by cultured algae and spread to a higher nutritional level through the food chains, resulting in a significant burden on marine ecology.
Internal challenges
Seaweed production and processing technology does not match its increasing demand. At present, the cultivation of seaweed is mainly developed in some underdeveloped areas. Only a small number of countries such as China, have realized industrialized seedling raising, large-scale offshore cultivation, and mechanized harvesting, forming an industrial chain from product processing to sales. However, most countries mainly focus on basic cultivation, the automation of large-scale harvesting and processing are not high. It results in the unguaranteed quality, low efficiency, high employment cost, and processing waste. Most seaweed processed products are mainly used as edible and industrial raw materials. In recent years, large amounts of bioactive compounds from seaweed have been studied. However, the value-added products is generally low because of the lack of advanced techniques for extraction and purification (Pérez et al. 2016).
Response measures
The large-scale human activities at sea should be restricted, while the implement staggered peak aquaculture of algae and timely issue relevant water quality protection policies should be encouraged. Algae with high temperature resistance and disease resistance need to be cultivated. The advantages of algae should be used to solve problems and realize a virtuous cycle. For example, macroalgae can absorb carbon, nitrogen, and phosphorus in seawater through photosynthesis. The absorption of CO2 can play the ability of marine carbon fixation. Algae can reduce nitrogen and phosphorus in the enrichment of waters by inorganic nutrients. Ulva ohnoi has been proved to be an ideal target species for bioremediation activities at land-based aquaculture facilities in eastern Australia (Lawton et al. 2013). Seaweed has also been used to treat anaerobic digestion piggery effluent (Nwoba et al. 2016). In the integrated multi-trophic aquaculture (Chopin et al. 2012), the waste nutrients released or excreted into the water in the aquaculture system can be used by algae as the source of nutrients, which can achieve the goal of recirculating aquaculture system and regulating water quality.
Conclusions
The development of seaweed farming is growing year by year. The seaweed farming technologies are constantly updated, and seaweed processed products are emerging. Therefore, seaweed plays a huge role in the economic, social, and ecological fields. It is rich in a variety of biological active substances as drug sources, cosmetics, and agricultural regulators, which have been largely developed. It is necessary to strengthen investment in seaweed farming and processing technologies and develop high value-added products with the integrated multi-trophic aquaculture, which have great market potential and need in-depth exploration.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Change history
02 November 2022
A Correction to this paper has been published: https://doi.org/10.1186/s43014-022-00113-0
Abbreviations
- FAO:
-
Food and Agriculture Organization
- ARA:
-
Arachidonic acid
- EPA:
-
Eicosapentaenoic acid
- DHA:
-
Docosahexaenoic acid
- LA:
-
Linoleic acid
- ALA:
-
Alpha-linolenic acid
- HRAP:
-
High rate algal ponds
- MAE:
-
Microwave-assisted extraction
- UAE:
-
Ultrasound-assisted extraction
- SFE:
-
Supercritical fluid extraction
- PSE:
-
Pressurized solvent extraction
- EAE:
-
Enzyme-assisted extraction
References
Abdul, Q. A., Choi, R. J., Jung, H. A., & Choi, J. S. (2016). Health benefit of fucosterol from marine algae: A review. Journal of the Science of Food and Agriculture, 96(6), 1856–1866. https://doi.org/10.1002/jsfa.7489
Abel, A., & Anoland, & Garateix. (2004). Bioactive peptides from marine sources: Pharmacological properties and isolation procedures-sciencedirect. Journal of Chromatography B Analytical Technologies in the Biomedical & Life Sciences, 803(1), 41–53. https://doi.org/10.1016/j.jchromb.2003.11.005
Adeniyi, O. M., Azimov, U., & Burluka, A. (2018). Algae biofuel: Current status and future applications. Renewable and Sustainable Energy Reviews, 90, 316–335. https://doi.org/10.1016/j.rser.2018.03.067
Aguero, J., Lora, J., Estrada, K., Concepcion, F., Nunez, A., Rodriguez, A., & Pino, J. A. (2003). Volatile components of a commercial sample of the blue-green algae Spirulina platensis. Journal of Essential Oil Research, 15(2), 114–117. https://doi.org/10.1080/10412905.2003.9712085
Ale, M. T., Maruyama, H., Tamauchi, H., Mikkelsen, J. D., & Meyer, A. S. (2011). Fucose-containing sulfated polysaccharides from brown seaweeds inhibit proliferation of melanoma cells and induce apoptosis by activation of caspase-3 in vitro. Marine Drugs, 9(12), 2605–2621. https://doi.org/10.3390/md9122605
Alonso, A., Fernández-Torroba, M. A., Tena, M. T., & Pons, B. (2003). Development and validation of a solid-phase microextraction method for the analysis of volatile organic compounds in groundwater samples. Chromatographia, 57(5–6), 369–378. https://doi.org/10.1016/j.chroma.2005.10.056
Alves, M., Barreto, F., Vasconcelos, M. A., Nascimento Neto, L., Carneiro, R. F., Silva, L., Nagano, C. S., Sampaio, A. H., & Teixeira, E. H. (2020). Antihyperglycemic and antioxidant activities of a lectin from the marine red algae, Bryothamnion seaforthii, in rats with streptozotocin-induced diabetes. International Journal of Biological Macromolecules, 158, 773–780. https://doi.org/10.1016/j.ijbiomac.2020.04.238
Amador-Castro, F., García-Cayuela, T., Alper, H. S., Rodriguez-Martinez, V., & Carrillo-Nieves, D. (2021). Valorization of pelagic sargassum biomass into sustainable applications: Current trends and challenges. Journal of Environmental Management, 283, 112013. https://doi.org/10.1016/j.jenvman.2021.112013
Ambati, R. R., Phang, S. M., Ravi, S., & Aswathanarayana, R. G. (2014). Astaxanthin: Sources, extraction, stability, biological activities and its commercial applications–a review. Marine Drugs, 12(1), 128–152. https://doi.org/10.3390/md12010128
Andrade, L. M., Andrade, C. J., Dias, M., Nascimento, C., & Mendes, M. (2018). Chlorella and Spirulina microalgae as sources of functional foods. Nutraceuticals, and Food Supplements, 6(1), 45–58.
André, R., Pacheco, R., Bourbon, M., & Serralheiro, M. L. (2021). Brown algae potential as a functional food against hypercholesterolemia: Review. Foods (basel, Switzerland), 10(2), 234. https://doi.org/10.3390/foods10020234
Aravind, S., Barik, D., Ragupathi, P., & Vignesh, G. (2021). Investigation on algae oil extraction from algae Spirogyra by Soxhlet extraction method. Materials Today: Proceedings, 43(1), 308–313. https://doi.org/10.1016/j.matpr.2020.11.668
Ávila-Román, J., García-Gil, S., Rodríguez-Luna, A., Motilva, V., & Talero, E. (2021). Anti-Inflammatory and anticancer effects of microalgal carotenoids. Marine Drugs, 19(10), 531. https://doi.org/10.3390/md19100531
Bae, H., Song, G., Lee, J. Y., Hong, T., Chang, M. J., & Lim, W. (2020). Laminarin-derived from brown algae suppresses the growth of ovarian cancer cells via mitochondrial dysfunction and er stress. Marine Drugs, 18(3), 152. https://doi.org/10.3390/md18030152
Banskota, A. H., Stefanova, R., Sperker, S., Lall, S. P., Craigie, J. S., Hafting, J. T., & Critchley, A. T. (2014). Polar lipids from the marine macroalga Palmaria palmata inhibit lipopolysaccharide-induced nitric oxide production in RAW264.7 macrophage cells. Phytochemistry, 101, 101–108. https://doi.org/10.1016/j.phytochem.2014.02.004
Batista, A. P., Niccolai, A., Fradinho, P., Fragoso, S., Bursic, I., Rodolfi, L., & Raymundo, A. (2017). Microalgae biomass as an alternative ingredient in cookies: Sensory, physical and chemical properties, antioxidant activity and in vitro digestibility. Algal Research, 26, 161–171. https://doi.org/10.1016/j.algal.2017.07.017
Battacharyya, D., Babgohari, M. Z., Rathor, P., & Prithiviraj, B. (2015). Seaweed extracts as biostimulants in horticulture. Scientia Horticulturae, 196, 39–48. https://doi.org/10.1016/j.scienta.2015.09.012
Bogolitsyn, K., Dobrodeeva, L., Druzhinina, A., Ovchinnikov, D., Parshina, A., & Shulgina, E. (2019). Biological activity of a polyphenolic complex of Arctic brown algae. Journal of Applied Phycology, 31(5), 3341–3348. https://doi.org/10.1007/s10811-019-01840-7
Buschmann, A. H., Camus, C., Infante, J., Neori, A., Israel, Á., Hernández-González, M., et al. (2017). Seaweed production: Overview of the global state of exploitation, farming and emerging research activity. European Journal of Phycology, 52(4), 391–406. https://doi.org/10.1080/09670262.2017.1365175
Cao, S., Yang, Y., Liu, S., Shao, Z., Chu, X., & Mao, W. (2022). Immunomodulatory activity In vitro and in vivo of a sulfated polysaccharide with novel structure from the green alga Ulvaconglobata kjellman. Marine Drugs, 20(7), 447. https://doi.org/10.3390/md20070447
Carlucci, M. J., Pujol, C. A., Ciancia, M., Noseda, M. D., Matulewicz, M. C., Damonte, E. B., & Cerezo, A. S. (1997). Antiherpetic and anticoagulant properties of carrageenans from the red seaweed Gigartina skottsbergii and their cyclized derivatives: Correlation between structure and biological activity. International Journal of Biological Macromolecules, 20(2), 97–105. https://doi.org/10.1016/S0141-8130(96)01145-2
Carpena, M., Garcia-Perez, P., Garcia-Oliveira, P., Chamorro, F., Otero, P., Lourenço-Lopes, C., Cao, H., Simal-Gandara, J., & Prieto, M. A. (2022). Biological properties and potential of compounds extracted from red seaweeds. Phytochemistry Reviews. https://doi.org/10.1007/s11101-022-09826-z
Cavone, L., Calosi, L., Cinci, L., Moroni, F., & Chiarugi, A. (2012). Topical mannitol reduces inflammatory edema in a rat model of arthritis. Pharmacology, 89(1–2), 18–21. https://doi.org/10.1159/000335094
Chandrapala, J., Oliver, C. M., Kentish, S., & Ashokkumar, M. (2013). Use of power ultrasound to improve extraction and modify phase transitions in food processing. Food Reviews International, 29(1), 67–91. https://doi.org/10.1080/87559129.2012.692140
Chen, Y., Liu, X., Wu, L., Tong, A., Zhao, L., Liu, B., & Zhao, C. (2018b). Physicochemical characterization of polysaccharides from Chlorella pyrenoidosa and its anti-ageing effects in Drosophila melanogaster. Carbohydrate Polymers, 185, 120–126. https://doi.org/10.1016/j.carbpol.2017.12.077
Chen, Y., Ouyang, Y., Chen, X., Chen, R., Ruan, Q., Farag, M. A., Chen, X., & Zhao, C. (2022). Hypoglycaemic and anti-ageing activities of green alga Ulva lactuca polysaccharide via gut microbiota in ageing-associated diabetic mice. International Journal of Biological Macromolecules, 212, 97–110. https://doi.org/10.1016/j.ijbiomac.2022.05.109
Chiaramonti, D., Prussi, M., Buffi, M., Rizzo, A. M., & Pari, L. (2017). Review and experimental study on pyrolysis and hydrothermal liquefaction of microalgae for biofuel production. Applied Energy, 185, 963–972. https://doi.org/10.1016/j.apenergy.2015.12.001
Chidambara Murthy, K. N., Vanitha, A., Rajesha, J., Mahadeva Swamy, M., Sowmya, P. R., & Ravishankar, G. A. (2005). In vivo antioxidant activity of carotenoids from Dunaliella salina–a green microalga. Life Sciences, 76(12), 1381–1390. https://doi.org/10.1016/j.lfs.2004.10.015
Choi, Y. K., Ye, B. R., Kim, E. A., Kim, J., Kim, M. S., Lee, W. W., Ahn, G. N., Kang, N., Jung, W. K., & Heo, S. J. (2018). Bis (3-bromo-4,5-dihydroxybenzyl) ether, a novel bromophenol from the marine red alga Polysiphonia morrowii that suppresses LPS-induced inflammatory response by inhibiting ROS-mediated ERK signaling pathway in RAW 264.7 macrophages. Biomedicine & Pharmacotherapy, 103, 1170–1177. https://doi.org/10.1016/j.biopha.2018.04.121
Chopin, T., Cooper, J., & A., Reid. G., Cross, S., & Moore, C. (2012). Open-water integrated multi-trophic aquaculture: Environmental biomitigation and economic diversification of fed aquaculture by extractive aquaculture. Review in Aquaculture., 4(4), 209–220. https://doi.org/10.1111/j.1753-5131.2012.01074.x
Ciliberti, M. G., Francavilla, M., Intini, S., Albenzio, M., Marino, R., Santillo, A., & Caroprese, M. (2017). Phytosterols from Dunaliella tertiolecta reduce cell proliferation in sheep fed flaxseed during post partum. Marine Drugs, 15(7), 216. https://doi.org/10.3390/md15070216
Cong, Q., Chen, H., Liao, W., Xiao, F., Wang, P., Qin, Y., Dong, Q., & Ding, K. (2016). Structural characterization and effect on anti-angiogenic activity of a fucoidan from Sargassum fusiforme. Carbohydrate Polymers, 136, 899–907. https://doi.org/10.1016/j.carbpol.2015.09.087
Cotas, J., Leandro, A., Monteiro, P., Pacheco, D., Figueirinha, A., Gonçalves, A., da Silva, G. J., & Pereira, L. (2020a). Seaweed phenolics: From extraction to applications. Marine Drugs, 18(8), 384. https://doi.org/10.3390/md18080384
Cotas, J., Leandro, A., Pacheco, D., Gonçalves, A., & Pereira, L. (2020b). A comprehensive review of the nutraceutical and therapeutic applications of red seaweeds (Rhodophyta). Life, 10(3), 19. https://doi.org/10.3390/life10030019
Cotas, J., Marques, V., Afonso, M. B., Rodrigues, C., & Pereira, L. (2020c). Antitumour potential of Gigartina pistillata carrageenans against colorectal cancer stem cell-enriched tumourspheres. Marine Drugs, 18(1), 50. https://doi.org/10.3390/md18010050
da Costa, E., Melo, T., Reis, M., Domingues, P., Calado, R., Abreu, M. H., & Domingues, M. R. (2021). Polar lipids composition, antioxidant and anti-inflammatory activities of the Atlantic red seaweed Grateloupia turuturu. Marine Drugs, 19(8), 414. https://doi.org/10.3390/md19080414
Dai, Y., Meng, Q., Mu, W., & Zhang, T. (2017). Recent advances in the applications and biotechnological production of mannitol. Journal of Functional Foods, 36, 404–409. https://doi.org/10.1016/j.jff.2017.07.022
Dawczynski, C., Schubert, R., & Jahreis, G. (2007). Amino acids, fatty acids, and dietary fibre in edible seaweed products. Food Chemistry, 103(3), 891–899. https://doi.org/10.1016/j.foodchem.2006.09.041
De la Coba, F., Aguilera, J., Figueroa, F. L., De Gálvez, M. V., & Herrera, E. (2009). Antioxidant activity of mycosporine-like amino acids isolated from three red macroalgae and one marine lichen. Journal of Applied Phycology, 21(2), 161–169. https://doi.org/10.1007/s10811-008-9345-1
Delazar, A., Nahar, L., Hamedeyazdan, S., & Sarker, S. D. (2012). Microwave-assisted extraction in natural products isolation. Methods in Molecular Biology, 864, 89–115. https://doi.org/10.1007/978-1-61779-624-1_5
Dembitsky, V. M., & Maoka, T. (2007). Allenic and cumulenic lipids. Progress in Lipid Research, 46(6), 328–375. https://doi.org/10.1016/j.plipres.2007.07.001
Denery, J. R., Dragull, K., Tang, C. S., & Li, Q. X. (2004). Pressurized fluid extraction of carotenoids from Haematococcus pluvialis and Dunaliella salina and kavalactones from Piper methysticum. Analytica Chimica Acta, 501(2), 175–181. https://doi.org/10.1016/j.aca.2003.09.026
Dias, M., Madusanka, D., Han, E. J., Kim, M. J., Jeon, Y. J., Kim, H. S., & Ahn, G. (2020). (-)-Loliolide isolated from Sargassum horneri protects against fine dust-induced oxidative stress in human keratinocytes. Antioxidants, 9(6), 474. https://doi.org/10.3390/antiox9060474
Ding, Y., Wang, L., Im, S., Hwang, O., Kim, H. S., Kang, M. C., & Lee, S. H. (2019). Anti-obesity effect of diphlorethohydroxycarmalol isolated from brown alga ishige okamurae in high-fat diet-Induced obese mice. Marine Drugs, 17(11), 637. https://doi.org/10.3390/md17110637
Dmytryk, A., Wieczorek, P. P., Rój, E., Łęska, B., Górka, B., Messyasz, B., Lipok, J., Mikulewicz, M., Wilk, R., Schroeder, G., & Chojnacka, K. (2015). Supercritical algal extracts: A source of biologically active compounds from nature. Journal of Chemistry, 597140, 1–14. https://doi.org/10.1155/2015/597140
Dong, H., Liu, M., Wang, L., Liu, Y., Lu, X., Stagos, D., Lin, X., & Liu, M. (2021). Bromophenol bis (2,3,6-Tribromo-4,5-dihydroxybenzyl) ether protects HaCaT skin cells from oxidative damage via Nrf2-mediated pathways. Antioxidants (basel, Switzerland), 10(9), 1436. https://doi.org/10.3390/antiox10091436
El-Baz, F. K., Hussein, R. A., Mahmoud, K., & Abdo, S. M. (2018). Cytotoxic activity of carotenoid rich fractions from Haematococcus pluvialis and Dunaliella salina microalgae and the identification of the phytoconstituents using LC-DAD/ESI-MS. Phytotherapy Research, 32(2), 298–304. https://doi.org/10.1002/ptr.5976
Eom, S. H., Lee, M. S., Lee, E. W., Kim, Y. M., & Kim, T. H. (2013). Pancreatic lipase inhibitory activity of phlorotannins isolated from Eisenia bicyclis. Phytotherapy Research, 27(1), 148–151. https://doi.org/10.1002/ptr.4694
Feng, W., Hu, Y., An, N., Feng, Z., Liu, J., Mou, J., Hu, T., Guan, H., Zhang, D., & Mao, Y. (2020). Alginate oligosaccharide alleviates monocrotaline-induced pulmonary hypertension via anti-oxidant and anti-inflammation pathways in rats. International Heart Journal, 61(1), 160–168. https://doi.org/10.1536/ihj.19-096
Francavilla, M., Franchi, M., Monteleone, M., & Caroppo, C. (2013). The red seaweed Gracilaria gracilis as a multi products source. Marine Drugs, 11(10), 3754–3776. https://doi.org/10.3390/md11103754
Froehlich, H. E., Afflerbach, J. C., Frazier, M., & Halpern, B. S. (2019). Blue growth potential to mitigate climate change through seaweed offsetting. Current Biology, 29(18), 3087–3093. https://doi.org/10.1016/j.cub.2019.07.041
Geetha Bai, R., & Tuvikene, R. (2021). Potential antiviral properties of industrially important marine algal polysaccharides and their significance in fighting a future viral pandemic. Viruses, 13(9), 1817. https://doi.org/10.3390/v13091817
Gille, A., Stojnic, B., Derwenskus, F., Trautmann, A., Schmid-Staiger, U., Posten, C., Briviba, K., Palou, A., Bonet, M. L., & Ribot, J. (2019). A lipophilic fucoxanthin-rich Phaeodactylum tricornutum extract ameliorates effects of diet-induced obesity in C57BL/6J Mice. Nutrients, 11(4), 796. https://doi.org/10.3390/nu11040796
Gomaa, H. H., & Elshoubaky, G. A. (2016). Antiviral activity of sulfated polysaccharides carrageenan from some marine seaweeds. Int. J. Curr. Pharm. Rev. Res, 7(1), 34–42.
Güçlü-Üstündağ, Ö., & Temelli, F. (2005). Solubility behavior of ternary systems of lipids, cosolvents and supercritical carbon dioxide and processing aspects. The Journal of Supercritical Fluids, 36(1), 1–15. https://doi.org/10.1016/j.supflu.2005.03.002
Guo, C., Zhu, Z., Yu, P., Zhang, X., Dong, W., Wang, X., Chen, Y., & Liu, X. (2019). Inhibitory effect of iota-carrageenan on porcine reproductive and respiratory syndrome virus in vitro. Antiviral Therapy, 24(4), 261–270. https://doi.org/10.3851/IMP3295
Han, R., Wang, L., Zhao, Z., You, L., Pedisić, S., Kulikouskaya, V., & Lin, Z. (2020). Polysaccharide from Gracilaria Lemaneiformis prevents colitis in Balb/c mice via enhancing intestinal barrier function and attenuating intestinal inflammation. Food Hydrocolloids, 109, 106048. https://doi.org/10.1016/j.foodhyd.2020.106048
Harley, C. D., Anderson, K. M., Demes, K. W., Jorve, J. P., Kordas, R. L., Coyle, T. A., & Graham, M. H. (2012). Effects of climate change on global seaweed communities. Journal of Phycology, 48(5), 1064–1078. https://doi.org/10.1111/j.1529-8817.2012.01224.x
Holdt, S. L., & Kraan, S. (2011). Bioactive compounds in seaweed: Functional food applications and legislation. Journal of Applied Phycology, 23(3), 543–597. https://doi.org/10.1007/s10811-010-9632-5
Horibe, S., Tanahashi, T., Kawauchi, S., Mizuno, S., & Rikitake, Y. (2016). Preventative effects of sodium alginate on indomethacin-induced small-intestinal Injury in mice. International Journal of Medical Sciences, 13(9), 653–663. https://doi.org/10.7150/ijms.16232
Huang, Z., Chi, X., Shu, Z., & Sun, J. (2015). Immunomodulatory effects of seaweed polysaccharide in aged mice. International Journal of Laboratory Medicine, 13, 1801–1803.
Jaballi, I., Sallem, I., Feki, A., Cherif, B., Kallel, C., Boudawara, O., Jamoussi, K., Mellouli, L., Nasri, M., & Amara, I. B. (2019). Polysaccharide from a Tunisian red seaweed Chondrus canaliculatus: Structural characteristics, antioxidant activity and in vivo hemato-nephroprotective properties on maneb induced toxicity. International Journal of Biological Macromolecules, 123, 1267–1277. https://doi.org/10.1016/j.ijbiomac.2018.12.048
Jung, H. A., Bhakta, H. K., Min, B. S., & Choi, J. S. (2016). Fucosterol activates the insulin signaling pathway in insulin resistant HepG2 cells via inhibiting PTP1B. Archives of Pharmacal Research, 39(10), 1454–1464. https://doi.org/10.1007/s12272-016-0819-4
Jung, H. A., Jin, S. E., Ahn, B. R., Lee, C. M., & Choi, J. S. (2013). Anti-inflammatory activity of edible brown alga Eisenia bicyclis and its constituents fucosterol and phlorotannins in LPS-stimulated RAW264.7 macrophages. Food and Chemical Toxicology, 59, 199–206. https://doi.org/10.1016/j.fct.2013.05.061
Jung, H. A., Jung, H. J., Jeong, H. Y., Kwon, H. J., Ali, M. Y., & Choi, J. S. (2014a). Phlorotannins isolated from the edible brown alga Ecklonia stolonifera exert anti-adipogenic activity on 3T3-L1 adipocytes by downregulating C/EBPα and PPARγ. Fitoterapia, 92, 260–269. https://doi.org/10.1016/j.fitote.2013.12.003
Jung, H. A., Jung, H. J., Jeong, H. Y., Kwon, H. J., Kim, M. S., & Choi, J. S. (2014b). Anti-adipogenic activity of the edible brown alga Ecklonia stolonifera and its constituent fucosterol in 3T3-L1 adipocytes. Archives of Pharmacal Research, 37(6), 713–720. https://doi.org/10.1007/s12272-013-0237-9
Jung, W. K., Choi, I., Oh, S., Park, S. G., Seo, S. K., Lee, S. W., Lee, D. S., Heo, S. J., Jeon, Y. J., Je, J. Y., Ahn, C. B., Kim, J. S., Oh, K. S., Kim, Y. M., Moon, C., & Choi, I. W. (2009). Anti-asthmatic effect of marine red alga (Laurencia undulata) polyphenolic extracts in a murine model of asthma. Food and Chemical Toxicology, 47(2), 293–297. https://doi.org/10.1016/j.fct.2008.11.012
Kadam, S. U., Tiwari, B. K., & O’Donnell, C. P. (2015). Extraction, structure and biofunctional activities of laminarin from brown algae. International Journal of Food Science & Technology, 50(1), 24–31. https://doi.org/10.1111/ijfs.12692
Karsten, U., Franklin, L. A., Lüning, K., & Wiencke, C. (1998). Natural ultraviolet radiation and photosynthetically active radiation induce formation of mycosporine-like amino acids in the marine macroalga Chondrus crispus (Rhodophyta). Planta, 205(2), 257–262. https://doi.org/10.1007/s004250050319
Karthikeyan, R., Somasundaram, S. T., Manivasagam, T., Balasubramanian, T., & Anantharaman, P. (2010). Hepatoprotective activity of brown alga Padina boergesenii against CCl4 induced oxidative damage in Wistar rats. Asian Pacific Journal of Tropical Medicine, 3(9), 696–701. https://doi.org/10.1016/S1995-7645(10)60168-X
Kasanah, N., Amelia, W., Mukminin, A., & Triyanto, & Isnansetyo, A. (2019). Antibacterial activity of Indonesian red algae Gracilaria edulis against bacterial fish pathogens and characterization of active fractions. Natural Product Research, 33(22), 3303–3307. https://doi.org/10.1080/14786419.2018.1471079
Kavalappa, Y. P., Rudresh, D. U., Gopal, S. S., Shivarudrappa, A. H., Stephen, N. M., Rangiah, K., & Ponesakki, G. (2019). β-carotene isolated from the marine red alga, Gracillaria sp. potently attenuates the growth of human hepatocellular carcinoma (HepG2) cells by modulating multiple molecular pathways. Journal of Functional Foods, 52, 165–176. https://doi.org/10.1016/j.jff.2018.11.015
Kavita, K., Singh, V. K., & Jha, B. (2014). 24-Branched Δ5 sterols from Laurencia papillosa red seaweed with antibacterial activity against human pathogenic bacteria. Microbiological Research, 169(4), 301–306. https://doi.org/10.1016/j.micres.2013.07.002
Khan, M. N., Cho, J. Y., Lee, M. C., Kang, J. Y., Park, N. G., Fujii, H., & Hong, Y. K. (2007). Isolation of two anti-inflammatory and one pro-inflammatory polyunsaturated fatty acids from the brown seaweed Undaria pinnatifida. Journal of Agricultural and Food Chemistry, 55(17), 6984–6988. https://doi.org/10.1021/jf071791s
Kim, C. J., Yoon, S. K., Kim, H. I., Park, Y. H., & Oh, H. M. (2006). Effect of Spirulina platensis and probiotics as feed additives on growth of shrimp fenneropenaeus chinensis. Journal of Microbiology & Biotechnology, 16(8), 1248–1254.
Kim, E. Y., Choi, Y. H., & Nam, T. J. (2018). Identification and antioxidant activity of synthetic peptides from phycobiliproteins of Pyropia yezoensis. International Journal of Molecular Medicine, 42(2), 789–798. https://doi.org/10.3892/ijmm.2018.3650
Kim, K. N., Yang, H. M., Kang, S. M., Kim, D., Ahn, G., & Jeon, Y. J. (2013). Octaphlorethol a isolated from Ishige foliacea inhibits α-MSH-stimulated induced melanogenesis via ERK pathway in B16F10 melanoma cells. Food and Chemical Toxicology, 59, 521–526. https://doi.org/10.1016/j.fct.2013.06.031
Koyande, A. K., Chew, K. W., Manickam, S., Chang, J. S., & Show, P. L. (2021). Emerging algal nanotechnology for high-value compounds: A direction to future food production. Trends in Food Science & Technology, 116, 290–302. https://doi.org/10.1016/j.tifs.2021.07.026
Kumar, L. R., Treesa Paul, P., Anas, K. K., Tejpal, C. S., Chatterjee, N. S., Anupama, T. K., & Mathew, S. (2020). Screening of effective solvents for obtaining antioxidant-rich seaweed extracts using principal component analysis. Journal of Food Processing and Preservation, 44(9), e14716. https://doi.org/10.1111/jfpp.14716
Lavie, C. J., Milani, R. V., Mehra, M. R., & Ventura, H. O. (2009). Omega-3 polyunsaturated fatty acids and cardiovascular diseases. Journal of the American College of Cardiology, 54(7), 585–594.
Lawton, R. J., Leonardo, M., Rocky, D. N., Paul, N. A., & Adrianna, I. (2013). Algal bioremediation of waste waters from land-based aquaculture using Ulva: Selecting target species and strains. PLoS ONE, 8(10), e77344. https://doi.org/10.1371/journal.pone.0077344
Lee, D., Nishizawa, M., Shimizu, Y., & Saeki, H. (2017). Anti-inflammatory effects of dulse (Palmaria palmata) resulting from the simultaneous water-extraction of phycobiliproteins and chlorophyll a. Food Research International, 100(Pt1), 514–521. https://doi.org/10.1016/j.foodres.2017.06.040
Lee, H. A., Kim, I. H., & Nam, T. J. (2015). Bioactive peptide from Pyropia yezoensis and its anti-inflammatory activities. International Journal of Molecular Medicine, 36(6), 1701–1706. https://doi.org/10.3892/ijmm.2015.2386
Lee, J. C., Hou, M. F., Huang, H. W., Chang, F. R., Yeh, C. C., Tang, J. Y., & Chang, H. W. (2013). Marine algal natural products with anti-oxidative, anti-inflammatory, and anti-cancer properties. Cancer Cell International, 13(1), 55. https://doi.org/10.1186/1475-2867-13-55
Lee, K. Y., & Mooney, D. J. (2012). Alginate: Properties and biomedical applications. Progress in Polymer Science, 37(1), 106–126. https://doi.org/10.1016/j.progpolymsci.2011.06.003
Lee, S., Lee, Y. S., Jung, S. H., Kang, S. S., & Shin, K. H. (2003). Anti-oxidant activities of fucosterol from the marine algae Pelvetia siliquosa. Archives of Pharmacal Research, 26(9), 719–722. https://doi.org/10.1007/BF02976680
Lee, Y., Oh, H., & Lee, M. (2018). Anti-inflammatory effects of Agar free-Gelidium amansii (GA) extracts in high-fat diet-induced obese mice. Nutrition Research and Practice, 12(6), 479–485. https://doi.org/10.4162/nrp.2018.12.6.479
LePape, M. A., Grua-Priol, J., & Demaimay, M. (2002). Effect of two storage conditions on the odor of an edible seaweed, Palmaria palmata, and optimization of an extraction procedure preserving its odor characteristics. Journal of Food Science, 67(8), 3135–3139. https://doi.org/10.1111/j.1365-2621.2002.tb08871.x
Li, J., & Zheng, G. (2016). Concurrent extraction and transformation of bioactive phenolic compounds from rapeseed meal using pressurized solvent extraction system. Industrial Crops and Products, 94, 152–159. https://doi.org/10.1016/j.indcrop.2016.08.045
Li, N., Liu, X., He, X., Wang, S., Cao, S., Xia, Z., Xian, H., Qin, L., & Mao, W. (2017). Structure and anticoagulant property of a sulfated polysaccharide isolated from the green seaweed Monostroma angicava. Carbohydrate Polymers, 159, 195–206. https://doi.org/10.1016/j.carbpol.2016.12.013
Li, X., Chen, Y., Gao, X., Wu, Y., El-Seedi, H. R., Cao, Y., & Zhao, C. (2021a). Antihyperuricemic effect of green alga Ulva lactuca ulvan through regulating urate transporters. Journal of Agricultural and Food Chemistry, 69(38), 11225–11235. https://doi.org/10.1021/acs.jafc.1c03607
Li, Y., Zheng, Y., Zhang, Y., Yang, Y., Wang, P., Imre, B., Wong, A., Hsieh, Y., & Wang, D. (2021b). Brown algae carbohydrates: Structures, pharmaceutical properties, and research challenges. Marine Drugs, 19(11), 620. https://doi.org/10.3390/md19110620
Lin, G. P., Wu, D. S., Xiao, X. W., Huang, Q. Y., Chen, H. B., Liu, D., Fu, H. Q., Chen, X. H., & Zhao, C. (2020). Structural characterization and antioxidant effect of green alga Enteromorpha prolifera polysaccharide in Caenorhabditis elegans via modulation of microRNAs. International Journal of Biological Macromolecules, 150, 1084–1092. https://doi.org/10.1016/j.ijbiomac.2019.10.114
Lin, G., Liu, X., Yan, X., Liu, D., Yang, C., Liu, B., & Zhao, C. (2018). Role of green macroalgae Enteromorpha prolifera polyphenols in the modulation of gene expression and intestinal microflora profiles in type 2 diabetic mice. International Journal of Molecular Sciences, 20(1), 25. https://doi.org/10.3390/ijms20010025
Liu, B., Liu, Q. M., Li, G. L., Sun, L. C., Gao, Y. Y., Zhang, Y. F., Liu, H., Cao, M. J., & Liu, G. M. (2019). The anti-diarrhea activity of red algae-originated sulphated polysaccharides on ETEC-K88 infected mice. RSC Advances, 9(5), 2360–2370. https://doi.org/10.1039/c8ra09247h
Liu, Q. M., Yang, Y., Maleki, S. J., Alcocer, M., Xu, S. S., Shi, C. L., Cao, M. J., & Liu, G. M. (2016). Anti-food allergic activity of sulfated polysaccharide from Gracilaria lemaneiformis is dependent on immunosuppression and inhibition of p38 MAPK. Journal of Agricultural and Food Chemistry, 64(22), 4536–4544. https://doi.org/10.1021/acs.jafc.6b01086
Liu, Q., Zhang, Y., Shu, Z., Liu, M., Zeng, R., Wang, Y., Liu, H., Cao, M., Su, W., & Liu, G. (2020). Sulfated oligosaccharide of Gracilaria lemaneiformis protect against food allergic response in mice by up-regulating immunosuppression. Carbohydrate Polymers, 230, 115567. https://doi.org/10.1016/j.carbpol.2019.115567
Liu, Q., Zhou, Y., Ma, L., Gu, F., Liao, K., Liu, Y., Zhang, Y., Liu, H., Hong, Y., Cao, M., Liu, W. H., Liu, C., & Liu, G. (2022). Sulfate oligosaccharide of Gracilaria lemaneiformis modulates type 1 immunity by restraining T cell activation. Carbohydrate Polymers, 288, 119377. https://doi.org/10.1016/j.carbpol.2022.119377
Liu, X., Liu, H., Zhai, Y., Li, Y., Zhu, X., & Zhang, W. (2017). Laminarin protects against hydrogen peroxide-induced oxidative damage in MRC-5 cells possibly via regulating NRF2. PeerJ, 5, e3642. https://doi.org/10.7717/peerj.3642
López-Hortas, L., Flórez-Fernández, N., Torres, M. D., Ferreira-Anta, T., Casas, M. P., Balboa, E. M., Falqué, E., & Domínguez, H. (2021). Applying seaweed compounds in cosmetics, cosmeceuticals and nutricosmetics. Marine Drugs, 19(10), 552. https://doi.org/10.3390/md19100552
Machu, L., Misurcova, L., Ambrozova, J. V., Orsavova, J., Mlcek, J., Sochor, J., & Jurikova, T. (2015). Phenolic content and antioxidant capacity in algal food products. Molecules, 20(1), 1118–1133. https://doi.org/10.3390/molecules20011118
Maheswari, M., Das, A., Datta, M., & Tyagi, A. K. (2021). Supplementation of tropical seaweed-based formulations improves antioxidant status, immunity and milk production in lactating murrah buffaloes. Journal of Applied Phycology., 33(4), 2629–2643. https://doi.org/10.1007/s10811-021-02473-5
Mahmoud, S. H., Salama, D. M., El-Tanahy, A. M., & Abd El-Samad, E. H. (2019). Utilization of seaweed (Sargassum vulgare) extract to enhance growth, yield and nutritional quality of red radish plants. Annals of Agricultural Sciences, 64(2), 167–175. https://doi.org/10.1016/j.aoas.2019.11.002
Manandhar, B., Wagle, A., Seong, S. H., Paudel, P., Kim, H. R., Jung, H. A., & Choi, J. S. (2019). Phlorotannins with potential anti-tyrosinase and antioxidant activity isolated from the marine seaweed Ecklonia stolonifera. Antioxidants, 8(8), 240. https://doi.org/10.3390/antiox8080240
Marchal, L., Mojaat-Guemir, M., Foucault, A., & Pruvost, J. (2013). Centrifugal partition extraction of β-carotene from Dunaliella salina for efficient and biocompatible recovery of metabolites. Bioresource Technology, 134, 396–400. https://doi.org/10.1016/j.biortech.2013.02.019
Martelli, F., Cirlini, M., Lazzi, C., Neviani, E., & Bernini, V. (2020). Edible seaweeds and spirulina extracts for food application: In vitro and in situ evaluation of antimicrobial activity towards foodborne pathogenic bacteria. Foods, 9(10), 1442. https://doi.org/10.3390/foods9101442
Mesquita, J. X., de Brito, T. V., Fontenelle, T., Damasceno, R., de Souza, M., de Souza Lopes, J. L., Beltramini, L. M., Barbosa, A., & Freitas, A. (2021). Lectin from red algae Amansia multifida Lamouroux: Extraction, characterization and anti-inflammatory activity. International Journal of Biological Macromolecules, 170, 532–539. https://doi.org/10.1016/j.ijbiomac.2020.12.203
Michalak, I., & Chojnacka, K. (2014). Algal extracts: Technology and advances. Engineering in Life Sciences, 14(6), 581–591. https://doi.org/10.1002/elsc.201400139
Miyashita, K. (2009). Function of marine carotenoids. Forum of Nutrition, 61, 136–146. https://doi.org/10.1159/000212746
Miyashita, K., Mikami, N., & Hosokawa, M. (2013). Chemical and nutritional characteristics of brown seaweed lipids: A review. Journal of Functional Foods, 5(4), 1507–1517. https://doi.org/10.1016/j.jff.2013.09.019
Mohd Fauziee, N. A., Chang, L. S., Wan Mustapha, W. A., Md Nor, A. R., & Lim, S. J. (2021). Functional polysaccharides of fucoidan, laminaran and alginate from Malaysian brown seaweeds (Sargassum polycystum, Turbinaria ornata and Padina boryana). International Journal of Biological Macromolecules, 167, 1135–1145. https://doi.org/10.1016/j.ijbiomac.2020.11.067
Morgan, K. C., Wright, J. L., & Simpson, F. J. (1980). Review of chemical constituents of the red alga Palmaria palmata (dulse). Economic Botany, 34(1), 27–50. https://doi.org/10.1007/BF02859553
Mu, J., Hirayama, M., Sato, Y., Morimoto, K., & Hori, K. (2017). A novel high-mannose specific lectin from the green alga Halimeda renschii exhibits a potent anti-influenza virus activity through high-affinity binding to the viral hemagglutinin. Marine Drugs, 15(8), 255. https://doi.org/10.3390/md15080255
Murata, M., & Nakazoe, J. I. (2001). Production and use of marine aIgae in Japan. Japan Agricultural Research Quarterly: JARQ, 35(4), 281–290. https://doi.org/10.6090/jarq.35.281
Namvar, F., Mohamed, S., Fard, S. G., Behravan, J., Mustapha, N. M., Alitheen, N. B. M., & Othman, F. (2012). Polyphenol-rich seaweed (Eucheuma cottonii) extract suppresses breast tumour via hormone modulation and apoptosis induction. Food Chemistry, 130(2), 376–382. https://doi.org/10.1016/j.foodchem.2011.07.054
Neumann, U., Derwenskus, F., Flaiz Flister, V., Schmid-Staiger, U., Hirth, T., & Bischoff, S. C. (2019). Fucoxanthin, a carotenoid derived from Phaeodactylum tricornutum exerts antiproliferative and antioxidant activities In vitro. Antioxidants (basel, Switzerland), 8(6), 183. https://doi.org/10.3390/antiox8060183
Nwoba, E. G., Moheimani, N. R., Ubi, B. E., Ogbonna, J. C., & Huisman, J. M. (2016). Macroalgae culture to treat anaerobic digestion piggery effluent (adpe). Bioresource Technology, 227, 15–23. https://doi.org/10.1016/j.biortech.2016.12.044
Olsen, E. K., Hansen, E., Isaksson, J., & Andersen, J. H. (2013). Cellular antioxidant effect of four bromophenols from the red algae. Vertebrata Lanosa. Marine Drugs, 11(8), 2769–2784. https://doi.org/10.3390/md11082769
Ouyang, Y., Liu, D., Zhang, L., Li, X., Chen, X., & Zhao, C. (2022). Green alga Enteromorpha prolifera oligosaccharide ameliorates ageing and hyperglycemia through gut-brain axis in age-matched diabetic mice. Molecular Nutrition & Food Research, 66(4), e2100564. https://doi.org/10.1002/mnfr.202100564
Palanisamy, S., Vinosha, M., Manikandakrishnan, M., Anjali, R., Rajasekar, P., Marudhupandi, T., Manikandan, R., Vaseeharan, B., & Prabhu, N. M. (2018). Investigation of antioxidant and anticancer potential of fucoidan from Sargassum polycystum. International Journal of Biological Macromolecules, 116, 151–161. https://doi.org/10.1016/j.ijbiomac.2018.04.163
Pallela, R., & Kim, S. K. (2011). Impact of marine micro- and macroalgal consumption on photoprotection. Advances in Food and Nutrition Research, 64, 287–295. https://doi.org/10.1016/B978-0-12-387669-0.00023-5
Pan, Q., Chen, M., Li, J., Wu, Y., Zhen, C., & Liang, B. (2013). Antitumor function and mechanism of phycoerythrin from Porphyra haitanensis. Biological Research, 46(1), 87–95. https://doi.org/10.4067/S0716-97602013000100013
Pantidos, N., Boath, A., Lund, V., Conner, S., & McDougall, G. J. (2014). Phenolic-rich extracts from the edible seaweed, ascophyllum nodosum, inhibit α-amylase and α-glucosidase: Potential anti-hyperglycemic effects. Journal of Functional Foods, 10, 201–209. https://doi.org/10.1016/j.jff.2014.06.018
Pape, M., Grua-Priol, J., Prost, C., & Demaimay, M. (2004). Optimization of dynamic headspace extraction of the edible red algae Palmaria palmata and identification of the volatile components. Journal of Agricultural & Food Chemistry, 52(3), 550–556. https://doi.org/10.1021/jf030478x
Park, H. Y., Han, M. H., Park, C., Jin, C. Y., Kim, G. Y., Choi, I. W., Kim, N. D., Nam, T. J., Kwon, T. K., & Choi, Y. H. (2011). Anti-inflammatory effects of fucoidan through inhibition of NF-κB, MAPK and Akt activation in lipopolysaccharide-induced BV2 microglia cells. Food and Chemical Toxicology, 49(8), 1745–1752. https://doi.org/10.1016/j.fct.2011.04.020
Paudel, P., Seong, S. H., Zhou, Y., Park, H. J., Jung, H. A., & Choi, J. S. (2019). Anti-alzheimer’s disease activity of bromophenols from a red alga, Symphyocladia latiuscula (Harvey) Yamada. ACS Omega, 4(7), 12259–12270. https://doi.org/10.1021/acsomega.9b01557
Peltomaa, E., Johnson, M. D., & Taipale, S. J. (2017). Marine cryptophytes are great sources of EPA and DHA. Marine Drugs, 16(1), 3. https://doi.org/10.3390/md16010003
Pérez, M. J., Falqué, E., & Domínguez, H. (2016). Antimicrobial action of compounds from marine seaweed. Marine Drugs, 14(3), 52. https://doi.org/10.3390/md14030052
Pradhan, B., Nayak, R., Patra, S., Jit, B. P., Ragusa, A., & Jena, M. (2020a). Bioactive metabolites from marine algae as potent pharmacophores against oxidative stress-associated human diseases: A comprehensive review. Molecules, 26(1), 37. https://doi.org/10.3390/molecules26010037
Pradhan, B., Patra, S., Nayak, R., Behera, C., Dash, S. R., Nayak, S., Sahu, B. B., Bhutia, S. K., & Jena, M. (2020b). Multifunctional role of fucoidan, sulfated polysaccharides in human health and disease: A journey under the sea in pursuit of potent therapeutic agents. International Journal of Biological Macromolecules, 164, 4263–4278. https://doi.org/10.1016/j.ijbiomac.2020.09.019
Fernando, P. S., & I., Kim, K. N., Kim, D., & Jeon, Y. J. (2019). Algal polysaccharides: Potential bioactive substances for cosmeceutical applications. Critical Reviews in Biotechnology, 39(1), 99–113. https://doi.org/10.1080/07388551.2018.1503995
Puspita, M., Déniel, M., Widowati, I., Radjasa, O. K., Douzenel, P., Marty, C., Vandanjon, L., Bedoux, G., & Bourgougnon, N. (2017). Total phenolic content and biological activities of enzymatic extracts from Sargassum muticum (Yendo) fensholt. Journal of Applied Phycology, 29(5), 2521–2537. https://doi.org/10.1007/s10811-017-1086-6
Ramluckan, K., Moodley, K. G., & Bux, F. (2014). An evaluation of the efficacy of using selected solvents for the extraction of lipids from algal biomass by the soxhlet extraction method. Fuel, 116, 103–108. https://doi.org/10.1016/j.fuel.2013.07.118
Reed, R. H., Davison, I. R., Chudek, J. A., & Foster, R. (1985). The osmotic role of mannitol in the Phaeophyta: An appraisal. Phycologia, 24(1), 35–47. https://doi.org/10.2216/i0031-8884-24-1-35.1
Régnier, P., Bastias, J., Rodriguez-Ruiz, V., Caballero-Casero, N., Caballo, C., Sicilia, D., Fuentes, A., Maire, M., Crepin, M., Letourneur, D., Gueguen, V., Rubio, S., & Pavon-Djavid, G. (2015). Astaxanthin from Haematococcus pluvialis prevents oxidative stress on human endothelial cells without toxicity. Marine Drugs, 13(5), 2857–2874. https://doi.org/10.3390/md13052857
Reighard, T. S., & Olesik, S. V. (1996). Bridging the gap between supercritical fluid extraction and liquid extraction techniques: Alternative approaches to the extraction of solid and liquid environmental matrices. Critical Reviews in Analytical Chemistry, 26(2–3), 61–99. https://doi.org/10.1080/10408349608050568
Ribeiro, N. A., Abreu, T. M., Chaves, H. V., Bezerra, M. M., Monteiro, H. S., Jorge, R. J., & Benevides, N. M. (2014). Sulfated polysaccharides isolated from the green seaweed Caulerpa racemosa plays antinociceptive and anti-inflammatory activities in a way dependent on HO-1 pathway activation. Inflammation Research, 63(7), 569–580. https://doi.org/10.1007/s00011-014-0728-2
Rodríguez-Luna, A., Ávila-Román, J., González-Rodríguez, M. L., Cózar, M. J., Rabasco, A. M., Motilva, V., & Talero, E. (2018). Fucoxanthin-containing cream prevents epidermal hyperplasia and UVB-induced skin erythema in mice. Marine Drugs, 16(10), 378. https://doi.org/10.3390/md16100378
Ruiz Rodríguez, L. G., Aller, K., Bru, E., De Vuyst, L., Hébert, E. M., & Mozzi, F. (2017). Enhanced mannitol biosynthesis by the fruit origin strain Fructobacillus tropaeoli CRL 2034. Applied Microbiology and Biotechnology, 101(15), 6165–6177. https://doi.org/10.1007/s00253-017-8395-1
Ruqqia, -, Sohail, N., Taj, D., Sarwar, G., Sultana, V., Ara, J., & Haque, S. E. (2020). Hypolipidemic potential of sterol containing fractions of Jolyna laminarioides: A brown alga. Pakistan Journal of Pharmaceutical Sciences, 33(1), 169–174.
Ruxton, C., Reed, S., Simpson, M., & Millington, K. (2007). The health benefits of omega-3 polyunsaturated fatty acids: A review of the evidence. Journal of Human Nutrition and Dietetics, 20(3), 275–285. https://doi.org/10.1111/j.1365-277X.2007.00770.x
Sato, M., Hosokawa, T., Yamaguchi, T., Nakano, T., Muramoto, K., Kahara, T., Funayama, K., Kobayashi, A., & Nakano, T. (2002). Angiotensin I-converting enzyme inhibitory peptides derived from wakame (Undaria pinnatifida) and their antihypertensive effect in spontaneously hypertensive rats. Journal of Agricultural and Food Chemistry, 50(21), 6245–6252. https://doi.org/10.1021/jf020482t
Schepers, M., Martens, N., Tiane, A., Vanbrabant, K., Liu, H. B., Lütjohann, D., Mulder, M., & Vanmierlo, T. (2020). Edible seaweed-derived constituents: An undisclosed source of neuroprotective compounds. Neural Regeneration Research, 15(5), 790–795. https://doi.org/10.4103/1673-5374.268894
Sebök, S., Herppich, W. B., & Hanelt, D. (2017). Development of an innovative ring-shaped cultivation system for a land-based cultivation of marine macroalgae. Aquacultural Engineering, 77, 33–41. https://doi.org/10.1016/j.aquaeng.2017.01.005
Seca, A., & Pinto, D. (2018). Overview on the antihypertensive and anti-obesity effects of secondary metabolites from seaweeds. Marine Drugs, 16(7), 237. https://doi.org/10.3390/md16070237
Shannon, E., Conlon, M., & Hayes, M. (2021). Seaweed components as potential modulators of the gut microbiota. Marine Drugs, 19(7), 358. https://doi.org/10.3390/md19070358
Shen, H. Y., Li, L. Z., Xue, K. C., Hu, D. D., & Gao, Y. J. (2017). Antitumor activity of fucoidan in anaplastic thyroid cancer via apoptosis and anti-angiogenesis. Molecular Medicine Reports, 15(5), 2620–2624. https://doi.org/10.3892/mmr.2017.6338
Shin, E. S., Hwang, H. J., Kim, I. H., & Nam, T. J. (2011). A glycoprotein from Porphyra yezoensis produces anti-inflammatory effects in liposaccharide-stimulated macrophages via the TLR4 signaling pathway. International Journal of Molecular Medicine, 28(5), 809–815. https://doi.org/10.3892/ijmm.2011.729
Ślusarczyk, J., Adamska, E., & Czerwik-Marcinkowska, J. (2021). Fungi and algae as sources of medicinal and other biologically active compounds: A review. Nutrients, 13(9), 3178. https://doi.org/10.3390/nu13093178
Souza, C., Bezerra, W. P., & Souto, J. T. (2020). Marine alkaloids with anti-inflammatory activity: Current knowledge and future perspectives. Marine Drugs, 18(3), 147. https://doi.org/10.3390/md18030147
Suetsuna, K., Maekawa, K., & Chen, J. R. (2004). Antihypertensive effects of Undaria pinnatifida (wakame) peptide on blood pressure in spontaneously hypertensive rats. The Journal of Nutritional Biochemistry, 15(5), 267–272. https://doi.org/10.1016/j.jnutbio.2003.11.004
Suleria, H. A. R., Osborne, S., Masci, P., & Gobe, G. (2015). Marine-based nutraceuticals: An innovative trend in the food and supplement industries. Marine Drugs, 13(10), 6336–6351. https://doi.org/10.3390/md13106336
Sun, X., Duan, M., Liu, Y., Luo, T., Ma, N., Song, S., & Ai, C. (2018). The beneficial effects of Gracilaria lemaneiformis polysaccharides on obesity and the gut microbiota in high fat diet-fed mice. Journal of Functional Foods, 46, 48–56. https://doi.org/10.1016/j.jff.2018.04.041
Sun, Z., Mohamed, M., Park, S. Y., & Yi, T. H. (2015). Fucosterol protects cobalt chloride induced inflammation by the inhibition of hypoxia-inducible factor through PI3K/Akt pathway. International Immunopharmacology, 29(2), 642–647. https://doi.org/10.1016/j.intimp.2015.09.016
Suzuki, A., Saeki, T., Ikuji, H., Uchida, C., & Uchida, T. (2016). Brown algae polyphenol, a prolyl isomerase pin1 inhibitor, prevents obesity by inhibiting the differentiation of stem cells into adipocytes. PLoS ONE, 11(12), e0168830. https://doi.org/10.1371/journal.pone.0168830
Tamama, K. (2021). Potential benefits of dietary seaweeds as protection against COVID-19. Nutrition Reviews, 79(7), 814–823. https://doi.org/10.1093/nutrit/nuaa126
Tanaka, K., Yamada, A., Noda, K., Hasegawa, T., Okuda, M., Shoyama, Y., & Nomoto, K. (1998). A novel glycoprotein obtained from Chlorella vulgaris strain CK22 shows antimetastatic immunopotentiation. Cancer Immunology, Immunotherapy: CII, 45(6), 313–320. https://doi.org/10.1007/s002620050448
Tanzi, C. D., Vian, M. A., & Chemat, F. (2013). New procedure for extraction of algal lipids from wet biomass: A green clean and scalable process. Bioresource Technology, 134, 271–275. https://doi.org/10.1016/j.biortech.2013.01.168
Tseng, C. K. (2001). Algal biotechnology industries and research activities in China. Journal of Applied Phycology, 13(4), 375–380. https://doi.org/10.1023/A:1017972812576
Tzachor, A. (2019). The future of feed: Integrating technologies to decouple feed production from environmental impacts. Industrial Biotechnology, 15(2), 52–62. https://doi.org/10.1089/ind.2019.29162.atz
Um, M. Y., Lim, D. W., Son, H. J., Cho, S., & Lee, C. (2018). Phlorotannin-rich fraction from Ishige foliacea brown seaweed prevents the scopolamine-induced memory impairment via regulation of ERK-CREB-BDNF pathway. Journal of Functional Foods, 40, 110–116. https://doi.org/10.1016/j.jff.2017.10.014
Ummat, V., Sivagnanam, S. V., Rajauria, G., O’Donnell, C., & Tiwari, B. K. (2021). Advances in pre-treatment techniques and green extraction technologies for bioactives from seaweeds. Trends in Food Science & Technology, 110, 90–106. https://doi.org/10.1016/j.tifs.2021.01.018
Van Ginneken, V. J., Helsper, J. P., De Visser, W., Van Keulen, H., & Brandenburg, W. A. (2011). Polyunsaturated fatty acids in various macroalgal species from North Atlantic and tropical seas. Lipids in Health and Disease, 10, 104. https://doi.org/10.1186/1476-511X-10-104
Vijayaraghavan, K., & Joshi, U. M. (2015). Application of seaweed as substrate additive in green roofs: Enhancement of water retention and sorption capacity. Landscape and Urban Planning, 143, 25–32. https://doi.org/10.1016/j.landurbplan.2015.06.006
Wan, X., Li, X., Liu, D., Gao, X., Chen, Y., Chen, Z., Fu, C., Lin, L., Liu, B., & Zhao, C. (2021). Physicochemical characterization and antioxidant effects of green microalga Chlorella pyrenoidosa polysaccharide by regulation of microRNAs and gut microbiota in Caenorhabditis elegans. International Journal of Biological Macromolecules, 168, 152–162. https://doi.org/10.1016/j.ijbiomac.2020.12.010
Wang, L., Kim, H. S., Oh, J. Y., Je, J. G., Jeon, Y. J., & Ryu, B. (2020a). Protective effect of diphlorethohydroxycarmalol isolated from Ishige okamurae against UVB-induced damage in vitro in human dermal fibroblasts and in vivo in zebrafish. Food and Chemical Toxicology, 136, 110963. https://doi.org/10.1016/j.fct.2019.110963
Wang, M., Chen, L., & Zhang, Z. (2021). Potential applications of alginate oligosaccharides for biomedicine - A mini review. Carbohydrate Polymers, 271, 118408. https://doi.org/10.1016/j.carbpol.2021.118408
Wang, R., Paul, V. J., & Luesch, H. (2013a). Seaweed extracts and unsaturated fatty acid constituents from the green alga Ulva lactuca as activators of the cytoprotective Nrf2-ARE pathway. Free Radical Biology & Medicine, 57, 141–153. https://doi.org/10.1016/j.freeradbiomed.2012.12.019
Wang, S., Wang, W., Hou, L., Qin, L., He, M., Li, W., & Mao, W. (2020b). A sulfated glucuronorhamnan from the green seaweed Monostroma nitidum: Characteristics of its structure and antiviral activity. Carbohydrate Polymers, 227, 115280. https://doi.org/10.1016/j.carbpol.2019.115280
Wang, X., Liu, F., Gao, Y., Xue, C. H., Li, R. W., & Tang, Q. J. (2018). Transcriptome analysis revealed anti-obesity effects of the Sodium alginate in high-fat diet-induced obese mice. International Journal of Biological Macromolecules, 115, 861–870. https://doi.org/10.1016/j.ijbiomac.2018.04.042
Wang, X., Zhang, Z., Yao, Z., Zhao, M., & Qi, H. (2013b). Sulfation, anticoagulant and antioxidant activities of polysaccharide from green algae Enteromorpha linza. International Journal of Biological Macromolecules, 58, 225–230. https://doi.org/10.1016/j.ijbiomac.2013.04.005
Wang, X., Zhang, Z., Zhou, H., Sun, X., Chen, X., & Xu, N. (2019). The anti-aging effects of Gracilaria lemaneiformis polysaccharide in Caenorhabditis elegans. International Journal of Biological Macromolecules, 140, 600–604. https://doi.org/10.1016/j.ijbiomac.2019.08.186
Wassie, T., Niu, K., Xie, C., Wang, H., & Xin, W. (2021). Extraction techniques, biological activities and health benefits of marine algae Enteromorpha prolifera polysaccharide. Frontiers in Nutrition, 8, 747928. https://doi.org/10.3389/fnut.2021.747928
Wei, J., Zhao, Y., Zhou, C., Zhao, Q., Zhong, H., Zhu, X., Fu, T., Pan, L., Shang, Q., & Yu, G. (2021). Dietary polysaccharide from Enteromorpha clathrata attenuates obesity and increases the intestinal abundance of butyrate-producing bacterium, Eubacterium xylanophilum, in mice fed a high-fat diet. Polymers, 13(19), 3286. https://doi.org/10.3390/polym13193286
Wijesinghe, W. A. J. P., & Jeon, Y. J. (2012). Biological activities and potential industrial applications of fucose rich sulfated polysaccharides and fucoidans isolated from brown seaweeds: A review. Carbohydrate Polymers, 88(1), 13–20. https://doi.org/10.1016/j.carbpol.2011.12.029
Woertz, I., Feffer, A., Lundquist, T., & Nelson, Y. (2009). Algae grown on dairy and municipal wastewater for simultaneous nutrient removal and lipid production for biofuel feedstock. Journal of Environmental Engineering, 135(11), 1115–1122. https://doi.org/10.1061/(asce)ee.1943-7870.0000129
Wu, D., Chen, Y., Wan, X., Liu, D., & Zhao, C. (2020). Structural characterization and hypoglycemic effect of green alga Ulva lactuca oligosaccharide by regulating micrornas in Caenorhabditis elegans. Algal Research, 51, 102083. https://doi.org/10.1016/j.algal.2020.102083
Wu, G. J., Shiu, S. M., Hsieh, M. C., & Tsai, G. J. (2016a). Anti-inflammatory activity of a sulfated polysaccharide from the brown alga Sargassum cristaefolium. Food Hydrocolloids, 53, 16–23. https://doi.org/10.1016/j.foodhyd.2015.01.019
Wu, M., Tong, C., Wu, Y., Liu, S., & Li, W. (2016b). A novel thyroglobulin-binding lectin from the brown alga Hizikia fusiformis and its antioxidant activities. Food Chemistry, 201, 7–13. https://doi.org/10.1016/j.foodchem.2016.01.061
Yan, X., Yang, C., Lin, G., Chen, Y., Miao, S., Liu, B., & Zhao, C. (2019). Antidiabetic potential of green seaweed Enteromorpha prolifera flavonoids regulating insulin signaling pathway and gut microbiota in type 2 diabetic mice. Journal of Food Science, 84(1), 165–173. https://doi.org/10.1111/1750-3841.14415
Yang, C. F., Lai, S. S., Chen, Y. H., Liu, D., Liu, B., Ai, C., Wan, X. Z., Gao, L. Y., Chen, X. H., & Zhao, C. (2019). Anti-diabetic effect of oligosaccharides from seaweed Sargassum confusum via JNK-IRS1/PI3K signalling pathways and regulation of gut microbiota. Food and Chemical Toxicology, 131, 110562. https://doi.org/10.1016/j.fct.2019.110562
Yang, F., Shi, Y., Sheng, J., & Hu, Q. (2006). In vivo immunomodulatory activity of polysaccharides derived from Chlorella pyrenoidosa. European Food Research and Technology, 224(2), 225–228. https://doi.org/10.1007/s00217-006-0315-z
Yende, S. R., Harle, U. N., & Chaugule, B. B. (2014). Therapeutic potential and health benefits of Sargassum species. Pharmacognosy Reviews, 8(15), 1–7. https://doi.org/10.4103/0973-7847.125514
Yu, B., Bi, D., Yao, L., Li, T., Gu, L., Xu, H., Li, X., Li, H., Hu, Z., & Xu, X. (2020). The inhibitory activity of alginate against allergic reactions in an ovalbumin-induced mouse model. Food & Function, 11(3), 2704–2713. https://doi.org/10.1039/d0fo00170h
Yun, E. J., Yu, S., Kim, Y. A., Liu, J. J., Kang, N. J., Jin, Y. S., & Kim, K. H. (2021). In vitro prebiotic and anti-colon cancer activities of agar-derived sugars from red seaweeds. Marine Drugs, 19(4), 213. https://doi.org/10.3390/md19040213
Zhang, L., Wang, H., Fan, Y., Gao, Y., Li, X., Hu, Z., Ding, K., Wang, Y., & Wang, X. (2017). Fucoxanthin provides neuroprotection in models of traumatic brain injury via the Nrf2-ARE and Nrf2-autophagy pathways. Scientific Reports, 7, 46763. https://doi.org/10.1038/srep46763
Zhang, Q., Fan, X. Y., Guo, W. L., Cao, Y. J., Lin, Y. C., Cheng, W. J., & Lv, X. C. (2020). The protective mechanisms of macroalgae Laminaria japonica consumption against lipid metabolism disorders in high-fat diet-induced hyperlipidemic rats. Food & Function, 11(4), 3256–3270. https://doi.org/10.1039/d0fo00065e
Zhao, C., Lin, G., Wu, D., Liu, D., You, L., Högger, P., Simal-Gandara, J., Wang, M., daCosta, J. G. M., Marunaka, Y., Daglia, M., Khan, H., Filosa, R., Wang, S., & Xiao, J. (2020). The algal polysaccharide ulvan suppresses growth of hepatoma cells. Food Frontiers, 1(1), 83–101. https://doi.org/10.1002/fft2.13
Zhao, C., Yang, C., Liu, B., Lin, L., Sarker, S. D., Nahar, L., Yu, H., Cao, H., & Xiao, J. (2018). Bioactive compounds from marine macroalgae and their hypoglycemic benefits. Trends in Food Science & Technology, 72, 1–12. https://doi.org/10.1016/j.tifs.2017.12.001
Zhao, D., Zheng, L., Qi, L., Wang, S., Guan, L., Xia, Y., & Cai, J. (2016). Structural features and potent antidepressant effects of total sterols and β-sitosterol extracted from Sargassum horneri. Marine Drugs, 14(7), 123. https://doi.org/10.3390/md14070123
Zheng, J., Manabe, Y., & Sugawara, T. (2020a). Siphonaxanthin, a carotenoid from green algae Codium cylindricum, protects Ob/Ob mice fed on a high-fat diet against lipotoxicity by ameliorating somatic stresses and restoring anti-oxidative capacity. Nutrition Research, 77, 29–42. https://doi.org/10.1016/j.nutres.2020.02.001
Zheng, L. X., Chen, X. Q., & Cheong, K. L. (2020b). Current trends in marine algae polysaccharides: The digestive tract, microbial catabolism, and prebiotic potential. International Journal of Biological Macromolecules, 151, 344–354. https://doi.org/10.1016/j.ijbiomac.2020.02.168
Zhong, Q. W., Zhou, T. S., Qiu, W. H., Wang, Y. K., Xu, Q. L., Ke, S. Z., Wang, S. J., Jin, W. H., Chen, J. W., Zhang, H. W., Wei, B., & Wang, H. (2021). Characterization and hypoglycemic effects of sulfated polysaccharides derived from brown seaweed Undaria pinnatifida. Food Chemistry, 341(Pt 1), 128148. https://doi.org/10.1016/j.foodchem.2020.128148
Zubia, M., Freile-Pelegrín, Y., & Robledo, D. (2014). Photosynthesis, pigment composition and antioxidant defences in the red alga Gracilariopsis tenuifrons (Gracilariales, Rhodophyta) under environmental stress. Journal of Applied Phycology, 26(5), 2001–2010. https://doi.org/10.1007/s10811-014-0325-3
Bereczki, D., Fekete, I., Prado, G. F., & Liu, M. (2007). Mannitol for acute stroke. The Cochrane Database of Systematic Reviews, 2007(3), CD001153. https://doi.org/10.1002/14651858.CD001153.pub2.
Billakanti, J. M.. (2012). Extraction of fucoxanthin from Undaria pinnatifida using enzymatic pre-treatment followed by DME & EtoH co-solvent extraction. International Symposium on Supercritical Fluids.1316.
Cai et al., 2021 J Cai A Lovatelli J Aguilar-Manjarrez L Cornish L Dabbadie A Desrochers X Yuan 2021 Seaweeds and microalgae: An overview for unlocking their potential in global aquaculture development FAO Fisheries and Aquaculture Circular 1229
Cha, S. H., Ahn, G. N., Heo, S. J., Kim, K. N., & Jeon, Y. J.. (2006). Screening of extracts from marine green and brown algae in jeju for potential marine angiotensin-i converting enzyme (ace) inhibitory activity. Journal of the Korean Society of Food Science & Nutrition, 35(3). https://doi.org/10.3746/jkfn.2006.35.3.307.
Chen, L., Chen, P., Liu, J., Hu, C., Yang, S., He, D., ... Zhang, X. (2018a). Sargassum fusiforme polysaccharide SFP-F2 activates the NF-κB signaling pathway via CD14/IKK and P38 axes in RAW264.7 cells. Marine Drugs, 16(8), 264. https://doi.org/10.3390/md16080264.
Cherry, P., O’Hara, C., Magee, P. J., McSorley, E. M., & Allsopp, P. J. (2019). Risks and benefits of consuming edible seaweeds. Nutrition Reviews, 77(5), 307–329. https://doi.org/10.1093/nutrit/nuy066.
FAO. (2021). The State of World Fisheries and Aquaculture 2021 (SOFIA).
García-Poza, S., Leandro, A., Cotas, C., Cotas, J., Marques, J. C., Pereira, L., & Gonçalves, A. (2020). The evolution road of seaweed aquaculture: cultivation technologies and the industry 4.0. International Journal of Environmental Research and Public Health, 17(18), 6528. https://doi.org/10.3390/ijerph17186528.
Gwon, W. G., Lee, M. S., Kim, J. S., Kim, J. I., Lim, C. W., Kim, N. G., & Kim, H. R. (2013). Hexane fraction from Sargassum fulvellum inhibits lipopolysaccharide-induced inducible nitric oxide synthase expression in RAW 264.7 cells via NF-κB pathways. The American Journal of Chinese Medicine, 41(3), 565–584. https://doi.org/10.1142/S0192415X13500407.
Hardoko, H., Febriani, A., & Siratantri, T. (2015). Invitro antidiabetic activities of agar, agarosa, and agaropectin from Gracilaria gigas seaweed. Jurnal Pengolahan Hasil Perikanan Indonesia, 18(2).
Hossain, M. B., Ba Rry-Ryan, C., Martin-Diana, A. B., & Brunton, N. P.. (2011). Optimisation of accelerated solvent extraction of antioxidant compounds from rosemary (Rosmarinus officinalis L.), marjoram (Origanum majorana L.) and oregano (Origanum vulgare L.) using response surface methodology. Food Chemistry, 126(1), 339–346. https://doi.org/10.1016/j.foodchem.2010.10.076.
Hu, L. B., Li, H. B., Sun, J. L., & Zeng, J. (2012). Effect of laminarin on Aspergillus flavus growth and aflatoxin production. In Advanced Materials Research (Vol. 343, pp. 1168–1171). Trans Tech Publications Ltd. https://doi.org/10.4028/www.scientific.net/AMR.343-344.1168.
Huang, P., Hong, J., Mi, J., Sun, B., Zhang, J., Li, C., & Yang, W. (2022). Polyphenols extracted from Enteromorpha clathrata alleviates inflammation in lipopolysaccharide-induced RAW 264.7 cells by inhibiting the MAPKs/NF-κB signaling pathways. Journal of Ethnopharmacology, 286, 114897. https://doi.org/10.1016/j.jep.2021.114897.
Jazzara, M., Ghannam, A., Soukkarieh, C., & Murad, H. (2016). Anti-Proliferative activity of λ-carrageenan through the induction of apoptosis in human breast cancer cells. Iranian Journal of Cancer Prevention, 9(4), e3836. https://doi.org/10.17795/ijcp-3836.
Ji, H. K., Lee, J. O., Ji, W. M., Kang, M. J., & Kim, H. S.. (2020). Laminarin from salicornia herbacea stimulates glucose uptake through ampk-p38 mapk pathways in l6 muscle cells. Natural Product Communications, 15(3), 1934578X2090140. https://doi.org/10.1177/1934578X20901409.
Jiang, P., Meng, J., Zhang, L., Huang, L., Wei, L., Bai, Y., Liu, X., & Li, S. (2021). Purification and anti-inflammatory effect of selenium-containing protein fraction from selenium-enriched Spirulina platensis. Food Bioscience, 45, 101469https://doi.org/10.1016/j.fbio.2021.101469.
Jing, R., Guo, K., Zhong, Y., Wang, L., Zhao, J., Gao, B., Ye, Z., Chen, Y., Li, X., Xu, N., & Xuan, X. (2021). Protective effects of fucoidan purified from Undaria pinnatifida against UV-irradiated skin photoaging. Annals of Translational Medicine, 9(14), 1185. https://doi.org/10.21037/atm-21-3668.
Joannes, C., Sipaut, S., Dayou, J., Yasir, S. M., & Mansa, F. (2015). The potential of using pulsed electric field (pef) technology as the cell disruption method to extract lipid from microalgae for biodiesel production. International Journal of Renewable Energy Research, 5(2), 598–621
Kite-Powell, J. (2018). See how algae could change our world. Forbes. June 15.
Lee, J. Y., Kim, Y. J., Kim, H. J., Kim, Y. S., & Park, W. (2012). Immunostimulatory effect of laminarin on RAW 264.7 mouse macrophages. Molecules (Basel, Switzerland), 17(5), 5404–5411. https://doi.org/10.3390/molecules17055404.
Leone, G. P., Balducchi, R., Mehariya, S., Martino, M., Larocca, V., Di Sanzo, G., Iovine, A., Casella, P., Marino, T., Karatza, D., Chianese, S., Musmarra, D., & Molino, A. (2019). Selective extraction of ω-3 fatty acids from Nannochloropsis sp. using supercritical CO2 extraction. Molecules, 24(13), 2406. https://doi.org/10.3390/molecules24132406.
Lewitus et al., 2012 AJ Lewitus RA Horner DA Caron E Garcia-Mendoza JF Tweddle 2012 Harmful algal blooms along the north American west coast region: History, trends, causes, and impacts Harmful Algae 19
Ma, Y., Ye, X., Wu, H., Zhou, Z., Wang, H., & Sun, Z. (2010). Advances in ultrasound-assisted extraction of bioactive compounds from plants. Food Science.
Nguyen, T. T., MD Mikkelsen, Tran, V., Trang, V., & Meyer, A. S. (2020). Enzyme-assisted fucoidan extraction from brown macroalgae Fucus distichus subsp. evanescens and saccharina latissima. Marine Drugs, 18(6), 296. https://doi.org/10.3390/md18060296.
Pangestuti and Kim, 2013 R Pangestuti SK Kim 2013 Marine bioactive peptide sources: Critical points and the potential for new therapeutics Marine Proteins and Peptides: Biological Activities and Applications 533–544
Paulert, R. , Talamini, V. , Cassolato, J. E. F. , Duarte, M. E. R. , Noseda, M. D. , & Smania, A. , et al. (2009). Effects of sulfated polysaccharide and alcoholic extracts from green seaweed Ulva fasciataon anthracnose severity and growth of common bean (Phaseolus vulgaris L.). Journal of Plant Diseases & Protection, 116(6), 263–270. https://doi.org/10.1007/BF03356321.
Qin, Y. (2018). Applications of bioactive seaweed substances in functional food products. In bioactive seaweeds for food applications (pp. 111–134). Academic Press. https://doi.org/10.1016/B978-0-12-813312-5.00006-6.
Sanjeewa, K. A., Jayawardena, T. U., Kim, H. S., Kim, S. Y., Ahn, G., Kim, H. J., ... & Jeon, Y. J. (2019). Ethanol extract separated from Sargassum horneri (Turner) abate LPS-induced inflammation in RAW 264.7 macrophages. Fisheries and Aquatic Sciences, 22(1), 1–10. https://doi.org/10.1186/s41240-019-0121-8.
Senthilkumar, K., Ramajayam, G., Venkatesan, J., Kim, S. K., & Ahn, B. C. (2017). Biomedical applications of fucoidan, seaweed polysaccharides. In Seaweed Polysaccharides (pp. 269–281). Elsevier. https://doi.org/10.1016/B978-0-12-809816-5.00014-1.
Surin, S., You, S., Seesuriyachan, P., Muangrat, R., Wangtueai, S., Jambrak, A. R., Phongthai, S., Jantanasakulwong, K., Chaiyaso, T., & Phimolsiripol, Y. (2020). Optimization of ultrasonic-assisted extraction of polysaccharides from purple glutinous rice bran (Oryza sativa L.) and their antioxidant activities. Scientific Reports, 10(1), 10410. https://doi.org/10.1038/s41598-020-67266-1.
Turner, C., & Waldebäck, M. (2013). Principles of pressurized fluid extraction and environmental, food and agricultural applications. In Separation, Extraction and Concentration Processes in the Food, Beverage and Nutraceutical Industries (pp. 39–70). Woodhead Publishing. https://doi.org/10.1533/9780857090751.1.67.
Vilakazi, H., Olasehinde, T. A., & Olaniran, A. O. (2021). Chemical characterization, antiproliferative and antioxidant activities of polyunsaturated fatty acid-rich extracts from Chlorella sp. S14. Molecules, 26(14), 4109. https://doi.org/10.3390/molecules26144109.
Wijesinghe, W. A. J. P., & Wedamulla, N. E. (2019). Exploring the potential of using Micro-and macroalgae in cosmetics. In Handbook of Algal Technologies and Phytochemicals (pp. 149–159). CRC Press.
Yanai, H., Masui, Y., Katsuyama, H., Adachi, H., Kawaguchi, A., Hakoshima, M., Waragai, Y., Harigae, T., & Sako, A. (2018). An improvement of cardiovascular risk factors by omega-3 polyunsaturated fatty acids. Journal of Clinical Medicine Research, 10(4), 281–289. https://doi.org/10.14740/jocmr3362w.
Yoo, M. S., Shin, J. S., Choi, H. E., Cho, Y. W., Bang, M. H., Baek, N. I., & Lee, K. T. (2012). Fucosterol isolated from Undaria pinnatifida inhibits lipopolysaccharide-induced production of nitric oxide and pro-inflammatory cytokines via the inactivation of nuclear factor-κB and p38 mitogen-activated protein kinase in RAW264.7 macrophages. Food Chemistry, 135(3), 967–975. https://doi.org/10.1016/j.foodchem.2012.05.039.
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The authors would like to thank the reviewers and Journal Editor for thoughtful reading of the manuscript and constructive comments.
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This work was supported by Key Project of the Natural Science Foundation of Fujian Province (2020J02032) and Fujian ‘Young Eagle Program’ Youth Top Talent Program.
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Lizhu Zhang, Wei Liao, and Yajun Huang: Formal analysis, Investigation, Resources, Writing- Original Draft, Writing- Review & Editing, Visualization. Yuxi Wen & Yaoyao Chu: Writing- Review & Editing. Chao Zhao: Conceptualization, Resources, Writing- Review & Editing, Visualization, Supervision, Funding acquisition. All authors read and approved the final manuscript.
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Zhang, L., Liao, W., Huang, Y. et al. Global seaweed farming and processing in the past 20 years. Food Prod Process and Nutr 4, 23 (2022). https://doi.org/10.1186/s43014-022-00103-2
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DOI: https://doi.org/10.1186/s43014-022-00103-2