Open access peer-reviewed chapter

Nutraceuticals from Microbes of Marine Sources

Written By

Charu Gupta and Dhan Prakash

Submitted: 30 August 2018 Reviewed: 02 November 2018 Published: 29 October 2019

DOI: 10.5772/intechopen.82369

From the Edited Volume

Nutraceuticals - Past, Present and Future

Edited by María Chávarri Hueda

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Abstract

Therapeutic compounds can be derived from various natural sources like plants, animals, marine organisms, and microorganisms. Although the marine biota accounts for around 50% of the total world biodiversity, but their potential as a rich source of bioactive products and their applications in both pharmaceutical and nutraceutical industries have only recently been identified through several scientific studies. Marine biotechnology is an upcoming area that involves about the study of marine microorganisms and animals including algae, sponges, and coral as a novel source of bioactive substances that can be used in the treatment of various human diseases like cancer, anemia, diarrhea, obesity, diabetes, atopic dermatitis, Crohn’s disease, etc. They are also potential sources of natural antioxidants, colors, immuno-suppressants, enzyme inhibitors, hypocholesterolemic agents, vitamins, enzymes, and antibiotics. However, marine microorganisms have not yet been given the attention they deserve and a very limited scientific data is available on bioactive potential of marine microorganisms. There is still scope for a higher magnitude of research and investigation to explore the potential of both marine organisms and marine microorganisms as producers of novel drugs. This chapter deals with the exploitation of microbes from marine sources as potential sources for various nutraceuticals and their possibilities for applications in variety of diseases and as functional food supplement.

Keywords

  • microbes
  • nutraceuticals
  • marine organisms
  • functional food
  • bioactive compounds

1. Introduction

It is well-known that more than 70% of our planet’s surface is covered by oceans. Experts estimate that the biological diversity in marine environment is higher than in tropical rain forests. Marine water contains enormous amounts of biodiversity which makes it as a source of huge amounts and wide varieties of novel bioactive compounds. The majority of the marine microbiota is soft bodied and follows a sedentary life style, thus requiring the other means of defense systems mainly by producing certain biochemical compounds that are generally toxic to the other animals. These toxic substances also aid them in detecting their harmful predators, and help them to protect themselves from their competitors or they can even paralyze their enemies. The biodiversity of marine microflora is overwhelming and there is an urgent need to explore and exploit their potential as biotherapeutic agents. These biotherapeutic compounds are usually synthesized as secondary metabolites by the marine microflora and fauna. The disadvantage is that since these natural products are synthesized and released extracellularly into the water so they are rapidly diluted and, therefore, their potency should be very high to show any effect. It is well-known that a large number of novel bioactive natural compounds are found in the oceans, and deep sea possessing various biological properties that can be exploited for discovering various drugs with improved efficacy and action in the treatment of various human diseases like cancer, anemia, diarrhea, obesity, diabetes, atopic dermatitis, Crohn’s disease, etc. [1, 2].

The oceans are the source of a large group of structurally unique natural products that are mainly accumulated in invertebrates such as sponges, tunicates, bryozoans, and mollusks.

Macroalgae (or seaweed) are one of the most well-known types of algae used in the production of various nutraceuticals or dietary supplements. They are a rich source of valuable bioactive substances with both therapeutic and preventative effect. They have been used to develop a great variety of food and food ingredients, especially in Asian countries including Korea, Japan, and China. It is estimated that China and Indonesia are by far the largest seaweed producers with over 23 million tons of aggregated production in 2014 [3]. About 2400 natural products have been isolated from macroalgae belonging to the classes Rhodophyceae, Phaeophyceae, and Chlorophyceae [4]. Presently, seaweeds constitute commercially important marine renewable resources which are providing valuable ideas for the development of new drugs against diabetes, microbial infections, and inflammations [5]. Algal constituents include acids, alkaloids, amines, antibacterial, antifungal, antiviral substances, lipids, sterols, steroids, fatty acids, phenolic compounds, phytochromes, pigments, proteins, peptides, amino acids, sugar, alcohols, and vitamins. Gracilaria opuntia belongs to the family Rhodophyceae (Red algae) and possesses various biological activities.

The potential of marine microorganisms in producing various bioactive metabolites is due to their unique biochemical and physicochemical properties inherited by them in order to survive in extreme environmental conditions in the marine environment. These unique bioactive “bioceuticals” have tremendous potential for use as active pharmaceutical ingredient (API) and in food supplements to design various nutraceuticals [6].

Most of the bioactive compounds are having numerous biological activities which are found to act as nutraceuticals for humans and animals. Thus, the marine microflora contributes an important source of various bioactive constituents. Due to the great diversity of the marine flora, the chemistry of its associated bioactive compounds is also novel [7]. The marine flora includes a wide range of organisms from sponges, tunicates, bryozoans, mollusks to bacteria, microalgae, macroalgae, and cyanobacteria. The bioactive metabolites produced as a result of their metabolic activity is therefore effective in treatment of both infectious and non-infectious diseases.

Marine microflora including algae are widely used in the development of various nutraceuticals and are also used as food source or food ingredients [8]. Algae include both the micro- and macroforms and both the types are used as nutraceuticals. Microalgae are the most primitive and simply organized algae present in marine environment. They are the rich sources of various food nutrients and vitamins such as beta-carotene (vitamin A), vitamin C, E, H, B1, B2, B6, and B12, astaxanthin, polysaccharides, and polyunsaturated fatty acids [9]. These bioactive compounds are extracted from the microalgae and are used as food additives, fortifying infant milk, and other dietary supplements [10]. These compounds (especially the tunicate metabolite ET-743) have also shown good pharmacological properties and can be used to develop new drugs for cancer treatment. Some other compounds such as ziconotide obtained from the mollusk (Conus magus) are used as analgesics and anti-inflammatory. Natural products localized in symbiotic bacteria or cyanobacteria from marine invertebrates exhibits striking structural similarities with the known microbial metabolites; suggesting that bacteria and microalgae are involved in their biosynthesis and are the true sources of these metabolites. Nowadays, molecular techniques are used to study the microbial diversity in marine sponges and to study the involvement of bacteria in the biosynthesis of the bryostatins in the bryozoan Bugula neritina [2].

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2. Marine microorganisms as source of nutraceuticals

A study reported that some unidentified prokaryotic communities, such as the JS1 and DSAG groups, occur widely in organic rich deep marine sediments associated with methane hydrates along the Pacific Ocean margin. The microflora is present in deep marine sediments and their community structure is affected by the surrounding geochemical and geological settings. Various studies have shown that many classes of microorganisms exist only in the sea [11]. Thus, limited scientific data is available on the growth media and culture techniques for culturing these marine microbes.

Many pharmaceutical industries have not been able to fully utilize this important resource. There is a general belief that marine microorganisms are difficult to culture; however, now there are a number of reports that showed that these marine microorganisms can be successfully cultured [12]. Thus, now many of the developed and underdeveloped countries have shifted their research focus on the marine habitat and new marine-oriented projects are emerging worldwide. Majority of microbes belonging to class bacteria and fungi are now the target of biomedical study. The coastal bacterial samples that grow under saline conditions are a source of novel antibiotics, antitumor, and anti-inflammatory compounds [13]. The symbiotic microbial consortia have also been proven to be a rich source of bioactive compounds with pharmaceutical potential. Many bacteria and fungi have been sampled from the surfaces of marine plants and the internal tissues of invertebrates, and they have been found to be of increasing interest [14].

2.1 Marine bacteria

Marine bacteria are prolific producers of valuable secondary metabolites as they thrive in harsh oceanic climates. The marine isolate Pseudomonas, Gram-negative, γ-proteo-bacteria is not well explored and only a limited number have been reported as producers of bioactive compounds. A bacterium strain KMM 3042 that is aerobic, non-pigmented, produces some bioactive substances such as pyrroles, pseudopeptide pyrrolidinedione, phloroglucinol, phenazine, benzaldehyde, quinoline, quinolone, phenanthren, phthalate, andrimid, moiramides, zafrin, and bushrin [15]. Some of these bioactive compounds are antimicrobial agents, and dibutyl phthalate and di-(2-ethylhexyl) phthalate have been reported to be cathepsin-B inhibitors [16].

Stenotrophomonas strains isolated from sponge, sea urchin, and ophiura specimens showed remarkable antimicrobial and antifungal inhibitory activity. However, they showed negligible activity against Candida albicans, but these strains could substantially inhibit Gram-positive microorganisms. Though Stenotrophomonas maltophilia is an opportunistic pathogen, it also possesses biocontrolling capabilities [17]. Low molecular weight antimicrobial metabolites have also been reported from marine ark shell Anadara broughtoni associated heterotrophic bacteria (butanol extracts) that exhibit strong antimicrobial, hemolytic, and surface activities [18]. Another recently discovered genus of bioactive substance producing marine bacteria is Pseudoalteromonas, the seawater species P. phenolica was reported to inhibit methicillin-resistant Staphylococcus aureus (MRSA) strains due to the presence of a brominated biphenyl compound, 3,3″,5,5″-tetrabromo-2,2″-diphenyldiol [19]. Some strains of Pseudoalteromonas luteoviolacea have also been shown to inhibit the growth of protists [20]. Other marine invertebrates have also been shown to be a source of novel bioactive compound which was later identified as a tambjamine (4-methoxypyrrole-containing bioactive compounds) like alkaloid and re-designated as YP1 [21]. Pseudoalteromonas tunicate is associated with them and produces a yellow pigment that possesses antifungal activity [20, 22]. These tambjamines are also known to possess antimicrobial, antitumorigenic, immunosuppressive, antiproliferative, and ichthyo-deterrent activities [20]. There are other evidences that points toward the colonizing bacteria present at the surface of higher organisms as the source of these compounds [23]. These studies have been further proven by Burke and colleagues by elucidation of YP1 biosynthetic pathway in Pseudoalteromonas tunicata [24].

2.2 Marine-derived fungi

Marine fungi have been known to produce a wide variety of bioactive metabolites that possess anticancer, antibacterial, antiplasmodial, anti-inflammatory, and antiviral activity [25, 26]. This is due to the presence of some unique and exceptional carbon frameworks in them. These novel compounds are used as new lead structures for medicine and for plant protection. The detailed procedure for their isolation and cultivation from various marine organisms (sponges, algae, and mangrove plants) has been given by Kjer et al. [27]. They have also elucidated the structure of secondary metabolites produced by these fungi. A novel anthraquinone derivative with naphtho [1,2,3-de]chromene-2,7-dione skeleton was isolated from a marine filamentous fungus, Aspergillus glaucus in the Fujian province of China and named aspergiolide A [28]. It was found to exhibit cytotoxicity against K562 and P388 cell lines. Similarly, Penicillium sp., isolated from deep ocean sediment was found to exhibit antitumor activities in their alkaloid-rich extracts due to the presence of meleagrin D and E and roquefortine H and I. However, they exhibited weak cytotoxicity in comparison to the previously reported meleagrin B and meleagrin that functions by inducing HL-60 cell apoptosis and can also arrest the cell cycle through G2/M phase, respectively. The mode of action was the distinct substitutions on the imidazole ring that have a significant influence on the cytotoxicity of these alkaloids [29]. Some other novel compounds and metabolites were also isolated and characterized from marine fungi Ampelomyces sp. that possesses potent antimicrobial and antifouling compounds. The antilarvicidal effect was due to the presence of compound 3-chloro-2,5-dihydroxybenzyl alcohol that effectively inhibited larval settlement of the tubeworm Hydroides elegans and of cyprids of the barnacle Balanus amphitrite. The compound is non-toxic and is also a potent antifoulant and/or antibiotic agent [30]. Another example of marine-derived fungus Cladosporium sp. also exhibited antibiotic and antifouling activity. It was later named as strain F14. The fungus produced the bioactive compounds in nutrient enriched cultivation media, in the presence of glucose or xylose [31]. Another study reported the marine-derived fungus Fusarium sp. (strain 05JANF165) to possess novel antimitotic and antifungal activity from its ethanol extracts. This compound was later identified and named as Fusarielin E [32].

Another marine-derived fungus of the genus Pseudallescheria was reported to produce a novel antibacterial dioxopiperazine, dehydroxybisdethiobis-methylthio-gliotoxin from its broth. All three compounds exhibited potent antibacterial activity against the methicillin-resistant and multidrug-resistant Staphylococcus aureus, whereas Gliotoxin showed a significant radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) [33].

A marine isolate of the fungus Exophiala was also reported to exhibit a mild antibacterial activity against Staphylococcus aureus due to the presence of two novel antibacterial aspyrone derivatives, viz., Chlorohydroaspyrones A and B, and the previously described aspyrone, asperlactone, and penicillic acid from its broth [34].

Marine fungi also exhibited nematicidal effect along with antimicrobial activity. The same activity has also been reported from marine ascomycete Lachnum papyraceum (Karst.) [35].

Another marine-derived Phoma herbarum strain was reported with significant radical scavenging activity against DPPH due to the presence of halogenated benzoquinones (bromochlorogentisylquinones A and B) [36].

2.3 Marine-derived actinomycetes

Actinomycetes are well-known to be the producers of secondary metabolites. Many well-known antibiotics, such as streptomycin, erythromycin, and tetracycline, with potent biological activities are produced by them [37]. Many marine-derived actinomycetes were found to be the producers of novel antitumor [38], antimalarial [39], and antimicrobial compounds [40, 41]. Another marine-derived actinomycete namely Nocardiopsis lucentensis produced four novel 3-methyl-4-ethylideneproline-containing peptides called as Lucentamycins A-D from their fermentation broth [42]. Only compound Lucentamycins A and B exhibited strong in vitro cytotoxicity against HCT-116 human colon carcinoma [42]. In a similar study, marine-derived isolate of Streptomyces sp. were found to produce four new derivatives, Mansouramycin A-D, and the known 3-methyl-7-(methylamino)-5,8-isoquinolinedione from their ethyl acetate extract. These bioactive compounds, exhibited strong cytotoxicity with great degree of selectivity for non-small cell lung cancer, breast cancer, melanoma, and prostate cancer cells [43] suggesting their potential as anticancer drugs. Similarly, Perez and coworkers [44] isolated a macrodiolide Tartrolon D from the fermentation broths of Streptomyces sp. MDG-04-17-069. The isolated tartrolon was found to exhibit strong cytotoxic activity against three human tumor cell lines, viz., lung (A549), colon (HT29), and breast (MDA-MB-231) [44]. In yet another study, the secondary metabolites of a marine Saccharomonospora sp. yielded a novel alkaloid Lodopyridone, was found to be cytotoxic to HCT-116 human colon cancer cells [45].

Besides their antitumor and anticancerous potential, marine actinomycetes are also known for their antimicrobial activities also. A marine actinomycete, Marinispora was used to isolate a series of chlorinated bisindole pyrroles, Lynamicins A–E that exhibited a broad-spectrum antimicrobial activity against both the groups of Gram-positive and Gram-negative bacteria. These compounds were also effective against important drug-resistant pathogens, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium [41]. In a similar study, Carlson et al. [46] isolated the two novel bioactive compounds namely dienoyl tetramic acids tirandamycin C and D from the marine environmental isolate Streptomyces sp. These compounds were effective against vancomycin-resistant Enterococcus faecalis and are structurally similar to the previously identified compounds Tirandamycins A and B with a slight variation in the pattern of pendant oxygenation on the bicyclic ketal system.

Similarly, ethyl acetate extract of Streptomyces sp. isolate B8652 was used to isolate Trioxacarcins A, B, and C along with three new derivatives designated as Trioxacarcins D, E, and F [47]. These types of trioxacarcins exhibited good antimicrobial, antitumor, and antimalarial activity. Similarly, the crude extract of a marine Streptomyces strain that was isolated from deep sea sediments, exhibited potent antifouling activity [48].

In yet another study, a marine-derived Actinomyces strain (NPS554) that was isolated from Japan yielded two trialkyl-substituted aromatic acids, Lorneic acid A and B. It was observed that Lorneic acid-A had significant inhibition activity against phosphodiesterase (PDE)5 [49]. PDE5 inhibitors are of great pharmacological importance as they are used in erectile dysfunctions and pulmonary hypertension.

2.4 Marine-derived microalgae

Cyanobacteria are a diverse group of Gram-Negative bacteria, also known as blue-green algae that produce an array of secondary metabolites with antifungal, antiviral, antibiotic, and other properties. They also exhibit selective bioactivity against vertebrates, invertebrates, plants, microalgae, fungi, bacteria, viruses, and cell lines [50]. Thus, they are of great pharmaceutical value. Besides, there are other anticancer compounds, which were initially thought to be obtained from marine sources, are now known to be produced by cyanobacteria [51]. Ulithiacyclamide and Patellamide A belong to Cyanobactins, produced by cyanobacteria; possess potent antimalarial, antitumor, and multidrug reversing activities [52].

Some other examples of marine cyanobacterial bioactive natural products are viridamides A and B. It was observed that Viridamide A produced by a blackish-green, mat-forming, filamentous cyanobacterium Oscillatoria nigroviridis showed antitrypanosomal, and antileishmanial activity [53]. In yet another study, the crude extracts of four green marine algae (Cladophora rupestris, Codium fragile sp. tomentosoides, Ulva intestinalis, and Ulva lactuca) were found to exhibit antiprotozoal activity [54]. All the algal extracts were active against T. brucei rhodesiense, and exhibited potent leishmanicidal activity [54]. This study was reportedly the first study to show antiprotozoal activity of British marine algae. Further, Desbois et al. [55] isolated an antibacterial polyunsaturated fatty acid, eicosapentaenoic acid (EPA) from the marine diatom, Phaeodactylum tricornutum Bohlin, which showed activity against a range of both Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) [55].

Both micro- and macroalgae are used as nutraceuticals. Studies have shown that microalgae are rich sources of all the vital nutrients such as beta-carotene, vitamins C, A, E, H, B1, B2, B6, and B12, astaxanthin, polysaccharides, and polyunsaturated fatty acids [9]. Thus, their bioactive molecules are produced commercially for use as food additives, infant milk formulations, and dietary supplements [10].

Macroalgae, are also commonly known as seaweeds. They are the most popular type of algae in the nutraceutical industry and are used in a great variety of food and food ingredients, especially in Asian countries like Korea, Japan, and China. Macroalgae are also well-known for the production of agarose. They are also an important source of many bioactive metabolites and natural products that possess many nutritional and therapeutic functions. Some of the examples of bioactive constituents are proteins, furanone, polyunsaturated fatty acids (PUFA), L-α kainic acid, phenotics, pigments, phlorotannins, phyco-colloids (carrageenan and agar), and minerals. Likewise, red and brown seaweeds are also good sources of many vitamins, minerals, proteins, and essential fatty acids [56, 57]. They are also used to prepare bioactive peptides and to improve protein digestibility. Further, antihypertensive bioactive peptides have also been isolated that can act as angiotensin-converting enzyme (ACE) inhibitors [58].

2.5 Symbiotic interaction between marine microbes

Symbiosis is the mutual association between any two organisms for their mutual benefit that can be in terms of their nutritional needs or protection from prey. Research studies have shown that a variety of secondary metabolites are produced as a result of this association especially obtained from algae and invertebrates. Their associated microbes perform various biological activities [59]. Some of the various marine fungi isolated are Haliclona simulans, Agaricomycotina, Mucoromycotina, Saccharomycotina, and Pezizomycotina [60]. A variety of media were used for their isolation and identification and their antimicrobial activities were also determined. Some of these isolates exhibited antimicrobial activity against Escherichia coli, Bacillus sp., Staphylococcus aureus, and Candida glabrata [60]. It has been found that sponge-microbial association is a potential chemical and ecological phenomenon that can serve as a sustainable resource for generating novel pharmaceutical leads. Thus, sponge microsymbionts are an important focus nowadays [61, 62]. In yet another study, a marine-derived fungal strain named M-3 was isolated from marine red alga Porphyra yezoensis. It was assessed for its antifungal activity against Pyricularia oryzae [63]. As a result, a novel compound diketopiperazine was isolated from the culture extracts and its structure was also elucidated by spectroscopic methods.

In another study, the butanol extracts of algal associated species Pseudoalteromonas issachenkonii were reported to show hemolysis and inhibition of Candida albicans. Their ethyl acetate extracts were also subjected to spectroscopic studies and revealed the presence of indole-2,3-dione, a type of isatin that was responsible for its antifungal activity [63]. In another study, a red-brown hemolytic pigment was also discovered [64]. Coral reefs widely prevalent in oceans are also unexplored source of novel bioactive compounds [65].

In another study, a marine gorgonian associated bacterium Bacillus amyloliquefaciens was isolated from the South China Sea gorgonian, Junceella juncea. The studies showed their antibacterial against Escherichia coli, Bacillus subtilis, and Staphyloccocus aureus and antilarval properties against the larvae of bryozoan Bugula neritina. In yet another study, an antimicrobial activity of about 42 marine bacterial strains belonging to genera Alteromonas, Pseudomonas, Bacillus, and Flavobacterium was reported [66]. Besides this, certain mycoparasitic and fungicolous fungi were also shown to colonize other fungal physiological structures and were known to produce various bioactive agents [67]. In a study, five new natural products, Phomadecalins A, B, C, D, and Phomapentenone A, were reported from cultures of Phoma sp., a mitosporic fungal colonist isolated from the stromata of Hypoxylon sp. These bioactive compounds were found to be active against Gram-positive bacteria, Bacillus subtilis (ATCC 6051) and Staphylococcus aureus (ATCC 29213) [68].

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3. Classification of marine nutraceuticals on the basis of chemical nature

Marine nutraceuticals can be broadly classified into Marine lipids (microalgal origin), polysaccharides derived from macro algae, marine probiotics, marine natural pigments, chitin and other related products, bioactive marine peptides/enzymes, and vitamins.

3.1 Lipids

Lipids derived from marine microalgae are used in larval nutrition of aquaculture, especially for enrichment of live feeds. Their other biological properties are anti-inflammatory, antiallergic, antiviral, and therapeutic. The wide spectrum of the properties is due to the presence of various components like polyunsaturated fatty acids (PUFA), highly unsaturated fatty acids (HUFA), and other substances. Various microalgal originated lipid/fatty acids and their activities [69] are given in Table 1.

Microalgal lipid/fatty acid Biological action/function
Eicosapentaenoic acid (EPA) Nutraceutical; antimicrobial and anti-inflammatory
Gamma-linolenic acid (GLA) Integrity of tissue and delay of aging
Arachidonic acid (ARA) Aggregative and vasoconstrictive of platelets
Docosahexaenoic acid (DHA) Nutraceutical and brain development
Brassicasterol and stingmasterol Hypercholesterolemic
Gamma-amino-butyric acid (GABA) Neuro-transmitter, antioxidant and anti-inflammatory
Okadaic acid Antifungal and promotion of the secretion of nerve growth factor (NGF)
Microcolin-A Immunosuppressive

Table 1.

Microalgal lipid/fatty acids and their activity.

3.2 Polysaccharides

Generally, bacterial capsules contain polysaccharides. They form one of the important classes of secondary metabolites that are also important from pharmaceutical point of view. Research studies have shown that these exopolysaccharides (EPS) particularly from marine bacteria can be used in various pharmaceutical and food processing agents. They can also be used in industries as thickeners, coagulating agents, adhesive agents, stabilizers, and as gelling agents. The exopolysaccharides possess good viscosity and pseudo-plastic properties that impart them ability to resist extremes of temperature, pH, and salinity. This increases their potential to be used as an industry friendly resource [70]. In a study, exopolysaccharides have been shown to possess immunomodulatory and antiviral properties on immunocompetent cells in a marine bacteria Geobacillus thermodenitrificans that was isolated from a shallow marine vent of Volcano Island (Italy). This bacterium not only produced secondary metabolites against other organisms, but also produced certain compounds which help in bioremediation [71]. Certain other marine bacterial species are known as prolific producers of biosurfactants, bioemulsifiers, and exopolysaccharides.

Some polysaccharides are also derived from macroalgae. Seaweeds contain higher amounts of the polysaccharides like agar, alginates, and carrageenan. These act as food fiber and are collectively called phyco-colloids or hydrocolloids. Being rich in fiber, seaweeds exhibit health benefits like reducing the absorption of toxins, anticarcinogenic, and antioxidant properties. Example of the few important bioactive polysaccharides isolated from macroalgae (seaweeds) that possess the potential to be used as nutraceuticals are Fucoidan, Sphinganine amide, and caulerpicin (green algae), Carrageenan, Alginic acid and xylofucans, Hyperoxaluria, Sulfated polysaccharides, and Alginates. All these compounds possess wide range of biological properties such as antioxidant, antiangiogenic, antibacterial, antiviral and antitumor activities anticoagulant, immuno-modulating, hypolipidemic, and anti-inflammatory [72]. In addition to the phyco-colloids, seaweeds are sources of biologically active phytochemicals like carotenoids, phycobilins, fatty acids, vitamins, sterols, tocopherol, phycocyanins, and others.

Macroalgae are also rich sources of insoluble and soluble dietary fiber. They contain chiefly indigestible sulfated polysaccharides. Some of the notable examples of structural and storage polysaccharides are fucan, agar, laminaran, carrageenan, and alginates that are found both in red and brown seaweeds. The alginates obtained from brown seaweeds are used as hydrocolloids and fucans from brown seaweeds are used in both food and cosmetics industries [73].

A research highlighted the role of marine bacteria Bacillus circulans in the biodegradation of anthracene (a polyaromatic hydrocarbon) [74]. The said bacteria also produced a novel type of biosurfactant that exhibited excellent emulsification properties. It was shown that Bacillus circulans utilized anthracene as a sole carbon source for the production of biosurfactant. The researchers also reported the production of another biosurfactant by an unnamed marine bacteria that has the ability to remove metal from solutions [75].

3.3 Bryostatins: bryozoan origin

The marine bryozoan, Bugula neritina, is the sole source of the bryostatins, a family of macrocyclic lactones with anticancer activity. Bryostatins are actually the bacterial products as B. neritina harbors the uncultivated gamma proteobacterial symbiont Candidatus Endobugula sertula. The clinical studies of bryostatins are also under going to study their potential for the treatment of leukemias, lymphomas, melanomas, and solid tumors [76]. Their mode of action is that they act through protein kinase C signal transduction to alter cellular activity.

3.4 Probiotics: marine lactic acid bacteria (LAB) origin

Microbial diversity of marine environments is very rich and can be helpful to develop safe and effective probiotics. Novel marine probiotics can be an effective alternative for fighting the antibiotic resistance. Lactobacillus and Bifidobacterium are found to possess antimutagenic [77] and immunomodulatory [78] activity in host animal. Different strains of marine probiotic bacteria are Lactobacillus (L. casei, L. acidophilus, L. rhamnosus GG (ATCC 53013), L. johnsonii La-1), Bifidobacterium (B. bifidum, B. longum, B. infantis, B. breve, B. adolescentis), Leuconostoc spp. (Ln. lactis, Ln. mesenteroides subsp. cremoris, Ln. mesenteroides subsp. dextranicum), and Streptococcus spp. (S. salivarius subsp. thermophiles).

The problem posed during the development of new marine probiotics is the isolation and identification of potential strain. Application of biotechnological and molecular biological tactics is necessary for the development of marine probiotic strains for use of aquatic industry [72].

3.5 Pigments: marine algae

Besides polysaccharides and lipids, marine macro- and microalgae also provide various types of the bioactive natural pigments. The natural pigments of the marine algae provide food by photosynthesis and also provide the pigmentation. In addition to these, the natural pigments are also found to exhibit health benefits which make them one of the important marine nutraceuticals. Chlorophyll-a, Lutein, zeaxanthin, and canthaxanthin possess antimutagenic properties; pheophytin-a exhibits neuroprotective, and anti-inflammatory action; Chlorophyll-a, Pheophorbide-a, Pyropheophytin-a, Phycoerythrobilin, Lutein, Fucoxanthin, Phycocyanin, Astaxanthin, Zeaxanthin, and Canthaxanthin are all good antioxidants. Alpha-Carotene is also used as a food additive [72].

3.6 Chitosan: chitin

Chitosan is a natural polymer derived from chitin and it is the second most abundant polysaccharide after cellulose. Chitin is recovered from processing discards of shrimp, crab, lobster, and crayfish following de-proteinization and demineralization. The chitin so obtained may then be deacetylated to afford chitosan. Fungal cell walls are also rich in chitin. Chitin and chitosan are used as biomaterials in a variety of application in edible film industry, additives, for improving nutritional quality, recovery of solid materials from food processing waste, in purification of water, etc. The other biological properties of chitosan are antioxidant, hypocholesterolemic, antimicrobial, and anti-inflammatory activities [79].

Chitosan disrupts the barrier properties of the outer membrane of Gram-negative bacteria due to ionic interaction between the cationic groups of the chitosan molecules and the anionic groups of the microbial cell membrane, which can rupture the cell membrane. Chitosan can also function as an antifungal agent by forming gas-permeable coats, interference with fungal growth and stimulation of various defense processes like, build-up of chitinases, production of proteinase inhibitors, and stimulators of callous synthesis.

The antioxidant property could be attributed to the ability of chitosan to chelate metals and combine with lipids. Derivatives of chitosan, namely, N,O-carboxymethyl chitosan, N,O-carboxymethyl chitosan lactate, N,O-carboxymethyl chitosan acetate, and N,O-carboxymethyl chitosan pyrrolidine carboxylate had also exhibited the antioxidant activity. Chitosan possesses special properties for use in pharmaceutical, biomedical, food industry, health, and agriculture due to its biocompatibility, biodegradability, and non-toxic nature. Through encapsulation, it is being used as a vehicle for nutraceutical compounds and pharmacological compounds. Chitosan derivatives may also be produced in order to obtain more effective products for certain applications [72].

3.7 Bioactive peptides/enzymes: marine origin

Peptides refer to the specific protein fragments that exhibit a specific biological activity. Some of the peptides may exhibit multifunctional properties like opioid, immunomodulatory, antibacterial, antithrombotic, and antihypertensive activity. Biofunctional peptides have a size range of 2–20 amino acid residues and are encrypted within the sequence of the parent protein and are released during processing. They can be formed either by acid or alkaline hydrolysis. The major bioactivities of peptides are antihypertensive (ACE inhibitory), antioxidant, antimicrobial, antihypoallergenic activity, and cell immunity [80].

Proteins isolated from bacteria such as Dunaliella, Phaeodactylum tricornutum, and Arthrospira platensis possess potent antioxidant and anti-inflammatory activity which can be effectively used in aquaculture practices. Similarly, enzymes such as superoxide dismutase and carbonic anhydrase derived from Porphyridium, Anabaena, Isochrysis galbana, and Amphidinium carterae play an important role in regulating the metabolite waste (CO2).

3.8 Vitamins: marine microalgal origin

Marine microalgae are also known to have good amount of alpha-carotene. Microalgae like, Arthrospira, Isochrysis galbana, Porphyridium cruentum, and Tetraselmis are rich in vitamin C, K, A, E, and alpha-carotene which possess strong antioxidant activity. Vitamins A specially provitamin-A or alpha-carotene and vitamin E or alpha-tocopherol function as source of strong antioxidant compounds and protect the cells from free radical damage by quenching these free radicals. Vitamin E, together with vitamin C and alpha-carotene, helps in improving antioxidant defenses in the body. Fat soluble vitamin K isolated from Pavlova helps in blood clotting or coagulation. The role of antioxidant vitamins in health and disease control has been well documented [73]. Some of the important marine microorganisms, their bioactive metabolites and biological activity are highlighted in Table 2 [20].

Microorganism Marine microbial metabolites Biological activity
Cyanobacteria Dolastatin-10 Antimicrotubule; and the synthetic analog, TZT-1027, as antitumor
Dolastatin-15 Antimicrotubule; and the synthetic analog, ILX-651, as antitumor
Curacin A Antimicrotubule
Toyocamycin Antifungal
Actinomycetes Resistoflavine Anticancerous and antibacterial
Marinomycin A Antitumor and antibiotic
Daryamide C Antitumor
Violacein Antiprotozoal
Bacteria Macrolactin S Antibacterial
Pyrone I and II Antibacterial
MC21-B Antibacterial
Fungi Meleagrin Antitumor
Oxaline Antitumor
Alternaramide Antibacterial
Algae Norharman Enzyme inhibitor
Calothrixin-A Antimalarial and anticancerous
Eicosapentanoic acid (EPA) Treats heart disease, anti-inflammatory agent (rheumatoid arthritis and immunodeficiency diseases)
Symbiotic microbes Macrolactin V Antibacterial and antilarval
DAPG Antibacterial (anti-MRSA, anti-VRSA and anti-VRE)
BE-43472B Antibacterial (anti-MRSA and anti-VRE)

Table 2.

Name and biological activity of some of the marine microbial metabolites.

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4. Classical examples of some marine microflora and their nutraceutical potential

The oceans harbor one of the most diverse flora and fauna on our earth surface. Its biodiversity serves as an inexhaustible source of variety of biologically active compounds such as antibiotic, antimicrobial, anti-inflammatory, anticancer, antioxidant, antimicrotubule, cytotoxic, photo-protective, and antifouling properties. A variety of novel range of microorganisms, such as bacteria (both free living and symbiotic), fungi, actinomycetes, microalgae-cyanobacteria, and diatoms, are found in the marine environment that are potent producers of important therapeutic compounds. They have also been found effective against many deadly infectious diseases such as AIDS, drug-resistant bacteria, including conditions of multiple bacterial infections. Only little research has been done on the biophysical and biochemical properties, their chemical structures and biotechnological applications of these marine bioactive substances, and their potential utilization in both cosmeceuticals and nutraceuticals. Some of the research studies on bioactive molecules from marine sources are discussed below.

Seaweeds provide a rich source of bioactive molecules. In this study, the antimicrobial potential of Red sea weed, Gracilaria opuntia was investigated against clinically important microorganism such as Escherichia coli, Staphylococcus aureus, Klebsiella pneumonia, and Pseudomonas putida that cause diseases in diabetic patients. Crude extracts prepared from aqueous, ethanol, and methanol extraction procedures revealed that aqueous extraction procedure have a wide range of antimicrobial activity against all the test pathogens. The overall antibacterial activity assessed from the above results indicates the presence of active constituents in the extractions of seaweeds, which can be explored for the production of significant molecules that could be used in pharmaceutical industry [81].

In a similar another study on Gracilaria edulis, their phytochemical, antibacterial, and antifungal activities of crude extracts were investigated. The methanol and aqueous extracts of Gracilaria edulis showed the presence of a number of metabolites such as alkaloids, saponin, phenols, terpenoids, proteins, flavonoids, glycosides, coumarins, and tannins. The red algae showed the significant antibacterial activity against the clinical pathogens of Pseudomonas aeroginosa, Staphylococcus aureus, Bacillus cereus, Bacillus subtilis, Streptococcus pyogenes, Salmonella typhi as well as the fungus Aspergillus niger, Aspergillus flavus, Rhizopus indicus, and Candida albicans. The methanol extract showed the broader spectrum of antibacterial and antifungal activity when compared with aqueous extract [82].

In yet another study, the phytochemical and biological evaluation of some Sargassum species from Persian Gulf was also studied. These plants contain important phytochemical constituents and have various potential biological activities. The study investigated the presence of phytochemical constituents and total phenolic quantity of the seaweeds Sargassum angustifolium, Sargassum oligocystum, and Sargassum boveanum. Cytotoxicity and antioxidant potential of these three Sargassum species was also analyzed. Sargassum angustifolium had the highest content of total phenolics and showed the highest antioxidant activity. Cytotoxic results showed that all species could inhibit cell growth effectively, for S. oligocystum, S. angustifolium, and S. boveanum, respectively. Thus considerable phytochemicals and moderate cytotoxic activity of S. angustifolium, S. oligocystum, and S. boveanum make them appropriate candidate for further studies and identification of their bioactive principles [83].

Further study on screening the algae for their phytochemicals from their extracts and testing on their antibacterial, antifungal and antioxidant potential was carried out. The algal strains were Tetraselmis sp., Dunaliella sp., Chlorella sp., Synechocystis sp., and Oscillatoria sp. Their extracts were prepared in an organic solvent and were used to screen for the presence of any phytochemicals. Later, their antimicrobial activity was also assessed against some selected bacterial and fungal species. Their antioxidant activity was also determined by DPPH scavenging assay and confirmed the presence of flavonoids in majority of the solvent extracts. In addition, the microalgal strains exhibited better antifungal activity as compared to bacterial. The solvent acetone from Dunaliella sp. showed highest antioxidant activity. The results showed the presence of Octadecanoic acid-4-hydroxy-methyl ester, benzoic acid, hexadecanoic acid, and Tetradecanoic acid, confirming the bioactive compounds in the algal extracts [84].

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5. Other marine sources of nutraceuticals

Besides the microbes (which contributes around 19%), there are other marine flora and fauna, such as sponges (38%), coelenterates (23%), algae (10%), echinoderms (7%), tunicates (7%), mollusks (3%), and bryozoans (2%), have also shown to exhibit their potential to produce various therapeutic compounds including some novel anticancer substances. These compounds can also work against infectious diseases and inflammation [85].

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6. Current market of nutraceuticals

Nutraceuticals, including functional foods and dietary supplements, have tremendous market potential. It has been estimated that the consumer demand of these health foods were around $250 billion only in 2014 alone and this figure is continue to rise and is expected to reach around $385 billion by 2020 [86].

Nutraceutical products are in demand throughout the world especially in developed countries, including United States of America (USA), Europe, Japan, Asia Pacific, Middle East, and Latin America. In particular, the global market is dominated by the United States of America, Europe, and Japan, which account for more than 85% of the market [87]. As per the Mintel survey carried out in the United Kingdom on vitamins and minerals supplements, it was observed that 25% of all adult populations were satisfied with the results of the nutraceutical products. The percentage of the usage varied according to the age of the consumers like the consumption of nutraceutical products was more common in elderly population as compared with the younger generation. There is a strong belief that in the coming years, nutraceutical industry would remain at the forefront market including the Asian countries such as India and China. This is because of greater consumer awareness toward their health, increasing income levels and greater confidence in traditional and complimentary medicines [73].

The consumption of nutraceutical products in the USA is comparatively higher and accounts for approx. 40% of adults; in Spain, the nutraceuticals are consumed by the population aged between 35 and 80 years, and only around 9% consume dietary supplements as the source of vitamins and minerals. Besides, about 72% educated women that are of age between 35 and 49 years are more likely to choose nutraceuticals and dietary supplements [88].

In addition, the geriatric populations are also the most common consumers of these health supplements as they are more prone to micronutrient deficiencies. Due to the steady rise of geriatric population in developed countries, there is an urgent need to encourage and maintain a healthy lifespan and prevent chronic illnesses associated with aging [89].

Thus individuals with healthy lifestyles are more commonly the users of nutraceutical products.

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7. Conclusion

From the above discussion, it is quite pertinent to conclude that the marine environment harbors variety of microbial flora that have capability to produce a wide array of bioactive metabolites that can be used both in nutrition and pharmaceuticals to formulate new drugs that are effective against various drug-resistant pathogens. Though the saga of marine microbial bioactive metabolites is continuing with new compounds being added day by day, our knowledge is still a miniscule of what exists deep in the oceans. Interdisciplinary research and collaborative endeavors are required amongst scientists, medical practitioners, marine microbiologists, and biotechnologists, to provide innovative approaches to marine based biomedical research. Thus, it is imperative to utilize our marine biodiversity and their bioactive metabolites for discovering new therapeutic compounds of nutraceutical importance. Recent biomedical tools, such as metabolomics and genetic engineering, can also be applied to increase their yield.

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Acknowledgments

Authors greatly acknowledge Dept. of Scientific & Industrial Research (DSIR), New Delhi for their financial support. The authors are also grateful to Dr. Ashok K. Chauhan, Founder President and Mr. Atul Chauhan, Chancellor, Amity University-UP, Noida, India for the motivation and research facilities.

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Conflict of interest

The author(s) confirm that this article content has no conflict of interest.

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Ethical issues

There is none to be declared.

Abbreviations

γ

gamma

DPPH

1,1-diphenyl-2-picrylhydrazyl

PDE

phosphodiesterase

EPA

eicosapentaenoic acid

MRSA

methicillin-resistant Staphylococcus aureus

ACE

angiotensin-converting enzyme

ATCC

American Type Culture Collection

PUFA

polyunsaturated fatty acids

HUFA

highly unsaturated fatty acids

GLA

gamma-linolenic acid

ARA

arachidonic acid

DHA

docosahexaenoic acid

GABA

gamma-amino-butyric acid

EPS

exopolysaccharides

LAB

lactic acid bacteria

CO2

carbon-di-oxide

HIV

Human Immunodeficiency Virus

References

  1. 1. Chapman AS, Stévant P, Larssen WE, Stévant P, Larssen WE. Food or fad? Challenges and opportunities for including seaweeds in a Nordic diet. Botanica Marina. 2015;58:423-433
  2. 2. Cornish M, Critchley A, Mouritsen O. Consumption of seaweeds and the human brain. Journal of Applied Phycology. 2017;29:2377-2398. DOI: 10.1007/s10811-016- 1049-3
  3. 3. Buschmann AH, Camus C, Infante J, Neori A, Israel Á, Hernández-González MC, et al. Seaweed production: Overview of the global state of exploitation, farming and emerging research activity. European Journal of Phycology. 2017;52(4):391-406. DOI: 10.1080/09670262.2017.1365175
  4. 4. Elena M. Mailiohydrin, a cytotoxic chamigrene dibromohydrin from a phillippine Laurencia species. Journal of Natural Products. 2003;64:790-791
  5. 5. Bhagavathy S, Sumathi P, Bell IJB. Green algae chlorococcumhumicola—A new source of bioactive compounds with antimicrobial activity. Asian Pacific Journal of Tropical Biomedicine. 2011;1:S1-S7. DOI: 10.1016/S2221-1691(11)60111-1
  6. 6. Dewapriya P, Se-kwon K. Marine microorganisms: An emerging avenue in modern nutraceuticals and functional foods. Food Research International. 2014;56:115-125. DOI: 10.1016/j.foodres.2013.12.022
  7. 7. Aneiros A, Garateix A. Bioactive peptides from marine sources: Pharmacological properties and isolation procedures. Journal of Chromatography, B: Analytical Technologies in the Biomedical and Life Sciences. 2004;803:41-53. DOI: 10.1016/j.jchromb.2003.11.005
  8. 8. Tseng CK. Algal biotechnology industries and research activities in China. Journal of Applied Phycology. 2001;13:375-380. DOI: 10.1023/A:1017972812576
  9. 9. Grobbelaar JU. Algal biotechnology: Real opportunities for Africa. South African Journal of Botany. 2004;70:140-144. DOI: 10.1016/S0254-6299(15)30274-X
  10. 10. Volkman JK. Sterols in microorganisms. Applied Microbiology and Biotechnology. 2003;60:495-506. DOI: 10.1007/s00253-002-1172-8
  11. 11. Inagaki F, Nunoura T, Nakagawa S, Teske A, Lever M, Lauer A, et al. Biogeographical distribution and diversity of microbes in methane hydrate-bearing deep marine sediments on the Pacific Ocean margin. Proceedings of the National Academy of Sciences of the United States of America. 2006;103:2815-2820. DOI: 10.1073/pnas.0511033103
  12. 12. Okami YJ. The search for bioactive metabolites forms marine bacteria. Marine Biotechnology. 1993;1:59-65
  13. 13. Trischman JA, Tapiolas DM, Jensen PR, Dwight R, McKee TC, Ireland CM, et al. Salinamides A and B: Anti-inflammatory depsipeptides from a marine Streptomycete. Journal of the American Chemical Society. 1994;116:757-758. DOI: 10.1021/ja00081a042
  14. 14. Belofsky GN, Jensen PR, Renner MK, Fenical W. New cytotoxic sesquiterpenoid nitrobenzoyl esters from a marine isolate of the fungus Aspergillus versicolor. Tetrahedron. 1998;54:1715-1724. DOI: 10.1016/S0040-4020(97)10396-9
  15. 15. Romanenko LA, Uchino M, Kalinovskaya NI, Mikhailov VV. Isolation, phylogenetic analysis and screening of marine mollusc-associated bacteria for antimicrobial, hemolytic and surface activities. Microbiological Research. 2008;163:633-644. DOI: 10.1016/j.micres.2006.10.001
  16. 16. Isnansetyo A, Kamei Y. Bioactive substances produced by marine isolates of Pseudomonas. Journal of Industrial Microbiology & Biotechnology. 2009;36:1239-1248. DOI: 10.1007/s10295-009-0611-2
  17. 17. Romanenko LA, Uchino M, Tanaka N, Frolova GM, Slinkina NN, Mikhailov VV. Occurrence and antagonistic potential of Stenotrophomonas strains isolated from deep-sea invertebrates. Archives of Microbiology. 2008;189:337-344. DOI: 10.1007/s00203-007-0324-8
  18. 18. Romanenko LA, Uchino M, Tebo BM, Tanaka N, Frolova GM, Mikhailov VV. Pseudomonas marincola sp. nov., isolated from marine environments. International Journal of Systematic and Evolutionary Microbiology. 2008;58:706-710. DOI: 10.1099/ijs.0.65406-0
  19. 19. Isnansetyo A, Kamei Y. MC21-A, a bactericidal antibiotic produced by a new marine bacterium, Pseudoalteromonas phenolica sp. nov. O-BC30T against methicillin-resistant Staphylococcus aureus. Antimicrobial Agents and Chemotherapy. 2003;47:480-488. DOI: 10.1128/AAC.47.2.480-488.2003
  20. 20. Bhatnagar I, Kim S-K. Immense essence of excellence: Marine microbial bioactive compounds. Marine Drugs. 2010;8:2673-2701. DOI: 10.3390/md8102673
  21. 21. Franks A, Haywood P, Holmström C, Egan S, Kjelleberg S, Kumar N. Isolation and structure elucidation of a novel yellow pigment from the marine bacterium Pseudoalteromonas tunicata. Molecules. 2005;10:1286-1291. DOI: 10.3390/10101286
  22. 22. Egan S, James S, Holmström C, Kjelleberg S. Correlation between pigmentation and antifouling compounds produced by Pseudoalteromonas tunicata. Environmental Microbiology. 2002;4:433-442. DOI: 10.1046/j.1462-2920.2002.00322.x
  23. 23. König G, Kehraus S, Seibert S, Abdel-Lateff A, Müller D. Natural products from marine organisms and their associated microbes. ChemBioChem. 2006;7:229-238. DOI: 10.1002/cbic.200500087
  24. 24. Burke C, Thomas T, Egan S, Kjelleberg S. The use of functional genomics for the identification of a gene cluster encoding for the biosynthesis of an antifungal tambjamine in the marine bacterium Pseudoalteromonas tunicata. Environmental Microbiology. 2007;9:814-818. DOI: 10.1111/j.1462-2920.2006.01177.x
  25. 25. Bhadury P, Mohammad BT, Wright PC. The current status of natural products from marine fungi and their potential as anti-infective agents. Journal of Industrial Microbiology & Biotechnology. 2006;33:325-337. DOI: 10.1007/s10295-005-0070-3
  26. 26. Newman DJ, Hill RT. New drugs from marine microbes: The tide is turning. Journal of Industrial Microbiology & Biotechnology. 2006;33:539-544. DOI: 10.1007/s10295-006-0115-2
  27. 27. Kjer J, Debbab A, Aly AH, Proksch P. Methods for isolation of marine-derived endophytic fungi and their bioactive secondary products. Nature Protocols. 2010;5:479-490. DOI: 10.1038/nprot.2009.233
  28. 28. Du L, Zhu T, Fang Y, Liu H, Gu Q , Zhu W. Aspergiolide A, a novel anthraquinone derivative with naphtho(1,2,3-de)chromene-2,7-dione skeleton isolated from a marine-derived fungus Aspergillus glaucus. Tetrahedron. 2007;63:1085-1088. DOI: 10.1016/j.tet.2006.11.074
  29. 29. Du L, Feng T, Zhao B, Li D, Cai S, Zhu T, et al. Alkaloids from a deep ocean sediment-derived fungus Penicillium sp. and their antitumor activities. The Journal of Antibiotics. 2010;63:165-170. DOI: 10.1038/ja.2010.11
  30. 30. Kwong TF, Miao L, Li X, Qian PY. Novel antifouling and antimicrobial compound from a marine-derived fungus Ampelomyces sp. Marine Biotechnology. 2006;8:634-640. DOI: 10.1007/s10126-005-6146-2
  31. 31. Xiong H, Qi S, Xu Y, Li M, Qian P-Y. Antibiotic and antifouling compound production by the marine-derived fungus Cladosporium sp. F14. Journal of Hydro-Environment Research. 2009;2:264-270
  32. 32. Gai Y, Zhao LL, Hu CQ , Zhang HP. Fusarielin E, a new antifungal antibiotic from Fusarium sp. Chinese Chemical Letters. 2007;18:954-956. DOI: 10.1016/j.cclet.2007.05.048
  33. 33. Li X, Kim SK, Nam KW, Kang JS, Choi HD, Son BW. A new antibacterial dioxopiperazine alkaloid related to gliotoxin from a marine isolate of the fungus Pseudallescheria. Journal of Antibiotics (Tokyo). 2006;59:248-250. DOI: 10.1038/ja.2006.35
  34. 34. Zhang D, Yang X, Kang JS, Choi HD, Son BW. Chlorohydroaspyrones A and B, antibacterial aspyrone derivatives from the marine-derived fungus Exophiala sp. Journal of Natural Products. 2008;71:1458-1460. DOI: 10.1021/np800107c
  35. 35. Stadler M, Anke H, Sterner O. Metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. III. Production of novel isocoumarin derivatives, isolation and biological activities. The Journal of Antibiotics. 1995;48:261-266. DOI: 10.7164/antibiotics.48.154
  36. 36. Nenkep VN, Yun K, Li Y, Choi HD, Kang JS, Son BW. New production of haloquinones, bromochlorogentisylquinones A and B, by a halide salt from a marine isolate of the fungus Phoma herbarum. The Journal of Antibiotics. 2010;63:199-201. DOI: 10.1038/ja.2010.15
  37. 37. Takahashi Y, Omura S. Isolation of new actinomycete strains for the screening of new bioactive compounds. The Journal of General and Applied Microbiology. 2003;49:141-154. DOI: 10.2323/jgam.49.141
  38. 38. Olano C, Méndez C, Salas JA. Antitumor compounds from marine actinomycetes. Marine Drugs. 2009;7:210-248. DOI: 10.3390/md7020210
  39. 39. Prudhomme J, McDaniel E, Ponts N, Bertani S, Fenical W, Jensen P, et al. Marine actinomycetes: A new source of compounds against the human malaria parasite. PLoS One. 2008;3:e2335. DOI: 10.1371/journal.pone.0002335
  40. 40. El-Gendy MM, Hawas UW, Jaspars M. Novel bioactive metabolites from a marine derived bacterium Nocardia sp. ALAA 2000. Journal of Antibiotics (Tokyo). 2008;61:379-386. DOI: 10.1038/ja.2008.53
  41. 41. McArthur KA, Mitchell SS, Tsueng G, Rheingold A, White DJ, Grodberg J, et al. Lynamicins A-E, chlorinated bisindole pyrrole antibiotics from a novel marine actinomycete. Journal of Natural Products. 2008;71:1732-1737. DOI: 10.1021/np800286d
  42. 42. Cho JY, Williams PG, Kwon HC, Jensen PR, Fenical W. Lucentamycins A–D, cytotoxic peptides from the marine-derived actinomycete Nocardiopsis lucentensis. Journal of Natural Products. 2007;70:1321-1328. DOI: 10.1021/np070101b
  43. 43. Hawas UW, Shaaban M, Shaaban KA, Speitling M, Maier A, Kelter G, et al. Cytotoxic isoquinolinequinones from a marine streptomycete. Journal of Natural Products. 2009;72:2120-2124. DOI: 10.1021/np900160g
  44. 44. Pérez M, Crespo C, Schleissner C, Rodríguez P, Zúñiga P, Reyes F. Tartrolon D, a cytotoxic macrodiolide from the marine-derived actinomycete Streptomyces sp. MDG-04-17-069. Journal of Natural Products. 2009;72:2192-2194. DOI: 10.1021/np9006603
  45. 45. Maloney KN, Macmillan JB, Kauffman CA, Jensen PR, Dipasquale AG, Rheingold AL, et al. Lodopyridone, a structurally unprecedented alkaloid from a marine actinomycete. Organic Letters. 2009;11:5422-5424. DOI: 10.1021/ol901997k
  46. 46. Carlson JC, Li S, Burr DA, Sherman DH. Isolation and characterization of Tirandamycins from a marine-derived Streptomyces sp. Journal of Natural Products. 2009;72:2076-2079. DOI: 10.1021/np9005597
  47. 47. Maskey RP, Helmke E, Kayser O, Fiebig HH, Maier A, Busche A, et al. Anti-cancer and antibacterial trioxacarcins with high anti-malaria activity from a marine Streptomycete and their absolute stereochemistry. Journal of Antibiotics (Tokyo). 2004;57:771-779. DOI: 10.7164/antibiotics.57.771
  48. 48. Xu Y, He H, Schulz S, Liu X, Fusetani N, Xiong H, et al. Potent antifouling compounds produced by marine Streptomyces. Bioresource Technology. 2010;101:1331-1336. DOI: 10.1016/j.biortech.2009.09.046
  49. 49. Iwata F, Sato S, Mukai T, Yamada S, Takeo J, Abe A, et al. Lorneic acids, trialkyl-substituted aromatic acids from a marine-derived actinomycete. Journal of Natural Products. 2009;72:2046-2048. DOI: 10.1021/np900353y
  50. 50. Lopes VR, Fernández N, Martins RF, Vasconcelos V. Primary screening of the bioactivity of brackish water cyanobacteria: Toxicity of crude extracts to Artemia salina larvae and Paracentrotus lividus embryos. Marine Drugs. 2010;8:471-482. DOI: 10.3390/md8030471
  51. 51. Luesch H, Harrigan GG, Goetz G, Horgen FD. The cyanobacterial origin of potent anticancer agents originally isolated from sea hares. Current Medicinal Chemistry. 2002;9:1791-1806. DOI: 10.2174/0929867023369051
  52. 52. Sivonen K, Leikoski N, Fewer DP, Jokela J. Cyanobactins-ribosomal cyclic peptides produced by cyanobacteria. Applied Microbiology and Biotechnology. 2010;86:1213-1225. DOI: 10.1007/s00253-010-2482-x
  53. 53. Simmons TL, Engene N, Ureña LD, Romero LI, Ortega-Barría E, Gerwick L, et al. Viridamides A and B, lipodepsipeptides with antiprotozoal activity from the marine cyanobacterium Oscillatoria nigro-Viridis. Journal of Natural Products. 2008;71:1544-1550. DOI: 10.1021/np800110e
  54. 54. Allmendinger A, Spavieri J, Kaiser M, Casey R, Hingley-Wilson S, Lalvani A, et al. Antiprotozoal, anti-mycobacterial and cytotoxic potential of twenty-three British and Irish red algae. Phytotherapy Research. 2010;24:1099-1103. PMID: 20077438
  55. 55. Desbois AP, Mearns-Spragg A, Smith VJ. A fatty acid from the diatom Phaeodactylum tricornutum is antibacterial against diverse bacteria including multi-resistant Staphylococcus aureus (MRSA). Marine Biotechnology. 2009;11:45-52. DOI: 10.1007/s10126-008-9118-5
  56. 56. Plaza M, Cifuentes A, Ibanez E. In the search of new functional food ingredients from algae. Trends in Food Science and Technology. 2008;19:31-39. DOI: 10.1016/j.tifs.2007.07.012
  57. 57. Gomez-Ordonez E, Jimenez-Escrig A, Ruperez P. Dietary fibre and physico-chemical properties of several edible seaweeds from the Northwestern Spanish coast. Food Research International. 2010;9:2289-2294. DOI: 10.1016/j.foodres.2010.08.005
  58. 58. Kim EY, Kim DG, Kim YR, Hwang HJ, Nam TJ, Kong IS. An improved method of protein isolation and proteome analysis with Saccharina japonica (Laminariales) incubated under different pH conditions. Journal of Applied Phycology. 2011;23:123-130. DOI: 10.1007/s10811-010-9550-6
  59. 59. Thomas TRA, Kavlekar DP, LokaBharathi PA. Marine drugs from sponge-microbe association—A review. Marine Drugs. 2010;8:1417-1468. DOI: 10.3390/md8041417
  60. 60. Baker PW, Kennedy J, Dobson ADW, Marchesi JR. Phylogenetic diversity and antimicrobial activities of Fungi associated with Haliclona simulans isolated from Irish coastal waters. Marine Biotechnology. 2009;11:540-547. DOI: 10.1007/s10126-008-9169-7
  61. 61. Gandhimathi R, Arunkumar M, Selvin J, Thangavelu T, Sivaramakrishnan S, Kiran GS, et al. Antimicrobial potential of sponge associated marine actinomycetes. Journal de Mycologie Médicale. 2008;18:16-22. DOI: 10.1016/j.mycmed.2007.11.001
  62. 62. Selvin J, Shanmughapriya S, Gandhimathi S, Kiran GS, Ravji TR, Natarajaseenivasan K, et al. Optimization and production of novel antimicrobial agents from sponge associated marine actinomycetes Nocardiopsis dassonvillei MAD08. Applied Microbiology and Biotechnology. 2009;83:435-445. DOI: 10.1007/s00253-009-1878-y
  63. 63. Byun HG, Zhang H, Mochizuki M, Adachi K, Shizuri Y, Lee WJ, et al. Novel antifungal diketopiperazine from marine fungus. Journal of Antibiotics (Tokyo). 2003;56:102-106. DOI: 10.7164/antibiotics.56.102
  64. 64. Kalinovskaya NI, Ivanova EP, Alexeeva YV, Gorshkova NM, Kuznetsova TA, Dmitronek AD, et al. Low-molecular-weight, biologically active compounds from marine Pseudoalteromonas species. Current Microbiology. 2004;48:441-446. DOI: 10.1007/s00284-003-4240-0
  65. 65. Radjasa OK. Marine invertebrate-associated bacteria in coral reef ecosystems as a new source of bioactive compounds. Journal of Coastal Development. 2004;7:65-70
  66. 66. Zheng L, Han X, Chen H, Lin W, Yan X. Marine bacteria associated with marine macro-organisms: The potential antimicrobial resources. Annales de Microbiologie. 2005;55:119-124
  67. 67. Soman AG, Gloer JB, Angawi RF, Wicklow DT, Dowd PF. Vertilecanins: New phenopicolinic acid analogs from Verticillium lecanii. Journal of Natural Products. 2001;64:189-192. DOI: 10.1021/np000094q
  68. 68. Che Y, Gloer JB, Wicklow DT. Phomadecalins A-D and Phomapentenone A: New bioactive metabolites from Phoma sp. NRRL 25697, a fungal colonist of Hypoxylon Stromata. Journal of Natural Products. 2002;65:399-402. DOI: 10.1021/np010519o
  69. 69. Raposo MFD, de Morais R, de Morais A. Health applications of bioactive compounds from marine microalgae. Life Sciences. 2013;93:479-486. DOI: 10.1016/j.lfs.2013.08.002
  70. 70. Satpute SK, Banat IM, Dhakephalkar PK, Banpurkar AG, Chopade BA. Biosurfactants, bioemulsifiers and exopolysaccharides from marine microorganisms. Biotechnology Advances. 2007;28:436-450. DOI: 10.1016/j.biotechadv.2010.02.006
  71. 71. Arena A, Gugliandolo C, Stassi G, Pavone B, Iannello D, Bisignano G, et al. An exopolysaccharide produced by Geobacillus thermodenitrificans strain B3-72: Antiviral activity on immunocompetent cells. Immunology Letters. 2009;123:132-137. DOI: 10.1016/j.imlet.2009.03.001
  72. 72. Ande MP, Syamala K, Rao PS, Mohan KM, Lingam SS. Marine nutraceuticals. Aquaculture Times. 2017;3(2):06-09
  73. 73. Suleria HAR, Osborne S, Masci P, Gobe G. Marine-based nutraceuticals: An innovative trend in the food and supplement industries. Marine Drugs. 2015;13:6336-6351. DOI: 10.3390/md13106336
  74. 74. Das P, Mukherjee S, Sen R. Improved bioavailability and biodegradation of a model polyaromatic hydrocarbon by a biosurfactant producing bacterium of marine origin. Chemosphere. 2008;72:1229-1234. DOI: 10.1016/j.chemosphere.2008.05.015
  75. 75. Das P, Mukherjee S, Sen R. Biosurfactant of marine origin exhibiting heavy metal remediation properties. Bioresource Technology. 2009;100:4887-4890. DOI: 10.1016/j.biortech.2009.05.028
  76. 76. Davidson SK, Allen SW, Lim GE, Anderson CM, Haygood MG. Evidence for the biosynthesis of bryostatins by the bacterial symbiont “Candidatus Endobugula sertula” of the Bryozoan Bugula neritina. Applied and Environmental Microbiology. 2001;67(10):4531-4537. DOI: 10.1128/AEM.67.10.4531-4537.2001
  77. 77. Chalova V, Lingbeck J, Kwon Y, Ricke S. Extracellular anti-mutagenic activities of selected probiotic Bifidobacterium and Lactobacillus spp. as a function of growth phase. Journal of Environmental Science and Health, Part B. 2008;43(2):193-198. DOI: 10.1080/03601230701795262
  78. 78. Forsythe P, Bienenstock J. Immunomodulation by commensal and probiotic bacteria. Immunological Investigations. 2010;39:429-448. DOI: 10.3109/08820131003667978
  79. 79. Je JY, Kim SK. Chitosan as potential marine nutraceutical. Advances in Food and Nutrition Research. 2012;65:121-135. DOI: 10.1016/B978-0-12-416003-3.00021-4
  80. 80. Kim SK. Marine medical foods: Implications and applications: Animals and microbes. Advances in Food and Nutrition Research. 2012;65:280. DOI: 10.1016/B978-0-12-416003-3.00001-9
  81. 81. Rayapu L, Makkar F, Chakraborty K, Valluru L. Phytochemical evaluation and antimicrobial activity of Gracilaria opuntia: An important anti-diabetic red marine macroalgae. International Journal of Current Pharmaceutical Research. 2017;9(6):37-41. DOI: 10.22159/ijcpr.2017v9i6.23426
  82. 82. Rajakumar R, Allwin Prem Singh Y. Preliminary phytochemical and antimicrobial studies on the crude extract of red algae Gracilaria edulis against clinical isolates. European Journal of Pharmaceutical and Medical Research. 2017;4(07):763-766
  83. 83. Mehdinezhad N, Ghannadi A, Yegdaneh A. Phytochemical and biological evaluation of some Sargassum species from Persian Gulf. Research in Pharmaceutical Sciences. 2016;11(3):243-249
  84. 84. Rajendran N, Selvan K, Sobana P, Logeswar V, Kathiresan E, Tamilselvi A, et al. Phytochemicals, antimicrobial and antioxidant screening from five different marine microalgae. Journal of Chemical and Pharmaceutical Sciences. 2014;(Special Issue 2):78-85
  85. 85. Blunt JW, Copp BR, Munro MHG, Northcote PT, Prinsep MR. Marine natural products. Natural Product Reports. 2004;21:1-49. DOI: 10.1039/b305250h
  86. 86. Mordor Intelligence Global Nutraceuticals Market—Growth, Trends and Forecasts (2015-2020). Available from: http://www.mordorintelligence.com/industry-reports/global-nutraceuticals-market-industry [Accessed: August 1, 2015]
  87. 87. Research and Markets: Nutraceuticals—2012. Global Strategic Business Report Annual Estimates and Forecasts for 2010-2018. 2012. Available from: http://www.researchandmarkets.com/research/n54vdx/nutraceuticals [Accessed: September 20, 2012]
  88. 88. Rovira MA, Grau M, Castañer O, Covas MI, Schröder H, REGICOR Investigators. Dietary supplement use and health-related behaviors in a Mediterranean population. Journal of Nutrition Education and Behavior. 2013;45(5):386-391
  89. 89. Gupta C, Prakash D. Nutraceuticals for geriatrics. Journal of Traditional and Complementary Medicine. 2015;5(1):5-14

Written By

Charu Gupta and Dhan Prakash

Submitted: 30 August 2018 Reviewed: 02 November 2018 Published: 29 October 2019