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β-Glucans: An Important Bioactive Molecule of Edible and Medicinal Mushrooms

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Edible mushrooms are important for their dietary value and their biologically active and health promoting compounds such as polysaccharides, polysaccharopeptides and polysaccharide-protein complexes. Mushroom β-glucans such as β-glucan, Schizophyllan, Ganoderan, Lentinan and Pleuran are the components of the cell wall. They consist of glucopyranose molecules linked through β (1→3), β (1→4) or β (1→6) linkages. The mushroom β-glucans are not digested in human gastrointestinal tract and are thus considered as a potential source of prebiotics. β-glucans possess profound health promoting properties like speeding up the transit of bowel contents, increasing fecal bulk and frequency, consequently protecting the body from colon cancer, diverticular diseases and irritable bowel syndrome. They stimulate the immune system by having immunomodulatory, antitumour, antioxidant activities and are identified as biological response modifiers. Mushroom β-glucans differ in their nutraceutical effect due to the difference in their molecular masses, solubility, degree of polymerization, their structures and helical conformation. Various mushroom β-glucans are available as pure extracts in the market which are used as therapeutic agents, however, no commercialized functional products are available which have been enriched with mushroom β-glucans. Furthermore, it has a great potential to be used as an ingredient in the near future in various food industries, such as breakfast cereals, sport nutrition products, dairy products, bakery such as biscuits and breads, salad dressings and fat replacer. The aim of this review is to present information on β-glucans of edible and medicinal mushrooms, emphasize their benefits and the usage potential in the functional food and nutraceuticals.
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1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
β-Glucans: An Important Bioactive Molecule of Edible and Medicinal
Mushrooms
Sanem BULAM1*, Nebahat Şule ÜSTÜN2, Aysun PEKŞEN3
1Giresun University, Faculty of Engineering, Department of Food Engineering, Giresun, Turkey;
sanem.bulam@giresun.edu.tr
2Ondokuz Mayıs University, Faculty of Engineering, Department of Food Engineering, Samsun, Turkey;
sustun@omu.edu.tr
3Ondokuz Mayıs University, Faculty of Agriculture, Department of Horticulture, Samsun, Turkey;
aysunp@omu.edu.tr
* Corresponding Author: sanem.bulam@giresun.edu.tr
Abstract
Edible mushrooms are important for their dietary value and their biologically active and health promoting
compounds such as polysaccharides, polysaccharopeptides and polysaccharide-protein complexes. Mushroom β-
glucans such as β-glucan, Schizophyllan, Ganoderan, Lentinan and Pleuran are the components of the cell wall.
They consist of glucopyranose molecules linked through β (1→3), β (1→4) or β (1→6) linkages. The mushroom
β-glucans are not digested in human gastrointestinal tract and are thus considered as a potential source of
prebiotics. β-glucans possess profound health promoting properties like speeding up the transit of bowel
contents, increasing fecal bulk and frequency, consequently protecting the body from colon cancer, diverticular
diseases and irritable bowel syndrome. They stimulate the immune system by having immunomodulatory,
antitumour, antioxidant activities and are identified as biological response modifiers. Mushroom β-glucans differ
in their nutraceutical effect due to the difference in their molecular masses, solubility, degree of polymerization,
their structures and helical conformation. Various mushroom β-glucans are available as pure extracts in the
market which are used as therapeutic agents, however, no commercialized functional products are available
which have been enriched with mushroom β-glucans. Furthermore, it has a great potential to be used as an
ingredient in the near future in various food industries, such as breakfast cereals, sport nutrition products, dairy
products, bakery such as biscuits and breads, salad dressings and fat replacer. The aim of this review is to present
information on β-glucans of edible and medicinal mushrooms, emphasize their benefits and the usage potential
in the functional food and nutraceuticals.
Keywords: Mushrooms, β-glucan, bioactivity, functional, nutraceutical, food industry.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
1. Introduction
β-glucans are polysaccharides of D-glucose monomers linked through β-glycosidic
bonds. The structures of β-glucans and chemically modified β-glucans were given in Figure 1.
(a) (b)
(c) (d)
(e) (f)
Figure 1. The structures of β-glucans and chemically modified β-glucans. (a) (1→3) β-glucans with
ramifications β (1→6); (b) (1→3) β-glucans with ramifications β (1→4); (c) CM β-glucan;
(d) Sulfated β-glucan; (e) Aminated β-glucan; (f) Cyclic glucan (Zhu et al., 2016).
As a kind of dietary fiber (DF), β-glucan could be found in a variety of natural sources
such as yeast, mushrooms, bacteria, algae, barley and oat (Zhu et al., 2015). β-glucan exhibits
a broad spectrum of biological activities including antitumour, immune-modulating (Rieder
and Samuelsen, 2012), antiaging, antimicrobial, antioxidant and antiinflammatory properties.
β-glucans have attracted attention because of their physical and chemical properties over the
years. β-glucans from different sources and with different molecular weights have different
biological activities (Du and Xu, 2014). Fungal β-glucan has been shown to be effective as an
immune system booster and an antitumour substance (Du et al., 2015). The results of clinical
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
research indicate that the presence of β-glucan is linked to the production and activation of
macrophages, NK-cells, T-cells, B-cells from the body’s natural defense system (Lindequist
et al., 2005).
2. Mushroom β-glucans
Mushroom β-glucan is a carbohydrate polymer derived from the cell wall of
mushrooms. β-glucan is known as biological response modifier (BRM), which refers to the
ability to up-regulate and down-regulate the response of biological systems (Brown and
Gordon, 2003; Novak and Vetvicka, 2009).
Mushroom β-glucans such as Schizophyllan, Ganoderan, Lentinan and Pleuran are the
components of the cell wall. They consist of glucopyranose molecules linked through β
(1→3), β (1→4) or β (1→6) linkages. Especially in Japan and China, Pleuran from Pleurotus
ostreatus, Lentinan from Lentinula edodes, Schizophyllan from Schizophyllum commune,
Grifolan (MD-fraction) from Grifola frondosa and Krestin from Trametes versicolor (PSK
and PSP) in addition to the major cancer therapies like surgical operation, radiotherapy and
chemotherapy are in clinical use for the adjuvant tumour therapy (immunotherapy)
(Lindequist et al., 2005; Chan et al., 2009; Novak and Vetvicka, 2009).
β-glucans are also present in many other mushrooms such as Auricularia auricula,
Calocybe indica (Calocyban), Flammulina velutipes, Ganoderma lucidum (Ganoderan/
Ganopoly), Grifola frondosa, and Pleurotus abalones (Lindequist et al., 2005; Villares et al.,
2012; Zhu et al., 2015).
2.1. β-glucan Amounts in Mushrooms
Important medical mushrooms containing β-glucan as bioactive compound are seen in
Table 1. The β-glucan contents of the mushrooms vary between 0.22 and 0.53 g/100 g on dry
weight basis. According to Manzi and Pizzoferrato (2000), Pleurotus pulmunarius seemed to
be the richest source of fungal β-glucans and it has been reported that L. edodes contains high
levels of β-glucans in the soluble fraction. Camelini et al. (2005) found that Agaricus
brasiliensis had higher (1→6)-β-glucan ratio and (1→3)-β-glucan increased with the
maturation of fruiting bodies.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Table 1. Important medicinal mushrooms with β-glucans as bioactive components (Chan et al., 2009).
Mushroom species
Common name
β-glucan structure
Type of β-glucan
Agaricus blazei
Brazilian sun-mushroom,
Himematsutake
mushroom
Protein bound β-1,6-
glucan
Agaricus polysaccharides
Coprinus comatus
Shaggy ink cap, lawyer's
wig, or shaggy mane
β-1,3-glucan
Coprinus polysaccharides
Coriolus versicolor
Yun Zhi
Protein bound β-
1,3;1,6-glucan
PSP (polysaccharide
peptide) PSK
(polysaccharide-Kureha or
polysaccharide-K, krestin)
Ganoderma lucidum
Lingzhi, Reishi
β-1,3;1,6-glucan
Ganoderma
polysaccharides, Ganopoly
Grifola frondosa
Maitake mushroom
β-1,3;1,6-glucan with
xylose and mannose
Maitake D-Fraction
Lentinula edodes
Shiitake mushroom
β-1,3;1,6-glucan
Lentinan
Pleurotus ostreatus
Oyster mushroom, píng
β-1,3-glucan with
galactose and mannose
Pleuran
Schizophyllan commune
Brazilian mushroom
β-1,3;1,6-glucan
Schizophyllan (SPG) or
sizofiran
It was determined that Bracket fungi Trametes versicolor, Piptoporus betulinus or
Phlebia tremellosa contained more than 50% β-glucans and in Boletus edulis (Bull. ex Fr.,
stipe part) or Piptoporus betulinus (Bull. ex Fr.) Karst. the amount was more than 50 g/100 g
dw. In most of the wild mushrooms analysed, the β-glucan contents were significantly higher
in stipes than in caps (Sari et al., 2017). Özcan and Ertan (2018) have determined that Boletus
edulis is the highest β-glucan containing wild mushroom (13.93%). It was followed by
Cantharellus cibarius and Hydnum repandum with 12.89 and 12.84% contents, respectively.
Synytsya et al. (2008) working with Pleurotus spp. mushrooms found that the β-glucan
content of the pilei was between 20.4-39.2% and the content of the stems was between 35.5-
50.0%. The results of a study comparing the β-glucan content of some wild mushrooms (Sari
et al., 2017) is presented in Table 2.
Table 2. β-glucan content of some wild mushrooms (not dividable in cap and stipe parts).
Dry matter
(%)
β-glucans
(g/100g dm)
% β-glucans/
all glucans
91.276
41.755±4.644
99.096
86.122
22.495±2.329
90.186
92.783
25.991±3.643
83.761
89.627
47.006±6.517
89.345
96.547
53.555±2.452
98.572
90.825
51.801±4.024
95.659
87.892
60.788±11.795
99.337
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
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2.2. Bioactive Properties of β-glucans in Mushrooms
Mushrooms polysaccharides having β-linkage have been demonstrated a boost in the
human immune system and the modulation of the immunological response under certain
conditions, thus they are commonly termed as biological response modifiers (BRM). As the
result of the activation of the host’s immune system, these polysaccharides show significant
antitumour, antiviral and antimicrobial activities besides their other effects (Villares et al.,
2012). A number of studies have been carried out on β-glucans that have a health-enhancing
effect in various important ways such as antitumour and immunomodulatory (Table 3),
antitumour, antiviral (Borchers et al., 2004; Moradali et al., 2007), cardiovascular (Wasser
and Weis, 1999), liver protective, antiinflammatory (Lindequist et al., 2005), radioprotective
(Pillai and Devi, 2013), antidiabetic (Kim et al., 2005), antioxidant (Deng et al., 2012),
antibacterial (Beattie et al., 2010), and antiobesity activities (Zhang et al., 2013). Antitumour
activity (Deng et al., 2012; Ren et al., 2012) and immunemodulating activity (Wasser, 2002)
of mushroom β-glucans have been documented in the previous reviews. Basically, their
health-promoting abilities are influenced by the molecular mass, branching configuration,
conformation, and chemical modification of the polysaccharides (Ren et al., 2012). In terms
of biological activity, β-1,3-D-glucans and β-1,6-D-glucans contained in oyster, shiitake, split
gill, and himematsutake mushrooms, as well as other Basidiomycetes, are considered to be the
most effective (Rop et al., 2009).
Table 3. Some mushroom β-glucans with antitumour and immunomodulatory activities (Zhang et al.,
2007; Novak and Vetvicka, 2008; Kothari et al., 2018).
Mushroom species
Type of β-glucan
Character of polymer
Degree of branching
Agaricus blazei
β-glucomannan
Branched
-
Dictyophora indusiata
T-4-N, T-5-N
Branched
-
Ganoderma lucidum
Ganoderan
Branched
-
Grifola frondosa
Grifolan
Branched
0.31-0.36
Inonotus obliquus
Xylogalactoglucan
Branched
-
Laminaria spp.
Laminaran
Linear
-
Lentinula edodes
Lentinan
Branched
0.23-0.33
Pleurotus ostreatus
Pleuran (HA-glucan)
Branched
0.25
Poria cocos
Pachymaran
Linear
0.015-0.020
Schizophyllum commune
Schizophyllan
Branched
0.33
Sclerotinia sclerotiorum
Sclerotinan (SSG)
Branched
0.50
2.3. Extraction and Production of Mushroom β-glucans
The methods used to extract and produce β-glucans from various edible/medicinal
mushrooms are given in Table 4.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Table 4. Production/extraction process of β-glucans from various edible/medicinal mushrooms.
Mushroom species
Production/Extraction process
References
Agaricus bisporus
Ultrasonic-assisted extraction, precipitation with
ethanol, centrifugation
Lyophilization, milled and submitted to successive cold
and hot aqueous extraction
Tian et al., 2012
Smiderle et al., 2013
Agaricus brasiliensis
Sequentially extracted with 350 ml water, concentrated,
dialyzed and DEAE-cellulose column chromatography
Lyophilization, milled and submitted to successive cold
and hot aqueous extraction
Camelini et al., 2005
Smiderle et al., 2013
Astraeus hygrometricus
Aqueous extraction, DEAE cellulose bag and Sepharose
6B column
Chakraborty et al.,
2004
Boletus edulis
The estimation of non-starch glucans was based on the
difference between glucose contents after total acidic
hydrolysis of glucans and specific enzymatic hydrolysis
of α-1,4-glucans
Özcan and Ertan, 2018
Boletus erythropus
Water extraction, centrifugation, DEAE Trisacryl M
column and S 400 HR column
Chauveau et al., 1996
Botryosphaeria rhodina
β-glucan production were monitored in a stirred-tank
bioreactor
Crognale et al., 2007
Cantharellus cibarius
The estimation of non-starch glucans was based on the
difference between glucose contents after total acidic
hydrolysis of glucans and specific enzymatic hydrolysis
of α-1,4-glucans
Özcan and Ertan, 2018
Flammulina velutipes
Successive hot extraction with water and KOH and
submitted to freeze-drying
Smiderle et al., 2006
Ganoderma lucidum
Extraction using dilute NaOH solution and Sephadex
G-15 gel-filtration chromatography
Kao et al., 2012; Nie et
al., 2013
Paenibacillus polymyxa
Seed culture was supplemented with carbon source to
induce glucan production
Jung et al., 2007
Pleurotus eryngii
The estimation of non-starch glucans was based on the
difference between glucose contents after total acidic
hydrolysis of glucans and specific enzymatic hydrolysis
of α-1,4-glucans
Washing with ethanol and distilled water, extraction
with boiling water, incubation with α-amylase, chemical
deproteinization, dialization and lyophilization
Synytsya et al., 2008
Synytsya et al., 2009
Pleurotus ostreatus
The estimation of non-starch glucans was based on the
difference between glucose contents after total acidic
hydrolysis of glucans and specific enzymatic hydrolysis
of α-1,4-glucans
Washing with ethanol and distilled water, extraction
with boiling water, incubation with α-amylase, chemical
deproteinization, dialization and lyophilization
Lyophilization, using of methanolic extraction, cold
water, hot water, hot aqueous NaOH solutions, enzyme
protease, and ethanol precipitation
Synytsya et al., 2008
Synytsya et al., 2009
Palacios et al., 2012
Ramaria botrytis
Hot water extraction followed by treating NaOH
Bhanja et al., 2014
Schizophyllum commune
Seed culture preparation, optimization of fermentation
medium and schizophyllan production
Kumari et al., 2008
Termitomyces eurhizus
Hot alkaline extraction, centrifugation, DEAE cellulose
bag and freeze dry
Chakraborty et al.,
2006
The detection methods of β-glucan from mushrooms are summarized as: (1) enzymic
method or McCleary method (Megazyme kit), (2) enzymelinked immunosorbent assay
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
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(ELISA) method, (3) fluorimetric method with aniline blue, and (4) colorimetric method with
Congo red (Zhu et al., 2015).
2.3.1 Extraction and Production of β-glucans from Fruiting Bodies of Mushrooms
Kim et al. (2005) extracted β-glucan from the fruiting bodies of Agaricus blazei using
hot water for 3 h. Bhanja et al. (2014) extracted and isolated two water-insoluble glucans from
fruiting bodies of Ramaria botrytis. Extraction in hot or boiling water is the most common
and convenient method for extracting water-soluble fungal polysaccharides (Yan et al., 2014).
Liu et al. (2014) obtained a purified β-glucan by precipitating a hot-water extract from fruiting
bodies of G. lucidum with 20% (V/V) ethanol. The total carbohydrate content was 95.9% in
prepared β-glucan.
2.3.2. Extraction and Production of β-glucans from the Mycelia of Mushrooms
Kim et al. (2009) provided a method for mass production of β-glucan from S. commune,
comprising subjecting mycelia of S. commune to liquid culture with an addition of a synthetic
adsorbent. In another study, a neutral polysaccharide, GLSA50-1B, was isolated from
sporoderm-broken spores of G. lucidum, by hot-water extraction, graded ethanol precipitation,
anion-exchange chromatography, and gel permeation chromatography (Dong et al., 2012).
Kim et al. (2013) demonstrated generation of high β-glucan producing mutant strains of
Sparassis crispa, additional culture optimization further increased β-glucan productivity of
the mutant strains. Recently, Park et al. (2014) enhanced the β-glucan content in the sawdust-
based cultivation of cauliflower mushroom (Sparassis latifolia) using three kinds of enzymes
(chitinase, β-glucuronidase, and lysing enzyme complex) as elicitors.
2.4. Chemical Modification and Purification of Mushroom β-glucans
β-glucan is an important bioactive compound for human health, but its low solubility
has led to the development of chemical modification technologies to improve bioavailability.
Several methods to modify β-glucan are laid out to improve their functional and technological
properties via physical and chemical crosslinking reactions (Ahmad et al., 2015). In this
respect, β-glucans can be chemically modified to obtain various derivatives with potential
industrial or medicinal importance (Synytsya and Novak, 2013).
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
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Ion-exchange chromatography and gel filtration chromatograph are the most common
and convenient methods for purifying polysaccharide. In general, the crude polysaccharide
extracts were further applied to a Sephadex column and eluted with water (Zhu et al., 2015).
3. Studies on Mushroom β-glucan for Food and Nutraceutical Applications
3.1. Food Applications and Some Patents
There have been some studies previously conducted by enriching a product with the
mushroom β-glucan agglomerated as food additive. β-glucans from P. ostreatus and L. edodes
have been demonstrated satisfactory results when they were added to yogurt (Hozova et al.,
2004) were used in the production of extruded snack products with low glycemic index
(Brennan et al., 2013). Also chicken burgers were enriched with P. sajor-caju, fiber and β-
glucans (Wan Rosli et al., 2011) as well as P. ostreatus was incorporated into sausages in an
effort to lower their fat content (Chockchaisawasdee et al., 2010). In a study to produce a
novel high-fibre and low-calorie functional food, Kim et al. (2011) used β-glucans from L.
edodes as a wheat flour substitute in baked foods. These glucans improved the pasting
properties of wheat flour and increased batter viscosity and shear-thinning elasticity without
any adverse effect on air holding capacity or hardness. β-glucans of Ganoderma amboinense,
Agaricus or Fomes yucatensis, or mixed mushrooms have also been tested for encapsulation
of pickling liquid to be released in soups or sauces during cooking (Watanabe, 2005).
3.2. Nutraceutical Applications, Some Clinical Studies and Patents
“Mushroom nutraceuticals” is nowadays a relatively common term which refers to a
refined polysaccharide, or a partially refined fruit body extract, or the dried biomass from
mycelium or the fruiting body of a mushroom, which is consumed in the form of capsules,
tablets, powder, syrups, solutions as a dietary supplement with some therapeutic properties
(Giavasis, 2014). Camelini et al. (2005) investigated the β-glucans of A. brasiliensis in
different stages of fruiting body maturity and their use in nutraceutical products. The results
showed that because of their important glucan contents, mature fruiting bodies of A.
brasiliensis should be used for nutraceutical products. Cap-opened, more fragile mature
fruiting bodies of A. brasiliensis should be selected over immature ones for the production of
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nutraceuticals. Synytsya et al. (2008) reported that the stems of Pleurotus eryngii and P.
ostreatus could be used for the preparation of biologically active polysaccharide complexes as
food supplements. Schizophyllan, produced by S. commune ATCC 38548 has attracted
attention as immunomodulatory and anti-neoplastic agent in pharmaceutical industry in the
recent years (Kumari et al., 2008). Akiyama et al. (2011) studied the effects of agaritine, a
hydrazine-derivative from hot-water extract of A. blazei Murrill on human leukemic
monocyte lymphoma (U937) cells. Agaritine induced DNA fragmentation, annexin V
expression, and cytochrome C release. Caspase-3, 8 and 9 activities were gradually increased
after agaritine treatment. A. blazei has been used as an adjuvant in cancer chemotherapy and
various types of anti-leukemic bioactive components have been extracted from it (Patel and
Goyal, 2012). It was proposed to mix β-glucan from mushroom with one or two substances
such as ubiquinone Q10 and ferments leading to a biologically active additive for food with a
wide range of action (Bragintseva et al., 2002). Suga et al. (2005) suggested converting
lentinan into superfine particles, improving absorption through mucosa.
In animal experiments, β-glucans have been shown to have varying activity against
sarcomas, mammary cancer, some chemically induced cancers, adenocarcinoma, colon cancer
and some leukemias. Lentinan has already been shown effective in gastric carcinomas
(Taguchi et al., 1985; Jeannin, et al., 1988). Furthermore, lentinan was reported to induce
apoptosis in murine skin carcinoma cell-lines (Gu and Belury, 2005). Even if mushrooms and
especially β-glucans have been used in Chinese medicine for decades, mechanisms need to be
elucidated. However, lot of these substances have already been patented for antitumour
treatments. Among them, β-glucan extracted from Agaricus mushroom was proposed,
together with fucoidan (Hosokawa, 2003). The use of Grifola frondosa extract has also been
patented, mixed with fucoidan and organic germanium (Sogabe, 1998).
Extracts of L. edodes markedly inhibited the growth of Sarcoma 180 (a retrovirus,
similar to HIV which uses reverse transcriptase for its tumourpromoting activity) (Chihara et
al., 1987). According to clinical studies, lentinan produces specific T-helper cell stimulation
in healthy humans as well as animals. It has also been recognized to stimulate lymphokine
activated killer activity in combination with Interleukin-2 (Suzuki et al., 1990). Other patents
concerning direct utilisation of -D-glucans such as G. frondosa extract (Sogabe, 1996) for
treating AIDS have been rare.
In 2003, an original application has been patented, proposing to use -glucan as a gene
carrier (Sakurai et al., 2003). In this patent, a hydrogen-bonding polymer with a triple-helix
structure (such as schizophyllan, curdlan, lentinan, scleroglucan) was used for binding to a
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nucleic acid. Thus, a nucleic acid-polymer complex was obtained and could be applied as a
vector. Moreover, this complex was also resistant to nuclease, allowing its use as a nucleic
acid-protecting agent. PSP derived from Coriolus versicolor (syn. Trametes versicolor), a
Chinese product commercially available since 1987 (Cui and Chisti, 2003), has been
documented to improve the quality of life in cancer patients by providing substantial pain
relief and enhancing immune status in 70-97% of patients with stomach, esophagus, lung,
ovary and cervical cancers. Both PSK and PSP boosted immune cell production, ameliorated
chemotherapy symptoms and enhanced tumour infiltration by dendritic and cytotoxic T-cells
(Kidd, 2000). From a commercial standpoint, pleuran from oyster (P. ostreatus) mushrooms
and lentinan from Shiitake (L. edodes) mushrooms are currently the most frequently used β-
glucans. Both of them show positive effects on the intestines. They increase the resistance of
intestinal mucosa to inflammation (Zeman et al., 2001) and inhibit the development of
intestinal ulcers (Nosalova et al., 2001). Lentinan also shows a positive effect on peristalsis
(Van Nevel et al., 2003).
3.3. Industrial Food Applications of Mushroom β-glucan in Functional Foods and
Dietary Supplements
According to literature data, β-glucan has the potential to perform functions in the food
industry such as thickening, water-holding, or oil-binding, gelling, film-making and
encapsulation agent, and emulsifying stabilizer (Ahmad et al., 2012a, b; Giavasis, 2013; Zhu
et al., 2016). Today, mushroom-glucans are found in the market more in the form of capsules
or tablets as food supplements and to a lesser extent as ingredients in the food products
(Eleftherios et al., 2014). In addition to food, β-glucans have potential applications in
medicine and pharmacy, cosmetic and chemical industries, in veterinary medicine and feed
production (Laroche and Michaud, 2007; Zhu et al., 2016). Besides, various mushroom β-
glucans are available as pure extracts in the market which are used as therapeutic agents. S.
commune glucan manufactured by Bioland Technology Co. Ltd. is commercially available in
the market (Zhu et al., 2016). There have been two patents on production technology of β-
glucan from S. commune, today (Kim et al., 2008; 2009). Polysachharides such as lentinan,
schizophyllan from shiitake and Schizophyllan mushrooms, PSK and PSP, the protein bound
polysachharides from turkey tail mushroom, have been developed as anticancer agents in
Japan and are now available worldwide (Lull, et al., 2005). There has also been a patent on
application on β-glucan process, additive and food product (Cahill et al., 2003). Although
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
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some of the most studied polysaccharides produced by mushrooms (e.g. schizophyllan and
lentinan) are already available and marketed as nutraceuticals (pharmaceutical formulation),
their addition to food in their purified form has not been commercialized, yet (Giavasis,
2013). Nevertheless, β-glucan has a great potential to be used as an ingredient in the near
future in various food industries, such as breakfast cereals, prebiotic sausage formulations,
sport nutrition products, dairy products such as yogurts, bakery products such as biscuits,
breads, cakes and ready-to-eat snacks, beverages, salad dressings and fat replacer that have
some functionalities such as noticeable effect on physical and sensory properties, calorie-
reducing and cholesterol-lowering actions and faster proteolysis, lower release of large
peptides and a higher proportion of free amino acids, the glycemic response manipulation,
controlling food intake and reducing 24 h energy intake and having good quality
characteristics (Zhu et al., 2016).
The polysaccharides extracted from A. brasiliensis, C. sinensis, G. lucidum, G.
frondosa, L. edodes, and T. versicolor are used to produce tablets for inhibiting the growth of
tumours and improving the immunity (Rai et al., 2005). Several mushroom products, mainly
polysaccharides such as β‐D‐glucans, have also proceeded successfully through clinical trials
and are used as drugs to treat cancer and chronic diseases (Morris et al., 2016).
Today, it is possible to find commercial dietary supplements originated from various
mushroom β-glucans in the form of powdered extracts, tablets, capsules, teas and syrups on
the market. Imunoglukan P4H® from P. ostreatus, LentinanXP in USA/Lentinex® in Europe
and Shiitake Gold and Pure Shiitake™ from L. edodes, Ganopoland Immulink MBG®
from G. lucidum, D-fraction, MD fraction, MaitakeGold 404® nutraceutical extract and Pure
Maitake™ from G. frondosa, Pure Turkey Tail™ from T. versicolor and Immune Assist™
from A. blazei, C. sinensis, G. lucidum, G. frondosa, L. edodes and T. versicolor can be given
as example (Point Institute, 2013; Morris et al., 2016; Reis et al., 2017; URL-1, 2018).
McCleary and Draga (2016) developed a robust and reliable method for the measurement of
β-glucan in mushroom and mycelial products. In the literature, there have also been some
clinical studies on pharmacological benefits and safe doses of these mushroom β-glucan
derived dietary supplements such as Lentinex® (Gaullier et al., 2011) and Imunoglukan
P4H® (Jesenak et al., 2012). A scientific documentation was published to carry out the
additional safety assessment for Lentinex®, an aqueous mycelial extract of L. edodes, as a
novel food ingredient (EFSA, 2010). On the other hand, Gründemann et al. (2015) have
reported that the standardisation of shiitake preparations is difficult because even preparations
with similar polysaccharide and β-glucan contents have different immunological properties.
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4. β-glucan Market by Food & Beverage Applications and Regions
The industries are adopting β-glucan to fortify foodstuff with high dietary fibres as
consumer interests in the nutraceutical products is on escalation. Furthermore β-glucan
actively impacts the metabolic parameters and help curing the chronic diseases. The
worldwide development of policies for inclusion of functional ingredients in industrial
products boosts the global β-glucan market. According to application segmentation, food and
beverage segment was accounted more than 25% value share in 2016. Increasing demand for
fibrous intake and concerns over blood cholesterol levels majorly drives the β-glucan market
in food and beverage applications. In addition, β-glucan allows food product manufacturers to
attract attention heart health claims in functional foods such as heart healthy biscuits, dairy
products, snack bars etc., which in turn aids in driving the global β-glucan market (URL-2,
2018).
Geographically, the Europe accounted major share in the global β-glucan market in
2016. Approval of health claims by EU, related to heart health, blood glucose, cholesterol
control and digestive health will be fueling the growth for β-glucan market in the region over
the forecast period. In Asia Pacific, the government initiatives for awareness on cancer,
women heart and maternal health are expected to drive the sales revenue of β-glucan during
the forecast period of 2017-2025 (URL-2, 2018).
5. Conclusion
Although there are many findings related to the biological effects of β-glucans in vitro
and in vivo, there are still some questions about structure activity and dose activity
relationships. Moreover, β-glucan content of mushroom products has not been standardised,
yet. To make better use of β-glucan, food manufacturers and processors must bring attention
not only to ensure sufficient concentration of β-glucan in the raw material but also to the
processing methods and physicochemical properties of β-glucan, decreasing mechanical and
enzymatic breakdown of the β-glucans in end-product and optimizing processing conditions.
Mushroom β-glucans have potential nutraceutical properties that could be explored in the
food and the pharmaceutical fields and might present different functional properties upon
modification through suitable means and continuity of detailed clinical studies for the
convinience of consumers.
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References
Ahmad, A., Anjum, F. M., Zahoor, T., Nawaz, H., and Dilshad, S. M. (2012a). Beta glucan: A
valuable functional ingredient in foods. Critical Reviews in Food Science and Nutrition, 52,
201-212.
Ahmad, A., Munir, B., Abrar, M., Bashir, S., Adnan, M., and Tabassum, T. (2012b). Perspective of β-
glucan as functional ingredient for food industry. Journal of Nutrition and Food Sciences, 2,
133.
Ahmad, N. H., Mustafa, S., and Che Man, Y. B. (2015). Microbial polysaccharides and their
modification approaches: A review. International Journal of Food Properties, 18, 332-347.
Akiyama, H., Endo, M., Matsui, T., Katsuda, .I, Emi, N., Kawamoto, Y., Koike, T., and Beppu, H.
(2011). Agaritine from Agaricus blazei Murrill induces apoptosis in the leukemic cell line
U937. Biochimica et Biophysica Acta, 1810, 519-525.
Beattie, K. D., Rouf, R., Gander, L., May, T. W., Ratkowsky, D., Donner, C. D., Gill, M., Grice, I. D.,
and Tiralongo, G. (2010). Antibacterial metabolites from Australian macrofungi from the genus
Cortinarius. Phytochemistry, 71, 948-955.
Bhanja, S. K., Rout, D., Patra, P., Sena, I. K., Nandan, C. I. K., and Islam, S. S. (2014). Water-
insoluble glucans from the edible fungus Ramaria botrytis. Bioactive Carbohydrates and
Dietary Fibre, 3(2), 52-58.
Borchers, A., Keen, C. L., and Gershwin, M. E. (2004). Mushrooms, tumors, and immunity: an
update. Experimental Biology and Medicine, 229, 393-406.
Bragintseva, L. M., Grigorash, A. I., Kovalenko, V. A., Maklanov, A. I, and Ustynjuk, T. K. (2002).
RU2177699.
Brennan, M. A., Derbyshire, E., Tiwari, B. K., and Brennan, C. (2013). Integration of β-glucan fibre
rich fractions from barley and mushrooms to form healthy extruded snacks. Plant Foods for
Human Nutrition, 68(1), 78-82.
Brown, G. D., and Gordon, S. (2003). Fungal beta-glucans and mammalian immunity. Immunity, 19,
311-315.
Cahill, A. P., Fenske, D. J., Freeland, M., and Hartwig, G. W. (2003). Beta-glucan process, additive
and food product. US patent 6749885 B2.
Camelini, C. M., Maraschin, M., Matos de Mendonça, M., Zucco, C., Ferreira, A. G., and Tavares, L.
A. (2005). Structural characterization of β-glucans of Agaricus brasiliensis in different stages
of fruiting body maturity and their use in nutraceutical products. Biotechnology Letters,
27(17), 1295-1299.
Chakraborty, I., Mondal, S., Pramanik, M., Rout, D., and Islam, S. S. (2004). Structural investigation
of a water-soluble glucan from an edible mushroom, Astraeus hygrometricus. Carbohydrate
Research, 339(13), 2249-2254.
Chakraborty, I., Mondal, S., Rout, D., and Islam, S. S. (2006). A water-insoluble (1→3)-beta-D-
glucan from the alkaline extract of an edible mushroom Termitomyces eurhizus. Carbohydrate
Research, 341(18), 2990-2993.
Chan, G. C. F., Chan, W. K., and Sze, D., M. Y. (2009). The effects of β-glucan on human immune
and cancer cells. Journal of Hematology & Oncology, 2, 25.
Chauveau, C., Talaga, P., Wieruszeski, J. M., Strecker, G., and Chavant, L. (1996). A water-soluble
beta-D-glucan from Boletus erythropus. Phytochemistry, 43(2), 413-415.
Chihara, G., Hamuro, J., Maeda, Y.Y., Arai, Y., and Fukuoka, F. (1987). Function and purification of
the polysaccharides with marked antitumor activity, especially Lentinan, from Lentinus edodes
(Berk.). Cancer Research, 30, 2776-2781.
Chockchaisawasdee, S., Namjaidee, S., Pochana, S., and Stathopoulos, C. E. (2010). Development of
fermented oyster mushroom sausage. Asian Journal of Food & Agro-Industry, 3, 35-43.
Crognale, S., Bruno, M., Fidaleo, M., Moresi, M., and Petruccioli, M. (2007). Production of β-glucan
and related glucan-hydrolases by Botryosphaeria rhodina. Journal of Applied Microbiology,
102, 860-871.
Cui, J, and Chisti, Y. (2003). Polysaccharopeptides of Coriolus versicolor: physiological activity,
uses, and production. Biotechnology Advances, 21(2), 109-22.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Deng, C., Hu, Z., Fu, H. T., Hu, M. H., Xu, X., and Chen, J. H., (2012). Chemical analysis and
antioxidant activity in vitro of a β-D-glucan isolated from Dictyophora indusiata. International
Journal of Biological Macromolecules, 51, 70-75.
Dong, Q., Wang, Y., Shi, L., Yao, J., Li, J., Ma, F., and Ding, K. (2012). A novel water-soluble β-D-
glucan isolated from the spores of Ganoderma lucidum. Carbohydrate Research, 353, 100-105.
Du, B., and Xu, B. J. (2014). Oxygen radical absorbance capacity (ORAC) and ferric reducing
antioxidant power (FRAP) of β-glucans from different sources with various molecular weight.
Bioactive Carbohydrate and Dietary Fibre, 3, 11-16.
Du, B., Lin, C. Y., Bian, Z. X., and Xu, B. J. (2015). An insight into anti-inflammatory effects of
fungal beta-glucans. Trends in Food Science & Technology, 41, 49-59.
EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA). (2010). Scientific opinion on the
safety of “Lentinus edodes extract” as a novel food ingredient. EFSA Journal, 8(7), 1685.
Eleftherios, E., Vassilis, M. G., and Cleanthes, I. (2014). The potential use of mushrooms β-glucans in
the food industry. International Journal of Biotechnology for Wellness Industries, 3, 15-18.
Gaullier, J. M., Sleboda, J., Øfjord, E. S., Ulvestad, E., Nurminiemi, M., Moe, C., Albrektsen, T., and
Gudmundsen, O. (2011). Supplementation with a soluble beta-glucan exported from shiitake
medicinal mushroom, Lentinus edodes (Berk.) Singer mycelium: A crossover, placebo-
controlled study in healthy elderly. International Journal of Medicinal Mushrooms, 13(4), 319-
326.
Giavasis, I. (2013). Production of microbial polysaccharides for use in food. In: Microbial production
of food ingredients, enzymes and nutraceuticals. United Kingdom: Woodhead Publishing.
Giavasis, I. (2014). Bioactive fungal polysaccharides as potential functional ingredients in food and
nutraceuticals. Current Opinion in Biotechnology, 26, 162-173.
Gründemann, C., Garcia-Käufer, M., Sauer, B., Scheer, R., Merdivan, S., Bettin, P., Huber, R., and
Lindequist, U. (2015). Comparative chemical and biological investigations of β-glucan-
containing products from shiitake mushrooms. Journal of Functional Foods, 18, 692-702.
Gu, Y. H., and Belury M. A. (2005). Selective induction of apoptosis in murine skin carcinoma cells
(CH72) by an ethanol extract of Lentinula edodes. Cancer Letters, 220, 21-28.
Hosokawa, J. (2003). JP2003055234.
Hozova, B., Kuniak, L., and Kelemova, B. (2004). Application of β-glucans isolated from mushrooms
Pleurotus ostreatus (pleuran) and Lentinula edodes (lentinan) for increasing the bioactivity of
yoghurts. Czech Journal of Food Sciences, 22, 204-214.
Jeannin, J. F., Lagadec, P., Pelletier, H., Reisser, D., Olsson, N. O., Chihara, G., and Martin, F. (1988).
Regression induced by lentinan of peritoneal carcinomatoses in a model of colon cancer in rat.
Interntional Journal of Immunopharmacology, 10(7), 855-861.
Jesenak, M., Majtan, J., Rennerova, Z., Kyselovic, J., Banovcin, P., and Hrubisko, M. (2012).
Immunomodulatory effect of pleuran (β-glucan from Pleurotus ostreatus) in children with
recurrent respiratory tract infections. International Immunopharmacology, 15, 395-399.
Jung, H. K., Hong, J. H., Park, S. C., Park, B. K., Nam, D. H., and Kim, S. D. (2007). Production and
physicochemical characterization of β-glucan produced by Paenibacillus polymyxa JB115.
Biotechnology and Bioprocess Engineering, 12, 713-719.
Kao, P. F., Wang, S. H., Hung, W. T., Liao, Y. H., Lin, C. M., and Yang, W. B. (2012). Structural
characterization and antioxidative activity of low-molecular-weights beta-1, 3-glucan from the
residue of extracted Ganoderma lucidum fruiting bodies. BioMed Research International, 1-8.
Kidd, P. M. (2000). The use of mushroom glucans and proteoglycans in cancer treatment. Alternative
Medicine Review, 5(1), 4-27.
Kim, Y. W., Kim, K. H., Choi, H. J., and Lee, D. S. (2005). Anti-diabetic activity of beta-glucans and
their enzymatically hydrolyzed oligosaccharides from Agaricus blazei. Biotechnology Letters,
7(7), 483-487.
Kim, M. S., Park, Y. D., and Lee, S. R. (2008). Preparation method of beta-glucan from Schizophyllum
commune and composition for experimental application comprising the same. US patent
0160043 A1.
Kim, M. S., Park, Y. D., and Lee, S. R. (2009). Method of using beta-glucan from Schizophyllum
commune. US patent 0023681 A1.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Kim, J., Lee, S. M., Bae, I. Y., Park, H. G., Gyu Lee, H., and Lee, S. (2011). (1-3)(1-6)-β-glucan-
enriched materials from Lentinus edodes mushroom as a high-fibre and low-calorie flour
substitute for baked foods. Journal of the Science of Food and Agriculture, 91, 1915-1919.
Kim, S. R., Kang, H. W., and Ro, H. S. (2013). Generation and evaluation of high β-glucan producing
mutant strains of Sparassis crispa. Mycobiology, 41(3), 159-163.
Kothari, D., Patel, S., and Kim, S. K. (2018).Anticancer and other therapeutic relevance of mushroom
polysaccharides: A holistic appraisal. Biomedicine & Pharmacotherapy, 105, 377-394.
Kumari, M., Survase, S. A., and Singhal, R. S. (2008). Production of schizophyllan using
Schizophyllum commune NRCM. Bioresource Technology, 99, 1036-1043.
Laroche, C., and Michaud, P. (2007). New developments and prospective applications for β-(1,3)
glucans. Recent Patents on Biotechnology, 1, 59-73.
Lindequist, U., Niedermeyer, T., and Jülich, W. D. (2005). The pharmacological potential of
mushrooms. Evidence-Based Complementary and Alternative Medicine, 2(3), 285-299.
Liu, Y., Zhang, J., Tang, Q., Yang, Y., Guo, Q., Wang, Q., Wu, D., and Cui, S. W. (2014).
Physicochemical characterization of a high molecular weight bioactive β-D-glucan from the
fruiting bodies of Ganoderma lucidum. Carbohydrate Polymers, 101, 968-974.
Lull, C., Wichers, H. J., and Savelkoul, H. F. (2005). Antiinflammatory and immunomodulating
properties of fungal metabolites. Mediators of Inflammation, 2, 63‐80.
Manzi, P., and Pizzoferrato, L. (2000). Beta-glucans in edible mushrooms. Food Chemistry, 68, 315-
318.
McClearly, B. V., and Draga, A. (2016). Measurement of β-glucan in mushrooms and mycelial
products. Journal of AOAC International, 99(2), 364-373.
Moradali, M. F., Mostafavi, H., Ghods, S., and Hedjaroude, G. A. (2007). Immunomodulating and
anticancer agents in the realm of macromycetes fungi (macrofungi). International
Immunopharmacology, 7, 701-724.
Morris, H. J., Llaurado, G., Beltran, Y., Lebeque, Y., Bermudez, R. C., Garcia, N., Gaime-Perraud, I.,
and Moukha, S. (2016). The use of mushrooms in the development of functional foods, drugs or
nutraceuticals. In: Wild Plants, Mushrooms and Nuts: Functional Food Properties and
Applications, pp. 123-157. John Wiley & Sons, Ltd.
Nie, S., Zhang, H., Li, W., and Xie, M. (2013). Current development of polysaccharides from
Ganoderma: Isolation, structure and bioactivities. Bioactive Carbohydrates and Dietary Fiber, 1,
10-20.
Novak, M., and Vetvicka, V. (2008). β-glucans, history, and the present: Immunomodulatory aspects
and mechanism of action. Journal of Immunotoxicology, 5, 47-57.
Novak, M., and Vetvicka, V. (2009). Glucans as biological response modifiers. Endoctrine, Metabolic
& Immune Disorders Drug Targets, 9, 6775.
Nosalova, V., Bobek, P., Cerna, S., Galbavy, S., and Stvrtina, S. (2001). Effects of pleuran (beta-
glucan isolated from Pleurotus ostreatus) on experimental colitis in rats. Journal of the
Physiological Research, 50, 575-581.
Özcan, Ö., and Ertan, F. (2018). Beta-glucan content, antioxidant and antimicrobial activities of some
edible mushroom species. Journal of Food Science and Technology, 6(2), 47-55.
Palacios, I., García-Lafuente, A., Guillamón, E., and Villares, A. (2012). Novel isolation of water-
soluble polysaccharides from the fruiting bodies of Pleurotus ostreatus mushrooms
Carbohydrate Research, 358, 72-77.
Patel, S., and Goyal, A. (2012). Recent developments in mushrooms as anti-cancer therapeutics: A
review. Biotechnology, 2, 1-15.
Park, H., Ka, K. H., and Ryu, S. R. (2014). Enhancement of β-glucan content in the cultivation of
cauliflower mushroom (Sparassis latifolia) by elicitation. Mycobiology, 42, 41-45.
Pillai, T. G., and Devi, U. P. (2013). Mushroom beta glucan: Potential candidate for post irradiation
protection. Mutation Research, 751, 109-115.
Point Institute. (2013). The use of mushroom-derived dietary supplements as immunomodulating
agents: An overview of evidence-based clinical trials and the mechanisms and actions of
mushroom constituents. Technical Report. Wisconsin: Stevens Point.
Rai, M., Tidke, G., and Wasser, S. P. (2005). Therapeutic potential of mushrooms. Natural Product
Radience, 4(4), 246-257.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Reis, F. S., Martins, A., Vasconcelos, M. H., Morales, P., and Ferreira, I. C. F. R. (2017). Functional
foods based on extracts or compounds derived from mushrooms. Trends in Food Science &
Technology, 66, 48-62.
Ren, L., Perera, C., and Hemar, Y. (2012). Antitumor activity of mushroom polysaccharides: A
review. Food & Function, 3, 1118-1130.
Rop, O., Mlcek, J., and Jurikova, T. (2009). Beta-glucans in higher fungi and their health effects.
Nutrition Reviews, 67(11), 624-631.
Rieder, A., and Samuelsen, A. B. (2012). Do cereal mixed-linked β-glucans possess immune-
modulating activities? Molecular Nutrition & Food Research, 56, 536-547.
Sakurai, K., Shinkai, S., Kimura, T., Tabata, K., Koumoto, K., and Gronwald, O. (2003).
US2003216346.
Sari, M., Prange, A., Lelley, J. I., and Hambitzer, R. (2017). Screening of beta-glucan contents in
commercially cultivated and wild growing mushrooms. Food Chemistry, 216, 45-51.
Smiderle, F. R., Carbonero, E. R., Mellinger, C. G., Sassaki, G. L., Gorin, P. A., and Iacomini, M.
(2006). Structural characterization of a polysaccharide and a beta-glucan isolated from the
edible mushroom Flammulina velutipes. Phytochemistry, 67(19), 2189-2196.
Smiderle, F. R., Alquini, G., Tadra-Sfeir, M. Z., Iacomini, M., Wichers, H. J., and Van Griensven, L.
J. L. D. (2013). Agaricus bisporus and Agaricus brasiliensis (1→6)-β-D-glucans show
immunostimulatory activity on human THP-1 derived macrophages. Carbohydrate Polymers,
94, 91-99.
Sogabe, T. (1996). JP8119874.
Sogabe, T. (1998). JP10033142.
Suga, T., Ogasawara, Y., Kaneko, Y., Kajiura, M., and Suga, Y. (2005). JP2005097308.
Suzuki, M., Higuchi, S., Taki, Y., Miwa, K., and Hamuro, J. (1990). Activity of Lentinan and
Interleukin 2. International Journal of Immunopharmacology, 12(6), 613-623.
Synytsya, A., Míčková, K., Jablonský, I., Sluková, M., and Čopíková, J. (2008). Mushrooms of genus
Pleurotus as a source of dietary fibres and glucans for food supplements. Czech Journal of Food
Sciences, 26, 441-446.
Synytsya, A., Míčková, K., Synytsya, A., Jablonský, I., Spěváček, J., Erban, V., Kovarikova, E., and
Čopíková, J. (2009). Glucans from fruit bodies of cultivated mushrooms Pleurotus ostreatus
and Pleurotus eryngii: Structure and potential prebiotic activity. Carbohydrate Polymers, 76(4),
548-556.
Synytsya, A., and Novak, M. (2013). Structural diversity of fungal glucans. Carbohydrate Polymers,
92, 792-809.
Taguchi, T., Furue, H., Kimura, T., Kondo, T., Hattori, T., Itoh, T., and Osawa, N. (1985). End-point
results of phase 111 study of Lentinan. Japanese Journal of Cancer and Chemotherapy, 12, 366-
371.
Tian, Y. T., Zeng, H. L., Xu, Z. B., Zheng, B. D., Lin, Y. X., Gand, C. J., and Lo, Y. M. (2012).
Ultrasonic-assisted extraction and antioxidant activity of polysaccharides recovered from white
button mushroom (Agaricus bisporus). Carbohydrate Polymers, 88, 522-529.
Toyoda, S., and Kimura, M. (2004). US2004047949.
URL-1: https://alohamedicinals.com/?s=beta+glucan, (Date of access: 30 September 2018).
URL-2: http://www.credenceresearch.com/report/beta-glucan-market, Beta glucan market by source
type (cereals, fungal & microbial), by application (food & beverage, pharmaceutical, cosmetics,
animal feed) - growth, future prospects and competitive analysis, 2017-2025, (Date of access:
24 September 2018).
Van Nevel, C. J., Decuypere, J. A., Dierick, N., and Molly, K. (2003). The influence of Lentinus
edodes (Shiitake mushroom) preparations on bacteorological and morphological aspects of the
small intestine piglets. Archives of Animal Nutrition, 57, 399-412.
Villares, A., Mateo-Vivaracho, L., and Guillamon, E. (2012). Structural features and healthy
properties of polysaccharides occurring in mushrooms. Agriculture, 2, 452-471.
Wan Rosli, W. I., Solihah, M. A., Aishah, M., Fakurudin, N. A., and Mohsin, S. S. J. (2011). Colour,
texture properties, cooking characteristics and fibre content of chicken patty added with oyster
mushroom (Pleurotus sajor-caju). International Food Research Journal, 18, 621-627.
1. INTERNATIONAL TECHNOLOGICAL SCIENCES AND DESIGN SYMPOSIUM
27-29 June 2018 - Giresun/TURKEY
Wasser, S. P., and Weis, A. L. (1999). Medicinal properties of substances occurring in higher
Basidiomycetes mushrooms: Current perspectives (Review). International Journal of Medicinal
Mushrooms, 1(1), 31-62.
Wasser, S. P. (2002). Medicinal mushrooms as a source of antitumor and immunomodulating
polysaccharides. Applied Microbiology and Biotechnology, 60, 258-274.
Watanabe, M. (2005). JP2005160326.
Yan, J. K., Wang, W. Q., and Wu, J. Y. (2014). Recent advances in Cordyceps sinensis
polysaccharides: mycelial fermentation, isolation, structure, and bioactivities: A review. Journal
of Functional Foods, 6, 33-47.
Zeman, M., Nosalova, V., Bobek, P., Zakalova, M., and Cerna, S. (2001). Changes of endogenous
melatonin and protective effect of diet containing pleuran and extract of black elder in colonic
inflammation in rats. Biologia. 56, 659-701.
Zhang, M., Cuia, S. W., Cheung, P. C. K and Wang, Q. (2007). Antitumor polysaccharides from
mushrooms: A review on their isolation process, structural characteristics and antitumor
activity. Trends in Food Science & Technology, 18, 4-19.
Zhang, Y., Xia, L., Pang, W., Wang, T., Chen, P., Zhu, B., and Zhang, J. (2013). A novel soluble β-1,
3-D-glucan salecan reduces adiposity and improves glucose tolerance in highfat diet-fed mice.
British Journal of Nutrition, 109, 254-262.
Zhu, F., Du, B., Bian, Z., and Xu, B. (2015). Beta-glucans from edible and medicinal mushrooms:
Characteristics, physicochemical and biological activities. Journal of Food Composition and
Analysis, 41, 165-173.
Zhu, F., Du, B., and Xu, B. (2016). A critical review on production and industrial applications of beta-
glucans. Food Hydrocolloids, 52, 275-288.
... The findings of this study rightly align with the report of Hozova et al. (2004) to indicate that if these mushrooms are consumed directly or as supplements, the glucans in them can enhance human hearthealth in which the report of Ciecierska et al. (2019) and Bulam et al. (2018), suggested that the glucans in mushrooms play important role in the proper functioning of gastrointestinal tract and preventing inflammation as well as colon cancer. ...
... This antiviral activity correlates with the antioxidant effect and anti-inflammatory cytokines induced by β-glucans (Shi et al., 2022). In addition, high molecular weight β-glucans show greater anticancer properties, although they are more difficult to extract due to the intermolecular interactions they usually form (Bulam, Ş ule Üstün, & Pekşen, 2018;Mirończuk-Chodakowska & Witkowska, 2020). The structural properties of β-glucans, in terms of branching degree and molecular conformation as well as their association with other cell wall components (such as mannoproteins, chitin or other polysaccharides) will determine their solubility and extractability. ...
... Yeung et al. (2018) stated the most popular topics focused on nutraceuticals and functional foods as prebiotics, probiotics, antioxidants, and phenolic contents. Nowadays, functional edible and medicinal mushrooms have been known as one of the potential natural sources for developing novel functional foods as well as dietary supplements, myconutraceuticals, mycocosmeceuticals, and mycopharmaceuticals (Morris et al., 2017;Reis et al., 2017;Bulam et al., 2018;Üstün et al., 2018;Bulam et al., 2019a, c, d;Cateni et al., 2021;Kaur et al., 2021;Niego et al., 2021;Venturella et al., 2021). ...
Article
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The oyster mushroom (Pleurotus ostreatus (Jacq. ex Fr.) P. Kumm.) is one of the most popular edible mushrooms. P. ostreatus contains important essential nutrients for human nutrition and is a natural source used in both traditional and modern medicine. Nowadays, P. ostreatus has been used in vitro studies as food additive in the development of value-added functional foods such as meat, bakery, and dairy products, traditional foods, and various alcoholic and non-alcoholic beverages. Fresh and other forms of P. ostreatus have been used for food fortification, the improvement of sensory quality and the physicochemical properties of foods and prolonging the shelf life of functional foods. In this review, potential of use of P. ostreatus as food additive in sustainable functional food production and its effects on food quality were emphasized.
... Sclerox becomes sensitive to environmental conditions giving a reversible sol-gel transition mediated by pH, commonly used for drug delivery. (Coviello et al., 2005) on the market, e.g., Imunoglukan P4H® from Pleurotus ostreatus and LentinanXP in USA/Lentinex® in Europe from Lentinula edodes (Bulam et al., 2018). β-1,3-glucan have been also used in several TE applications, such as bone scaffolds composed of chitosan/β-1,3-glucan/calcium phosphate ceramic (Belcarz et al., 2013;Borkowski et al., 2015;Przekora & Ginalska, 2015;Przekora et al., 2014) and wound dressing nanofiber scaffolds based on β-1,3-glucan/polyvinyl alcohol (PVA) (Basha et al., 2017). ...
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Fungal exopolysaccharides (EPSs) are natural biopolymers with diverse potential applications in the biomedical, packaging, cosmetic, and food industries. Fungal EPSs are easy to extract and purify polysaccharides that are biodegradable, biocompatible, with low immunogenicity, bioadhesion ability, antibacterial activity, and contain different reactive groups such as hydroxyl, carboxyl, and amine for chemical modifications. Despite fast progress in identifying and characterization fungal EPSs for biomedical applications, i.e., wound healing, drug, and gene delivery, only a few products have been commercialized based on fungal EPSs. This review critically discusses potential biomedical applications of fungi sourced EPSs in tissue engineering (TE), drug and gene delivery.
... Among the different polysaccharides, β-glucans are the most abundant in mushrooms, and are found primarily in the fungal cell wall. They are the most versatile metabolite, with a wide spectrum of biological activity [132]. Detailed studies of β-glucans demonstrated their beneficial impact on human life. ...
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Macrofungi production and economic value have been increasing globally. The demand for macrofungi has expanded rapidly owing to their popularity among consumers, pleasant taste, and unique flavors. The presence of high quality proteins, polysaccharides, unsaturated fatty acids, minerals, triterpene sterols, and secondary metabolites makes macrofungi an important commodity. Macrofungi are well known for their ability to protect from or cure various health problems, such as immunodeficiency, cancer, inflammation, hypertension, hyperlipidemia, hypercholesterolemia, and obesity. Many studies have demonstrated their medicinal properties, supported by both in vivo and in vitro experimental studies, as well as clinical trials. Numerous bioactive compounds isolated from mushrooms, such as polysaccharides, proteins, fats, phenolic compounds, and vitamins, possess strong bioactivities. Consequently, they can be considered as an important source of nutraceuticals. Numerous edible mushrooms have been studied for their bioactivities, but only a few species have made it to the market. Many species remain to be explored. The converging trends and popularity of eastern herbal medicines, natural/organic food product preference, gut-healthy products, and positive outlook towards sports nutrition are supporting the growth in the medicinal mushroom market. The consumption of medicinal mushrooms as functional food or dietary supplement is expected to markedly increase in the future. The global medicinal mushroom market size is projected to increase by USD 13.88 billion from 2018 to 2022. The global market values of promising bioactive compounds, such as lentinan and lovastatin, are also expected to rise. With such a market growth, mushroom nutraceuticals hold to be very promising in the years to come.
... Furthermore, previous studies showed that the β-glucans in mushroom could not be digested in the human gastrointestinal tract and were thus considered as a potential source of prebiotics. Mushroom β-glucans possess profound health promoting properties like speeding up the transit of bowel contents, increasing fecal bulk and frequency, consequently protecting the body from colon cancer, diverticular diseases and irritable bowel syndrome [27]. Although many studies on the SCPs have been carried out, data on the fermentation characteristics of SCPs and their effects on the intestinal microbes in mice are limited and the underlying mechanism of the effects of SCPs on intestinal microbes are still largely unclear. ...
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Cosmeceutical formulations containing naturally derived active ingredients are currently preferred by consumers worldwide. Mushrooms are one of the potential sources for cosmeceutical ingredients but relevant research is still lacking. In this study, hot-and cold-water extractions were performed on four locally-cultivated mushrooms-Pleurotus ostreatus, Ganoderma lucidum, Auricularia polytricha and Schizophyllum commune-with the aim to assess the cosmeceutical potential of these mushroom fruitbody extracts. Total phenolics, polysaccharide and glucan content were determined. Antioxidant property of the mushroom extracts was assessed by determining the DPPH radical scavenging, ferric-reducing (FRAP) and superoxide anion (SOA) scavenging activity. Anti-hyaluronidase activity was used as an indicator for the anti-aging and anti-inflammatory property, while anti-tyrosinase activity was evaluated to assess the anti-pigmentation or whitening property of these extracts. Our results showed that total polysaccharide content of P. ostreatus extracts was the highest (235.8-253.6 mg GE/g extract), while extracts from G. lucidum contained the lowest glucan (10.12-10.67%). Cold-water extract from S. commune exhibited substantial tyrosinase inhibition activity (98.15%) and SOA scavenging activity (94.82%). The greatest hyaluronidase activity was exhibited by G. lucidum hot-water extract, with the value of 72.78%. The findings from the correlation analyses suggest that the cosmeceutical properties of these mushrooms can be attributed mainly to the combination of different types of compound such as polysaccharides and phenolics. Overall, cold-water extract of S. commune and hot-water extract of G. lucidum showed the best results and may be further investigated.
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The obesity prevalence in the world continues to increase yearly, which further cause clinical problems related to metabolic syndrome and lipid peroxidation. This study aims to determine the effect of ß-glucan extract from oyster mushrooms on lipid peroxidation markers, namely serum MDA levels in rats. Therefore, Sprague dawley rats were divided into four groups, namely the KN group, which was fed with AIN-93M standard diet, the KP group was given the AIN-93M modified HFHF diet, the PI group was fed with AIN-93M modified HFHF + ß-glucan diet 125 mg/kgBW, and the P2 group was given the AIN-93M modified HFHF + ß-glucan diet 375 mg/kgBW. The ß-glucan detection test in oyster mushroom extract used an FTIR spectrophotometer, while the content analysis used the Mega-Calc™ from Megazyme, and also, the MDA levels were determined through the TBARS method. Furthermore, based on FTIR spectrum results, it was proven that oyster mushroom extract contained ß-glucan. The provision of HFHF diet for 14 weeks caused the rats to be pre-obese, resulting in lipid peroxidation due to the free radicals induction. The average Fee index rats at the end of treatment were 294.00 + 6.40 (KN), 292.78 + 6.37 (KP), 291.85 + 9.60 (PI), and 286.88 + 10.60 (P2), with a p value of 0.687. Meanwhile, the average serum MDA level (ng/mF) obtained were 507.833 + 35.95 (KN), 504.184 + 29.17 (KP), 540.397 + 29.80 (PI), and 553.996 + 86.78 (P2), with a p value of 0.001. The values of serum MDA levels that were statistically significant were KN vs P2, KP vs P1, KP vs P2, and P1 vs P2. These results showed that the dose and duration of ß-glucan administered were not sufficient to prevent the lipid peroxidation process.
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Mushrooms are becoming a vital component of the human diet for the prevention and treatment of various diseases. The use of mushrooms for developing functional foods, drugs, and nutraceuticals is reviewed in this chapter, with emphasis on present or potential medical implications. As functional foods, mushrooms represent a paradigm of integrating tradition and novelty, due to their wide spectrum of pharmacological properties. Their bioactive components can be extracted or concentrated as nutraceuticals, and/or a diverse class of dietary supplements. Functional foods and nutraceuticals, particularly mushrooms, are immunoceuticals with antitumor and immunomodulatory effects which target and modulate biological processes that foster the development of diseases. Several mushroom products, mainly polysaccharides such as β‐D‐glucans, have proceeded successfully through clinical trials and are used as drugs to treat cancer and chronic diseases. In sum, the present status and future prospects open new avenues for upgrading mushroom species from functional food to translational mushroom medicine.
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A robust and reliable method has been developed for the measurement of β-glucan in mushroom and mycelial products. Total glucan (plus free glucose and glucose from sucrose) was measured using controlled acid hydrolysis with H2SO4 and the glucose released specifically was measured using glucose oxidase/peroxidase reagent. α-Glucan (starch/glycogen) plus free glucose and glucose from sucrose were specifically measured after hydrolysis of starch/glycogen to glucose with glucoamylase and sucrose to glucose plus fructose with invertase and the glucose specifically measured with GOPOD reagent. β-Glucan was determined by the difference. Several acid and enzyme-based methods for the hydrolysis of the β-glucan were compared, and the best option was the method using H2SO4. For most samples, similar β-glucan values were obtained with both the optimized HCl and H2SO4 procedures. However, in the case of certain samples, specifically Ganoderma lucidum and Poria cocus, the H2SO4 procedure resulted in significantly higher values. Hydrolysis with 2 N trifluoroacetic acid at 120°C was found to be much less effective than either of the other two acids evaluated. Assays based totally on enzymatic hydrolysis, in general, yielded much lower values than those obtained with the H2SO4 procedure.
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The objective of the model experiment was to examine the microbiological (yeasts, moulds, coliform bacteria) and sensory (appearance, colour, consistency, taste) qualities as well as the lifetime of white and fruit yoghurts enriched with different additions of two types of hydrogels of beta-D-glucan, namely pleuran (from Pleurotus ostreatus) and lentinan (from Lentinus edodes). The yoghurts were stored for 30 days under the refrigerator conditions (5degreesC +/- 2degreesC), the sampling being done on the 1(st), 15(th) and 30(th) day of the storage. The results obtained by the analyses of yoghurts with the addition of pleuran and lentinan showed that the fermentation ability of white and fruit yoghurts was not inhibited by the addition of hydrogels before this process; the acid equivalent (degreesSH) and pH of samples showed values typical for this kind of product during a month-lasting storage; the groups of microorganisms followed (coliform bacteria, yeasts and moulds) did not appear during the whole storage period (< 1 CFU/g); the application of both hydrogels added to yoghurts had no negative influence on the sensory acceptability of the products; all samples maintained a very good quality during the whole storage period and did not differ significantly from one another in the individual parameters evaluated.
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The optical and textural properties of chicken patty formulated with different level of grey oyster mushroom (Pleurotus sajor-caju) at 0, 25 or 50% to replace chicken meat were investigated. The addition of up to 50% oyster mushroom to chicken patty formulations did not change colour a* (redness), compared with the control patty. Chicken patties containing oyster mushroom had lower L* value ranging from 51.02 - 52.65 compared to that of the control patty (57.86). All oyster mushroom-based patties had lower colour b* (yellowness) value compared to chicken patty without mushroom. The hardness of chicken patty decreased proportionally with the level of oyster mushroom. On the other hand, oyster mushroom-based patties were springier than the control patty. Chicken which was replaced with 25% of fresh mushroom, recorded the highest moisture retention (77.19%) and cooking yield (80.71%), respectively. However, replacement of 25% of oyster mushroom with chicken breast in chicken patty formulation was not change the moisture retention, fat retention and cooking yield compared to control patty. Chicken patty added with 50% ground oyster mushroom the highest concentration of total dietary fibre (TDF) at 4.90 g/100 g compared to chicken patty containing 25% of mushroom (3.40 g/100 g) and control (1.90 g/100 g). In summary, the addition of oyster mushroom in chicken patties has decreased the lightness, yellowness, hardness and chewiness while no changes were noted in the redness of the patties.
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Background Due to an aging population and illnesses related to current lifestyles, health-related concerns are becoming increasingly more important. Moreover, today's society is more aware of the potential side effects of medicines and is looking for innovative therapeutic alternatives. Hence, the use of natural compounds in the prevention of various diseases and health maintenance has been studied. Among the natural products studied are mushrooms, which are well known for their nutritional value and health-promoting properties. These have been considered as both functional foods and a source of nutraceuticals. Scope and approach The present review is aimed at collecting and critically examining current data on the bioactive properties of mushrooms as well as their classification as functional foods and source of nutraceuticals. It also intended to describe the state of the art regarding mushroom formulations currently available on the market, and to highlight what could be done to improve this market in order to make a variety of quality and duly-certified products that promote human well-being available. Key findings and conclusions Mushrooms are natural matrices of excellence. Their bioactivity has been proved and therefore, their incorporation in foods has been studied. However, these new food products have not yet gone to market and most of the mushrooms and their compounds are mainly consumed in their natural form or in dietary supplements. Despite interest in such products having grown over the years, in Western countries, mushroom products are not as common as in Asia and legislation needs to be implemented to permit an increase in their consumption.
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Many edible mushrooms are considered as “functional” foods having immunomodulatory and anticancer properties. The ability of mushrooms to exert biological effects and modulate immune functions is due to the presence of bioactive compounds with most important the polysaccharides β-glucans. B-glucans are found in bacteria, fungi and plants and act on several immune cell receptors resulting in both innate and adaptive response. The incorporation of β-glucans in various foods and animal feed has the potential of creating novel “functional” food products, with many health benefits to human and animal nutrition.
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Mushrooms have unique sensory properties and nutritional values as well as health benefits due to their bioactive compounds, especially beta-glucans. Well-known edible and medicinal mushroom species as well as uncommon or unknown species representing interesting sources of bioactive beta-glucans have been widely studied. Commercially cultivated and wild growing mushrooms were analysed for their beta-glucan contents. Enzymatic determinations of all glucans, alpha-glucans and beta-glucans in 39 mushrooms species were performed, leading to very remarkable results. Many wild growing species present high beta-glucan contents, especially Bracket fungi. The well-known cultivated species Agaricus bisporus, Lentinula edodes and Cantharellus cibarius as well as most screened wild growing species show higher glucan contents in their stipes than caps.