<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FNS</journal-id><journal-title-group><journal-title>Food and Nutrition Sciences</journal-title></journal-title-group><issn pub-type="epub">2157-944X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fns.2023.1410061</article-id><article-id pub-id-type="publisher-id">FNS-128767</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  &lt;i&gt;β&lt;/i&gt;-Glucans: Characterization, Extraction Methods, and Valorization
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ana</surname><given-names>Chioru</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aurica</surname><given-names>Chirsanova</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Food and Nutrition, Technical University of Moldova, Chisinau, Republic of Moldova</addr-line></aff><pub-date pub-type="epub"><day>11</day><month>10</month><year>2023</year></pub-date><volume>14</volume><issue>10</issue><fpage>963</fpage><lpage>983</lpage><history><date date-type="received"><day>29,</day>	<month>June</month>	<year>2023</year></date><date date-type="rev-recd"><day>28,</day>	<month>October</month>	<year>2023</year>	</date><date date-type="accepted"><day>31,</day>	<month>October</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  β
  -glucans are bioactive compounds with a wide range of biological properties, including anticancer, anti-inflammatory, antioxidant, and immune-modulating properties. Due to their specific physical properties, such as (in)solubility, viscosity, and gelation, β-glucans are increasingly being used in the food, pharmaceutical, and cosmetic industries. The purpose of this review is to provide an overview of the different types of β-glucans, their sources, especially Saccharomyces cerevisiae yeasts, and the methods of extraction, isolation, and purification of β-glucans, with the aim of optimizing these methods for the efficient production process. Moreover
  ,
   the physico-chemical properties, modifications, current applications and future prospects of the use of β-glucans in food, medicines, cosmetics and other potential value-added products are summarized. The data presented indicate that β-glucans will play an increasingly important role in the sector of special
  -
  purpose food products as well as in other current and future areas.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;β&lt;/i&gt;-Glucans</kwd><kwd> Yeast</kwd><kwd> Extraction</kwd><kwd> Valorization</kwd><kwd> Value-Added Products</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>β-glucans are polymers of glucose with different glycosidic bonds [<xref ref-type="bibr" rid="scirp.128767-ref1">1</xref>] . Most β-glucans play a crucial role in the structure of the cell wall, while others are used as an energy source for metabolism [<xref ref-type="bibr" rid="scirp.128767-ref2">2</xref>] . Despite their simple monosaccharide composition, glucans exhibit a high structural variability [<xref ref-type="bibr" rid="scirp.128767-ref2">2</xref>] . β-glucans are recognized as biologically active substances with immunomodulatory [<xref ref-type="bibr" rid="scirp.128767-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref4">4</xref>] , antioxidant [<xref ref-type="bibr" rid="scirp.128767-ref5">5</xref>] , anti-inflammatory [<xref ref-type="bibr" rid="scirp.128767-ref6">6</xref>] , antitumor [<xref ref-type="bibr" rid="scirp.128767-ref7">7</xref>] , cholesterol [<xref ref-type="bibr" rid="scirp.128767-ref8">8</xref>] and glucose [<xref ref-type="bibr" rid="scirp.128767-ref9">9</xref>] lowering properties. In addition, β-glucans are used in the food industry for the production of functional food products [<xref ref-type="bibr" rid="scirp.128767-ref10">10</xref>] and nutraceuticals [<xref ref-type="bibr" rid="scirp.128767-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref12">12</xref>] .</p><p>In recent decades, β-glucans have gained increasing attention from scientists, with a particular focus on identifying potential β-glucan sources and valorizing agro-food waste. In this context, the Republic of Moldova, being an agrarian country, has a wide variety of agro-food residues that can be utilized [<xref ref-type="bibr" rid="scirp.128767-ref13">13</xref>] . All of these studies have been significant because, at the initiative of the German company Leiber GmbH, β-glucans were recognized as a new food ingredient at the European level in 2017. Thus, studying the applicability and specific functionality in different branches is very topical.</p><p>Carbohydrates are widely used as food for humans and animals. In the food industry, they are used to produce alcoholic beverages, as food additives, and in the pharmaceutical industry. Vegetable carbohydrates present in foods consumed by humans and animals contain polymer-like fibers. Thus, there are two types of dietary fiber, soluble and insoluble, which are distinguished by their solubility in water. Insoluble fibers (cellulose, lignin, and some hemicelluloses) are insoluble in water, while soluble fibers (hemicelluloses and pectin) form viscous solutions in water. β-glucans are polysaccharides that can be classified into the hemicellulose group [<xref ref-type="bibr" rid="scirp.128767-ref14">14</xref>] .</p><p>Although beta-glucans have been studied extensively, their multiple health-promoting effects are still being investigated, including their effects on the skin [<xref ref-type="bibr" rid="scirp.128767-ref15">15</xref>] ; the human gut [<xref ref-type="bibr" rid="scirp.128767-ref16">16</xref>] , as well as the gut of pigs [<xref ref-type="bibr" rid="scirp.128767-ref17">17</xref>] , fish [<xref ref-type="bibr" rid="scirp.128767-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref19">19</xref>] , and other animals; the kidneys [<xref ref-type="bibr" rid="scirp.128767-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref21">21</xref>] ; the gallbladder [<xref ref-type="bibr" rid="scirp.128767-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref23">23</xref>] ; the liver [<xref ref-type="bibr" rid="scirp.128767-ref24">24</xref>] ; the brain [<xref ref-type="bibr" rid="scirp.128767-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref26">26</xref>] . The most common sources of beta-glucans are cereals and microorganisms. Beta-glucans are known for their unique immunomodulation properties through their ability to interact with macrophages, triggering a specific beneficial immune response and enhancing the activity of the immune system without overactivation. They have been suggested as vaccine adjuvants for COVID-19. Additionally, they are considered to be safer on the basis of nutritional supplements [<xref ref-type="bibr" rid="scirp.128767-ref27">27</xref>] .</p><p>However, the review of the production, physical properties, and industrial applications of β-glucans from other promising sources has received little attention and needs further and more in-depth study. The purpose of this work is to provide an overview based on published scientific data. We have also presented the physical properties of β-glucans. Finally, we have included the potential applications of β-glucan in food, cosmetics, the pharmaceutical industry, and other health products.</p></sec><sec id="s2"><title>2. General Description of β-Glucans</title><sec id="s2_1"><title>2.1. Legal Provisions</title><p>According to the document published by EFSA (European Food Safety Authority) in 2011, “Scientific Opinion on the safety of ‘beta-glucans from yeast’ as a new food ingredient”, β-glucans have been recognized as safe products that can be used in both soluble and insoluble forms. For dietary supplements or foods intended for special nutritional uses, a daily dose of 375 mg to 600 mg is recommended [<xref ref-type="bibr" rid="scirp.128767-ref28">28</xref>] . Following this opinion, the European Union adopted Decision (EU) 2017/2048 in 2017, which extended the use of β-glucans from yeast S. cerevisiae to other foods, such as juices (1.3 g/kg), breakfast cereals (15.3 g/kg), biscuits (6.7 g/kg), milk powder (25.5 g/kg), and dairy products (3.8 g/kg). This decision of the European Union was revised in 2019, and the necessary purity of β-glucans was added, which must be greater than 80%. Similarly, more products in which the use of β-glucans is allowed have been added, such as: cereal bars, fermented dairy products, soups, chocolate and sweets, jam, marmalade, and other spreadable fruit products [<xref ref-type="bibr" rid="scirp.128767-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref29">29</xref>] .</p></sec><sec id="s2_2"><title>2.2. Classification of β-Glucans</title><p>β-glucans can be classified by their structure and source of origin, and these are interdependent. Based on their origin, β-glucans are divided into cereal and non-cereal β-glucans. In cereals, β-glucans are predominantly found in barley and oats. Other rich sources of β-glucans include mushrooms, seaweed, bacteria, and seafood. β-glucans in cereals have a different structure than non-cereal β-glucans [<xref ref-type="bibr" rid="scirp.128767-ref30">30</xref>] .</p><p>β-glucans can also be classified by their structure. Ruiz-Herrera [<xref ref-type="bibr" rid="scirp.128767-ref31">31</xref>] classified β-glucans into seven categories based on their structure:</p><p>&#183; Non-branched 1,3-β-glucans;</p><p>&#183; 1,3-β-glucans with a few branches;</p><p>&#183; 1,6-β-glucans formed from a single glucose unit;</p><p>&#183; β-glucans containing 1,3 and 1,4 glucose fragments;</p><p>&#183; β-glucans formed from 1,3, 1,4, and β 1,6 glucose fragments</p><p>&#183; 1,3-β-glucans phosphorylated;</p><p>&#183; 1,3-β-glucans with significant 1,6 branching;</p><p>&#183; β-glucans formed predominantly from 1,6-linked glucose units.</p><p>This classification is based on the type of linkages between the glucose molecules in the β-glucan chain. Non-branched 1,3-β-glucans are the simplest type of β-glucans. They are long, straight chains of β-glucose molecules linked by 1,3-β linkages. Other types of β-glucans have more complex structures. For example, 1,3-β-glucans with a few branches have 1,3-β linkages between most of the glucose molecules, but some of the glucose molecules are linked by 1,6-β linkages. The structure of β-glucans affects their properties, such as their solubility and ability to form gels [<xref ref-type="bibr" rid="scirp.128767-ref31">31</xref>] . The nutritional value of β-glucans from different sources varies depending on the source and the processing method [<xref ref-type="bibr" rid="scirp.128767-ref32">32</xref>] . Therefore, the structure of b-glucans will also influence the digestibility of β-glucans. In general, β-glucans have been shown to be more resistant to digestion in the small intestine, which allows them to reach the large intestine, where they can be fermented by beneficial bacteria [<xref ref-type="bibr" rid="scirp.128767-ref33">33</xref>] . The fermentation of β-glucans by beneficial bacteria produces short-chain fatty acids [<xref ref-type="bibr" rid="scirp.128767-ref34">34</xref>] .</p></sec><sec id="s2_3"><title>2.3. Sources of β-Glucans</title><p>As mentioned, the structure of β-glucans presents significant differences based on their sources. <xref ref-type="table" rid="table1">Table 1</xref> shows different types of β-glucans from different sources. Cereal β-glucans from different sources vary in their tri- to tetramer ratio, the share of longer cellulosic fragments and the ratio between two types of glycosidic bonds. The main source of various structural types of glucans is fungal cell walls, which consist mainly of structural polysaccharides and glycoproteins. These β-glucans commonly have trivial names according their fungal origin (grifolan, lentinan, pachyman, pleuran, schizophylan, scleroglucan, etc.) [<xref ref-type="bibr" rid="scirp.128767-ref2">2</xref>] . The yeast-derived beta-(1→3)(1→6)-glucan purportedly has greater biological activity than the (1→3)(1→4)-counterparts [<xref ref-type="bibr" rid="scirp.128767-ref14">14</xref>] . Cereals are considered as the most common β-glucans source, so the unbranched β-glucans are currently more widely used [<xref ref-type="bibr" rid="scirp.128767-ref35">35</xref>] .</p></sec><sec id="s2_4"><title>2.4. The Structure of β-Glucans</title><p>Depending on the interchain linkage, glucans are divided into α and β glucans. In general, some α glucans are amorphous and soluble in hot water and play the role of energy storage material. Examples of these are glycogen in fungi and animals, and starch in algae and plants. Those present in the walls of fungi are insoluble in water. Most β-glucans are insoluble in water and almost all solvents, they are mostly crystalline. Examples of β-glucans are cellulose in plants and various 1,3 β-glucans in yeasts [<xref ref-type="bibr" rid="scirp.128767-ref31">31</xref>] . <xref ref-type="fig" rid="fig1">Figure 1</xref> shows the basic, simple units of β-glucans. All β-glucans are homo-polysaccharides and essentially composed of glucose units linked together and thus have a characteristic 1,3 linked backbone. The structural difference occurs at branching off this backbone, which is dictated by source. β-glucans can be unbranched or branched [<xref ref-type="bibr" rid="scirp.128767-ref30">30</xref>] .</p><p>β-glucans in cereals consist of a mixture of β-(1,3) and β-(1,4) glycosidic linkages, without branching. Cereal derived β-glucans are generally located in the aleurone (proteins stored as granules), in the sub-aleurone or in the cell wall of endospores, which are all located in oat, barley, wheat [<xref ref-type="bibr" rid="scirp.128767-ref37">37</xref>] . <xref ref-type="fig" rid="fig2">Figure 2</xref> shows the basic structure of cereal β-glucans.</p><p>Whereas, non-cereal β-glucans do not have β-(1,4) linkages. For example, β-glucans in mushrooms are formed from linear β-(1,3) glycosidic linkages with a single β-(1,6) branching linkage every third linear linkage. β-glucans in the cell wall of the yeast Saccharomyces cerevisiae are a large molecule, consisting of linear chains made up of 30 simple β-(1,3) glycosidic units, the chains are linked together by branched β-(1,6) glycosidic linkages. Approximately 60% of the β-d-glucans in yeasts have a long chain of 1500 glucose residues linked by β-(1-3)-glycosidic linkages, and a molecular weight of approximately 100 - 200 kDa [<xref ref-type="bibr" rid="scirp.128767-ref28">28</xref>] . <xref ref-type="fig" rid="fig3">Figure 3</xref> shows the comparative structure of glucans from mushrooms and yeasts.</p><p>The conformation of polysaccharides is determined by the interplay of intermolecular and intramolecular forces, such as hydrogen bonds. Polysaccharides can exist in a variety of conformations, including single helices, double helices, triple helices, random coils, aggregates, rod-like structures, and worm-like structures [<xref ref-type="bibr" rid="scirp.128767-ref10">10</xref>] .</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Sources of β-glucans</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Name of β-glucan</th><th align="center" valign="middle"  colspan="2"  >The source of provenance of β-glucan</th><th align="center" valign="middle"  colspan="5"  >Literature</th></tr></thead><tr><td align="center" valign="middle" >Source</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >Title</td><td align="center" valign="middle" >Authors</td><td align="center" valign="middle" >Journal of Publication</td><td align="center" valign="middle" >Publication Year</td><td align="center" valign="middle" >References</td></tr><tr><td align="center" valign="middle" >(1→3)-β-D-glucan</td><td align="center" valign="middle" >Bacterias Seaweeds Lichens</td><td align="center" valign="middle" >Agrobacterium, Rhizobium, Cellulomonas, Bacillus, Alcaligenes faecalis Euglena, Astasialonga, Pavlovamesolychnon Stereocaulonramulosum, Ramalina, Cladonia</td><td align="center" valign="middle" >Chemistry, physico-chemistry and applications linked to biological activities of β-glucans β-Glucan in Foods and Its Physiological Functions</td><td align="center" valign="middle" >Barsanti L, Passarelli V, Evangelista V, Nakashima A, Yamada K, Iwata O</td><td align="center" valign="middle" >Nat Prod Rep Journal of Nutritional Science and Vitaminology</td><td align="center" valign="middle" >2011 2018</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref36">36</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref37">37</xref>]</td></tr><tr><td align="center" valign="middle" >(1→6)-β-D-glucan</td><td align="center" valign="middle" >Lichens Fungus</td><td align="center" valign="middle" >Lasalliapustulata Guignardiacitricarpa</td><td align="center" valign="middle" >Structural analysis of glucans</td><td align="center" valign="middle" >Synytsya A, Novak M</td><td align="center" valign="middle" >Ann Transl Med</td><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref2">2</xref>]</td></tr><tr><td align="center" valign="middle" >(1→3)(1→2)-β-D-glucan</td><td align="center" valign="middle" >Bacterias</td><td align="center" valign="middle" >Streptococuspneumonie</td><td align="center" valign="middle" >Chemistry, physico-chemistry and applications linked to biological activities of β-glucans</td><td align="center" valign="middle" >Barsanti L, Passarelli V, Evangelista V</td><td align="center" valign="middle" >Nat Prod Rep</td><td align="center" valign="middle" >2011</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref36">36</xref>]</td></tr><tr><td align="center" valign="middle" >(1→3)(1→4)-β-D-glucan</td><td align="center" valign="middle" >Cereals Lichens Fungus</td><td align="center" valign="middle" >Barley, Oats, Wheat Cetrariaislandica Calocybe indica</td><td align="center" valign="middle" >A Concise Review on the Molecular Structure and Function Relationship of β-Glucan Recent advances in enzymatic synthesis of β-glucan and cellulose</td><td align="center" valign="middle" >Du B, Meenu M, Liu H, Xu B Bulmer GS, de Andrade P, Field RA, van Munster JM</td><td align="center" valign="middle" >IJMS Carbohydrate Research</td><td align="center" valign="middle" >2019 2021</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref38">38</xref>]</td></tr><tr><td align="center" valign="middle" >(1→3)(1→6)-β-D-glucan</td><td align="center" valign="middle" >Fungus Seaweeds Bacterias</td><td align="center" valign="middle" >Lentinula edodes, Grifolafrondosa, Schizophyllan commune, Sclerotium, Pleurotusostreatus, Botryosphaeria, Saccharomyces cerevisae, Schizosaccharomyces pombe, Aspergillus fumigatus, Candida albicans, Aspergillus oryzae Chaetcerosmulleri, Ochromonas, Haramonasdimorpha, Phaeodactylumtricornutum, Xanthomonas campestris, Bacillus natto</td><td align="center" valign="middle" >A Concise Review on the Molecular Structure and Function Relationship of β-Glucan Structural analysis of glucans Evaluating comparative β-glucan production aptitude of Saccharomyces cerevisiae, Aspergillus oryzae, Xanthomonas campestris, and Bacillus natto β-Glucan in Foods and Its Physiological Functions</td><td align="center" valign="middle" >Du B, Meenu M, Liu H, Xu B Synytsya A, Novak M Utama GL, Dio C, Sulistiyo J, Nakashima A, Yamada K, Iwata O</td><td align="center" valign="middle" >IJMS Ann Transl Med Saudi Journal of Biological Sciences Journal of Nutritional Science and Vitaminology</td><td align="center" valign="middle" >2019 2014 2021 2018</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref39">39</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref37">37</xref>]</td></tr><tr><td align="center" valign="middle" >(1→4)(1→6)-β-D-glucan</td><td align="center" valign="middle" >Fungus</td><td align="center" valign="middle" >Auricularia auricula-judae, Coriolusversicolor</td><td align="center" valign="middle" >Chemistry, physico-chemistry and applications linked to biological activities of β-glucans</td><td align="center" valign="middle" >Barsanti L, Passarelli V, Evangelista V,</td><td align="center" valign="middle" >Nat Prod Rep</td><td align="center" valign="middle" >2011</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref36">36</xref>]</td></tr></tbody></table></table-wrap></sec><sec id="s2_5"><title>2.5. Properties of β-Glucans</title><sec id="s2_5_1"><title>2.5.1. Solubility of β-Glucans</title><p>The solubility of β-glucans is a critical factor that determines their functional properties, such as stability, emulsifying capacity, and membrane formation [<xref ref-type="bibr" rid="scirp.128767-ref10">10</xref>] . β-glucans in the cell wall are classified into 3 categories based on solubility: water-soluble (1→6 β-glucans, short polymers), alkali-soluble (1→3 β-glucans not linked to chitin), and alkali-insoluble (1→3, 6 β-glucans and linked to chitin) [<xref ref-type="bibr" rid="scirp.128767-ref40">40</xref>] . β-glucans are very hydrophilic due to the abundance of hydroxyl groups that participate in hydrogen bonds with water, giving the molecule the ability to retain water in both soluble and insoluble forms [<xref ref-type="bibr" rid="scirp.128767-ref41">41</xref>] . A study carried out by</p><p>Kim, H.J. showed that β-glucan from oats with molecular weight between 2.42 &#215; 105 and 1.61 &#215; 105 g/mol has the highest water solubility of 83.4% to 87.3% [<xref ref-type="bibr" rid="scirp.128767-ref42">42</xref>] . Another study reported that an increase in the molecular weight of oat β-glucan from 1.13 &#215; 105 to 9.04 &#215; 105 g/mol and from 1.65 &#215; 105 to 8.51 &#215; 105 g/mol leads to a significant decrease in its solubility in water from 72.8% to 68.2% and 72.3% to 67.2%, respectively [<xref ref-type="bibr" rid="scirp.128767-ref43">43</xref>] . A method for reducing the molecular weight of β-glucans and increasing their solubility is sulfation. The incorporation of ionic groups increases the amount of small β-glucan fragments.</p></sec><sec id="s2_5_2"><title>2.5.2. Rheological Properties of β-Glucans</title><p>The water retention capacity and mode of water retention of β-glucans are influenced by several factors, including: structure, purity, extraction method, and isolation method. β-glucans are a type of dietary fiber that forms a viscous solution when mixed with water [<xref ref-type="bibr" rid="scirp.128767-ref44">44</xref>] . In aqueous solutions, β-glucans have a high viscosity due to their high molecular weight, conformation, and interactive properties [<xref ref-type="bibr" rid="scirp.128767-ref45">45</xref>] . The study conducted by Petravić-Tominac demonstrated that the rheological properties of β-glucans are influenced by the extraction and drying methods used to obtain them [<xref ref-type="bibr" rid="scirp.128767-ref46">46</xref>] . Due to their rheological properties, β-glucans can be used in the food industry as thickeners, texture enhancers, stabilizers, and fortified ingredients.</p></sec></sec><sec id="s2_6"><title>2.6. β-Glucans from the Cell Wall of the Yeast Saccharomyces cerevisiae</title><p>Saccharomyces cerevisiae is a non-pathogenic, non-toxic yeast that is commonly used in fermentation processes. It produces β-glucans, which are a component of its cell wall [<xref ref-type="bibr" rid="scirp.128767-ref47">47</xref>] . The earliest studies of the structure of fungal glucans were made with those produced by S. cerevisiae secreted during protoplast regeneration. Saccharomices cerevisiae yeasts have a thick cell wall composed of polysaccharides and proteins that protect the inner compartments of the cell. The most abundant polysaccharide in the yeast cell wall is β-glucan, which constitutes 65% - 90% of the total polysaccharides [<xref ref-type="bibr" rid="scirp.128767-ref31">31</xref>] . The cell wall of these yeasts is composed of 55% β-glucans with 1,3 linkages and 12% 1,6 β-glucans. In total, the mixture of 1,3 and 1,6 β-glucans constitutes between 9% and 18% of the yeast cell mass [<xref ref-type="bibr" rid="scirp.128767-ref48">48</xref>] .</p><p>The cell wall of S. cerevisiae yeasts represents 15% - 30% of the dry weight of the cell, and has a thickness of 105 - 200 nm [<xref ref-type="bibr" rid="scirp.128767-ref49">49</xref>] . The cell wall is composed of 40% manoproteins, 60% β-glucans, and a small amount of chitin. The composition and organization of the cell wall vary at different stages of the cell cycle [<xref ref-type="bibr" rid="scirp.128767-ref50">50</xref>] . The process of glucan formation takes place in the plasma membrane [<xref ref-type="bibr" rid="scirp.128767-ref51">51</xref>] . Structurally, manoproteins are linked indirectly to β-1,6-glucan via a glycosylphosphatidylinositol (GPI) anchor and directly to β-1,3-glucan. This outer part of the cell wall, with a thickness of 30 - 40 nm, contains a protein fragment that can be partially removed chemically, while the rest of the cell wall requires enzymatic treatment [<xref ref-type="bibr" rid="scirp.128767-ref1">1</xref>] . The schematic representation of the yeast cell wall and distribution of β-glucans in Saccharomices cerevisiae is shown in <xref ref-type="fig" rid="fig4">Figure 4</xref>.</p><p>β-glucans in the cell wall of yeasts, unlike plant cell walls, are 80% - 85% insoluble in hot alkalis, due to covalent association with chitin and other polysaccharides [<xref ref-type="bibr" rid="scirp.128767-ref1">1</xref>] . Following the isolation of β-glucans from yeasts, there is co-isolation of glycogen, an α-1,4-glucan similar to starch. The removal of glycogen, in order to obtain the most accurate results, is difficult [<xref ref-type="bibr" rid="scirp.128767-ref52">52</xref>] .</p></sec></sec><sec id="s3"><title>3. Methods of the Extraction of β-Glucans from Yeasts</title><p>The extraction of β-glucans from the cell wall of Saccharomyces cerevisiae consists of two steps: 1). Cell disruption: β-glucan is located in the cell wall, so it is necessary to lyse the cells and separate the insoluble cell wall from the cytoplasm; 2). Extraction of β-glucan from the insoluble cell wall [<xref ref-type="bibr" rid="scirp.128767-ref49">49</xref>] . To be used as a drug, β-glucan must be biologically active and soluble in water. Numerous studies have focused on transforming β-glucan into a water-soluble form through chemical modifications [<xref ref-type="bibr" rid="scirp.128767-ref53">53</xref>] . Molecular modifications of β-glucans can affect their structure and molecular weight, with a significant impact on their bioactivity. To date, several molecular modification methods have been developed, including carboxymethylation, phosphorylation, sulfation, ultrasonic disruption,</p><p>selenylation, and polysaccharide degradation. Molecular modifications can affect the physical and chemical properties of polysaccharides, such as solubility, molecular weight, and intrinsic viscosity. Modified polysaccharides have superior biological properties [<xref ref-type="bibr" rid="scirp.128767-ref54">54</xref>] .</p><sec id="s3_1"><title>3.1. Mechanical Modification</title><p>This method consists of molecular modification by mechanical action, causing the rupture of the main chain of the glucan macromolecule, which will lead to the solubilization and functionalization of the polysaccharide, without destroying the basic molecular structure of the yeast β-glucan. By this method, fractions of β-glucans with a lower molecular weight, better water solubility, and modification of the conformation in solutions are obtained. This method is more efficient when used in combination with other methods.</p></sec><sec id="s3_2"><title>3.2. Thermal Degradation</title><p>Thermal degradation of β-glucans is a simple method for reducing their molecular weight. In 2018, a study was conducted [<xref ref-type="bibr" rid="scirp.128767-ref55">55</xref>] that involved thermal degradation of yeast β-glucan for solubilization. It was found that it was efficiently solubilized after being treated in an aqueous suspension at 135˚C for several hours. Another study conducted in 2022 involved autolysis-extraction with warm water (50˚C for 48 h.) and treatment at 121˚C for 6 hours in an autoclave for the extraction of fresh β-glucan [<xref ref-type="bibr" rid="scirp.128767-ref56">56</xref>] .</p></sec><sec id="s3_3"><title>3.3. Irradiation</title><p>Irradiation of β-glucans leads to their physicochemical modification. The application of ionizing radiation, such as gamma rays, X-rays, and electron beams, leads to a significant decrease in the molecular weight of β-glucans, depending on the radiation dose. Additionally, irradiation improves the solubility and decreases the viscosity of β-glucans [<xref ref-type="bibr" rid="scirp.128767-ref54">54</xref>] .</p></sec><sec id="s3_4"><title>3.4. The Treatment with Ultrasound</title><p>This method involves treating with low-frequency and high-intensity ultrasound, which leads to depolymerization and breakage of the side chain of the molecules. Following this treatment, the molecular weight of the polysaccharides also decreases, the viscosity decreases, and the solubility in water increases [<xref ref-type="bibr" rid="scirp.128767-ref57">57</xref>] . A study from 2022 showed that ultrasound-assisted H<sub>2</sub>O<sub>2</sub> treatment is a simple and efficient method for reducing the molecular weight and increasing the solubility of yeast β-glucans [<xref ref-type="bibr" rid="scirp.128767-ref58">58</xref>] .</p></sec><sec id="s3_5"><title>3.5. Chemical Modification</title><p>Chemical modification is the most commonly used method, as it can significantly increase the solubility in water and respective bioactivity of polysaccharides. The most common chemical modification methods are sulfation, alkylation, carboxymethylation, phosphorylation, selenization, and acetylation [<xref ref-type="bibr" rid="scirp.128767-ref41">41</xref>] .</p></sec><sec id="s3_6"><title>3.6. Sulfation</title><p>Sulfated polysaccharides are synthesized by replacing hydroxyl, carboxyl, or amino terminal groups with sulfate groups, with improved biological activities. The solubility of the modified glucan is increased due to the hydrophilicity of the sulfate group. The good aqueous solubility of the resulting polysaccharide has represented a huge progress in its application, especially in pharmaceutical products.</p></sec><sec id="s3_7"><title>3.7. Carboxymethylation</title><p>Carboxymethylation is used to increase the water solubility of macromolecular polysaccharides, such as cellulose, scleroglucan, and chitin. To prepare carboxymethylated polysaccharides, chloroacetic acid or sodium monochloroacetate is used as a substrate, reacting with polysaccharides in basic 2-propanone.</p></sec><sec id="s3_8"><title>3.8. Phosphorylation</title><p>Phosphorylation is a method by which a phosphate group is introduced into a polysaccharide. Several studies have shown that both naturally occurring and artificially modified phosphorylated polysaccharides have specific medicinal properties. The presence of charged phosphate groups can lead to improved water solubility, changes in molecular weight, and changes in the conformation of the polysaccharide chain [<xref ref-type="bibr" rid="scirp.128767-ref41">41</xref>] .</p></sec><sec id="s3_9"><title>3.9. Biological Modification - Enzymatic</title><p>Biological modification of polysaccharides refers specifically to enzymatic modification, which consists in the degradation of β-glucans due to the catalysis of enzymes. Compared to chemical modification, this is a gentler and promising method, due to its high specificity and efficiency. The most used enzymatic modification is depolymerization, used especially in industry [<xref ref-type="bibr" rid="scirp.128767-ref54">54</xref>] .</p><p>Numerous studies have shown that both the extraction method and the drying method of yeasts play a crucial role on their properties. The most common methods for extracting β-glucans from yeasts are: acid extraction, alkaline extraction, combined acid-base extraction, enzymatic extraction, and enzymatic-alkaline extraction [<xref ref-type="bibr" rid="scirp.128767-ref59">59</xref>] . For example, acid-base extraction can be performed using different reagents: NaOH/HCl extraction, NaOH/CH<sub>3</sub>COOH extraction, NaOH/NaClO extraction, and NaClO/DMSO extraction [<xref ref-type="bibr" rid="scirp.128767-ref32">32</xref>] . Alkaline extraction involves treatment with a 6% NaOH solution (g/v) at 90˚C for 2 hours, followed by centrifugation [<xref ref-type="bibr" rid="scirp.128767-ref60">60</xref>] . Several studies have shown that certain characteristics, such as the physicochemical parameters, chemical structure, and molecular weight of β-glucans, determine how they will interact with the immune system [<xref ref-type="bibr" rid="scirp.128767-ref52">52</xref>] . The most appropriate extraction method depends on the sources and the structures of β-glucans. The cost of β-glucans production is influenced by several factors, including the source of the beta glucans, the desired purity and properties of the final product, and the scale of production. Oats are a relatively inexpensive source of beta glucans, and they can be processed using relatively simple methods. Another way to reduce costs is to optimize the extraction process. For example, the extraction temperature and pH can be adjusted to optimize the yield and purity of the beta glucans. Additionally, the use of enzymes and other additives can help to improve the efficiency of the extraction process [<xref ref-type="bibr" rid="scirp.128767-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref61">61</xref>] . The list of the most widespread methods of methods of extraction and analysis of β-glucans is presented in <xref ref-type="table" rid="table2">Table 2</xref>.</p></sec></sec><sec id="s4"><title>4. Valorization of β-Glucans in Industrial Practice</title><p>The growing awareness of the potential of some food components to protect people against different diseases has led to an increased demand for functional foods. As a result, consumers are increasingly looking for natural foods that are safe, attractive, and provide valuable nutrients that can help to improve human health and contribute to a healthy lifestyle. This trend presents a challenge for food scientists, whose task is to develop and identify sources of foods with specific properties that can improve health.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Methods of extraction and analysis of β-glucans</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Source of β-glucan</th><th align="center" valign="middle"  rowspan="2"  >Extraction method</th><th align="center" valign="middle"  rowspan="2"  >Analysismethod</th><th align="center" valign="middle"  colspan="5"  >Literature</th></tr></thead><tr><td align="center" valign="middle" >Title</td><td align="center" valign="middle" >Authors</td><td align="center" valign="middle" >Journal of Publication</td><td align="center" valign="middle" >Publication Year</td><td align="center" valign="middle" >References</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae dry yeast cells</td><td align="center" valign="middle" >-The acid-base extraction method (NaOH, 80˚C, 2 h, CH<sub>3</sub>COOH)</td><td align="center" valign="middle" >Spectroscopicanalysis FTIR</td><td align="center" valign="middle" >Enhancement of β-Glucan Biological Activity Using a Modified Acid-Base Extraction Method from Saccharomyces cerevisiae. Biotechnological β-glucan Production from Returned Baker’s Yeast and Yeast Remaining after Ethanol Fermentation</td><td align="center" valign="middle" >Mahmoud Amer E, Saber SH, Abo Markeb A, Zohri AE-N, Moubasher H, Abdel-Hay H, Orban M</td><td align="center" valign="middle" >Molecules Egyptian Sugar Journal</td><td align="center" valign="middle" >2021 2019</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref62">62</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref63">63</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae pure culture</td><td align="center" valign="middle" >-Modified acid-base extraction method (NaOH, 80˚C, 2 h, DMSO)</td><td align="center" valign="middle" >Spectroscopic analysis FTIR</td><td align="center" valign="middle" >Extraction of β-glucan from Saccharomyces cerevisiae: Comparison of different extraction methods and in vivo assessment of immunomodulatory effect in mice</td><td align="center" valign="middle" >Pengkumsri N, Sivamaruthi BS, Sirilun S,</td><td align="center" valign="middle" >Food Sci Technol</td><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref64">64</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae, pure culture NRRL Y-567</td><td align="center" valign="middle" >-Alkaline-acid extraction method assisted with ultrasound (NaOH, 90˚C, 1 h, 40 kHz during 15 min, CH<sub>3</sub>COOH, 85˚C, 1 h, -Ultrasound-assisted autolysis (50˚C, 24 h, 40 kHz during 15 min, CH<sub>3</sub>COOH, 85˚C, 1 h</td><td align="center" valign="middle" >Spectroscopic analysis FTIR</td><td align="center" valign="middle" >A new isolation method of β-d-glucans from spent yeast Saccharomyces cerevisiae</td><td align="center" valign="middle" >Liu X, Wang Q, Cui S, Liu H</td><td align="center" valign="middle" >Food Hydrocolloids</td><td align="center" valign="middle" >2008</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref65">65</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae residual yeasts from beer production</td><td align="center" valign="middle" >-Induced autolysis (3% NaCl, 55˚C, 24 h) + treatment with water and organic solvent (121˚C, 4 h), homogenization and protease hydrolysis</td><td align="center" valign="middle" >Electron microscopy</td><td align="center" valign="middle" >Optimized methodology for extraction of (1 → 3)(1 → 6)-β-d-glucan from Saccharomyces cerevisiae and in vitro evaluation of the cytotoxicity and genotoxicity of the corresponding carboxymethyl derivative Application of different methods for the extraction of yeast β-glucan</td><td align="center" valign="middle" >Magnani M, Calliari CM, de Macedo FC VassileiosVarelas, P. Tataridis, M. Liouni, T. Nerantzis</td><td align="center" valign="middle" >Carbohydrate Polymers e-Journal of Science &amp; Technology</td><td align="center" valign="middle" >2009 2016</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref66">66</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref67">67</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae VIN 13 S</td><td align="center" valign="middle" >-Enzyme treatment + NaOH -Induced autolysis (3% NaCl), hot water extraction, sonication, extraction of lipids and proteins with the help of enzymes</td><td align="center" valign="middle" >Enzymatic assay kit (Megazyme International)</td><td align="center" valign="middle" >Effect of preparation methods on physiochemical and functional properties of yeast β-glucan</td><td align="center" valign="middle" >Fu W, Zhao G, Liu J</td><td align="center" valign="middle" >LWT</td><td align="center" valign="middle" >2022</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref56">56</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae dry yeast cells Angel Yeast Co., Ltd (China)</td><td align="center" valign="middle" >-Autolysis (55˚C, 48 h), hot water extraction (121˚C, 6 h), deproteinization treatment (proteases)</td><td align="center" valign="middle" >Enzymatic assay kit (Megazyme International)</td><td align="center" valign="middle" >Enzymatic process for the fractionation of baker’s yeast cell wall (Saccharomyces cerevisiae)</td><td align="center" valign="middle" >Borchani C, Fonteyn F, Jamin G</td><td align="center" valign="middle" >Food Chemistry</td><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref68">68</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae cell wall in the form of powder</td><td align="center" valign="middle" >-Extraction by the enzymatic method (hot water extraction 125˚C, 5 h, treatment with proteases, treatment with lipases)</td><td align="center" valign="middle" >Enzymatic assay kit (Megazyme International)</td><td align="center" valign="middle" >New method for preparing purity β-D-glucans (beta-Glucan) from baker’s yeast (Saccharomyces cerevisiae)</td><td align="center" valign="middle" >Khanh Pham, Nguyen Nhut, Nguyen Cuong</td><td align="center" valign="middle" >STDJ</td><td align="center" valign="middle" >2020</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref69">69</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae baker’s yeast powder Saf-Viet</td><td align="center" valign="middle" >-Extraction using the ionic solution (ionic solution 1-butyl-3-methyl- imidazolium Chloride, stirring 30 min at 80˚C)</td><td align="center" valign="middle" >1D- and 2D-NMR spectroscopy</td><td align="center" valign="middle" >Optimization of β-glucan extraction from waste brewer’s yeast saccharomyces cerevisiae using autolysis, enzyme, ultrasonic and combined enzyme – ultrasonic treatment</td><td align="center" valign="middle" >Tran Minh Tam, Nguyen Quoc Duy</td><td align="center" valign="middle" >American Journal of Research Communication</td><td align="center" valign="middle" >2013</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref70">70</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae residual yeasts from beer production</td><td align="center" valign="middle" >-Combined enzymatic and ultrasound extraction</td><td align="center" valign="middle" >Enzymatic assay kit (Megazyme International)</td><td align="center" valign="middle" >A Simple and Efficient Mechanical Cell Disruption Method Using Glass Beads to Extract β-Glucans from Spent Brewer’s Yeast</td><td align="center" valign="middle" >Avramia I, Amariei S</td><td align="center" valign="middle" >Applied Sciences</td><td align="center" valign="middle" >2022</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref71">71</xref>]</td></tr><tr><td align="center" valign="middle" >Saccharomyces cerevisiae residual yeasts from beer production</td><td align="center" valign="middle" >-Mechanical damage of yeast cells, acid-base extraction</td><td align="center" valign="middle" >Spectroscopicanalysis FTIR</td><td align="center" valign="middle" >Antioxidant Activity of β-Glucan</td><td align="center" valign="middle" >Kofuji K, Aoki A, Tsubaki K</td><td align="center" valign="middle" >ISRN Pharmaceutics</td><td align="center" valign="middle" >2012</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.128767-ref72">72</xref>]</td></tr></tbody></table></table-wrap><p>This review focused on the potential for the utilization of β-glucans -an important ingredient for the development of new products in the food industry. Over time, the immunomodulatory activity of various polysaccharides, either from plants or microorganisms, has been observed. β-glucans belong to this group. Generically, these are called biological response modifiers (BRM) [<xref ref-type="bibr" rid="scirp.128767-ref73">73</xref>] , [<xref ref-type="bibr" rid="scirp.128767-ref74">74</xref>] . In addition, various studies have shown that β-glucans also have other therapeutic properties in the human body, such as antioxidant activity [<xref ref-type="bibr" rid="scirp.128767-ref75">75</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref76">76</xref>] hypoglycemic [<xref ref-type="bibr" rid="scirp.128767-ref44">44</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref77">77</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref78">78</xref>] , hypolipidemic (reduction of lipid content) [<xref ref-type="bibr" rid="scirp.128767-ref79">79</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref80">80</xref>] , prebiotic activity [<xref ref-type="bibr" rid="scirp.128767-ref59">59</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref81">81</xref>] , antitumor action [<xref ref-type="bibr" rid="scirp.128767-ref82">82</xref>] [<xref ref-type="bibr" rid="scirp.128767-ref83">83</xref>] reduces inflammation in acute respiratory infections, including in the case of covid-19 [<xref ref-type="bibr" rid="scirp.128767-ref84">84</xref>] . Therefore, β-glucans can be added to products as a dietary supplement in: juices, cereal bars, breakfast cereals, biscuits, dairy products, chocolate, soups, sauces, and powdered milk.</p><p>In addition to their therapeutic effects, β-glucans can be used in the food industry as functional ingredients: thickener, water retention agent, texturizer, stabilizer, emulsifier and fat substitute [<xref ref-type="bibr" rid="scirp.128767-ref85">85</xref>] . Numerous studies show that β-glucans show positive results used in different products as functional agents. The study carried out by Mykhalevych [<xref ref-type="bibr" rid="scirp.128767-ref40">40</xref>] regarding the use of β-glucans in dairy products showed that in dairy drinks with additions it is possible to replace carrageenans with β-glucans, for example in a drink based on orange juice the addition of 0.5% of barley β-glucans and 1.5% whey protein isolate, the drink becomes more structured, less acidic. Another study published by Chiozzi [<xref ref-type="bibr" rid="scirp.128767-ref35">35</xref>] reports that the addition of 0.6% oat β-glucan in fermented dairy products does not affect the fermentation time and leads to an increase in the viscosity of the product. In sausages, a 10:1 mixture of oat β-glucan and marine collagen peptides allows the replacement of 50% of fats. Study conducted by Ramandeep Kaur [<xref ref-type="bibr" rid="scirp.128767-ref86">86</xref>] demonstrates the positive effect of β-glucans on the rheological, physicochemical, sensory properties of yogurt, effects that are maintained during the storage period of the product compared to the control sample. In the same way, β-glucans also improved the nutritional values of yogurt, acting as a prebiotic. It should be noted that the sensory characteristics of yogurt samples with the addition of beta-glucans in different amounts do not influence the smell of yogurts obtained. At the same time, the external appearance and consistency are changed in essentially: the consistency of the curd becomes firmer but still remains without gas bubbles, with poor elimination of whey [<xref ref-type="bibr" rid="scirp.128767-ref87">87</xref>] . Another study shows that bifidobacterial are capable of utilizing all of the structurally diversified β-glucansas a substrate of fermentation comparably to the known prebioticinulin [<xref ref-type="bibr" rid="scirp.128767-ref20">20</xref>] .</p><p>The use of β-glucans from yeasts was studied by Marinescu G. [<xref ref-type="bibr" rid="scirp.128767-ref88">88</xref>] for the preparation of mayonnaise. In this study, 50% of the oil was replaced with β-glucan, so the added mayonnaise is less caloric and has a more stable storage stability than mayonnaise without β-glucan.</p><p>β-glucans can be used in meat products for the partial substitution of carrageenans and starch, this shows the study conducted by Sandra M. Vasquez Mejia [<xref ref-type="bibr" rid="scirp.128767-ref89">89</xref>] . They play the role of stabilizer, water retention agent and lead to the reduction of the curtains during baking. A significant decrease in hardness and fracture values was also observed, while maintaining the structural cohesiveness of the samples, in part due to the increase in moisture content.</p></sec><sec id="s5"><title>5. Conclusion</title><p>β-glucans are among the compounds that will be increasingly studied for their potential applications in various industrial sectors. This is supported by the scientific studies that highlight their diverse multifunctional properties; by the growing trend of consumers who prefer products with “clean labels” without additives, and by other factors that lead to the development of new functional ingredients, such as β-glucans. Currently, β-glucans have a wide range of applications in the food, pharmaceutical, and cosmetic industries. However, their potential is not yet fully realized. Further research is needed to optimize the extraction, purification, drying, and use of β-glucans from yeast in various fields.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The research was made possible by the project: “Valorisation de co-produits vinicole moldaves: identification et caract&#233;risation d’agents multifonctionnels” supported by the Francophone University Agency (AUF), held within the Department of Food and Nutrition, Faculty of Food Technology of the Technical University of Moldova.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s8"><title>Cite this paper</title><p>Chioru, A. and Chirsanova, A. (2023) β-Glucans: Characterization, Extraction Methods, and Valorization. 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