Carbohydrates

"Oligosaccharides consist of three to six monosaccharide units but are not frequently found in natural sources." [Egbuna FFN]

"Polysaccharides are polymer of monosaccharides that may be branched or unbranched. Starch and cellulose are two main examples of polysaccharides which are considered as slow releasing carbohydrates." [Egbuna FFN]

"Cellulose, the most common organic substrate in nature, is a linear polymer of 10,000–15,000 glucose units linked by ß-1,4 bonds and synthesized by plants and microorganisms (e.g., Glucon- acetobacter xylinum)." [Benckiser BAPS]

"Structural analogues of cellulose are homo- or heteropolymer hemicelluloses. They consist largely of ß-glucosidal (ß-1,4, ß-1,6, ß-1,3, etc.) linked D-xylose, D- mannose, L-arabinose, D- glucose, D-galactose, and D-glucuronic acid. Hemicelluloses with ß-1,4-D-glucose and D-mannose are glucomannans, ß-1,3-xylans are hemicelluloses with a xylose backbone and glucoronic acid- arabinose side chains esterified to aromatic (phenolic) acids. Hemicelluloses probably are the second most important carbohydrate source in nature." [Benckiser BAPS]

Degredation

"Anaerobic soil microorganisms degrade about 5–10% of the cellulose." [Benckiser BAPS]

Yeast

"Baker’s yeasts in general are capable of utilizing a variety of sugars present in flour: glucose, fructose, mannose, maltose, and sucrose. On the other hand, they do not utilize the pentoses xylose or arabinose, and consume raffinose only partially. In addition, S. exiguus is unable to take up maltose, a trait it may have developed during the development of its symbiotic relationship with the sourdough lactobacterium L. sanfrancisco." [Kulp HDF]

"Glucose and fructose are the first sugars to be used during fermentation. Sucrose is rapidly broken down to glucose and fructose by yeast enzymes already present outside the cell membrane, whereas maltose is not consumed until glucose is almost exhausted. Because amylase, a starch-degrading enzyme in flour, is constantly generating new glucose and maltose from flour starch, maltose levels may actually increase in the early stages of fermentation in a yeast-only dough." [Kulp HDF]

Alchol production

"There are four major classes of carbohydrate that are of general interest: monosaccharides, disaccharides, oligosaccharides and polysaccharides." [Jacques AT]

"Disaccharides encompass sugars such as sucrose, which is an important transport carbohydrate in plants. Lactose, a disaccharide of glucose and galactose, is commonly called milk sugar." [Jacques AT] "A compound sugar that yields two monosaccharide units on hydrolysis. For example, lactose yields glucose and galactose, sucrose yields glucose and fructose, while maltose yields two glucose units." [Jacques AT]

"Oligosaccharides (Greek oligos, ‘few’) are made up of short chains of monosaccharide units joined together by covalent bonds. Most oligosaccharides in nature do not occur as free entities but are joined as side chains to polypeptides in glycoproteins and proteoglycans." [Jacques AT]

"Polysaccharides consist of long chains of hundreds or even thousands of linked monosaccharide units and, as will be discussed, exist in either linear or branched chain form. Knowledge of the terminology associated with the organizational structure of monosaccharides, such as D-glucose, is fundamental to an understanding of how polysaccharides differ and how polysaccharide-degrading enzymes, such as amylases, function." [Jacques AT]

"For fermentation purposes, polysaccharides must be subjected to hydrolysis to yield their component fermentable monosaccharides." [Jacques AT]

"Saccharomyces cerevisiae is the primary microorganism involved in the transformation of starch to ethyl alcohol, and corn starch remains the major raw material for industrial alcohol fermentation although potato starch also has limited use, particularly in Europe." [Jacques AT]

"The starting compound for alcohol synthesis by yeast is glucose (dextrose), which is a six- carbon sugar. Once fermented, each molecule of glucose yields two molecules of ethanol and carbon dioxide, respectively." [Jacques AT]

"The sequence of biosynthetic reactions by which yeast converts glucose to ethanol is termed the Embden-Meyerhof-Parnas (glycolytic) pathway (Figure 1). In this pathway, glucose is phosphorylated, then split into two phosphorylated 3-carbon derivatives, glyceraldehyde-3-phosphate and dihydroxy- acetone phosphate. Both products are subsequently converted into pyruvic acid, which under anaerobic conditions yields ethanol and carbon dioxide. It is obvious from Figure 1 that the yeast, S. cerevisiae, is very well equipped to ferment glucose and fructose. This is why wine fermentations are technically very simple. Grape pressings deliver pure glucose and, of course, the required yeast are already present on the surface of the grapes. Likewise, molasses represents a readily assimilated feedstock for yeast since the predominant sugar in molasses is the disaccharide, sucrose. Yeast contains the enzyme sucrase, which cleaves sucrose into its constituent monosaccharides, glucose and fructose." [Jacques AT]

"Starch, however, cannot be fermented directly by S. cerevisiae, because the organism lacks the requisite starch-degrading or amylolytic enzymes to liberate glucose from this storage polysaccharide. Whether the starch is derived from corn, potatoes, sorghum (milo), barley or other cereal grains, the bonds between the glucose subunits in the starch chain must first be hydrolyzed to liberate free glucose molecules which yeast can utilize. Brewers achieve this by exploiting the endogenous starch-digesting enzymes produced by seeds when they germinate. Grains, such as barley, destined for fermentation, are first sprouted to initiate enzyme synthesis within the seeds. This process is termed malting. The malted grains are then steeped in hot water to allow the enzymes to convert starch to fermentable sugar. This mashing phase is then followed by a lautering or mash filtration stage to separate the solids from the glucose-rich liquid ‘wort’ to which yeast is added." [Jacques AT]

"Normal sorghum also known as non-waxy types contain 70–80 % amylopectin and 20–25 % amylose, while the waxy varieties contain 5 % or even lesser amylose." [Lichtfouse SAR 16]
"Wu et al. (2007) reported that low amylose content in sorghum grain may be associated with increased ethanol conversion efficiency. Waxy sorghums are more preferred in brewing industry, since they gelatinize more rapidly." [Lichtfouse SAR 16]


Starch (Amylose & Amylopectin)

"The term starch is used to describe a biopolymer system comprising predominantly two polysaccharides – amylose and amylopectin – which are made of glucose monomers." [Eastaugh PC] "Starch is made up of a mixture of two α-glucans built upon mainly α-(1,4) linkages." [Rolland-Sabaté et al.,2012]
"Amylose... occupies approximately 15–30% of starch, while amylopectin, the major component (70–85%), is a larger molecule with highly α-1,6 branched chains. Starch granules are thought to have alternative layers of crystalline and amorphous regions constructed by amylopectin and amylose." [Srichuwong et al.,2005] "A starch granule usually contains 20% to 30% amylose, 70% to 80% amy- lopectin, and in some cases up to 20% phytoglycogen." [Heldt PB]

"Starch is the most abundant storage reserve carbohydrate in plants. It is found in many different plant organs including seeds, fruits and many roots and tubers." [Rolland-Sabaté et al.,2012]
"Starch granules are the plant’s reserve glucose, and are concentrated in storage organs such as seeds, fruits, roots and tubers, but also occur in other plant parts such as starchy stems (Gott et al. 2006)." [Outram SSP]
"Botanical source greatly affected the composition and functional properties of starch. Our results reveal the influences of amylopectin unit-chain length distribution on thermal properties and α-amylase digestibility of different starches." [Srichuwong et al.,2005]

"Starch is insoluble but is subject to (reversible) swelling since it is permeable to water, and gelatinizes under heat and/or certain chemical conditions." [Outram SSP]

Detection

"Amylose, amylopectin, and phytoglycogen form blue- to violet-colored complexes with iodine molecules (Table 9.1). This makes it very easy to detect starch in a leaf by a simple iodine test." [Heldt PB] "amylose ... soluble in water; stains blue with iodine) and amylopectin ... insoluble in water; stains brown with iodine)." [Hostettmann HCBPAM]

Removal of Starch

"If the starting material contained starch, starch may be isolated as well and then has to be removed, for example, by repeated treatment with amylase. The used amylases must be free of other glycanase activities. For long and repeated amylase treatment, a contamination with microorganisms must be avoided. Another method to remove starch is its solubilization and extraction in dimethyl sulfoxide (DMSO) (90%), for example, for 12 h at 25oC. Finally, DMSO can be removed by washing steps with ethanol (70%). Besides starch, however, also some other polysaccharides (e.g., highly acetylated polysaccharides) can be soluble in DMSO at thus may be lost (Aspinall, 1982a; Selvendran, Stevens, and O’Neill, 1985; Fry, 1988)." [Hostettmann HCBPAM]

Conversion into simple sugars

Yam: "In Bolivia some producers sweeten up their tubers by putting them in a sunny place for up to 2 weeks. In a previous test, the sucrose content tripled and the starch dropped by 80 percent after 3 months of storage at 12.5oC. Paull, R.E., and N.J. Chen. 1988. Compositional changes in yam bean during storage. Hortscience 23:194–196." [LCAV2]

Use as an Additive: "Starch is not infrequently mentioned as an addition to paint, either as an adulterant or extender, or as a substrate for dyestuffs." and "Carlyle (2001) found various mentions of starch used not directly as a pigment, but to gelatinise oil paint[Eastaugh PC] "Starch-rich raw materials are widely used in the food industry. Their functionality and end-use applications are markedly influenced by starch characteristics. Starches with varying amylose (AM) and amylopectin (AP) content are of particular interest due to their ability to influence and modify the texture, quality and stability of starch-based food products." [Schirmer, M., et al.,2013]

Use as Biopolymers

"Natural polymers by themselves are a class of polymers which refer to polymers sourced from nature (plants or animals). They include mainly carbohydrates and proteins which exist in plants and animals providing mainly structural support." [Olatunji NP]

"Like synthetic polymers, natural polymers can be grouped based on their formation method as addition and condensation polymers. Most natural polymers are condensation polymers which are formed as a result of monomer units combining to form a small molecule (usually water) as a by-product. Additional polymers are those formed by direct combination of the monomer units making up the polymer without any by-product. Polymers existing in nature can be grouped into six main classifications with respect to their sources: Proteins, polysaccharides polynucleotides, polyisoprenes, polyesters, and lignin (Atkins 1987)." [Olatunji NP]

"Starch is one of the commonly used plant-based polymers for food packaging and preparation of edible coatings [54]. Its solubility in water due to the amylopectin and amylose chains is of considerable importance for its usage. In addition, relative advantages of cost-effectiveness, availability, ease of processing, of natural origin, and barrier properties against oxygen makes it a choice material for selection when formulating edible coatings [25]. However, in solitude, starch has a few limitations especially relating to its mechanical strength such as tensile strength and elongation and must be prepared as a composite with other materials by casting, chem- ical modification, blending, plasticizing, extrusion, or by combination of two or more of these operations [55]. To reduce its brittleness, starch is often plasticized with xylitol, urea, sorbitol, polyethers, or glycerol." [Chhikara FF]

"Starch is one of the less expensive biodegradable materials used for many non-food items such as textile sizing, cardboard, and paper making. In recent times, starch has been employed as the major polymer in thermoplastic compositions and has been processed into various materials such as utensils and it also has been used as raw material for film production (Canigueral et al. 2009)." [Olatunji NP]

"Starch and cellulose are not plastics in their native form, but are converted into plastics through various approaches, including extrusion cooking, functionalization, and plasticization. Starch is one of the least expensive biodegradable materials available in the world market today. It is a versatile biopolymer with immense potential for use in non-food industries. Starch-based polymers can be produced from corn, rice, wheat, or potatoes." [Mohanty NFBB]

Modified Starch: "Starches and modified starches are used by the food industry for cake mixes, pie fillings, frozen and canned foods, and jellies (Chinachoti, 1995). When starch granules are heated at 56-68~ (or higher) in water, all of the hydrogen bonds between its chains lose contact with each other and, instead associate with water. The result of heating is a viscous suspension, or gelatination. To prevent the re-formation of a solid gel, with heating, the food industry adds phosphate groups to the hydroxyl residues of starch, to add a repelling force between adjacent chains of sugars, thus maintaining the starch in gel form." [NB Brody]

"The starches purified from some plants, such as cassava (tapioca starch) or potato, are too viscous for use by the food industry. They create a gummy texture in foods and reduce their palatability. These root starches develop a rubbery texture when cooked. Some starches, such as corn starch and wheat starch, form the desired texture when cooked, but with cooling these starches form a gel that eventually loses its water-binding properties. This process, which results in water separation, is called syneresis. Syneresis occurs with freezing or storage at low temperatures. The foregoing problems (gumminess and syneresis) can be avoided by modifying food starch prior to adding it to the food. Modification can be effected by acid treatment, hypochlorite treatment (oxidation), and by drying the starch and heat- ing it (Wurzburg, 1995)." [NB Brody]

"Acid treatment results in partial hydrolysis of the sugar-to-sugar bonds in the starch, i.e., an event similar or identical to that catalyzed, during digestion, by amylase. Hypochlorite treatment results in the conversion of hydroxyl groups to carboxyl groups, aldehyde groups, or ketones.
In making candy (gumdrops), corn starch is added to the hot, liquified product. Pouring this liquid into the candy mold is difficult, unless the starch is first processed by acid treatment. Oxidized starches are mainly used in breaded foods. This additive improves adhesion of the batter to fish or meat. Dry heat converts starch to a product called dextrin. Dextrins are used for coating candies, for imparting a gloss to baked goods, and for encapsulating oils and oily flavors to form a dry powder (Wurzburg, 1995)." [NB Brody]

Selective Breeding

"Plant breeding has led to specialty starches with atypical proportions of amylose and amylopectin. Waxy maize starch with nearly 100 percent amylopectin is inherently stable to retrogradation. Chemically cross-linked waxy maize starch is a very high-quality modified starch. High-amylose starches have become available more recently and have led to lower caloric starches. Because of the crystallinity of these starches they are partially resistant to digestion by intestinal amylases and behave as dietary fiber when analyzed by the official methods of analysis for dietary fiber. Some of these high-amylose starches contain as high as 60 percent dietary fiber when analyzed." [Katz EFC]

"Inbreeding is also helpful for detecting useful genes and one of these is the waxy locus (Wx), which encodes the starch granule-bound glucosyl transferase (GBSS). The ‘waxy’ starch lacks amylose, and starch composed exclusively of amylopectin is advantageous for commercial appli- cations. A clone resulting from the screening of self populations has been shown to present a naturally occurring mutation on the Wx locus and the strategy is now to transfer this mutation to other genotypes. It is expected that about 25% of the progenies obtained from the second cycle of crosses will be homozygous for the Wx locus and will produce amylose-free starch (Ceballos et al., 2008)." [Lebot TRTC]

Digestability

"Carbohydrates generally supply about 45% of our energy requirement. Dietary carbohydrates include monosaccharides (such as glucose and fructose), disaccharides (such as sucrose and lactose), and the longer-chain oligo- and polysaccharides. (Polysaccharides with fewer than 15 monosaccharide units are classed as oligosaccharides.) Dietary polysaccharides include starches, such as amylose and amylopectin, and some of the dietary fibers." [NB Brody]

"The nutritional value of uncooked (ungelatinized) starchy foods (cereal grains, potato, peas, and beans) is relatively poor. Our digestive enzymes do not readily convert the native granular starch of uncooked fruits and vegetables into glucose that would be absorbed in the small intestine. Undigested starch passes into the large intestine where, along with dietary fiber, it is broken down to glucose and fermented to short-chain fatty acids. Some of these short-chain acids are absorbed from the large intestine resulting in recovery of some of the caloric value of the native starch." [Katz EFC]

"The starch in plants occurs in small microscopic granules that have a core of starch surrounded by a network of protein. In the granules, amylopectin has an orderly crystalline structure, whereas amylose is somewhat amorphous. The orderly structure of the starch molecules may impair digestion by pancreatic amylase. The occurrence of starch in granules, whether in wheat, potatoes, bananas, or other foods, may prevent the digestion of up to 50% of the starch in these foods when they are consumed in the raw state. Cooking results in hydration of the starch molecules and in the swelling and gelatinization of the starch granules, increasing the susceptibility of the starch to enzymatic hydrolysis, with a consequent increase in digestibility." [NB Brody]

"The susceptibility of starch to hydrolysis by α-amylase has been shown to vary with botanical origin; nevertheless, it is not clear what structural features affect the degree of digestion. Extent of digestibility is known to be related to crystalline polymorphic forms, and it is accepted that starch with ‘A’ type X-ray diffraction is more susceptible to amylolysis than that with a ‘B’ type pattern (Jane et al., 1997, Planchot et al., 1997, Valetudie et al., 1993). The inferior crystallites composing linked branch points and the shorter double helices of A-type starch would be more readily digested by α-amylase (Jane et al., 1997). In addition to the crystalline polymorphic form, the fraction of crystalline structures in the starch (Planchot et al., 1997), molecular associations between starch components (Dreher, Berry, & Dreher, 1984), amylose content (Fuwa et al., 1977, Noda et al., 2002), granule size (Snow and O'Dea, 1981, Valetudie et al., 1993), granule shape (Valetudie et al., 1993) and surface pores (Jane et al., 1997) have all been mentioned in enzyme digestibility. Among these factors, granular structure is considered to be the most important in defining the rate and extent of enzymatic hydrolysis (Zhang & Oates, 1999). Electron microscopy studies have shown that α-amylase attacks the granule surface before penetrating through internal channels then hydrolyzing the granule from inside out (Li, Vasanthan, Hoover, & Rossnagel, 2004). External chains of amylopectin that construct the crystalline structures of starch granules likely affect the rate of hydrolysis; nevertheless, information concerning the contribution of amylopectin unit-chain length distribution to the enzyme digestibility of various starches has not been reported." [Srichuwong et al.,2005]

Bananas

"The starch content in plant foods changes with the age of the plant, that is, it decreases during the ripening process, with the concomitant production of free glucose. Starch may account for 3-82% of the dry matter of bananas, depending on ripeness (Table 3.1). Apparently bananas are good sources of carbohydrate, whether unripe or overripe. However, are unripe bananas really good sources of carbohydrates? The ripening process involves the hydrolysis of the starch in the ripening plant. This activity is a form of autolysis (self-digestion). The starch also can be broken down after consumption via the action of pancreatic (x-amylase, as well as other enzymes. The effect of amylase in cleaving banana starch is illustrated.... The data show the effects of attempts to digest banana starch in a test tube. The starch was mixed with hog pancreas amylase and incubated. Then the extent of hydrolysis was measured. As indicated in the table, different treatments were used. About half the starch in a raw banana resisted hydrolysis, but all the starch in a cooked banana was hydrolyzed. On cooling a cooked banana, a small fraction of the starch lost its susceptibility to hydrolysis." [NB Brody]

"Cooking disrupts the structure of the starch molecules in the grains, resulting in a marked increase in their digestibility. With cooling, the starch molecules regain a more orderly structure, resulting in a slight increase in resistance to enzymatic hydrolysis, as illustrated in the study with banana starch. The reversion to an organized structure with cooling is called the "crystallization" of starch. Although this process may not result in a significant effect on the nutritional value of the food, it may detract from its aesthetic value. For example, freshly baked bread may be quite appealing. With storage for a day or so, the bread loses its appeal and is called "stale." The original consistency of the bread can be revived by heating it. The staling effect occurs because of the crystallization of the bread starch. The revival by heating results because of the disruption of its orderly structure." [NB Brody]

Sources of Starch

Species: Amylose (%) Amylopectin (%) References
Banana 17 83 [NB Brody]
Cassava Root 17 83 [NB Brody]
Corn 25-28 72-75 [NB Brody]
Kodo millet 24 76 [Farooq NUC]
Potato 21-23 77-79 [NB Brody]
Rice 15-35/12-19 65-83/81-88 [NB Brody]/[Farooq NUC]
Wheat 20-28 72-80 [NB Brody]

"In millets starch percentage ranges from 65-80%. The percentage of amylose and amylopectin content vary among the grains which ranges from 16-28% and 72-84%, respectively. Total sugars present in the grain ranges from 1.5 to 2.1 %. Sucrose is the predominant sugar in millets and constitutes 1.5% of its total sugar weight [46]." [Chhikara FF]

Ipomoea batatas (sweet potato) - "Sweet potato starch granules are made up of amylopectin and amylose molecules. Starches isolated from three Chinese cultivars have been shown to differ in granule size and particle size distribution but the amylose contents are similar (19.3–20.0%)." [Lebot TRTC]

"Most cereals contain 70–75% amylopectin. Almost all the starch disappears in the gastro-intestinal tract, only a small portion of the starch (1–5%) resists enzymatic hydrolysis when cereal foods are thermally abused. Thus, the residual starch can be quantified as soluble dietary fiber residue which could be highly susceptible to fermentation in the large intestine [45, 46]. Millet fiber is more concentrated in its bran, which is termed as complex unavailable polysaccharides and therefore produces more health benefits. Due to higher viscosity, glycemic index and water holding capacity dietary fibres that are potent in reduction of blood glucose level as well as insulin response [47, 48]." [Chhikara FF]

Fiber

"Fiber is grouped by its physical properties and is called soluble, insoluble or resistant starch. It was found that millet contains 6.3% insoluble fiber and 0.6% soluble fiber [11]. The most abundant fiber constituents in cereals are cellulose, hemicelluloses, lignin, pectins, and gums and almost all fiber types listed are present in millets." [Chhikara FF]


Gums

"Gums are polymers acquired from shrubs and trees from Africa and Asia. Gums are complex polysaccharides made of units of galactose and mannose. Gums are used by the food industry to prevent ice crystal formation in ice cream and candy; to prevent separation of oils and water in various beverages, and to prevent the leakage of water from proc- essed cheese." [NB Brody]


Hemicellulose

Xylan - cell wall polysaccharide. "associated with cellulose, can replace cellulose in some green and red algae" [Hostettmann HCBPAM]

"The main hemicelluloses found in plants are xylans (1,4-linked polymers of the pentose sugar xylose), but arabans (polyarabinose), galactans (polygalactose), mannans and copolymers (e.g. glucomannans and galactoglucomannans) are also encountered. The major angiosperm hemicellulose is a xylan with up to 35% of the xylose residues acetylated, and it is also substituted with 4-O-methylglucuronic acid in dicotyledonous plants. Enzymes responsible for hemicellulose degradation are named according to their substrate specificity; for example, mannanases degrade mannans, xylanases degrade xylans, etc. As xylans predominate in plant walls, more is known about xylanases." [Moore 21stFungi]

"Xylanases can be induced by their substrate, the response being for the fungus to produce a complex of enzymes rather than a single one. The complex consists of at least two endoxylanases and a b-xylosidase. The endoxylanases degrade xylan to xylobiose and other oligosaccharides while the xylosidase degrades these smaller sugars to xylose. Some arabinose is also formed, showing that the xylanase complex is able to hydrolyse the branch points in xylan." [Moore 21stFungi]


Simple Sugars

Monosaccharides

Arabinose

Fructose (levulose)

Fucose

Galactose

Glucose (dextrose)

"glucose sugar or monosaccharide, C6H12O6, that is the most important carbohydrate in plants and animals. In plants and algae, glucose is formed by photosynthesis." [Mouritsen Seaweeds]

Hexoses

Hexoses

Mannose

Pentoses

Ribose

Trioses

Xyloses

Disaccharides

Galactose

Lactose

Lactulose

Maltose

Sucrose


Algae-derived carbohydrates

"From a general point of view, green seaweeds contain sulfuric acid polysac- charides, sulfated galactans, and xylans (see the section Green Macroalgae), while brown algae contain alginic acid, fucoidan (sulfated fucose), and laminaran (β-1,3 glucan) (see the section Brown Macroalgae). Red algae contain agars, carrageenans, xylans, floridean starch (amylopectin-like glucan), and water-soluble sulfated galac- tan, as well as porphyran as mucopolysaccharides located in the intercellular spaces (see Red Macroalgae; Table 8.1; Kumar et al., 2008). Contents of both total and species-specific polysaccharides show seasonal variations." [Fleurence SHDP]

"Among the various ingredients, carbohydrates are the most abundant constituents of marine algae [1,10,11]. Based on degrees of polymerization (DPs), carbohydrates, also called saccharides, exist in marine algae as various forms of monosaccharides, disaccharides, oligosaccharides and polysaccharides [1]. Marine carbohydrates have been utilized in cosmeceutical industries due to their chemical and physical properties [12,13]. Fucoidans/alginate from brown algae, ulvans from green algae and carrageenans/agar from red algae are used as gelling, thickening and stabilizing agents [2,6,12,14]. In addition, accumulating reports suggest that marine carbohydrates have been proven to exhibit potential benefits for skin [2,12]." [Kim, Ji Hye, et al.,2018]

"In 2002, Fujimura’s group found that topical application of brown algae Fucus vesiculosus (Bladder wrack) aqueous extracts improved the thickness and elasticity of human cheek skin [20]. These results suggest that the F. vesiculosus extract possesses anti-aging activities and may be useful for a variety of cosmetics [20]." [Kim, Ji Hye, et al.,2018]

"Brown seaweeds contain several nutraceutical components (laminaran, fucoidan, polyphenols) that can positively influence human health (Plaza et al., 2008). Of these, laminaran modulates the immune response (Neyrinck et al., 2007) among other activities, such as anti-tumor (Jolles et al., 1963) and anti-apoptosis (Kim et al., 2006), that have been discovered for this compound. Fucoidan, by contrast, affects the secretion of extracellular matrix proteins (Moon et al., 2008), influences the proliferation of cells (Haroun-Bouhedja et al., 2000, Koyanagi et al., 2003) and can activate apoptosis (Aisa et al., 2005). Anticoagulant, anti-tumor, anti-thrombosis, anti-inflammatory and antiviral properties are also well known for fucoidan (Berteau and Mulloy, 2003, Boisson-Vidal et al., 1995). Furthermore, these biological activities are dominated by the structure of the polysaccharides, which vary for each seaweed species."[Rioux et al.,2010]

"Numerous in vitro and in vivo studies showed that marine algae extracts and algal carbohydrates showed various biological activities against skin disorders including hyperpigmentation, wrinkles, dry skin disorders, skin inflammation and skin cancer. However, although diverse biological activities of marine carbohydrates have been determined, their detailed molecular mechanisms and target proteins are not fully understood." [Kim, Ji Hye, et al.,2018]

"Among marine algae, brown algae have been reported to contain fucoxanthin (FUCO), nonstarch polysaccharides and lipids (phospho- and glycolipids), which are widely studied for their versatile functions like anti-oxidant, anti-inflammatory and anti-cancerous [12]. FUCO is the primary carotenoid found in the brown algae chloroplast and is recognized for its weight reduction, antioxidant, anti-inflammatory properties [13]. Dietary FUCO is hydrolyzed to fucoxanthinol (FXOH) in the intestine that is readily absorbed and enters systemic circulation through the lymph and functions as a superior antioxidant than the parent molecule FUCO [14]. Seaweed polysaccharides (PS) are majorly composed of laminaran, fucoidan and alginate [15]...." [Sharma&Baskaran.,2021]

"In the terrestrial blue-green alga, Nostoc flagelliforme, the main carbohydrate has been identified as nostoflan, which is composed mainly of glucose, galactose, xylose and mannose, and less of fucose that is common in the brown sea algae (Kanekiyo et al., 2008). Shimonaga et al. (2007) reported that red algae produce mainly floridean starch, and the unicellular species, Porphyridium purpureum, produces both amylopectin-type and amylose-type α-Polyglucans. Another species, Cynadium caldarium, synthesises glycogen-type polyglucans rather than starch. Laminarin, a β-glucan, has been identified in other seaweeds (Deville et al., 2007) and may be less digestible by animal enzymes and therefore be more suitable as prebiotic than products that are predominantly α-glucan in nature." [Dominguez FIAFN]

Seaweed oligosaccharides

-

Other Seaweed Carbohydrates

"Porphyran has been reported to scavenge oxidative radicals in vitro [55], and to increase antioxidant enzyme activity and antioxidant capacity in aging mice [56,57]." [Kim, Ji Hye, et al.,2018]


Polysaccharides

"Polysaccharides fulfil two main functions in living organisms: as food reserves and as structural elements. Plants accumulate starch as their main food reserve, a material that is composed entirely of glucopyranose units, but in two types of molecule." [MNP Dewick]

"Polysaccharides are of various types depending on their structure or function. In terms of function there are three main types; storage polysaccharides such as starch and glycogen, structural polysaccharides such as cellulose and chitin, and gel forming polysaccharides such as alginic acid and mucopolysaccharides (Yui 2005). They can also be branched or straight chained polymers, ionic or nonionic (cationic and anionic) polymers." [Olatunji NP]

Polysaccharides
Source Polymer Reference
Cells walls of plants Pectin [Olatunji NP]
Seeds and roots Galactomannans [Olatunji NP]
Seaweeds Carragenans, alginates, agar [Olatunji NP]
Animal cell walls Hyaluronan [Olatunji NP]
Shells of aquatic animals Chitin [Olatunji NP]
Wood Cellulose, lignin, hemicellulose [Olatunji NP]
Skins and bones of animals and scales of fish Gelatin [Olatunji NP]
Bacteria Xanthan, hyaluronan, gellan [Olatunji NP]
Fungi Cardlan, scleroglucan, schizophyllan [Olatunji NP]

Levan (Phlein) - storage polysaccharide. Poaceae. [Hostettmann HCBPAM]
Galacturonan - cell wall polysaccharide. Structural element of pectin [Hostettmann HCBPAM]
Rhamno-galacturonan I - cell wall polysaccharide. Structural element of pectin [Hostettmann HCBPAM]
Arabinogalactan - "As natural gum (gum Arabic) of Acacia sp., as main component of arabinogalactan protein (AGP) in cell walls, as sulfated polymers in green seaweeds" [Hostettmann HCBPAM]
Inulin - storage polysaccharide. Asteraceae. [Hostettmann HCBPAM] "A less common storage polysaccharide found in certain plants of the Compositae/Asteraceae and Campanulaceae is inulin ..., which is a relatively small polymer of fructofuranose, linked through β2→1 bonds." [MNP Dewick]
Rhamno-galacturonan II - cell wall polysaccharide. Structural element of pectin, contains rare sugars.[Hostettmann HCBPAM]
Xyloglucan - cell wall polysaccharide. [Hostettmann HCBPAM]
Glucomannan - cell wall polysaccharide. [Hostettmann HCBPAM]
β-(1→3)(1→4)-Glucan - cell wall polysaccharide and storage polysaccharide, in lichens (Lichenan) and cereals [Hostettmann HCBPAM]

Seaweed Polysaccharides

"Alginic acid ... is a linear polysaccharide formed principally by β1->4 linkage of d-mannuronic acid residues, though sometimes residues of the C-5 epimer l-guluronic acid are also part of the structure. Alginic acid is the main cell wall constituent of brown algae (seaweeds). Some bacteria also produce alginates; the human pathogen Pseudomonas aeruginosa secretes alginates as a viscous coating when it infects lung tissue in cystic fibrosis. Salts of algal alginic acid are valuable thickening agents in the food industry, and the insoluble calcium salt is the basis of absorbable alginate surgical dressings." [MNP Dewick]

"Alginic acid (Figure 8.20) is obtained by alkaline (Na2CO3) extraction of a range of brown seaweeds, chiefly species of Laminaria (Laminariaceae) and Ascophyllum (Phaeophyceae) in Europe, and species of Macrocystis (Lessoniaceae) on the Pacific coast of the USA. The carbohydrate material constitutes 20–40% of the dry weight of the algae. The acid is usually converted into its soluble sodium salt or insoluble calcium salt. Sodium alginate finds many applications as a stabilizing and thickening agent in a variety of industries, particularly food manufacture, and also the pharmaceutical industry, where it is of value in the formulation of creams, ointments, and tablets. Calcium alginate is the basis of many absorbable haemostatic surgical dressings. Alginic acid or alginates are incorporated into many aluminium- and magnesium-containing antacid preparations to protect against gastro-oesophageal reflux. Alginic acid released by the action of gastric acid helps to form a barrier over the gastric contents." [MNP Dewick]

"Fucoidans are major sulfated polysaccharides (SPs) found in the cell wall of some brown algae [10]. Numerous studies have reported the benefits of fucoidans for diverse skin disorders including pigmentation, skin aging, atopic dermatitis and skin carcinogenesis." [Kim, Ji Hye, et al.,2018]

"In recent years, fucoidan extracts have attained regulatory approvals in a number of global jurisdictions for use in foods and dietary supplements." [Fitton et al.,2019]

"The oral bioavailability of fucoidan preparations is generally low, although recent studies have elegantly demonstrated the uptake and tissue distribution of Fucus vesiculosus fucoidan in a rat model [25]. A Japanese study has further confirmed the bioavailability of fucoidan and its excretion in urine, after ingestion of whole seaweed [26]. This follows their earlier work demonstrating the uptake of orally delivered fucoidan in serum and urine [27].... The recently described observations of clinical efficacy of orally delivered fucoidan for chronic renal failure indicate probable systemic uptake [5] in humans." [Fitton et al.,2019]

"... a clinical topical study using a cream containing 4% fucoidan was found to be effective for treating oral herpes [38]. This topical application is supported by a substantial body of research indicating excellent inhibitory activity against herpes viruses [39]." [Fitton et al.,2019]

"The use of fucoidans as potential agents in oncology has been recently reviewed by others and is briefly expanded upon here [3,15]. The mechanism by which fucoidans could induce either a direct or indirect anticancer effect is better understood. The modulation of immune activity by fucoidans shows promise, not only as an anti-inflammatory agent, but also as a potential vaccine adjuvant. This immune-modulatory effect may also represent an additional anticancer mechanism for fucoidans. Observations in elderly Japanese subjects showed that oral administration of a fucoidan extract enhanced their response to influenza vaccines [16]. The mechanism for this useful activity may be associated with the ability of fucoidans to bind to Toll-like receptors [17]. Another emerging application in the literature is the use of fucoidans in ocular diseases [18], particularly age-related macular degeneration due to their ability to interfere with the activity of vascular endothelial growth factor (VEGF) [19]." [Fitton et al.,2019]

"Fucoidans continue to be developed as bioactive oral supplements and will likely increase their market presence in the future. Gut health, oral health and anti-inflammatory applications are already partly commercialised for use in humans, livestock and pets, with the recent suite of regulatory approvals for fucoidan extracts in the US and EU likely to spur further growth in these sectors.
... Regulatory approval of a fucoidan preparation for chronic renal failure has provided clinically useful outcomes in China. Fucoidans have enormous potential as part of drug delivery systems and devices, and they show particular near-market potential in imaging and in treatments for thrombosis. Safety studies on radiolabelled fucoidan have been carried out with a view to regulatory approval for clinical imaging applications....
Orally bioavailable adjunct therapies for neurological disease, bacterial and viral infections, and oncology also appear to be commercial possibilities with research now progressing into the clinical trial phase." [Fitton et al.,2019]

"The presence and position of sulfate groups is important to the biological activities of fucoidans. Fucoidan extracted from Fucus vesiculosus is commercially available and is composed of 44.1% fucose, 26.3% sulfate, and 31.1% ash, and a little aminoglucose. Other sources of fucoidan include the edible species Cladosiphon okamuranus, Fucus serratus, Sargassum polycystum, Sargassum oligocystum, and Undaria pinnatifida [70]. These compounds reportedly have multiple inhibitory actions in vivo and in vitro including antithrombin, antiproliferative, antioxidant, anticomplement, anticancer, and antineutrophil migration effects. Fucans may block various binding events at cell surfaces including cell–cell binding through integrin–selectin molecules or by binding thrombin or complement in the blood or fucose receptors on cell surfaces. Such activity is thought to be responsible for anti-inflammatory properties, namely, inhibition of lymphocyte or neutrophil binding to vascular endothelial cells that might prevent the invasion of these cells into a tissue compartment with subsequent inflammation [71, 72]." [Marine Algae]

"Laminaran (also known as laminarin) is one of the major non-SPs found in brown algae. The biological activities of fucoidans have been well-studied, while those of laminaran have been poorly understood to date. Laminaran from the brown algae Saccharina longicruris has been reported to show skin anti-aging induced by UVA/UVB in an in vivo model [50]." [Kim, Ji Hye, et al.,2018]

"The brown algae have storage laminaran (β-D-glucopyranose), a combination of soluble and insoluble chains of the type β-1,3 and β-1,6-D-glucans." [ECOStud-219]

"Laminaran, a polysaccharide extracted from marine algae, exhibits attractive properties being non-toxic, hydrophilic and biodegradable." [Sellimi, Sabrine, et al.,2018] "Laminaran is a ß-glucan that has shown anti-apoptotic and anti-tumoral activities". [Rioux et al.,2010]

"Laminaran has many advantages, including low cellular toxicity, biodegradability, and high biocompatibility [11]. A diverse array of bioactivities has been reported for laminaran, such as anti-apoptotic [12], anti-inflammatory [13], immunoregulatory [14, 15], antitumor [16], anticoagulant [17] and antioxidant activities [18]." [Sellimi, Sabrine, et al.,2018]

"It is present in either soluble or insoluble forms. The first form is characterized by complete solubility in cold water, while the other is only soluble in hot water (Black and Dewar, 1973, Percival and McDowell, 1967). The solubility is also influenced by the presence of branching, with the higher the branching content the higher the solubility in cold water. Two types of laminaran have been described, one type with chains that are terminated by d-mannitol residues (M-series) and another type with chains terminated by d-glucose residues (G-series) (Nelson and Lewis, 1974). Laminaran is composed of d-glucose with β-(1,3) linkages (Barry, 1939), with β-(1,6) intrachain branching (Peat et al., 1958). Ratios of the two types of laminaran, as well as their structures, can vary according to the seaweed species, as well as environmental factors such as nutritive salts and frond age (Chizhov et al., 1998, Rioux et al., 2009). These factors are also believed to influence the biological activity of laminaran." [Rioux et al.,2010]

Anticancer: "In the last decade, numerous studies reported promising anti-cancer effects of laminarin involving enhanced apoptotic cellular death, colony formation inhibition and angiogenic potential inhibition...." [Zargarzadeh et al.,2020]

"Ji and colleagues reported on laminarin’s capacity to inhibit human colorectal adenocarcinoma (LoVo) cell proliferation and induce apoptosis via mitochondrial or death receptor pathways (Ji & Ji, 2014; Ji, Ji, & Zhang, 2012)." [Zargarzadeh et al.,2020]

"These polysaccharides have been found to exert potent immunomodulating, radioprotective, and anticancer activities (Kadam, Tiwari, & O’Donnell, 2015). Recently it was reported that sulfated derivatives of laminarans are more effective than native laminarans in the inhibition of proliferation, colony formation, migration, and induction of apoptosis of cancer cells (Ji, Ji, & Meng, 2013; Malyarenko et al., 2017; Park, Kim, Kim, & Nam, 2012)." [Malyarenkob et al.,2019]

"Native and sulfated laminarans from the brown alga D. dichotoma exhibited significant anticancer activity against melanoma cells when administered at non-toxic doses. At low doses the polysaccharides were able to selectively sensitize melanoma cells to X-ray irradiation, resulting in significant inhibition of cell proliferation, colony formation, and cancer cell migration. The molecular mechanism of this effect was found to involve the down-regulation of MMP-2 and MMP-9 protein kinase activity,..." [Malyarenkob et al.,2019]

Antibacterial: "The results showed that LME extract [from Sargassum crassifolium] at a concentration of 250 mg/mL is bacteriostatic against Gram-positive [Bacillus subtilis and Staphylococcus aureus] and –negative bacteria [Salmonella typhimurium and Escherichia coli]." [Chamidah et al.,2017]

Conversion into glucose: "Laminarin can be hydrolysed to glucose using a laminarinase, which cleaves the ß-1,3-linkages of d-glucan to form oligosaccharides with 2 to 10 residues. Laminarinase is an endo-ß-glucanase that may cleave either (1 -> 3), (1 -> 4), (1 -> 6) or mixed (1 -> 3), (1 -> 4), (1 -> 6) linkages into glucose units [11]. Beta-glucanases are specifically used as biocatalysts in industrial processes, such as the brewing, poultry and biofuel industries. These enzymes form part of the glycoside hydrolase (GH) family and are relatively widespread among microorganisms, including various filamentous fungi and yeasts [12]." [Rocher et al.,2021]

"The yeast S. cerevisiae remains the ideal host organism for industrial bioethanol production, since it can tolerate high ethanol concentrations [15]. However, S. cerevisiae cannot produce enough of its native laminarinase-like enzyme for effective hydrolysis of laminarin. Microorganisms known to produce efficient amounts of laminarinase, such as T. viride, T. reesei and R. emersonii, have a lower ethanol tolerance, thus reducing their potential use in industry. Efficient conversion of the laminarin from brown macroalgae into bioethanol thus requires the development of recombinant S. cerevisiae yeast strains that express effective laminarinases." [Rocher et al.,2021]

Ulvans

"Ulvan represents a class of sulfated heteropolysaccharide extracted from the cell wall of green seaweeds like Ulva, Enteromorpha, and Utricularia belonging to Ulvales that is responsible for maintaining osmotic stability and provides protection to the cell. It constitutes about 8–29% of the algal dry weight [116, 117]." [Marine Algae]

"The composition of ulvan has been extensively debated and has been shown to vary according to several factors including the period of collection, the ecophysiological growth conditions, taxonomic origins, and the postcollection treatment of the algal sources. It is composed mainly of rhamnose, glucuronic acid, iduronic acid, xylose, glucose, with sulfate and traces of galactose." [Marine Algae]

"Ulvans are sulfated heteropolysaccharides extracted from the cell wall of green algae Ulva pertusa [52]. Ulvans are water-soluble sulfated polysaccharides and their main constituents are rhamnose, xylose, glucose, uronic acid and sulfate." [Kim, Ji Hye, et al.,2018]

"The most striking feature that distinguishes the chemical composition of ulvan from that of the other polysaccharides of marine origin is the presence of the uncommon sugars, iduronic, and sulfated rhamnose. The ubiquitous occurrence of rhamnose in this algal polysaccharide can be considered as an advantage, particularly for the treatment of skin pathologies. In general, rhamnose-rich polysaccharides demonstrate anti-inflammatory properties, diminish skin bacterial adhesion, protect it from UV-induced and age-related injuries, and stimulate cellular proliferation and collagen biosynthesis [129, 130]." [Marine Algae]

Floridean starch

"The storage polysaccharide of the red algae is known as floridean starch" [Dominguez FIAFN]

"In Rhodophyta, carbohydrates synthesized from carbon fixation are stored as floridean starch, which is characterized by a1,4-D and a1,6-glucans." [ECOStud-219]

"Floridean starch, which is formed in the cytoplasm outside the chloroplasts, is chemically similar to the amylopectin of higher plant starches." [GPOD]

Floridean starch "... has a similar structure as starch without amylose. However, it was confirmed that some species of red algae form also amylose units. Another difference is the imposition of granules of floridean starch outside the plastids (Shimonaga et al., 2007)." [HMA]


Other Carbohydrates

Chitosan: "Chemical deacetylation of chitin provides chitosan, a valuable industrial material used for water purification because of its chelating properties and in wound-healing preparations." [MNP Dewick]

Chondroitin: "Chondroitin is another glycosaminoglycan widely distributed in animal tissues, particularly connective tissue, and is a major component of cartilage, lubricating and cushioning joints. It is based on a repeating disaccharide unit of glucuronic acid linked β1-> to N-acetylgalactosamine, with the disaccharide units then connected β1→4. It is typically found as chondroitin sulfate, the polymer having varying sulfation patterns, though mainly monosulfation at positions 4 and 6 of the GalNAc residues". sup>[MNP Dewick]

Glycogen: "The mammalian carbohydrate storage molecule is glycogen, which is analogous to amylopectin in structure, but is larger and contains more frequent branching, about every 10 residues." [MNP Dewick]

"This is the polysaccharide reserve that’s found in animal tissues, and in the fungi themselves. Most fungi are likely to encounter glycogen in their surroundings, as they are likely to be surrounded by dead and dying fungal cells." [Moore 21stFungi]

"Extracellularly, glycogen, like starch, is degraded by components of the amylase enzyme complex." [Moore 21stFungi]

Heparin: "The mammalian blood anticoagulant heparin (Figure 8.21) is also a carbohydrate polymer containing glucosamine derivatives, but these alternate with uronic acid residues. Polymers of this kind are known as mucopolysaccharides or glycosaminoglycans. Heparin consists of two repeating disaccharide units, in which the amino functions and some of the hydroxyls are sulfated, producing a heterogeneous polymer. The carboxyls and sulfates together make heparin a strongly acidic water-soluble material." [MNP Dewick]

"heparin carbohydrate of the glucosamino-glycan type; used as a very effective anticoagulant to prevent blood clots." [Mouritsen Seaweeds]

Heparan sulfate: "Heparan sulfate is structurally related to heparin, but the chains are longer and more heterogeneous. Heparin is secreted only by mast cells, whereas heparan sulfate is more widely distributed and found in different cell types and tissues." [MNP Dewick]


Hyaluronic acid: "Hyaluronic acid (Figure 8.21) is a similar polymer based on glucuronic acid and N-acetylglucosamine, though not modified by sulfation; it is a major component of the extracellular matrix and plays an important role in tissue regeneration and wound healing." [MNP Dewick]

Peptidoglycan:


Diseases Related to Carbohydrates

"Glycogen storage diseases or glycogenoses occur when there is a defect in the enzymes that are involved in the metabolism of glycogen, resulting in growth abnormalities, weakness, and confusion. These diseases are caused by lack of an enzyme needed to convert glucose into glycogen and break down glycogen into glucose. Typical symptoms include weakness, sweating, confusion, kidney stones, and stunted growth." [Eddouks PMDH]

"About 1 in 20,000 infants has some form of glycogen storage disease. The specific symptoms, age at which symptoms start and their severity vary considerably among these diseases." [Eddouks PMDH]

"Galactosemia or a high blood level of galactose is caused by lack of one of the enzymes necessary for metabolizing galactose (a sugar in lactose, fruits and vegetables). A deficient enzyme or liver dysfunction can alter the metabolism, leading to high levels of galactose in the blood (galactosemia). There are different forms of galactosemia, but in classic galactosemia a toxic metabolite to the liver and kidneys builds up, that damages the eye lens, causing cataract." [Eddouks PMDH]

"Fructose intolerance, is a hereditary disorder caused by lack of the enzyme needed to metabolize fructose. As a result, a by-product of fructose accumulates in the body, blocking the formation of glycogen and its conversion to glucose for use as energy." [Eddouks PMDH]

"Mucopolysaccharidoses, are a group of hereditary disorders when complex sugar molecules are not broken down normally due to the lack of necessary enzymes responsible for its break down and storage, leading to its accumulation in harmful amounts in the tissues." [Eddouks PMDH]


References

Carbohydrate Monographs

Acacia (gum arabic)

"Acacia (gum arabic) is a dried gum from the stems and branches of the tree Acacia senegal (Leguminosae/Fabaceae), abundant in the Sudan and Central and West Africa. Trees are tapped by removing a portion of the bark. The gum is used as a suspending agent and as an adhesive and binder for tablets. The carbohydrate is a complex branched-chain material which yields l-arabinose, d-galactose, d-glucuronic acid, and l-rhamnose on hydrolysis. Occluded enzymes (oxidases, peroxidases, and pectinases) can cause problems in some formulations, unless inactivated by heat." [MNP Dewick]

References


Alginic acid

References


Alginates

Classification: Polysaccharide

"Most of the large brown seaweeds are potential sources of alginate. The properties of the alginate varies from one species to another, so the choice of which seaweeds to harvest is based on both the availability of particular species and the properties of the alginate that they contain. The main commercial sources are species of Ascophyllum, Durvillaea, Ecklonia, Laminaria, Lessonia, Macrocystis, Sargassum and Turbinaria. Of these the most important are Laminaria, Macrocystis and Ascophyllum." [McHugh, Dennis J.,1987]

Use in Textile Printing

"In textile printing, alginates are used as thickeners for the paste containing the dye. These pastes may be applied to the fabric by either screen or roller printing equipment. An excellent review by Hilton (1969) discusses the role of the thickener in the printing of fabrics and the advantages/disadvantages of sodium alginate in different printing processes. Alginates became, important thickeners with the advent of reactive dyes which combine chemically with cellulose at its hydroxyl groups. Many of the standard thickeners, such as starch, also react with these dyes and this leads to lower colour yields and sometimes insoluble products which are not easily washed out and which can result in a fabric with poor handle. Alginates react minimally with reactive dyes, they wash out of the finished textile readily and are the best thickeners for these dyes. They are also used with other types of dyes." [McHugh, Dennis J.,1987]

"The viscosity of the paste can be varied according to the application and the equipment. Thick pastes with short flow characteristics are useful when the extent of penetration into the fabric must be limited but thinner pastes with long flow are required for fine-patterned prints. For alginates containing small quantities of calcium, viscosity can be controlled by adding sequestering agents such as polyphosphates. However these pastes are more likely to lose viscosity as shear rate increases and a paste which is less shear sensitive can be made using a high concentration of a lower viscosity alginate. This latter kind of paste is especially useful for printing disperse dyes on synthetic fibres. Most alginate manufacturers can supply basic recipes for the different types of dyes and printing processes (for example, Protan, 1985) which are a useful starting point; the quantities of alginate can vary from 1.5% of high viscosity alginate to 5% of low viscosity alginate." [McHugh, Dennis J.,1987]

Food Use

"Alginates have a long history of use in foods and these uses are based mainly on their thickening, gelling and general colloidal properties. Thickening is useful in sauces, syrups and toppings for ice cream, etc., pie fillings (it reduces moisture retention by the pastry), cake mixes (it thickens the batter aids moisture retention), and canned meat and vegetables (it can give either temporary or delayed-action Chickening). Gel formation leads to uses in instant milk desserts and jellies, bakery filling cream, fruit pies, animal foods and reformed fruit. General colloidal properties are difficult to define but are illustrated by the results obtained by adding sodium alginate to ice cream and water ices, or propylene glycol alginate to stabilize beer foam or the suspended solids in fruit drinks (Leigh, 1979)." [McHugh, Dennis J.,1987]

"One of the more recent developments is the use of alginates in restructured meat products. The US Department of Agriculture approved the use of alginate as a binder in these products last year (September, 1986) and this should lead to a new market for alginate. Restructuring is the process of taking flaked, sectioned or chunked meat and binding the pieces to resemble intact cuts of meat. The final products can be shaped as nuggets, roasts, loaves and steaks. Until now most restructured products have been sold frozen or cooked, so they could retain their shape. With the use of binders, the restructured products can be sold fresh or raw. The binder is a powder of sodium alginate, calcium carbonate, lactic acid and calcium lactate. When mixed with the raw meat, they form a calcium alginate gel which binds the meat. This binding mixture can be used to replace the sodium chloride and phosphate salts commonly used, thereby reducing the sodium level in the restructured products. Up to 1% sodium alginate is permitted." [McHugh, Dennis J.,1987]

"Alginates have been used for other re-formed foods. Morimoto (1984) patented a process for making shrimp or crabmeat analogue products using alginate and proteins such as soy protein concentrate or sodium caseinate. A mixture of the two is extruded into a calcium chloride bath to form edible fibres which are then frozen, thawed, chopped, coated with sodium alginate and formed in an appropriately shaped mould. After further freezing and thawing a product analogous to natural shrimp is obtained. Wylie (1976) described the manufacture of analogue fish fillets (sole) using minced white fish and a calcium alginate gel; the products could be grilled or cooked with sauce. A meat substitute has been formed from an aqueous mixture of protein and alginate by a process of freezing, slicing, gelling and heat setting; a well defined fibre structure results (Shenouda, 1983)." [McHugh, Dennis J.,1987]

"The principles used for making structured fruit products have been extended to making structured potato products such as croquettes and french fries (Anon., 1983). A synthetic potato skin shell containing alginate can be filled with mashed potato and browned to produce 'baked potatoes' in the fast-food market (Ooraikul and Aboagye, 1986). A patent by Cox (1982) for forming simulated, shaped, edible products includes the production of caviar and cottage cheese as examples." [McHugh, Dennis J.,1987]

"There has been an increased interest in the use of alginate-pectin mixed gels with potential for use in jams, fruit flans and mayonnaise (Thom et al., 1982; Toft, 1982; Morris and Chilvers, 1984). New dessert gels from alginate have been reviewed by Kelco (1983) while Protan (1986a) has discussed alginates as stabilizers in bakery creams, jams and jellies." [McHugh, Dennis J.,1987]

"The reasons for the effectiveness of alginate as a stabilizer in ice cream have never been fully understood; Muhr and Blanshard (1984) have studied the mechanism for the reduction of crystal growth but their work is not yet conclusive." [McHugh, Dennis J.,1987]

"A moisture barrier which allows breaded or batter-covered products to come in contact with a sauce or filling can be made using a coating of soluble alginate which is then treated with calcium chloride (Earle and McKee, 1986). Alginates are being used to make improved rice pasta and vegetable pasta (Hsu, 1985, 1985a). Calcium alginate can be formed as a fibrous precipitate and is used to simulate the texture of natural fruit and vegetables (Anon., 1980)." [McHugh, Dennis J.,1987]

"Alginate may be partiall~ though not completely, digested, as indicated by the finding that the consumption of 15 g alginate has a laxative effect in humans (McNeely and Kovacs, 1975). Carrageenan is thought not to be digested or absorbed by humans or animals. The typical daily intake of carrageenan is only 25-35 mg/day. Hence, there is little reason to believe that our intake of this seaweed polysaccharide contributes to or detracts from normal metabolism (Stancioff and Renn, 1975)." [NB Brody]

Wound Dressing

"The use of alginate as a wound dressing dates back to the Roman times. In folklore, seaweeds were used by sailors to stem blood loss and by doctors in the eighteenth-century Scotland to drain abdominal wall abscesses [29]." [Marine Algae]

"Alginate is both a biopolymer and a polyelectrolyte and is considered to be biocompatible, nontoxic, nonimmunogenic, and biodegradable." [Marine Algae]

"A number of alginate dressings ... are available on the market. They are available in various forms ranging from flat sheets for superficial wounds to ropes and ribbons for light cavity wounds. In addition, there are superabsorbent and self-adhesive versions of alginate dressings. If the dressing is not self-adhesive, a secondary dressing is required." [Marine Algae]

"Alginate dressings have three main characteristics that influence their use. These are: their ability to provide an in situ moist environment at the wound bed, good fluid-handling properties, and hemostasis. Alginate fibers, typically as calcium salt, may absorb wound exudates up to 20 times their weight, which makes them a good choice for heavily exuding wounds." [Marine Algae]

"Alginate dressings lower the bioburden and reduce odor. The high level of bioactivity in these dressings is believed to be because of the presence of an endotoxin in alginates [41]." [Marine Algae]

"The different brands of alginate dressings show differences in characteristics such as fluid retention, adherence, and dressing residues.... an in-depth knowledge of their features and wound type is important to determine applicability. They have been found to be effective in pressure ulcers, venous leg ulcers, diabetic foot ulcers, postoperative wounds, cavity, traumatic and malignant wounds, pilonidal sinus wounds, donor sites, and partial thickness burns. Generally, alginate dressings can be left in place for 5–7 days depending on the level of the exudates with change required when the dressing has completely gelled and saturated [52]. However, they are not recommended for dry or slightly moist wound beds because they will dehydrate the wound by forming a sticky plaque that needs traction for removal." [Marine Algae]

References

  • [McHugh, Dennis J.,1987] McHugh, Dennis J. "Production, properties and uses of alginates." Production and Utilization of Products from Commercial Seaweeds. FAO. Fish. Tech. Pap 288 (1987): 58-115. https://www.fao.org/4/x5822e/x5822e04.htm

Agar

Classification: Polysaccharide

"According to the US Pharmacopeia, agar can be defined as a hydrophilic colloid extracted from certain seaweeds of the Rhodophyceae class. It is insoluble in cold water but soluble in boiling water. A 1.5% solution is clear and when it is cooled to 34-43°C it forms a firm gel which does not melt again below 85°C. It is a mixture of polysaccharides whose basic monomer is galactose. These polysaccharides can be sulphated in very variable degrees but to a lesser degree than in carrageenan. For this reason the ash content is below those of carrageenan, furcelleran (Danish agar) and others. A 5% maximum ash content is acceptable for agar although it is normally maintained between 2.5-4%." [Armisen&Galatas,1987]

"Different seaweeds used as the raw material in agar production have given rise to products with differences in their behaviour, although they can all be included in the general definition of agar. For this reason, when agar is mentioned, it is customary to indicate its original raw material as this can affect its applications (Figure 1). Hence we talk about Gelidium agar, Gracilaria agar, Pterocladia agar, etc. To describe the product more accurately, it is usual to mention the origin of the seaweeds, since Gracilaria agar from Chile has different properties from Gracilaria agar from Argentina and Gelidium agar from Spain differs from Gelidium agar from Mexico." [Armisen&Galatas,1987]

"Nowadays the world agar industry basically uses the following seaweeds:
(1) Different species of Gelidium harvested mainly in Spain, Portugal, Morocco, Japan, Korea, Mexico, France, USA, People's Republic of China, Chile and South Africa.
(2) Gracilaria of different species harvested in Chile, Argentina, South Africa, Japan, Brazil, Peru, Indonesia, Philippines, People's Republic of China including Taiwan Province, India and Sri Lanka.
(3) Pterocladia capillace from Azores (Portugal) and Pterocladia lucida from New Zealand.
(4) Gelidiella from Egypt, Madagascar, India, etc." [Armisen&Galatas,1987]

Chemical Structure

"Agar is now considered to consist of two fractions, agarose and agaropectin. These were first separated by Araki (1937) and the results were published in Japanese so they were not readily available to some research workers. For example Jones and Peats (1942) assigned a single structure to agar defining it as a long D-galactose chain residue, joined by 1,3-glycosidic links; in the proposed structure, this chain was ended by a residue of L-galactose joined to the chain at C-4 and with C-6 semi-esterified by sulfuric acid. This false structure is still mentioned in some books on natural polymers and even in recently published encyclopedias." [Armisen&Galatas,1987]

Uses

"Agar was the first phycocolloid to be used in the human food industry. In the beginning it was only used in the Far East, but the applications have been extending all over the world for more than a century. The increasing range of applications is due to the particular gelling characteristics which are not present in any other phycololloid, gum or gelatin. As a result the price for food grade agar is higher than that of other phycocolloids with gelling properties which are also permitted as food additives. In addition, these characteristics allow agar to be used successfully and even exclusively in certain scientific and industrial applications. Some earlier reviews have also discussed uses of agar (Selby and Wynne, 1973; Meer, 1980; Glicksman, 1983)." [Armisen&Galatas,1987]

"In the human food industry, agar is used mainly as a gelling agent and in a secondary way as a stabilizing agent and for controlling viscosity. It is used as an additive, not as a nutrient. The gelling power of agar is so high that it is used at 1% maximum concentration; for viscosity control and as a stabilizing agent the proportion used is 1/100 or less. For this reason the ingested quantities are very small and, because agar is not easily digested by the human body, its calorie contribution is negligible and thus agar can be used in special diet food. Agar digestion by the human body is imperfect, studies have shown that less than 10% of the polysaccharide is assimilated. Therefore due to the small proportions in which it is used in human food, its importance as a nutrient is very small." [Armisen&Galatas,1987]

Marketing

"The data for all these applications refers to industrial agars that are sold worldwide in powder form with different meshes, generally included between 60-100 mesh, ASTM standards, in the Orient there is a considerable household consumption of natural agar with much lower gel strengths, in the range 150-400 g/cm2, with which daily food is prepared at home. This agar is marketed in "strips" or "square" (the appearance is string-like or bar-like respectively, Figure 15) produced always by freezing, thawing, draining, and drying without breaking the strips or squares, that are prepared at the gel stage. This popular method of presentation helps the housewife with her measurements. Such agar, produced basically in Japan, Korea, People's Republic of China and its Taiwan Province, is consumed locally and exported mainly to neighbouring countries with some quantities being sold in Western countries, mainly in health food stores. In Japan the sale of industrial agar for these uses is successfully presented in a pill form of the same content as a bar, to help the housewife with her measurement of it for cooking purposes." [Armisen&Galatas,1987]

References

  • [Armisen&Galatas,1987] Armisen, Rafael, and Fernando Galatas. "Production, properties and uses of agar." Production and utilization of products from commercial seaweeds. FAO Fish. Tech. Pap 288 (1987): 1-57. https://www.fao.org/4/x5822e/x5822e03.htm

Agarose

References


Carrageenan

Classification: Polysaccharide

"Carrageenans are commercially important hydrophilic colloids (water-soluble gums) which occur as matrix material in numerous species of red seaweeds (Rhodophyta) wherein they serve a structural function analogous to that of cellulose in land plants. Chemically they are highly sulfated galactans. Due to their half-ester sulfate moieties they are strongly anionic polymers. In this respect they differ from agars and alginates, the other two classes of commercially exploited seaweed hydrocolloids." [Stanley,Norman.,1987]

"Carrageenan from red algae is linear SP composed of 3,6-anhydro-D-galactose (D-AHG) and d-galactose. Carrageenan has been utilized in cosmetic products as a stabilizer, emulsifier and moisturizer due to its chemical and physical properties. In addition, carrageenan is known to exhibit various beneficial effects on skin health...." [Kim, Ji Hye, et al.,2018]

"There are three main types of carrageenans: kappa (κ), iota (ι), and lambda (λ) differing in the number and position of the sulfate groups and the possible presence of a three–six anhydrogalactose bridge." [Marine Algae]

Uses

"Carrageenans are used to gel, thicken, or suspend; therefore they are used in emulsion stabilization, for syneresis control, and for bodying, binding and dispersion. Major uses are in foods, particularly dairy applications." [Stanley,Norman.,1987]

"All carrageenans have the ability to form gels by cooling a solution of the carrageenan in hot milk. Even lambda-carrageenan, which does not gel in water regardless of the cations present, will form a gel at levels of 0.2% or more by weight of the milk. This gelation is ascribed to the formation of carrageenan-casein bonds, as previous described." [Stanley,Norman.,1987]

"The use of iota-carrageenan in dessert gel formulations affords gels which have textures very similar to those of gelatin gels. They have an advantage over gelatin gels in that their melting point is higher, so that they find a ready market in tropical climates or where refrigeration is not available. This is offset to some extent by the different mouth-feel, since these gels do not "melt in the mouth", as does gelatin. A further advantage is that iota gels retain their tender structure on aging, whereas gelatin tends to toughen. This is important for ready-to-eat desserts, an item popular in Europe." [Stanley,Norman.,1987]

"In toothpastes carrageenans function as a "binder" to impart the desired rheological properties to the paste and to provide the cosmetic quality of "sheen". Toothpastes consist of ingredients which interact in complex and poorly understood ways and the carrageenan often must be carefully tailored to achieve satisfactory performance in a particular formulation. Carrageenan suffers severe competition in the U.S. domestic market from sodium carboxymethylcellulose, a much cheaper gum. Despite this, business has been retained - and regained - due to the superior quality and appearance carrageenan imparts to a toothpaste. Outside the United States carrageenan has maintained a strong position in this application, due, among other factors, to its immunity to degradation by enzymes which attack cellulose gums." [Stanley,Norman.,1987]

"The Carrageenan market is worth US $527 million with most carrageenan being used as human food grade semire- fined carrageenan (90%) and the rest going into pet food." [Marine Algae]

"Though carrageenans are known for their antithrombotic, anticoagulant, antiviral, antitumor, antifungal, antibacterial, antioxidant, and immunomod- ulating activities [74], their use is limited in wound management because of toxicity issues." [Marine Algae]

Source Material

"Chondrus crispus .... The carrageenan from C. crispus, which comprises a mixture of kappa- and lambda-carrageenan, is much valued as the preferred type for applications such as chocolate milk stabilization." [Stanley,Norman.,1987]

"Furcellaria fastigiata yields furcellaran ("Danish agar"), often treated in the literature as a polysaccharide distinct from carrageenan but now considered, on the basis of chemical evidence (Lawson, et al., 1973), to be a member of the carrageenan family of polysaccharides." [Stanley,Norman.,1987]

"Gigartina acicularis and G. pistillata occur and are harvested together along the coasts of southern France, Spain, Portugal, and Morocco. The latter two species are unique in that they yield a nongelling, predominantly lambda or xi type carrageenan." [Stanley,Norman.,1987]

"Gigartina radula is harvested in Chile and comprises a major resource for carrageenan production. The taxonomy of Chilean G. radula is a subject of controversy, with some algologists holding to the earlier classification of this seaweed as one or more Iridea species." [Stanley,Norman.,1987]

"Gymnogongrus furcellatus, harvested in Peru, has been used as a source of iota-type carrageenan." [Stanley,Norman.,1987]

"Hypnea musciformis has been harvested along the south-eastern coast of the United States, in Brazil, and in Senegal. It yields a kappa or furcellaran type carrageenan. It is no longer used by the major carrageenan manufacturers due to difficulty in processing and low yield." [Stanley,Norman.,1987]

References

  • [Kim, Ji Hye, et al.,2018] Kim, Ji Hye, et al. "Beneficial effects of marine algae-derived carbohydrates for skin health." Marine drugs 16.11 (2018): 459.
  • [Stanley,Norman.,1987] Stanley, Norman. "Production, properties and uses of carrageenan." Production and utilization of products from commercial seaweeds. FAO Fisheries Technical Paper 288 (1987): 116-146. https://www.fao.org/4/x5822e/x5822e05.htm

Cellulose

"Cellulose is reputedly the most abundant organic material on earth, being the main constituent in plant cell walls. It is composed of glucopyranose units linked β1→4 in a linear chain." [MNP Dewick]

"Cellulose (Figure 8.19) may be extracted from wood pulp and is usually partially hydrolysed with acid to give micro-crystalline cellulose. These materials are used as tablet diluents. Semi-synthetic derivatives of cellulose, e.g. methylcellulose, hydroxymethylcellulose, and carboxymethylcellulose, are used as emulsifying and suspending agents. Cellulose acetate phthalate is cellulose with about half the hydroxyl groups acetylated and the remainder esterified with phthalic acid. It is used as an acid-resistant enteric coating for tablets and capsules." [MNP Dewick]

References


Chitin

"Chitin occurs as cell walls in fungi, algae, and some plants, and as exoskeletons of invertebrates and represents the third most important natural carbohydrate source consisting of (1-4)-ß-linked N-acetyl-glucosamine." [Benckiser BAPS]

"[Chitin] is the second most abundant polymer on Earth as it occurs in the exoskeletons of arthropods and, of course, in fungal cell walls." [Moore 21stFungi]

"Chitin is degraded by chitinase, a glucan hydrolase which attacks the b1,4-glycosidic bonds, eventually producing the disaccharide chitobiose which is then converted to the monosaccharide N-acetylglucosamine by chitobiase (Seidl, 2008). Chitinase may also be involved in fungal wall synthesis...." [Moore 21stFungi]

References


Cyclitols

References


Dermatan

References


Dextran

References


Hyaluronate

References


Inulin

Type: polysaccharide [MNP Dewick]

"A less common storage polysaccharide found in certain plants of the Compositae/Asteraceae and Campanulaceae is inulin ..., which is a relatively small polymer of fructofuranose, linked through β2→1 bonds." [MNP Dewick]

References


Karaya

"Karaya or sterculia gum is a dried gum obtained from the trunks of the tree Sterculia urens (Sterculiaceae) or other Sterculia species found in India. It exudes naturally or may be obtained by incising through the bark. It contains a branched polysaccharide comprising l-rhamnose, d-galactose, and with a high proportion of d-galacturonic acid and d-glucuronic acid residues. The molecule is partially acetylated, and the gum typically has an odour of acetic acid. It is used as a bulk laxative and as a suspending agent. It has proved particularly effective as an adhesive for stomal appliances, rings of the purified gum being used to provide a non-irritant seal between the stomal bag and the patient’s skin." [MNP Dewick]

References


Levans

References


Mannitol

References


Pectins

"Pectins consist of chains of b1,4-linked galacturonic acids, in which about 20% to 60% of the carboxyl groups are esterified with methanol. They occur primarily in the middle lamella between plant cells. As this represents only a small proportion of the plant wall they are correspondingly of little importance as a component of the bulk of plant litter. However, extensive breakdown of the middle lamella of living plants is brought about by necrotrophic parasites. Pectinases, therefore, are of great importance during fungal invasion of plant tissue (Byrde, 1982)." [Moore 21stFungi]

"Polygalacturonases and pectin lyases attack the true pectins, while arabanases and galactanases degrade the neutral sugar polymers associated with them. These activities have drastic effects on the structural integrity of the tissues which may extend to death of the cell due to osmotic stresses imposed by damage to the wall." [Moore 21stFungi]

References


Raffinose

References


Sorbitol

First found in the ripe berries of the mountain ash Pyrus aucuparia Ehrh. (L.) (Sorbus aucuparia L.), Rosaceae. Occurs also in many other berries (except grapes) and in cherries, plums, pears, apples, seaweed and algae. Has been detected in blackstrap molasses. Isoln from berries: Embden, Griesbach, Z. Physiol. Chem. 91, 268 (1914). Prepd industrially from glucose by high pressure hydrogenation or by electrolytic reduction. [Merck]

Properties: Sweet taste, ~60% as sweet as sugar (w/w). In the healthy human organism 1.0 g of sorbitol yields 3.994 calories which is comparable to 3.940 calories from 1.0 g of cane sugar. Seventy percent of orally ingested sorbitol is converted to CO2 without appearing as glucose in the blood.
Freely sol in water (up to 83%). High % sorbitol solns are much more viscous than corresp glycerol solns. Quite sol in hot alcohol, sparingly sol in cold alcohol. Also sol in methanol, isopropanol, butanol, cyclohexanol, phenol, acetone, acetic acid, DMF, pyridine, acetamide solns. Practically insol in most other organic solvents. Not attacked in the cold when mixed with dil acids, alkalies or mild oxidizing substances. [Merck]

Most bacteria are unable to use sorbitol for energy, but it can be slowly fermented in the mouth by streptococcus mutans, a species of bacteria that cause tooth decay unlike many other sugar alcohols such as isomalt and xylitol, which are considered to be non-acidogenic.[9][10] [Wiki]

Hazards: "Ingesting large amounts of sorbitol can lead to abdominal pain, flatulence, and mild to severe diarrhea. Habitual sorbitol consumption of over 20 grams (0.7 oz) per day as sugar-free gum has led to severe diarrhea, causing unintended weight loss or even requiring hospitalization.[33] In early studies, a dose of 25g of sorbitol, eaten through the day, produced a laxative effect in only 5% of individuals.[34] As a result of the large molecular weight of sorbitol, when large amounts of sorbitol are ingested, only a small amount of sorbitol is absorbed in the small intestine, and most of the sorbitol enters the colon, with consequent gastrointestinal effects.[30]" [Wiki]

Use: In manuf of sorbose, ascorbic acid, propylene glycol, synthetic plasticizers and resins; as humectant (moisture conditioner) on printing rolls, in leather, tobacco. In writing inks to insure a smooth flow and to prevent crusting on the point of the pen. In antifreeze mixtures with glycerol or glycols. In candy manuf to increase shelf life by retarding the solidification of sugar; as humectant and softener in shredded coconut and peanut butter; as texturizer in foods; as sequestrant in soft drinks and wines. Used to reduce the undesirable aftertaste of saccharin in foodstuffs; as sugar substitute for diabetics. Pharmaceutic aid (flavor; tablet excipient); to increase absorption of vitamins and other nutrients in pharmaceutical preparations [Merck]

Melting point: mp 110-112° [Merck] 94-96°C [1-Wiki] 97-112°C [ChemSpider]
Boiling point: 494.9oC [ChemSpider]
Solubility: Water 36mg/ml (MedChem Express) [ChemSpider]

Therap-Cat: Laxative.[Merck]

Therap-Cat-Vet: In ruminant ketosis, osmotic diuretic, laxative. [Merck]

References

  • [ChemSpider] Sorbitol, http://www.chemspider.com/Chemical-Structure.5576.html, Accessed Jan 27, 2019
    • MedChem Express, https://www.medchemexpress.com/d-sorbitol.html?redir=1
  • [Merck] The Merck Index, 13th Ed. 2001 Merck & Co, New Jersey, U.S.A
  • [Wiki] https://en.wikipedia.org/wiki/Sorbitol, Accessed Jan 27, 2019
    • [1] Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
    • [9] Hayes, C. (October 2001). "The effect of non-cariogenic sweeteners on the prevention of dental caries: a review of the evidence". Journal of Dental Education. 65 (10): 1106–1109.
    • [10] Nicolas, Guillaume G.; Lavoie, Marc C. (January 2011). "[Streptococcus mutans and oral streptococci in dental plaque]". Canadian Journal of Microbiology. 57 (1): 1–20.
    • [30] Islam, M. S.; Sakaguchi, E (2006). "Sorbitol-based osmotic diarrhea: Possible causes and mechanism of prevention investigated in rats". World Journal of Gastroenterology. 12: 7635–7641. doi:10.3748/wjg.v12.i47.7635.
    • [33] Kathleen Doheny (2008-01-10). "Sweetener Side Effects: Case Histories". WebMD Medical News. Retrieved 2008-01-10.
    • [34] Peters, Ronald; Lock, R. H. (1958-09-13). "Laxative Effect of Sorbitol". British Medical Journal. 2 (5097): 677–678. doi:10.1136/bmj.2.5097.677. ISSN 0007-1447. PMC 2026423. PMID 13572866.

Stachyose

References


Tragacanth

"Tragacanth is a dried gummy exudate obtained from Astragalus gummifer (Leguminosae/Fabaceae) and other Astragalus species, small shrubs found in Iran, Syria, Greece, and Turkey. It is usually obtained by deliberate incision of the stems. This material swells in water to give a stiff mucilage with an extremely high viscosity, and provides a useful suspending and binding agent. It is chemically a complex material, and yields d-galacturonic acid, d-galactose, l-fucose, l-arabinose, and d-xylose on hydrolysis. Some of the uronic acid carboxyls are methylated." [MNP Dewick]

References

Trehalose

References


Xanthan

References


Index

Acacia (gum arabic)
Alginic acid
Alginates
agar
agarose
Cellulose
Carrageenan
chitin
cyclitols
dermatan
dextran
hyaluronate
inulin
Karaya (sterculia gum)
levans
mannitol
pectins
raffinose
Sorbitol
stachyose
Tragacanth
trehalose
xanthan