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Chemical and Functional Properties of Food Saccharides

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© 2004 by CRC Press LLC<br />

Alginates are widely used as thickeners <strong>and</strong> stabilizers as well as for their gelforming<br />

properties <strong>and</strong> are found in ice creams, dairy products such as milk shakes,<br />

soups, <strong>and</strong> sauces. They are also an important ingredient in beer manufacture to<br />

stabilize dissolved solids in commercial beer <strong>and</strong> prevent sedimentation. Alginate<br />

gels are popular in the dessert <strong>and</strong> bakery sectors for pie fillings <strong>and</strong> also for<br />

restructuring meat. Alginates can also be used to form films that can be used as<br />

edible packaging. An important market for alginates uses chemically modified alginate,<br />

mainly propylene glycol alginate PGA. PGA has greater acid solubility than<br />

native alginate <strong>and</strong> can therefore be used in a range <strong>of</strong> applications where native<br />

alginate would start to precipitate out.<br />

15.6.2 AGARS<br />

Agars are obtained from red seaweeds (Rhodophyta) mainly from the genus Gelidium,<br />

<strong>of</strong> which some 15 species are now used to produce agar from the cell wall<br />

mucilage. The main center <strong>of</strong> production has historically been Japan, <strong>and</strong> this bias<br />

continues to this day. Production involves aqueous extraction <strong>of</strong> seaweed in hot<br />

water, with the extract frozen <strong>and</strong> thawed to precipitate polysaccharides <strong>and</strong> remove<br />

water-soluble contaminants. Agarose is a purified form <strong>of</strong> agar with typically shorter<br />

chains <strong>and</strong> a lower molecular weight.<br />

Agars are formed from linear chains <strong>of</strong> both L- <strong>and</strong> D-galactose residues linked<br />

alternately α(1-3) <strong>and</strong> β(1-4) <strong>and</strong> can be sulfated at the 2, 4, or 6 positions. Some<br />

<strong>of</strong> the L-galactose residues are converted to 3,6-anhydrogalactose by the formation<br />

<strong>of</strong> a bridging bond across the ring between the C-3 <strong>and</strong> C-6. Formation <strong>of</strong> the 3,6anhydrogalactose<br />

changes the conformation <strong>of</strong> the sugar ring <strong>and</strong> favors the formation<br />

<strong>of</strong> a helix by the polysaccharide chain. 95 Gelling can occur by formation <strong>of</strong><br />

junctions between the helical regions <strong>of</strong> two agar chains that intertwine to form a<br />

double helix. Agar gels are thermoreversible <strong>and</strong> show significant hysteresis, a large<br />

difference between the melting (80–90°C) <strong>and</strong> gelling temperatures (35–45°C),<br />

which reflects the slow rate <strong>of</strong> double-helix formation <strong>and</strong> the strength <strong>of</strong> the<br />

association once it is formed. 96<br />

Agar gels are formed at low concentration <strong>and</strong> are hard <strong>and</strong> brittle. Generally,<br />

they are too hard for many food uses <strong>and</strong> are therefore more commonly used in<br />

nonfood applications. <strong>Food</strong> uses include confectionery <strong>and</strong> sweets, icings, <strong>and</strong><br />

restructured meat pie fillings.<br />

15.6.3 CARRAGEENANS<br />

Carrageenans are a family <strong>of</strong> sulfated polymers with a linear chain <strong>of</strong> D-galactose<br />

linked alternately α(1-3) <strong>and</strong> β(1-4). The sulfate groups are present at the 2, 4, or<br />

6 positions. An important feature <strong>of</strong> carrageenan structure is that some <strong>of</strong> the<br />

galactose residues are converted to 3,6-anhydrogalactose by the formation <strong>of</strong> a<br />

bridging bond across the ring between the C-3 <strong>and</strong> C-6. This transformation can<br />

occur after chain synthesis catalyzed by an enzyme in the algae or it can be promoted<br />

during extraction by the use <strong>of</strong> alkaline conditions which result in the loss <strong>of</strong> some<br />

sulfate groups from galactose residues. Formation <strong>of</strong> 3,6-anhydrogalactose changes

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