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Chemical and Functional Properties of Food Saccharides

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© 2004 by CRC Press LLC<br />

values, showing a very pronounced increase in the rate with increasing F A. NMR<br />

studies <strong>of</strong> enzymatic degradation <strong>of</strong> chitosans 32,33 give more direct information on<br />

the specificities with respect to cleavage <strong>of</strong> the four differerent glycosidic linkages<br />

(A–A, A–D, D–A, <strong>and</strong> D–D) as determined by the identity <strong>of</strong> the new reducing <strong>and</strong><br />

nonreducing ends, <strong>and</strong> in some cases also the variation in the identity <strong>of</strong> the nearest<br />

neighbours to the new reducing <strong>and</strong> nonreducing ends. From both viscometric <strong>and</strong><br />

enzymatic studies <strong>of</strong> lysozyme (using both hen egg white <strong>and</strong> human lysozyme)<br />

degradation <strong>of</strong> chitosans, it was concluded that minimum four A-units had to be<br />

contained in the active site <strong>of</strong> lysozyme in order to obtain maximum degradation<br />

rates, explaining the dependence <strong>of</strong> lysozyme degradation rates <strong>of</strong> chitosans on F As<br />

given in Table 14.2. It was also found that chitosans with a low degree <strong>of</strong> Nacetylation<br />

may bind specifically to lysozyme 34,35 without cleaving the polysaccharide,<br />

which was recently demonstrated by using immobilized lysozyme to fractionate<br />

chitosan chains containing A-units from fully de-N-acetylated chains. 36<br />

14.6 TECHNICAL PROPERTIES<br />

14.6.1 FILM-FORMING PROPERTIES<br />

Chitin <strong>and</strong> especially chitosan have been extensively studied for applications as films<br />

or membranes. The use <strong>of</strong> such films to improve the quality <strong>of</strong> foods has been<br />

examined 37 <strong>and</strong> is especially interesting due to the antimicrobial action <strong>of</strong> chitosan. 38<br />

The preparation <strong>of</strong> a composite film <strong>of</strong> cellulose <strong>and</strong> an almost fully de-N-acetylated<br />

<strong>and</strong> highly viscous chitosan has been reported. 39 A Schiff's base is formed between<br />

the carbonyl groups on the cellulose <strong>and</strong> the amino groups on chitosan, resulting in<br />

a film in which the chitosan does not dissolve in water <strong>and</strong> has good wet tensile<br />

strengths. Uragami has reported the preparation <strong>and</strong> characteristics <strong>of</strong> different<br />

chitosan membranes. 40<br />

14.6.2 GELLING PROPERTIES<br />

The preparation <strong>of</strong> chitin gels has been reported. 41–43 The preparation <strong>and</strong> characterization<br />

<strong>of</strong> a few hydrogels <strong>of</strong> chitosan have also been reported, such as thermoreversible<br />

chitosan-oxalate gels. 44,45 So far, no simple ionic <strong>and</strong> nontoxic cross-linking<br />

agent has been found that gives reproducible chitosan gels at low concentrations,<br />

such as calcium ions for gelling <strong>of</strong> alginates. However, aqueous chitosan gels crosslinked<br />

with molybdate polyoxy-anions have been reported, resulting in transparent,<br />

thermoirreversible gels that are able to swell several times their original size in<br />

aqueous solutions, depending on the ionic strength. 46<br />

Different chitosan gels made with covalent cross-linking have been reported,<br />

with cross-linking with glutaraldehyde being the most widely applied. 47–49 Recently,<br />

an enzymatic gelling system with chitosan has been reported. 50,51<br />

14.6.3 ANTIMICROBIAL PROPERTIES<br />

Although the mechanism(s) involved in the antimicrobial activity <strong>of</strong> chitosans has<br />

not been explained, a number <strong>of</strong> studies support that the polycation chitosan does

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