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Chemical and Functional Properties of Food Saccharides

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18<br />

CONTENTS<br />

© 2004 by CRC Press LLC<br />

Chemistry <strong>of</strong> the<br />

Maillard Reaction in<br />

<strong>Food</strong>s<br />

Tomas Davidek <strong>and</strong> Jiri Davidek<br />

18.1 Introduction<br />

18.2 Formation <strong>of</strong> Glycosylamines <strong>and</strong> Rearrangement to Amino<br />

Deoxysugars<br />

18.3 Other Reactions <strong>of</strong> Glycosylamines<br />

18.4 Degradation <strong>of</strong> Amino Deoxysugars<br />

18.5 Degradation <strong>of</strong> 3-Deoxy-2-Osuloses<br />

18.6 Degradation <strong>of</strong> 1-Deoxy-2,3-Diuloses<br />

18.7 Degradation <strong>of</strong> 1-Amino-1,4-Dideoxydiketoses<br />

18.8 Strecker Degradation <strong>of</strong> Amino Acids<br />

18.9 Melanoidins<br />

18.10 Closing Remarks<br />

References<br />

18.1 INTRODUCTION<br />

The term Maillard reaction is used for a complex network <strong>of</strong> reactions involving<br />

carbonyl compounds, namely reducing sugars, <strong>and</strong> amino compounds, for example<br />

amino acids or peptides. These reactions are also called nonenzymatic browning, as<br />

they are accompanied by the formation <strong>of</strong> brown pigments (melanoidins). However,<br />

other reactions, such as caramelization, can also cause nonenzymatic browning <strong>of</strong><br />

foods. Thus, the Maillard reaction should be considered as a special case <strong>of</strong> nonenzymatic<br />

browning.<br />

The reaction is named after the French chemist Louis-Camille Maillard, who<br />

first described flavor <strong>and</strong> colour development on heating reducing sugars with amino<br />

acids. 1 Since then, the Maillard reaction has become <strong>of</strong> fundamental interest to food<br />

chemists <strong>and</strong> technologists, <strong>and</strong> also to scientists working in medicine <strong>and</strong> nutrition.

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