Maillard redox reaction

In the course of the Maillard reaction, de-oxyosones and reductones, e. g., acetylformoin (cf. Ill, Formula 4.67), are formed. They cttn react to give enol and triketo compounds via an addition with disproportionation (Formula 4.86). Redox reactions of this type can explain the formation of products which are not possible according to the reactions described till now. In fact, it has recently been found that, for example, glucose 6-phosphate and fructose-1,6-diphosphate, which occur in baker s yeast and muscle, form 4-hydroxy-2,5-dimethyl-3(2H)-furanone to a large extent. Since the formation from hexoses (or hexose phosphates) is not explainable, reduction of the intermediate acetylformoin (Formula 4.87) must have occurred. As shown, this reduction can proceed through acetylformoin itself or other reductones, e. g., ascorbic acid. Such re-... 

Ten aspects of the Maillard reaction will be considered in this chapter the effect on a,, on pH, on redox potential, on solubility, on texture, on foamability and foam stability, on emulsifying power, on volatile formation on storage, on binding of volatiles, and on other functionalities. The third of these has received by far the most attention and this is reflected here. 

Increased reducing power, i.e., increased antioxidant activity or more negative redox potential, is also one of the symptoms of the Maillard reaction (see Chapter 1). This has considerable significance, because, as far as foods are concerned, one of the main ways in which they deteriorate chemically is through oxidation, particularly of unsaturated fats and oils, leading to oxidative rancidity. The topic has considerable physiological significance as well (see Chapter 8). 

Fig. 8.27. Maillard reaction involved in the non-enzymic oxidative browning of plant tissues, (a) Formation of an imine by an amino acid reacting with an aldose (Ri = H) or ketose (Ri H). (b) Enolization of the imine to enaminol, then to an Amadori (Ri = H) or Heyns (Ri H) intermediate, (c) Breaking of the preceding intermediates, with the appearance of a reductone in redox equilibrium with an a-dicarbonylated compound, responsible for the non-enzymic oxidation phenomenon...

Particle size effects on the ORR, the peak positions of the Pt/PtO redox process, and the CO oxidation reaction are nicely reviewed by Hayden and Maillard (Hayden 2009 Maillard 2009). 

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