The
Maillard reaction is a
chemical reaction between an
amino acid and a
reducing sugar, usually requiring
heat. Like
caramelization, it's a form of
non-enzymatic browning. The reactive
carbonyl group of the sugar interacts with the
nucleophilic amino group of the
amino acid, and interesting but poorly characterized odor and flavor molecules result. This process accelerates in an alkaline environment because the
amino groups don't neutralize. This reaction is the basis of the
flavoring industry, since the type of
amino acid determines the resulting flavor.
In the process, hundreds of different flavor compounds are created. These compounds in turn break down to form yet more new flavor compounds, and so on. Each type of food has a very distinctive set of flavor compounds that are formed during the Maillard reaction. It is these same compounds that
flavor scientists have used over the years to create artificial flavors.
Although used since ancient times, the reaction is named after the chemist
Louis-Camille Maillard who investigated it in the
1910s.
Foods and products with Maillard reactions
The Maillard reaction is responsible for many colors and flavors in foods:
6-acetyl-1,2,3,4-tetrahydropyridine (1) is responsible for the biscuit or cracker-like flavor present in baked goods like
bread,
popcorn,
tortilla products. 2-acetyl-1-pyrroline (2) flavors aromatic varieties of cooked
rice. Both compounds have
odor thresholds below 0.06
ng/
l .
Caramelization is an entirely different process from Maillard browning, though the results of the two processes are sometimes similar to the naked eye (and tastebuds). Caramelization may sometimes cause browning in the same foods in which the Maillard reaction occurs, but the two processes are distinct. They both are promoted by heating, but the Maillard reaction involves amino acids, as discussed above, while caramelization is simply the
oxidation of certain sugars. The following things are a result of the Maillard browning reaction:
caramel made from milk and sugar, especially in candies; NB: milk is high in protein (amino acids) and browning of food involving this complex ingredient would most likely include maillard reactions. See references below.
chocolate and maple syrup
lightly roasted peanuts
The process
The carbonyl group of the sugar reacts with the amino group of the amino acid, producing N-substituted glycosylamine and water
The unstable glycosylamine undergoes Amadori rearrangement, forming ketosamines
There are several ways for the ketosamines to react further:
Factors
High temperature, high relative humidity, and alkaline conditions all promote the Maillard reaction.
The rate of Maillard reactions increases as the water activity increases, reaching a maximum at water activities in the range of 0.6 to 0.7. However, as the Maillard reaction produces water, further increases in water activity may inhibit Maillard reactions.
Pentose sugars react more than hexoses, which react more than disaccharides. Different amino acids produce different amounts of browning.
External results
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