Acrylamide from Maillard reaction products
Richard H. Stadler (),
Imre Blank,
Natalia Varga,
Fabien Robert,
Jörg Hau,
Philippe A. Guy,
Marie-Claude Robert and
Sonja Riediker
Additional contact information
Richard H. Stadler: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Imre Blank: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Natalia Varga: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Fabien Robert: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Jörg Hau: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Philippe A. Guy: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Marie-Claude Robert: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Sonja Riediker: Nestlé Research Center, Nestec, Vers-chez-les-Blanc
Nature, 2002, vol. 419, issue 6906, 449-450
Abstract:
Abstract The discovery of the adventitious formation of the potential cancer-causing agent acrylamide in a variety of foods during cooking1,2 has raised much concern3,4, but the chemical mechanism(s) governing its production are unclear. Here we show that acrylamide can be released by the thermal treatment of certain amino acids (asparagine, for example), particularly in combination with reducing sugars, and of early Maillard reaction products (N-glycosides)5. Our findings indicate that the Maillard-driven generation of flavour and colour in thermally processed foods can — under particular conditions — be linked to the formation of acrylamide.
Date: 2002
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:419:y:2002:i:6906:d:10.1038_419449a
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DOI: 10.1038/419449a
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