4.6 Review

Key Aspects of Amadori Rearrangement Products as Future Food Additives

Journal

MOLECULES
Volume 26, Issue 14, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26144314

Keywords

flavor; Amadori rearrangement products; flavor additives; taste enhancing

Funding

  1. USDA National Institute of Food and Agriculture through the New Jersey Agricultural Experiment Station [1025755, NJ10181]

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Flavor is crucial in attracting consumers and enhancing food quality, with the Maillard reaction playing a significant role in flavor formation. Amadori rearrangement products, as intermediates of the Maillard reaction, show promise as potential flavor additives due to their stability and fresh flavor formation ability. Research is ongoing to explore the future applications of Amadori rearrangement products in flavorings, with a focus on their stability, chemical nature, and flavor-enhancing effects.
Flavor is one of the most important factors in attracting consumers and maximizing food quality, and the Maillard reaction (MR) is highly-involved in flavor formation. However, Maillard reaction products have a big drawback in their relatively low stability in thermal treatment and storage. Amadori rearrangement products (ARPs), MR intermediates, can alternatively act as potential flavor additives for their better stability and fresh flavor formation ability. This review aims to elucidate key aspects of ARPs' future application as flavorings. The development of current analytical technologies enables the precise characterization of ARPs, while advanced preparation methods such as synthesis, separation and drying processes can increase the yield of ARPs to up to 95%. The stability of ARPs is influenced by their chemical nature, pH value, temperature, water activity and food matrix. ARPs are associated with umami and kokumi taste enhancing effects, and the flavor formation is related to amino acids/peptides of the ARPs. Peptide-ARPs can generate peptide-specific flavors, such as: 1,6-dimethy-2(1H)-pyrazinone, 1,5-dimethy-2(1H)-pyrazinone, and 1,5,6-trimethy-2(1H)-pyrazinone. However, further research on systematic stability and toxicology are needed.

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