Trapping of Carbonyl Compounds by Epicatechin: Reaction Kinetics and Identification of Epicatechin-adducts in Stored UHT Milk.

The kinetics of the reaction between epicatechin and various carbonyl compounds typically formed in cooked and stored foods were evaluated in model systems at pH 7.4 and 37 °C, and the corresponding reaction products in stored UHT milk added epicatechin were identified by HPLC-MS/MS. The rate constants for the reactions of carbonyl compounds with epicatechin decreased in the following the order: methylglyoxal; 1.6 ± 0.2 M-1 s-1 > glyoxal; (5.9 ± 0.3) × 10-2 M-1 s-1 ≥ 5-(hydroxymethyl)furfural; (4.0 ± 0.2) × 10-2 M-1 s-1 ≥ acetaldehyde; (2.6 ± 0.3) ×10-2 M-1 s-1 ≥ phenylacetaldehyde; (2.1 ± 0.2) ×10-2 M-1 s-1 ≥ furfural; (4.3 ± 0.1) × 10-3 M-1 s-1 > 2-methylbutanal and 3-methylbutanal; ~ 0 M-1 s-1. Reaction products generated by epicatechin and methylglyoxal, glyoxal, 5-(hydroxymethyl)furfural and acetaldehyde were detected in UHT milk samples by incubating milk samples with epicatechin at 37 °C for 24 h. The lack of reaction between epicatechin and phenylacetaldehyde, furfural, 2-methylbutanal and 3-methylbutanal in stored UHT milk may be due to their slow reaction rates or low concentration in stored UHT milk. It is demonstrated that epicatechin traps 5-(hydroxymethyl)furfural, acetaldehyde, glyoxal and methylglyoxal, and may thereby reduce off-flavour formation in UHT milk during storage both by trapping of precursors (methylglyoxal and glyoxal) for off-flavour formation and by direct trapping of off-flavours.

[1]  Mahesha M. Poojary,et al.  Effect of pH on the reaction between naringenin and methylglyoxal: A kinetic study. , 2019, Food chemistry.

[2]  Biying Pan,et al.  Impacts of epicatechin on the formation of advanced lipid oxidation end products (ALEs) in a fish oil oxidation model , 2019, LWT.

[3]  M. Petersen,et al.  Effect of green tea catechins on physical stability and sensory quality of lactose-reduced UHT milk during storage for one year , 2019, International Dairy Journal.

[4]  Ezgi Doğan Cömert,et al.  Kinetic evaluation of the reaction between methylglyoxal and certain scavenging compounds and determination of their in vitro dicarbonyl scavenging activity. , 2019, Food research international.

[5]  Li Wang,et al.  Epicatechin Adducting with 5-Hydroxymethylfurfural as an Inhibitory Mechanism against Acrylamide Formation in Maillard Reactions. , 2018, Journal of agricultural and food chemistry.

[6]  Bing Li,et al.  Reduction of Nε-(carboxymethyl) lysine by (-)-epicatechin and (-)-epigallocatechin gallate: The involvement of a possible trapping mechanism by catechin quinones. , 2018, Food chemistry.

[7]  L. B. Larsen,et al.  Maillard reaction progress in UHT milk during storage at different temperature levels and cycles , 2018 .

[8]  Mahesha M. Poojary,et al.  Green Tea Polyphenols Decrease Strecker Aldehydes and Bind to Proteins in Lactose-Hydrolyzed UHT Milk. , 2017, Journal of agricultural and food chemistry.

[9]  F. Hidalgo,et al.  Model Studies on the Effect of Aldehyde Structure on Their Selective Trapping by Phenolic Compounds. , 2017, Journal of agricultural and food chemistry.

[10]  C. Ray,et al.  Control of Maillard Reactions in Foods: Strategies and Chemical Mechanisms. , 2017, Journal of agricultural and food chemistry.

[11]  R. Elias,et al.  Reaction of Acetaldehyde with Wine Flavonoids in the Presence of Sulfur Dioxide. , 2016, Journal of agricultural and food chemistry.

[12]  A. Waterhouse,et al.  (1)H NMR: A Novel Approach To Determining the Thermodynamic Properties of Acetaldehyde Condensation Reactions with Glycerol, (+)-Catechin, and Glutathione in Model Wine. , 2016, Journal of agricultural and food chemistry.

[13]  M. Pischetsrieder,et al.  Investigations on the Reaction of C3 and C6 α-Dicarbonyl Compounds with Hydroxytyrosol and Related Compounds under Competitive Conditions. , 2016, Journal of agricultural and food chemistry.

[14]  F. Morales,et al.  Mechanism of reactive carbonyl species trapping by hydroxytyrosol under simulated physiological conditions. , 2015, Food chemistry.

[15]  S. Sang,et al.  Quercetin inhibits advanced glycation end product formation by trapping methylglyoxal and glyoxal. , 2014, Journal of agricultural and food chemistry.

[16]  D. Peterson,et al.  Control of Maillard-type off-flavor development in ultrahigh-temperature-processed bovine milk by phenolic chemistry. , 2014, Journal of agricultural and food chemistry.

[17]  L. B. Larsen,et al.  Lactose-hydrolyzed milk is more prone to chemical changes during storage than conventional ultra-high-temperature (UHT) milk. , 2014, Journal of agricultural and food chemistry.

[18]  Chi-Tang Ho,et al.  Essential Structural Requirements and Additive Effects for Flavonoids to Scavenge Methylglyoxal. , 2014, Journal of agricultural and food chemistry.

[19]  D. Peterson,et al.  Response surface methodology as optimization strategy for reduction of reactive carbonyl species in foods by means of phenolic chemistry. , 2013, Food & function.

[20]  Paul J Thornalley,et al.  Dicarbonyls (Glyoxal, Methylglyoxal, and 3-Deoxyglucosone) , 2012 .

[21]  V. Gökmen,et al.  Model studies on the role of 5-hydroxymethyl-2-furfural in acrylamide formation from asparagine. , 2012, Food chemistry.

[22]  Na Li,et al.  Degradation kinetics of catechins in green tea powder: effects of temperature and relative humidity. , 2011, Journal of agricultural and food chemistry.

[23]  K. Sze,et al.  Trapping of phenylacetaldehyde as a key mechanism responsible for naringenin's inhibitory activity in mutagenic 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine formation. , 2008, Chemical research in toxicology.

[24]  T. Labuza,et al.  Effect of green tea flavonoids on Maillard browning in UHT milk , 2007 .

[25]  I. Pianet,et al.  A kinetic study of the reactions of (+)-catechin with aldehydes derived from toasted oak , 2007 .

[26]  D. Peterson,et al.  Epicatechin carbonyl-trapping reactions in aqueous maillard systems: Identification and structural elucidation. , 2006, Journal of agricultural and food chemistry.

[27]  T. Henle Protein-bound advanced glycation endproducts (AGEs) as bioactive amino acid derivatives in foods , 2005, Amino Acids.

[28]  D. Peterson,et al.  Inhibition of key aroma compound generated during ultrahigh-temperature processing of bovine milk via epicatechin addition. , 2005, Journal of agricultural and food chemistry.

[29]  Dongman Kim,et al.  Interaction of Flavanols in Green Tea Extract during Heat Processing and Storage , 2002 .

[30]  V. Cheynier,et al.  Study of the reactions between (+)-catechin and furfural derivatives in the presence or absence of anthocyanins and their implication in food color change. , 2000, Journal of agricultural and food chemistry.

[31]  V. Cheynier,et al.  Competition between (+)-catechin and (-)-epicatechin in acetaldehyde-induced polymerization of flavanols. , 1999, Journal of agricultural and food chemistry.

[32]  M. T. Veciana-Nogués,et al.  Changes in Furfural Compounds during Storage of Infant Milks , 1998 .

[33]  V. Viswanadhan,et al.  Configurational statistics of C(4)-C(8) linked homopolymers of (+)-catechin or (-)-epicatechin , 1987 .

[34]  W. Luo,et al.  Maillard Reaction in Processed Foods—Reaction Mechanisms , 2018 .

[35]  V. Yaylayan,et al.  The Maillard reaction and food quality deterioration. , 2010 .

[36]  Gilles Trystram,et al.  Accumulation of 5-hydroxymethyl-2-furfural in cookies during the backing process: Validation of an extraction method , 2006 .