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1.
J Agric Food Chem ; 63(38): 8493-500, 2015 Sep 30.
Article in English | MEDLINE | ID: mdl-26365517

ABSTRACT

We have previously found that fatty acids can mask the bitterness of certain nitrogenous substances through direct molecular interactions. Using isothermal titration calorimetry, we investigated the interactions between sodium oleate and 22 bitter substances. The hydrochloride salts of quinine, promethazine, and propranolol interacted strongly with fatty acids containing 12 or more carbon atoms. The (1)H NMR spectra of these substances, obtained in the presence of the sodium salts of the fatty acids in dimethyl sulfoxide, revealed the formation of hydrogen bonds between the nitrogen atoms of the bitter substances and the carboxyl groups of the fatty acids. When sodium laurate and the hydrochloride salt of quinine were mixed in water, an equimolar complex formed as insoluble heterogeneous needlelike crystals. These results suggested that fatty acids interact directly with bitter substances through hydrogen bonds and hydrophobic interactions to form insoluble binary complexes that mask bitterness.


Subject(s)
Flavoring Agents/chemistry , Lauric Acids/chemistry , Quinine/chemistry , Hydrogen Bonding , Models, Chemical
2.
J Agric Food Chem ; 60(18): 4492-9, 2012 May 09.
Article in English | MEDLINE | ID: mdl-22502602

ABSTRACT

Bitterness-masking compounds were identified in a natural white mold cheese. The oily fraction of the cheese was extracted and further fractionated by using silica gel column chromatography. The four fractions obtained were characterized by thin-layer chromatography and nuclear magnetic resonance spectroscopy. The fatty acid-containing fraction was found to have the highest bitterness-masking activity against quinine hydrochloride. Bitterness-masking activity was quantitated using a method based on subjective equivalents. At 0.5 mM, the fatty acid mixture, which had a composition similar to that of cheese, suppressed the bitterness of 0.008% quinine hydrochloride to be equivalent to that of 0.0049-0.0060% and 0.5 mM oleic acid to that of 0.0032-0.0038% solution. The binding potential between oleic acid and the bitter compounds was estimated by isothermal titration calorimetry. These results suggest that oleic acid masked bitterness by forming a complex with the bitter compounds.


Subject(s)
Cheese/analysis , Oleic Acid/analysis , Taste Buds/metabolism , Humans , Oleic Acid/metabolism , Quinine/antagonists & inhibitors , Quinine/pharmacology , Taste , Taste Buds/drug effects
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