2022
DOI: 10.3390/molecules27092942
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Effects of Organic Acids on the Release of Fruity Esters in Water: An Insight at the Molecular Level

Abstract: It is well known that organic acids (OAs) could affect the flavour of fruit juices and beverages. However, the molecular mechanism of aroma release is still unclear. In this study, the effects of citric acid (CA), L-(-)-malic acid (MA) and L-lactic acid (LA) on the release of six selected esters and their sensory perception were investigated by means of HS-GC-MS analyses and odour detection threshold determination, respectively. Meanwhile, the density functional theory (DFT) calculation was employed to explore… Show more

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Cited by 8 publications
(5 citation statements)
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“…From this, it was inferred that specific intermolecular forces in the non-volatile compound-aldehyde system induced various aldehyde release behaviors in the TM, thereby affecting human olfactory perception, leading to a higher threshold. This phenomenon is consistent with previous research in which it was shown that low concentrations of organic acids can cause higher detection thresholds for many odorants ( Liu, Xi, Fu, Li, Sun, & Zong, 2022 ).
Fig.
…”
Section: Resultssupporting
confidence: 93%
“…From this, it was inferred that specific intermolecular forces in the non-volatile compound-aldehyde system induced various aldehyde release behaviors in the TM, thereby affecting human olfactory perception, leading to a higher threshold. This phenomenon is consistent with previous research in which it was shown that low concentrations of organic acids can cause higher detection thresholds for many odorants ( Liu, Xi, Fu, Li, Sun, & Zong, 2022 ).
Fig.
…”
Section: Resultssupporting
confidence: 93%
“…The masking effect observed among aroma compounds may be attributed to intermolecular forces (such as hydrogen bonding), which influence their volatility, thereby affecting their odor perceptibility. , Acetic acid, butyric acid, hexanoic acid, and isovaleric acid contain the carboxyl group ( −COOH ), where the oxygen atom of the carbonyl group exhibits high electronegativity, enabling it to act as a hydrogen bond acceptor. Conversely, the hydrogen atom in the hydroxyl group ( OH ) serves as a hydrogen bond donor.…”
Section: Resultsmentioning
confidence: 99%
“…The IGM diagram is rendered by VMD. The theoretical calculation is based on the ratio of polysaccharide, linoleic acid, and water at 1:2:7 …”
Section: Methodsmentioning
confidence: 99%
“…The theoretical calculation is based on the ratio of polysaccharide, linoleic acid, and water at 1:2:7. 43 2.6. Morphology of Emulsion.…”
Section: Preparation Of High Internal Phase Emulsion (Hipe)mentioning
confidence: 99%