| Literature DB >> 32429177 |
Mina K Kim1, Hae Won Jang2, Kwang-Geun Lee3.
Abstract
The objective of this study was to characterize the key aroma-active compounds isolated from omija fruits using gas chromatography-mass spectrometry (GC-MS), orthonasal threshold testing, and descriptive sensory analysis techniques. Omija fruits were prepared using four different methods: raw, pureed, freeze-dried, and hot-air dried. The aromatic compounds were extracted with ethanol. Flavor compounds were further isolated using distillation under reduced pressure, followed by liquid-liquid extraction, and were then identified using GC-MS. A total of 40 volatile compounds were identified in omija fruits; nine were further identified as key aroma-active compounds found in omija fruits. The odor-active values for key flavor compounds were calculated, and aroma descriptions perceived by humans were determined using a highly trained panel. This study found that compounds high in omija fruit extracts were not necessarily the odor active compounds and 4-terpineol (1.84) and α-terpineol (2.58) were high odor-active compounds in omija fruits. Samples with high levels of the two compounds (hot air- and freeze-dried omija fruit) had high intensities of "spicy" and "wet-wood" aromatics.Entities:
Keywords: GC-MS; descriptive analysis; flavor analysis; odor activity value; omija; sensory threshold
Year: 2020 PMID: 32429177 PMCID: PMC7278746 DOI: 10.3390/foods9050638
Source DB: PubMed Journal: Foods ISSN: 2304-8158
Instrumental flavor analysis results of omija fruit extracts.
| Peak No. | Compound | Kovats Index 1 | mg/kg | |||||
|---|---|---|---|---|---|---|---|---|
| ID Method | KI | KI (Ref) | Raw Omija Fruit | Pureed Omija Fruit | Freeze Dried Omija Fruits | Hot Air-Dried Omija Fruits | ||
| 1 | MS, Co, KI | 1177 | 1172 | 1.88 | 2.5 | 0.74 | ||
| 2 | 1,8-Cineol | MS, Co, KI | 1232 | 1224 | 0.22 | 0.13 | 0.71 | 0.37 |
| 3 | MS, Co, KI | 1264 | 1261 | 0.63 | 1.49 | 0.14 | ||
| 4 | MS, Co | 1245 | 0.84 | 1.03 | ||||
| 6 | 4-Cymene | MS, Co, KI | 1289 | 1287 | 0.76 | |||
| 7 | Cyclohexenone | MS | 0.37 | 0.67 | ||||
| 8 | Cyclohexenol | MS | 0.27 | 0.74 | 1.15 | 0.22 | ||
| 9 | Bornyl acetate | MS, Co, KI | 1611 | 1613 | 0.54 | 2.51 | 1.19 | 0.81 |
| 10 | Undecanone | MS, Co, KI | 1619 | 1615 | 0.34 | |||
| 11 | 4-Terpineol | MS, Co, KI | 1631 | 1633 | 3.74 | 4.82 | 6.08 | 3.73 |
| 12 | Dimethyloctadiene | MS | 1.00 | 3.42 | ||||
| 13 | Citronellylpropianoate | MS | 2.42 | |||||
| 14 | MS, Co, KI | 1724 | 1756 | 0.77 | 4.07 | 5.87 | ||
| 15 | α-Terpineol | MS, Co, KI | 1586 | 1576 | 1.51 | 1.63 | 2.58 | 2.16 |
| 16 | MS | 0.91 | 5.82 | 0.23 | 2.26 | |||
| 17 | α-Selinene | MS | 0.55 | 3.4 | 3.16 | |||
| 18 | MS, Co, KI | 1783 | 1774 | 1.41 | 1.07 | 1.9 | ||
| 19 | MS, Co, KI | 1683 | 1674 | 1.76 | 0.82 | 1.23 | 0.94 | |
| 20 | MS | 0.23 | ||||||
| 21 | MS | 0.27 | ||||||
| 22 | α-Copaene | MS, KI | 1515 | 1509 | 1.19 | |||
| 23 | Bicyclosesqui-phellandrene | MS, KI | 1795 | 1782 | 0.86 | 1.12 | ||
| 24 | Ylangene | MS, Co, KI | 1515 | 1499 | 0.2 | |||
| 25 | α-Cadinol | MS, Co, KI | 2264 | 2264 | 3.85 | 4.22 | 2.17 | 0.77 |
| 26 | 11-Selinenol | MS, KI | 5.02 | 0.21 | 2.3 | |||
1) Identification methods of volatile compounds compared with mass spectrum (MS) in Wiley mass database, compared to the Kovat Index (KI) on a DB-wax column and co-injection (CO) with authentic chemicals.
Best estimate threshold (BET) values and odor activity values (OAVs) for key aroma compounds.
| Peak No. | Compound | BET (µg/kg) | OAV | |||
|---|---|---|---|---|---|---|
| Raw Omija Fruit Extract | Pureed Omija Fruit Extract | Freeze Dried Omija Fruit Extract | Hot Air-Dried Omija fruit Extract | |||
| 1 | 9.46 | 0.20 | 0.00 | 0.26 | 0.08 | |
| 2 | 1,8-Cineol | 1.86 | 0.12 | 0.07 | 0.38 | 0.20 |
| 3 | 389.40 | 0.00 | 0.00 | 0.00 | 0.00 | |
| 4 | 38.51 | 0.02 | 0.00 | 0.00 | 0.03 | |
| 9 | Bornyl acetate | 13.13 | 0.04 | 0.19 | 0.09 | 0.06 |
| 10 | Undecanone | 98.50 | 0.00 | 0.00 | 0.00 | 0.00 |
| 11 | 4-Terpineol | 3.31 | 1.13 | 1.46 | 1.84 | 1.13 |
| 15 | 1.00 | 1.51 | 1.63 | 2.58 | 2.16 | |
| 18 | 3.02 | 0.47 | 0.35 | 0.00 | 0.63 | |
BET values were collected in the water matrix; odor activity values (OAV) were calculated for each compound using the concentration found in Table 1 and the orthonasal BET values in this study.
Descriptive analysis result of omija fruit extracts.
| Aroma Attribute | Definition | Raw Omija Fruit Extract | Pureed Omija Fruit Extract | Freeze Dried Omija Fruit Extract | Hot Air-Dried Omija Fruit Extract | |
|---|---|---|---|---|---|---|
| Overall Aroma Intensity | Overall aroma impact | 1.23 b | 1.77 b | 2.50 a | 2.83 a | 0.002 |
| Cough syrup | Characteristic aromatics associated with cherry cough syrup (Reference: Bruffen®, Samil-pharm) | 1.23 a | 1.00 a | 1.03 a | 1.77 a | 0.053 |
| Spicy | Characteristic aromatics associated with whole black pepper (Reference: whole black pepper, Ottugi®) | 0.53 b | 0.83 b | 1.43 a | 1.90 a | 0.002 |
| Smoky aromatics | Characteristic aromatics associated with burning wood at campfire | 0.70 a | 0.17 b | 0.17 b | 0.67 a | 0.033 |
| Wet wood | Characteristic aromatics associated with wet wood | 1.50 a | 0.50 b | 1.50 a | 2.17 a | 0.014 |
| Lemon | Characteristic aromatics associated with cooked lemon (Reference: freshly shaved lemon peel) | 0.90 a | 0.60 a | 0.73 a | 0.67 a | 0.606 |
| Tomato ketchup | Characteristic aromatics associated with tomato ketchup (Reference: tomato ketchup, Ottugi®) | 1.17 a | 0.43 b | 0.00 b | 0.00 b | 0.001 |
| Alcohol | Characteristic aromatics associated with ethyl alcohol (Reference: 10% ( | 1.10 c | 1.23 c | 1.83 b | 3.27 a | <0.0001 |
Numbers represent the mean value of aroma intensity of each sensory term, on a 15-pt universal scale using the Spectrum™ method; Means in a row that do not share the same alphabetical letter represent significant differences at p < 0.05.
Figure 1(a) Principal component bioplot of sensory and instrumental flavor analyses on four omija samples with PC1 and PC2. (b) Principal component bioplot of sensory and instrumental flavor analyses on four omija samples with PC1 and PC3.