| Literature DB >> 32545821 |
Martyna Lubinska-Szczygeł1, Żaneta Polkowska1, Tomasz Dymerski1, Shela Gorinstein2.
Abstract
In the presented study, an overall Jaffa sweetie evaluation was made to find a correlation between Citrus grandis Osbeck × Citrus paradisi Macf. and its parent fruits' (Citrus grandis Osbeck, Citrus paradisi Macf.) properties. Based on the sensory analysis, it was found that the taste and aroma of the new hybrid fruit are close to pummelo. By the use of chromatographic analysis, the selected monoterpenes present in the fruits were quantified. α-terpineol was typed as the main monoterpene compound in the headspace of sweetie and grapefruit, with the concentrations: 20.96 and 87.9 μg/g, respectively. In turn, γ-terpinene was chosen as the most important monoterpene determining the flavor of sweetie fruit. Based on two-dimensional gas chromatography (GC × GC-TOF-MS) and principal component analysis (PCA) of the data, several volatile compounds were associated with analyzed fruits' aroma. Jaffa Sweetie is the hybrid fruit with sensory properties similar to pummelo with a higher content of monoterpenes, which improves its health benefits compared to the parent fruit. The research presents an instrumental method for assessing the aroma properties of the fruit as a reference method for sensory analysis, commonly used in the industry.Entities:
Keywords: flavoromics; fruit hybridization; gas chromatography; sensory analysis; terpenes
Year: 2020 PMID: 32545821 PMCID: PMC7357158 DOI: 10.3390/molecules25122748
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Physical and visual evaluation of the citrus fruits.
| Property of Fruit | Sweetie | Grapefruit | Pummelo |
|---|---|---|---|
| Diameter at the widest point [mm] | 129.7 ± 5.1 | 145.3 ± 7.2 | 189 ± 11 |
| Peel color | yellow-green | yellow | light green |
| Thickness of peel [mm] | 17.00 ± 0.80 | 16.70 ± 0.40 | 19.5 ± 1.2 |
| Flesh colors | grey-yellow | yellow | straw |
| Presence of seed | not noticed | few | many |
| Shape | round, slightly flattened | round, slightly flattened | round, elongated |
| Weight [g] | 259 ± 27 | 283 ± 10 | 875 ± 86 |
Figure 1Cross-section of analyzed fruits.
Figure 2Results of sensory analysis of pummelo, sweetie, and grapefruit: (a) heat map of panelists’ choices and (b) radar plot of average values of main sensory properties.
Figure 3Two-dimensional gas chromatography (GC × GC) contour plots in total ion current (TIC) mode of (A) grapefruit, (B) sweetie, and (C) pummelo samples.
Identification of selected volatiles compounds in sweetie, pummelo and grapefruit samples using HS-GC × GC-TOFMS technique.
| Chemical Compound | CAS Number | Average | ID | S | G | P | Odor Type | Flavor Type | |
|---|---|---|---|---|---|---|---|---|---|
| RT1 [s] | RT2 [s] | ||||||||
| Terpenes | |||||||||
| p-Menthane | 99-82-1 | 862 | 1.16 | MS | + | + | + | pine | n.d. |
| p-Cymene | 99-87-6 | 938 | 1.58 | MS | + | + | + | terpenic | terpenic |
| Ocimene | 6874-44-8 | 970 | 1.41 | MS, RT | + | + | + | fruity | n.d. |
| γ-Terpinene | 99-85-4 | 926 | 1.36 | MS, RT | + | + | + | terpenic | terpenic |
| β-Myrcene | 123-35-3 | 878 | 1.38 | MS, RT | + | + | + | spicy | woody |
| Limonene | 138-86-3 | 950 | 1.38 | MS, RT | + | + | + | citrus | citrus |
| α-Pinene | 80-56-8 | 790 | 1.22 | MS, RT | + | + | + | herbal | woody |
| Citronellene | 2436-90-0 | 806 | 1.20 | MS | + | + | + | floral | n.d. |
| β-Pinene | 127-91-3 | 858 | 1.30 | MS, RT | + | + | + | herbal | pine |
| α-Terpineol | 98-55-5 | 1186 | 2.67 | MS, RT | + | - | + | terpenic | citrus |
| Alcohols | |||||||||
| Hexanol | 111-27-3 | 654 | 3.47 | MS | + | + | + | herbal | green |
| Pentanol | 71-41-0 | 486 | 3.66 | MS | + | + | + | fermented | fusel |
| 3-Hexenol | 928-97-2 | 638 | 0.15 | MS | + | + | + | green | green |
| 2-Hexenol | 2305-21-7 | 658 | 0.27 | MS | + | + | + | fruity | fruity |
| Octanol | 111-87-5 | 1002 | 2.69 | MS | + | + | + | waxy | waxy |
| Aldehydes | |||||||||
| Hexanal | 66-25-1 | 518 | 1.84 | MS | + | + | + | green | green |
| Heptanal | 111-71-7 | 702 | 1.79 | MS | + | + | + | green | solvent |
| Nonanal | 124-19-6 | 1046 | 1.70 | MS | + | + | + | aldehydic | aldehydic |
| Octanal | 124-13-0 | 878 | 1.76 | MS | + | + | + | aldehydic | aldehydic |
| Esters | |||||||||
| Ethyl 2-methylbutyrate | 7452-79-1 | 626 | 1.44 | MS | + | + | + | fruity | fruity |
| Ethyl butanoate | 105-54-4 | 534 | 1.56 | MS | + | + | + | fruity | fruity |
| Ethyl hexanoate | 123-66-0 | 882 | 1.50 | MS | + | + | + | fruity | fruity |
| Ethyl isobutyrate | 97-62-1 | 470 | 1.43 | MS | + | + | + | fruity | ethereal |
| Ethyl octanoate | 106-32-1 | 1190 | 1.49 | MS | + | + | + | waxy | waxy |
| Hydrocarbons | |||||||||
| 2,6-Dimethyl-2,6-octadiene | 2792-39-4 | 902 | 1.23 | MS | + | + | + | n.d. | n.d. |
| Octane | 111-65-9 | 554 | 1.08 | MS | + | + | + | gasoline | n.d. |
| Nonane | 111-84-2 | 734 | 1.08 | MS | + | + | + | gasoline | n.d. |
| 4-Decene | 19689-18-0 | 766 | 1.10 | MS | + | + | + | n.d. | n.d. |
| Tetradecane | 629-59-4 | 1362 | 1.10 | MS | + | + | + | n.d. | n.d. |
| Ketones | |||||||||
| 3-Octanone | 106-68-3 | 854 | 1.68 | MS | + | + | + | herbal | mushroom |
| 6-Methyl-5-hepten-2-one | 110-93-0 | 850 | 2.06 | MS | + | + | + | citrus | n.d. |
| 2-Heptanone | 110-43-0 | 686 | 1.82 | MS | + | + | + | cheesy | cheesy |
| 4-Nonanone | 4485-09-0 | 998 | 1.58 | MS | + | − | + | n.d. | n.d. |
| 6-Dodecanone | 6064-27-3 | 1482 | 1.56 | MS | + | − | + | n.d. | n.d. |
| Others | |||||||||
| 2-Pentylfuran | 3777-69-3 | 874 | 1.55 | MS | + | + | + | fruity | green |
ID—Method of identification: MS—identification by comparison with National Institute of Standards and Technology (NIST) mass spectral libraries; RT—identification by comparison with the retention time of analytical standard compound; Odor and flavor types were taken from The Good Scents Company; S—Sweetie, P—Pummelo, and G—Grapefruit, +/- — detected/not detected.
Figure 4Distribution of volatiles by chemical classes.
Quantitation of selected monoterpenes present in the volatile fraction of sweetie, pummelo, and grapefruit (μg/g).
| Monoterpene | R2 | S | P | G | LOQ | LOD |
|---|---|---|---|---|---|---|
| α-Pinene | 0.999 | 0.8241 ± 0.0096 | <LOQ | 2.851 ± 0.015 | 0.657 | 0.219 |
| Limonene | 0.996 | 5.298 ± 0.058 | 2.75 ± 0.54 | 15.79 ± 0.30 | 1.416 | 0.472 |
| Ocimene | 0.995 | 1.600 ± 0.097 | <LOQ | 2.057 ± 0.078 | 1.504 | 0.501 |
| β-Myrcene | 0.991 | 4.1 ± 0.14 | <LOQ | 3.22 ± 0.029 | 2.077 | 0.692 |
| γ-Terpinene | 0.997 | 7.27 ± 0.34 | <LOQ | 2.566 ± 0.026 | 1.152 | 0.384 |
| α-Terpineol | 0.992 | 20.96 ± 0.70 | <LOQ | 87.9 ± 2.0 | 1.928 | 0.643 |
LOQ—Limit of quantitation, LOD—Limit of detection, S—Sweetie, P—Pummelo, and G—Grapefruit.
Figure 5Ishikawa diagram presenting the influence of parameters on the analytical process for the determination of monoterpenes in citrus fruit samples.
Selected volatile compounds determined in sweetie, grapefruit, and pummelo with their respective odor threshold and odor active compounds (OAC).
| Chemical Compound | OT [ppm] | Sweetie | Pummelo | Grapefruit |
|---|---|---|---|---|
| OAV + SD [-] | ||||
| α-Pinene | 0.19 | 4.335 ± 0.051 | - | 15.01 ± 0.080 |
| Limonene | 0.2 | 26.49 ± 0.29 | 13.8 ± 2.7 | 78.95 ± 1.5 |
| Ocimene | 0.034 | 47.1 ± 2.9 | - | 60.5 ± 2.3 |
| β-Myrcene | 0.1 | 41 ± 1.4 | - | 32.20 ± 0.29 |
| γ-Terpinene | 0.26 | 28.0 ± 1.3 | - | 9.86 ± 0.10 |
| α-Terpineol | 5 | 4.2 ± 0.14 | - | 17.58 ± 0.40 |
OT—odor threshold values were taken from the literature [32].
Figure 6Principal component analysis (PCA) biplots of the assignments of sweetie, grapefruit and pummelo fruits in respect of individual volatile organic compounds (VOCs).
Figure 7The process of sample preparation for analysis.
Parameters and conditions of GC × GC-TOF-MS analysis.
| Element | Parameter | Value |
|---|---|---|
| Carrier gas | Hydrogen | 1 mL/min |
| Front inlet | Temperature | 250 °C |
| Temperature program | Initial temperature | I. column 40 °C |
| II column 45 °C | ||
| Modulator 60 °C | ||
| Time to maintain the initial temperature | I, II column, modulator 210 s | |
| Temperature rate | I, II. column, modulator 6 °C/min | |
| Final temperature | I column 250 °C | |
| II. column 255 °C | ||
| Modulator 265 °C | ||
| Time to maintain the set temperature | I column 300 s | |
| II column, modulator 350 s | ||
| Modulation | Modulation period | 4 s |
| Modulation | Hot pulse time | 0.80 s |
| Modulation | Cool time between stages | 1.20 s |
| Cooling medium | Type of medium | Liquid nitrogen |
| Detector | Mass range | 40–400 u |
| Detector | Voltage | 1600 V |
| Detector | Acquisition rate | 125 spectra/s |
| Detector | Electron Energy | −70 V |