| Literature DB >> 30223605 |
Siti Raihan Zakaria1, Norashikin Saim2, Rozita Osman3, Zaibunnisa Abdul Haiyee4, Hafizan Juahir5.
Abstract
This study analyzed the volatile organic compounds (VOCs) of three mango varieties (Harumanis, Tong Dam and Susu) for the discrimination of authentic Harumanis from other mangoes. The VOCs of these mangoes were extracted and analysed nondestructively using Head Space-Solid Phase Micro Extraction (HS-SPME) coupled to Gas Chromatography-Mass Spectrometry (GC-MS). Prior to the analytical method, two simple sensory analyses were carried out to assess the ability of the consumers to differentiate between the Harumanis and Tong Dam mangoes as well as their preferences towards these mangoes. On the other hand, chemometrics techniques, such as principal components analysis (PCA), hierarchical clustering analysis (HCA), and discriminant analysis (DA), were used to visualise grouping tendencies of the volatile compounds detected. These techniques were successful in identifying the grouping tendencies of the mango samples according to the presence of their respective volatile compounds, thus enabling the identification of the groups of substances responsible for the discrimination between the authentic and unauthentic Harumanis mangoes. In addition, three ocimene compounds, namely beta-ocimene, trans beta-ocimene, and allo-ocimene, can be considered as chemical markers of the Harumanis mango, as these compounds exist in all Harumanis mango, regardless the different sources of the mangoes obtained.Entities:
Keywords: Harumanis; Mangifera indica L.; VOCs; authentication; chemometrics; chromatographic; sensory analysis
Mesh:
Substances:
Year: 2018 PMID: 30223605 PMCID: PMC6225100 DOI: 10.3390/molecules23092365
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Figure 1Harumanis (A), Tong Dam (B) and Susu (C) mangoes.
Number of agree judgment of respondents (n = 30) on a Duo Trio test.
| Reference | Number of Agree Judgments | |
|---|---|---|
| Tong Dam | Tong Dam | Harumanis |
| 30 | 17 | 13 |
Figure 2Acceptance test of the parameters for (a) whole Harumanis and Tong Dam samples and (b) slices of Harumanis and Tong Dam samples, evaluated using a 9-point hedonic sensory evaluation. Different letters indicate significant differences of mean concentrations (p ≤ 0.05) between the two mango cultivars.
Figure 3Chromatograms of the real Harumanis mango in three locations with three marker compounds. (a) beta-ocimene, (b) trans-beta-ocimene and (c) allo-ocimene.
Figure 4Chromatograms of Harumanis, Susu, and Tong Dam mangoes with three chemical compounds appearing in Harumanis: (a) beta-ocimene, (b) trans-beta ocimene and (c) allo-ocimene.
Figure 5Dendrogram of the authentic (CI) and unauthentic (CII) Harumanis mango.
Classification matrix of VOCs in different variety of mangoes.
| Source | % Correct | Source Assigned by DA | ||
|---|---|---|---|---|
| Harumanis | Susu | Tong Dam | ||
| Standard DA mode | ||||
| Harumanis | 100 | 10 | 0 | 0 |
| Susu | 100 | 0 | 6 | 0 |
| Tong Dam | 100 | 0 | 0 | 7 |
| Total | 100 | 10 | 6 | 7 |
Figure 6PCA plots of the three mangoes varieties; Susu (CI), Harumanis (CII), and Tong Dam (CIII).
Loadings of volatile organic compounds (VOCs) for Harumanis mango samples from point sources.
| Parameters | F1 | F1 | F1 | F1 | F1 | F1 | F1 |
|---|---|---|---|---|---|---|---|
| ethyl acetate |
| −0.0668 | 0.1046 | −0.1006 | 0.3285 | 0.2685 | 0.0473 |
| cyclotrisiloxane | −0.2479 |
| 0.0398 | −0.1300 | 0.0020 | −0.0686 | 0.0354 |
| 1 |
| −0.0557 | −0.4895 | 0.1708 | −0.5931 | −0.0475 | −0.0058 |
| 2,6,6-Trimethyl | −0.4089 | 0.6959 | 0.1444 | 0.0552 | 0.0072 | −0.2591 | −0.2182 |
| camphene |
| −0.6812 | −0.0450 | −0.1776 | 0.0228 | −0.2657 | 0.2247 |
|
| −0.5703 | −0.0208 | −0.1859 | 0.0216 | −0.3885 | −0.0783 | |
|
| −0.1486 | 0.1526 | 0.0816 | −0.175 | −0.0822 | −0.0206 | |
| hexanoic acid | 0.4131 | −0.0892 | −0.2776 | 0.2624 |
| −0.2539 | −0.047 |
| (+)-3-carene |
| 0.4894 | 0.1065 | −0.0780 | 0.0180 | −0.3210 | −0.4591 |
| 3-heptene | −0.2235 |
| 0.0822 | −0.0053 | 0.0053 | −0.1772 | 0.4339 |
| (+)-4-carene |
| −0.6359 | 0.0472 | 0.1751 | −0.0037 | −0.1551 | 0.2726 |
| 1,3-cyclohexadiene |
| 0.0028 | 0.2105 | 0.5431 | −0.0393 | 0.0828 | −0.0138 |
|
| −0.0689 | 0.2047 | 0.5145 | −0.0273 | −0.1676 | 0.3267 | |
| 0.4162 | −0.1325 |
| −0.2094 | −0.2824 | 0.0615 | 0.0085 | |
| 0.4108 | −0.133 |
| −0.2078 | −0.2764 | 0.058 | 0.0078 | |
| −0.445 | −0.1911 | 0.1321 | 0.4781 | −0.0441 |
| −0.3439 | |
| undecane | −0.4981 |
| −0.0366 | −0.0694 | 0.0025 | 0.3551 | −0.1115 |
|
| −0.1314 | −0.2506 | 0.2139 | −0.1572 | −0.1157 | −0.0287 | |
| octanoic acid |
| −0.1241 | −0.0111 | 0.2726 | 0.54 | −0.2734 | −0.062 |
| ethyl ( |
| −0.0501 | −0.3193 | 0.0568 | 0.1252 | 0.2036 | 0.0299 |
| decanoic acid |
| −0.1302 | −0.0043 | 0.215 | 0.6032 | −0.0902 | −0.0292 |
|
| 0.1662 | 0.0649 | 0.048 | 0.0043 | 0.105 | 0.5499 | |
| germacrene D |
| −0.1102 | 0.2001 | 0.2503 | 0.1101 | −0.2713 | −0.0247 |
| heneicosane |
| −0.1997 | 0.4348 | 0.1317 | 0.0326 | −0.2029 | −0.0434 |
| Eicosane |
| −0.1034 | 0.2084 | 0.5369 | −0.0353 | −0.1027 | −0.2779 |
| eigenvalue | 8.3184 | 3.265 | 2.2706 | 1.8592 | 1.6844 | 1.3503 | 1.3106 |
| variability (%) | 31.9939 | 12.5577 | 8.733 | 7.1509 | 6.4786 | 5.1935 | 5.0408 |
| cumulative (%) | 31.9939 | 44.5515 | 53.2845 | 60.4354 | 66.9141 | 72.1076 | 77.1484 |
Note: Strong loadings (>0.75) are shown in bold and moderate loading (0.5–0.75) in italic.