Abstract
In this study, the flavor substances of soypaste were extracted by a simultaneous distillation method and identified by GC-MS. The characteristic aroma components of soypaste were determined by the GC-O technique and the FD value of the characteristic aroma components was determined by AEDA method. It could be inferred that the aroma of the soypaste should be attributed to the presence of heterocyclic compounds and organic acids, with the heterocyclic compounds playing a prominent role.
Keywords: flavor; soypaste; aroma; GC-MS, GC-O; FD value; AEDA
1. Introduction
Soypaste is a kind of special seasoning produced by microbial fermentation using soybean and wheat flour as the main raw materials. Traditional soypaste has a unique aroma due to the natural fermentation production method. However, the production of the soypaste suffers from a long production cycle, high costs and low output. Many soypaste manufacturers use artificial fermentation installations and other industrial fermentation processes to expand the scale of production and reduce the cost, but significant differences in aroma are noted by the consumers, which has also become a major factor in markg acceptance. Thus, the aroma of soypaste is considered as one of the important indicators to evaluate the quality of soypaste.
Until recently, soypaste aroma research of was still in the development. The research was focused on the identification and the extraction methods of aroma components [1,2,3,4] and the results only showed the aroma substances in the samples by similar methods such as solid-phase micro-extraction and the direct distillation method, which could not further specify which were the main flavor ingredients. As a result, it was difficult to establish the industrial standard from the aspect of the characristic aroma and the functions of different favor components in traditional soypaste still could not be determined. In this study, the flavor substances of soypaste were extracted by simultaneous distillation method and identified by GC-MS. Then the characteristic aroma components in the soypaste were determined by the GC-O analysis technique and the FD values of the characteristic aroma components were measured by the AEDA method. The results obtained could be used to understand the aroma of traditional soypaste and help standardize the modern product of soypaste.
2. Results and Discussion
The GC profile of the volatile components extracted from the soypaste by SDE (simultaneous distillation and extraction) is shown in Figure 1. One hundred and eight eight components were detected in soypaste extracts, among which 103 compounds were identified by searching the MSDChem NIST02.1 MS library (similarity ratio >75%). Through the data processing system of the MSDChem ChemStation, the relative contents of the various components in the volatile oil were determined by the peak area normalization method and the identified compounds thus accounted for over 80% of the overall aroma components.
In accordance with the order of the peaks, the main identified compounds were as follows: 2-methyl propionaldehyde (0.6568%), ethyl acetate (0.9856%), 3-butyraldehyde (4.4674%), ethanol (16.0962%), 2-methyl-1-propanol (0.5181%), formic acid ester (0.1137%), heptanal (0.0137), iso-amyl alcohol (1.5799%), 2-pentylfuran (0.1063%), 2,5-dimethylpyrazine (0.2044%), 2,6-dimethylpyrazine (0.1038%), ethyl lactate (0.2514%), dimethyl trisulfide (0.1145%), 3-methylpyrazine (0.1862%), acetic acid (2.1983%), 3-methylthiopropionaldehyde (0.168%), furfural (7.5069%), 2-acetylfuran (0.2062%), benzaldehyde (0.9816%), 2-methylpropionic acid (0.9689%), 5-methylfurfural (0.7121%), phenyl-acetaldehyde (6.5578%), furfuryl alcohol (2.1997%), 3-methyl-pentanoic acid (7.0269%), ethyl phenylacetate (0.188%), guaiacol (0.6268 %), phenethyl alcohol (0.7545%), 2-acetylpyrrole (0.9778%), 4-ethylguaiacol (3.2858%), 4-ethylphenol (0.2072%) and palmitic acid ethyl ester (0.8126%).
In this study, 103 volatile compounds were identified in traditional soypaste, mainly esters, alcohols, aldehydes, acids, ketones, and heterocyclic compounds. The contents of alcohols and acids were the highest, followed by the contents of esters and aldehydes. Although the contents of alcohols were high, they had a relatively high threshold, which made their contribution to the flavor small. Esters were the main component present in the soypaste aroma volatile components, providing sweet bean paste, fruit fragrance, and a variety of floral aromas. The aldehydes and ketones had the lowest thresholds and produced fruit fragrances and nut aromas. The heterocyclic compounds were the main component of the cconstituted the main body of the baking aroma. High contents of some compounds such as ethyl acetate, benzoin aldehyde, 5-methylfurfural, benzene, acetaldehyde, furfural, 3-butyric aldehyde, 2,3,5-trimethylpyrazine, etc., some of which had been identified as flavor compounds, have been detected in the soypaste.
The characteristic aroma components of the soypaste were determined by the GC-O technique. During the GC-O analysis, there were three professional evaluators to detect 22 kinds of odor active volatile compounds (Log3 FD> 1). These compounds were classified according to the sequence in Table 1, Table 2, Table 3, Table 4 and Table 5. Many different odors were sniffed at the GC-O sniffing port, including coke flavor, fried potato flavor, fruit fragrance, flower fragrance, butter flavor and so on. All the compounds could be detected in GC-MS. The Log3 FD values of 18 compounds were more than 3. Of these 2,3,5-trimethyl-pyrazine (a strong aroma of fried potatoes), isovaleric (smelly sock smell), 4-ethylguaiacol (slightly sweet herbal incense), acetic acid Ding esters (strong fruit aroma), ethyl phenylacetate (similar to honey fragrant ester), phenethyl alcohol (sweet floral aroma), 3-methyl-pentanoic acid (sour herb smell, slightly green grass aroma), 2,6-dimethylpyrazine (roasted coffee, peanuts, potato aroma), furfural (sweet, roasted, woody), maltol (with butter, sugar, like a special focus fragrant aroma), lactic acid (mild cream aroma), benzaldehyde (bitter almond aroma), ethyl lactate (baked apple aroma), n-octanol (green fragrance, fruit, incense), 4-ethylphenol (phenolic wood aroma, slightly sweet aroma), 2,5-dimethyl-pyrazine (a strong focus scent), 2-acetylpyrrole (bread aroma) all had very high FD values (Log3 FD ≥ 4 ), which could account for the overall flavor of soypaste. Among them, the FD values of 2,3,5-trimethylpyrazine, isovalerate and 4-ethylguaiacol were as high as 2187 (Log3 FD = 7), which formed the bean flavor of the special paste aroma. According to the other similar studies [5], 2,3,5-trimethyl-pyrazine and 4-ethylguiacol were thought to be the characteristic compounds in the fermented bean aroma. It could be broadly inferred that the characteristic aroma of the soypaste should be attributed to the heterocyclic compounds and the organic acids. The role of heterocyclic compounds was particularly prominent, constituting the basis of the soy flavor. The results of this study should help us to control the fermentation process and improve the aroma of soypaste.
Table 1.
Name | RI | Smell description | Log3 FD | ||
---|---|---|---|---|---|
WAX | DB-5 | ||||
1 | 2-Butyraldehyde | 910 | 650 | Nut odor | 1 |
2 | 3-Butyraldehyde | 914 | 664 | Apple odor | 3 |
3 | Hexanal | 1074 | 809 | Aldehyde odor | <1 |
4 | Heptaldehyde | 1174 | 909 | Fruit flavor, rose oil odor, perilla oil odor | 3 |
5 | 5-n-Octyl aldehyde | 1278 | 1014 | Fruits, fat aroma and citrus odor | <1 |
6 | Nonanal | 1380 | 1102 | Citrus and vinegar smell | 2 |
7 | 3-Methylthiopropionaldehyde | 1392 | 925 | Potato and sauce smell | 2 |
8 | Furfural | 1442 | 841 | Sweet, roasted, woody, bread aroma | 5 |
9 | Benzaldehyde | 1498 | 966 | Bitter almonds, woody odor | 4 |
10 | 5-Methylfurfural | 1014 | 771 | Thick, sweet, spicy odor, | 2 |
11 | Phenylacetaldehyde | 1623 | 1059 | Ocean narcissus elegant aroma, a strong wind letter sub-aroma, cherry flavor | 2 |
12 | 2,3-Butanedione | 973 | 606 | Sweet cream, butter aroma | 3 |
13 | 2,3-Pentanedione | 1074 | 702 | Sweet odor, cream odor. | 2 |
14 | 3-Penten-2-one | 1121 | — | Fruit and spicy aroma | <1 |
Table 2.
No | Name | RI | Smell description | Log3 FD | |
---|---|---|---|---|---|
WAX | DB-5 | ||||
1 | Ethanol | 930 | — | 2 | |
2 | iso-propyl carbinol | 1080 | — | Artificial musk aroma | <1 |
3 | 3-Methylbutanol | 1205 | 739 | Wines and ether smell | <1 |
4 | Hexanol | 1349 | 889 | Fruit flavor | <1 |
5 | 1-Octen-3-ol | 1443 | 978 | Mushrooms, lavender, rose and hay aroma | 2 |
6 | Octanol | 1550 | 1086 | Citrus, sweet orange, aldehydes fragrant, sweet floral, fragrant aroma and green incense | 4 |
7 | Furfuryl alcohol | 1660 | — | Bitter and spicy smell | 2 |
8 | 3-Methylthiopropanol | 1436 | 1099 | A strong aroma and taste of meat and broth, a strong smell of garden onions and meat, butter flavor when diluted | 1 |
9 | 2-Methoxyphenol, guaiacol | 1859 | 1102 | Aromatic smell | <1 |
10 | Phenylethanol | 1885 | 1131 | Sweet, floral aroma, and fruit, fat taste, rose aroma | 6 |
11 | Phenol | 1920 | — | Special smell, sweet smell | <1 |
12 | 4-Ethyl-2-methoxyphenol, | 2032 | — | Barbecue flavour | 7 |
13 | 4 - Ethylphenol | 2086 | — | Wood phenol aroma, slightly sweet aroma | 4 |
14 | Maltol | 1968 | 1108 | butter, sugar, coke special aroma incense, strawberry flavor | 5 |
Table 3.
No | Name | RI | Smell description | Log3 FD | |
---|---|---|---|---|---|
WAX | DB-5 | ||||
1 | Ethyl acetate | 885 | <600 | Ether fragrance, sweet fruit such as pineapple | 3 |
2 | Ethyl 2-methylbutyrate | 1051 | 845 | Strong apple skin, pineapple skin and immature sweet aroma of plum skin | <1 |
3 | n-Butyl acetate | 1070 | 820 | Strong fruit aroma, similar to pear, banana aroma | 6 |
4 | Ethyl 3-methylbutyrate | 1134 | — | Similar to apple, bananas aromas and sweet and sour smell | <1 |
5 | Ethyl caproate | 1235 | 996 | Fragrant fruits like pineapple and wine | 4 |
6 | Ethyl lactate | 1293 | 825 | Sweet, fruit, roasted, old rum aroma, wine aroma | |
7 | Octanoic acid ethyl ester | 1431 | 1209 | Brandy aroma, wax incense, milk and cream, fruit, wine | <1 |
8 | Ethyl benzoate | 1647 | 1188 | Fruit, medicine fragrant aroma | 1 |
9 | Ethyl phenylacetate | 1765 | 1258 | Strong and sweet fragrance of honey. Significant and sweet incense rose | 6 |
10 | Ethyl palmitate | >2000 | — | Incense wax smell, butter aroma | 2 |
Table 4.
No | Name | RI | Smell description | Log3 FD | |
---|---|---|---|---|---|
WAX | DB-5 | ||||
1 | 2-Pentylfuran | 1225 | 996 | bean aroma, fruity, green fragrance, vegetables, fragrant soil, root incense aroma | 2 |
2 | 2,5-Dimethylpyrazine | 1316 | 925 | Pungent aroma of fried flowers and chocolate, butter odor, roasted barley aroma, fried potatoes, fried potato chips | 4 |
3 | 2,6-Dimethylpyrazine | 1319 | 925 | Roasted, coffee, peanuts, potato aroma and chocolate flavor | 6 |
4 | 2,3,5-Trimethyl-pyrazine | 1391 | 999 | Baked goods, roasted barley, cocoa, coffee and pork, beef, popcorn, baked potatoes, roasted peanut odor | 7 |
5 | 3-Ethyl-2, 5-dimethyl- pyrazine | 1439 | 1071 | Fried barley, cocoa products, coffee, peanut, hazelnut, soybean odor | 3 |
6 | 2-Acetylfuran | 1497 | — | Almonds, nuts, fermented aroma, milk and sweet caramel-like aroma | 1 |
7 | 1-Methoxy-4-(1- propenyl)-benzene, anethole | 1682 | 1244 | A special aroma of fennel | <1 |
8 | 2-Acetylpyrrole | 1952 | — | Bread aroma, bakery aroma | 4 |
Table 5.
No | Name | RI | Smell description | Log3 FD | |
---|---|---|---|---|---|
WAX | DB-5 | ||||
1 | Acetic acid | 1413 | 671 | Acetic, vinegar odor | 2 |
2 | 2-Methylpropionic acid | 1468 | — | Pungent odor, rancid oil odor | 3 |
3 | Butyric acid | 1546 | — | Milk, cream, butter, cheese, fruity aroma | 2 |
4 | 3-Methylpentanoic acid | 1597 | 882 | Sour herbal aroma, slightly green grass aroma | 6 |
5 | Isovaleric acid | 1638 | 966 | Old sock odor | 7 |
6 | Hexanoic acid | 1826 | 1209 | Strong rancid cheese aroma | 1 |
7 | Lactic acid | >2000 | 1296 | Mild and pleasant cheese aroma | 5 |
8 | Nonanoic acid | >2000 | 1308 | Fats, wax, cheese, coconut fragrance | <1 |
3. Experimental
3.1. Materials and chemicals
Soypaste was obtained from Fang Yuan Food Ltd. Company of Lan Yang City, Shang Dong Province. Other chemical were of analytical grade.
3.2. Fermentation process
After removing the impurities, the soybeans and wheat were cooked, cooled and mixed in a ratio of 6:4. The obtained mixture was used as the starter-material and fermented in a fermentation tank for six months. After the fermentation, it was collected as the soypaste.
3.3. SDE Preparation of aroma components from soypaste
The bean paste (200 g) was mixed with distilled water (300 mL) and a small amount of zeolite in a 1000 mL round-bottomed flask. The mixture was placed in a simultaneous distillation extraction instrument (Anhui Tianchang Excellent Letter Electrical Equipment Co., Ltd.) and extracted at 40 °C for 3 h. The extract was concentrated and dried by sodium sulfate for the subsequent GC-O and GC analysis.
3.4. Analysis of GC and GC-MS
GC-MS analysis was performed on an Agilent 6890NGC-5973IMS GC-MS. The gas chromatograph was equipped with a HP-INNO Wax Polyethylene Glycol capillary column 60 m × 0.25 mm coated with 0.25 μm film thickness. Carrier gas (helium) at flow rate of 1 mL/min. Column temperature program was 40 °C (3 min) isotherm, increased to 130 °C at a rate of 3 °C/min, maintained at 130 °C for 2 min, then increased to 200 °C at a rate of 4 °C/min and held at 200 °C for 5 min. The mass spectrometer was used in EI scan mode with a scan range of masses from 33 to 450 m/z. Ionization was set at 70 eV. Injector temperature was 250 °C. The compounds were identified by searching NIST02.1 database of the MSDChem workstation.
GC-O analysis was performed on an Agilent 7980 gas chromatograph interfaced to an ALPHA-MOS sniffer sniffing device (France ALPHA-MOS Corporation). The gas chromatograph was equipped with an Rtx-WAX capillary column 30 m × 0.25 mm coated with 0.25 μm film thickness (Agilent, USA). Carrier gas (helium) at flow rate of 1 mL/min. Column temperature program was 40 °C (3 min) isotherm, increased to 130 °C at a rate of 3 °C/min, maintained at 130 °C for 2 min, then increased to 200 °C at a rate of 4 °C/min and held at 200 °C for 5 min. The split ratio of the effluent into the FID and the ALPHA-MOS sniffer was 1:1.
3.5. Analysis of AEDA [6]
The extract was diluted according to the volume ratios of 1:3, 1:9, 1:81, 1:243, respectively. The obtained sample (2 μL) was injected for the GC-O analysis until the evaluators at the GC-O terminal could not feel the smell. The obtained highest dilution ratio was defined as the FD factor. There were three professional evaluators from Central Research Institute of Ting Hsin International Group who performed the AEDA.
4. Conclusions
In this study, the flavor substances of soypaste were extracted by simultaneous distillation method and subjected to standard analysis by GC-MS. The characteristic aroma components of soypaste were determined by the GC-O technique, and at the same time the FD values of the characteristic aroma components were determined by the AEDA method. The results could be used to evaluate the quality of soypaste.
Footnotes
Sample Availability: Samples of the compounds are available from the authors.
References and Notes
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