Sensory-directed f lavor analysis of key odorants compounds development of French fries and oils in the break-in, optimum and degrading frying stage
2023-01-22LirongXuGangchengWuJianhuaHuangHuiZhangQingzheJinXingguoWang
Lirong Xu, Gangcheng Wu, Jianhua Huang, Hui Zhang, Qingzhe Jin, Xingguo Wang,*
a Institute of Nutrition and Health, Qingdao University,Qingdao 266071, China
b Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China
Keywords:French fries Frying stages Off-flavor Odor activity value Aroma recombination
A B S T R A C T The flavor is a decisive sensory characteristic that determines the popularity of French fries (FFs). During high-oleic rapeseed oil (RO) frying, the flavor development of FFs showed three noticeable stages including break-in (3.5%–7.5% of total polar compounds (TPC)), optimum (7.5%–22.18% of TPC), and degrading stages (above 22.18% of TPC). Further, in order to distinguish the key aroma compounds in each stage, the FFs prepared in RO at TPC of 3.5% (FF4), 14.5% (FF15), and 26.96% (FF27) and their relevant oils (RO4,RO15, RO27) were selected for sensory-directed analysis. The results revealed that the FF4 had low contents of (E,E)-2,4-decadienal (deep-fried odor) which also caused lower sensory score in FF4 sample. The higher contents of (E,E)-2,4-decadienal in FF15 induced its higher deep-fried odor. The FF27 had higher hexanoic acid (sweaty odor), heptanoic acid, nonanoic acid, benzene acetaldehyde (stale odor), and trans-4,5-epoxy-(E)-2-decenal (metallic odor) compared with FF4 and FF15, thus leading to the undesirable flavor of FF27.Moreover, the decrease of 2,5-dimethylpyrazine and 2-ethyl-6-methyl-pyrazine in FF27 induced the lower roasty flavor, which may also lead to the decline of the sensory score. Similarly, the higher contents of(E)-2-undecenal, hexanoic acid, heptanoic acid, and nonanoic acid in RO27 lead to increase its rancid score and thus lower the sensory score.
1. Introduction
Frying is a popular and fast cooking practice that has been used domestically and commercially for decades to improve the sensory quality of food products [1]. The f lavor of fried food is one of the fundamental and the decisive sensory characteristics which ultimately determines the acceptance of deep-fried food [2]. From the perspective of practicability and economic eff iciency, the frying oil is continuously used in the household kitchen, restaurants and catering industries, it is also widely used in the fast-food industry, and snack processing enterprises. When the oil was heated, the temperature increased constantly, and several aroma compounds e.g. (E,E)-2,4-decadienal, (E,E)-2,4-heptadienal, octanal, nonanal, appeared,ultimately directly affecting the food flavor [3]. During the frying process, the oil will undergo a series of complex chemical reactions,which further induce changes in components of fried food such as triacylglycerols, polysaccharides, and proteins. During prolonged deep frying, the degradation of oil will inevitably contribute to the losses of vital potato nutrients. These reactions could induce volatile products, and determine the sensorial values of fried products. Among these reactions, lipid oxidation acted as a protagonist, and decided the fried f lavor through the formation of hydroperoxides to be eventually broken down into aroma compounds (e.g., aldehydes, ketones, and alcohols) [4]. Consequently, it is important to explore the degradation of oil when frying and the influence of oil on fried food, contributing to the acquisition of high-quality fried food.
The study carried out by Blumenthal proposed a “Frying Oil Quality Curve”, which introduced five stages of oil degradation(break-in, fresh, optimum, degrading, and runaway stages) that explained the relationship between the changes of oil and the quality of food. Fried products prepared in the first stage were raw with light color and smell [5]. As oil degraded further, the frying process entered in the “fresh” and “optimum” stages with improved food quality,golden brown colored and desired smell. Finally, the oil continued to degrade and entered in the “degrading” and “runaway” stages. In the last stage, the long-term usage of frying oil resulted in the excessive lipid oxidation which finallly obtained a lower sensory score [6].However, this curve did not point out which compounds have a meaningful influence on food flavor because the conclusion was only based on the sensory evaluation, nonetheless, the detailed quantitative information of aroma compounds need further investigation.Numerous studies evaluated the impact of oil types on the French fries (FFs) flavor [7,8]. Furthermore, only a few studies evaluated the fried food sensory, one of which was carried out by Enríquez-Fernández et al., who reported an influence of oil type and freshness on the sensory perception of FFs, without determining the volatile compounds [9]. Also, the study of Santos et al. compared the sensory quality of potatoes during deep-frying in three commercial oils [10].Further, this study revealed that the volatile compounds of potatoes was only characterized roughly neglecting the detailed change of each aroma-active compounds.
In recent studies, the sensory-directed flavor analysis was used for a comprehensive analysis of the key aroma-active compounds in oil and other food matrices [11,12]. Therefore, the aim of this study is to characterize and compare the quantitative information related to the key odor-active flavor compounds in FFs and high-oleic rapeseed oil (RO) during break-in, optimum, and degrading stages using sensory-directed flavor analysis. Moreover, this study will provide new insights regarding the mechanism underlying the generation of desirable and off-flavors after deep-frying in different stages, and the total polar compounds (TPC) value at the turning point of each stage.Results obtained from this study will assist in limiting the off-flavors formation and improving the aroma of fried food. Furthermore,the present study may benefit food industries for the control and standardization of flavor.
2. Materials and methods
2.1 Materials and reagents
Fresh potatoes (Solanum tuberosum L, Helan15 cultivar)were obtained from a farm located in Shandong, China. The higholeic RO (Brassica napus) was donated by (Cargill Cereals &Oils (Nantong) Co., Ltd.), without additives, was stored at 4 °C.The reagents and volatile compound standards were purchased from Sigma (St. Louis, MO, USA).
2.2 Frying procedure
A commercial deep fryer (Aigoli, China) with a maximum capacity of 2.5 L was used for frying. A batch of (100 ± 2) g of potatoes was fried in the RO for 5 min at 170 °C. Then, the next frying cycle was done after 55 min. The overall time was 3 days(8 h/day). The FFs and the RO were collected for further analysis after each cycle.
2.3 Determination of fatty acid composition
The fatty acid composition was determined according to the method reported by Li et al. [13] with methyl nonadecanoate as an internal standard. The fatty acid composition was analyzed by gas chromatography using Agilent 7820 (Agilent, USA) and the conditions were referred from our previous research [14].
2.4 Determination of AV, PV, p-AnV, TOTOX and TPC
The acid value (AV), peroxide value (PV),p-Anisidine value(p-AnV) and TPC were determined according to AOCS official method 3a-63 [15], Cd 8b-90 (AOCS, 2003) [16], Cd18-90 (AOCS, 2011) [17],and Cd 20-91 with minor modifications (AOCS,1993), respectively. The total oxidation (TOTOX) value was calculated using values of PV andp-AnV according to the AOCS official method Cg 3-91.
2.5 Determination of moisture and total oil contents and color of FFs
The moisture content of the samples was determined by the oven drying method [19]. The oil content of FFs was determined by the Soxhlet extraction method [10]. Color of the FFs sample was expressed as lightness (L*), yellowness (b*) and redness (a*), and was measured by using a high-precision spectrophotometer (UltraScan Pro 1166, HunterLab Inc., USA). Color change (ΔE) and the browning index were calculated according to the study of Yost et al. [20].
2.6 Sensory evaluation
The FFs were analyzed by an 80 sensory panel members (65%female; 18–40 years old, from Jiangnan University) for flavor desirability on a 7-point hedonic scale, from 1 (extremely undesirable flavor) to 7 (extremely desirable flavor), the panelists were trained according to the national standard method (GB/T 16291). The FFs were placed in paper cups which were marked with 3-digit ofrandom numbers, and were presented to each assessor. Furthermore, twelve trained panelists (6 males and 6 females; with an average age of 30 years) from Jiangnan University were employed to evaluate the sensory attributes of RO and FFs in three different frying stages. Prior to analysis, several aroma qualities were selected by a descriptive test as reported by Thürer et al. [8]. A reference solution in refined sunflower oil was provided for each descriptor as follows: hexanal for green, (E,E)-2,4-decadienal for deep-fried, (E)-2-nonenal for fatty,butyric acid for sweaty,trans-4,5-epoxy-(E)-2-decenal for metallic,hexanoic acid for rancid, 3-(methylthio) propanal for cooked potatolike, 2,6-dimethyl-pyrazine for roasty, 2,5-dimethyl-4-hydroxy-3(2H)-furanone for caramel, and benzene acetaldehyde for stale/beeswax-like. The intensities of selected odor attributes (green/grassy,metallic, deep-fried, fatty, sweaty, rancid for RO and cooked potatolike, roasty, caramel, deep-fried, fatty, stale, metallic, and rancid for FFs) were rated by a trained sensory panelist on a linear scale from 0(not perceivable) to 3 (strongly perceivable) on a seven-point scale in step. Each sample was evaluated thrice by each panelist.
2.7 Aroma extract dilution analysis by gas chromatographyolfactometry-mass spectrometry (GC-O-MS) analysis
A GC-MS (QP-2010, Shimadzu, Shimane, Japan) combined with an olfactory port was used to analyze the samples. GC-O analysis was performed on DB-WAX column (30 m × 0.25 mm × 0.25 μm),experimental conditions were in accordance with GC-MS. The volatile extracts were obtained by HS-SPME, and the sample was diluted by increasing the GC inlet split ratio from 4:1 to 16:1, 64:1,256:1. The flavor dilution (FD) factor was defined as the maximum dilution at which the aroma compound could be detected.
2.8 Quantitation of the aroma-active compounds and calculation of odor activity values (OAVs)
The SPME method was referred from the study carried out by Santos et al. [10], with minor modification. The FFs (1.50 ± 0.02) g were placed in a 20 mL vial, while 5ml of saline solution and 20 μL of standard solution (1,2-dichlorobenzene, 51.55 μg/mL) were added to each sample before extraction. For frying oil analysis, (3.00 ± 0.02) g oil samples and 20 μL of standard solution (1,2-dichlorobenzene,1 031 μg/mL) were added to a 20 mL vial. The 50 μm/30 μm DVB/CAR/PDMS fiber (Supelco Inc., Bellefonte, PA, USA) was used for headspace sampling. Volatile compounds were analyzed on GC-MS apparatus using a TSQ Quantum XLS (Thermo, USA)operating in electron ionization mode (EI, 70 eV) with the DBWAX MS column (30 m × 0.25 mm × 0.25 μm). The odor-active compounds were quantified by an external standard method with mass spectra, and detected in a selected ion monitoring mode. Prior to quantitative analysis, the FFs were further treated to obtain an artificial odorless matrix as described in the previous study with minor modification [21]. The odorless refined rapeseed oil was obtained by molecular distillation. OAVs were calculated as the ratio of the concentration of each odorant to its respective threshold in oil, and the threshold was obtained from the previous study [22].
2.9 Aroma recombination and omission experiment
All flavor standards with OAVs ≥ 1 were added in the odorless FFs and the odorless refined RO, as shown in the recombination model 1. Then, each standard was omitted in the recombination model 2 to compare the difference from original samples. The aroma of model 2 was differed from that of the original samples, indicating that the lacked aroma compounds were key aroma compound. Finally,the selected key aroma compounds were recombined as model 3.Recombination model 3 was evaluated based on whether it was consistent with the original FFs and RO by panelists as described above for APA.2.10 Statistical analyses
All analyses were conducted in triplicates. One-way analysis of variance (ANOVA) and Duncan’s multiple range tests were performed using the IBM SPSS Statistics for Macintosh (Version 22.0).
3. Results and discussion
3.1 Physicochemical analysis
3.1.1 Fatty acids compositions of frying oil
The changes in fatty acids composition of RO during the frying process are showed in Table 1. Remarkably, oleic acid (72.79 g/100 g)was recovered with the most predominant fatty acid in fresh RO. The oxidative susceptibility of lipids was correlated with their fatty acid composition and resulted in different volatile compounds degraded from fatty acids [23]. Furthermore, our results showed that the oleic acid was decreased from 72.79 g/100 g to 60.42 g/100 g in the RO over the frying process. While, the degradation of polyunsaturated fatty acids was increased with the frying time. Further, the contents of the linoleic and linolenic acids were decreased in the RO. At the end of the frying process, linoleic and linolenic acids were decreased by 4.29 and 1.84 g/100 g, respectively, in RO. Moreover, the saturated fatty acids similarly showed a declining trend with frying time(10.47 g/100 g to 7.87 g/100 g). These results were consistent with the previous study of Liu et al. [23]. Also, the trans fatty acids (TFA)were observed to be a common indicator for oil thermal degradation.The TFA in the RO was increased with frying time (from 0.23 g/100 g to 0.31 g/100 g) which is in accordance with the increasing trend for canola oil and olive oil during 28 h of frying [10].
3.1.2 The change of AV, PV, p-AnV, TOTOX and TPC of frying oil
As shown in Table 2, the AV was rapidly increased over frying time in the RO and reached 4.70 mg/g after 16 h of frying. The PV in the RO showed an initial sharp increasing trend until it reached the highest value (17.40 meq/kg) at 16 h. Thep-AnV indicated the degree of secondary oxidation by measuring the content of aldehydes. Thep-AnV was low in fresh oil (0.73) and then it was sharply increased by 144.38 after 8 h of deep-frying. Then, the value showed a moderate increasing trend (form 146.80 to 157.70) until the end of the frying time. The TOTOX value was used to describe the degree of overall oxidation [24]. The TOTOX value was low (3.63) in the fresh oil, then showed a continuously increasing trend (from 3.63 to 192.49) during 16 h of frying. The TPC content was one of the greatest representative indicators, which described the degree of oil deterioration in frying oils. According to the Chinese national standard (GB 2716–2018),when the TPC is over 27%, the frying oils should be discarded [14].The TPC content of RO was gradually increased during the prolonged frying period and reached 26.96% at 16 h of the frying.
3.1.3 The moisture, oil content and color change of FFs
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