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Article

Characterization of Volatile Component Changes in Jujube Fruits during Cold Storage by Using Headspace-Gas Chromatography-Ion Mobility Spectrometry

by
Lvzhu Yang
1,2,
Jie Liu
1,2,
Xinyu Wang
1,2,
Rongrong Wang
3,*,
Fang Ren
4,
Qun Zhang
2,
Yang Shan
2 and
Shenghua Ding
1,2,*
1
Longping Branch Graduate School, Hunan University, Changsha 410125, China
2
Provincial Key Laboratory for Fruits and Vegetables Storage Processing and Quality Safety, Agricultural Product Processing Institute, Hunan Academy of Agricultural Sciences, Changsha 410125, China
3
College of Food Science and Technology, Hunan Agricultural University, Changsha 410128, China
4
G.A.S. Department of Shandong Hanon Science Instrument Co., Ltd., Jinan 253000, China
*
Authors to whom correspondence should be addressed.
Molecules 2019, 24(21), 3904; https://doi.org/10.3390/molecules24213904
Submission received: 20 September 2019 / Revised: 28 October 2019 / Accepted: 28 October 2019 / Published: 30 October 2019
(This article belongs to the Special Issue Volatile Compounds and Smell Chemicals (Odor and Aroma) of Food)
Browse Figures
Versions Notes

Abstract

:
Volatile components in jujube fruits from Zizyphus jujuba Mill. cv. Dongzao (DZ) and Zizyphus jujuba Mill. cv. Jinsixiaozao (JS) were analyzed under different cold storage periods via headspace-gas chromatography-ion mobility spectrometry (HS-GC-IMS). Results identified 53 peaks that corresponded to 47 compounds and were mostly alcohols, aldehydes, esters, and ketones. Differences in the volatile components of jujube fruits were revealed in topographic plots and fingerprints. For DZ, 3-pentanone was the characteristic component of fresh fruits. After storage for 15 days, dipropyl disulfide became the most special substance. Moreover, when stored for 30 and 45 days, the fruits had some same volatile components, like 2-pentyl furan and diallyl sulfide. However, for DZ stored for 60 days, esters were the prominent constituent of the volatile components, simultaneously, some new alcohols appeared. For JS, 2-ethyl furan was the representative of fresh fruits, and 2-butoxyethanol content was the most abundant after 15 and 30 days of storage. Different from that in DZ, the content of ester in JS increased after storage for 45 days. Substances such as amyl acetate dimer, methyl salicylate, and linalool greatly contributed to the jujube flavor during the late storage period. Principal component analysis (PCA) showed that fresh samples and refrigerated fruits were effectively distinguished. Heat map clustering analysis displayed the similarity of volatile components in different samples and was in accordance with PCA results. Hence, the volatile components of jujube fruits can be readily identified via HS-GC-IMS, and jujube fruits can be classified at different periods based on the difference of volatile components.

1. Introduction

Jujube (Zizyphus jujuba Mill) tree belongs to the Rhamnaceae family, which is indigenous to China and is distributed worldwide, in places such as Asia, northern Africa, southern Europe, the Middle East, and the southwestern USA. This tree has a history of more than 4000 years, with over 700 cultivars found in China [1,2,3]. Phytochemical analytical studies showed that jujube fruits are rich in nutrients, including fiber, sugars, organic acids, amino acids, vitamins, and trace minerals [4]. They also contain high levels of functional components, such as polysaccharides, triterpene acids, phenolics, and cyclic nucleotides, which exhibit multiple health-promoting properties, such as antioxidant and anti-inflammatory properties and liver protection [5,6,7,8,9]. Recognized for its delicious taste and health beneficial properties, jujube fruits have been consumed for thousands of years as ordinary fruits and Chinese traditional medicine.
In addition to their nutritional and biological activity, jujube fruits are favored as food by consumers due to their unique flavor. Fresh jujube fruits show an extraordinary flavor, but they are highly perishable when not handled properly due to their high moisture content, which leads to the loss of their commercial value. Cold storage is a common means of delaying the deterioration of quality and prolonging shelf-life effectively, which can affect the physicochemical properties of jujube fruits. Liu et al. found that the contents of chlorophyll, ascorbic acid, and soluble solids in fresh-cut jujubes without any treatment were reduced after storage at 4 °C for a certain period [10]. Kou et al. [11] reported that when jujube fruits were stored at 0 °C, the contents of total soluble solids, ascorbic acid, and chlorophylls continuously declined, and the anthocyanin content firstly increased and then decreased. Furthermore, Günther et al. [12] studied kiwifruit and found that cold storage also affected flavor. Simultaneously, changes in post-harvest metabolic and anaerobic environment greatly influence the fruit flavor, anaerobic conditions can enhance the flavor quality of fruits by producing certain aromatic compounds during storage [13]. Aroma profiles are important characteristics to evaluate the quality of fruits. Several studies have reported that the volatile compounds of jujube fruits are affected by many factors, such as growth period [14], extraction methods [15], the load [16], and processing methods [17,18,19,20]. However, few reports have been associated with changes in volatile compounds of jujube fruits during cold storage, which should be considered. The difference in volatile compounds among different periods of jujube fruit cold storage is unclear. Therefore, the purpose of this study was to monitor the changes in flavor and identify its characteristics at different times.
Ion mobility spectrometry (IMS) is an instrumental analytical technique of separating the ions of detected substances based on their ion mobility velocity under atmospheric pressure [21]. It is a convenient and efficient instrument with the advantages of simple sample preparation, easy operation, high sensitivity, and quick analytical speed. Even trace volatile compounds can also be detected in a short time [22,23]. Furthermore, ion mobility notably allows the separation of isomers and isobaric compounds, which cannot be separated even with ultra-high resolution instruments [24]. At first, compounds extracted from the sample enter the ionization chamber directed by a carrier gas, and the analyte is charged after being ionized. Then, a series of reactions occur and reactant ions [H+(H2O)n] are generated. In an IMS instrument, if the proton affinity of the analyte is higher than the proton affinity of water, it will react with the reactant ions. Based on the content of the analyte, their chemical nature or the drift tube temperature, product ions such as protonated monomers or proton-bound dimers were produced [25]. Subsequently, analyte ions enter the drift region through the Bradbury–Nielsen–Shutter. Analyte ions react against the reverse drift gas under the action of the electric field and migrate to the right end to reach the right detector, the drift velocity of ions depends on their charge, mass, and shape [26]. Finally, the Faraday–Plate detects ions and outputs electrical signals. The results are expressed in terms of voltage units. IMS has been used for chemical warfare agents [27], illicit drug detection [28], analysis of explosives [29], and environmental monitoring [30]. The instrument is highly sensitive to high electronegativity and high proton affinity compounds, which can detect a large number of compounds from different chemical families, such as alcohols, aldehydes, aromatics, esters, and ketones [30]. Combining IMS with other instruments is a good way to increase its advantages and produce a good analysis result. In recent years, HS-GC-IMS has been extensively applied to investigate volatile compounds in food science, such as Tricholoma matsutake Singer [22], jujube fruits [31], eggs [26], Iberian ham [32,33], and honey [25]. As a consequence, HS-GC-IMS could be used to identify the volatile components of jujube fruits at different periods.
In this study, HS-GC-IMS was used to analyze the variations in the volatile compositions of jujube fruits at different storage periods, and the fingerprints were established to confirm the characteristic substance of each period. The results will provide a new method for studying the flavor of jujube fruits, which will help to rapidly select the best storage time of jujube fruits.

2. Results and Discussion

2.1. Volatile Components Identification of All Samples at Different Storage Periods

The aromatic components of fruits undergo many complicated changes during storage, such as vitamin degradation and phenol oxidation, resulting in changes in fruit flavor. Rodrigo et al. [34] found that the aroma of peaches was related to storage conditions and fruit quality characteristics. As the refrigeration progressed, the aroma of peaches dropped considerably, and the flavor and fruit sweetness, juiciness, and texture were strongly correlated. In this study, the volatile components of jujube fruits at different storage periods were determined by HS-GC-IMS. The samples were ionized in the column and then identified using ion mobility systems based on retention and drift times. The qualitative analysis of volatile components in jujube fruits is shown by numbers in Figure 1, where the ordinate represented the retention time, and the abscissa represented the drift time. A total of fifty-three peaks, forty-seven components were identified from the GC×IMS library (Figure 1 and Table 1), including fourteen alcohols, six aldehydes, nine esters, six ketones, two organic acids, two furans, three pyrazines, four sulfur-containing compounds, linalool oxide, and 2-methoxy-4-cresol. Among them, sulfur-containing compounds, linalool oxide, and 2-methoxy-4-cresol were detected in jujube fruits for the first time. This finding may be ascribed to the differences in detection methods and essential differences of raw materials. The identified components are listed in Table 1, which includes the compound name, CAS number, molecular formula, molecular weight, retention index, retention time, and drift time. Moreover, other substances with signals were detected but could not be determined were not listed. When moving through the drift region, due to the formation of adducts between the analyzed ions and neutral molecules (such as dimers and trimers), multiple signals were observed for a single compound [35]. The compounds of 1-octen-3-one, 3-hydroxy-2-butanone, 1-pentanol, heptanal, amyl acetate, and ethyl propanoate exhibited two peaks due to the presence of both monomer and dimer.

2.2. Differential Analysis of the Topographic Plots of Volatile Components in Jujube Fruits at Different Storage Periods

For an intuitive observation and comparison, topographic plots were used to characterize the substances of different jujube fruits during storage. From the 3D topographic plot (Figure 2), it can be clearly observed that with prolonged storage periods, the content of some compounds decreased, and new substances were formed. For DZ, some of the volatile components in the yellow circles disappeared after 15 days of storage but new peaks appeared after 60 days. Moreover, new peaks with high retention time were found after 45 days of storage, as indicated by the black circles (Figure 2A). For JS, more new peaks appeared when the storage time was extended to 45 days (Figure 2B). Hence, compared with fresh jujube fruits, volatile components were formed during the storage process [36]. During fruit ripening, the production of aroma volatiles (especially esters) was regulated by ethylene signaling pathways. Moreover, the production of volatile aroma components was strongly hampered in ethylene-suppressed fruits [37]. It could be inferred that after a certain time of refrigeration, the increase in ethylene synthesis led to more aroma components.
Considering that the 3D spectrum was rough, the overhead view was used for comparison, as represented in Figure 3. Different volatile organic components (VOCs) were different points in the picture, which was highly convenient for observation and analysis. The red vertical line at the abscissa was the reactive ion peak (RIP) at normalized drift times for DZ and JS of 7.79 and 7.81, respectively. The differential contrast model was used to compare the differences among the samples. The fresh sample was selected as the reference, and the spectrum of the other samples deducted the reference. The background after deduction was white showed that the VOCs were the same. Red spots indicate that the content of the substance was higher than the reference, and blue spots indicate that the content was lower than that of the reference. Compared with that of untreated fruits, more red spots are located in the retention time range of 900–1400 s of DZ after storage, and the VOCs changed inconspicuously in the retention time range of 100–600 s at the topographic plot (Figure 3A). For JS, many red spots appeared, and the entire retention time was covered. Especially after 45 days, most of the signals were much higher than that of fresh fruits. This finding indicated that the VOCs of two species varied at different refrigeration times and were affected by variety when the fruits were under similar conditions. Further ripening of the jujube fruits during storage promoted the synthesis of certain volatile components. The formation of fruit flavor was a dynamic process in which the fruit continuously synthesized volatile aroma substances [38]. In the post-harvest ripening stage of bananas, the ester content in the yellow ripening period increased, and the alcohol content in the over-ripe period increased [39].

2.3. Fingerprints of VOCs in Jujube Fruits at Different Storage Periods

Although the topographic plots showed the tendency of volatile components, it is difficult to make an accurate judgment for the dense material on the map. The use of fingerprint was a good way to solve this problem. According to the peak signal of the topographic plots, the fingerprints of jujube fruits were formed (Figure 4 and Figure 5). In the fingerprints, each row represents the entire signal peak of one sample, and each column represents the same substance in different samples. Each cell represents the content of a substance at different times. Colors represent the content of volatile compounds. The brighter the color, the higher the content. Two compounds with the same name in the fingerprints were the monomers and their dimers. The drift time of dimers was increased due to their proton affinity and higher content [40]. By utilizing the fingerprints, the VOCs between different samples can be compared intuitively, moreover, the dynamic changes of each substance can be revealed. The unidentified substances are represented by numbers in the fingerprints. During the whole storage period, the volatile components detected in JS were more than those in DZ, which may be caused by the differences in the varieties and genetic factors of the two jujube fruits.
The VOCs of the jujube fruits constantly changed during storage. By comparing the intensity of spot for the profiles of VOCs at different stages, changes in the substances during storage (increased, decreased, disappeared or fluctuated) can be determined. Substances in the green-framed areas of Figure 4A and Figure 5A were the most abundant in fresh jujube fruits but dramatically decreased or even disappeared during the later period of storage. For DZ, 2-propanol, 3-methyl-2-butanol, 3-pentanone, and heptanal dimer were detected, while amyl acetate, ethyl octanoate, (E)-2-octenal, and 1-pentanol dimers were detected in JS. Simultaneously, it can be clearly seen that, compared to other periods, the relative amount percentage of these substances was the highest in fresh fruits during the entire storage period (Table S1). This finding may be due to the degradation of these substances during refrigeration.
By contrast, with prolonged storage time, some new compounds appeared, which showed strong signal intensity and bright color (the red-framed areas of Figure 4A and Figure 5A). These substances included linalool, ethyl isobutanoate, propyl acetate, ethyl ester, and methyl salicylate. This finding may be attributed to the complex physiological metabolism in fruits during storage, which mainly were a series of reactions, such as fatty acid, amino acid, and carbohydrate metabolism. Esters, which are mainly derived from the lipoxygenase pathway and amino acid metabolism are associated with the “fruity” attributes of fruit flavor, and its levels typically increase in the later periods of the ripening process [41]. Moreover, peaches stored after pre-storage were sweeter and had higher levels of propyl acetate, amyl acetate, and 2-methyl-1-butanol than control fruits [42]. The VOCs of the unframed part in the fingerprints presented few changes during the whole storage period, indicating that these substances were relatively stable during the cold storage of jujube fruits.

2.4. Changes of VOCs during Different Storage Periods

Changes in volatile components during different storage periods have been observed from the fingerprints. To compare the changes of each substance clearly, the fingerprint of each jujube fruit was divided into two parts based on the characteristic volatiles presented in different parts (Figure 4B and Figure 5B). The representative VOCs detected in fresh DZ and JS were found in the region a of Figure 4B and region c of Figure 5B, respectively. The same ingredients included 1-octen-3-one, 2-ethylfuran, (E)-2-octenal, (E)-2-heptenal, 2,3-butanedione, (E)-3-hexen-1-ol, and heptanal. Chen et al. [43] studied ten different varieties of Chinese jujube fruits and found that aldehydes had the highest content and contributed to the aroma of fresh jujube fruits, moreover, (E)-2-hexenal, hexanal, (Z)-2-heptenal, benzaldehyde, and (E)-2-nonenal were the common volatile components in fresh jujube fruits. This finding differed from our results, presumably due to differences in varieties and detection methods. Heredity can determine precursors, enzymes, and their activity in the formation of flavor components in jujube fruits. Compared with fresh jujube fruits, these parameters decreased significantly after 15 days of storage in DZ and 30 days in JS. Aldehydes significantly affected the flavor of fresh jujube fruits, which generated from the oxidation of fatty acids and the metabolism of amino acids [44]. They can affect the overall aroma of samples at low content for their low odor threshold values [45]. (E)-2-Heptenal was characterized by soap and almond flavor, (E)-2-octenal was associated with roasted, cucumber, nutty, and fatty characteristics, and heptanal has a fishy, nutty and sweet apricot note flavor [46].
Many different changes of VOCs have been observed during storage. As shown in Figure 4B, the contents of 3-methyl-2-butanol, heptanal dimer, 2-ethyl-6-methylpyrazine, dimethyldisulphide, (E)-3-hexen-1-ol, (E)-2-octenal, (E)-2-heptenal, 2-ethylfuran, and 1-octen-3-one dimer in fresh DZ were much higher than that after storage. During storage, their contents continuously declined, (E)-2-octenal, (E)-2-heptenal, 2-ethylfuran, and 1-octen-3-one dimer vanished after storage. It showed that 2-methylpropanoic acid, 3-pentanone, 2,3-butanedione, 2-methoxy-4-cresol, and 1-octen-3-one were important for the flavor of fresh DZ. The contents of 3-pentanone and 2,3-butanedione were initially the highest in DZ, which decreased significantly after a certain period of storage and increased slightly after 60 days, while in JS, 3-pentanone with low content in fresh fruits. Low-carbon saturated ketones have a special aroma, and many ketones have been found in cheese, which are the main volatile constituents of cheese with a unique flavor [47]. In addition, it can be observed that the change of 2-methylpropanoic acid was consistent with 3-pentanone and 2,3-butanedione. However, 2-methylbutanoic acid was different from them, it appeared with a strong signal at 60 days, which was not detected during the storage time of 0–45 days. Additionally, its relative amount percentage was up to 100% when stored for 60 days, before this period, this value was basically less than 10% (Table S1). Interestingly, only these two short-chain organic acids were identified in the two cultivars of jujube fruits. In JS, they appeared in storage for 45 days and then enhanced (Figure 5B). Organic acid is derived from the oxidation of fatty acids, which affects the flavor of jujube fruits [48]. During ripening, fruits undergo an esterification reaction, consuming a large amount of acid. When the jujube fruits are ripe, the amount of acids becomes low [49]. However, long-term storage resulted in the oxidation and decomposition of fatty acids. Besides, it should be noted that high content of organic acids can damage fruit quality and deteriorate the flavor of jujube fruits. In addition, processing methods also affect the content of organic acids. Chen et al. reported that acids were the major group among all the volatile chemicals in dried jujube fruits. Moreover, pre-treatment of jujube fruits with 5% CO2 can induce a decrease in acid content during drying, which is mainly caused by a decrease in lauric acid and nutmeg acid content [18]. 2-Methoxy-4-cresol was a newly detected component in the VOCs of jujube fruits, which appeared with high content in fresh DZ but not found in fresh JS and showed a pleasant clove-like flavor [50]. For DZ, its signal intensity was almost invisible after storage for 15–30 days, then gradually strengthened. In JS, it appeared after 45 days with a bright color in the fingerprint plot.
Some volatile compounds, mostly including esters, were rare in fresh samples of two jujube fruits but abundant in the later storage period, which were the most important volatile components at the end of storage (Figure 4B and Figure 5B), including hexyl acetate, ethyl acetate, ethyl propanoate, propyl acetate, ethyl isobutanoate, and methyl salicylate. Most of these compounds show a typical fruity or floral flavor, which may greatly affect the aroma of fruits. Zhou et al. found that low-temperature treatment could prevent the loss of aromatic esters during the ripening of ‘Nanguo’ pears at room temperature [51]. During the cold storage period, although complete ripening of the jujube fruits was inhibited, ripening proceeded at a slower pace, thus generating more esters. It can be found that the relative amount percentage of ethyl propanoate, propyl acetate, ethyl isobutanoate, and methyl salicylate was lower in the two cultivars of jujube at 0–30 days of storage and increased after 45 days. Moreover, it is worth noting that long-term storage at low temperatures inhibits the activity of enzymes, such as lipoxygenase and alcohol acyltransferase, which are the key enzymes in the aroma metabolism of fruits esters, resulting in a reduction in fruit flavor [52]. The jujube fruits in this investigation were refrigerated for 45–60 days, showed a good flavor. However, some substances had an adverse effect on the flavor of jujube fruits when the content was too high. The odor of high content of ethyl acetate was not described as “fruity” but rather as an off-flavor. Its elevated levels are usually associated with the over-ripeness and/or anaerobic metabolism of the fruit [53].
Two alcohols, including linalool and citronellol, showed the same variation tendency of the whole storage period, which was not detected at the initial stages of storage but appeared at a later time. For DZ they were detected with high signal intensity when the storage time was 60 days, but they appeared earlier in JS, showing a high content after 45 days of storage. This condition might have occurred because, with the prolongation of storage time, the glycoside precursors and other precursors for linalool and citronellol synthesis were formed in the jujube fruits. He et al. found that the content of linalool was closely related to the temperature of lemon-flavored hard tea during storage. At room temperature, its content increased slightly but decreased significantly when the temperature increased [54]. An interesting phenomenon was that the monoterpene alcohol of transgenic citrus peels could induce resistance against fungal invasion [55]. Therefore, whether jujube fruits were infected by fungi in the late storage period was uncertain, and the increased in linalool and citronellol content may be related to the self-defensive mechanism of fruits.
Meanwhile, 2-ethylpyrazine and acetylpyrazine with weak signal in fresh jujube fruits, and eye-catching signals have emerged in the fingerprints until storage for 45 days. Pyrazines were the characteristic flavor of the Maillard reaction and were often found in dried jujube fruits, which show a roasted or nutty flavor [56]. During drying, heat treatment could accelerate the progress of the Maillard reaction, resulting in more furans and pyrazines were formed. In this study, jujube fruits were stored at low temperature, which did not provide a good condition for the formation of pyrazines compared with drying.
Some substances with the highest content during the middle of storage. Amyl acetate, 2-pentyl furan, 2-butoxyethanol, diallyl sulfide, heptanal, 1-pentanol dimer, and (E)-2-undecenal were the characteristic VOCs when DZ was stored at 4 °C for 15–30 days. Among these compounds, 2-pentyl furan, 2-butoxyethanol, and (E)-2-undecenal were the characteristic VOCs in JS in the same period. Heptanal, 2-methyl-1-propanol, and 2-butoxyethanol remained in DZ and were maintained at a high content during the subsequent storage period. In addition, the content of furfuryl alcohol continued to increase during storage, reaching a maximum of 60 days. Linalool and citronellol were synthesized in large quantities at the late storage stage. Most alcohols showed increased contents in the later stages, indicating that aldehydes were reduced and converted into corresponding alcohols at this stage, thus promoting the esterification of alcohols with acids produced by anaerobic respiration during storage. However, the signal intensity of 2-butoxyethanol disappeared later in JS, but the heptanal dimer was largely accumulated.
Dipropyl disulfide was only detected when the storage period was 15 days in DZ samples, but its content increased in JS after storage for 45 days. Three other sulfide compounds, namely, dimethyl sulfide, diallyl sulfide, and dimethyldisulphide were identified. The signal of dimethyl sulfide was observed in the whole storage process, and minor changes in signal intensity were observed in all samples. Diallyl sulfide and dimethyldisulphide were the characteristic VOCs of fresh JS and DZ, respectively. Sulfur-containing compounds are widely found in vegetables [57]. Diallyl sulfide was the characteristic flavor of garlic, dipropyl disulfide was associated with onion, and dimethyldisulphide was abundant in the volatile components of cabbage. Sulfur-containing compounds commonly arise from sulfur-bearing precursors, and in jujube fruits, sulfur-containing amino acids primarily exist, such as methionine. Low content of sulfur compounds can enhance the aromatic flavor of jujube fruits. Pyrazines and sulfur-containing compounds had low odor thresholds, and they acted with other compounds to enhance the overall aroma in jujube fruits [58,59]. Some substances, such as ethyl propanoate, amyl acetate dimer, 2-methyl-3-heptanone, and 3-hydroxy-2-butanone, existed in all periods of two jujube fruits, and the signal had minor changes.

2.5. PCA of Jujube Fruits at Different Storage Periods

PCA is a multivariate statistical analysis method that uses multiple variables to linearly transform to select a few significant variables. The main features are extracted for linear analysis by reducing the dimensionality of the data, and the main information is retained in several unrelated principal components [60]. Generally, when the cumulative contribution rate reaches 60%, PCA model is selected as the separation model [61]. Li et al. found the volatile components of different tissue parts of tomato showed disparate distributions among four varieties by PCA [62]. In this study, PCA was performed to analyzed the variation of 53 identified volatile compounds in the two cultivars of jujube. Firstly, all data were normalized to calculate the covariance matrix and its eigenvalues and eigenvectors, which derived from the corresponding peak area of each volatile component of jujube fruits. Then, the principal component was determined, and the corresponding contribution rate was calculated. Finally, a classification program was adopted in a smaller space to illustrate the relationship of jujube fruits during different storage periods. The results were shown in Figure 6 and Figure 7, a clear separation trend of jujube fruits at different storage periods in two principal components can be observed.
As shown in Figure 6 and Figure 7, the first principal component (PC1) and the second principal component (PC2) explained 82% and 84.6% of the total variables of the model in DZ and JS, respectively. A remarkable difference was found between fresh jujube fruits and refrigerated ones in volatile components. On the axis, a large distance is found between fresh DZ and the other samples, the four other samples in different storage periods can be distinguished easily. Among them, the ones stored for 15 days and 30 days are closer (Figure 6A), which indicates that the volatile components of DZ in these two periods are similar. In JS, changes of the sample are distributed from right to left in the PCA, as the storage time was extended (Figure 7A). Jujube fruits stored for 0–30 days are distributed in the right quadrant, while the ones stored for 45–60 days are in the left quadrant with a higher similarity. Based on the PCA, the jujube fruits at different periods of two cultivars are separated well. Additionally, some information on the volatile compounds was lost during the statistical re-modeling. As shown in the loading plots (Figure 6B and Figure 7B), the length of the arrow reflects the extent of information loss, the shorter the arrow, the more information lost [20]. For example, linalool oxide and 5-methyfurfural suffered the most with the loss of their information of DZ, but in JS, dimethyl sulfide loss was the highest.
To get more details, the biplots were used (Figure 6C and Figure 7C). From the biplots, it can be clearly seen that 2-methoxy-4-cresol, heptanal and some ketones (1-octen-3-one and 2,3-butanedione) were positively related to the fresh DZ. However, for JS, 3-hydroxy-2-butanone contributed a lot to the flavor of the fresh fruits. When storage for 15 days, (E)-undecenal and 2-penty furanl were closely related to the DZ, 2-butoxyethanol was positively related to JS. In the biplots, the relationship between specific volatile components and jujube fruits in a certain period was demonstrated. While at the end of the storage, most esters were positively related to the jujube fruits, while 2-methylbutanoic acid and 2-methylpropanoic acid were found to be positively related to JS. These results were in accordance with the above fingerprints.

2.6. Cluster Analysis of VOCs of Jujube Fruits from Different Periods Based on the Heat Map

To further understand the differences in VOCs of two jujube fruits at different storage periods, cluster analysis was performed using a heat map (Figure 8). According to the vertical direction of the heat map, all samples were classified into two main categories. Jujube fruits from JS that were stored for 45 and 60 days and those from DZ that were stored for 60 days were clustered together to form a group (J45, J60, and D60 in Figure 8), the rest of the samples were clustered together to form another group (J0 to J30, and D0 to D45 in Figure 8). At the late period of storage, the volatile components of DZ were very similar to those in JS and were quite different from those in the early storage period. The second group can also be divided into four categories. Among them, fresh jujube fruits from different cultivars were clustered into two different groups. Jujube fruits from JS, which were stored for 15 and 30 days, were grouped together (J15 and J30 in Figure 8), and those from DZ were stored for 15, 30 and 45 days, which were from the same class (D15, D30, and D45 in Figure 8).
According to the above results, we can infer that the volatile components of DZ and JS largely differ due to the differences in their varieties. The content of 1-octen-3-one and 2-methoxy-4-cresol was higher in fresh DZ than that in JS. Samples from D60, J45, and J60 were similar in 2-pentyl furan, 1-octen-3-one, ethyl acetate and propyl acetate content. Cluster analysis show that the storage time greatly influenced the volatile components of jujube fruits, and the flavor of jujube fruits varied during different periods. This finding was consistent with the fingerprint and PCA.

3. Materials and Methods

3.1. Experimental Materials

Two cultivars of jujube fruits were used for this experiment, namely, Zizyphus jujuba Mill. cv. ‘Dongzao’ and Zizyphus jujuba Mill. cv. ‘Jinsixiaozao’. Fresh DZ were harvested in September 2018, from a garden in Zhanhua County, Shandong province, China (118°7′56″ E, 37°4′53″ N). JS were harvested from an experimental field station in Qidong County, Hengyang City, Hunan Province, China (111°59′14″ E, 26°48′3″ N). After harvest, they were transported to the laboratory within 24 h with a cold chain. Jujube fruits with intact appearance, similar morphological properties, and free from visible blemish, disease, and mechanical injury were selected as raw materials. Samples were stored at 4 °C with a humidity of 90% and obtained every 15 days until storage for 60 days. The collected samples (500 g) were de-nucleated and freeze-dried, then the dried jujube fruits were crushed into powder with a grinder (RoyalstarRS-FS1401, Zhongshan Rongshida Kitchen & Bathroom Appliance Co., Ltd., Zhongshan, China), after that, collected samples were passed through a 60-mesh sieve, sealed, and stored at −80 °C for subsequent analyses.

3.2. Apparatuses

Vacuum freeze dryer LGJ-25C (Beijing Sihuan Instrument Factory Co., Ltd. Beijing, China), HS-GC-IMS instrument: the GC-IMS FlavourSpec® Gesellschaft für Analytische Sensorsysteme mbH (G.A.S., Dortmund, Germany). The device was equipped with an autosampler unit (CTC Analytics AG, Zwingen, Switzerland).

3.3. HS-GC-IMS Analysis

Analyses of jujube fruits were performed using the HS-GC-IMS instrument as described by Xin et al. with slight modifications [31]. Specifically, 1.0 g of fine powder was weighed and placed into a 20 mL headspace-glass sampling vial. The samples were incubated at 60 °C for 10 min. After incubation, 500 μL of headspace was automatically injected into the injector under splitless injection mode with a syringe at 85 °C. The GC was performed with an RTX-WAX (30 m, 0.53 mm ID, 1 μm film thickness, Restek Co., Bellefonte, PA, USA) capillary column to separate volatile components and coupled to IMS at 45 °C. Nitrogen (99.999% purity) was used as the carrier gas under the following programmed flow: 2 mL/min for 2 min and maintenance for 8 min, 20 mL/min for 10 min and 50 mL/min for 15 min, and flow then stopped. The instrument was performed under ambient pressure. The analytes were separated at 40 °C in the column and then ionized in the IMS ionization chamber of 45 °C. The drift gas (nitrogen gas) was set at 150 mL/min.
In this experiment, the instrument was standardized with n-ketones whose retention index was linear, because IMS had no response to alkanes. The retention index (RI) of volatile compounds was calculated by using n-ketones C4-C9 (Sinopharm Chemical Reagent Beijing Co., Ltd., Beijing, China) as external references. Volatile compounds were identified by comparing RI and the drift time (the time it takes for ions to reach the collector through drift tube, in milliseconds) of standard in the GC-IMS library (Gesellschaft für Analytische Sensorsysteme mbH, Dortmund, Germany).

3.4. Data Analysis

The instrumental analysis software included laboratory analytical viewer (LAV, G.A.S., Dortmund, Germany), three plug-ins (G.A.S., Dortmund, Germany), and GC × IMS library search, which can be used for sample analysis from different perspectives. The spectra were analyzed using the LAV software, and the difference profiles and fingerprints of volatile components were constructed using the Reporter and Gallery plug-ins. The NIST and IMS databases were built into the software for qualitative analysis of the materials. The principal component analysis (PCA) and heat map were used for clustering analysis of samples. The heat map and PCA were generated using Origin 2018 software (OriginLab, Northampton, MA, USA).

4. Conclusions

In this study, 47 volatile compounds were identified in jujube fruits at different storage periods at 4 °C via HS-GC-IMS. Among the identified substances, alcohols, esters, ketones and aldehydes were predominant, and a few organic acids were found. At the same time, some new compounds were found, namely, four sulfur-containing compounds (dimethyldisulphide, dimethyl sulfide, dipropyl disulfide, diallyl sulfide), linalool oxide, and 2-methoxy-4-cresol. The differences of the volatile compounds at different cold storage times between varieties and individuals were revealed by using topographic plots and fingerprints. Aldehydes and ketones were the main volatile components in fresh fruits and the early storage, while esters changed obviously and became the main VOCs at the end of the storage, which synthesized in large quantities at 45 days (JS) and 60 days (DZ), respectively. According to the PCA and heat map, the samples from different periods were well separated, the stored jujube fruits kept a long distance from the fresh one on the PCA map. The results showed that HS-GC-IMS could identify the characteristic volatile compounds of jujube fruits. It could provide an efficient method for determining the storage period of jujube fruits due to simple sample preparation steps and shorter analysis time.

Supplementary Materials

The following are available online, Table S1: Relative amount percentage (%) of the same compound at different refrigerated times.

Author Contributions

L.Y. performed the experiments, conducted the analyses, and wrote the original draft. S.D. and R.W. conceived the experiment. J.L., X.W., Q.Z., F.R., and Y.S. critically revised the manuscript from format to content.

Funding

The study was supported by the National Natural Science Foundation of China (31501543), Key Research Project of Hunan Province, China (2017NK2112), and Agricultural Science and Technology Innovation Project of Hunan Province, China (2019JG01, 2019TD04).

Conflicts of Interest

The authors declare that there is no conflict of interest.

Abbreviations

HS-GC-IMSheadspace-gas chromatography-ion mobility spectrometry
DZZizyphus jujuba Mill. cv. Dongzao
JSZizyphus jujuba Mill. cv. Jinsixiaozao
VOCsvolatile organic compounds
PCAPCA principal component analysis

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Sample Availability: Samples of the compounds are not available from the authors.
Molecules 24 03904 g001 550
Figure 1. Ion migration spectra of jujube fruits stored for different times at 4 °C. The numbers are identified volatile components.
Figure 1. Ion migration spectra of jujube fruits stored for different times at 4 °C. The numbers are identified volatile components.
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Figure 2. 3D-topographic plots of jujube fruits at different times. Jujube fruits are Dongzao shown in (A), D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. Jujube fruits are Jinsixiaozao shown in (B), J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively.
Figure 2. 3D-topographic plots of jujube fruits at different times. Jujube fruits are Dongzao shown in (A), D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. Jujube fruits are Jinsixiaozao shown in (B), J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively.
Molecules 24 03904 g002
Molecules 24 03904 g003 550
Figure 3. 2D-topographic plots of jujube fruits at different times. Jujube fruits are Dongzao shown in (A), D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. Jujube fruits are Jinsixiaozao shown in (B), J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively.
Figure 3. 2D-topographic plots of jujube fruits at different times. Jujube fruits are Dongzao shown in (A), D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. Jujube fruits are Jinsixiaozao shown in (B), J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively.
Molecules 24 03904 g003
Molecules 24 03904 g004 550
Figure 4. Fingerprint of volatile compounds of Dongzao samples. (A) Fingerprint of all Dongzao, (B) two parts of the fingerprint.
Figure 4. Fingerprint of volatile compounds of Dongzao samples. (A) Fingerprint of all Dongzao, (B) two parts of the fingerprint.
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Figure 5. Fingerprint of volatile compounds of Jinsixiaozao samples. (A) Fingerprint of all Jinsixiaozao, (B) two parts of the fingerprint.
Figure 5. Fingerprint of volatile compounds of Jinsixiaozao samples. (A) Fingerprint of all Jinsixiaozao, (B) two parts of the fingerprint.
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Molecules 24 03904 g006a 550Molecules 24 03904 g006b 550
Figure 6. PCA analysis of Dongzao. (A) score plot of the first two principal components, D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. (B) loading plot of different variances, (C) biplot of PCA.
Figure 6. PCA analysis of Dongzao. (A) score plot of the first two principal components, D0, D15, D30, D45, and D60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. (B) loading plot of different variances, (C) biplot of PCA.
Molecules 24 03904 g006aMolecules 24 03904 g006b
Molecules 24 03904 g007a 550Molecules 24 03904 g007b 550
Figure 7. PCA analysis of Jinsixiaozao. (A) Score plot of the first two principal components, J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. (B) Loading plot of different variances, (C) biplot of PCA.
Figure 7. PCA analysis of Jinsixiaozao. (A) Score plot of the first two principal components, J0, J15, J30, J45, and J60 represent refrigeration for 0, 15, 30, 45, and 60 days, respectively. (B) Loading plot of different variances, (C) biplot of PCA.
Molecules 24 03904 g007aMolecules 24 03904 g007b
Molecules 24 03904 g008 550
Figure 8. Heat map and cluster analysis of jujube fruits at different periods. D0, D15, D30, D45, and D60 represent DZ refrigerated for 0, 15, 30, 45, and 60 days, respectively; J0, J15, J30, J45, and J60 represent JS refrigerated for 0, 15, 30, 45, and 60 days, respectively.
Figure 8. Heat map and cluster analysis of jujube fruits at different periods. D0, D15, D30, D45, and D60 represent DZ refrigerated for 0, 15, 30, 45, and 60 days, respectively; J0, J15, J30, J45, and J60 represent JS refrigerated for 0, 15, 30, 45, and 60 days, respectively.
Molecules 24 03904 g008
Table
Table 1. The information on identified compounds of jujube fruits.
Table 1. The information on identified compounds of jujube fruits.
NO.CompoundCAS#FormulaMWRIRt (Sec)Dt
(RIP Relative)		CommentIdentification Approach
1Furfuryl alcoholC98000C5H6O298.11661.41226.8861.1116 RI, Dt
2Octan-2-olC123966C8H18O130.21401.0704.6881.4313 RI, Dt
3(E)-3-Hexen-1-olC928972C6H12O100.21327.8562.2411.2529 RI, Dt
42-ButoxyethanolC111762C6H14O2118.21400.9704.4001.5715 RI, Dt
52-HeptanolC543497C7H16O116.21291.4500.1901.3920 RI, Dt
61-PentanolC71410C5H12O88.11262.0456.4111.2576monomerRI, Dt
71-PentanolC71410C5H12O114.21262.0456.4111.5164dimerRI, Dt
82-Methyl-1-butanolC137326C5H12O88.11215.7397.4451.2367 RI, Dt
92-HexanolC626937C6H14O102.21194.9374.1601.2880 RI, Dt
103-Methyl-2-butanolC598754C5H12O88.11124.2306.5041.4417 RI, Dt
112-PropanolC67630C3H8O60.1908.5188.3391.2264 RI, Dt
122-Methyl-1-propanolC78831C4H10O74.11090.2279.7041.3727 RI, Dt
13LinaloolC78706C10H18O154.31496.8896.9131.2161 RI, Dt
14CitronellolC106229C10H20O156.31742.81390.3071.3610 RI, Dt
153-OctanolC589980C8H18O130.21397.5697.6571.4073 RI, Dt
16(E)-2-OctenalC2548870C8H14O126.21438.5779.9301.3345 RI, Dt
17(E)-2-HeptenalC18829555C7H12O112.21326.9560.6841.6667 RI, Dt
18HeptanalC111717C7H14O114.21191.5370.3811.3412monomerRI, Dt
19HeptanalC111717C7H14O114.21193.2372.2701.6841dimerRI, Dt
203-MethylbutanalC590863C5H10O86.1917.4190.7411.1796 RI, Dt
21(E)-2-undecenalC53448070C11H20O168.31736.91378.4771.5700 RI, Dt
225-MethylfurfuralC620020C6H6O2110.11562.01027.521.4726 RI, Dt
231-Octen-3-oneC4312996C8H14O126.21308.2527.7161.2773monomerRI, Dt
241-Octen-3-oneC4312996C8H14O126.21308.2527.7161.6826dimerRI, Dt
251-Hydroxypropan-2-oneC116096C3H6O274.11295.3506.3071.2352 RI, Dt
263-Hydroxy-2-butanoneC513860C4H8O288.11298.6511.7791.0710monomerRI, Dt
273-Hydroxy-2-butanoneC513860C4H8O288.11295.5506.6291.3273dimerRI, Dt
282,3-ButanedioneC431038C4H6O286.11021.6233.3751.1507 RI, Dt
293-PentanoneC96220C5H10O86.1989.2215.9611.3600 RI, Dt
302-Methyl-3-heptanoneC13019200C8H16O128.21169.0347.2921.2730 RI, Dt
31Ethyl octanoateC106321C10H20O2172.31401.0704.6881.4841 RI, Dt
32Amyl acetate C628637C7H14O2130.21150.4329.4601.3196monomerRI, Dt
33Amyl acetateC628637C7H14O2130.21134.6315.3341.3240dimerRI, Dt
34Ethyl propanoateC105373C5H10O2102.1942.6197.9471.1418monomerRI, Dt
35Ethyl acetateC141786C4H8O288.1866.3176.9301.3333 RI, Dt
36Hexyl acetateC142927C8H16O2144.21230.8415.5021.4044 RI, Dt
37Ethyl propanoateC105373C5H10O2102.1964.6205.5021.4486dimerRI, Dt
38Propyl acetateC109604C5H10O2102.1968.8207.0901.5065 RI, Dt
39Ethyl isobutanoateC97621C6H12O2116.2970.1207.6191.5604 RI, Dt
40Methyl salicylateC119368C8H8O3152.11732.11368.7331.2162 RI, Dt
412-Methylpropanoic acidC79312C4H8O288.11562.11027.8021.1494 RI, Dt
422-Methylbutanoic acidC116530C5H10O2102.11632.91169.8461.2188 RI, Dt
432-EthylpyrazineC13925003C6H8N2108.11365.8634.5301.1116 RI, Dt
442-Ethyl-6-methylpyrazineC13925036C7H10N2122.21345.4594.9361.1737 RI, Dt
45AcetylpyrazineC22047252C6H6N2O122.11654.41212.8571.1463 RI, Dt
462-Pentyl furanC3777693C9H14O130.21253.1444.1791.2477 RI, Dt
472-EthylfuranC3208160C6H8O96.1975.6209.9001.0454 RI, Dt
48DimethyldisulphideC624920C2H6S294.21074.6268.2021.1262 RI, Dt
49Dimethyl sulfideC75183C2H6S62.1737.5142.1020.9636 RI, Dt
50Dipropyl disulfideC629196C6H14S2150.31356.5616.3301.4603 RI, Dt
51Diallyl sulfideC592881C6H10S114.21118.4301.6871.1088 RI, Dt
52Linalool oxideC60047178C10H18O2170.31417.2737.2071.2585 RI, Dt
532-Methoxy-4-cresolC93516C8H10O2138.21921.71749.1501.1921 RI, Dt
MW: molecular mass; RI: retention index; Rt: retention time; Dt: drift time.

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MDPI and ACS Style

Yang, L.; Liu, J.; Wang, X.; Wang, R.; Ren, F.; Zhang, Q.; Shan, Y.; Ding, S. Characterization of Volatile Component Changes in Jujube Fruits during Cold Storage by Using Headspace-Gas Chromatography-Ion Mobility Spectrometry. Molecules 2019, 24, 3904. https://doi.org/10.3390/molecules24213904

AMA Style

Yang L, Liu J, Wang X, Wang R, Ren F, Zhang Q, Shan Y, Ding S. Characterization of Volatile Component Changes in Jujube Fruits during Cold Storage by Using Headspace-Gas Chromatography-Ion Mobility Spectrometry. Molecules. 2019; 24(21):3904. https://doi.org/10.3390/molecules24213904

Chicago/Turabian Style

Yang, Lvzhu, Jie Liu, Xinyu Wang, Rongrong Wang, Fang Ren, Qun Zhang, Yang Shan, and Shenghua Ding. 2019. "Characterization of Volatile Component Changes in Jujube Fruits during Cold Storage by Using Headspace-Gas Chromatography-Ion Mobility Spectrometry" Molecules 24, no. 21: 3904. https://doi.org/10.3390/molecules24213904

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