1. Introduction
Volatile organic compounds may play a key role as a quality parameter in table grape production due to their contribution to berry flavor [
1]. Several families of volatile compounds, including alcohols, terpenes, esters, C
13 norisoprenoids, C6 compounds, aldehydes, fatty acids, among others, are responsible for the varietal aroma of fruits [
2]. These aromatic compounds may influence consumer preference and acceptance and provide important information about the nutritional value of foods [
3]. Grapes are a popular fruit consumed worldwide and berry development has a complex dynamic process that involves a series of biochemical changes [
1,
4]. Since the content of volatile organic compounds changes during berry development (ripening), harvest time is crucial to provide a fruit of high organoleptic quality [
1].
Berry development follows a double sigmoid curve, which presents three main stages: from berry formation to lag phase (Stage I), from lag phase to veraison (Stage II) and post-veraison (Stage III) [
5]. The first phase is characterized by a period of rapid cell division and the berry expands in volume and accumulates solutes such as tartaric and malic acids but little amounts of sugar [
5]. The second phase is characterized by the slow growth of the berry, the embryo within the seeds matures, the seed coat lignifies, and, finally, the berries start to soften [
5]. The post-veraison period is defined as the resumption of growth, and the significant accumulation of anthocyanin and sugars is carried out in the berries [
5]. The bound glycoside forms of many volatile compounds in grapes, such as C
13 norisoprenoids, C6 compounds and terpenes have been identified and quantified during these stages [
4].
Grape berries are mostly characterized by their terpene composition, predominantly in varieties that are identified by their Muscat aroma [
6]. Terpene composition discriminates among muscat, terpenic and neutral profiles in different grape varieties [
7]. Thus, grapes are classified according to their free monoterpene concentrations into neutral, non-Muscat aromatic and Muscat varieties [
8]. In Muscat grape cultivars, monoterpenes are the primary compounds [
9]. Previous studies have reported differences in volatile organic compounds in berries of different grapevine varieties, including also differences in their composition along berry ripening [
10,
11]. Some recent studies have investigated the evolution of free volatiles from fruit set to berry ripeness in some neutral and non-Muscat aromatic varieties [
10,
12,
13]. Zhang et al. [
13] reported that terpenes content decreased from pre-veraison to veraison, probably due to an inactivation in their biosynthetic pathways, whereas Wu et al. [
14] showed that at pre-softening, the volatile compounds content was regulated by expansion dilution, and berry terpene concentration significantly decreased, resulting in a minimum terpene content at softening. Due to the above, the planning of the harvest date must consider these aspects, based on the characteristics desired by consumers.
The Italia (Vitis vinifera L.) grape variety is widely grown in Marmara, Aegean, Central Anatolia and Southeastern Anatolia regions in Turkey. Italia is a seeded variety characterized by a mid-late ripeness, a vigorous vegetative behavior and a slight Muscat flavor of berries. Bronx Seedless is an interesting variety and preferred by consumers due to its pink berries that are characterized by their strawberry flavor. To our knowledge, there is little available information about the characterization of berry volatile composition of table grapes along berry ripeness, even more in varieties such as Italia and Bronx Seedless. Thus, the aim of this research was to study the changes in varietal volatile organic compounds in Italia and Bronx Seedless table grapes throughout berry ripeness.
3. Discussion
To our knowledge, there is little available information about the study of the volatile composition of table grapes in the scientific literature, neither is there a local contribution from Turkey, whose viticultural production is of the utmost importance as a world supplier. Based on the results exposed, β-ionone presented the highest odor activity value (OAV) in Italia and Bronx Seedless table grapes, which coincided with the findings exposed by Wu et al. [
15]. These authors concluded that β-ionone and octanal may be useful indicators for the improvement of breeding in table grapes. Bronx Seedless grapes presented a higher OAV for (Z)-3-hexenal and cedrol than Italia grapes. These volatile compounds present aromatic descriptors related to green aromas, such as grass and camphor (
Table 8). Based on this, it is probable that to achieve better aromatic quality, Bronx Seedless should be harvested later than Italia.
Bronx Seedless is characterized by its foxy taste, whereas Italia by its Muscat aroma. Methyl anthranilate is considered the most important contributor to its foxy aroma, but this compound is not necessarily identified by SPME due to its high boiling point and low volatility [
12,
16]. In this way, methyl anthranilate was not detected in Bronx Seedless and Italia table grapes in the present study. Wu et al. [
12] reported that foxy aroma varieties presented lower contents of D-limonene, (E)-β-ocimene, geraniol, α-terpineol, neral, terpinolene, geranic acid, linalool, nerol, citronellol, geranial, (Z)-β-ocimene, nonanal and rose oxide II (cis), and higher contents of ethyl benzoate, methyl salicylate, benzyl alcohol, ethyl 3-hydroxybutyrate, ethyl heptanoate, ethyl pentanoate, ethyl hexanoate, 2-hexenoic acid ethyl ester, ethyl acetate, phenylacetaldehyde, ethyl butyrate, ethyl 3-methylbutanoate, ethyl propionate and ethyl octanoate than Muscat aromatic varieties. The current results show that only α-terpineol, neral, geranic acid and linalool presented these differences between Bronx Seedless (foxy taste) and Italia (Muscat taste) variety. Ruiz-García et al. [
17] reported that rose oxide is the key compound to identify and select varieties with a Muscat aroma. Bronx Seedless grapes presented a lower content of rose oxide I (
trans) than Italia grapes. Terpene content at commercial harvest (BBCH-89) in Italia and Bronx Seedless table grapes was lower than 1.0 mg L
−1 (749.44 ± 10.56 and 757.23 ± 67.34 μg L
−1, respectively). In this way, the grapevine varieties could be grouped into Muscat (≥6 mg L
−1), non-Muscat aromatic (1–4 mg L
−1) and neutral varieties (<1 mg L
−1), regarding their monoterpene levels [
8]. Despite the above-mentioned, the Italia and Bronx Seedless varieties could be considered as aromatically neutral based on their terpene levels.
The results exposed showed that esters, fatty acids, terpenes and C6 compounds were the most abundant families of volatile compounds in Italia and Bronx Seedless table grapes, in which hexanoic acid, ethyl 3-hydroxybutyrate, ethyl octanoate, 2-hexenoic acid and octanoic acid exhibited the most important concentrations. Regarding OAVs, the most important family of volatile compounds were C
13-norisoprenoids, followed by esters and C6 compounds. Wu et al. [
15] reported that C6 compounds, terpenes and C
13 norisoprenoids were the main contributors to the aroma in different table grapes obtained from a vineyard located in Shanghai, China. Ubeda et al. [
18] reported that C6 compounds were the most abundant family of volatile compounds in new seedless table grapes (Timco
TM, Magenta
TM, Krissy
TM and Arra15
TM), followed by aldehydes and ketones. C6 compounds derive from linoleic and linolenic acid and have been described to contribute to the green flavor in table grape berries [
12,
15]. Hexanal, hexanol and (E)-2-hexenal were the major C6 compounds found in Bronx Seedless and Italia varieties (
Table 4 and
Table 8). The hexanal to (E)-2-hexenal ratio was correlated to sweetness, an important attribute for table grape production [
19]. In this way, (E)-2-hexenal was positively correlated to sourness and crunchiness and negatively to neutral flavor and sweetness [
19]. As ripening advanced from BBCH-77 to BBCH-89, this ratio decreased (1.67–1.66, respectively), whereas Italia grapes showed a higher hexanal-to-(E)-2-hexenal ratio than Bronx Seedless grapes (1.69–1.54, respectively).
The concentration of most of the volatile compounds analyzed increased as ripening progressed, except (Z)-3-hexenal, (E)-2-hexenol, heptanol, phenylethyl alcohol, butyl acetate, β-pinene, β-myrcene, rose oxide II (cis) and 4-terpineol (
Table 1,
Table 2,
Table 3,
Table 4,
Table 5,
Table 6 and
Table 7). Maoz et al. [
19] mentioned that the concentration of some volatile compounds, such as 1-hexanal, 1-hexanol, methyl hexanoate, 1-nonanal, benzaldehyde, rose-oxide, and linalool, often increases during berry development. Contrary to this, the concentration of other volatile compounds, such as geraniol, (E)-2-octenal, and 1-pentanal, often decreases during berry ripening, whereas the levels of other volatile compounds, such as 1-decanal, (E)-2-hexenal, 1-heptanal, geraniol, 2-phenylethanol, and β-ionone, have been suggested to depend on the variety [
19]. Yang et al. [
10] reported that alcohols, carbonyls, C6 compounds and terpenoids were found in high amounts before veraison, while most of the esters were detected at or after veraison. C6 compounds increased in the early period of berry ripening and then decreased [
10].
4. Conclusions
The results showed that Bronx Seedless table grapes presented higher contents of α-pinene, phellandrene, D-limonene, P-cymene, geranial, nerol, cedrol, 3-methylbutanal, octanal, nonanal, total aldehydes, 2-hexenoic acid, 1-octen-3-ol, heptanol, phenylethyl alcohol, total alcohols and (E)-3-hexenol, and lower contents of β-myrcene, γ-terpinene, rose oxide I (trans), nerol oxide, linalool, 4-terpineol, hotrienol, neral, α-terpineol, myrtenol, geranic acid, hexanoic acid, ethyl acetate, ethyl isobutyrate, butyl acetate, ethyl hexanoate, nonanol, hexanal, (E)-2-hexenal, hexanol, (E)-2-hexenol and total C6 compounds than Italia table grapes. The concentration of most of the volatile compounds analyzed increased from BBCH-77 to BBCH-89, except (Z)-3-hexenal, (E)-2-hexenol, heptanol, phenylethyl alcohol, butyl acetate, β-pinene, β-myrcene, rose oxide II (cis) and 4-terpineol. Based on terpene content, Italia and Bronx Seedless varieties could be classified as neutral varieties. β-ionone presented the highest odor activity value (OAV) in Italia and Bronx Seedless table grapes. Bronx Seedless table grapes presented higher OAVs for (Z)-3-hexenal (grass) and cedrol (camphor) than Italia grapes. In addition, Italia grapes showed a higher hexanal-to-(E)-2-hexenal ratio than Bronx Seedless grapes. Therefore, it is probable that to achieve a better aromatic quality, Bronx Seedless should be harvested later than Italia.
5. Materials and Methods
5.1. Plant Material and Sample Preparation
The research was performed during the 2021 season on twenty-year-old Italia (Bicane × Muscat Hamburg) and Bronx Seedless (New York 8536 × Sultanina) vines grafted onto 5 BB rootstock in the Manisa Viticulture Research Institute, Manisa Province, Aegean Region, Turkey (38°37′57.14″ North Latitude and 27°23′ 57.36″ East Longitude at an altitude of 31.3 m.a.s.l.). Italia is a seeded (formation of seeds) variety and Bronx seedless is a seedless (no formation of seeds) variety. Spur-pruned vines were trained to a high trunk (about 1 m) cordon trellis system with one bunch per shoot and 12–15 shoots per vine at a north–west orientation. Italia and Bronx Seedless vines were planted at a distance of 3.0 m × 2.0 m. Exactly 450 healthy berries from both varieties were randomly harvested in triplicate from both sides of six clusters per vine. Sampling began in the first week before veraison (27 July) and the latest sampling was performed at harvest (28 August), accounting for a total of six sampling phases during berry ripeness. Sampling was performed following different growth stages of the grapevines, according to a BBCH scale published by Lorenz et al. [
20]. Grapes were harvested differentially in six different states as follows: BBCH-77 (begin of berry touch), BBCH-79 (berry touch complete), BBCH-81 (berries begin to brighten in color), BBCH-83 (berries brightened), BBCH-85 (softening of berries) and BBCH-89 (berries ripe for harvest), each following the sampling time. Grape samples were harvested and put into bags, then transported immediately in refrigerated conditions (2 to 5 °C) to the laboratory and stored at −80 °C until further analyses.
5.2. Chemicals and Reagents
Methanol HPLC grade from Merck (Darmstadt, Germany), NaCl (analytical grade) was obtained from Sigma–Aldrich (Millipore, Bedford, MA, USA) and pure water was obtained from the Milli-Q purification system (Millipore, Bedford, MA, USA). The standards (purity > 95%) used for the quantification and identification of the volatile compounds and the chemical standards were obtained as follows: (E)-2-hexenal, geranic acid, (Z)-3-hexenal, 2-octanol, hexanal, phellandrene, β-damascenone, β-myrcene, D-limonene, benzyl alcohol, citronellol, neral, geranial, α-terpineol, (Z)-rose oxide II, geraniol, (E)-rose oxide I and phenylethyl alcohol from Sigma (St. Louis, MO, USA); hexanoic acid, benzaldehyde, octanoic acid, octanal, nonanal, pentanal, 3-methylbutanal, 1-octen-3-ol, (Z)-3-hexenol, heptanol, ethyl butyrate, ethyl acetate, butyl acetate, ethyl pentanoate, ethyl isobutyrate, methyl salicylate, (E)-2-hexenoic acid, hexyl acetate, terpinolene, P-cymene, linalool, geranyl acetone, 4-terpineol, β-ionone and ethyl hexanoate was obtained from Nu-Chek Prep (Elysian, MN, USA); hexanol, octanol, (E)-2-hexenol from Chem Service Inc. (West Chester, PA, USA). The automatic solid phase microextraction (SPME) fibers of 50/30 μm divinylbenzene/polydimethylsiloxane/carboxen (DVB/PDMS/CAR) were obtained from Supelco (Bellefonte, PA, USA).
5.3. Extraction of Volatile Compounds
Volatile organic compounds from the two grape variety samples were extracted by headspace solid phase micro-extraction (HS-SPME) and determined by gas chromatography–mass spectrometry (GC–MS) based on the methodology exposed by Lan et al. [
21]. After removing stems and seeds, 120 g of each grape berry sample were mashed and de-seeded and then blended with 1 g polyvinylpolypyrrolidone (PVPP). Subsequently, the obtained samples were crushed by treatment with liquid nitrogen and centrifuged to obtain a clear juice after maceration at 4 °C for 4 h. After this procedure, 5 mL of grape juice were added into a 20 mL flask containing a magnetic stirrer, previously mixed with 10 μL of internal standard (4-methyl-2-pentanol, 1.0018 mg mL
−1) and 1 g NaCl. Then, the samples were stirred at 40 °C for 30 min on a heating agitation platform. After this, the pre-treated SPME fiber (50/30 μm DVB/Carboxen/PDMS, Supelco, Bellefonte, PA, USA) was inserted into the headspace and extracted for another 30 min with continued agitation and heating. For the GC/MS analysis, the fiber was instantly desorbed into the GC injector.
Free volatile compounds were detected in grapes directly using the above juice. The aroma precursors for the samples were extracted using adsorption on a Cleanert PEP-SPE cartridge (150 mg 6 mL−1; Bonna-Agela Technologies, Wilmington, DE, USA) and then eluted by using methanol. The methanolic elutions were concentrated to dryness and then reconstituted in 100 μL of the glycosidase AR2000, and 5 mL of 0.2 mol L−1 citrate–phosphate-buffered solution (pH 5.0) (Rapidase, DSM Food Specialties, Delft, The Netherlands).
5.4. Analysis of Volatile Compounds by GC-MS
The oven temperature was programmed as follows: 50 °C for 4 min, increased to 220 °C at 5 °C min
−1, and then ramped at 20 °C min
−1 to 220 °C and kept in these conditions for 5 min. The operating conditions in the identification and quantification were determined as follows: ion source, 230 °C, interface, 280 °C and injector, 250 °C. The GC inlet was set in the splitless mode and helium was the carrier gas (1 mL min
−1). Six independent detections were calculated for each sample from three replicates. Then, retention indices were calculated by analyzing a C6–C24
n-alkane series (Supelco) under the same chromatographic conditions. Volatile compounds for samples were identified according to their retention indices and their mass spectra matching in the standard NIST08 library. Quantification procedure for samples was performed according to a previous report published by Wu et al. [
22]. Calibration curves obtained from samples were determined with regression coefficients above 98%. The volatile compounds without calibration curves were semi-quantitative determined using the internal standard. Odor activity values (OAV) of each volatile compound were calculated by dividing the concentration of the compound by its odor threshold obtained from the literature [
12,
15].
5.5. Statistical Analysis
The variables were analyzed considering a complete randomized design with factorial arrangement, accounting for two varieties in six phenological stages. The variables were subjected to a multifactorial analysis (MANOVA) that was performed using the Statgraphics Centurion XVI.I (The Plains, VA, USA) statistical package. The significance of the differences was determined by Duncan’s test (p ≤ 0.05).