Volatile Constituents of Jambolan (<Emphasis Type="Italic">Syzygium cumini</Emphasis> L.) Fruits at Three Maturation Stages and Optimization of HS-SPME GC-MS Method Using a Central Composite Design

The volatile compounds of jambolan (Syzygium cumini L.) fruit were determined at three different maturity stages (unripe, half-ripe, and ripe) by headspace solid-phase microextraction (HS-SPME)–gas chromatography-mass spectrometry (GC-MS) technique using five different fibers (Fused silica PDMS/DVB, DVB/CAR/PDMS, PEG, Stable flex PDMS/DVB, and PDMS). The optimal extraction conditions were evaluated using different variables such as adsorption temperature (minimum 25 °C, maximum 55 °C), salt quantity (minimum 0, maximum 30.0%), and extraction time (min 10, max 30 min). The major classes of compounds identified were ester, terpene, alcohol, aldehyde, and carboxylic acid. Ninety volatile compounds with characteristics aroma attributes were identified, and the primary compounds linked with development of characteristics aroma of ripe jambolan fruit pulp were trans-β-ocimene, β-ocimene, caryophyllene, humulene, D-α-pinene, L-β-pinene, β-pinene, D-limonene, α-terpineol, neo-allo-ocimene, 2-hexenal (E), δ-cadinene, 3-hexen-1-ol, (Z) β-linalool, terpinolene, eremophilene, valencene, 1-hexanol, longipinene, γ-terpinene, γ-muurolene, endo-borneol, o-cymene, nonanal, terpinen-4-ol, β-terpineol, α-muurolene, fenchol, α-fenchene, β-thujene, benzaldehyde, (E)-2-hexenal, β-cadinene, and decanal.     

Exploring <Emphasis Type="Italic">nuruk</Emphasis> aroma; Identification of volatile compounds in commercial fermentation starters

Volatile compounds of 7 commercial fermentation starters, including 4 traditional nuruk, 2 ipguk, and 1 crude amylolytic enzyme, were extracted using solvent-assisted flavor evaporation (SAFE), and extracts were analyzed using GC-MS. A total of 70 volatile compounds, including 4 esters, 10 acids, 16 alcohols, 16 hydrocarbons, 9 ketones, 5 aldehydes, 3 volatiles phenols, and 7 miscellaneous components were identified. Concentrations of volatile compounds, including 4,6-dimethylundecane, methyl 2-hydroxybenzoate, 1-hexanol, 2-phenylethanol, 3-methylbutanoic acid, and hexanoic acid were higher in 4 traditional nuruk starters than in others. The major volatile components in 2 ipguk starters were the hydrocarbones dodecane, heptadecane, octadecane, and nonadecane. Concentrations of 2-methoxy-4-vinylphenol and 3-hydroxy-2-butanone were highest in the crude amylolytic enzyme starter. Compositions and amounts of volatile compounds were different among the 7 commercial fermentation starters.     

Quantitative analysis of volatile flavor components in Korean alcoholic beverage and Japanese sake using SPME-GC/MS

Quantitative analysis of the volatile flavor components in Korean alcoholic beverages (makgeolli and yakju) and Japanese sake was carried out using SPME-GC/MS. Fusel oils (n-butyl alcohol, isobutyl alcohol, isoamyl alcohol, and phenethyl alcohol), ethyl esters (ethyl acetate, isoamyl acetate, ethyl caproate, ethyl caprylate, and ethyl caprate) and aldehydes (furfural and benzaldehyde) were analyzed quantitatively by an 85 μm SPME fiber (carboxen/polydimethylsiloxane) using internal standards (1-pentanol-1-¹³C and methyl nonanoate). Phenethyl alcohol (85-216 ppm) and isoamyl alcohol (38-115 ppm) constituted the majority of fusel oils in all the samples. Acetic acid was detected in sour makgeolli at a high level (0.02-0.14 ppm) compared with yakju and sake. A very high level of total ethyl esters (ethyl acetate, isoamyl acetate, ethyl caprate, and phenethyl acetate), having fruit and flower flavor, was found in makgeolli. Processing the volatile flavor data by multivariate partial least squares discriminant analysis, makgeolli, yakju, and sake showed cluster separation.     

Change in profiles of volatile compounds from two types of <Emphasis Type="Italic">Fagopyrum esculentum</Emphasis> (buckwheat) <Emphasis Type="Italic">soksungjang</Emphasis> during fermentation

Fagopyrum esculentum (buckwheat) soksungjang is one of the traditional soybean pastes in Korea. This study profiled and compared volatile compounds between traditionally manufactured (TBS) and commercially modified buckwheat soksungjang (CBS) according to their fermentation periods. More volatile compounds were generated and non-uniform increases or decreases in volatiles were more common during TBS fermentation. In addition, the changes in and differences between the volatiles from TBS and CBS during the fermentation process (after 0, 1, 2, and 5 weeks) were investigated in partial least squares-discriminant analysis models. The changes were accelerated during CBS fermentation in comparison with TBS fermentation. Several major volatile compounds, such as methyl decanoate, 3-hydroxy-2,6-dimethylpyran-4-one, and methyl heptanoate were found in the final stage of fermentation in TBS, in contrary, tridecane, (Z)-hex-3-en-1-ol, furan-2-carbaldehyde, and ethyl tetradecanoate were contributed to the latest of fermentation in CBS.     

Ridgetail White Prawn (<Emphasis Type="Italic">Exopalaemon carinicauda</Emphasis>) K Value Predicting Method by Using Electronic Nose Combined with Non-linear Data Analysis Model

In this paper, ridgetail white prawn (Exopalaemon carinicauda) K value predicting model by electronic nose (EN) was studied. Human sensory evaluation (HSE), weight loss, color, total viable counts (TVC), GC-MS, and K value were examined to provide quality references for EN detection. EN responses to prawns were recorded and processed by principal component analysis (PCA) and stochastic resonance (SR). Results indicated that prawn K value rapidly increased due to microbiology propagation. The volatile gases emitted by prawns increased with the increase of storage time based on GC-MS results. PCA method could not discriminate the prawns in different qualities, and SR signal-to-noise ratio (SNR) maximum (SNR_max) values successfully discriminated all samples. K value predicting model was developed by linear fitting regression between K values and SNR_maxvalues (R²?=?0.97). The proposed method will promote the applications of EN in aquatic product quality rapid determination.     

Effect of heat-treated <Emphasis Type="Italic">Nuruk</Emphasis> on the quality characteristics of aged <Emphasis Type="Italic">Yakju</Emphasis>

Long-term aging of Yakju, a traditional Korean liquor made of rice and Nuruk (a fermentation agent), causes browning and odor and flavor development. This study investigated the effects of heat-treated Nuruk (50–80 °C, 30 min) on Yakju quality. The saccharogenic powers and glucoamylase, α-amylase, and carboxypeptidase activities were similar in non-heat-treated Nuruk and that treated at 50 °C. However, acidic protease and alcohol dehydrogenase decreased above 50 °C. The content of nitrogen-containing compounds was inversely proportional to the heat-treatment temperature. Compounds that cause off-flavors decreased at 50–60 °C, but increased at 70–80 °C, whereas compounds that provide fragrance increased at 50–60 °C. Sensory evaluation indicated that bad taste attributes were higher in Yakju produced using non-heat-treated Nuruk. Therefore, heat treatment of Nuruk at 50 °C can be adopted as a method for improving Yakju quality, as enzymatic activities that affect color, aroma, and taste are regulated.     

Chemical compositions and volatile compounds of <Emphasis Type="Italic">Tricholoma matsutake</Emphasis> from different geographical areas at different stages of maturity

Tricholoma matsutake is a commercially important edible fungus. Volatile compounds, chemical compositions, and nutritional values of fruiting bodies at different stages of maturity from different geographical areas were analyzed. The main volatile compounds in T. matsutake fruiting bodies were (E)-2-octenal, phenylacetaldehyde, 3-octanone, methyl cinnamate, benzaldehyde, and 1- octen-3-ol. Kinds and levels of volatile compounds from different geographical areas varied. As the fruiting bodies aged, levels of methyl cinnamate and 1-octen-3-ol gradually declined. Potassium was the most abundant element in T. matsutake fruiting bodies. Of 17 amino acids detected in fruiting bodies, glutamate was the most abundant. Volatile compounds, chemical compositions, and nutritional values of T. matsutake varied with age and geographical origin and can serve as chemical indicators for classication of T. matsutake from different geographical areas and at different stages of maturity.     

In vitro antifungal activity and chemical composition of Warionia saharae essential oil against 3 apple phytopathogenic fungi

Essential oil of aerial parts of Warionia saharae was obtained by hydrodistillation and analyzed by GC and GC-MS. Thirty-nine compounds were identified, accounting for 93.2% of the total oil. β-Eudesmol (34.9%), nerolidol-E (23%), and linalool (15.2%) were the most abundant components. The antifungal activity of the W. saharae oil was tested by poisoned food (PF) technique and the volatile activity (VA) assay against 3 phytopathogenic causing the deterioration for apple. The results indicated that the W. saharae oil inhibited significantly the mycelial growth of all strains tested (p<0.05). The minimum inhibitory concentration against Alternaria sp. was 2 μL/mL air in VA assay, whereas >2 μL/mL in PF technique for all strains. Fungal spore production was completely inhibited at 1 μL/mL air for Alternaria sp. and at 2 μL/mL air for Penicillium expansum and Rhizopus stolonifer.     

Influence of keeping system on the fatty acid composition in the <Emphasis Type="Italic">longissimus</Emphasis> muscle of bulls and odorants formed after pressure-cooking

German Simmental bulls were kept either in a stable (group 1) or on a pasture (group 2). For both groups the intramuscular fat content of the longissimus muscle and the fatty acid composition in phospholipids and triacylglycerols were investigated. Significant influences of feeding were shown in most fatty acids measured in both lipid classes. In concentrate-fed bulls a higher content of linoleic acid (C18:2n-6) was detected, corresponding to the large amount of linoleic acid found in concentrate used as feed. In contrast, bulls fed grass proved to have a higher linolenic acid (C18:3n-3) content, also correlating well with the larger amount of linolenic acid found in grass. Pressure-cooking of the beef followed by an analysis of eight important meat odorants revealed that, in line with the higher concentrations of the precursor fatty acids C18:3n-3 and C18:1 in muscle of group 2, (E,Z)-2,6-nonadienal (from C18:3n-3) as well as nonanal and octanal (from C18:1) were much higher in the processed meat of animals fed grass. On the other hand, the much higher amounts of C18:2n-6 in bulls fed concentrate were well-reflected by higher concentrations of five aroma compounds known to be formed by a thermal degradation of this acid, e.g. (E,E)-2,4-decadienal.     

The Comparison of Cinnamomi Cortex and <Emphasis Type="Italic">Cinnamomum burmannii</Emphasis> Blume Using <Superscript>1</Superscript>H NMR and GC-MS Combined with Multivariate Data Analysis

Cinnamomi Cortex (CC, rougui) is the stripped trunk bark of Cinnamomum cassia Presl (CCP) and commonly is used to treat dyspepsia, gastritis, blood circulation disturbances, and inflammatory diseases. However, Cinnamomum burmannii Blume (CBB), an edible ingredient in food from a different Cinnamomum, sometimes replaces CC due to their similar functions and appearance. To identify and distinguish CC from CBB, we investigated the metabolite differences in polar and non-polar extracts of these species by high-resolution ¹H nuclear magnetic resonance (¹H NMR) spectroscopy and gas chromatography–mass spectrometry (GC-MS) combined with multivariate statistical analyses. The results showed a significantly higher separation in GC-MS analysis (non-polar extracts) than ¹H NMR analysis (polar extracts). One-way ANOVA revealed that polar extracts (acetate, α-glucose, sucrose, glycerol, fructose) and non-polar extracts (trans-cinnamaldehyde, α-copaene, δ-cadinene, 2-methoxycinnamaldehyde, (?)-calamenene, α-muurolene, γ-muurolene, α-calacorene, cubenol and α-muurolol) contributed greatly to the comparison of CC and CBB. These results indicate that the ¹H NMR- and GC-MS-based metabolomic approach can effectively differentiate the phytochemical compositions among different species in plants, which in turn could identify important metabolites with known pharmacological activity.     

Kinetic Study of High-Intensity Ultrasound-Assisted Maillard Reaction in a Model System of D-Glucose and L-Methionine

A Maillard reaction (MR) model system of D-glucose and L-methionine at pH of 10.0 assisted by high-intensity ultrasound was studied based on a MR scheme. Activation energy (E _a ) values for the depletion of D-glucose and the generation of intermediate MR products (MRPs), including 1-deoxyglucosone (1-DG) and 3-deoxyglucosone (3-DG), were calculated. The E _a values in ultrasonic MR were further compared with those obtained using a conventionally thermal treatment under the same processing temperature and duration. Results indicated that the E _a values for the depletion of D-glucose and the generation of 1-DG and 3-DG in ultrasonic MR were significantly lower than those in thermal MR, whereas the E _a values for the isomerization of D-glucose in ultrasonic MR was significantly higher than that in thermal MR. Moreover, melanoidins and methional generated in ultrasonic MR were found to have always significantly higher concentrations than those in thermal MR. Similarly, the concentration of another volatile MRP in ultrasonic MR, i.e., 2,5-dimethylpyrazine, was higher than that in thermal MR but not always significantly. Lastly, the samples processed by ultrasound had significantly higher free radical scavenging capacities compared with the samples by thermal MR at 60 °C; however, no significant difference was found at relatively high processing temperatures, i.e., 70 and 80 °C. These findings may be due to active hydroxyl radicals (·OH) generated by cavities under a high temperature and pressure environment that was produced by high-intensity ultrasound wave.     

Extraction and in vitro antioxidant capacity evaluation of phenolic compounds from pigmented aromatic rice (<Emphasis Type="Italic">Oryzae sativa</Emphasis> L.) cultivars

The aroma generating volatile components profile and in vitro antioxidant capacities of different aromatic rice cultivars was determined by GC–MS analysis and in terms of DPPH scavenging activity, lipid peroxidation inhibition, phosphomolybdenum reduction and reducing power assay. The total phenolic content including both free and bound forms in the analyzed aromatic rice cultivars, Mushki budgi (1.62 mg GAE/g), Mushki kandi (1.63 mg GAE/g) and Kamad (1.60 mg GAE/g) were found double the amount as compared to non-aromatic Koshkari (0.86 mg GAE/g) cultivar. The aromatic rice cultivars had also shown higher total flavonoid content and antioxidant activity than non-aromatic rice cultivar (Koshkari). The GC–MS results indicated 21-aromatic compounds present in sufficient quantities in aromatic cultivars and some of them were unique to these cultivars. Among the compounds identified, aldehydes were found in higher quantity followed by alkanes, ketones and esters. Among the aromatic rice cultivars, Mushki budgi and Mushki kandi were found possessing higher quantity of flavoring components such as benzaldehyde, a carcinostatic agent. The cultivars Mushki budgi and Mushki kandi indicated positive correlation of TPC, TFC and the in vitro antioxidant components largely, while the less aromatic Kamad, correlate with only two components viz DPPH and lipid peroxidation.     

Characterization of volatile compounds in Cowart muscadine grape (<Emphasis Type="Italic">Vitis rotundifolia</Emphasis>) during ripening stages using GC-MS combined with principal component analysis

Muscadine grape (Vitis rotundifolia) is a popular fruit in the Southeastern United States because of its unique aroma and strong antioxidant capacity. Volatile compounds of a locally cultivated muscadine cultivar Cowart were characterized by solid-phase microextraction coupled with GC-MS. Twenty-eight volatile compounds, including fruity short-chain esters, alcohols, terpenes, and carbonyl compounds, were detected based on mass spectra and Kovats indices. Based on principal component analysis and hierarchical clustering, the grapes in stages I and II had relatively similar flavor patterns, which were different from that in stage III. Butyl-2-butenoate, hexyl acetate, propyl acetate, ethyl trans-2-butenoate, hexyl-2-butenoate, ethyl acetate, butyl acetate, 1-octanol, ethyl hexanoate, and β- citral were present as distinct volatile chemicals in stage III, while nonanal, decanal, and β-citronellol were distinct in stage II, and myrcenol, β-ocimene, and l-limonene were biomarkers in stage I. Understanding volatile compounds at each stage can assist farmers in choosing the optimal time to harvest muscadine grapes.     

The preservation effect of <Emphasis Type="Italic">Metschnikowia pulcherrima</Emphasis> yeast on anthracnose of postharvest mango fruits and the possible mechanism

This study aimed to determine the effects of Metschnikowia pulcherrima yeast on storage quality of ‘Tainong’ mango, and elucidate it’s possible anti–disease mechanism. The results showed that M. pulcherrima could inhibit the changes in peel colour, fruit firmness, the contents of total soluble solids, total acid and vitamin C, and maintain the storage quality of mango fruits. An investigation of the mechanism showed that M. pulcherrima competed not only for the primary carbon source, but also for living space with Colletotrichum gloeosporioides. In addition, M. pulcherrima promoted the activities of defence-related enzymes, including ß-1,3-glucanase(GLU) and chitinase (CHT), and secreted a small amount of antimicrobial substances composed of volatile and nonvolatile anti-fungal compounds. The results strongly demonstrated that antagonistic yeast M. pulcherrima could be applied as a biocontrol agent for deducing the spoilage and decay of mango fruit.     

Phenolics and eudesmanolide from aged common sage exudate with sugar

Nineteen compounds including one new flavanone were isolated from the juice of aged common sage exudate with sugar (ACSE). The isolated compounds were identified by NMR and MS analyses as levodopa methyl ester (1), 3,4-dihydroxybenzoic acid (2), (S)-8-hydroxy-4-hydroxy-phenylpropanoic acid (3), 4-hydroxybenzoic acid ethyl ester (4), cis-caffeic acid (5), trans-caffeic acid (6), esculetin (7), (S)-8-hydroxy-3,4-dihydroxy-phenylpropanoic acid ethyl ester (8), cis-rosmarinic acid (9), trans-rosmarinic acid (10), trans-rosmarinic acid methyl ester (11), 6-methoxy-7,8,3′,5′-tetrahydroxyflavanone (12), nepetin (13), trans-caffeic acid ethyl ester (14), luteolin (15), cis-caffeic acid ethyl ester (16), 6-methoxynaringenin (17), 1α-acetoxy-2-oxo-eudesman-3,7(11)-dien-8β,12-olide (18), and hispidulin (19). Compound 12 was isolated for the first time from nature and seven compounds (1, 3, 4, 7, 8, 14, and 18) were newly identified from common sage. Of them, 15 isolated phenolic compounds (1–3, 5–8, 10–15, 17, and 19) were detected in ACSE juice, while only 10 was detected in the fresh common sage.     

Antioxidant Activity and Determination of Phenolic Compounds from <Emphasis Type="Italic">Eugenia involucrata</Emphasis> DC. Fruits by UHPLC-MS/MS

Fruits have been the focus of several studies aimed at finding new antioxidant sources for protection against the damage caused by reactive species. In this study, the antioxidant activity and the presence of phenolic compounds in all parts (peel, pulp, and seeds) of Eugenia involucrata DC. fruits were evaluated. DPPH^·, ABTS^·+, and ORAC methods were used to determine the antioxidant activity, and an UHPLC-MS/MS method was developed for determining the phenolic compounds (gallic, chlorogenic, ferulic, p-coumaric and ellagic acids, quercetin, and myricetin). In the determination of both antioxidant activity and phenolic composition, the efficiency of solvents with different polarities—methanol/H₂O (80:20, v/v), ethanol/H₂O (80:20, v/v), methanol/acidified water with phosphoric acid pH 3.00 (80:20, v/v), and ethyl acetate—for the extraction of the phenolic compounds, was also evaluated. All parts of E. involucrata fruits showed antioxidant activity, in the range of 36.68 ± 1.44 to 873.87 ± 18.24 μmol TE g^?1, being the highest values found in the seeds and peel when more polar extraction solvents were used. Six, five, and three phenolic compounds were identified and quantified in the pulp, peel, and seeds, respectively, with the highest abundance as p-coumaric acid (14 ± 2 mg kg^?1) in the pulp, quercetin (47 ± 5 mg kg^?1) in the peel, and gallic acid (74 ± 4 mg kg^?1) in the seeds, also when more polar solvents were used. Although antioxidant activity methods suggested that the peel and seeds have more antioxidant potential, a wider variety of compounds were determined in the pulp.     

Comprehensive metabolic profiles of mulberry fruit (<Emphasis Type="Italic">Morus alba</Emphasis> Linnaeus) according to maturation stage

In this study, comprehensive metabolic profiles of mulberry fruits (Morus alba Linnaeus) at various maturation stages were determined using GC-MS and HPLC. In total, 48 compounds, including 3 alcohols, 16 amino acids, 7 organic acids, 2 sugars, 4 phenolics, 2 terpenes, 3 vitamins, 9 fatty acids, and 2 cyanidins were identified in the mulberry samples. Levels of chlorogenic acid, cryptochlorogenic acid, neochlorogenic acid, ascorbic acid, and δ-tocopherol, and total fatty acid content were significantly higher in the semi-matured mulberry fruits. Furthermore, levels of glycerol, citrate, fructose, glucose, 3-O-glucoside, and cyanidin-3-O-rutinoside were significantly higher at the fully matured stage than at the other stages. Twelve biosynthetic pathways were suggested as major pathways involved in mulberry fruit maturation. The information obtained in this study will provide a basis for future investigations toward quality control or metabolic engineering for development of mulberry fruits possessing commercially valuable characteristics.     

Effect of different solvents on volatile and non-volatile constituents of red bell pepper (<Emphasis Type="Italic">Capsicum annuum</Emphasis> L.) and their in vitro antioxidant activity

The fresh fruit of Capsicum annuum L. (red bell pepper) was successively extracted using n-hexane, chloroform, ethyl acetate, ethanol and their percentage yield was calculated. The effectiveness of each extract on chemical composition and antioxidant activity was studied. The qualitative phytochemical evaluation of each extract of bell pepper was done by HPTLC and Gas chromatography–mass spectroscopy (GC-MS) analysis. The total content of phenols, flavonoids and carotenoids were estimated by standard chemical methods. Further, the antioxidant potential of each extract was measured via DPPH and reducing power assays. Gas chromatography–mass spectroscopy analysis showed that the majority of compounds were related to phenols and flavonoids. Further analysis of the extract by HPTLC verified the presence of different types of phenolic compounds in addition to flavonoids and carotenoids. Among the different solvent extracts analyzed, total phenolic content was higher in ethanol extract (7.136?±?0.03%, w/w) whereas ethyl acetate extract showed the presence of higher flavonoid content (4.0521?±?0.03%, w/w). The ethanol and ethyl acetate extracts of the fruit of C. annuum exhibited the highest radical scavenging activity with inhibition percentage of 53.66 and 49.55% at a concentration of 254 µg/ml. Based on the biochemical analysis and phytochemical screening, we conclude that C. annuum possess potent antioxidant potential and this ability of the extract is attributed to the presence of rich polyphenolic compounds.