We investigated the effect of various cooking methods (boiling, steaming, stir-frying, and roasting) and three cooking times (5, 10, and 15 min) on the antioxidant properties of red pepper. Raw and cooked peppers were measured for proximate composition, ascorbic acid (AsA) content, total carotenoid content (TCC), total polyphenol content (TP), and 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging activities. Results showed that the proximate composition, AsA content, TCC, TP, and antioxidant activities were significantly (p<0.05) affected by the cooking procedure; the loss rate varied among individual compounds. Boiling and steaming significantly reduced AsA content (24.3~66.5%), TP (13.9~ 54.9%), and antioxidant activity (21.7~60.5%) in red pepper, while stir-frying and roasting slightly reduced AsA content (2.7~25.9%), TP (1.8~4.9%), and antioxidant activity (4.9~17.9%). The highest loss was observed after boiling, followed by steaming, roasting, and stir-frying. Stir-frying and roasting better preserved AsA content, TCC, TP, and antioxidant activity. In conclusion, dry-heat cooking methods such as stir-frying and roasting may be preferred to retain the nutrient compositions and antioxidant properties of red pepper.

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Zingiberaceae is the large diverse family comprised of rhizomatous plants with a higher concentration of phenolic compounds. The normal ginger (Zingiber officinale Rosc.) and black ginger (Kaempferia parviflora Wall.) belongs to this family and have similar morphological characteristics of rhizome, but their phenolic composition revealed differently. On this study, the phenolic composition of normal ginger (from Ethiopia and Korea) and black gingers (from Korea and Thailand) were profiled using ultra performance liquid chromatography coupled with diode array detector, quadrupole time-of-flight mass spectrometry (UPLC-DAD-QToF-MS). The result revealed that gingerol-related phenolic acid was detected only in normal gingers while, the methoxyflavones were identified exclusively in black gingers. 6-gingerol, 8-gingerol, 10-gingerol, 1-dehydro-6-gingerdione, and diacetoxy-8-gingerdiol were the major constituents among 18 phenolic acids detected from normal gingers, and 3,5,7,3′,4′-pentamethoxyflavone and 5,7,4′-trimethoxyflavone were confirmed as predominant constituents among 13 methoxyflavones from black gingers. The total phenolic content was 434.7 and 698.1 mg/100 g dry weight (DW) in Korean and Ethiopian sample, respectively. The total methoxyflavone concentration was 4388.0 mg/100 g DW and 3940.2 mg/100 g DW in Korean and Thai black ginger sample, respectively. The higher concentration of methoxyflavones is from advanced biosynthetic pathway related to accumulated color of black ginger. In addition, new possible structural fragmentation was proposed for gingerol homologous series as additional pathway under the positive ionization mode, and further rationalized that ferulic acid moiety is the biosynthetic precursor. The result suggested that despite the morphological similarity, normal and black ginger showed distinct biosynthetic difference to synthesis their major secondary metabolites.Electronic supplementary material The online version of this article (https ://doi.org/10.1007/s0021 7-018-3188-z) contains supplementary material, which is available to authorized users. Graphical AbstractKeywords Kaempferia parviflora Wall. · Phenolic compounds · UPLC-DAD-QToF-MS · Zingiberaceae · Zingiber officinale Rosc.

Graphical abstract

Most previous studies have been focused on the variation of tea chemical composition by fermentative processes as well as different cultivars and regions. The detailed changes of flavonoid profiles were described for the first time by each processing step of green and black tea leaves in this study. A total of 24 flavonoid derivatives including catechins, theaflavins, and flavonols were separated and identified from the tea samples based on UPLC-DAD-QToF/MS data and constructed library. Among these, the fragmentation pathway of theaflavins was proposed specifically in positive ionization mode for structural interpretation. During leaf processing, the individual flavonols were changed as diverse patterns according to their aglycone types and glycosylated forms, but their total content showed a slight difference. EGCG and ECG were increased after roasting approximately twofold higher than that of fresh leaves (EGCG, 2709.5 →6085.6; ECG, 1548.0 →2318.2 mg/100 g dry weight, respectively) in green tea while considerably decreased their contents due to oxidation and conversion to theaflavins after fermentation during black tea processing. Especially, the drying steps also found to be factor to influence positively to increase the flavonoid contents in both tea processing. Therefore, this result indicated that detailed conditions of each processing step played important roles in changing the flavonoid profiles from tea leaves.

Most previous studies have been focused on isoflavone profile with biological activities from soybean seed and its related products. However, in the present study, eighty-three flavonoid derivatives (55 flavonols, 9 flavones and 19 isoflavones) were comprehensively identified and quantified from young leaves of 21 core-collected soybean cultivars based on ultra-performance liquid chromatography-diode array detector with quadrupole time of flight/mass spectrometry (UPLC-DAD-QToF/MS). Among total content (342.5-992.7 mg/100 g, dry weight) of 83 derivatives found in these soybean leaves (SLs), the abundant flavonols (83.6%, 275.1–854.0) were primarily composed of 26 di- and 23 tri- glycosides combined to the aglycones (K, kaempferol; Q, quercetin; I, isorhamnetin), and distributed in the order of K, Q and I. Particularly, K-rich SLs (yellow coated seed), Nongrim 51 (breeding line) and YJ208-1 (landrace) contained mainly kaempferol 3-O-(2"-O-glucosyl-6"-O-rhamnosyl)galactoside and 3-O-(2",6"-di-O-rhamnosyl)galactoside, and were expected to be superior cultivars by their higher flavonoids. Besides, the new tri-I-glycosides (soyanins Ⅰ~Ⅴ) were presented as predominant components in Junyeorikong (landrace, black). Thus, these detailed profiles will support breeding of superior varieties with excellent biological activities as well as relationship with seed anthocyanins production, and suggest that the SLs can be considered as a valuable edible resource due to their rich flavonoids.

Platycodon grandiflorum (PG) is known as a high-potential material in terms of its biological activity. The objective of this report is to provide chromatographic and mass fragment ion data of 38 simultaneously identified saponins, including novel compounds, by analyzing them through ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-QToF/MS). In so doing, we investigated their diverse conditions, including morphological parts (stems, roots, buds, and leaves), peeling (or not), and blanching of PG. The total contents of individual saponins indicated an order of roots (containing peel, 1674.60 mg/100 g, dry weight) > buds (1364.05) > roots (without peel, 1058.83) ≈ blanched roots (without peel, 945.17) ≈ stems (993.71) ≈ leaves (881.16). When considering three types of aglycone, the platycodigenin group (55.04 ~ 68.34%) accounted for the largest proportion of the total content, whereas the platycogenic acid A group accounted for 17.83 ~ 22.61%, and the polygalacic acid group represented 12.06 ~ 22.35%. As they are classified as major compounds, novel saponins might be utilized for their role in healthy food for human consumption. Additionally, during blanching, the core temperature of PG was satisfied with the optimal condition, thus activating the enzymes related to biotransformation. Furthermore, through the use of this comprehensive data, additional studies related to buds, as well as roots or the characterization of individual saponins, can be conducted in a rapid and achievable manner.

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