Kye Man Cho’s research while affiliated with Gyeongsang National University and other places

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Publications (189)


Amending Metagenomic Bacterial Community in Soybean-Cultivated Soils to Enhance Phytoestrogen in Soybean Roots by Communicating with Mixture of Culturable Rhizospheric Bacteria
  • Preprint

January 2025

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10 Reads

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Hee Yul Lee

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Kye Man Cho

Fig. 1. The light distribution of the 2W4R (A) and 1W8R (B) treatments in a cultivation area for baby leaf soybean under the location of the red chips. The points from 1 to 15 indicate positions from left to right on the LED bar. Each point is located on a vertical line between the LED bar and the cultivation bed.
Fig. 2. Correlation between baby leaf soybean's heights and the red light distribution of LED bars treated with 2W4R (A) and 1W8R (B). The bars represent the plant height of the soybeans grown at each location and the red line represents the measured red photon flux density at each location.
Fig. 3. The stem thickness index of baby leaf soybean exposed to different light sources (n = 6). Statistically significant differences are detected at p < 0.05 in Duncan's multiple-range test. *** is p < 0.001. Different letters a and b indicate statistical differences between the treatments, DW is Dry weight.
Fig. 5. Correlation between kale biomass and the red-light distribution of the LED bar in the 2W4R (A, C) and 1W8R (B, D) treatments. Kale fresh weight (A) and dry weight (C) in the 2W4R treatment, and kale fresh weight (B) and dry weight (D) in the 1W8R treatment. The points represent the plant biomass of kale grown at each location and the red line represents the measured red photon flux density at each location.
Fig. 6. The leaf thickness index of kale exposed to different light sources (n = 6). Statistically significant differences were identified using Duncan's multiple-range test. * is p < 0.05, DW is Dry weight.
Lighting design affects the uniformity and growth of plants in a vertical farming system
  • Article
  • Full-text available

December 2024

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89 Reads

Plant Science Today

Light is essential for plant production and has various effects on plant quality. Vertical farms typically use light-emitting diodes (LEDs) as light sources. However, the cost of LEDs varies with wattage and the initial installation costs are generally high. Therefore, to explore more cost-effective LED designs, we aimed to investigate the impact of red LED chips density on light distribution and plant growth under the same total electricity consumption. To this end, we exposed baby leaf soybean (Glycine max (L.) Merr.; 5 days) and kale (Brassica oleracea var. acephala; 18 days) to LEDs light with different arrangements of red and white chips. Plants were exposed to either 2 W chips with a red: white ratio of 4: 64 (2W4R treatment) or 1 W chips with a red: white ratio of 8: 64 (1W8R treatment) across the entire LED bar. We observed that the distribution of red light in the cultivation room differed depending on the density of the red LED chips. We found that arranging low-power red LED chips at narrow intervals resulted in uniform light distribution across the entire cultivation bed, positively affecting crop growth. Baby leaf soybean and kale exhibited uniform growth under 1W8R and growth was particularly enhanced in kale. This may be because of the dense leaf structure of kale, which promotes photosynthesis under a uniform light environment. The results of this study demonstrate that a favorable light environment can be created by altering the position and distribution of red LED chips, thereby inducing uniform growth in plants.

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Fig. 1. Comparison of fatty acids in the DrIESLs, StIESLs, and FeIESLs. (A) and (B) 2D score plot with principal component analysis, and (C) heatmap analysis. Processing stages: DrIESLs, dried isoflavone-enriched soybean leaves; StIESLs, steamed isoflavone-enriched soybean leaves; FeIESLs, fermented isoflavone-enriched soybean leaves.
Fig. 2. Comparison of free amino acids in the DrIESLs, StIESLs, and FeIESLs. (A) and (B) 2D score plot with principal component analysis, and (C) heatmap analysis. Processing stages: DrIESLs, dried isoflavone-enriched soybean leaves; StIESLs, steamed isoflavone-enriched soybean leaves; FeIESLs, fermented isoflavone-enriched soybean leaves.
Fig. 3. Comparison of water-soluble vitamin contents in DrIESLs, StIESLs, and FeIESLs. (A) Water-soluble vitamin contents, (B) 2D scores plot with principal component analysis, and (C) heatmap analysis. Processing stages: DrIESLs, dried isoflavone-enriched soybean leaves; StIESLs, steamed isoflavone-enriched soybean leaves; FeIESLs, fermented isoflavone-enriched soybean leaves. All values are presented as the mean ± SD of pentaplicate determination, and different small letters correspond to the significant differences relating to the fermentation time and starter using Duncan's multiple tests (p < 0.05).
Fig. 7. Comparison of total phenolic and total flavonoid contents in the DrIESLs, StIESLs, and FeIESLs. (A) Total phenolic and flavonoid contents, and (B) 2D scores plot with principal component analysis. Processing stages: DrIESLs, dried isoflavone-enriched soybean leaves; StIESLs, steamed isoflavone-enriched soybean leaves; FeIESLs, fermented isoflavone-enriched soybean leaves. All values are presented as the mean ± SD of pentaplicate determination, and different small letters correspond to the significant differences relating to the fermentation time and starter using Duncan's multiple tests (p < 0.05).
Fig. 8. Comparison of antioxidant and digestive enzyme inhibitory activities in the DrIESLs, StIESLs, and FeIESLs. (A) DPPH radical-scavenging activity, (B) ABTS
Changes in nutritional compositions and digestive enzyme inhibitions of isoflavone-enriched soybean leaves at different stages (drying, steaming, and fermentation) of food processing

November 2024

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17 Reads

Food Chemistry X

Isoflavone-enriched soybean leaves (IESLs) were processed for drying, steaming, and fermentation, and bioactive compounds and biological activities were analyzed. During food processing, the content of fatty acids, water-soluble vitamins, total phenolics, total flavonoids, and isoflavone-aglycones increased from dried IESLs (DrIESLs) to fermented IESLs (FeIESLs). Especially, oleic acid (53.4 → 113.1 mg/100 g, 2.1-folds), γ-aminobutyric acid (357.36 → 435.48 mg/100 g, 1.2-folds), niacin (19.0 → 130.6 mg/100 g, 6.9-folds), folic acid (9.7 → 25.5 mg/100 g, 2.6-folds), daidzein (270.02 → 3735.10 μg/100 g, 13.8-folds), and genistein (121.18 → 1386.01 μg/100 g, 11.4-folds) dramatically increased. Correspondingly, the antioxidant and digestive enzyme inhibitory activities increased. Therefore, solid-state lactic acid fermentation (SLAF) was suggested as a suitable technique for mass-processing IESLs. FeIESLs with SLAF have the potential to be utilized as a functional food.


Effects of fermented and aged mountain‐cultivated ginseng sprout extract (FAMCGSE) on RAW 264.7 macrophage cell activation and viability in response to LPS treatment. (A) Morphological changes of RAW 264.7 cells exposed to LPS and treated with varying concentrations of FAMCGSE (0.001%–0.1%). The upper panel shows differential interference contrast (DIC) images, and the lower panel shows nuclear red (NR)‐stained images. The black and red arrows indicate LPS‐induced cell spreading and vacuoles in activated cells, respectively. Symbols are applied only to the LPS treatment group. Scale bars, 50 μm. (B) Effect of FAMCGSE on cell viability in response to LPS. (C, D) Analysis of the proportion of spread and vacuolized cells in response to LPS in the presence of FAMCGSE. Cells were pre‐treated with FAMCGSE (0.001% to 0.1%) for 2 h, followed by stimulation with 1 μg/mL of LPS for 16 h. Hydrogen peroxide (H2O2, 300 μM) treatment was used to control cell death induction. Bar graphs are presented as mean ± SD (n = 9). Plus and minus symbols represent with and without treatment, respectively. *p < 0.05 compared to control without LPS treatment. †p < 0.05 compared to LPS. #p < 0.05 compared to LPS + 0.01% FAMCGSE.
Anti‐inflammatory and antioxidant effects of FAMCGSE. (A) ABTS and DPPH radical scavenging activity of FAMCGSE at different doses. (B) Antioxidant effect of FAMCGSE on LPS‐induced ROS generation in RAW264.7 cells. The cells were pretreated with FAMCGSE (0.01% and 0.1%) for 2 h and stimulated with LPS (1 μg/mL) for 16 h. Intracellular ROS generation was determined using dichlorodihydrofluorescein (H2DCFDA), and the fluorescence intensity was measured using a microplate reader. Scale bars, 50 μm. (C) Inhibitory effect of main components of FAMCGSE on COX‐2 activity. CK and F2 at concentrations above 1 μM showed a significant difference from 0.1 μM, and Rg3 at concentrations above 3 μM showed significant difference from 0.1 μM. (D) Inhibitory effect of CK, F2, and Rg3 on LPS‐induced NO production. RAW264.7 cells were pretreated with FAMCGSE and then stimulated with 1 μg/mL LPS for 16 h. Culture media were collected to determine the amount of NO using the Griess reagent system. Bar graphs are presented as mean ± SD (n = 4). Plus symbols represent treatment with LPS. *p < 0.05 compared to control without LPS treatment. †p < 0.05 compared to LPS.
Suppression of proinflammatory mediators in LPS‐stimulated RAW 264.7 macrophages by FAMCGSE treatment. (A, B) Semi‐quantitative PCR analysis of TNF‐α, IL‐1β, IL‐6, iNOS, and COX‐2 mRNA expression levels. (C) Western blot analysis of iNOS and COX‐2 protein levels. The cells were pretreated with FAMCGSE at concentrations of 0.01% and 0.1% before LPS stimulation. GAPDH and β‐Actin were used as the loading control for PCR and Western blotting assays, respectively. (D) Concentration of TNF‐α, IL‐1β, IL‐6, NO, and PGE2 produced in LPS‐exposed cells. Bar graphs are presented as mean ± SD (n = 4). Plus and minus symbols represent with and without treatment, respectively. *p < 0.05 compared to control without LPS treatment. †p < 0.05 compared to LPS. #p < 0.05 compared to LPS + 0.01% FAMCGSE.
Effects of FAMCGSE on MAPK and NF‐κB p65 activation in LPS‐stimulated RAW 264.7 macrophages. (A) Western blot analysis showing the phosphorylation levels of MAPK proteins (ERK1/2, p38, and JNK) in LPS‐stimulated RAW 264.7 macrophages after treatment with FAMCGSE (0.01% and 0.1%). (B) Analysis of the nuclear and cytoplasmic distribution of NF‐κB p65 in LPS‐stimulated RAW 264.7 macrophages treated with FAMCGSE or CK. Lamin A and α‐tubulin were used as nuclear and cytoplasmic markers, respectively. The accompanying bar graph indicates that FAMCGSE significantly decreased the nuclear translocation of NF‐κB p65. Data are presented as mean ± SD of four independent experiments. *p < 0.05 compared to control without LPS treatment. †p < 0.05 compared to LPS.
Reduction of NF‐κB activation by MAPK inhibition. (A) ELISA results showing the phosphorylation of NF‐κB p65 in RAW 264.7 cells treated with FAMCGSE, CK, or specific MAPK inhibitors (PD98059, SB203580, SP600125) or NF‐κB and AP‐1 inhibitors (Bay11‐7085, SR11302, SP100030). (B) Combined effects of FAMCGSE or CK and MAPK inhibitors on NF‐κB activation induced by LPS in RAW264.7 cells. Data are presented as mean ± SD of three independent experiments. Plus and minus symbols represent with and without treatment, respectively. *p < 0.05 compared to control without LPS treatment. †p < 0.05 compared to LPS. #p < 0.05 compared to LPS + 0.01% FAMCGSE or LPS + CK.
Anti‐Inflammatory Effects of Fermented and Aged Mountain‐Cultivated Ginseng Sprouts via Suppression of MAPK‐NF‐κB Pathway in Lipopolysaccharide‐Stimulated RAW264.7 Macrophages

October 2024

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45 Reads

Fermented and aged mountain‐cultivated ginseng sprouts (FAMCGS) exhibit superior antioxidant and anti‐inflammatory properties compared to mountain‐cultivated ginseng sprouts (MCGS). However, the mechanisms behind these properties of FAMCGSE remain unclear. This study explores the anti‐inflammatory effects of FAMCGS extract (FAMCGSE) on LPS‐stimulated RAW 264.7 macrophages and the underlying mechanisms. The MTT assay confirmed that FAMCGSE (0 to 0.1%) maintained cell viability without inducing morphological changes. Pretreatment with FAMCGSE significantly mitigated LPS‐induced morphological alterations dose‐dependently. RT‐PCR and Western blot analyses showed that FAMCGSE significantly reduced the mRNA and protein levels of proinflammatory mediators such as TNF‐α, IL‐1β, IL‐6, iNOS, and COX‐2. Additionally, FAMCGSE decreased the production of TNF‐α, IL‐1β, IL‐6, nitric oxide, and PGE2 in LPS‐activated RAW264.7 cells. Mechanistically, FAMCGSE inhibited the phosphorylation of mitogen‐activated protein kinases (MAPKs; ERK, p38, and JNK) and prevented the LPS‐induced nuclear translocation of NF‐κB, with effects comparable to compound K (CK) or dexamethasone. Notably, FAMCGSE was particularly effective in inhibiting ERK and JNK activation, with less impact on p38, suggesting a specific inhibitory action on certain MAPK pathways. These findings highlight FAMCGSE's potential as an inhibitor of MAPK and NF‐κB pathways, indicating that FAMCGSE, including its main component CK, may be a promising therapeutic agent for inflammation‐related conditions.


Comparison in Bioactive Compounds and Antioxidant Activity of Cheonggukjang Containing Mountain-Cultivated Ginseng Using Two Bacillus Genus

October 2024

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24 Reads

In this study, the nutrients, phytochemicals (including isoflavone and ginsenoside derivatives), and antioxidant activities of cheonggukjang with different ratios (0%, 2.5%, 5%, and 10%) of mountain-cultivated ginseng (MCG) were compared and analyzed using microorganisms isolated from traditional cheonggukjang. The IDCK 30 and IDCK 40 strains were confirmed as Bacillus licheniformis and Bacillus subtilis, respectively, based on morphological, biological, biochemical, and molecular genetic identification, as well as cell wall fatty acid composition. The contents of amino acids and fatty acids showed no significant difference in relation to the ratio of MCG. After fermentation, isoflavone glycoside (such as daidzin, glycitin, and genistin) contents decreased, while aglycone (daidzein, glycitein, and genistein) contents increased. However, total ginsenoside contents were higher according to the ratio of MCG. After fermentation, ginsenoside Rg2, F2, and protopanaxadiol contents of cheonggukjang decreased. Conversely, ginsenoside Rg3 (2.5%: 56.51 → 89.43 μg/g, 5.0%: 65.56 → 94.71 μg/g, and 10%: 96.05 → 166.90 μg/g) and compound K (2.5%: 28.54 → 69.43 μg/g, 5.0%: 41.63 → 150.72 μg/g, and 10%: 96.23 → 231.33 μg/g) increased. The total phenolic and total flavonoid contents were higher with increasing ratios of MCG and fermentation (fermented cheonggukjang with 10% MCG: 13.60 GAE and 1.87 RE mg/g). Additionally, radical scavenging activities and ferric reducing/antioxidant power were significantly increased in fermented cheonggukjang. This study demonstrates that the quality of cheonggukjang improved, and cheonggukjang with MCG as natural antioxidants may be useful in food and pharmaceutical applications.


Nutritional components and physiological activities of kombucha containing ginseng sprouts

August 2024

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6 Reads

In this study, the physicochemical properties, nutritional components, and antioxidant activities of kombucha containing ginseng sprouts (control kombucha, CT; strawberry kombucha, ST ; strawberry kombucha with 2% ginseng sprout, ST+GS) were analyzed for comparison of quality characteristics. The total content of free amino acids in ST+GS (273.38 mg/100 mL) was 3.2-14.5 times higher than in CT (18.9 mg/100 mL) and ST (84.9 mg/100 mL). The total mineral content in ST+GS (63.99 mg/100 mL) was 3.3-4.1 times higher than those of CT and ST (15.45 and 19.28 mg/100 mL). The contents of soluble phenolic and soluble flavonoid were 1.2 mg GAE/mL and 0.14 mg RE/mL in ST+GS. Several ginsenosides were detected only in ST+GS; ginsenoside Rg2 (2.4 mg/100 mL), Rh1 (4.5 mg/100 mL), F2 (9.0 mg/100 mL), Rg3 (4.6 mg/100 mL), and compound K (7.8 mg/100 mL) were detected. The content of phenolic acids was 1.2-1.5 times higher in ST+GS than in CT and ST. The amount of flavonol of ST+GS was not significantly different from CT but was 1.4 times higher than in ST. In terms of antioxidant activities, the values of ST+GS were significantly higher in comparison to other kombucha samples. These results confirmed that incorporating ginseng sprouts amplifies the advantages of kombucha.


Nutritional components and physiological activities of kombucha containing ginseng sprouts

August 2024

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10 Reads

In this study, the physicochemical properties, nutritional components, and antioxidant activities of kombucha containing ginseng sprouts (control kombucha, CT; strawberry kombucha, ST ; strawberry kombucha with 2% ginseng sprout, ST+GS) were analyzed for comparison of quality characteristics. The total content of free amino acids in ST+GS (273.38 mg/100 mL) was 3.2-14.5 times higher than in CT (18.9 mg/100 mL) and ST (84.9 mg/100 mL). The total mineral content in ST+GS (63.99 mg/100 mL) was 3.3-4.1 times higher than those of CT and ST (15.45 and 19.28 mg/100 mL). The contents of soluble phenolic and soluble flavonoid were 1.2 mg GAE/mL and 0.14 mg RE/mL in ST+GS. Several ginsenosides were detected only in ST+GS; ginsenoside Rg2 (2.4 mg/100 mL), Rh1 (4.5 mg/100 mL), F2 (9.0 mg/100 mL), Rg3 (4.6 mg/100 mL), and compound K (7.8 mg/100 mL) were detected. The content of phenolic acids was 1.2-1.5 times higher in ST+GS than in CT and ST. The amount of flavonol of ST+GS was not significantly different from CT but was 1.4 times higher than in ST. In terms of antioxidant activities, the values of ST+GS were significantly higher in comparison to other kombucha samples. These results confirmed that incorporating ginseng sprouts amplifies the advantages of kombucha.




Fig. 1. Changes in NEAAs and EAAs using amino acid analyzer from the 50 % ethanol extracts through aging processes of ginseng sprouts: (A) DGS; (B) RGS; (C) BGS; Phosphoetanolamine (3.3 min), Proline (36.6 min), Aspartic acid (12.0 min), Threonine (17.1 min), Serine (18.7 min), Glutamic acid (23.5 min), Sarcosine (28.8 min), Aminoadipic acid (31.4 min), Glycine (38.3 min), Alanine (40.1 min), Citrulline (41.6 min), α-Aminobutyric acid (43.2 min), Valine (45.4 min), Cystine (46.9 min), Methionine (47.9 min), Cystathionine (49.1 min), Isoleucine (51.1 min), Leucine (52.6 min), Tyrosine (54.9 min), Phenylalanine (58.8 min), β-Alanine (63.1 min), β-Aminoisobutyric acid (64.6 min), γ-Aminobutyric acid (70.3 min), Aminoethanol (78.1 min), Hydroxyproline (89.1 min), Ornithine (93.8 min), Lysine (98.4 min), 1-Methylhistidine (101.0 min), Histidine (103.5 min), 3-Methylhistidine (107.1 min), Anserine (110.3 min), and Arginine (119.4 min).
Changes in phenolic acids and flavonols through different aging processes from ginseng sprouts.
Investigating alterations of nutritional constituents, antioxidant abilities, and physicochemicals in aging processes of ginseng sprouts

July 2024

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19 Reads

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1 Citation

Heliyon

This study was the first to document the fluctuations of nutritional constituents, antioxidant capacities, and physicochemical characteristics during the aging processes of red ginseng sprouts (RGS) and black ginseng sprouts (BGS) from dried ginseng sprouts (DGS). Total ginsenoside levels differed with 54.72 (DGS) → 57.15 (RGS) and 6.98 (BGS) mg/g, specifically, ginsenoside F2 and Rd2 in RGS remarkably increased with 1.97 → 5.88 and 2.41 → 5.49 mg/g, respectively. Phenolics increased dramatically as 297.02 → 1770.01 (6.0-fold); 1834.94 (6.2-fold) μg/g in DGS → RGS; BGS with abundance contents of benzoic acid (>15.3-fold), chlorogenic acid (>9.5-fold), and catechin (>4.2-fold), whereas amino acids markedly decreased (3686.81 → 1505.00; 364.64 mg/100 g), with arginine showing a significant decrease. Moreover, beneficial factors (total phenolic content: TPC; total flavonoid content: TFC; maillard reaction products: MRP) displayed increase tendencies (approximately 2.0-fold) with BGS > RGS > DGS, and antioxidant patterns significantly increased with potential capacities as follows: ABTS (48.3: DGS → 65.8: RGS; 70.2 %: BGS) > DPPH (18.5 → 44.6; 59.2 %) > hydroxyl (23.2 → 35.4; 39.9 %) > FRAP (0.6 → 1.8; 1.8 %) at 500 μg/mL. In particular, DNA protection exhibited excellent rates of 100 %, in the order of BGS (25 μg/mL) > RGS (50 μg/mL) > DGS (500 μg/mL). These findings suggest that processed ginseng sprouts can be excellent agents for natural antioxidants.


Citations (68)


... Adding substances enriched with polyphenols can effectively improve the antioxidant activity of the bread, such as green coffee extracts, ginger powder, and grapeseed [13] . Additionally, owing to the strong reducing properties of some polyphenols, they could interact with proteins in gluten and result in changes in the secondary and tertiary structures of the proteins, affecting the ductility and elasticity of the gluten, and ultimately improving the quality of the bread [14] . ...

Reference:

Fortification effect of mixed fermentation product of Russula vinosa Lindblad supplementation on physicochemical, sensory and antioxidant properties of wheat bread
Comparison of primary and secondary metabolites and antioxidant activities by solid-state fermentation of Apios americana Medikus with different fungi
  • Citing Article
  • August 2024

Food Chemistry

... Phenolic acid and flavonol analyses were performed by modifying a previously published method [55]. Here, the analysis was performed by HPLC using an Agilent 1200 platform (Agilent Technologies). ...

Examining the Alterations in Metabolite Constituents and Antioxidant Properties in Mountain-Cultivated Ginseng (Panax ginseng C.A. Meyer) Organs during a Two-Month Maturation Period

... To gain more information on the antioxidant ratios of the MCG plant, the DNA protection activities of recombinant 50% ethanol extracts from the organs through maturation times were evaluated. A nicked DNA system through super-coiled plasmid DNA pUC18 was investigated in an MCO apparatus [25,26,32]. According to the preliminary results of the radical scavenging effects and FRAP values, the DNA protection assay documented the percentage values in five different concentrations (50, 100, 250, 500, and 1000 μg/mL). ...

Comparative Assessment of Nutritional Metabolites in Yellow Soybeans at Different Growth Years and Their Antioxidant and α-Glucosidase Inhibition Properties

... Free amino acid analysis was performed using a previously published method with some modifications [54]. Briefly, 1 mL of centrifuged fermentation supernatant and 4 mL of HPLC water were first mixed in a test tube, after which hydrolysis was performed at 60 • C for 1 h. ...

Changes in Nutrient Components and Digestive Enzymatic Inhibition Activities in Soy Leaves by Ethephon Treatment

... Ginseng sprouts have a short cultivation period and are harvested from the whole plant (shoot and root), containing high ginsenosides content (Chang et al., 2020). Korean ginseng is a well-known commercial medicinal crop, and many studies have attempted to produce ginseng sprouts in vertical farms (Park et al., 2019;Lee et al., 2023a). In this study, several types of white LED with different CCT and CRI values were used to investigate the effects on the growth, canopy net photosynthetic rate (P n ), and the content of bioactive compounds, specifically saponin and ginsenosides, of ginseng sprouts in a vertical farm module. ...

Comparison of Growth Patterns and Metabolite Composition of Different Ginseng Cultivars (Yunpoong and K-1) Grown in a Vertical Farm

... Skin aging is an inherent physiological phenomenon, characterized by increased fragility, lower tissue integrity, and a decline in repair ability [1][2][3][4]. External factors, especially ultraviolet radiation, can further accelerate skin aging [5][6][7][8][9]. Traditional anti-aging methods, such as the use of cosmetological care products, medicines, or dermal fillers, are developed to improve skin elasticity and reduce wrinkles [10][11][12][13][14][15][16]. ...

Photoprotective Effect of Fermented and Aged Mountain-Cultivated Ginseng Sprout (Panax ginseng) on Ultraviolet Radiation-Induced Skin Aging in a Hairless Mouse Model

... Analysis of total phenolic and flavonoid contents and antioxidant capacity was performed according to the methods described by Cho et al. (2022) and Lee et al. (2022). Extracts, prepared by shaking 1 g samples of leaf or root powder from each treatment group with 20 mL of 50% methanol for 14 h at room temperature, were used for total phenolic and flavonoid contents and antioxidant capacity analysis. ...

Comprehensive comparison of the primary and secondary metabolites and antioxidant activity of Polygoni multiflori Radix by processing methods
  • Citing Article
  • December 2022

Journal of Applied Biological Chemistry

... Additionally, molecular dynamics (MD) simulations of the protein-ligand complex for both the wild-type and H113P mutant proteins revealed significant differences in key structural parameters, including RMSD, RMSF, radius of gyration, and SASA profiles. The simulations were conducted over a 100 ns timeframe, consistent with previously established studies [65][66][67][68]. These variations in structural dynamics strongly indicate that the H113P mutation is likely to disrupt the normal function of the CXCR4 protein, potentially leading to alterations in its stability, flexibility, and ligand-binding behavior. ...

Unveiling chlorpyrifos mineralizing and tomato plant-growth activities of Enterobacter sp. strain HSTU-ASh6 using biochemical tests, field experiments, genomics, and in silico analyses

... Ferroptosis is implicated in numerous lung disorders, including chronic obstructive pulmonary disease, cystic fibrosis, and obstructive sleep apnea [16]. Furthermore, increasing studies indicate that ferroptosis has a pivotal role in the development of asthma [17,18]. Iron metabolism, lipid metabolism, reactive oxygen species (ROS) production, and amino acid metabolism are biological processes associated with ferroptosis, and they are all related to asthma [19]. ...

Fermented and Aged Ginseng Sprouts (Panax ginseng) and Their Main Component, Compound K, Alleviate Asthma Parameters in a Mouse Model of Allergic Asthma through Suppression of Inflammation, Apoptosis, ER Stress, and Ferroptosis

... A diversity of microorganisms, including fungi, yeast, and lactic acid bacteria (LAB), are used for fermentation. According to previous reports, LAB fermentation can convert to fatty acids, amino acids, and isoflavones in fermentation substrates, which from linolenic acid, glutamic acid, and glycoside isoflavones to conjugated linoleic acid, γ-aminobutyric acid (GABA), and aglycone isoflavones (Lee et al., 2018;Lee et al., 2022). These converted compounds have health benefits such as anti-obesity, reduced blood pressure, and anti-diabetes (Chen et al., 2018;Lee et al., 2018;Lee et al., 2022). ...

Changes of γ-Aminobutyric Acid, Phytoestrogens, and Biofunctional Properties of the Isoflavone-Enriched Soybean (Glycine max) Leaves during Solid Lactic Acid Fermentation

Fermentation