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15 pages, 3181 KiB  
Article
Effect of EGCG–Methacrylate-Functionalized Resin Infiltrant on White Spot Lesions: An In Vitro Study
by Karin Landmayer, Bruna de Oliveira Iatarola, Talita Portela Pereira, Raquel Shimizu Mori, Alyssa Teixeira Obeid, Mariele Vertuan, Daniela Alvim Chrisostomo, Ana Carolina Magalhães, Lulwah Alreshaid, Paulo Henrique dos Santos, Anuradha Prakki and Luciana Fávaro Francisconi-dos-Rios
J. Funct. Biomater. 2025, 16(1), 6; https://doi.org/10.3390/jfb16010006 (registering DOI) - 29 Dec 2024
Viewed by 89
Abstract
This study evaluated the color change (ΔE00) and penetration depth (PD) of white spot lesions (WSLs) infiltrated with the resin infiltrant (Icon®) functionalized with methacrylate epigallocatechin-3-gallate (EGCG). To introduce polymerizable double bonds, EGCG was reacted with methacryloyl chloride (EM). [...] Read more.
This study evaluated the color change (ΔE00) and penetration depth (PD) of white spot lesions (WSLs) infiltrated with the resin infiltrant (Icon®) functionalized with methacrylate epigallocatechin-3-gallate (EGCG). To introduce polymerizable double bonds, EGCG was reacted with methacryloyl chloride (EM). Subsequently, the Icon resin infiltrant (I) was loaded with neat EGCG (IE) or EGCG–methacrylate (IEM) at 2 wt% each. WSLs were created on bovine enamel blocks and treated with I, IE, or IEM. Sound and untreated enamel surfaces were used as controls (C). Infiltrant PD (%) was determined by Confocal Laser Scanning Microscopy (CLSM, n = 12) analysis. For color change (ΔE00) determination (n = 14), ΔL, Δa, and Δb, half of each sample was kept sound as a reference area. The color was determined with a spectrophotometer. Data were statistically evaluated (p = 0.05). Surface morphology was obtained as a qualitative response variable using 3D CLSM. PD (%) did not differ statistically for I, IE, and IEM (p = 0.780). Groups I and IEM showed similar performance on color change (ΔE00) compared to the control group, while IE exhibited intermediate results, with no significant difference observed between the untreated, I, and IEM groups (p < 0.001). IEM promoted the masking of the WSL color without interfering with the PD. Full article
(This article belongs to the Special Issue Biomaterials in Restorative Dentistry and Endodontics)
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<p>Representative transverse microradiography (TMR) images of enamel white spot lesion from sample 1 (<b>A</b>), sample 2 (<b>B</b>), and sample 3 (<b>C</b>). All samples exhibited an outer surface layer corresponding to the pseudo-intact surface layer over the body of lesion typical of caries white spot lesions.</p>
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<p>Illustrative images obtained by CLSM according to experimental groups, as follows: (<b>A</b>) resin infiltrant (I-Icon); (<b>B</b>) EGCG-functionalized Icon (IE); (<b>C</b>) EGCG–methacrylate-functionalized Icon (IEM). Rhodamine B dye (reddish areas) indicates the infiltrated region, while sodium fluorescein (greenish areas) highlights the non-infiltrated porous areas.</p>
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<p>Data (25%/median/75%) of ΔE<sub>00</sub> values of the control group (C), untreated white spot lesion (L), groups treated with Icon (I), epigallocatechin-3-gallate (EGCG)-functionalized Icon (IE), or EGCG–methacrylate-functionalized Icon (IEM). Different letters indicate statistically significant differences.</p>
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<p>Data (25%/median/75%) of ΔL values of the control group (C), untreated white spot lesion (L), groups treated with Icon (I), EGCG-functionalized Icon (IE), or EGCG–methacrylate-functionalized Icon (IEM). Different letters indicate statistically significant differences.</p>
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<p>Data (25%/median/75%) of Δa values color coordinates (green–red axis) of the control group (C), untreated white spot lesion (L), groups treated with Icon (I), EGCG-functionalized Icon (IE), or EGCG–methacrylate-functionalized Icon (IEM). Different letters indicate statistically significant differences.</p>
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<p>Means and standard deviations of Δb values color coordinate (blue–yellow axis) of the control group (C), untreated white spot lesion (L), groups treated with Icon (I), EGCG-functionalized Icon (IE), or EGCG–methacrylate-functionalized Icon (IEM). Different letters indicate statistically significant differences.</p>
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<p>Surface morphology images obtained by CLSM according to experimental groups, as follows: (<b>A</b>) control (C), (<b>B</b>) untreated white spot lesion (L), (<b>C</b>) Icon resin infiltrant (I); (<b>D</b>) EGCG-functionalized Icon (IE); (<b>E</b>) EGCG-methacrylate-functionalized Icon (IEM).</p>
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14 pages, 11724 KiB  
Article
Transcriptomics Analysis Reveals Differences in Purine and Phenylpropanoid Biosynthesis Pathways Between Camellia sinensis var. Shuchazao and Camellia ptilophylla
by Waqar Khan, Peng Zheng, Binmei Sun and Shaoqun Liu
Horticulturae 2025, 11(1), 8; https://doi.org/10.3390/horticulturae11010008 - 26 Dec 2024
Viewed by 159
Abstract
Tea production and quality are largely determined by the many genetic and biochemical characteristics that occur in tea plant cultivars. Worldwide, tea is consumed for its pleasing and refreshing effects due to its caffeine content. The present study performed transcriptomics analyses of two [...] Read more.
Tea production and quality are largely determined by the many genetic and biochemical characteristics that occur in tea plant cultivars. Worldwide, tea is consumed for its pleasing and refreshing effects due to its caffeine content. The present study performed transcriptomics analyses of two tea species (Camellia sinensis var. Shuchazao (SCZ) and Camellia ptilophylla (CAF)) and identified diversity in the gene expression levels and major regulatory transcription factors (TFs) for the characterization of purine alkaloids and phenylpropanoid biosynthesis pathways. The RNA-seq analysis of two species (SCZ and CAF) revealed the differences in caffeine and catechins synthesis. In the purine alkaloid biosynthesis pathway, the S-adenosyl methionine (SAM) and adenosine monophosphate (AMP) pathway genes were significantly related to xanthosine synthesis in contrasting purine alkaloids among (Camellia sinensis var. Shuchazao (SCZ) and Camellia ptilophylla (CAF)). The significant expression of SAMS-5, PPAT-2, IMPDH-2, TCS-2, TCS-3, XMT-1, XMT-13, and XDH-4 in the xanthosine degradation pathway in CAF is attributed to higher theobromine content as compared to SCZ. Moreover, the transcription factors (TFs) AP2/ERF (20%), WRKY (12%), NAC (11%), and MYB (8%) were significantly correlated. The upregulated expression of caffeine synthesis genes in SCZ was correlated with MYB and AP2/ERF transcription factors. This study provides the basis for differences in the genetic mechanism in purine alkaloids, phenylpropanoid, and flavonoid biosynthesis pathways, which would be helpful in the development and selection of tea plant species with high or low caffeine concentrations. This study also provides a road map for future genetic improvement in tea species and cultivars. Full article
(This article belongs to the Special Issue Tea Tree: Cultivation, Breeding and Their Processing Innovation)
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<p>Pearson correlation coefficient of three replicates of CAF and SCZ species.</p>
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<p>The volcano map of differentially expressed genes (DEGs) in CAF and SCZ species. The percentage distribution of upregulated and downregulated genes is also shown in the figure.</p>
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<p>GO analysis of differentially expressed genes (DEGs) in CAF and SCZ species.</p>
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<p>(<b>A</b>) The DEGs’ KEGG pathways between CAF and SCZ. The three pathways with red color were further analyzed. (<b>B</b>) The scatterplot of RNA-seq transcript abundance folds change RNA-seq values (x-axis) against the qRT-PCR expression values (y-axis).</p>
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<p>Caffeine biosynthesis pathway and expression profiles of genes in CAF and SCZ species. Five pathways towards caffeine synthesis: (1) de novo route, (2) AMP pathway, (3) SAM cycle, (4) NAD pathway, and (5) GMP pathway were listed. Genes in the respective pathways are shown in the heat map with their expression levels. A list of abbreviations is given in <a href="#app1-horticulturae-11-00008" class="html-app">Supplementary Table S6</a>.</p>
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<p>Phenylpropanoid and flavonoid biosynthesis pathways and gene expression in CAF and SCZ species. Genes involved in the respective pathways are shown in the heat map with their expression levels. A list of abbreviations is given in the <a href="#app1-horticulturae-11-00008" class="html-app">Supplementary Materials</a>, <a href="#app1-horticulturae-11-00008" class="html-app">Table S6</a>.</p>
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<p>Coexpression network of TFs and purine alkaloid and phenylpropanoid biosynthesis genes, shown with colored lines (Pearson’s correlation test, <span class="html-italic">p</span> ≤ 0.01). The gene correlation expression networks were visualized using Cytoscape software. The size and color of nodes depend on the degree of coexpression.</p>
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25 pages, 2684 KiB  
Article
Effect of Foliar Application of Calcium and Salicylic Acid on Fruit Quality and Antioxidant Capacity of Sweet Pepper (Capsicum annuum L.) in Hydroponic Cultivation
by Anna Sobczak-Samburska, Ewelina Pióro-Jabrucka, Jarosław L. Przybył, Leszek Sieczko, Stanisław Kalisz, Janina Gajc-Wolska and Katarzyna Kowalczyk
Agriculture 2025, 15(1), 26; https://doi.org/10.3390/agriculture15010026 - 25 Dec 2024
Viewed by 262
Abstract
The aim of this study was to investigate the effect of foliar application of calcium and salicylic acid on improving the physicochemical quality, sensory quality and antioxidant potential of pepper fruits grown hydroponically in mineral wool substrate. Two sweet pepper varieties with red [...] Read more.
The aim of this study was to investigate the effect of foliar application of calcium and salicylic acid on improving the physicochemical quality, sensory quality and antioxidant potential of pepper fruits grown hydroponically in mineral wool substrate. Two sweet pepper varieties with red fruit type were used: block Aifos and elongated Palermo. Fruit quality was tested from four plant treatment combinations: (1) water (control), (2) calcium nitrate 0.7% (Ca), (3) salicylic acid 0.03% (SA), (4) calcium nitrate and salicylic acid combined (Ca+SA). Fruits of both varieties showed high concentrations of health-promoting constituents, including potassium, phosphorus, vitamin C (over 47 mg 100 g−1 of FW (fresh weight)), and carotenoids, with capsanthin being the most abundant (more than 1226 μg 100 g−1 of FW). The results of the sensory evaluation demonstrated that the attributes tested scores above 7 out of 10, indicating a high sensory quality. The antioxidant activity of pepper fruits was determined by three different methods: DPPH (method for measuring the antioxidant activity of DPPH), ABTS (method for measuring the antioxidant activity of ABTS) and TPC (total polyphenol content) and averaged more than 86%, 78% RSC (radical scavenging capacity) and almost 54 mg CE (catechin) 100 g−1 of FW for both cultivars, respectively. Fruit quality results were analysed using PCA (principal component analysis). The first two principal components (PC1 and PC2) explained almost 54% of the variation, highlighting the strong correlations of PC1 with dry matter content, soluble sugars, potassium, acidity and sensory characteristics of pepper fruit such as skin hardness and flesh firmness. The application of SA to peppers resulted in an increase in the carotenoid content of the fruit. Furthermore, a notable positive correlation was detected between total sugars and the sugar/acid ratio when Ca+SA was combined in both cultivars. Palermo fruit showed better quality parameters and higher antioxidant activity, making this sweet pepper variety particularly valuable in a health-promoting context. Full article
(This article belongs to the Section Agricultural Product Quality and Safety)
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical and sensory quality parameters in the space of two main components (PC1, PC3) explaining in total more than 46% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical and sensory quality parameters in the space of two main components (PC1, PC2) explaining in total close to 54% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical parameters and antioxidant properties of pepper fruit in the space of two main components (PC1, PC2) explaining in total more than 57% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical parameters and antioxidant properties of pepper fruit in the space of two main components (PC2, PC3) explaining in total more than 49% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical parameters and antioxidant properties of pepper fruit in the space of two main components (PC1, PC3) explaining in total more than 51% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical parameters of pepper fruit and yield parameters in the space of two main components (PC1, PC2) explaining in total more than 55% of the total variability.</p>
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<p>Principal component analysis (PCA) biplot showing the analysed components based on the physicochemical parameters of pepper fruit and yield parameters in the space of two main components (PC2, PC3) explaining in total more than 43% of the total variability.</p>
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17 pages, 942 KiB  
Article
Phytochemical Characterization and Biological Activity of Two Anacardiaceae Species from Guinea-Bissau
by Quintino Malú, Maryam Malmir, Gonçalo Infante Caldeira, Sofia Encarnação, Katelene Lima, Luís Catarino, Beatriz Silva Lima, João Rocha and Olga Silva
Plants 2025, 14(1), 8; https://doi.org/10.3390/plants14010008 - 24 Dec 2024
Viewed by 263
Abstract
The dried leaves of Lannea velutina A.Rich. and Sorindeia juglandifolia Planch. ex Oliv. are commonly used in traditional medicine throughout West Africa to treat inflammatory diseases. The aim of the present study was to evaluate the anti-inflammatory activity of the standardized hydroethanolic (70%) [...] Read more.
The dried leaves of Lannea velutina A.Rich. and Sorindeia juglandifolia Planch. ex Oliv. are commonly used in traditional medicine throughout West Africa to treat inflammatory diseases. The aim of the present study was to evaluate the anti-inflammatory activity of the standardized hydroethanolic (70%) extracts of these plants and to investigate the underlying mechanisms, with a focus on their antioxidant properties. The anti-inflammatory effects were evaluated using a rat model of induced paw edema, while the antioxidant activity was evaluated by DPPH radical scavenging and iron-reducing antioxidant power assays. Chemical fingerprint was achieved by LC-UV/DAD-ESI/MS and the main classes of secondary metabolites were quantified by colorimetric analysis. The results showed that Sorindeia juglandifolia extract significantly inhibited the increase in paw edema volume, with the maximum effect observed at doses of 100 and 200 mg/kg (20.51 ± 1.07% and 35.50 ± 6.90%, respectively). For L. velutina, the strongest inhibition was observed at 200 and 400 mg/kg (47.48 ± 11.37% and 35.40 ± 1.70%, respectively). Both extracts also showed remarkable antioxidant activity. Phenol derivatives were identified as the main classes of secondary metabolites, with L. velutina containing 350.1 ± 20.6 mg GAE/g DE and S. juglandifolia containing 463.4 ± 29.4 mg GAE/g DE. Ten phenolic markers were identified in L. velutina and six in S. juglandifolia extracts. The main components of L. velutina include myricetin-3-O-glucuronide, quercetin-3-O-glucuronide, catechin, and gallic acid, while S. juglandifolia contains gallic acid, isoquercitrin, and ethyl gallate. These results confirm the anti-inflammatory potential of L. velutina and S. juglandifolia and highlight their prospects as candidates for the development of standardized anti-inflammatory herbal medicines based on their chemical and biological properties. Full article
(This article belongs to the Special Issue Plant Extracts: Bioactive Substances and Active Ingredient)
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<p>LC/MS chromatographic profiles of 70% hydroethanolic extracts of <span class="html-italic">L. velutina</span> (Lv) and <span class="html-italic">S. juglandifolia</span> (Sj) leaves.</p>
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<p>Anti-inflammatory activity of 70% hydroethanolic extracts of <span class="html-italic">L. velutina</span> and <span class="html-italic">S. juglandifolia</span> leaves by inhibition of carrageenan-λ-induced paw edema (1%) in male Wistar rats. The data are displayed as averages and their default errors. <b>Abbreviations</b>: Sal—saline; Car—carrageenan; Ind—indomethacin; Tro—Trolox; Tem—Tempol; <span class="html-italic">S. juglandifolia</span>; <span class="html-italic">L. velutina</span> **** <span class="html-italic">p</span> &lt; 0.0001; *** <span class="html-italic">p</span> &lt; 0.001; ** <span class="html-italic">p</span> &lt; 0.01; versus carrageenan group; # <span class="html-italic">p</span> &lt; 0.0001 versus saline (control) group.</p>
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17 pages, 3951 KiB  
Article
Inhibitory Effect and Mechanism of Dancong Tea from Different Harvesting Season on the α-Glucosidase Inhibition In Vivo and In Vitro
by Rourou Wen, Xianghua Chai, Pingping Wang, Kegang Wu, Xuejuan Duan, Jiasi Chen, Tong Zhang and Liya Zeng
Foods 2024, 13(24), 4183; https://doi.org/10.3390/foods13244183 - 23 Dec 2024
Viewed by 466
Abstract
Tea polyphenols have been reported to decrease the rate of starch hydrolysis by inhibiting α-glucosidase. However, the effect of the tea harvesting season and the structure of catechin monomers on the inhibitory activity of α-glucosidase is not understood. In this study, the inhibitory [...] Read more.
Tea polyphenols have been reported to decrease the rate of starch hydrolysis by inhibiting α-glucosidase. However, the effect of the tea harvesting season and the structure of catechin monomers on the inhibitory activity of α-glucosidase is not understood. In this study, the inhibitory effect and underlying mechanism of four seasons of Dancong tea against α-glucosidase were investigated by in vivo and in vitro experiments, multi-spectroscope and molecular dynamic. The Dancong tea harvested in spring and winter showed a stronger inhibitory effect on α-glucosidase due to a higher content of catechin, especially EGCG ((-)-epigallocatechin-3-gallate). The results of in vivo and in vitro experiments showed that EGCG and ECG ((-)-epicatechin-3-gallate) with a higher content of gallate and hydroxyl groups exhibited a stronger inhibitory effect on starch hydrolysis, rise of postprandial blood glucose and activities of α-glucosidase compared to EGC ((-)-epigallocatechin) and EC ((-)-epicatechin). These gallate and hydroxy groups were more effective in interacting with the amino acid residues in the active site of α-glucosidase, leading to structural changes in the enzyme. Certainly, the inhibitory effect of Dancong tea on α-glucosidase explains one of the mechanisms by which it helps alleviate diabetes; the other hypoglycaemic mechanisms of Dancong tea will be further explored. Full article
(This article belongs to the Special Issue Tea Technology and Resource Utilization)
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<p>Effect of tea harvesting season on α-glucosidase inhibition (<b>A</b>); Contents of the catechin monomers in Dancong four season tea (<b>B</b>); HPLC analysis chromatogram of the catechin monomers in spring tea (<b>C</b>), summer tea (<b>D</b>), autumn tea (<b>E</b>), and winter tea (<b>F</b>).</p>
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<p>Effect of the catechin monomers on in vitro digestion of starch (<b>A</b>,<b>B</b>); in vivo postprandial blood glucose content (<b>C</b>) and α-glucosidase inhibition (<b>E</b>); the calculated area under the curve of glucose content (<b>D</b>) and IC50 values (<b>F</b>). Different letters (a–e) in <a href="#foods-13-04183-f002" class="html-fig">Figure 2</a>D,F indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Fluorescence quenching effects on α-glucosidase by EGCG (<b>A</b>), ECG (<b>B</b>), EGC (<b>C</b>), EC (<b>D</b>).</p>
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<p>The CD spectra of α-glucosidase with various concentrations of EGCG (<b>A</b>), ECG (<b>B</b>), EGC (<b>C</b>), EC (<b>D</b>).</p>
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<p>The effect of EGCG (<b>A</b>), ECG (<b>B</b>), EGC (<b>C</b>), EC (<b>D</b>) on the synchronous fluorescence spectra of α-glucosidase at Δλ = 15 nm.</p>
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<p>The optimal 3D docking conformation of EGCG (<b>A</b>), ECG (<b>B</b>), EGC (<b>C</b>), EC (<b>D</b>) with α-glucosidase. The molecular dynamic results of RMSD (<b>E</b>), RMSF (<b>F</b>), Rg (<b>G</b>), Lennard–Jones potential (<b>H</b>), Coulomb interaction energy (<b>I</b>), hydrogen bond profile (<b>J</b>) of α-glucosidase–EGCG/ECG/EGC/EC complex.</p>
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37 pages, 3583 KiB  
Review
Phytochemistry, Anti-cancer, and Anti-diabetic Properties of Plant-Based Foods from Mexican Agrobiodiversity: A Review
by Adriana García-Gurrola, Ana Laura Martínez, Abraham Wall-Medrano, Francisco J. Olivas-Aguirre, Estefania Ochoa-Ruiz and Alberto A. Escobar-Puentes
Foods 2024, 13(24), 4176; https://doi.org/10.3390/foods13244176 - 23 Dec 2024
Viewed by 634
Abstract
Type 2 diabetes mellitus (T2DM) and cancer are significant contributors to morbidity and mortality worldwide. Recent studies have increasingly highlighted the potential of phytochemicals found in plants and plant-based foods for preventing and treating these chronic diseases. Mexico’s agrobiodiversity provides a valuable resource [...] Read more.
Type 2 diabetes mellitus (T2DM) and cancer are significant contributors to morbidity and mortality worldwide. Recent studies have increasingly highlighted the potential of phytochemicals found in plants and plant-based foods for preventing and treating these chronic diseases. Mexico’s agrobiodiversity provides a valuable resource for phytochemistry. This review presents an examination of essential phytochemicals found in plants and foods within Mexican agrobiodiversity that have shown promising anti-cancer and anti-diabetic properties, including their roles as antioxidants, insulin sensitizers, and enzyme inhibitors. Notable compounds identified include flavonoids (such as quercetin and catechins), phenolic acids (chlorogenic, gallic, and caffeic acids), methylxanthines (like theobromine), xanthones (such as mangiferin), capsaicinoids (capsaicin), organosulfur compounds (like alliin), and various lipids (avocatins). Although these phytochemicals have shown promise in laboratory and animal studies, there is a significant scarcity of clinical trial data involving humans, underscoring an important area for future research. Full article
(This article belongs to the Section Food Nutrition)
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Graphical abstract
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<p>Mexican plants and plant-based foods representative of Mexican agrobiodiversity.</p>
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<p>Mechanisms of anti-diabetic and anti-cancer effects of Mexican plants and plant-based foods. The anti-diabetic mechanisms of phytochemicals are primarily based on their ability to inhibit glycolytic enzymes and reduce glucose absorption in the intestines. They also promote the secretion of glucagon-like peptide-1 (GLP-1). At the pancreatic level, these compounds decrease oxidative stress and support the proper differentiation of β-cells while enhancing insulin secretion. Additionally, phytochemicals facilitate the translocation of glucose transporters (GLUT4) in muscle tissue, aiding in the cellular uptake of glucose. They also promote the correct metabolism and homeostasis of glucose in the liver. In terms of cancer, phytochemicals positively influence various stages of the disease. During the initiation phase, they regulate the cell cycle and improve the antioxidant environment by increasing levels of antioxidant enzymes such as superoxide dismutase (SOD), glutathione S-transferase (GST), and glutathione peroxidase (GPx). In the promotion phase, phytochemicals downregulate the production of cytokines associated with tumor progression, precisely tumor necrosis factor (TNF-α) and nuclear factor kappa light-chain enhancer of activated B cells (NF-κB). During the progression phase, they activate pro-apoptotic genes (like P53) and pro-apoptotic proteins (Caspase-3/9 and BAX). Finally, in the metastasis phase, phytochemicals reduce the activity of NF-κB and Wnt/B-catenin pathways.</p>
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19 pages, 5387 KiB  
Article
Cytotoxic Natural Products from Cryptomeria japonica (Thunb. ex L.) D.Don
by Bjørn Tobiassen Heieren, Anja Strandvoll Dyrdal, Lars Herfindal, Bjarte Holmelid, Cato Brede, Heidi Lie Andersen and Torgils Fossen
Int. J. Mol. Sci. 2024, 25(24), 13735; https://doi.org/10.3390/ijms252413735 - 23 Dec 2024
Viewed by 213
Abstract
Cryptomeria japonica is a commercially important tree native to Japan. The tree belongs to the ancient genus Cryptomeria and has found important uses as a medicinal plant, as well as a main source of timber in Japan. In recent years, there has been [...] Read more.
Cryptomeria japonica is a commercially important tree native to Japan. The tree belongs to the ancient genus Cryptomeria and has found important uses as a medicinal plant, as well as a main source of timber in Japan. In recent years, there has been an increased interest in discovering extended uses of C. japonica as a source of novel bioactive natural products with potential applications as lead compounds for active principles of future drugs. The compounds were isolated by a combination of two-phase extraction, XAD-7 Amberlite column chromatography, Sephadex LH-20 column chromatography and preparative High Performance Liquid Chromatography (HPLC). The structures were determined by a combination of several 1D and 2D Nuclear Magnetic Resonance (NMR) experiments and high-resolution mass spectrometry. Here, we report on the isolation and characterization of the novel biflavone glucoside hinokiflavone 7″-O-β-glucopyranoside, in addition to sixteen known compounds including the flavonols quercetin, quercetin 3-O-α-rhamnopyranoside and quercetin 3-O-β-galactopyranoside, the dihydroflavonols taxifolin 3-O-β-glucopyranoside, taxifolin 7-O-β-glucopyranoside, the flavanones naringenin, naringenin 7-O-β-galactopyranoside and eriodictyol 4′-O-β-glucopyranoside, the flavanol catechin, the biflavonoid amentoflavone, the dihydrochalcone phloretin 2′-O-β-glucopyranoside, the sesquiterpenoid roseoside, the polyphenolic compounds chlorogenic acid, methyl chlorogenate and the flavanocoumarins catechin-(7,8)-7″-(3,4 dihydroxyphenyl)-dihydro-8″(3H)-pyranone, and mururin A. The compounds exhibited low-to-moderate cytotoxic activity against MOLM-13 leukemia cells. Full article
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<p><span class="html-italic">Cryptomeria japonica</span> grown in the Arboretum of University of Bergen. Photo: Heidi Lie Andersen. Photo was taken on 14 November 2024.</p>
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<p>Molecular structures of quercetin (<b>1</b>), quercetin 3-<span class="html-italic">O</span>-<span class="html-italic">α</span>-rhamnopyranoside (<b>2</b>), quercetin 3-<span class="html-italic">O</span>-<span class="html-italic">β</span>-galactopyranoside (<b>3</b>), taxifolin 3-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>4</b>), taxifolin 7-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>5</b>), naringenin (<b>6</b>), naringenin 7-<span class="html-italic">O</span>-<span class="html-italic">β</span>-galactopyranoside (<b>7</b>), eriodictyol 4′-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>8</b>), catechin (<b>9</b>), amentoflavone (<b>10</b>), phloretin 2′-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>11</b>), roseoside (<b>12</b>), chlorogenic acid (<b>13</b>), and methyl chlorogenate (<b>13m</b>), in addition to the rare natural products catechin-(7,8)-7″-(3,4-dihydroxyphenyl)-dihydro-8″(3H)-pyranone (<b>14</b>), hinokiflavone 7″-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>15</b>), and Mururin A (<b>16</b>).</p>
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<p>Expanded regions of the 2D <sup>1</sup>H-<sup>13</sup>C HMBC spectrum (<b>left</b>) and the 2D <sup>1</sup>H-<sup>1</sup>H ROESY spectrum (<b>right</b>) of hinokiflavone 7″-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>15</b>) showing important crosspeaks for determination of linkages between the substructures of the compound. Blue arrows highlight the observed correlations in the molecular structure.</p>
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19 pages, 1349 KiB  
Article
Increasing the Content of Bioactive Compounds in Apple Juice Through Direct Ultrasound-Assisted Extraction from Bilberry Pomace
by Violeta Nour
Foods 2024, 13(24), 4144; https://doi.org/10.3390/foods13244144 - 21 Dec 2024
Viewed by 299
Abstract
The increasing trend of diet-related chronic diseases has stimulated research into developing new food products and beverages with health-promoting potential. At the same time, new resources, including plant by-products, are currently being investigated as a sustainable source of bioactive compounds. In this context, [...] Read more.
The increasing trend of diet-related chronic diseases has stimulated research into developing new food products and beverages with health-promoting potential. At the same time, new resources, including plant by-products, are currently being investigated as a sustainable source of bioactive compounds. In this context, the present study focused on the enrichment of apple juice with anthocyanins and other phenolic compounds by direct ultrasound-assisted extraction (UAE) from bilberry pomace. Response surface methodology combined with a Box–Behnken design was used to find the optimal extraction conditions for maximizing the total anthocyanin content (TAC), total phenolic content (TPC) and DPPH radical scavenging activity (RSA) in the enriched apple juices and to characterize their phenolic profile as influenced by the extraction temperature. UAE from 15% bilberry pomace during 15 min in apple juice at 80 °C resulted in the highest TAC (262.73 mg CGE/L), TPC (1700.91 mg GAE/L) and RSA (8.93 mmol Trolox/L) of the enriched apple juice. The chromatographic polyphenolic profile of the control and enriched juices showed that, besides anthocyanins, phenolic acids (chlorogenic, gallic, caffeic, 3-hydroxybenzoic, p-coumaric, ellagic and protocatechuic acids) and flavonoids (epigallocatechin and catechin) were extracted from the bilberry pomace directly in the apple juice, while the extraction temperature differently impacted the content of individual phenolic compounds. Full article
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<p>Response surface plots of total anthocyanin content (mg CGE/L) as a function of temperature and extraction time at 10% solid percent (<b>A</b>), temperature and solid percent at 60 min extraction time (<b>B</b>) and extraction time and solid percent at 50 degrees Celsius temperature (<b>C</b>) and Pareto chart for total anthocyanin content (<b>D</b>).</p>
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<p>Response surface plots of total phenolic content (mg GAE/L) as a function of temperature and extraction time at 10% solid percent (<b>A</b>), temperature and solid percent at 60 min extraction time (<b>B</b>) and extraction time and solid percent at 50 degrees Celsius temperature (<b>C</b>) and Pareto chart for total phenolic content (<b>D</b>).</p>
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<p>Response surface plots of DPPH radical scavenging activity (mmol Trolox/L) as a function of temperature and extraction time at 10% solid percent (<b>A</b>), temperature and solid percent at 60 min extraction time (<b>B</b>) and extraction time and solid percent at 50 degrees Celsius temperature (<b>C</b>) and Pareto chart for DPPH radical scavenging activity (<b>D</b>).</p>
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<p>Representative HPLC-DAD chromatograms of phenolic compounds in apple juice (AJ) and in apple juices enriched with bioactive compounds through direct ultrasound-assisted extraction from bilberry pomace at 20 °C (AJBP20), 50 °C (AJBP50) and 80 °C (AJBP80) (λ = 280 nm; extraction time = 30 min, solid percent = 10%). Peak identification: (1) gallic acid; (2) epigallocatechin; (3) catechin; (4) chlorogenic acid; (5) caffeic acid; (6) hydroxybenzoic acid; (7) cyanidin 3-glucoside; (8) p-coumaric acid; (9) ellagic acid; (10) ferulic acid; (11) protocatechuic acid; (12) resveratrol; (13) quercetin; (14) kaempferol.</p>
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22 pages, 4996 KiB  
Article
Localization of Secondary Metabolites in Relict Gymnosperms of the Genus Sequoia In Vivo and in Cell Cultures In Vitro, and the Biological Activity of Their Extracts
by Rima N. Kirakosyan, Elena A. Kalasnikova, Elizaveta A. Bolotina, Abdulrahman Saleh, Anastasiya A. Balakina and Svetlana M. Zaytseva
Life 2024, 14(12), 1694; https://doi.org/10.3390/life14121694 - 20 Dec 2024
Viewed by 714
Abstract
In order to scientifically search for new sources of secondary metabolites with valuable qualities for phytopharmacognosy, tasks requiring a step-by-step solution were set. The primary task is the development of technologies for obtaining in vitro highly productive biomass of cells of relict gymnosperms [...] Read more.
In order to scientifically search for new sources of secondary metabolites with valuable qualities for phytopharmacognosy, tasks requiring a step-by-step solution were set. The primary task is the development of technologies for obtaining in vitro highly productive biomass of cells of relict gymnosperms of the genus Sequoia, capable of accumulating various classes of secondary metabolites. The study of the accumulation and localization of secondary metabolites allowed us to evaluate the biological activity and cytotoxicity of in vitro Sequoia cultures. In our study, histochemical methods were used to determine the localization of secondary compounds (phenolic and terpenoid in nature) in plant tissues. Secondary metabolites—polyphenols, catechins, and terpenoids—are mainly localized in the epidermal, parenchymal, and conductive tissues of Sequoia leaves and stems. In callus and suspension cultures of Sequoia, secondary metabolites were localized in cell walls and vacuoles. The mineral composition of the nutrient medium (MS and WPM), the light source (photoperiod), and the endogenous content of polyphenols in the primary explant influenced the initiation and growth characteristics of the in vitro culture of Sequoia plants. Inhibition of growth in suspension cultures on the WPM nutrient medium was noted. The cultivation of Sequoia cell lines at a 16 h photoperiod stimulated the formation of polyphenols but had a negative effect on the growth of callus cultures. Extractive substances obtained from intact and callus tissues of evergreen Sequoia demonstrate high biological (fungicidal) activity and cytotoxicity. The inhibitory effect on Fusarium oxisporum was noted when 200 mg/L of Sequoia extract was added to the nutrient medium. Extracts of redwood callus cultures were low in toxicity to normal FetMSC cells but inhibited the growth of lines of “immortal” cervical HeLa cancer cells and human glioblastoma A172. Intact tissues of Sequoia plants and cell cultures initiated from them in vitro are producers of secondary metabolites with high biological activity. Full article
(This article belongs to the Special Issue Plants as a Promising Biofactory for Bioactive Compounds: 2nd Edition)
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<p>Appearance of evergreen <span class="html-italic">Sequoia</span> plants (<b>a</b>) in a greenhouse and (<b>b</b>) cuttings used as explants for in vitro cultivation.</p>
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<p>Localization of phenolic compounds in (<b>a</b>) meristematic, protective (<b>b</b>,<b>c</b>), and conducting (<b>d</b>–<b>f</b>) tissues of <span class="html-italic">Sequoia</span> used as explants for initiating callus cultures. (Reaction with vanillin reagent for flavonoids (<b>a</b>,<b>c</b>) and total phenolic content with Fast Blue reagent (<b>b</b>)). Reaction with NADH reagent for the presence of terpenoids (<b>g</b>–<b>i</b>).</p>
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<p>Formation of primary callus tissue at wound sites: cultivation of explants in darkness on WPM medium (<b>a</b>) and MS medium (<b>b</b>); cultivation of explants in the presence of light under a 16 h photoperiod on WPM medium (<b>c</b>) and MS medium (<b>d</b>).</p>
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<p>Formation of callus tissue on nutrient media with varying mineral content and under different light conditions: without light access on MS medium (<b>a</b>) and WPM medium in darkness (<b>b</b>); callus tissue from the third passage cultivated in darkness (<b>c</b>); callus tissue from the third and fourth passages (<b>d</b>,<b>e</b>) cultivated under a 16 h photoperiod inducing singular morphogenesis (<b>f</b>,<b>g</b>).</p>
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<p>Initiation of callus tissue from <span class="html-italic">Sequoia sempervirens</span> (D.Don) Endl. on MS media (<b>a</b>,<b>d</b>,<b>e</b>) and WPM (<b>b</b>,<b>c</b>,<b>f</b>), and its subsequent cultivation for four (<b>c</b>,<b>d</b>) and twelve (<b>f</b>) months under light in vertical tubes.</p>
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<p>Suspension cultures of <span class="html-italic">Sequoia sempervirens</span> (D.Don) Endl. cultivated on liquid nutrient media MS (<b>a</b>) and WPM (<b>a</b>) for 6 months, as well as their subsequent transfer to solid nutrient media according to the WPM formulation (<b>b</b>).</p>
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<p>Localization of phenolic compounds during the initiation of callus tissue on the explant (<b>a</b>,<b>b</b>), in the cells of primary callus tissue (<b>c</b>), and in the third passage callus of <span class="html-italic">Sequoia</span> cultivated in the absence of light (<b>d</b>–<b>f</b>). Reaction to the sum of soluble phenolic compounds with Fast Blue reagent (<b>a</b>,<b>b</b>,<b>c</b>,<b>f</b>) and with vanillin reagent for the localization of flavonoids (<b>d</b>,<b>e</b>). Reaction with NADI reagent for the presence of terpenoids in the primary callus (<b>g</b>,<b>h</b>) and third passage (<b>i</b>).</p>
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<p>Callus tissue obtained in the presence of light (<b>a</b>), localization of phenolic compounds during callus initiation on the explant (<b>b</b>), and in the poorly viable callus tissue after 3 months of subculturing in the presence of light (<b>c</b>–<b>e</b>). Reaction to the sum of soluble phenolic compounds with Fast Blue reagent (<b>d</b>) and with vanillin reagent for the localization of flavonoids (<b>b</b>,<b>c</b>,<b>e</b>).</p>
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<p>Localization of secondary metabolites in the morphogenic callus of <span class="html-italic">Sequoia</span>. Reaction for the total soluble phenolic compounds with Fast Blue reagent (<b>a</b>) and vanillin reagent for the localization of flavonoids (<b>b</b>). Reaction with NADI reagent for the presence of terpenoids (<b>c</b>,<b>d</b>).</p>
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<p>Localization of phenolic compounds (<b>a</b>–<b>c</b>) and terpenoids (<b>d</b>) in suspension culture of <span class="html-italic">Sequoia</span>. Reaction for the total soluble phenolic compounds with Fast Blue reagent (<b>a</b>,<b>b</b>) and vanillin reagent for the localization of flavonoids (<b>c</b>). Reaction with NADI reagent for the presence of terpenoids (<b>d</b>).</p>
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<p>Fungicidal activity. Changes in the growth of fungal mycelium under the influence of extracts obtained from intact plants (<b>a</b>,<b>b</b>) and sequoia callus tissue (<b>c</b>) at a concentration of 200 mg/L extract, 400 mg/L extract and 500 mg/L extract, respectively.</p>
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<p>Effect of <span class="html-italic">Sequoia</span> extract on the viability of normal and tumor cells. HepG2—human hepatocellular carcinoma cell line; HeLa—“immortal” cervical cancer cell line; FetMSC—mesenchymal stem cells from the bone marrow of a 5–6-week-old human embryo; A172 A-172 —human glioblastoma cell line. Cells stained with MTT, with the control taken as 100%. On the graphs, the x-axis represents the final concentration of dry matter in the culture medium, and the y-axis represents the intensity of MTT staining as a percentage of the control.</p>
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27 pages, 4683 KiB  
Article
Evaluation of the Antioxidant Properties of Black Acacia (Acacia mearnsii) Tannin in Vulcanized Natural Rubber Using Different Vulcanization Systems
by Matheus da Silva Filgueira, Leandro Ferreira Pinto, Carlos Toshiyuki Hiranobe, Amanda de Sousa Martinez de Freitas, Jéssica de Souza Rodrigues, André Luis de Oliveira, Marystela Ferreira, Samara Araújo Kawall, Dener da Silva Souza, Erivaldo Antonio da Silva, Eduardo Soares Nascimento, Michael Jones da Silva, Flávio Camargo Cabrera, Elmer Mateus Gennaro and Renivaldo José dos Santos
Sustainability 2024, 16(24), 11213; https://doi.org/10.3390/su162411213 - 20 Dec 2024
Viewed by 448
Abstract
Given the growing interest of the rubber industry in seeking alternatives that contribute to environmental sustainability, this work aims to present a study of the mechanical, thermal, and structural properties of natural rubber composites using tannin extracted from Acacia mearnsii as an antioxidant [...] Read more.
Given the growing interest of the rubber industry in seeking alternatives that contribute to environmental sustainability, this work aims to present a study of the mechanical, thermal, and structural properties of natural rubber composites using tannin extracted from Acacia mearnsii as an antioxidant agent. Tannin is a natural and biodegradable product, rich in polyphenols and known for its antioxidant properties. The analyses assessed the effectiveness of incorporating tannins (0, 1, 1.5, and 2 parts per hundred rubber) into sulfur-crosslinked natural rubber composites using a binary accelerator system across three distinct vulcanization schemes: conventional, semi-efficient, and efficient. Initially, tannin characterization tests were conducted, revealing characteristic polyphenol bands of proanthocyanidin catechins, a high total phenolic content, and a substantial reduction in antioxidant activity. These findings highlight the significant antioxidant potential of tannins, particularly for industrial and biological applications. The analyses of the characteristics of natural rubber composites with tannin incorporation indicated that the type of vulcanization process directly affects the antioxidant action of the plant tannin, with the tannins being most effective in the efficient system due to the formation of monosulfidic and disulfidic bonds. Furthermore, the incorporation of tannin did not compromise the physical and chemical properties of the materials, highlighting it as a viable additive for the rubber industry. Full article
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<p>Spectra of Black Acacia Vegetable Tannin.</p>
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<p>Rheometric parameters of the composites in their respective curing systems: (<b>A</b>) minimum torque, (<b>B</b>) maximum torque, (<b>C</b>) torque variation, (<b>D</b>) scorch time, (<b>E</b>) optimum cure time, and (<b>F</b>) cure rate index.</p>
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<p>Specific Density of Composites in Different Crosslinking Systems.</p>
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<p>FTIR-ATR spectra of the samples without exposure to UV-C radiation: (<b>A</b>) conventional system, (<b>B</b>) semi-efficient system, and (<b>C</b>) efficient system.</p>
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<p>FTIR-ATR spectra of samples vulcanized in the conventional system after exposure to UV-C radiation with tannin content of (<b>A</b>) 0.0 phr, (<b>B</b>) 1.0 phr, (<b>C</b>) 1.5 phr, and (<b>D</b>) 2.0 phr.</p>
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<p>FTIR-ATR spectra of samples vulcanized in the semi-efficient system after exposure to UV-C radiation with tannin content of (<b>A</b>) 0.0 phr, (<b>B</b>) 1.0 phr, (<b>C</b>) 1.5 phr, and (<b>D</b>) 2.0 phr.</p>
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<p>FTIR-ATR spectra of samples vulcanized in the efficient system after exposure to UV-C radiation with tannin content of (<b>A</b>) 0.0 phr, (<b>B</b>) 1.0 phr, (<b>C</b>) 1.5 phr, and (<b>D</b>) 2.0 phr.</p>
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<p>Comparison of the hydroxyl index concerning the tannin concentration in the samples of composites crosslinked in the (<b>A</b>) conventional system, (<b>B</b>) semi-efficient system, and (<b>C</b>) efficient system.</p>
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<p>Water contact angles of the surface of the composites before light exposure and after one week of accelerated aging.</p>
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<p>Shore A Hardness tests in different vulcanization systems.</p>
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<p>Abrasion Resistance Tests in Different Vulcanization Systems.</p>
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<p>Thermogravimetric curves of the crosslinked composites in the (<b>A</b>) conventional system, (<b>B</b>) semi-efficient system, and (<b>C</b>) efficient system.</p>
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<p>DTG curve of the crosslinked composites in the (<b>A</b>) conventional system, (<b>B</b>) semi-efficient system, and (<b>C</b>) efficient system.</p>
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18 pages, 4707 KiB  
Article
Investigation of Effects of Cushioning Packaging on the Physiological and Quality Changes in Chinese Olive Fruits During Cold Chain Transportation
by Han Lin, Fanghao Fu, Jinghai Li, Jiahui Liu, Kaiyang Du, Bingxia Zhu, Zhixiong Guo, Tengfei Pan and Wenqin She
Foods 2024, 13(24), 4133; https://doi.org/10.3390/foods13244133 - 20 Dec 2024
Viewed by 217
Abstract
To gain a deeper understanding of the mechanisms by which cushioning packaging preserves the quality of Chinese olive fruits during cold chain transportation and extends their shelf life, this study simulated cold chain conditions and investigated the effects of cushioning packaging on the [...] Read more.
To gain a deeper understanding of the mechanisms by which cushioning packaging preserves the quality of Chinese olive fruits during cold chain transportation and extends their shelf life, this study simulated cold chain conditions and investigated the effects of cushioning packaging on the physiology, antioxidant capacity, and secondary metabolites of fruits during a 20-day shelf life. The results indicated that the decay rate in cushioning-packaging-treated fruit was 75% lower than that in the unbuffered packaging fruit at day 20 of shelf life. Simultaneously, cushioning packaging treatment mitigated the damage severity of the cell membrane structure and kept the cell membrane permeability at a low level, which was 15.34% lower than that in the unbuffered packaging fruit at day 20 of shelf life. Additionally, cushioning packaging effectively restrained the increases in malondialdehyde (MDA) content and alleviated the decline in chlorophyll and total flavonoid contents. It kept a balance among reactive oxygen species (ROS), antioxidant levels, and antioxidant enzyme activities, thereby reducing mechanical-damage-induced decay rates in Chinese olive fruits during the shelf life. Furthermore, metabolome analysis of Chinese olives during the shelf life was performed comparing those without buffered packaging to those with buffered packaging. The metabolome analysis found that the flavonoid biosynthetic pathway exhibited a higher accumulation of chrysin, neohesperidin, naringenin chalcone, sakuranetin, quercetin, catechin, and naringenin metabolites in cushion-packaging treatment compared to those without cushioning treatment. Furthermore, within the phenylalanine metabolic pathway, the accumulation of phenylalanine, p-coumaraldehyde, p-coumaric acid, coniferin and caffeoyl quinic acid metabolites was significantly higher in buffered-packaging groups compared to those without buffering. Together, these findings suggest that cushioning packaging can effectively sustain the integrity of cell membranes and enhance the shelf-life quality of Chinese olive fruits by regulating the balance of ROS and mitigating oxidative stress during cold chain transportation. Full article
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<p>Effect of cushion packaging during cold chain transportation on (<b>A</b>) the delay rate, (<b>B</b>) weight loss rate, (<b>C</b>) chlorophyll content, (<b>D</b>) total flavonoid content, (<b>E</b>) MDA content, and (<b>F</b>) cell membrane permeability of Chinese olives during the shelf life. Asterisks indicate the significant differences between the Chinese olives invaded with unbuffered packing and the control fruit, with * and ** representing the significant levels at <span class="html-italic">p</span> &lt; 0.01 or <span class="html-italic">p</span> &lt; 0.05, respectively, on the same storage day. Symbols indicate the significant differences between the fruit treated with buffered packaging and the fruit subjected to unbuffered packaging, with * and ** denoting the significant levels at <span class="html-italic">p</span> &lt; 0.01 or <span class="html-italic">p</span> &lt; 0.05, respectively, based on the same shelf life.</p>
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<p>Effect of buffered packaging during cold chain transportation on AsA (<b>A</b>) and GSH(<b>B</b>) contents and activities of CAT (<b>C</b>), APX (<b>D</b>), PPO (<b>E</b>), POD (<b>F</b>), and LOX (<b>G</b>) in Chinese olives during the shelf life. The data presented in the figures are expressed as the mean ± SD of three biological replicates. Asterisks indicate the significant differences between the Chinese olives invaded with unbuffered packing and the control fruit, with * and ** representing the significant levels at <span class="html-italic">p</span> &lt; 0.01 or <span class="html-italic">p</span> &lt; 0.05, respectively, on the same storage day. Symbols indicate the significant differences between the fruit treated with buffered packaging and the fruit subjected to unbuffered packaging, with * and ** denoting the significant levels at <span class="html-italic">p</span> &lt; 0.01 or <span class="html-italic">p</span> &lt; 0.05, respectively, based on the same shelf life.</p>
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<p>(<b>A</b>) The PCA shows the metabolic shift of Chinese olive fruits in different groups. Fruit samples of CK0d, CK5d, CK15d, CK20d, CctQ0d, CctQ5d, CctQ15d, CctQ20d, Cct0d, Cct5d, Cct15d, and Cct20d were mixed in equal volumes for use as the quality control (QC). (<b>B</b>) The OPLS-DA for different comparison groups.</p>
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<p>(<b>A</b>) Pie chart showing the different categories of metabolites identified in Chinese olives during the shelf life. (<b>B</b>) Volcano plots of the DAMs in CctQ-0d vs. Cct-0d, CctQ-5d vs. Cct-5d, CctQ-15d vs. Cct-15d, and CctQ-20d vs. Cct-20d. (<b>C</b>) KEGG enrichment analysis of differential metabolites in CctQ-0d vs. Cct-0d, CctQ-5d vs. Cct-5d, CctQ-15d vs. Cct-15d, and CctQ-20d vs. Cct-20d. (The red boxes indicated the pathways related to antioxidant capacity).</p>
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<p>DAMs identified in the different comparison groups that are functionally associated with phenylpropanoid biosynthesis and flavonoid biosynthesis pathway.</p>
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21 pages, 4339 KiB  
Article
A Combined Extract from Dioscorea bulbifera and Zingiber officinale Mitigates PM2.5-Induced Respiratory Damage by NF-κB/TGF-β1 Pathway
by In Young Kim, Hyo Lim Lee, Hye Ji Choi, Yeong Hyeon Ju, Yu Mi Heo, Hwa Rang Na, Dong Yeol Lee, Won Min Jeong and Ho Jin Heo
Antioxidants 2024, 13(12), 1572; https://doi.org/10.3390/antiox13121572 - 20 Dec 2024
Viewed by 491
Abstract
This research evaluated the protective role of a combined extract of Dioscorea bulbifera and Zingiber officinale (DBZO) against respiratory dysfunction caused by particulate matter (PM2.5) exposure in BALB/c mice. The bioactive compounds identified in the DBZO are catechin, astragalin, 6-gingerol, 8-gingerol, [...] Read more.
This research evaluated the protective role of a combined extract of Dioscorea bulbifera and Zingiber officinale (DBZO) against respiratory dysfunction caused by particulate matter (PM2.5) exposure in BALB/c mice. The bioactive compounds identified in the DBZO are catechin, astragalin, 6-gingerol, 8-gingerol, and 6-shogaol. DBZO ameliorated cell viability and reactive oxygen species (ROS) production in PM2.5-stimulated A549 and RPMI 2650 cells. In addition, it significantly alleviated respiratory dysfunction in BALB/c mice exposed to PM2.5. DBZO improved the antioxidant systems in lung tissues by modulating malondialdehyde (MDA) content, as well as levels of reduced glutathione (GSH) and superoxide dismutase (SOD). Likewise, DBZO restored mitochondrial dysfunction by improving ROS levels, mitochondrial membrane potential, and ATP production. Moreover, DBZO modulated the levels of neutrophils, eosinophils, monocytes, and lymphocytes (specifically CD4+, CD8+, and CD4+IL-4+ T cells) in blood and IgE levels in serum. DBZO was shown to regulate the c-Jun N-terminal kinase (JNK) pathway, nuclear factor kappa B (NF-κB) pathway, and transforming growth factor β (TGF-β)/suppressor of mothers against decapentaplegic (Smad) pathway. Histopathological observation indicated that DBZO mitigates the increase in alveolar septal thickness. These findings indicate that DBZO is a promising natural agent for improving respiratory health. Full article
(This article belongs to the Special Issue Oxidative Stress Induced by Air Pollution, 2nd Edition)
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<p>Ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) chromatogram of a combined extract from <span class="html-italic">Dioscorea bulbifera</span> and <span class="html-italic">Zingiber officinale</span> (DBZO).</p>
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<p>Effects of DBZO of particulate matter (PM<sub>2.5</sub>)-stimulated A549 and RPMI 2650 cells. Cell viability in (<b>a</b>) A549 and (<b>b</b>) RPMI 2650 cells and intracellular oxidative stress levels in (<b>c</b>) A549 and (<b>d</b>) RPMI 2650 cells. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on antioxidant system in the lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Malondialdehyde (MDA) contents, (<b>b</b>) reduced glutathione (GSH) levels, and (<b>c</b>) superoxide dismutase (SOD) levels. The results are presented as mean ± SD (<span class="html-italic">n</span> = 5). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on mitochondrial function in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Mitochondrial reactive oxygen species (ROS) production, (<b>b</b>) mitochondrial membrane potential, and (<b>c</b>) mitochondrial ATP content. The results are presented as mean ± SD (<span class="html-italic">n</span> = 4). Data are statistically represented with * = significantly different from the NC group, and # = significantly different from the PM<sub>2.5</sub> group; * and # = <span class="html-italic">p</span> &lt; 0.05 and ** and ## = <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effects of DBZO on inflammatory cells in whole blood and immunoglobulin E (IgE) levels in serum of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Flow cytometry plots, frequency of (<b>b</b>) CD3<sup>+</sup>CD4<sup>+</sup> T cells, (<b>c</b>) CD3<sup>+</sup>CD8<sup>+</sup> T cells, (<b>d</b>) CD3<sup>+</sup>CD4<sup>+</sup>IL-4<sup>+</sup> T cells in whole blood, and (<b>e</b>) IgE levels in serum. The results are presented as mean ± SD (<b>b</b>–<b>d</b>, <span class="html-italic">n</span> = 5; e, <span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on alveolar size in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Histopathological sections and (<b>b</b>) alveolar area. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on inflammation-related protein expression levels in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Western blot images, protein expression levels of (<b>b</b>) IL-33, (<b>c</b>) MyD88, (<b>d</b>) p-IκB-α, (<b>e</b>) p-NF-κB, (<b>f</b>) IL-1β, and (<b>g</b>) TNF-α. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on apoptosis-related protein expression levels in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Western blot images, protein expression levels of (<b>b</b>) p-JNK, (<b>c</b>) BCl-2, (<b>d</b>) BAX, (<b>e</b>) BAX/BCl-2 ratio, and (<b>f</b>) caspase-3. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on apoptosis-related protein expression levels in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Western blot images, protein expression levels of (<b>b</b>) p-JNK, (<b>c</b>) BCl-2, (<b>d</b>) BAX, (<b>e</b>) BAX/BCl-2 ratio, and (<b>f</b>) caspase-3. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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<p>Effects of DBZO on pulmonary fibrosis-related protein expression levels in lung tissues of PM<sub>2.5</sub>-exposed BALB/c mice. (<b>a</b>) Western blot images, protein expression levels of (<b>b</b>) TGF-β1, (<b>c</b>) p-Smad2, (<b>d</b>) p-Samd3, (<b>e</b>) MMP-2, and (<b>f</b>) MMP-9. The results are presented as mean ± SD (<span class="html-italic">n</span> = 3). Data were statistically considered at <span class="html-italic">p</span> &lt; 0.05, and different small letters represent the statistical differences.</p>
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15 pages, 2076 KiB  
Article
Bioactive Content and Antioxidant Properties of Spray-Dried Microencapsulates of Peumus boldus M. Leaf Extracts
by Valentina Polanco, Débora Cerdá-Bernad, Issis Quispe-Fuentes, Claudia Bernal and Jéssica López
Antioxidants 2024, 13(12), 1568; https://doi.org/10.3390/antiox13121568 - 20 Dec 2024
Viewed by 420
Abstract
Boldo (Peumus boldus M.), an plant endemic to central and southern Chile, has been recognized as a medicinal herb, especially its leaves that are rich in bioactive compounds with beneficial properties, such as antioxidant, anti-inflammatory, sedative, and antimicrobial properties, among others. This [...] Read more.
Boldo (Peumus boldus M.), an plant endemic to central and southern Chile, has been recognized as a medicinal herb, especially its leaves that are rich in bioactive compounds with beneficial properties, such as antioxidant, anti-inflammatory, sedative, and antimicrobial properties, among others. This research aimed to evaluate solid-liquid extraction using a response surface methodology to obtain phenolic-rich extracts from boldo leaves and to encapsulate them through spray-drying. A Box-Behnken design was applied to optimize extraction process variables (temperature, time, and solid-liquid ratio). Extracts were characterized in terms of their total phenolic content, with the maximum value obtained being 37.78 mg GAE/g using extraction conditions of a temperature of 100 °C, a time of 60 min, and a solid-liquid ratio of 1:100. The developed microcapsules containing the optimal boldo extracts were characterized (moisture, water activity, scanning electron microscopy, zeta potential, FTIR, total phenolic compounds, antioxidant capacity, and phenolic profile by HPLC-DAD), highlighting their high phenolic content (5.38–5.49 mg GAE/g) and antioxidant capacity, as well as their bioactive content in terms of catechin (445 ± 37 mg/100 g), pyrogallol (304 ± 24 mg/100 g), and epigallocatechin (156 ± 12 mg/100 g). Overall, this study revealed an efficient technique by which to isolate and stabilize bioactive compounds from boldo leaves, with the microcapsules being promising candidates as high added-value ingredients. Full article
(This article belongs to the Special Issue Phenolic Antioxidants)
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<p><span class="html-italic">P. boldus</span> M. plant and its dried leaves.</p>
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<p>Response surface plot representing the effects of time and solid-liquid ratio and temperature on Total Phenolic Content (TPC) from boldo leaves, with the temperature constant at 100 °C. Lower values are represented in blue and higher values in red.</p>
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<p>SEM micrographs of microcapsules. (<b>a</b>) Treatment N°1 microencapsulation (130 °C, 2 mL/min); (<b>b</b>) Treatment N°2 microencapsulation (150 °C, 2 mL/min); (<b>c</b>) Treatment N°3 microencapsulation (130 °C, 4 mL/min); (<b>d</b>) Treatment N°4 microencapsulation (150 °C, 4 mL/min).</p>
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<p>FTIR spectra for different samples. BOLDO extract (blue line), maltodextrin (black line), and Treatment 3 as a model (red line).</p>
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24 pages, 1296 KiB  
Article
Screening of Nutritionally Important Components in Standard and Ancient Cereals
by Vesna Dragičević, Milena Simić, Vesna Kandić Raftery, Jelena Vukadinović, Margarita Dodevska, Sanja Đurović and Milan Brankov
Foods 2024, 13(24), 4116; https://doi.org/10.3390/foods13244116 - 19 Dec 2024
Viewed by 392
Abstract
Sustainable nutrition and food production involve dietary habits and farming systems which are eco-friendly, created to provide highly nutritious staple crops which could serve as a functional food at the same time. This research sought to provide a comprehensive analysis of whole-grain cereals, [...] Read more.
Sustainable nutrition and food production involve dietary habits and farming systems which are eco-friendly, created to provide highly nutritious staple crops which could serve as a functional food at the same time. This research sought to provide a comprehensive analysis of whole-grain cereals, and some ancient grains toward important macro- (protein), micro-nutrients (mineral elements), and bioactive compounds, such as dietary fiber (arabinoxylan and β-glucan) and antioxidants (phytic acid, total glutathione, yellow pigment, and phenolic compounds) to provide functionality in a sustainable diet. Genotypes, such as durum wheat, triticale, spelt, emmer wheat, and barley, could be considered important and sustainable sources of protein (ranging 11.10–15.00%), as well as prebiotic fiber (β-glucan and arabinoxylan, ranging 0.11–4.59% and 0.51–6.47%, respectively), essential elements, and various antioxidants. Ancient grains can be considered as a source of highly available essential elements. Special attention should be given to the Cimmyt spelt 1, which is high in yellow pigment (5.01 μg·g−1) and has a capacity to reduce DPPH radicals (186.2 µmol TE·g−1), particularly Zn (70.25 mg·kg−1). The presence of phenolics, dihydro-p-coumaric acid, naringin, quercetin, epicatechin in grains of oats (Sopot), as well as catechin in barley grains (Apolon and Osvit) underline their unique chemical profile, making them a desirable genetic pool for breeding genotypes. This research provides a comprehensive assessment of different nutritional aspects of various cereals (some of which are commonly used, while the others are rarely used in diet), indicating their importance as nutraceuticals. It also provides a genetic background that could be translated the genotypes with even more profound effects on human health. Full article
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<p>Dendrogram presenting the concentration of mineral elements in standard and ancient grains.</p>
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<p>Dendrogram presenting ratio of Phy and essential elements in standardgrains and ancient grains.</p>
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<p>Dendrogram presenting concentrations of antioxidants in the grain of examined standard and ancient grains.</p>
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<p>PCA for evaluated phytochemicals in tested genotypes: (<b>A</b>) score and (<b>B</b>) loading plot. Abbreviations: protein (Prot), inorganic phosphorus (Pi), phytic phosphorus (Pphy), yellow pigment (YP), total phenolic compounds (TPCs), total glutathione(GSH), β-glucan (β-glu), arabinoxylan (Arab), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), sodium (Na), iron (Fe), manganese (Mn), zinc (Zn), copper (Cu), naringin (NA),p-coumaric acid(p-CoumA), ferulic acid (FA), and quercetin (QUE).</p>
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14 pages, 1326 KiB  
Article
Evaluation of Cellulase, Pectinase, and Hemicellulase Effectiveness in Extraction of Phenolic Compounds from Grape Pomace
by Natalia Stanek-Wandzel, Alicja Krzyszowska, Magdalena Zarębska, Katarzyna Gębura, Tomasz Wasilewski, Zofia Hordyjewicz-Baran and Magdalena Tomaka
Int. J. Mol. Sci. 2024, 25(24), 13538; https://doi.org/10.3390/ijms252413538 - 18 Dec 2024
Viewed by 313
Abstract
Grape pomace, the solid residue from winemaking, is a rich source of polyphenolic compounds with significant antioxidant properties. However, the efficient extraction of these valuable compounds remains a challenge. This study focuses on optimizing the conditions for the enzyme-assisted extraction of polyphenolic compounds [...] Read more.
Grape pomace, the solid residue from winemaking, is a rich source of polyphenolic compounds with significant antioxidant properties. However, the efficient extraction of these valuable compounds remains a challenge. This study focuses on optimizing the conditions for the enzyme-assisted extraction of polyphenolic compounds from red grape pomace using cellulase, hemicellulase, and pectinase. The key variables investigated in this study were enzyme concentration, extraction time, and solid/liquid ratio. The results highlight the importance of selecting enzymes based on target compounds, as different enzymes were found to be more effective for specific phenolic fractions. Hemicellulase was most effective for phenolic acids, cellulase for catechins, and pectinase for anthocyanins. Enzyme-assisted extraction significantly increased the yield of phenolic compounds and resulted in higher total phenolic content and antioxidant activity compared to control samples treated with solid/liquid extraction without enzyme addition. These findings confirm that enzyme-assisted extraction is a promising approach for enhancing the recovery of polyphenolic compounds from grape pomace. Full article
(This article belongs to the Section Bioactives and Nutraceuticals)
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<p>Response surface plots showing the relationships between total phenolic content and antioxidant activity extracts and reaction parameters: extraction time, cellulase amount, and solid-to-liquid ratio value.</p>
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<p>Proportion of phenolic compounds in grape pomace extracts depending on the enzymes used. Blue color—phenolic acids, yellow color—catechins, grey color—anthocyanins, and green color—other flavonoids.</p>
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<p>Spectra of extracts after extraction without and with cellulase enzyme for grape pomace.</p>
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