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22 pages, 1920 KiB  
Article
Antioxidant Bio-Compounds from Chestnut Waste: A Value-Adding and Food Sustainability Strategy
by Roberta Barletta, Alfonso Trezza, Andrea Bernini, Lia Millucci, Michela Geminiani and Annalisa Santucci
Foods 2025, 14(1), 42; https://doi.org/10.3390/foods14010042 - 27 Dec 2024
Viewed by 328
Abstract
In an era of escalating environmental challenges, converting organic residues into high-value bioactive compounds provides a sustainable way to reduce waste and enhance resource efficiency. This study explores the potential of the circular bioeconomy through the valorization of agricultural byproducts, with a focus [...] Read more.
In an era of escalating environmental challenges, converting organic residues into high-value bioactive compounds provides a sustainable way to reduce waste and enhance resource efficiency. This study explores the potential of the circular bioeconomy through the valorization of agricultural byproducts, with a focus on the antioxidant properties of specific chestnut burr cultivars. Currently, over one-third of food production is wasted, contributing to both humanitarian and environmental crises. Through circular bioeconomy, we can transform biological waste into valuable products for use in fields like food innovation and sustainability. The antioxidant effects of three chestnut cultivars, Bastarda Rossa, Cecio, and Marroni, were assessed through in vitro assays, highlighting their potential to combat oxidative stress—an important factor for health-related applications. The characterization of the three cultivars showed the major presence of ellagic acid and gallic acid in the extract, renowned for their antioxidant activity. In vitro assays evaluated the phenolic and flavonoid content, as well as the antioxidant activity of the three extracts, confirming the cultivar Cecio as the richest in these bioactive compounds and the most performative in antioxidant assays. In vitro antioxidant and oxidative stress recovery assays on SaOS-2, fibroblast, and chondrocyte cell lines displayed a strong antioxidant activity. Furthermore, the cytotoxicity assay demonstrated the safety of all three extracts in the tested human cell lines. In silico docking simulations further validated the biological relevance of these compounds by predicting strong hydrophobic and polar interactions with oxidative stress-related protein targets. Overall, this study demonstrates the antioxidant properties of chestnut byproducts. The findings contribute to the development of functional foods, nutraceuticals, and other applications, underscoring the role of chestnut cultivars in advancing circular bioeconomy practices. Full article
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<p>DPPH assay. Absorbance decrease in three cultivar extracts analyzed compared to control, ascorbic acid (AA). Antioxidant activity (expressed as %AA) of chestnut varieties was measured at varying extract concentrations (0–500 µg/mL). (<b>A</b>–<b>C</b>) represent cultivars <span class="html-italic">Bastarda Rossa</span>, <span class="html-italic">Cecio</span>, and <span class="html-italic">Marroni</span>, respectively.</p>
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<p>(<b>A</b>) The 1H NMR spectrum of an aqueous extract. (<b>B</b>) The aromatic region of the spectrum shows signals of gallic acid (*) and ellagic acid (+) for the cultivar <span class="html-italic">Bastarda Rossa</span> (RB, blue), <span class="html-italic">Cecio</span> (RC, red), and <span class="html-italic">Marroni</span> (RM, green). Signal integration allowed for polyphenol quantification, reported in <a href="#foods-14-00042-t005" class="html-table">Table 5</a>.</p>
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<p>13C NMR normalized spectra of <span class="html-italic">Bastarda Rossa</span> (RB, blue), <span class="html-italic">Cecio</span> (RC, red), and <span class="html-italic">Marroni</span> (RM, green).</p>
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<p>Cytotoxicity of chestnut extracts (RM: <span class="html-italic">Marroni</span>, RB: <span class="html-italic">Bastarda Rossa</span>, RC: <span class="html-italic">Cecio</span>) on SaOS-2 cells at varying concentrations (31.5–500 µg/mL) after 24 h (<b>top panel</b>) and 48 h (<b>bottom panel</b>) of treatment. Cell viability was measured using the MTT assay, and the results are expressed as a percentage of the untreated control group (CTR). Extract concentrations ranged from 31.5 to 500 µg/mL, with bars representing the mean ± standard deviation from three independent experiments.</p>
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<p>Cytotoxicity of chestnut extracts (RM: <span class="html-italic">Marroni</span>, RB: <span class="html-italic">Bastarda Rossa</span>, RC: <span class="html-italic">Cecio</span>) on chondrocyte varying concentrations (31.5–500 µg/mL) after 24 h (<b>top panel</b>) and 48 h (<b>bottom panel</b>) of treatment. Cell viability was measured using the MTT assay, and the results are expressed as a percentage of the untreated control group (CTR). Extract concentrations ranged from 31.5 to 500 µg/mL, with bars representing the mean ± standard deviation from three independent experiments.</p>
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<p>Cytotoxicity of chestnut extracts (RM: <span class="html-italic">Marroni</span>, RB: <span class="html-italic">Bastarda Rossa</span>, RC: <span class="html-italic">Cecio</span>) on fibroblasts at varying concentrations (31.5–500 µg/mL) after 24 h (<b>top panel</b>) and 48 h (<b>bottom panel</b>) of treatment. Cell viability was measured using the MTT assay, and the results are expressed as a percentage of the untreated control group (CTR). Extract concentrations ranged from 31.5 to 500 µg/mL, with bars representing the mean ± standard deviation from three independent experiments.</p>
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<p>Oxidative stress recovery in various cell lines treated with chestnut extracts. RM = <span class="html-italic">Marroni</span>; RB = <span class="html-italic">Bastarda Rossa</span>; RC = <span class="html-italic">Cecio</span>. (<b>A</b>) SaOS-2; (<b>B</b>) chondrocytes; and (<b>C</b>) fibroblasts, at different concentrations (3.125–100 µg/mL). Oxidative stress was induced in cells using hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), with untreated stressed cells (CNS) and untreated non-stressed cells (CS) serving as controls. Cell viability was measured using MTT, and results are expressed as a percentage of the untreated non-stressed control (CS). Data represent the mean ± standard deviation from three independent experiments.</p>
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<p>An overview of the target/ligand complexes. (<b>A</b>) is ellagic acid in complex with the NEK6 kinase 3D structure; (<b>B</b>) is gallic acid in complex with the carbonic anhydrase III 3D structure. The enlarged pictures display the interaction network established among the target-binding residues and the ligand. The binding residues involved in hydrogen bonds, salt bridges, and hydrophobic interactions are labeled cyan, yellow, and gray, respectively. Hydrogen bonds and salt bridges are pictured as orange and blue dashed lines, respectively.</p>
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18 pages, 1736 KiB  
Article
Drying: A Practical Technology for Blueberries (Vaccinium corymbosum L.)—Processes and their Effects on Selected Health-Promoting Properties
by Elsa Uribe, Antonio Vega-Galvez, Alexis Pasten, Kong Shun Ah-Hen, Nicol Mejias, Lorena Sepúlveda, Jacqueline Poblete and Luis S. Gomez-Perez
Antioxidants 2024, 13(12), 1554; https://doi.org/10.3390/antiox13121554 - 18 Dec 2024
Viewed by 496
Abstract
The global dried blueberry market is steadily growing, driven by the creation of innovative blueberry-based products. This trend presents an opportunity to explore a previously untapped segment of the blueberry market in Chile. In this study, a comprehensive assessment of four drying techniques [...] Read more.
The global dried blueberry market is steadily growing, driven by the creation of innovative blueberry-based products. This trend presents an opportunity to explore a previously untapped segment of the blueberry market in Chile. In this study, a comprehensive assessment of four drying techniques (hot-air drying [HAD], vacuum drying [VD], infrared drying [IRD], and freeze-drying [FD]) was conducted to determine best operating conditions and preserve the health-promoting properties of blueberries. Drying kinetics, proximate composition, color, anthocyanin content, individual phenols, and antioxidant, antiproliferative, and antidiabetic potential of blueberries were evaluated. VD showed the highest drying rates, reaching equilibrium moisture more rapidly (Deff value of 3.44 × 10−10 m2/s). Drying caused an increase in lipid content but a decrease in protein content. The color parameter L* increased in all dried samples, and C* reflected color intensification. FD best retained anthocyanin content, which decreased significantly in the other drying processes. Chlorogenic acid and rutin predominated in HAD, IRD, and FD samples. The antioxidant potential in ORAC assays increased for all drying methods but decreased in DPPH assays. Blueberry extracts from FD and HAD exhibited the greatest antiproliferative effect against A549 and H1299 cell lines, respectively. HAD showed the best inhibitory effect on α-glucosidase, with an IC50 value of 0.276 mg/mL, similar to acarbose (IC50 = 0.253 mg/mL). Given the significant retention of health-promoting properties and bioactive compounds in HAD-dried samples, this method is advisable as a sustainable option for drying blueberries in Chile. Full article
(This article belongs to the Special Issue Antioxidant Research in Chile)
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<p>(<b>A</b>) Effects of drying methods on the moisture ratio (MR) versus drying time curve of blueberries. (<b>B</b>) Drying rate (DR) versus drying time curve for blueberries with different drying methods. Values are the means of triplicate analyses (<span class="html-italic">n</span> = 3), and error bars are the standard deviation. Hot-air drying (HAD), vacuum drying (VD), infrared drying (IRD), and freeze-drying (FD).</p>
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<p>Qualitative analytical results of the phenolic profile in (<b>A</b>) control and (<b>B</b>) representative dried samples of blueberries by HPLC-DAD. <b>1</b> Protocatechuic acid; <b>2</b> Chlorogenic acid; <b>3</b> Epigallocatechin; <b>4</b> Caffeic acid; <b>5</b> Rutin; <b>6</b> Naringin; <b>7</b> Quercetin.</p>
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<p>Antioxidant potential of blueberries as affected by drying methods: (<b>A</b>) 2,2-diphenyl-1-picryl-hydrazyl (DPPH) and (<b>B</b>) Oxygen Radical Absorbance Capacity (ORAC) assays. Values are the means of triplicate analyses (<span class="html-italic">n</span> = 3), and error bars are the standard deviation. TE: Trolox equivalents. Different alphabet letters presented on the bars indicate significant differences at <span class="html-italic">p</span> &lt; 0.05 among different drying methods. Hot-air drying (HAD), vacuum drying (VD), infrared drying (IRD), and freeze-drying (FD).</p>
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<p>Antiproliferative effects estimated at various concentrations of extracts obtained from blueberries dried by different methods against (<b>A</b>) H1299 cell lines and (<b>B</b>) A549 cell lines. Data are expressed as mean ± SEM of three independent experiments (<span class="html-italic">n</span> = 3). Hot-air drying (HAD), vacuum drying (VD), infrared drying (IRD), and freeze-drying (FD).</p>
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<p>α-Glucosidase inhibitory activity estimated at various concentrations of extracts obtained from blueberries dried by different methods. Acarbose is a known anti-diabetic drug (positive control). Values are the means of triplicate analyses (<span class="html-italic">n</span> = 3), and error bars are the standard deviation. Hot-air drying (HAD), vacuum drying (VD), infrared drying (IRD), and freeze-drying (FD).</p>
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12 pages, 1172 KiB  
Article
Effects of Tithonia diversifolia Extract as a Feed Additive on Digestibility and Performance of Hair Lambs
by Olga Teresa Barreto-Cruz, Juan Carlos Henao Zambrano, Maria Alejandra Ospina Barrero and Román David Castañeda-Serrano
Animals 2024, 14(24), 3648; https://doi.org/10.3390/ani14243648 - 17 Dec 2024
Viewed by 395
Abstract
Animal production requires efficiency, safety and environmental sustainability. Bioactive compounds from tropical plants could modulate ruminal fermentation, providing an alternative method to antibiotic treatment and addressing concerns about antibiotic resistance. In this study, the aim was to determine the effects of Tithonia diversifolia [...] Read more.
Animal production requires efficiency, safety and environmental sustainability. Bioactive compounds from tropical plants could modulate ruminal fermentation, providing an alternative method to antibiotic treatment and addressing concerns about antibiotic resistance. In this study, the aim was to determine the effects of Tithonia diversifolia extract (TDE) on performance, intake, digestibility and blood parameters [i.e., glucose, blood urea nitrogen (BUN), aspartate aminotransferase (AST), alanine aminotransferase (ALT)] in crossbreed sheep. The main biocompounds of the TDE include caffeic acid (CA), quercetin (QCT), luteolin (LT) and apigenin (AP). Experiment 1: An in vitro dry matter digestibility (IVDMD) study was conducted to determine the optimal inclusion levels. The IVDM values were 73.09a, 82.03b, 81.01b, 73.20a and 74.51a for the control, 5, 10, 15 and 20 g/kg for the DM treatments, respectively (R-Sq adj = 0.857). The levels of 5 and 10 g were selected for the in vivo experiment. Experiment 2: Twenty-eight male crossbred hair lambs were assigned to four treatments (n = 7): control, 20 mg monensin/day, 5 g TDE/day and 10 g TDE/day groups. No differences in animal performance were observed, including body weight and feed conversion (p > 0.05). The TDE at 10 g/day improved NDF digestibility) (61.32%) and reduced the ruminal acetate to propionate ratio. The total digestible nutrients (TDN) were higher in 10 g TDE treatment with 66.41% and the lowest acetate production (67.82%) (p = 0.042), and propionate production (21.07%) were observed. The TDE were safe at 5 g and 10 g/day for liver function and exhibited lower BUN levels suggesting an improvement in protein metabolism. TDE extract at 10 g/day (TDE10), showed improvements in total tract digestibility of NDF and reduced the ruminal acetate to propionate ratio. However, due to TDE10 reducing the DM intake, the improvements in digestibility and ruminal fermentation were not reflected in growth performance improvements. Full article
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<p>Biosynthesis of the main polyphenols found in leaves of aqueous extracts of <span class="html-italic">Tithonia diversifolia</span>.</p>
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<p>In vitro digestibility of dry matter (IVDMD) in a diet with a forage to concentrate ratio of 60:40 at different inclusion levels of TDE.</p>
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<p>Polynomial regression of in vitro digestibility of dry matter (IVDMD) in a diet with forage to concentrate ratio of 66:34 at different inclusion levels of TDE.</p>
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14 pages, 4704 KiB  
Article
Macroalgae Compound Characterizations and Their Effect on the Ruminal Microbiome in Supplemented Lambs
by Adriana Guadalupe De la Cruz Gómez, Huitzimengari Campos-García, German D. Mendoza, Juan Carlos García-López, Gregorio Álvarez-Fuentes, Pedro A. Hernández-García, José Alejandro Roque Jiménez, Oswaldo Cifuentes-Lopez, Alejandro E Relling and Héctor A. Lee-Rangel
Vet. Sci. 2024, 11(12), 653; https://doi.org/10.3390/vetsci11120653 - 14 Dec 2024
Viewed by 565
Abstract
The impact of macroalgae species on rumen function remains largely unexplored. This present study aimed to identify the biocompounds of the three types of marine macroalgae described: Macrocystis pyrifera (Brown), Ulva spp. (Lettuce), Mazzaella spp. (Red) and their effect on species-specific modulations of [...] Read more.
The impact of macroalgae species on rumen function remains largely unexplored. This present study aimed to identify the biocompounds of the three types of marine macroalgae described: Macrocystis pyrifera (Brown), Ulva spp. (Lettuce), Mazzaella spp. (Red) and their effect on species-specific modulations of the rumen microbiome. The macroalgae were characterized using GC-MS. Twelve Rambouillet lambs were randomly assigned to one of four experimental diets (n = 3 per treatment): (a) control diet (CD); (b) CD + 5 g of Red algae; (c) CD + 5 g of Brown algae; and (d) CD + 5 g of Lettuce algae. After the lambs ended their fattening phase, they donated ruminal fluid for DNA extraction and 16S rRNA gene V3 amplicon sequencing. Results: The tagged 16S rRNA amplicon sequencing and statistical analysis revealed that the dominant ruminal bacteria shared by all four sample groups belonged to phyla Firmicutes and Bacteroidota. However, the relative abundance of these bacterial groups was markedly affected by diet composition. In animals fed with macroalgae, the fibrinolytic and cellulolytic bacteria Selenomonas was found in the highest abundance. The diversity in chemical composition among macroalgae species introduces a range of bioactive compounds, particularly VOCs like anethole, beta-himachalene, and 4-ethylphenol, which demonstrate antimicrobial and fermentation-modulating properties. Full article
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<p>Chromatogram of total ion of the volatile compounds in Red algae by CG-MS: 1. 2-Methylbutane; 2. Diethyl ether; 3. 1,1-Dichloroethene; 4. Propanon-2-one; 5. Ethene, 1,2-dichloro-, (E)-; 6. 1-Propanol; 7. 2-butanol; 8. Benzene; 9. 1,2-Dichloroethane; 10. Pental-2-ol; 11. Octane; 12. Ethyl isovalerate; 13. 2-Isopropyl-3-methoxypyrazine; 14. p-menthatriene; 15. etenyl-dimethylpyrazine; 16. 3-nonenal; 17. ethyl 3-(methylthio)propanoate; 18. Limonene oxide; 19. Anethole; 20. Tetradecane; 21. Carbamothioic acid; 22. beta-Himachalene; 23. 2-methyl-1,4-naphthalenedione.</p>
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<p>Chromatogram of total ion of the volatile compounds in Lettuce algae by CG-MS: 1. Diethyl ether; 2. Ethyl isovalerate; 3. Acetilpyrazine; 4. ethenyl-dimethylpirazine; 5. 1-2-Cyclopentanedione, 3,4; 6. Methyl salicylate; 7. Nerol; 8. trans-2-Undecenal; 9. beta-ionone; 10. 1,4-Naftalenedion; 11. Clorotalonil.</p>
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<p>Chromatogram of total ion of the volatile compounds in Brown algae by CG-MS: 1. Butane; 2. Ethanol; 3. propanona-2-one; 4. Diethyl ether; 5. 1-Propanol; 6. Carbon disulfide; 7. butan-2-one; 8. Tri-chloroethane; 9. 1,2-Dichloropropane; 10. Methyl butanoate; 11. Octane; 12. 1-Heptanol; 13. Al-pha-Phellandrene; 14. Butylbenzene; 15. p-Menthatriene; 16. 4-Ethylphenol; 17. Anethole; 18. trans-2-undecenal; 19. delta-decalactone; 20. Octadecane.</p>
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<p>(<b>A</b>) Rarefaction curves of the four feeding treatments in lambs. (<b>B</b>) Box and whisker plots of three α-diversity indices (Pielou evenness, Richness, and Shannon diversity index) of bacterial communities in each treatment. Different letters above the whiskers denote significant differences between groups determined by Kruskal–Wallis tests (<span class="html-italic">p</span> &lt; 0.05). (<b>C</b>) Nonmetric multidimensional scaling (NMDS) of bacterial communities, clustering based on Bray–Curtis similarities. (<b>D</b>) Relative abundances of bacterial genera in microbial composition among lambs fed with different diets.</p>
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<p>Bacterial community composition at family (<b>A</b>) and genus (<b>B</b>) levels in the rumen of four feed treatments in lambs.</p>
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23 pages, 5190 KiB  
Article
Microencapsulation of Anthocyanins from Zea mays and Solanum tuberosum: Impacts on Antioxidant, Antimicrobial, and Cytotoxic Activities
by Carlos Barba-Ostria, Yenddy Carrero, Jéssica Guamán-Bautista, Orestes López, Christian Aranda, Alexis Debut and Linda P. Guamán
Nutrients 2024, 16(23), 4078; https://doi.org/10.3390/nu16234078 - 27 Nov 2024
Viewed by 579
Abstract
Objectives: This study investigates the biological activities of microencapsulated anthocyanins extracted from two Andean ancestral edible plants, Solanum tuberosum, and Zea mays, with a focus on their potential applications in functional foods and therapeutics. The primary objective was to evaluate their [...] Read more.
Objectives: This study investigates the biological activities of microencapsulated anthocyanins extracted from two Andean ancestral edible plants, Solanum tuberosum, and Zea mays, with a focus on their potential applications in functional foods and therapeutics. The primary objective was to evaluate their antioxidant, antimicrobial, and cytotoxic properties alongside structural and functional analyses of the microencapsulation process. Methods: Anthocyanins were extracted and microencapsulated using maltodextrin as a carrier. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were employed to analyze the stability and structure of the microencapsulated particles. The antioxidant, antimicrobial, and cytotoxic activities of the microencapsulated were assessed through established assays. Results:S. tuberosum exhibited superior antioxidant capacity and potent anticancer activity against HepG2 and THJ29T cell lines, while Z. mays demonstrated significant antimicrobial efficacy against multidrug-resistant bacterial strains and biofilm-forming pathogens. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) confirmed the stabilization of anthocyanins within a maltodextrin matrix, enhancing their bioavailability and application potential. Conclusions: These results highlight the versatility of microencapsulated anthocyanins as bioactive agents for industrial and therapeutic applications. Future studies should explore in vivo validation and synergistic formulations to optimize their efficacy and broaden their use in nutraceutical and pharmaceutical fields. Full article
(This article belongs to the Special Issue Bioactive Compounds and Functional Foods in Human Health)
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<p>SEM image of <span class="html-italic">S. tuberosum</span> L. microencapsulated particles prepared by spray drying, captured with a TESCAN MIRA 3 SEM at 134× magnification and a 200 µm scale bar.</p>
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<p>SEM image of <span class="html-italic">Z. mays</span> L. microencapsulated particles prepared by spray drying, captured with a TESCAN MIRA 3 SEM at 1000× magnification and a 50 µm scale bar.</p>
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<p>Particle size distribution analysis of <span class="html-italic">S. tuberosum</span> L. microencapsulated spheres. Particle size distribution and cumulative distribution curve of <span class="html-italic">S. tuberosum</span> L microencapsulated spheres, measured using FIJI software (version 2.9.0).</p>
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<p>Particle size distribution analysis of <span class="html-italic">Z. mays</span> L. microencapsulated spheres. Particle size distribution and cumulative distribution curve of <span class="html-italic">Z. mays</span> microencapsulated spheres were measured using FIJI software (version 2.9.0).</p>
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<p>Antioxidant activity (% DPPH inhibition) of microencapsulated anthocyanins from <span class="html-italic">S. tuberosum</span> L. and <span class="html-italic">Z. mays</span> L. The plot illustrates the relationship between anthocyanin concentration and % DPPH inhibition. Data points represent the mean % DPPH inhibition, with <span class="html-italic">S. tuberosum</span> depicted as dark goldenrod cross and <span class="html-italic">Z. mays</span> as orange cross. Cubic polynomial fits (dashed lines).</p>
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<p>Antimicrobial activity of microencapsulated <span class="html-italic">S. tuberosum</span> anthocyanin extract against different bacterial strains. Heatmap showing the inhibition zones (in mm) with standard deviations for <span class="html-italic">S. aureus</span>, <span class="html-italic">L. monocytogenes</span>, <span class="html-italic">P. aeruginosa</span>, <span class="html-italic">B. cereus</span>, and <span class="html-italic">E. coli</span> at various concentrations (534.1 to 26.7 mg/mL) of the microencapsulated <span class="html-italic">S. tuberosum</span> extract. Antibiotic (gentamicin) was used at the standard concentration.</p>
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<p>Antimicrobial activity of microencapsulated <span class="html-italic">Z. mays</span> anthocyanin extracts against different bacterial strains. Heatmap showing the inhibition zones (in mm) with standard deviations for <span class="html-italic">S. aureus</span>, <span class="html-italic">L. monocytogenes</span>, <span class="html-italic">P. aeruginosa</span>, <span class="html-italic">B. cereus</span>, and <span class="html-italic">E. coli</span> at various concentrations (534.1 to 26.7 mg/mL) of the microencapsulated <span class="html-italic">S. tuberosum</span> extract. Antibiotic (gentamicin) was used at the standard concentration.</p>
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<p>Dose–response curves of the cytotoxic effects of <span class="html-italic">Z. mays</span> and <span class="html-italic">S. tuberosum</span> L. The <span class="html-italic">X</span>-axis (log scale) represents the concentration of anthocyanin extract in mg/mL, while the <span class="html-italic">Y</span>-axis shows the percentage of viable cells. Data points for <span class="html-italic">Z. mays</span> are depicted as black circles, with the fitted sigmoid curve shown as a solid black line. Red circles denote data points for <span class="html-italic">S. tuberosum</span>, with the corresponding fitted curve represented by a red line.</p>
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22 pages, 2004 KiB  
Review
Pulsed Electric Field Treatment in Extracting Proteins from Legumes: A Review
by Ramya Ramaswamy and Sivaneasan Bala Krishnan
Processes 2024, 12(12), 2667; https://doi.org/10.3390/pr12122667 - 26 Nov 2024
Viewed by 621
Abstract
A healthy diet rich in plant proteins can help in preventing chronic degenerative diseases. Plant-based protein consists of derivatives from algae, fungi (like mushrooms) and other plant products including stems, leaves, fruits, vegetables, grains, seeds, legumes and nuts. These sources are not only [...] Read more.
A healthy diet rich in plant proteins can help in preventing chronic degenerative diseases. Plant-based protein consists of derivatives from algae, fungi (like mushrooms) and other plant products including stems, leaves, fruits, vegetables, grains, seeds, legumes and nuts. These sources are not only rich in protein, but also contain a high percentage of iron, calcium, folates, fiber, carbohydrates, fats etc. Hence, it is essential to explore plant-based protein sources and their other nutritional components to address existing food insecurity issues. Nowadays, the impact of food processing has produced promising results in extracting valuable bio-compounds including proteins from the plant matrix. In this view, PEF technology has secured an exceptional place in solving food quality issues through minimized thermal effects in the samples, improved extraction capabilities at a shorter time, higher extraction levels, high nutritional content of extracted samples, greater shelf-life extension and increased microbial killing efficiency. It is an energy efficient process which is used as a pre-treatment to increase selective extraction of intracellular compounds through electroporation technique. Here, the processing parameters play a significant role in obtaining enhanced extraction levels. These parameters have also considerably influenced the protein digestibility and amino acid modification. So far, PEF has been producing remarkable results in plant protein extraction research. Among various plant sources mentioned above, there is a limited literature available on the use of PEF-assisted protein extraction from legumes. In this review, the authors have discussed essential legumes and their nutritional components and have highlighted how PEF can be beneficial in extracting the protein levels from these sources. Further research should focus on PEF-assisted protein extraction from legumes, specifically analyzing the properties of protein quality and quantity. Full article
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<p>Proportion of total protein intake from animal and plant sources [Reproduced with permission from Elsevier. License number: 5871670317304] [<a href="#B8-processes-12-02667" class="html-bibr">8</a>].</p>
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<p>Nutritional composition of lentils [<a href="#B20-processes-12-02667" class="html-bibr">20</a>].</p>
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<p>Nutritional composition of (<b>a</b>) Desi and (<b>b</b>) Kabuli chickpea varieties [<a href="#B44-processes-12-02667" class="html-bibr">44</a>].</p>
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<p>Nutritional composition of dry pea [<a href="#B59-processes-12-02667" class="html-bibr">59</a>].</p>
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<p>Nutritional composition of black bean [<a href="#B62-processes-12-02667" class="html-bibr">62</a>].</p>
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<p>Nutritional composition of mung bean [<a href="#B74-processes-12-02667" class="html-bibr">74</a>].</p>
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<p>Nutritional composition of soybean [<a href="#B76-processes-12-02667" class="html-bibr">76</a>,<a href="#B79-processes-12-02667" class="html-bibr">79</a>,<a href="#B80-processes-12-02667" class="html-bibr">80</a>].</p>
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<p>Block diagram of PEF setup (continuous mode).</p>
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16 pages, 4413 KiB  
Article
Metal–Organic Framework-Derived CeO2/Gold Nanospheres in a Highly Sensitive Electrochemical Sensor for Uric Acid Quantification in Milk
by Miloš Ognjanović, Milena Marković, Vladimír Girman, Vladimir Nikolić, Sanja Vranješ-Đurić, Dalibor M. Stanković and Branka B. Petković
Chemosensors 2024, 12(11), 231; https://doi.org/10.3390/chemosensors12110231 - 3 Nov 2024
Viewed by 1199
Abstract
In this work, CeBTC (a cerium(III) 1,3,5-benzene-tricarboxylate), was used as a precursor for obtaining CeO2 nanoparticles (nanoceria) with better sensor performances than CeO2 nanoparticles synthesized by the solvothermal method. Metal–organic framework-derived nanoceria (MOFdNC) were functionalized with spheric gold nanoparticles (AuNPs) to [...] Read more.
In this work, CeBTC (a cerium(III) 1,3,5-benzene-tricarboxylate), was used as a precursor for obtaining CeO2 nanoparticles (nanoceria) with better sensor performances than CeO2 nanoparticles synthesized by the solvothermal method. Metal–organic framework-derived nanoceria (MOFdNC) were functionalized with spheric gold nanoparticles (AuNPs) to further improve non-enzymatic electrode material for highly sensitive detection of prominent biocompound uric acid (UA) at this modified carbon paste electrode (MOFdNC/AuNPs&CPE). X-ray powder diffraction (XRPD) and transmission electron microscopy (TEM) analysis were used for morphological structure characterization of the obtained nanostructures. Cyclic voltammetry and electrochemical impedance spectroscopy, both in an [Fe(CN)6]3−/4− redox system and uric acid standard solutions, were used for the characterization of material electrocatalytic performances, the selection of optimal electrode modifier, and the estimation of nature and kinetic parameters of the electrode process. Square-wave voltammetry (SWV) was chosen, and the optimal parameters of technique and experimental conditions were established for determining uric acid over MOFdNC/AuNPs&CPE. Together with the development of the sensor, the detection procedure was optimized with the following analytical parameters: linear operating ranges of 0.05 to 1 µM and 1 to 50 µM and a detection limit of 0.011 µM, with outstanding repeatability, reproducibility, and stability of the sensor surface. Anti-interference experiments yielded a stable and nearly unchanged current response with negligible or no change in peak potential. After minor sample pretreatment, the proposed electrode was successfully applied for the quantification of UA in milk. Full article
(This article belongs to the Special Issue Chemical and Biosensors Based on Metal-Organic Frames (MOFs))
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<p>(<b>a</b>) XRPD diffractograms of solvothermal-prepared CeO<sub>2</sub> and MOFdCeO<sub>2</sub>. The standard diffraction pattern of CeO<sub>2</sub> JCPDS #43-1002 is given as a reference. (<b>b</b>,<b>c</b>) TEM micrographs of solvothermal-prepared CeO<sub>2</sub>. (<b>d</b>–<b>f</b>) TEM micrographs of MOFdCeO<sub>2</sub>/AuNP nanocomposites.</p>
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<p>(<b>a</b>) CV responses of pristine CPE, solvothermal-synthesized nanoceria and MOF-derived nanoceria-modified CPEs, and CPE modified with binary nanocomposite MOF-derived nanoceria/AuNPs. (<b>b</b>) EIS responses of the pristine and modified electrodes.</p>
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<p>(<b>a</b>) CV profiles of 20 µM of UA at pristine and MOFdNC/AuNP-modified CPE in BR buffer at pH 6. (<b>b</b>) Effect of pH on CV profiles at MOFdNC/AuNPs&amp;CPE (scan rate of 100 mV/s).</p>
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<p>The suggested electro-oxidation mechanism of UA at MOFdNC/AuNPs&amp;CPE.</p>
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<p>(<b>a</b>) Effect of the scan rate (20 µM of UA at various scan rates from 10 to 125 mV/s at MOFdNC/AuNPs&amp;CPE in BR buffer at pH 6). (<b>b</b>) Plot of peak potential vs. log of the scan rate, derived from the graph in a. (<b>c</b>) Plot of the peak current vs. the scan rate. (<b>d</b>) Plot of log of the peak current vs. log of the scan rate. (<b>f</b>) Taffel plot derived from CV recorded at 50 mV/s, as presented in graph (<b>e</b>).</p>
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<p>SW voltammograms of different concentrations of UA in BR buffer at pH 6 at MOFdNC/AuNPs&amp;CPE in (<b>a</b>) the whole investigated concentration range and (<b>b</b>) for a range of lower concentrations. The corresponding calibration curves (<b>c</b>,<b>d</b>) are given below each voltammetric profile. (<b>e</b>) The calibration curve for low concentrations ranging from 0.05 to 1 µM.</p>
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<p>(<b>a</b>) The interfering effect of selected biocompounds on 1 μM of UA at MOFdNC/AuNPs&amp;CPE. (<b>b</b>) Determination of UA in treated milk sample 1 (insert graph—milk protein interfering effect).</p>
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27 pages, 1753 KiB  
Review
Prospecting Pharmacologically Active Biocompounds from the Amazon Rainforest: In Vitro Approaches, Mechanisms of Action Based on Chemical Structure, and Perspectives on Human Therapeutic Use
by Andryo O. de Almada-Vilhena, Oscar V. M. dos Santos, Milla de A. Machado, Cleusa Y. Nagamachi and Julio C. Pieczarka
Pharmaceuticals 2024, 17(11), 1449; https://doi.org/10.3390/ph17111449 - 30 Oct 2024
Viewed by 912
Abstract
The Amazon rainforest is an important reservoir of biodiversity, offering vast potential for the discovery of new bioactive compounds from plants. In vitro studies allow for the investigation of biological processes and interventions in a controlled manner, making them fundamental for pharmacological and [...] Read more.
The Amazon rainforest is an important reservoir of biodiversity, offering vast potential for the discovery of new bioactive compounds from plants. In vitro studies allow for the investigation of biological processes and interventions in a controlled manner, making them fundamental for pharmacological and biotechnological research. These approaches are faster and less costly than in vivo studies, providing standardized conditions that enhance the reproducibility and precision of data. However, in vitro methods have limitations, including the inability to fully replicate the complexity of a living organism and the absence of a complete physiological context. Translating results to in vivo models is not always straightforward, due to differences in pharmacokinetics and biological interactions. In this context, the aim of this literature review is to assess the advantages and disadvantages of in vitro approaches in the search for new drugs from the Amazon, identifying the challenges and limitations associated with these methods and comparing them with in vivo testing. Thus, bioprospecting in the Amazon involves evaluating plant extracts through bioassays to investigate pharmacological, antimicrobial, and anticancer activities. Phenolic compounds and terpenes are frequently identified as the main bioactive agents, exhibiting antioxidant, anti-inflammatory, and antineoplastic activities. Chemical characterization, molecular modifications, and the development of delivery systems, such as nanoparticles, are highlighted to improve therapeutic efficacy. Therefore, the Amazon rainforest offers great potential for the discovery of new drugs; however, significant challenges, such as the standardization of extraction methods and the need for in vivo studies and clinical trials, must be overcome for these compounds to become viable medications. Full article
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<p>Comparison of the advantages and disadvantages of in vitro studies.</p>
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20 pages, 6172 KiB  
Article
Bacterial Community Structure and Patterns of Diversity in the Sediments of Mountain Rock Basins from a National Park
by Amaya de Cos-Gandoy, Andrea Serrano-Bellón, María Macías-Daza, Blanca Pérez-Uz, Richard A. J. Williams, Abel Sanchez-Jimenez and Mercedes Martín-Cereceda
Diversity 2024, 16(9), 544; https://doi.org/10.3390/d16090544 - 4 Sep 2024
Viewed by 3488
Abstract
Bacterial microbiomes influence global carbon and nutrient cycling as the environment changes. Rain-fed rock basins are ephemeral aquatic systems, potentially subject to extreme environmental stress, that can host a wide variety of biological communities, including bacteria. However, bacterial communities are barely described in [...] Read more.
Bacterial microbiomes influence global carbon and nutrient cycling as the environment changes. Rain-fed rock basins are ephemeral aquatic systems, potentially subject to extreme environmental stress, that can host a wide variety of biological communities, including bacteria. However, bacterial communities are barely described in these habitats. Here we provide a detailed description on the occurrence, diversity and distribution patterns of the bacterial communities within and between rain-fed granite mountain rock basins located in the Sierra de Guadarrama National Park, Spain, using high-throughput sequencing of 16S RNA. We recovered a highly diverse community consisting of 3174 operational taxonomic units (OTUs) belonging to 32 phyla. In total, 50% of OTUs were shared among basins and 6–10% were basin-exclusive OTUs, suggesting a robust global bacterial metacommunity colonizes the basins. The existence of 6% replicate-exclusive OTUs and the fact that at least four replicates were required to catalogue 90% of the basin bacterial community emphasized the heterogeneity of these habitats. Both environmental filtering and random dispersal are likely to be involved in the arrangement of the bacterial communities. The taxa identified in this study are versatile in metabolism, and some have biotechnological potential. The taxonomic affiliation of many of the OTUs found suggests that rain-fed rock basins could be a resource for mining novel bacterial biocompounds. Full article
(This article belongs to the Special Issue Montane Ecosystems and Diversity)
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<p>Rock basins sampled in the Sierra de Guadarrama National Park (La Pedriza). (<b>A</b>): Basin A; (<b>B</b>): Basin B; (<b>C</b>): Basin C.</p>
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<p>Venn diagrams representing the exclusive and shared OTUs among the three basins (<b>a</b>) and within the replicates of each basin (<b>b</b>). A-1 to A-5: Represent replicates of basin A; B-1 to B-5 represent replicates of Basin B; C-1 to C-5 represent replicates of basin C.</p>
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<p>Species accumulation curves for the three basins combined (<b>a</b>) and within each basin (<b>b</b>). A, B and C represent the three basins sampled.</p>
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<p>Normalised rarefaction curves of the number of OTUs for the three basins. A, B and C represent the three basins sampled.</p>
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<p>Relative abundances (%) of the phyla at each basin. Only groups with relative abundances ≥1% are depicted. (<b>A</b>–<b>C</b>) represent the three basins sampled.</p>
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<p>Relative abundances (in a scale of 0 to 1) of phyla in each of the 15 replicates collected from the sediments of the three basins (A, B, C).</p>
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<p>Box plots for OTU richness and Shannon and inverse Simpson diversity indices in each basin (<span class="html-italic">N</span> = 5), by OTU (<b>a</b>) and by phyla (<b>b</b>). Boxes represent the interquartile range and thick lines are the median. Whiskers indicate the highest and lowest values. Outliers are presented as dots. A, B and C represent the three basins sampled.</p>
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<p>Bray–Curtis dissimilarity heatmap between replicates of the basins. A, B and C represent the three basins sampled.</p>
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<p>Mean values of the chemical variables in each basin (A, B and C) (<span class="html-italic">N</span> = 15). Standard deviation is shown in red. Open circles represent the individual data points (dot plots). The <span class="html-italic">p</span>-values represent differences between basins and were computed using one-way ANOVA.</p>
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<p>Bray–Curtis based non-metric multidimensional scaling (NMDS) plot for the total OTUs (<b>a</b>) and phyla (<b>b</b>). A, B and C represent the three basins sampled.</p>
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<p>Abundance and statistical significance of the OTUs associated with each of the three basins (revealed by ISA, Indicator Species Analysis; see M and M for details on the analysis). Size of the circles represents the mean relative abundance of the OTU in that basin, and colour of the circles represents <span class="html-italic">p</span>-values. Circles coloured in grey represent insignificant taxa.</p>
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<p>Redundance analysis (RDA) for the OTUs selected in the indicator species analysis. 488—<span class="html-italic">Xanthobacteraceae</span>; 531—<span class="html-italic">Isosphaeraceae</span>; 534—<span class="html-italic">WD2101_soil_group</span>; 560—<span class="html-italic">Bryobacter</span>; 636—<span class="html-italic">Thermobaculum</span>; 644—<span class="html-italic">Gemmataceae</span>; 668—<span class="html-italic">Gemmata</span>; 743—<span class="html-italic">RB41</span>; 789—<span class="html-italic">SHA-26</span>; 801—<span class="html-italic">IMCC26207</span>; 847—<span class="html-italic">C0119</span>; 898—<span class="html-italic">Isosphaeraceae</span>; 958—<span class="html-italic">AKIW781</span>; 978—<span class="html-italic">SC-I-84</span>; 983—<span class="html-italic">Gaiellales</span>; 1031—<span class="html-italic">Isosphaeraceae</span>; 1033—<span class="html-italic">Chitinophagaceae</span>; 1060—<span class="html-italic">Gaiellales</span>; 1064—<span class="html-italic">TK10</span>; 1145—<span class="html-italic">TK10</span>; 1297—<span class="html-italic">TK10</span>; 1299—<span class="html-italic">Ethanoligenenaceae</span>; 1350—<span class="html-italic">Acidibacter</span>; 1370—<span class="html-italic">Thermobacillus</span>; 1441—<span class="html-italic">Hyphomicrobium</span>; 1484—<span class="html-italic">Ktedonobacteraceae</span>; 1515—<span class="html-italic">Roseisolibacter</span>; 1612—<span class="html-italic">Gemmataceae</span>; 1750—<span class="html-italic">Isosphaeraceae</span>; 1753—<span class="html-italic">Rhizorhapis</span>; 2035—<span class="html-italic">Nitrososphaeraceae</span>; 2972—<span class="html-italic">Occallatibacter</span>; 2998—<span class="html-italic">Sporomusaceae</span>; 3000—<span class="html-italic">Paenibacillus</span>; 3207—<span class="html-italic">Aquisphaera</span>; 3470—<span class="html-italic">Craurococcus-Caldovatus</span>; 3483—<span class="html-italic">Armatimonadota</span>; 3791—<span class="html-italic">B12-WMSP1</span>; 3803—<span class="html-italic">TK10</span>. A, B and C represent the three basins sampled.</p>
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18 pages, 1352 KiB  
Review
Unraveling the Valorization Potential of Pineapple Waste to Obtain Value-Added Products towards a Sustainable Circular Bioeconomy
by Sarah L. Paz-Arteaga, Edith Cadena-Chamorro, Ricardo Goméz-García, Liliana Serna-Cock, Cristóbal N. Aguilar and Cristian Torres-León
Sustainability 2024, 16(16), 7236; https://doi.org/10.3390/su16167236 - 22 Aug 2024
Viewed by 3291
Abstract
The pineapple (Ananas comosus) is one of the most commercialized tropical fruits worldwide. Its high processing and consumption generate huge quantities of organic waste and severe economic and environmental issues. Embracing the circular bioeconomy concept, this fruit waste can be applied [...] Read more.
The pineapple (Ananas comosus) is one of the most commercialized tropical fruits worldwide. Its high processing and consumption generate huge quantities of organic waste and severe economic and environmental issues. Embracing the circular bioeconomy concept, this fruit waste can be applied as a bioresource (raw material) for the obtention of a wide range of high-valued biocompounds by applying innovative and ecofriendly technologies. In this paper, we critically describe pineapple-derived waste, from their chemical composition to their functional and biological properties, as well as the latest advances on valorization technologies, particular solid and submerged fermentations. Notably, this article highlights the possibility of using pineapple waste to obtain bioactive compounds such as bromelain, phenolic compounds, and dietary fiber, which have important biological properties such as antioxidant, anticancer, antimicrobial, and prebiotic capacities. Indeed, pineapple wastes can become valued materials by using green and biotechnological technologies that allow us to maximize their potential and might avoid wastage and environmental issues. Nevertheless, it is necessary to further investigate the biomolecules present in the waste derived from different pineapple varieties and their health beneficial effects as well as emerging technologies in order to obtain a full spectrum of natural value-added compounds that industries and society demand today. Full article
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<p>By-product generation chain (crown, core, and shell) and food loss (stem and leaves) of pineapple.</p>
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<p>Pineapple by-product fermentation process.</p>
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17 pages, 2349 KiB  
Article
Wounding Citrus Peel By-Products as Abiotic Stress to Induce the Synthesis of Phenolic Compounds?
by Rosa Zapata, Lorena Martínez-Zamora, Marina Cano-Lamadrid and Francisco Artés-Hernández
Horticulturae 2024, 10(8), 885; https://doi.org/10.3390/horticulturae10080885 - 21 Aug 2024
Viewed by 806
Abstract
Wounding stress stimulates secondary metabolism and induces the phytochemical accumulation of fresh-cut fruit and vegetables. This research aims to study the biosynthesis of secondary metabolites in citrus peel by-products after different wounding intensities. Orange, grapefruit, and lemon peels were cut into rectangular shapes [...] Read more.
Wounding stress stimulates secondary metabolism and induces the phytochemical accumulation of fresh-cut fruit and vegetables. This research aims to study the biosynthesis of secondary metabolites in citrus peel by-products after different wounding intensities. Orange, grapefruit, and lemon peels were cut into rectangular shapes of 8.5 × 2 cm (CTRL), 1 × 1 cm dices (D), and 0.25 cm grates (G). Samples were stored at 15 °C and 65% relative humidity. Their total phenolic content (TPC), total antioxidant capacity (TAC), and individual organic and phenolic compounds were analyzed after 0, 4, 8, 24, 28, and 36 h. The results showed that the metabolite content decreased with the incubation time, so it is recommended to sample by-products between the first 8 h to achieve the maximum content. Grating, the most severe abiotic stress, was not a suitable technique to induce the synthesis of biocompounds because it allowed the full recovery of flavedo, but partial of albedo. However, it was different for CTRL and D, whose TPCs were ~170 and ~200%, ~98 and ~78%, and ~8 and ~36% higher for orange, grapefruit, and lemon, respectively, compared to G. A principal component analysis confirmed differences between the fruit species and cutting shapes combining all factors. Wounding citrus peels induces the accumulation of phytochemical compounds, but the layer of peel recovered in the cut is crucial in the concentration of phytochemicals extracted. It could be an innovative tool to revalorize these inedible parts of citrus, but further research is still needed. Full article
(This article belongs to the Special Issue From Farm to Table in the Era of a New Horticulture in Spain)
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<p>Incubation of lemon, grapefruit, and orange cut peels (CTRL, D, and G) for 0, 4, 8, 24, 28, and 36 h at 15 °C and 65% RH (n = 3).</p>
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<p>Total phenolic content of orange (<b>a</b>), grapefruit (<b>b</b>), and lemon (<b>c</b>) peels after different cutting intensities (CTRL, dices, and grated peel) and incubation time (h) at 15 °C and 65% RH. *: significant differences (<span class="html-italic">p</span> &lt; 0.05) among cutting intensity regarding CTRL samples within each incubation time. <sup>Δ</sup>: significant differences (<span class="html-italic">p</span> &lt; 0.05) among incubation time regarding the same cutting at time 0 h.</p>
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<p>Total antioxidant capacity of orange (<b>a</b>), grapefruit (<b>b</b>), and lemon (<b>c</b>) peels determined by DPPH assay after different cutting intensities (CTRL, dices, and grated peel) and incubation time (h) at 15 °C and 65% RH. *: significant differences (<span class="html-italic">p</span> &lt; 0.05) among cutting intensity regarding CTRL samples within each incubation time. <sup>Δ</sup>: significant differences (<span class="html-italic">p</span> &lt; 0.05) among incubation time regarding the same cutting at time 0 h.</p>
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<p>Total antioxidant capacity of orange (<b>a</b>), grapefruit (<b>b</b>), and lemon (<b>c</b>) peels determined by ABTS assay after different cutting intensities (CTRL, dices, and grated peel) and incubation time (h) at 15 °C and 65% RH. *: significant differences (<span class="html-italic">p</span> &lt; 0.05) among cutting intensity regarding CTRL samples within each incubation time. <sup>Δ</sup>: significant differences (<span class="html-italic">p</span> &lt; 0.05) among incubation time regarding the same cutting at time 0 h.</p>
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<p>Total antioxidant capacity of orange (<b>a</b>), grapefruit (<b>b</b>), and lemon (<b>c</b>) peels determined by FRAP assay after different cutting intensities (CTRL, dices, and grated peel) and incubation time (h) at 15 °C and 65% RH. *: significant differences (<span class="html-italic">p</span> &lt; 0.05) among cutting intensity regarding CTRL samples within each incubation time. <sup>Δ</sup>: significant differences (<span class="html-italic">p</span> &lt; 0.05) among incubation time regarding the same cutting at time 0 h.</p>
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<p>Pearson correlation between studied variables of orange, grapefruit, and lemon peels after different cutting intensities (CTRL, dices, and grated peel) and incubation time (h) at 15 °C and 65% RH.</p>
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<p>(<b>a</b>) The 2D-PCA scores plot and (<b>b</b>) 2D-PCA loadings plot of orange, lemon, and grapefruit peel samples considering their experimental analyses of TPC, TAC (by DPPH, ABTS, and FRAP assays), and individual phenolic and organic compounds.</p>
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<p>The 3D-PCA scores plot of orange, lemon, and grapefruit peels comparing different cutting intensities considering their experimental analyses of TPC, TAC (by DPPH, ABTS, and FRAP assays), and individual compound content.</p>
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20 pages, 1292 KiB  
Article
Evaluating Biocompounds in Discarded Beetroot (Beta vulgaris) Leaves and Stems for Sustainable Food Processing Solutions
by Carolina Mella, Natalia Rojas, Hector Calderon-Bravo and Loreto A. Muñoz
Foods 2024, 13(16), 2603; https://doi.org/10.3390/foods13162603 - 20 Aug 2024
Viewed by 1516
Abstract
The current trend focuses on reducing food waste, with scientific studies exploring the nutritional value of discarded food components to identify potential health benefits. Beetroot (Beta vulgaris L.) is highly consumed, but its stems and leaves are often discarded. This work aims [...] Read more.
The current trend focuses on reducing food waste, with scientific studies exploring the nutritional value of discarded food components to identify potential health benefits. Beetroot (Beta vulgaris L.) is highly consumed, but its stems and leaves are often discarded. This work aims to characterize the chemical properties and bioactive compounds in beet stems and leaves and assess their applicability in food products. The stems and leaves were subjected to different drying temperatures (50 to 70 °C) to determine the optimal temperature for preserving their bioactive compounds. They are then nutritionally and physiochemically characterized and incorporated into a food matrix. The optimal drying temperature was 60 °C. The leaves and stems contain approximately 30 and 15 g/100 g of protein, 30 and 32 g/100 g of dietary fiber, 4 and 0.45 g/100 g of lipids, and 24 and 25 g/100 g of ash, respectively. Both provide approximately 50% of the amino acid requirements established by the WHO/FAO/UNU and are rich in iron and potassium. The stems presented 53% more betalainic compounds (0.58 mg/g) and a higher nitrate content (359 mg/kg) than did the leaves, which presented a higher polyphenol content. The incorporation of flour from beet stems and leaves into food products is economical, reduces food waste, and enhances nutrition and health. Full article
(This article belongs to the Section Nutraceuticals, Functional Foods, and Novel Foods)
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<p>Effects of drying temperature on the moisture content curves of beetroot by-products over time. The values are means of triplicate analyses (<span class="html-italic">n</span> = 3) and the error bars represent the standard deviation.</p>
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<p>Composition of amino acids (mg/g protein) based on the FAO/WHO/UNU (Food and Agriculture Organization/World Health Organization/United Nations University) standard reference pattern (g/100 g protein). The values are expressed as mean ± standard deviation (<span class="html-italic">n</span> = 3). Different lowercase letters indicate significant differences according to Tukey’s multiple range test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of drying temperature on betalain content. Values are averages (<span class="html-italic">n</span> = 3). Different lowercase letters indicate significant differences according to Tukey’s multiple range test (<span class="html-italic">p</span> &lt; 0.05).</p>
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20 pages, 1281 KiB  
Article
A Survey on Potentially Beneficial and Hazardous Bioactive Compounds in Cocoa Powder Samples Sourced from the European Market
by Luigi Esposito, Matteo Perillo, Carla Daniela Di Mattia, Annalisa Scroccarello, Flavio Della Pelle, Dario Compagnone, Giampiero Sacchetti, Dino Mastrocola and Maria Martuscelli
Foods 2024, 13(15), 2457; https://doi.org/10.3390/foods13152457 - 3 Aug 2024
Viewed by 1180
Abstract
Cocoa (Theobroma cacao, L.) represents an important market that gained relevance and became an esteemed commodity thanks to cocoa powder, chocolate, and other related products. This work analyzed 59 cocoa powder samples from the European market. Three distinct subgroups were identified: [...] Read more.
Cocoa (Theobroma cacao, L.) represents an important market that gained relevance and became an esteemed commodity thanks to cocoa powder, chocolate, and other related products. This work analyzed 59 cocoa powder samples from the European market. Three distinct subgroups were identified: organic or conventional, alkalized or not alkalized, and raw or roasted processing. The impact of the technological process on their pH, color, and compositional traits, as well as their content of biogenic amines and salsolinol, was evaluated. The phenolic fraction was also investigated through both common and emerging methods. The results depict that the influence of the agronomical practices (organic/conventional) did not significantly (p < 0.05) affect the composition of the cocoa powders; similarly, the roasting process was not a determinant of the compounds traced. On the other hand, the alkalinization process greatly impacted color and pH, no matter the cocoa’s provenience or obtention or other processes, also resulting in reducing the phenolic fraction of the treated samples. Principal component analysis confirmed that the alkali process acts on pH, color, and phenolic composition but not on the content of other bioactive molecules (biogenic amines and salsolinol). All the samples were safe, while the alkalized powders saw a great reduction in beneficial biocompounds. A novel strategy could be to emphasize on the label whether cocoa powder is non-alkalized to meet the demand for more beneficial products. Full article
(This article belongs to the Section Food Quality and Safety)
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<p>Heat map diagram displaying the loadings of variables for principal components PC1, PC2, PC3, and PC4. Different intensities are shown on the far right-hand side: deep blue and red coloration represents extremes of low and high intensity, respectively. SPM (spermine), SPD (spermidine), HIS (histamine), SER (serotonin), DOP (dopamine), ETH (ethanolamine), C (Chroma), a_b (ratio of colorimetric coordinates a* and b*), b (b* blueness/yellowness), a (a* redness/greenness), H (hue angle), L (lightness), nSensor (electrochemical nanostructured sensor), AuNPs (gold nanoparticle-based sensor).</p>
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<p>Loading plot of variables for the first two components. Different contributions are shown on the far right-hand side: deep green and orange coloration represents extremes of low and high contributions, respectively. SPM (spermine), SPD (spermidine), HIS (histamine), SER (serotonin), DOP (dopamine), ETH (ethanolamine), C (Chroma), a_b (ratio of colorimetric coordinates a* and b*), b (b*blueness/yellowness), a (a* redness/greenness), H (hue angle), L (lightness), nSensor (electrochemical nanostructured sensor), AuNPs (gold nanoparticle-based sensor).</p>
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<p>Score plot obtained by principal component analysis of pH, colorimetric parameters, biogenic amine content, and polyphenol content in cocoa powder samples under different technological treatments. Legend: circle, alkalized cocoa powder; triangle, non-alkalized samples; blue circle, non-organic cocoa powder; red circle, organic samples; light blue symbol, cocoa powder from roasted beans; light red symbol, cocoa samples from raw beans.</p>
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47 pages, 5907 KiB  
Review
Marine Antioxidants from Marine Collagen and Collagen Peptides with Nutraceuticals Applications: A Review
by Emin Cadar, Ana-Maria Pesterau, Irina Prasacu, Ana-Maria Ionescu, Carolina Pascale, Ana-Maria Laura Dragan, Rodica Sirbu and Cezar Laurentiu Tomescu
Antioxidants 2024, 13(8), 919; https://doi.org/10.3390/antiox13080919 - 29 Jul 2024
Cited by 1 | Viewed by 2337
Abstract
Collagen peptides and marine collagen are enormous resources currently utilized. This review aims to examine the scientific literature to determine which collagen peptides derived from marine sources and which natural active antioxidants from marine collagen have significant biological effects as health-promoting nutraceuticals. Marine [...] Read more.
Collagen peptides and marine collagen are enormous resources currently utilized. This review aims to examine the scientific literature to determine which collagen peptides derived from marine sources and which natural active antioxidants from marine collagen have significant biological effects as health-promoting nutraceuticals. Marine collagen is extracted from both vertebrate and invertebrate marine creatures. For vertebrates, this includes fish skin, bones, scales, fins, and cartilage. For invertebrates, it includes mollusks, echinoderms, crustaceans, and poriferans. The method used involved data analysis to organize information for isolating and identifying marine biocompounds with antioxidant properties. Specifically, amino acids with antioxidant properties were identified, enabling the use of hydrolysates and collagen peptides as natural antioxidant nutraceuticals. The methods of extraction of hydrolyzed collagen and collagen peptides by different treatments are systematized. The structural characteristics of collagen, collagen peptides, and amino acids in fish skin and by-products, as well as in invertebrate organisms (jellyfish, mollusks, and crustaceans), are described. The antioxidant properties of different methods of collagen hydrolysates and collagen peptides are systematized, and the results are comparatively analyzed. Their use as natural antioxidant nutraceuticals expands the range of possibilities for the exploitation of natural resources that have not been widely used until now. Full article
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<p>Marine sources for the preparation of marine collagen.</p>
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<p>Scheme for obtaining marine collagen through (<b>A</b>) acid-soluble collagen method; (<b>B</b>) pepsin-soluble collagen method and (<b>C</b>) collagen peptides.</p>
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<p>Advantages and disadvantages of marine collagen extraction procedures.</p>
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<p>Structure of collagen fibers, collagen fibrils, and amino acid chains. Reprinted with permission from reference [<a href="#B34-antioxidants-13-00919" class="html-bibr">34</a>], 2023, Emin Cadar.</p>
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<p>Amino acids (EAA) in marine-derived collagen and collagen peptides.</p>
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<p>Type of methods used to demonstrate antioxidant activity.</p>
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<p>Diseases treated with antioxidant nutraceuticals that have in their compositions peptides and collagen hydrolysates.</p>
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20 pages, 6724 KiB  
Article
Comprehensive Nutritional and Functional Characterization of Novel Mycoprotein Derived from the Bioconversion of Durvillaea spp.
by Catalina Landeta-Salgado, Nicolás Salas-Wallach, Javiera Munizaga, María Paz González-Troncoso, César Burgos-Díaz, Lhaís Araújo-Caldas, Patricia Sartorelli, Irene Martínez and María Elena Lienqueo
Foods 2024, 13(15), 2376; https://doi.org/10.3390/foods13152376 - 27 Jul 2024
Viewed by 1497
Abstract
This study aimed, for the first time, to determine the nutritional composition, beta-glucan and ergosterol contents, phenolic compound composition, and biological and functional activities of a novel mycoprotein produced through a bioconversion process of Durvillaea spp., a brown seaweed. An untargeted metabolomics approach [...] Read more.
This study aimed, for the first time, to determine the nutritional composition, beta-glucan and ergosterol contents, phenolic compound composition, and biological and functional activities of a novel mycoprotein produced through a bioconversion process of Durvillaea spp., a brown seaweed. An untargeted metabolomics approach was employed to screen metabolites and annotate molecules with nutraceutical properties. Two products, each representing a distinct consortia of co-cultured fungi, named Myco 1 and Myco 2, were analysed in this study. These consortia demonstrated superior properties compared to those of Durvillaea spp., showing significant increases in total protein (~238%), amino acids (~219%), and β-D-glucans (~112%). The protein contains all essential amino acids, a low fatty acid content, and exhibits high antioxidant activity (21.5–25.5 µmol TE/g). Additionally, Myco 2 exhibited the highest anti-alpha-glucosidase activity (IC50 = 16.5 mg/mL), and Myco 1 exhibited notable anti-lipase activity (IC50 = 10.5 mg/mL). Among the 69 top differentially abundant metabolites screened, 8 nutraceutical compounds were present in relatively high concentrations among the identified mycoproteins. The proteins and polysaccharides in the mycoprotein may play a crucial role in the formation and stabilization of emulsions, identifying it as a potent bioemulsifier. In conclusion, the bioconversion of Durvillaea spp. results in a mycoprotein with high-quality protein, significant nutritional and functional value, and prebiotic and nutraceutical potential due to the production of unique bioactive compounds. Full article
(This article belongs to the Topic Future Foods from the Sea)
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<p>Beta-glucan content (<b>a</b>) and ergosterol content (<b>b</b>) in Myco 1, Myco 2, and <span class="html-italic">Durvillaea</span> spp. samples. Values are presented as mean ± SD. Bars with different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). All values are based on dry weight (dw) analysis. The different bar colours are used solely for visual distinction between the data for Myco and <span class="html-italic">Durvillaea</span> spp. and do not represent any additional variable.</p>
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<p>Images of the O/W emulsions stabilized by Myco 1 and Myco 2 at different concentrations (1–5%, <span class="html-italic">w</span>/<span class="html-italic">w</span>).</p>
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<p>Optical micrographs of the O/W Pickering emulsions stabilized at different Myco 1 concentrations (1.0–5.0%, <span class="html-italic">w</span>/<span class="html-italic">w</span>). The images were acquired at 40× magnification.</p>
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<p>Optical micrographs of the O/W Pickering emulsions stabilized at different Myco 2 concentrations (1.0–5.0%, <span class="html-italic">w</span>/<span class="html-italic">w</span>). The images were acquired at 40× magnification.</p>
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