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18 pages, 4884 KiB  
Article
Genome-Wide Identification of B-Box Family Genes and Their Potential Roles in Seed Development under Shading Conditions in Rapeseed
by Si Chen, Yushan Qiu, Yannong Lin, Songling Zou, Hailing Wang, Huiyan Zhao, Shulin Shen, Qinghui Wang, Qiqi Wang, Hai Du, Jiana Li and Cunmin Qu
Plants 2024, 13(16), 2226; https://doi.org/10.3390/plants13162226 (registering DOI) - 11 Aug 2024
Abstract
B-box (BBX) proteins, a subfamily of zinc-finger transcription factors, are involved in various environmental signaling pathways. In this study, we conducted a comprehensive analysis of BBX family members in Brassica crops. The 482 BBX proteins were divided into five groups based on gene [...] Read more.
B-box (BBX) proteins, a subfamily of zinc-finger transcription factors, are involved in various environmental signaling pathways. In this study, we conducted a comprehensive analysis of BBX family members in Brassica crops. The 482 BBX proteins were divided into five groups based on gene structure, conserved domains, and phylogenetic analysis. An analysis of nonsynonymous substitutions and (Ka)/synonymous substitutions (Ks) revealed that most BBX genes have undergone purifying selection during evolution. An analysis of transcriptome data from rapeseed (Brassica napus) organs suggested that BnaBBX3d might be involved in the development of floral tissue-specific RNA-seq expression. We identified numerous light-responsive elements in the promoter regions of BnaBBX genes, which were suggestive of participation in light signaling pathways. Transcriptomic analysis under shade treatment revealed 77 BnaBBX genes with significant changes in expression before and after shading treatment. Of these, BnaBBX22e showed distinct expression patterns in yellow- vs. black-seeded materials in response to shading. UPLC-HESI-MS/MS analysis revealed that shading influences the accumulation of 54 metabolites, with light response BnaBBX22f expression correlating with the accumulation of the flavonoid metabolites M46 and M51. Additionally, BnaBBX22e and BnaBBX22f interact with BnaA10.HY5. These results suggest that BnaBBXs might function in light-induced pigment accumulation. Overall, our findings elucidate the characteristics of BBX proteins in six Brassica species and reveal a possible connection between light and seed coat color, laying the foundation for further exploring the roles of BnaBBX genes in seed development. Full article
(This article belongs to the Special Issue Molecular Genetics and Breeding of Oilseed Crops—2nd Edition)
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<p>Phylogenetic tree of B-box genes from <span class="html-italic">Arabidopsis</span> and six <span class="html-italic">Brassica</span> U-triangle species. The phylogenetic tree, constructed using the protein matrix with iq-tree, is grouped into five clades (I–V) labeled with different colors. The phylogenetic tree was visualized using B-box genes from Arabidopsis, <span class="html-italic">B. rapa</span>, <span class="html-italic">B. nigra</span>, <span class="html-italic">B. oleracea</span>, <span class="html-italic">B. juncea</span>, <span class="html-italic">B. napus</span>, and <span class="html-italic">B. carinata</span>.</p>
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<p>WebLogos of conserved domains of BBX family members in six <span class="html-italic">Brassica</span> plants. (<b>A</b>–<b>C</b>) Typical WebLogos of B-box1, B-box2, and CCT domains in the A, B, and C subgenomes. The <span class="html-italic">x</span>-axis depicts the conserved sequences of the structural domains, where the height of each letter signifies the degree of conservation of each residue across all proteins. The <span class="html-italic">y</span>-axis indicates the relative entropy scale, which represents the conservation degree of each amino acid.</p>
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<p>Number of BBX family gene pairs in the six <span class="html-italic">Brassicaceae</span> species. (<b>A</b>) Number of BBX genes in <span class="html-italic">B. rapa</span> (Bra), <span class="html-italic">B. nigra</span> (Bni), <span class="html-italic">B. oleracea</span> (Bol), <span class="html-italic">B. napus</span> (Bna), <span class="html-italic">B. juncea</span> (Bju), and <span class="html-italic">B. carinata</span> (Bca). (<b>B</b>) Number of BBX family gene pairs in the A subgenome. (<b>C</b>) Number of BBX family gene pairs in the B subgenome. (<b>D</b>) Number of BBX family gene pairs in the C subgenome.</p>
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<p>Heatmap of the expression patterns of <span class="html-italic">BnaBBXs</span> across different tissues and organs. The expression profiles of each <span class="html-italic">BnaBBX</span> gene are based on log2-transformed values (FPKM value + 1). FPKM, fragments per kilobase of exon model per million mapped fragments; DAF, days after flowering.</p>
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<p>Expression patterns of BnaBBXs under shading conditions. (<b>A</b>,<b>B</b>) Phenotypes of L1262 (<b>A</b>) and L1263 (<b>B</b>) seeds under shading conditions (TR) and control conditions (CK, seeds under normal conditions) at different time points. D, days after shading. Scale bars, 2 mm. (<b>C</b>) Phenotypes of mature L1262 and L1263 seeds under shading conditions and the corresponding controls. Scale bars, 2 mm. (<b>D</b>) Heatmap of RNA-seq data of BnaBBX genes of seeds under shading. Three biological replicates for each type of sample were used. The transcriptome data of each <span class="html-italic">BnaBBX</span> gene are based on log<sub>2</sub>-transformed values (FPKM value + 1); (<b>D</b>) days after shading. (<b>E</b>) Venn diagram of genes with significant changes in expression (TR/CK, fold change ≥ 2 or fold change ≤ 0.5) before and after shading. (<b>F</b>) qRT-PCR analysis of BnaBBX family genes. The expression level of BnaActin7 was used to normalize the qRT-PCR data. <span class="html-italic">p</span>-values were calculated using multiple Student <span class="html-italic">t</span>-tests, comparing the levels in L1262CK (black-seeded material) and L1263CK (yellow-seeded material). * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; ****<span class="html-italic">p</span> &lt; 0.0001; ns, no difference. Error bars denote the standard deviation (SD) from three independent biological replicates. D, days after shading; TR, shading treatment.</p>
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<p>Validation of protein–protein interactions between BnaBBX22e and BnaA10.HY5. (<b>A</b>) Changes in metabolite contents before and after shading. Black blocks indicate that data were not available. The color scale represents the fold change in metabolite contents before and after shading, with red, blue, and yellow blocks indicating fold change ≥ 2, fold change ≤ 0.5, and fold change &gt; 0.5 and &lt;2, respectively. (<b>B</b>) The relationships among BnaBBX proteins and metabolites (|R value| ≥ 0.8, <span class="html-italic">p</span>-value ≤ 0.05). (<b>C</b>) Protein–protein interaction networks among BnaBBX proteins and BnaA10.HY5 proteins. The two red arrows point to BnaBBX22e and BnaBBX22f. (<b>D</b>) Yeast point-to-point validation between BnaBBX22e and BnaA10.HY5 as well as between BnaBBX22e and BnaA10.HY5. pGBKT7-53 and pGADT7-T, positive control; pGBKT7-lam and pGADT7-T, negative control; empty pGBKT7 and prey vector, testing for autoactivation and toxicity; bait vector and empty pGADT7, testing for autoactivation and toxicity.</p>
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14 pages, 902 KiB  
Article
Solid-State Fermentation for Phenolic Compounds Recovery from Mexican Oregano (Lippia graveolens Kunth) Residual Leaves Applying a Lactic Acid Bacteria (Leuconostoc mesenteroides)
by Israel Bautista-Hernández, Ricardo Gómez-García, Cristóbal N. Aguilar, Guillermo C. G. Martínez-Ávila, Cristian Torres-León and Mónica L. Chávez-González
Agriculture 2024, 14(8), 1342; https://doi.org/10.3390/agriculture14081342 (registering DOI) - 11 Aug 2024
Abstract
The Mexican oregano by-products are a source of bioactive molecules (polyphenols) that could be extracted using solid-state fermentation (SSF). This study fermented the by-products via SSF (120 h) with a lactic acid bacteria (LAB) Leuconostoc mesenteroides. Sequentially, a bioactive and chemical determination [...] Read more.
The Mexican oregano by-products are a source of bioactive molecules (polyphenols) that could be extracted using solid-state fermentation (SSF). This study fermented the by-products via SSF (120 h) with a lactic acid bacteria (LAB) Leuconostoc mesenteroides. Sequentially, a bioactive and chemical determination was made according to the phenolic content, antioxidant activity (DPPH/FRAP), bioactive properties (α-amylase inhibition and antimicrobial activity against Escherichia coli), and chemical composition (HPLC-MS). The results showed that the total phenolics and flavonoid content, as well as the antioxidant activity, increased (0.60, 2.55, and 3.01 times, respectively) during the SSF process compared with unfermented material. Also, the extracts showed antimicrobial activity against E. coli and α-amylase inhibition. These inhibitory results could be attributed to bioactive compounds identified via HPLC, such as gardenin B, trachelogenin, ferulic acid, and resveratrol 3-O-glucoside. Therefore, the application of L. mesenteroides under SSF on oregano by-products comprises an eco-friendly strategy for their valorization as raw materials for the recovery of phenolic compounds that could be natural alternatives against synthetic antioxidant and antimicrobial agents, promoting a more circular and sustainable supply system within the oregano industry. Full article
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<p>General process diagram of bioactive activity and chemical evaluation of <span class="html-italic">Lippia graveolens</span> by-product valorization through SSF process.</p>
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<p>Polyphenolic compounds concentration in fermentative extracts obtained from SSF process using <span class="html-italic">L. mesenteroides</span>. (<b>A</b>) Total polyphenolic content (TPC) and (<b>B</b>) total flavonoid content (TFC). Different letters show significant differences (α = 0.05).</p>
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<p>Antioxidant activity of fermentative extracts via the SSF process using <span class="html-italic">L. mesenteroides</span>; (<b>A</b>) FRAP assay and (<b>B</b>) DPPH<sup>●</sup> assay. The different letters show significant differences (α = 0.05).</p>
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30 pages, 1072 KiB  
Review
Dietary Flavonoids: Mitigating Air Pollution’s Cardiovascular Risks
by Oscar Andrés Rocha-Velasco, María Morales-Suárez-Varela and Agustín Llopis-González
Nutrients 2024, 16(16), 2647; https://doi.org/10.3390/nu16162647 (registering DOI) - 10 Aug 2024
Viewed by 370
Abstract
Air pollution significantly impacts cardiovascular health, yet pollution reduction strategies in cardiovascular disease prevention remain limited. Dietary flavonoids show promise in protecting cardiovascular health, but their potential to mitigate air-pollution-induced risks is unexplored. This study investigates this research gap. Following PRISMA-ScR guidelines, literature [...] Read more.
Air pollution significantly impacts cardiovascular health, yet pollution reduction strategies in cardiovascular disease prevention remain limited. Dietary flavonoids show promise in protecting cardiovascular health, but their potential to mitigate air-pollution-induced risks is unexplored. This study investigates this research gap. Following PRISMA-ScR guidelines, literature from 2014–2024 was searched across MedLine/PubMed, ScienceDirect, and MDPI databases. Of 463 identified studies, 53 were eligible for analysis based on PICO criteria. Findings revealed significant impacts of air pollution on cardiovascular health, including increased disease risks and mortality. Flavonoid intake demonstrated protective effects against these risks. Flavonoid mechanisms include improved endothelial function, antioxidant and anti-inflammatory effects, blood pressure regulation, antiplatelet effects, cardioprotection, and enhanced lipid and glucose metabolism. Higher flavonoid intake was consistently associated with reduced cardiovascular risks. While reducing pollution remains crucial, promoting flavonoid-rich diets is a promising complementary strategy. Public health initiatives should raise awareness about these benefits. Further research on direct interactions between flavonoid intake and air pollution exposure is needed. Current evidence supports integrating dietary interventions into broader strategies to reduce air pollution’s cardiovascular impacts. Full article
(This article belongs to the Section Clinical Nutrition)
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<p>Chemical structures of flavonoids. (<b>a</b>) Flavones (<b>b</b>) Flavonols (<b>c</b>) Flavanones (<b>d</b>) Flavanols (<b>e</b>) Isoflavones (<b>f</b>) Anthocyanidins.</p>
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<p>PRISMA flow diagram for the study selection and article eligibility process [<a href="#B49-nutrients-16-02647" class="html-bibr">49</a>].</p>
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15 pages, 1248 KiB  
Article
Impact of Incorporating Dried Chaga Mushroom (Inonotus obliquus) into Gluten-Free Bread on Its Antioxidant and Sensory Characteristics
by Zbigniew Kobus, Monika Krzywicka, Agata Blicharz-Kania, Alicja Bosacka, Anna Pecyna, Eva Ivanišová, Katarzyna Kozłowicz and Eva Kovačiková
Molecules 2024, 29(16), 3801; https://doi.org/10.3390/molecules29163801 (registering DOI) - 10 Aug 2024
Viewed by 208
Abstract
Gluten-free bread is increasingly popular among individuals with celiac disease, and The incorporation of mushroom flour offers a novel method to enhance its nutritional profile, antioxidant content, and sensory properties. This study aimed to evaluate the antioxidant and sensory characteristics of gluten-free bread [...] Read more.
Gluten-free bread is increasingly popular among individuals with celiac disease, and The incorporation of mushroom flour offers a novel method to enhance its nutritional profile, antioxidant content, and sensory properties. This study aimed to evaluate the antioxidant and sensory characteristics of gluten-free bread with varying amounts of chaga mushroom flour (5%, 10%, 15%, 20%). The total contents of polyphenols and flavonoids were measured using a spectrophotometric method. Antioxidant activity was assessed through DPPH and FRAP methods, while textural properties were evaluated using the TPA test. Bread colour was analysed using the CIELab system, and sensory evaluation was performed by a panel of trained consumers. The results showed that gluten-free bread enriched with chaga flour had increased polyphenol and flavonoid content and enhanced antioxidant activity. The highest levels of polyphenols, flavonoids, DPPH, and FRAP activity were found in bread with 20% chaga. The addition of chaga mushroom significantly affected the bread’s hardness, cohesiveness, and chewiness. Specifically, 20% chaga flour had the most pronounced effect on hardness and elasticity, while 15% chaga flour had the greatest impact on chewiness and cohesiveness. The bread’s colour darkened with higher chaga concentrations. The results of sensory evaluation showed a negative correlation between consumer preferences and bread fortified with chaga mushroom flour. The overall consumer acceptability score indicates that only a small addition of mushroom flour (up to 10%) can be used to bake gluten-free bread. Full article
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<p>Gluten-free bread with chaga: 0, 5, 10, 15, 20% respectively (from left).</p>
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<p>Sensory evaluation of gluten-free bread with the addition of chaga mushroom.</p>
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19 pages, 777 KiB  
Review
Regulation of Intestinal Inflammation by Walnut-Derived Bioactive Compounds
by Kexin Dai, Neel Agarwal, Alexander Rodriguez-Palacios and Abigail Raffner Basson
Nutrients 2024, 16(16), 2643; https://doi.org/10.3390/nu16162643 (registering DOI) - 10 Aug 2024
Viewed by 399
Abstract
Walnuts (Juglans regia L.) have shown promising effects in terms of ameliorating inflammatory bowel disease (IBD), attributed to their abundant bioactive compounds. This review comprehensively illustrates the key mechanisms underlying the therapeutic potential of walnuts in IBD management, including the modulation of [...] Read more.
Walnuts (Juglans regia L.) have shown promising effects in terms of ameliorating inflammatory bowel disease (IBD), attributed to their abundant bioactive compounds. This review comprehensively illustrates the key mechanisms underlying the therapeutic potential of walnuts in IBD management, including the modulation of intestinal mucosa permeability, the regulation of inflammatory pathways (such as NF-kB, COX/COX2, MAPCK/MAPK, and iNOS/NOS), relieving oxidative stress, and the modulation of gut microbiota. Furthermore, we highlight walnut-derived anti-inflammatory compounds, such as polyunsaturated fatty acids (PUFA; e.g., ω-3 PUFA), tocopherols, phytosterols, sphingolipids, phospholipids, phenolic compounds, flavonoids, and tannins. We also discuss unique anti-inflammatory compounds such as peptides and polysaccharides, including their extraction and preparation methods. Our review provides a theoretical foundation for dietary walnut supplementation in IBD management and provides guidance for academia and industry. In future, research should focus on the targeted isolation and purification of walnut-derived anti-inflammatory compounds or optimizing extraction methods to enhance their yields, thereby helping the food industry to develop dietary supplements or walnut-derived functional foods tailored for IBD patients. Full article
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<p>The mechanism of walnuts regulating IBD. (1) An illustration of the intestinal mucosal barrier and the effect of walnuts on permeability. (2) A depiction of the antioxidant effects of walnuts on ROS. (3) A pathway map showing NF-κB, COX/COX-2 and MAPK signaling modulation by walnuts. (4) Diagram showing changes in gut microbiota composition due to walnut consumption.</p>
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15 pages, 2283 KiB  
Article
Immunomodulatory Effects of Anadenanthera colubrina Bark Extract in Experimental Autoimmune Encephalomyelitis
by Karla A. Ramos, Igor G. M. Soares, Larissa M. A. Oliveira, Mariana A. Braga, Pietra P. C. Soares, Gracimerio J. Guarneire, Elaine C. Scherrer, Fernando S. Silva, Nerilson M. Lima, Felipe A. La Porta, Teresinha de Jesus A. S. Andrade, Gagan Preet, Sandra B. R. Castro, Caio César S. Alves and Alessandra P. Carli
Curr. Issues Mol. Biol. 2024, 46(8), 8726-8740; https://doi.org/10.3390/cimb46080515 (registering DOI) - 10 Aug 2024
Viewed by 304
Abstract
This study aimed to evaluate the efficacy of the ethanolic extract of Anadenanthera colubrina in modulating the immune response in the Experimental Autoimmune Encephalomyelitis (EAE) model. The ethanolic extract of the dried bark was analyzed by ESI (+) Orbitrap-MS to obtain a metabolite [...] Read more.
This study aimed to evaluate the efficacy of the ethanolic extract of Anadenanthera colubrina in modulating the immune response in the Experimental Autoimmune Encephalomyelitis (EAE) model. The ethanolic extract of the dried bark was analyzed by ESI (+) Orbitrap-MS to obtain a metabolite profile, demonstrating a wide variety of polyphenols, such as flavonoids and phenolic acids. Various parameters were evaluated, such as clinical signs, cytokines, cellular profile, and histopathology in the central nervous system (CNS). The ethanolic extract of A. colubrina demonstrated significant positive effects attenuating the clinical signs and pathological processes associated with EAE. The beneficial effects of the extract treatment were evidenced by reduced levels of pro-inflammatory cytokines, such as IL1β, IL-6, IL-12, TNF, IFN-γ, and a notable decrease in several cell profiles, including CD8+, CD4+, CD4+IFN-γ, CD4+IL-17+, CD11c+MHC-II+, CD11+CD80+, and CD11+CD86+ in the CNS. In addition, histological analysis revealed fewer inflammatory infiltrates and demyelination sites in the spinal cord of mice treated with the extract compared to the control model group. These results showed, for the first time, that the ethanolic extract of A. colubrina exerts a modulatory effect on inflammatory processes, improving clinical signs in EAE, in the acute phase of the disease, which could be further explored as a possible therapeutic alternative. Full article
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<p>Clinical signs of EAE. Animals (n = 8/group) were monitored daily for clinical signs of EAE after immunization with 100 µg of MOG<sub>35–55</sub> peptide. Mice were treated with 200 mg/kg of the ethanolic extract of <span class="html-italic">A. colubrina</span> barks (EtAc) for six days. The dotted line indicates the start of treatment. Each dot represents the arithmetic mean ± SEM. * indicates <span class="html-italic">p</span> &lt; 0.05 compared to induced and PBS-treated animals (EAE), analyzed by two-way ANOVA with Dunnett’s correction. CN = negative control (not induced and treated with PBS).</p>
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<p>Histopathology of the spinal cord of mice. Histopathology of the spinal cord of mice immunized or not immunized with 100 µg of MOG<sub>35–55</sub> (n = 8/group). Figures are representative of the histological analysis of each experimental group: CN= non-immunized and PBS-treated group (<b>A</b>,<b>B</b>), EAE = immunized and PBS-treated group (<b>C</b>,<b>D</b>), EtAc = immunized and treated with 200 mg/kg ethanolic extract of <span class="html-italic">A. colubrina</span> barks for six days (<b>E</b>,<b>F</b>). The examined groups representative sections (5 µm) were stained with hematoxylin and eosin (H&amp;E) to analyze the cell infiltrate. Original magnification: 10× objective (<b>A</b>,<b>C</b>,<b>E</b>), 40× (<b>B</b>,<b>D</b>,<b>F</b>). Scale bars = 100 µm (10×) and 50 µm (40×). Arrows indicate cellular infiltrates.</p>
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<p>Demyelination of the spinal cord of mice. Histopathology of spinal cords of mice immunized or not immunized with 100 µg of MOG35–55 (n = 8/group). Figures are representative of the histological analysis of each experimental group: CN= non-immunized and PBS-treated group (<b>A</b>), EAE = immunized and PBS-treated group (<b>B</b>), EtAc = immunized and treated with 200 mg/kg ethanolic extract of <span class="html-italic">A. colubrina</span> barks for six days (<b>C</b>). Representative sections (8 µm) of the examined groups, stained with Luxol fast blue, for analysis of the demyelination. Original magnification: 10× objective. Scale bars = 100 µm. Delimited areas = areas of demyelination.</p>
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<p>Cellular profile. Mononuclear cell counts (<b>A</b>,<b>E</b>) and cellular profile determination (<b>B</b>–<b>D</b>,<b>F</b>–<b>H</b>) in the brains (<b>A</b>–<b>D</b>) and spinal cords (<b>E</b>–<b>H</b>) of mice immunized or not immunized with 100 µg of MOG<sub>35–55</sub> (n = 8/group). Mice were treated with 200 mg/kg of the ethanolic extract of <span class="html-italic">A. colubrina</span> barks (EtAc) for six days. Each bar represents the arithmetic mean ± SEM. * indicates <span class="html-italic">p</span> &lt; 0.05 compared to induced and PBS-treated animals (EAE). CN = negative control (not induced and treated with PBS).</p>
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<p>Absolute intensity of the most abundant phenolic acids (cinnamic acid, gallic acid, and <span class="html-italic">p</span>-coumaric acid) and flavonoids (apigenin, catechin, quercetin, and myricetin) annotated through ESI (+) Orbitrap-MS analysis of the ethanolic extract from <span class="html-italic">A. colubrina</span> bark.</p>
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<p>ESI (+) Orbitrap-MS-based metabolite profiling of <span class="html-italic">A. colubrina</span> showing the major classes identified in bark ethanolic extract.</p>
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21 pages, 2255 KiB  
Article
Kalanchoe tomentosa: Phytochemical Profiling, and Evaluation of Its Biological Activities In Vitro, In Vivo, and In Silico
by Jorge L. Mejía-Méndez, Gildardo Sánchez-Ante, Yulianna Minutti-Calva, Karen Schürenkämper-Carrillo, Diego E. Navarro-López, Ricardo E. Buendía-Corona, Ma. del Carmen Ángeles González-Chávez, Angélica Lizeth Sánchez-López, J. Daniel Lozada-Ramírez, Eugenio Sánchez-Arreola and Edgar R. López-Mena
Pharmaceuticals 2024, 17(8), 1051; https://doi.org/10.3390/ph17081051 (registering DOI) - 9 Aug 2024
Viewed by 366
Abstract
In this work, the leaves of K. tomentosa were macerated with hexane, chloroform, and methanol, respectively. The phytochemical profiles of hexane and chloroform extracts were unveiled using GC/MS, whereas the chemical composition of the methanol extract was analyzed using UPLC/MS/MS. The antibacterial activity [...] Read more.
In this work, the leaves of K. tomentosa were macerated with hexane, chloroform, and methanol, respectively. The phytochemical profiles of hexane and chloroform extracts were unveiled using GC/MS, whereas the chemical composition of the methanol extract was analyzed using UPLC/MS/MS. The antibacterial activity of extracts was determined against gram-positive and gram-negative strains through the minimal inhibitory concentration assay, and in silico studies were implemented to analyze the interaction of phytoconstituents with bacterial peptides. The antioxidant property of extracts was assessed by evaluating their capacity to scavenge DPPH, ABTS, and H2O2 radicals. The toxicity of the extracts was recorded against Artemia salina nauplii and Caenorhabditis elegans nematodes. Results demonstrate that the hexane and chloroform extracts contain phytosterols, triterpenes, and fatty acids, whereas the methanol extract possesses glycosidic derivatives of quercetin and kaempferol together with sesquiterpene lactones. The antibacterial performance of extracts against the cultured strains was appraised as weak due to their MIC90 values (>500 μg/mL). As antioxidants, treatment with extracts executed high and moderate antioxidant activities within the range of 50–300 μg/mL. Extracts did not decrease the viability of A. salina, but they exerted a high toxic effect against C. elegans during exposure to treatment. Through in silico modeling, it was recorded that the flavonoids contained in the methanol extract can hamper the interaction of the NAM/NAG peptide, which is of great interest since it determines the formation of the peptide wall of gram-positive bacteria. This study reports for the first time the biological activities and phytochemical content of extracts from K. tomentosa and proposes a possible antibacterial mechanism of glycosidic derivatives of flavonoids against gram-positive bacteria. Full article
13 pages, 1884 KiB  
Article
Anti-Skin Aging and Cytotoxic Effects of Methanol-Extracted Solanum betaceum Red Fruit Seed Extract on Ca9-22 Gingival Carcinoma Cells
by Yen-Hua Huang and Cheng-Yang Huang
Plants 2024, 13(16), 2215; https://doi.org/10.3390/plants13162215 (registering DOI) - 9 Aug 2024
Viewed by 202
Abstract
The tamarillo, or Solanum betaceum, recognized for its comprehensive nutritional profile, has long been valued for its diverse ethnobotanical uses. This study delves into the potential therapeutic applications of S. betaceum by analyzing its polyphenolic content (TPC), total flavonoid content (TFC), anti-skin [...] Read more.
The tamarillo, or Solanum betaceum, recognized for its comprehensive nutritional profile, has long been valued for its diverse ethnobotanical uses. This study delves into the potential therapeutic applications of S. betaceum by analyzing its polyphenolic content (TPC), total flavonoid content (TFC), anti-skin aging activities against key enzymes like elastase, tyrosinase, and hyaluronidase, and its cytotoxic effects on oral carcinoma cells. Extracts from the seeds, pulp, and peel of red and yellow fruits were prepared using methanol, ethanol, and acetone. The highest TPC was found in the methanol extract from red fruit seeds (9.89 mg GAE/g), and the highest TFC was found in the methanol extract of yellow fruit peel (3.02 mg QUE/g). Some of these extracts significantly inhibited skin aging-associated enzymes with the red fruit seed extract (100 μg/mL) showing up to 50.4% inhibition of tyrosinase. Additionally, the red fruit seed extract obtained using methanol demonstrated potential anticancer effects against Ca9-22 oral carcinoma cells by inhibiting cell survival, migration, and proliferation as well as inducing apoptosis. These results underscore the potential of S. betaceum fruit extracts, especially from red fruit seeds, as promising agents for anti-skin aging and anticancer applications, meriting further exploration for therapeutic uses. Full article
(This article belongs to the Special Issue Biological Activities of Plant Extracts 2023)
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<p>Anticancer potential of methanol-extracted red fruit seeds on Ca9-22 gingival carcinoma cells. (<b>A</b>) The impact of the seed extract on cell survival, migration, proliferation, and nuclear condensation in Ca9-22 cells. The black and white dashed lines indicate the positions of cell migration before and after treatment with the extract. (<b>B</b>) Trypan blue exclusion assay results demonstrating cell viability after exposure to various concentrations of the seed extract. (<b>C</b>) Wound-healing assay depicting Ca9-22 cell migration before and 24 h after treatment at different concentrations of the extract. (<b>D</b>) Clonogenic assay assessing the ability of individual cells to form colonies, indicating the survival and proliferative potential of Ca9-22 cells treated with the seed extract. (<b>E</b>) Hoechst staining results showing levels of apoptosis and DNA fragmentation at various seed extract concentrations. Statistical significance is denoted by * (<span class="html-italic">p</span> &lt; 0.05), ** (<span class="html-italic">p</span> &lt; 0.01), and *** (<span class="html-italic">p</span> &lt; 0.001) compared to control. ns, not significant.</p>
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18 pages, 25183 KiB  
Article
Physiological and Transcriptome Responses of Sweet Potato [Ipomoea batatas (L.) Lam] to Weak-Light Stress
by Jin Yang, Huanhuan Qiao, Chao Wu, Hong Huang, Claude Nzambimana, Cheng Jiang, Jichun Wang, Daobin Tang, Weiran Zhong, Kang Du, Kai Zhang and Changwen Lyu
Plants 2024, 13(16), 2214; https://doi.org/10.3390/plants13162214 (registering DOI) - 9 Aug 2024
Viewed by 224
Abstract
In the relay intercropping system of maize/sweet potato, the growth of the sweet potatoes is seriously limited by weak light stress in the early stage due to shade from maize plants. However, it is not clear how the weak light affects sweet potatoes [...] Read more.
In the relay intercropping system of maize/sweet potato, the growth of the sweet potatoes is seriously limited by weak light stress in the early stage due to shade from maize plants. However, it is not clear how the weak light affects sweet potatoes and causes tuberous root loss. By setting two light intensity levels (weak light = 30% transmittance of normal light), this study evaluated the responses of two sweet potato cultivars with different tolerances to weak light in a field-based experiment and examined the divergence of gene expression related to light and photosynthesis in a pot-based experiment. The results showed that under weak light, the anatomic structure of functional leaves changed, and the leaf thickness decreased by 39.98% and 17.32% for Yuhongxinshu-4 and Wanshu-7, respectively. The ratio of S/R increased, and root length, root superficial area, and root volume all decreased. The photosynthetic enzyme rubisco was weakened, and the net photosynthetic rate (Pn) declined as well. The level of gene expression in Wanshu-7 was higher than that of Yuhongxinshu-4. The KEGG analysis showed that differentially expressed genes from the two cultivars under weak-light stress used the same enrichment pathway, mainly via glutathione metabolism and flavonoid biosynthesis. After full light levels were restored, the differentially expressed genes were all enriched in pathways such as photosynthesis, photosynthetic pigment synthesis, and carbon metabolism. These findings indicated that weak light changed the plant morphology, photosynthetic physiology and gene expression levels of sweet potatoes, which eventually caused losses in the tuberous root yield. The more light-sensitive cultivar (Wanshu-7) had stronger reactions to weak light. This study provides a theoretical basis and strategy for breeding low-light-tolerant varieties and improving relay intercropping production in sweet potatoes. Full article
(This article belongs to the Section Plant Genetics, Genomics and Biotechnology)
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<p>Effects of weak-light stress on root morphology of different sweet potato cultivars. The column height represents the LSD value at each sampling date, and different letters indicate the significance at <span class="html-italic">p</span> &lt; 0.05. (<b>A</b>) total root length, (<b>B</b>) root surface, (<b>C</b>) root volume, (<b>D</b>) root mean diameter.</p>
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<p>Anatomy of a sweet potato leaf after 45 days of shading.</p>
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<p>Effects of weak light stress on leaf anatomical structure of different sweet potato cultivars. The columns height represents the LSD value at each sampling date, and different letters indicate the significance at <span class="html-italic">p</span> &lt; 0.05. (<b>A</b>) leaf thickness, (<b>B</b>) palisade tissue thickness, (<b>C</b>) palisade tissue thickness, (<b>D</b>) ratio of palisade tissue to sponge tissue.</p>
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<p>Effects of weak-light stress on photosynthetic gas exchange parameters of different sweet potato cultivars. The column height represents the LSD value at each sampling date, and different letters indicate the significance at <span class="html-italic">p</span> &lt; 0.05. (<b>A</b>–<b>D</b>) represent Pn, Gs, Ci and Tr, respectively.</p>
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<p>Effects of weak-light stress on the activity of rubisco enzymes in leaves of different sweet potato cultivars. The column height represents the LSD value at each sampling date, and different letters indicate the significance at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The number of differentially expressed genes in different treatments. YNT: leaf sample of Yuhongxinshu-4 in natural light at 30 DPT; YWT: leaf sample of Yuhongxinshu-4 in weak light at 30 DPT; YNR: leaf sample of Yuhongxinshu-4 in natural light at 15 DPR; YWR: leaf sample of Yuhongxinshu-4 in weak light at 15 DPR; WNT: leaf sample of Wanshu-7 in natural light at 30 DPT; WWT: leaf sample of Wanshu-7 in weak light at 30 DPT; WNR: leaf sample of Wanshu-7 in natural light at 15 DPR; WWR: leaf sample of Wanshu-7 in weak light at 15 DPR. (<b>A</b>) The number of differentially expressed genes for every treatment, (<b>B</b>) The number of differentially expressed genes co-expressed.</p>
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<p>GO enrichment of differentially expressed genes under weak-light stress. Shading period data: (<b>A</b>) GO biological process of Yuhongxinshu-4, (<b>B</b>) GO molecular function of Yuhongxinshu-4, (<b>C</b>) GO biological process of Wanshu-7, (<b>D</b>) GO molecular function of Wanshu-7. Restore data after lighting: (<b>E</b>) GO biological process of Yuhongxinshu-4, (<b>F</b>) GO molecular function of Yuhongxinshu-4, (<b>G</b>) GO biological process of Wanshu-7, (<b>H</b>) GO molecular function of Wanshu-7.</p>
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18 pages, 5252 KiB  
Article
The Identification of Bioactive Compounds in the Aerial Parts of Agrimonia pilosa and Their Inhibitory Effects on Beta-Amyloid Production and Aggregation
by Chung Hyeon Lee, Min Sung Ko, Ye Seul Kim, Kwang Woo Hwang and So-Young Park
Separations 2024, 11(8), 243; https://doi.org/10.3390/separations11080243 - 9 Aug 2024
Viewed by 366
Abstract
Alzheimer’s disease (AD) is a progressive neurodegenerative condition characterized by memory and cognitive decline in older individuals. Beta-amyloid (Aβ), a significant component of senile plaques, is recognized as a primary contributor to AD pathology. Hence, substances that can inhibit Aβ [...] Read more.
Alzheimer’s disease (AD) is a progressive neurodegenerative condition characterized by memory and cognitive decline in older individuals. Beta-amyloid (Aβ), a significant component of senile plaques, is recognized as a primary contributor to AD pathology. Hence, substances that can inhibit Aβ production and/or accumulation are crucial for AD prevention and treatment. Agrimonia pilosa LEDEB. (A. pilosa) (Rosaceae), specifically its aerial parts, was identified in our previous screening study as a promising candidate with inhibitory effects on Aβ production. Therefore, in this study, A. pilosa extract was investigated for its anti-amyloidogenic effects, and its bioactive principles were isolated and identified. The ethanol extract of A. pilosa reduced the levels of sAPPβ and β-secretase by approximately 3% and 40%, respectively, compared to the DMSO-treated control group in APP-CHO cells (a cell line expressing amyloid precursor protein), which were similar to those in the positive control group. In addition, the ethanol extract of A. pilosa also hindered Aβ’s aggregation into fibrils and facilitated the disaggregation of Aβ aggregates, as confirmed by a Thioflavin T (Th T) assay. Subsequently, the active constituents were isolated using a bioassay-guided isolation method involving diverse column chromatography. Eleven compounds were identified—epi-catechin (1), catechin (2), (2S, 3S)-dihydrokaempferol 3-O-β-D-glucopyranoside (3), (-)-epiafzelechin 5-O-β-D-glucopyranoside (4), kaempferol 3-O-β-D-glucopyranoside (5), apigenin 7-O-β-D-glucopyranoside (6), dihydrokaempferol 7-O-β-D-glucopyranoside (7), quercetin 3-O-β-D-glucopyranoside (8), (2S, 3S)-taxifolin 3-O-β-D-glucopyranoside (9), luteolin 7-O-β-D-glucopyranoside (10), and apigenin 7-O-β-D-methylglucuronate (11)—identified through 1D and 2D NMR analysis and comparison with data from the literature. These compounds significantly decreased Aβ production by reducing β- and γ-secretase levels. Moreover, none of the compounds affected the expression levels of sAPPα or α-secretase. Further, compounds 1, 2, 4, 8, and 10 demonstrated a dose-dependent reduction in Aβ aggregation and promoted the disaggregation of pre-formed Aβ aggregates. Notably, compound 8 inhibited the aggregation of Aβ into fibrils by about 43% and facilitated the disassembly of Aβ aggregates by 41% compared to the control group containing only Aβ. These findings underscore the potential of A. pilosa extract and its constituents to mitigate a crucial pathological aspect of AD. Therefore, A. pilosa extract and its active constituents hold promise for development as therapeutics and preventatives of AD. Full article
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<p>The effect of APE on the levels of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase. (<b>A</b>) The amounts of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase were assessed using Western blot analysis in the APP-CHO cells treated with varying concentrations (100, 50, 25, and 12.5 μg/mL) of APE. The graphs depict the levels of sAPP<span class="html-italic">β</span> (<b>B</b>) and <span class="html-italic">β</span>-secretase (<b>C</b>) relative to those in the DMSO-treated control group. Data are presented as means ± SD of three independent experiments, with the values expressed as a percentage relative to the DMSO-treated control group. * <span class="html-italic">p</span> &lt; 0.05 indicates statistical significance compared to the control group (CTR:DMSO-treated control, PC: positive control, extract of <span class="html-italic">D. crassirhizoma</span> roots, APE: ethanol extract of <span class="html-italic">A. pilosa</span>).</p>
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<p>The effects of the solvent-partitioned fractions on sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase. (<b>A</b>) The amounts of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase in APP-CHO cells treated with the 4 solvent-partitioned fractions (50 μg/mL) were assessed using Western blot analysis. (<b>B</b>,<b>C</b>) The graphs display the levels of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase, presented as a percentage of the DMSO-treated control group. Data are presented as means ± SD of three independent experiments, with values expressed as a percentage relative to the DMSO-treated control group. * <span class="html-italic">p</span> &lt; 0.05 indicates statistical significance compared to the control group (CTR: DMSO-treated control, PC: positive control, extract of <span class="html-italic">D. crassirhizoma</span> roots, Hx: <span class="html-italic">n</span>-hexane, DCM: dichloromethane, EA: ethyl acetate, DW: water).</p>
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<p>The effect of APE and its solvent-partitioned fractions on A<span class="html-italic">β</span> aggregation and disaggregation. (<b>A</b>) A<span class="html-italic">β</span> was exposed to concentrations of 100, 20, and 4 μg/mL of APE and the solvent-partitioned fractions. Following a 24 h incubation period, A<span class="html-italic">β</span> aggregation was assessed using the Th T assay. (<b>B</b>) A<span class="html-italic">β</span> aggregates that had been pre-formed for 24 h were exposed to APE and the solvent-partitioned fractions at concentrations of 100, 20, and 4 μg/mL. Following an additional 24 h incubation, the extent of A<span class="html-italic">β</span> aggregation was assessed using the Th T assay. All data are presented as means ± SD of three independent experiments. * <span class="html-italic">p</span> &lt; 0.05, significantly different from the A<span class="html-italic">β</span>-only group (PC: positive control, quercetin, 50 μg/mL).</p>
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<p>The structures of the compounds isolated and identified from the EA fraction of APE.</p>
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<p>HPLC chromatogram of the APE, EA fraction, and isolated compounds. (<b>A</b>) A chromatogram of compounds <b>1</b>–<b>11</b>, (<b>B</b>) APE, and (<b>C</b>) EA fraction recorded at wavelength of 280 nm (APE: <span class="html-italic">A. pliosa</span>, 20 mg/mL; EA: ethyl acetate fraction of <span class="html-italic">A. pliosa</span>, 20 mg/mL; C1: compound <b>1</b>; C2: compound <b>2</b>; C3: compound <b>3</b>; C4: compound <b>4</b>; C5: compound <b>5</b>; C6: compound <b>6</b>; C7: compound <b>7</b>; C8: compound <b>8</b>; C9: compound <b>9</b>; C10: compound <b>10</b>; and C11: compound <b>11</b>; all isolated compounds were analyzed at 1 mg/mL).</p>
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<p>The effects of compounds <b>1</b>–<b>11</b> on sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase. (<b>A</b>–<b>C</b>,<b>J</b>–<b>L</b>) The supernatant and cell lysates obtained from APP-CHO cells treated with the compounds (50 and 10 μg/mL) were subjected to Western blot analysis to determine the levels of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase, respectively. (<b>D</b>–<b>I</b>,<b>M</b>–<b>R</b>) Graphs showing changes in the levels of sAPP<span class="html-italic">β</span> and <span class="html-italic">β</span>-secretase proteins. Data are presented as means ± SD of three independent experiments, with values expressed as a percentage relative to the DMSO-treated control group. * <span class="html-italic">p</span> &lt; 0.05 indicates statistical significance (PC: positive control, extract of <span class="html-italic">D. crassirhizoma</span> roots).</p>
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<p>The effects of compounds <b>1</b>–<b>11</b> on the levels of <span class="html-italic">γ</span>-secretase. (<b>A</b>–<b>C</b>, <b>G</b>–<b>I</b>) APP-CHO cells treated with 50 and 10 μg/mL of compounds were subjected to Western blot analysis in order to determine the levels of <span class="html-italic">γ</span>-secretase in the cell lysates. (<b>D</b>–<b>F</b>, <b>J</b>–<b>L</b>) Graphs showing changes in the <span class="html-italic">γ</span>-secretase proteins. Data are presented as means ± SD of three independent experiments, with values expressed as a percentage relative to the DMSO-treated control group. * <span class="html-italic">p</span> &lt; 0.05 indicates statistical significance compared to the control group. * <span class="html-italic">p</span> &lt; 0.05 indicates a significant differences compared to the control group (PC: positive control, extract of <span class="html-italic">D. crassirhizoma</span> roots).</p>
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<p>The effects of compounds <b>1</b>–<b>11</b> on sAPP<span class="html-italic">α</span> and <span class="html-italic">α</span>-secretase. (<b>A</b>–<b>C</b>,<b>J</b>–<b>L</b>) APP-CHO cells treated with 50 and 10 μg/mL of compounds were subjected to Western blot analysis in order to determine the levels of sAPP<span class="html-italic">α</span> in the supernatant and those of <span class="html-italic">α</span>-secretase in the cell lysates. (<b>D</b>–<b>I</b>,<b>M</b>–<b>R</b>) Graphs showing changes in the levels of sAPP<span class="html-italic">α</span> and <span class="html-italic">α</span>-secretase proteins. Data are presented as means ± SD of three independent experiments, with values expressed as a percentage relative to the DMSO-treated control group. * <span class="html-italic">p</span> &lt; 0.05 indicates statistical significance compared to the control group.</p>
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<p>The effects of the compounds on the aggregation and disaggregation of A<span class="html-italic">β</span>. (<b>A</b>) The compounds isolated from APE were incubated with A<span class="html-italic">β</span> at concentrations of 100, 50, and 10 μg/mL. After 24 h, the aggregation of A<span class="html-italic">β</span> was assessed using the Th T assay. (<b>B</b>) The compounds isolated from APE were added to A<span class="html-italic">β</span> aggregates pre-formed for 24 h at concentrations of 100, 50, and 10 μg/mL. After an additional 24 h, the disaggregation of A<span class="html-italic">β</span> was evaluated using the Th T assay. All data are presented as means ± SD of three independent experiments. * <span class="html-italic">p</span> &lt; 0.05, significantly different from the A<span class="html-italic">β</span>-only group (PC: positive control, quercetin, 50 μg/mL).</p>
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16 pages, 1037 KiB  
Article
Foliar Co-Applications of Nitrogen and Iron on Vines at Different Developmental Stages Impacts Wine Grape (Vitis vinifera L.) Composition
by Xiaoke Fu, Xi Chen, Yiwen Chen, Yueran Hui, Rui Wang and Yaqi Wang
Plants 2024, 13(16), 2203; https://doi.org/10.3390/plants13162203 - 9 Aug 2024
Viewed by 187
Abstract
The co-application of N and Fe can improve wine grape composition and promote the formation of flavor compounds. To understand the effects of foliar co-application of N and Fe on wine grape quality and flavonoid content, urea and EDTA-FE were sprayed at three [...] Read more.
The co-application of N and Fe can improve wine grape composition and promote the formation of flavor compounds. To understand the effects of foliar co-application of N and Fe on wine grape quality and flavonoid content, urea and EDTA-FE were sprayed at three different developmental stages. Urea and EDTA-Fe were sprayed during the early stage of the expansion period, at the end of the early stage of the expansion period to the late stage of the veraison period, and during the late stage of the veraison period. The results demonstrated that the co-application of urea and EDTA-Fe, particularly N application during the late stage of the veraison period and Fe application during the early stage of the berry expansion period (N3Fe1), significantly improved grape quality. Specifically, the soluble solid content of berries increased by 2.78–19.13%, titratable acidity decreased by 6.67–18.84%, the sugar-acid ratio became more balanced, and yield increased by 13.08–40.71%. Further, there was a significant increase in the relative content of amino acids and flavonoids. In conclusion, the application of Fe and N fertilizers at the pre-expansion and late veraison stages of grapes can significantly improve the quality and yield of berries; ultimately, this establishes a foundation for future improvement in the nutritional value of grapes and wine. Full article
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<p>Chlorophyll content in wine grape leaves treated with co-applications of N and Fe. Effect of N and Fe co-application on the chlorophyll of wine grape leaves. Different lowercase letters (abcd) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of co-application of N, Fe, and leaves/petiole on N and Fe contents in leaves and petioles of wine grapes at different developmental stages. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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11 pages, 4059 KiB  
Communication
Effect of Plant Growth Promoting Rhizobacteria on the Development and Biochemical Composition of Cucumber under Different Substrate Moisture Levels
by Gerardo Zapata-Sifuentes, Manuel Fortis-Hernández, Jorge Sáenz-Mata, Christian Silva-Martínez, Liliana Lara-Capistran, Pablo Preciado-Rangel and Luis Guillermo Hernández-Montiel
Microbiol. Res. 2024, 15(3), 1505-1515; https://doi.org/10.3390/microbiolres15030102 - 9 Aug 2024
Viewed by 255
Abstract
Cucumis sativus L. plants are subjected to stress during production, affecting their growth, development, and fruit quality due to abiotic factors. Thus, the aim of this research is to evaluate Pseudomonas paralactis, Sinorhizobium meliloti, and Acinetobacter radioresistens plant growth promoting rhizobacteria [...] Read more.
Cucumis sativus L. plants are subjected to stress during production, affecting their growth, development, and fruit quality due to abiotic factors. Thus, the aim of this research is to evaluate Pseudomonas paralactis, Sinorhizobium meliloti, and Acinetobacter radioresistens plant growth promoting rhizobacteria (PGPR) effect on C. sativus plants under three substrate moisture levels (100, 75, and 50%). A randomized complete block design (RCBD) was used with an A x B arrangement: (1) factor A (inoculant) with four levels; (2) PGPR and control (without bacterium); (3) factor B (substrate moisture content) with three levels. Plant height, root length, and fresh weight increased by inoculating PGPR (121%, 135%, and 134%, respectively); likewise, these variables increased with higher moisture content (177%, 204%, and 234%, respectively), while the effect of the interactions of the PGPR and the moisture content in the substrate showed statistical differences in plant height increasing of 197% and root length of 267%. On the other hand, the content of phenols, flavonoids, and antioxidant capacity was statistically different (p ≤ 0.05) in inoculated plants, with PGPR increasing by 117%, 126%, and 150% respectively. In the moisture content of the substrate, statistical differences were observed, with an increase in the flavonoid content (114%) and antioxidant capacity (116%). The assimilation of nitrogen was higher by 274% and phosphorus by 124% with the PGPR inoculation, the moisture content increased the nitrogen content in the plant (257%) and the phosphorus content in plant (135%), showing significant differences (p ≤ 0.05). However, the interaction of PGPR and moisture content only presented statistical differences in nitrogen assimilation. PGPR can be considered as an alternative to obtain vigorous cucumber seedlings. Full article
(This article belongs to the Special Issue Plants, Mycorrhizal Fungi, and Bacteria)
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> height. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) and moisture content interaction effect on <span class="html-italic">Cucumis sativus</span> height. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> root length. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) and substrate moisture content interaction effect on <span class="html-italic">Cucumis sativus</span> root length. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> fresh weight. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> total phenol content. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> flavonoid content. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (PGPR) inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> antioxidant capacity. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria inoculation (<b>a</b>) and substrate moisture content (<b>b</b>) effect on <span class="html-italic">Cucumis sativus</span> nitrogen (N) content. Columns with different letters are statistically different (Tukey’s <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria interaction and substrate moisture content effect on <span class="html-italic">Cucumis sativus</span> nitrogen content. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Plant growth promoting rhizobacteria (<b>a</b>) and substrate moisture content (<b>b</b>) on <span class="html-italic">Cucumis sativus</span> phosphorus content. Columns with different letters are statistically different (Tukey’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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12 pages, 2544 KiB  
Article
Comparative Analysis of the Characteristics of Two Hardy Kiwifruit Cultivars (Actinidia arguta cv. Cheongsan and Daebo) Stored at Low Temperatures
by Hyun Ji Eo, Chul-Woo Kim, Uk Lee and Yonghyun Kim
Plants 2024, 13(16), 2201; https://doi.org/10.3390/plants13162201 - 9 Aug 2024
Viewed by 185
Abstract
A cold storage system is useful for maintaining the quality of hardy kiwifruit. However, extended cold storage periods inevitably result in cold stress, leading to lower fruit marketability; the severity of chilling injury depends on fruit types and cultivars. In this study, the [...] Read more.
A cold storage system is useful for maintaining the quality of hardy kiwifruit. However, extended cold storage periods inevitably result in cold stress, leading to lower fruit marketability; the severity of chilling injury depends on fruit types and cultivars. In this study, the impact of cold storage conditions on the physicochemical properties and antioxidant capacity of two phenotypically different hardy kiwifruit cultivars—‘Cheongsan’ (large type) and ‘Daebo’ (small type)—stored at low (L; 3 °C, relative humidity [RH]; 85–90%) and moderate-low (ML; 5 °C, RH; 85–90%) temperatures was determined. Significant differences in fruit firmness and titratable acidity between treatments L and ML were observed in both cultivars during the experimental storage period. Meanwhile, the browning and pitting rates of the ‘Cheongsan’ fruits in treatment L increased for 8 weeks compared with those of the ‘Daebo’ fruits in treatments L and ML; nonetheless, fruit decay was observed in the ‘Daebo’ fruits in treatment ML after 6 weeks. The total chlorophyll, carotenoid, flavonoid, and ascorbic acid concentrations as well as the antioxidant activities of both the cultivars significantly differed between treatments L and ML. After 2 weeks of storage, the ‘Cheongsan’ fruits in treatment L had lower antioxidant activities and ascorbic acid content than those in treatment ML. These results demonstrate that the quality attributes and antioxidant activity of hardy kiwifruit are influenced by the low-temperature storage conditions and the specific kiwifruit cultivars. Our findings suggest that optimal cold storage conditions, specific to each hardy kiwifruit cultivar, promise to maintain fruit quality, including their health-promoting compounds, during long-term storage. Full article
(This article belongs to the Section Phytochemistry)
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<p>Changes in the physicochemical properties of the ‘Cheongsan’ and ‘Daebo’ hardy kiwi cultivars during cold storage. Weight loss, firmness, total soluble solids content, and titratable acidity were measured for 8 weeks. The asterisks indicate a significant difference for each cultivar between treatments L and ML according to Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05 and *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Incidence of physiological disorders in the hardy kiwifruits during cold storage. Shriveling, browning, pitting, and decay rates were evaluated based on a 6-point scale: 0 = 0%, 1 = 1–20%, 2 = 21–40%, 3 = 41–60%, 4 = 61–80%, and 5 = 81–100% of the corresponding affected area on the fruit surface. The asterisks indicate a significant difference for each cultivar between treatments L and ML according to Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001; <span class="html-italic">n</span> = 17–20).</p>
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<p>‘Cheongsan’ and ‘Daebo’ fruits stored at 3 °C and 5 °C after 6 weeks of storage. Bars indicate 2 cm.</p>
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<p>Changes in the Hunter values were monitored during the storage period and compared between the storage temperatures. The asterisks indicate a significant difference for each cultivar between treatments L and ML according to Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001; <span class="html-italic">n</span> = 20).</p>
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<p>Changes in the starch and soluble sugar content in the hardy kiwifruits during storage. The asterisks indicate a significant difference for each cultivar between treatments L and ML according to Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001; <span class="html-italic">n</span> = 3).</p>
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<p>Changes in the content of the health-promoting compounds and antioxidant activity. The asterisks indicate a significant difference for each cultivar between treatments L and ML according to Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001; <span class="html-italic">n</span> = 3).</p>
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14 pages, 2201 KiB  
Article
The Impact of Lighting Treatments on the Biosynthesis of Phenolic Acids in Black Wheat Seedlings
by Hongjie Lan, Chunping Wang, Zhengfei Yang, Jiangyu Zhu, Weiming Fang and Yongqi Yin
Foods 2024, 13(16), 2499; https://doi.org/10.3390/foods13162499 - 9 Aug 2024
Viewed by 257
Abstract
Light, as a crucial environmental determinant, profoundly influences the synthesis of secondary metabolites in plant metabolism. This study investigated the impacts of the red light combined with ultraviolet-A (UV-A) and ultraviolet-B (UV-B) treatments on phenolic acid biosynthesis in black wheat seedlings. The results [...] Read more.
Light, as a crucial environmental determinant, profoundly influences the synthesis of secondary metabolites in plant metabolism. This study investigated the impacts of the red light combined with ultraviolet-A (UV-A) and ultraviolet-B (UV-B) treatments on phenolic acid biosynthesis in black wheat seedlings. The results demonstrate that the red light combined with UV-A and UV-B treatments significantly enhanced the levels of phenolic acids in black wheat seedlings, at 220.4 μg/seedling and 241.5 μg/seedling, respectively. The content of bound phenolic acids in black wheat seedlings increased by 36.0% under the UV-B treatment. The application of the UV-A/UV-B treatments markedly enhanced the activities of phenylalanine ammonia-lyase, 4-coumarate CoA ligase, and cinnamate 4-hydroxylase in black wheat seedlings while also promoting the expression levels of genes related to phenolic acid synthesis. The expression levels of fructose-1,6-bisphosphate aldolase and NADP-malic enzyme related to photosynthesis were significantly upregulated. This resulted in an augmentation in the chlorophyll content, thereby enhancing photosynthesis in black wheat seedlings. Nevertheless, the UV-A and UV-B treatments also had a significant constraining effect on the growth and development of black wheat seedlings. In addition, the UV-A and UV-B treatments increased the activity and gene expression levels of antioxidant enzymes while significantly increasing the contents of total flavonoids and anthocyanins, activating the antioxidant system. The findings reveal that light-source radiation serves as an effective method for promoting the biosynthesis of phenolic acids in black wheat seedlings. Full article
(This article belongs to the Section Plant Foods)
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Figure 1
<p>Schematic diagram of the treatments used to study the effects of the red light combined with UV-A and UV-B on black wheat seedlings.</p>
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<p>Effects of red light combined with the UV-A and UV-B treatments on the physiological and oxidative damage indexes of black wheat seedlings. The lowercase letters represent significant differences between different treatments at the same time.</p>
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<p>Effects of red light combined with the UV-A and UV-B treatments on the contents of phenols in black wheat seedlings. The lowercase letters represent significant differences between different treatments at the same time.</p>
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<p>Effects of the red light treatment combined with UV-A and UV-B treatments on the chlorophyll contents and relative genes’ expression levels of photosynthesis in black wheat seedlings. The lowercase letters represent significant differences between different treatments at the same time.</p>
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<p>Effects of the red light treatment combined with UV-A and UV-B treatments on the antioxidant enzyme activity and relative gene expression levels in black wheat seedings. The lowercase letters represent significant differences between different treatments at the same time.</p>
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<p>Effects of the red light combined with UV-A and UV-B treatments on the enzyme activities and relative genes’ expression levels of phenolic acid synthesis in black wheat seedlings. The lowercase letters represent significant differences between different treatments at the same time.</p>
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<p>Hypothesis of the mechanisms of the red light combined with UV-A and UV-B treatments on black wheat seedling growth and the regulation of phenolic acid enrichment.</p>
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26 pages, 875 KiB  
Review
Citrus limon var. pompia Camarda var. nova: A Comprehensive Review of Its Botanical Characteristics, Traditional Uses, Phytochemical Profile, and Potential Health Benefits
by Anna Maria Posadino, Paola Maccioccu, Ali H. Eid, Roberta Giordo, Gianfranco Pintus and Grazia Fenu
Nutrients 2024, 16(16), 2619; https://doi.org/10.3390/nu16162619 - 8 Aug 2024
Viewed by 327
Abstract
Citrus limon var. pompia Camarda var. nova, commonly known as pompia, is a distinctive citrus ecotype native to Sardinia, notable for its unique botanical, phytochemical, and potential health benefits. It holds cultural significance as a traditional food product of Sardinia, recognized by [...] Read more.
Citrus limon var. pompia Camarda var. nova, commonly known as pompia, is a distinctive citrus ecotype native to Sardinia, notable for its unique botanical, phytochemical, and potential health benefits. It holds cultural significance as a traditional food product of Sardinia, recognized by the Italian Ministry of Agricultural Food and Forestry Policies. This comprehensive review examines pompia’s traditional uses, taxonomic classification, pomological characteristics, phytochemical profile, and potential health benefits. Pompia phytochemical analyses reveal a rich composition of flavonoids and terpenoids, with notable concentrations of limonene, myrcene, and various oxygenated monoterpenes. Pompia essential oils are primarily extracted from its peel and leaves. Peel essential oils exhibit a high concentration of the monoterpene limonene (82%) and significantly lower quantities of myrcene (1.8%), geranial (1.7%), geraniol (1.5%), and neral (1.4%). In its rind extract, flavanones such as naringin (23.77 µg/mg), neoeriocitrin (46.53 µg/mg), and neohesperidin (44.57 µg/mg) have been found, along with gallic acid (128.3 µg/mg) and quinic acid (219.67 µg/mg). The main compounds detected in the essential oils from pompia leaves are oxygenated monoterpenes (53.5%), with limonene (28.64%), α-terpineol (41.18%), geranial (24.44%), (E)-β-ocimene (10.5%), linalool (0.56%), and neryl acetate (13.56%) being particularly prominent. In pompia juice, the presence of phenolic compounds has been discovered, with a composition more similar to lemon juice than orange juice. The primary flavonoid identified in pompia juice is chrysoeriol-6,8-di-C-glucoside (stellarin-2) (109.2 mg/L), which has not been found in other citrus juices. The compound rhoifolin-4-glucoside (17.5 mg/L) is unique to pompia juice, whereas its aglycone, rhoifolin, is found in lemon juice. Other flavonoids identified in pompia juice include diosmetin 6,8-C-diglucoside (54.5 mg/L) and isorhamnetin 3-O-rutinoside (79.4 mg/L). These findings support the potential of pompia in developing nutraceuticals and natural health products, further confirmed by its compounds’ antioxidant, anti-inflammatory and antibacterial properties. Future research should focus on optimizing extraction methods, conducting clinical trials to evaluate efficacy and safety, and exploring sustainable cultivation practices. The potential applications of pompia extracts in food preservation, functional foods, and cosmetic formulations also warrant further investigation. Addressing these areas could significantly enhance pompia’s contribution to natural medicine, food science, and biotechnology. Full article
(This article belongs to the Section Phytochemicals and Human Health)
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