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15 pages, 2958 KiB  
Article
Application of Antimicrobial Rubber-Coated Cotton Gloves for Mangosteen-Peel-Extract-Mediated Biosynthesis of Ag–ZnO Nanocomposites
by Montri Luengchavanon, Ekasit Anancharoenwong, Sutida Marthosa, Theerakamol Pengsakul and Jidapa Szekely
Polymers 2025, 17(1), 32; https://doi.org/10.3390/polym17010032 (registering DOI) - 26 Dec 2024
Abstract
Nanocomposites based on metal nanoparticles (MNP) prepared with mangosteen (mgt) peel extract-mediated biosynthesis of Agmgt/Znmgt have attracted considerable interest due to their potential for various practical applications. In this study, their role in developing antibacterial protection for rubber [...] Read more.
Nanocomposites based on metal nanoparticles (MNP) prepared with mangosteen (mgt) peel extract-mediated biosynthesis of Agmgt/Znmgt have attracted considerable interest due to their potential for various practical applications. In this study, their role in developing antibacterial protection for rubber cotton gloves is investigated. The process of mangosteen-peel-extract-mediated biosynthesis produced Agmgt/Znmgt nanocomposites with respective diameters of 23.84 ± 4.08 nm and 30.99 ± 5.73 nm, which were assessed in the context of antimicrobial rubber-coated gloves. The rubber glover surface exhibited a very dense deposition of the Ag+Znmgt nanocomposite, which subsequently demonstrated level 4 resistance to punctures under the ANSI-ISEA 105-2016 standard. This could be attributed to the Zn-cellulose double formation on the rubber surface. Notably, on testing the inhibition of bacterial growth, the extract with the Agmgt nanoparticles presented the least concentration capable of growth inhibition in comparison to the extracts with Znmgt and Ag+Znmgt nanoparticles. Each of the mangosteen extracts was shown to inhibit bacterial growth when tested against both Gram-positive cocci and Gram-negative bacilli, with MIC in the range 40–320 µg/mL. The growth of drug-resistant bacteria (MRSA) could also be inhibited with an MIC value of 160 µg/mL, and with 30 min of contact, gloves with respective coatings of Znmgt and Ag+Znmgt extract nanocomposites were shown to inhibit K. pneumoniae and MRSA. However, while effective bacterial inhibition occurred with the suspensions, the coatings on glove surfaces required a lengthy incubation period (contact time) of at least 30 min for efficacy. Full article
(This article belongs to the Special Issue Advances in Functional Rubber and Elastomer Composites II)
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Figure 1

Figure 1
<p>The Ag<sub>mgt</sub>, Zn<sub>mgt</sub>, and Ag+Zn<sub>mgt</sub> nanocomposites were prepared and sprayed onto rubber gloves.</p>
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<p>SEM image samples of Ag<sub>mgt</sub> and Zn<sub>mgt</sub> nanocomposites. (<b>A</b>,<b>B</b>) show the SEM images for Ag<sub>mgt</sub> at 50,000× and 200,000× magnifications. (<b>C</b>,<b>D</b>) show the SEM images of Zn<sub>mgt</sub> at 50,000× and 200,000× magnifications.</p>
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<p>The XRD patterns of Ag<sub>mgt</sub> and Zn<sub>mgt</sub> nanocomposites: (<b>A</b>) the crystalline peaks of Ag<sub>mgt</sub> nanocomposite and (<b>B</b>) the crystalline peaks of Zn<sub>mgt</sub> nanocomposite.</p>
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<p>SEM image samples of the surfaces of rubber gloves; Ag<sub>mgt</sub>-coated rubber glove, Zn<sub>mgt</sub>-coated rubber glove, and Ag+Zn<sub>mgt</sub>-coated rubber glove. (<b>A</b>,<b>B</b>) show the SEM images of the surface of the rubber glove at 200× and 1000× magnifications. (<b>C</b>,<b>D</b>) show the SEM images of the surface of the Ag<sub>mgt</sub>-coated rubber glove at 200× and 1000× magnifications. (<b>E</b>,<b>F</b>) show the SEM image of the surface of the Zn<sub>mgt</sub>-coated rubber glove at 200× and 1000× magnifications. (<b>G</b>,<b>H</b>) show the SEM image of the surface of the Ag+Zn<sub>mgt</sub>-coated rubber glove at 200× and 1000× magnifications.</p>
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<p>Schematic cross-sections of rubber gloves when sprayed with Ag+Zn<sub>mgt</sub>, Ag<sub>mgt</sub>, and Zn<sub>mgt,</sub> to coat the surface of rubber gloves related to <a href="#polymers-17-00032-f003" class="html-fig">Figure 3</a> and <a href="#polymers-17-00032-f004" class="html-fig">Figure 4</a>. The XRD patterns indicated the Ag<sub>mgt</sub> and Zn<sub>mgt</sub> nanocomposites, while SEM exhibited the surfaces of the Ag<sub>mgt</sub> coated rubber glove, Zn<sub>mgt</sub> coated rubber glove, and Ag+Zn<sub>mgt</sub>-coated rubber glove.</p>
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<p>Antimicrobial activities at different concentrations of Ag+Zn<sub>mgt</sub>, Zn<sub>mgt</sub>, and Ag<sub>mgt</sub> nanoparticles.</p>
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<p>A comparison of (1) the bactericidal activity of the untreated glove, (2) Ag+Zn<sub>mgt</sub>, (3) Zn<sub>mgt</sub>, and (4) Ag<sub>mgt</sub> spray coated on gloves, at contact times of 0, 10, 20, and 30 min.</p>
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20 pages, 6521 KiB  
Article
Genome-Wide Identification and Expression Analysis of Eggplant Reveals the Key MYB Transcription Factor Involved in Anthocyanin Synthesis
by Jiaqi Ai, Wuhong Wang, Tianhua Hu, Haijiao Hu, Yaqin Yan, Jinglei Wang, Yunzhu Wang, Na Hu, Hongtao Pang, Chonglai Bao and Qingzhen Wei
Horticulturae 2025, 11(1), 12; https://doi.org/10.3390/horticulturae11010012 (registering DOI) - 26 Dec 2024
Abstract
MYB transcription factors (TFs) represent one of the largest gene families in plants, and previous studies have demonstrated their involvement in regulating anthocyanin synthesis. Eggplant is an important anthocyanin-rich solanaceae vegetable crop. In this study, a total of 219 MYB gene-family members were [...] Read more.
MYB transcription factors (TFs) represent one of the largest gene families in plants, and previous studies have demonstrated their involvement in regulating anthocyanin synthesis. Eggplant is an important anthocyanin-rich solanaceae vegetable crop. In this study, a total of 219 MYB gene-family members were identified using the complete and high-quality eggplant genome, comprising 105 1R-MYBs, 107 R2R3-MYBs, 5 3R-MYBs, and 2 4R-MYBs. Using phylogenetic analysis, we divided them into 33 subfamilies. Members of the SmeMYB gene family are unevenly distributed on 12 chromosomes, but are mainly concentrated at the upper and lower ends of the chromosomes. In addition, the expression levels of R2R3-MYBs in differently colored eggplant tissues (peel, calyx, stem, flower, and leaf) were investigated with RNA-seq (RNA sequencing). A total of 13 differentially expressed R2R3-MYB transcription factors related to the synthesis of anthocyanins in different eggplant tissues were screened out. SmeMYB110, SmeMYB175, and SmeMYB182 were also found to play significant roles in this process. Furthermore, 10 MYB TFs were identified as potential genes regulating anthocyanin synthesis in different tissues. The quantitative real-time PCR (qRT-PCR) analysis results showed that SmeMYB175 was regarded as the most likely key transcription factor regulating anthocyanin synthesis in calyx. These results not only deepen our understanding of the MYB gene family in eggplant but also lay a solid foundation for further research on the regulation of SmeR2R3-MYBs in anthocyanin synthesis across diverse eggplant tissues. Full article
(This article belongs to the Special Issue A Decade of Research on Vegetable Crops: From Omics to Biotechnology)
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Figure 1
<p>Chromosomal mapping of the MYB gene family in eggplant.</p>
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<p>Collinearity analysis of MYB gene-family members in eggplant.</p>
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<p>Phylogenetic relationships, gene structures, and motif composition of SmeR2R3-MYB gene-family members: (<b>a</b>) phylogenetic tree of SmeR2R3-MYB gene-family members; (<b>b</b>) conserved motifs of SmeR2R3-MYBs; and (<b>c</b>) gene structure of SmeR2R3-MYBs.</p>
Full article ">Figure 4
<p>Sequence logos of the conserved R2 and R3 repeats of the SmeR2R3-MYB domain: (<b>a</b>) sequence logo of R2 in SmeR2R3-MYBs; (<b>b</b>) sequence logo of R3 in SmeR2R3-MYBs.</p>
Full article ">Figure 5
<p>Phylogenetic tree of R2R3-MYB for major vegetable crops in the Solanaceae family. The major vegetable crops in the Solanaceae family include tomato (SlR2R3-MYB), eggplant (SmeR2R3-MYB), pepper (CaR2R3-MYB), and potato (StR2R3-MYB). The phylogenetic evolutionary tree was constructed and divided into 39 subfamilies (E1–E39). The corresponding Arabidopsis subfamilies (S1–S28) were also labeled.</p>
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<p>Expression levels of SmeR2R3-MYB DEGs in different colors of different tissues. The patches of different colors indicate the expression levels of SmeR2R3-MYB DEGs in different colors of different tissues. The connecting lines on the left represent cluster analysis. (<b>a</b>) Expression levels of DEGs in dark-purple stem (DPS), purple-green stem (PGS), and green stem (GS); (<b>b</b>) DEG expression levels in dark-purple calyx (DPC), purple-green calyx (PGC), and green calyx (GC); (<b>c</b>) DEG expression levels in dark-purple flower (DPF), purple flower (PF), and white flower (WF); (<b>d</b>) DEG expression levels in purple-black peel (B), purple-red peel (P), green peel (G), and white peel (W); and (<b>e</b>) DEG expression levels in dark-purple leaf (DPL), purple-green leaf (PGL), and green leaf (GL).</p>
Full article ">Figure 7
<p>Relative expression levels of candidate gene of calyx in eggplant. Relative expression levels of (<b>a</b>) <span class="html-italic">SmeMYB26</span> in different colors of calyx, (<b>b</b>) <span class="html-italic">SmeMYB110</span> in different colors of calyx, (<b>c</b>) <span class="html-italic">SmeMYB175</span> in different colors of calyx, and (<b>d</b>) <span class="html-italic">SmeMYB186</span> in different colors of calyx.</p>
Full article ">
28 pages, 27768 KiB  
Article
Nootkatone Derivative Nootkatone-(E)-2-iodobenzoyl hydrazone Promotes Megakaryocytic Differentiation in Erythroleukemia by Targeting JAK2 and Enhancing JAK2/STAT3 and PKCδ/MAPK Crosstalk
by Yang Pan, Feng Xiao, Chaolan Pan, Hui Song, Peng Zhao, Meijun Chen, Liejun Huang, Jue Yang and Xiaojiang Hao
Cells 2025, 14(1), 10; https://doi.org/10.3390/cells14010010 (registering DOI) - 26 Dec 2024
Abstract
Erythroleukemia, a complex myeloproliferative disorder presenting as acute or chronic, is characterized by aberrant proliferation and differentiation of erythroid cells. Although nootkatone, a sesquiterpene derived from grapefruit peel and Alaska yellow cedar, has shown anticancer activity predominantly in solid tumors, its effects in [...] Read more.
Erythroleukemia, a complex myeloproliferative disorder presenting as acute or chronic, is characterized by aberrant proliferation and differentiation of erythroid cells. Although nootkatone, a sesquiterpene derived from grapefruit peel and Alaska yellow cedar, has shown anticancer activity predominantly in solid tumors, its effects in erythroleukemia remain unexplored. This study aimed to investigate the impact of nootkatone and its derivatives on erythroleukemia. Our results demonstrate that the nootkatone derivative nootkatone-(E)-2-iodobenzoyl hydrazone (N2) significantly inhibited erythroleukemia cell proliferation in a concentration- and time-dependent manner. More importantly, N2 induced megakaryocytic differentiation, as evidenced by significant morphological changes, and upregulation of megakaryocytic markers CD41 and CD61. In vivo, N2 treatment led to a marked increase in platelet counts and megakaryocytic cell counts. Mechanistically, N2 activated a crosstalk between the JAK2/STAT3 and PKCδ/MAPK signaling pathways, enhancing transcriptional regulation of key factors like GATA1 and FOS. Network pharmacology and experimental validation confirmed that N2 targeted JAK2, and knockdown of JAK2 abolished N2-induced megakaryocytic differentiation, underscoring JAK2’s critical role in erythroleukemia differentiation. In conclusion, N2 shows great promise as a differentiation therapy for erythroleukemia, offering a novel approach by targeting JAK2-mediated signaling pathways to induce megakaryocytic differentiation. Full article
(This article belongs to the Section Cell Signaling)
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Figure 1

Figure 1
<p>Nootkatone derivative N2 inhibits cell proliferation in erythroleukemia HEL and K562 cells. (<b>A</b>) Chemical structure of nootkatone derivative N2. (<b>B</b>) Scatter diagram presentation of the influence of nootkatone and its derivatives (20 μM) on cell viability of HEL and K562 cells for 72 h. The inhibition rate was measured by MTT assays, with the 0.1% DMSO group serving as the negative control. Inhibition rate = (negative control group—treatment group)/negative control group × 100%. (<b>C</b>,<b>D</b>) HEL and K562 cells were treated with varying concentrations of the nootkatone derivative N2 for 72 h, and cell viability was evaluated using MTT assays. (<b>E</b>,<b>F</b>) The influence of N2 on the proliferation of HEL and K562 cells was quantified through MTT assays. (<b>G</b>,<b>H</b>) Effects of N2 on morphological changes in HEL and K562 cells. Magnification: ×200. Scale bar: 100 µm. Data represented the mean ± SD of three independent experiments. * <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 vs. the DMSO group.</p>
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<p>Nootkatone derivative N2 enhances multinucleation and CD41a expression in HEL and K562 cells. (<b>A</b>,<b>B</b>) Morphological analysis of HEL (<b>A</b>) and K562 (<b>B</b>) cells following treatment with varying concentrations of N2 for 72–96 h. Cells were subjected to Wright–Giemsa staining for morphological assessment. Magnification: ×400. Scale bar: 50 µm. (<b>C</b>,<b>D</b>) Immunofluorescence analysis was conducted on HEL (<b>C</b>) and K562 (<b>D</b>) cells treated with either DMSO or N2 for 72 h, revealing CD41a expression (green). Nuclear staining was performed using DAPI (blue). Magnification: ×400. Scale bar: 50 µm.</p>
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<p>Nootkatone derivative N2 increases the expression of megakaryocyte-specific markers in HEL cells. (<b>A,B</b>) Expression of CD41a and CD61 megakaryocyte-specific markers analyzed using flow cytometry in HEL cells. (<b>C</b>,<b>D</b>) Quantification of the percentage of CD41a<sup>+</sup> cells and CD61<sup>+</sup> cells in HEL cells. Data represent the mean ± SD of three independent experiments. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group.</p>
Full article ">Figure 4
<p>Nootkatone derivative N2 increases the expression of megakaryocyte-specific markers in K562 cells. (<b>A</b>,<b>B</b>) Expression of CD41a and CD61 megakaryocyte-specific markers analyzed using flow cytometry in K562 cells. (<b>C</b>,<b>D</b>) Quantification of the percentage of CD41a<sup>+</sup> cells and CD61<sup>+</sup> cells in K562 cells. Data represent the mean ± SD of three independent experiments. *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group.</p>
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<p>Effect of nootkatone derivative N2 on cell cycle distribution in HEL and K562 cells. (<b>A</b>–<b>F</b>) HEL (<b>A</b>) and K562 (<b>D</b>) cells were exposed to indicated concentrations of N2 for either 72 h or 96 h. The cells were stained with PI and the percentage of cell cycle distribution was analyzed by flow cytometry. The proportions of cell cycle distribution at G1, S, and G2 phases in HEL (<b>B</b>,<b>C</b>) and K562 (<b>E</b>,<b>F</b>) cells at various time points. Data are expressed as the mean ± SD, with each experiment conducted in triplicate. *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group.</p>
Full article ">Figure 6
<p>N2 treatment was associated with an increase in polyploidy in HEL and K562 cells. (<b>A</b>–<b>D</b>) Polyploid cells in N2-treated HEL (<b>A</b>) and K562 (<b>C</b>) cells were analyzed by flow cytometry. The proportion of polyploid cells in HEL (<b>B</b>) and K562 (<b>D</b>) cells. Data are expressed as the mean ± SD. Each experiment was repeated in triplicate. * <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 vs. the DMSO group.</p>
Full article ">Figure 7
<p>Nootkatone derivative N2 activates the PKCδ/MAPK signaling pathway and its downstream megakaryocytic differentiation-related transcription factors. (<b>A</b>–<b>D</b>) Upon treating with N2 (2, 4, 8 μM), the expression levels of p-PKCδ, PKCδ, p-MEK, MEK, p-ERK, ERK, and GATA1 detected using Western blotting in HEL (<b>A</b>) and K562 (<b>C</b>) cells. Densitometry analysis of these proteins in HEL (<b>B</b>) and K562 (<b>D</b>) cells. (<b>E</b>,<b>F</b>) Effects of N2 on the mRNA expression levels of seven transcription factors relevant to megakaryocytic differentiation in HEL (<b>E</b>) and K562 (<b>F</b>) cells. All data are expressed as the mean ± SD. GAPDH was used as loading control. Each experiment was repeated in triplicate. * <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 vs. the DMSO group.</p>
Full article ">Figure 8
<p>Nootkatone derivative N2 activates the JAK2/STAT3 signaling pathway in HEL and K562 cells. (<b>A</b>) JAK2 was identified as a potential target based on the intersection of N2-predicted targets with established targets associated with acute myeloid leukemia. (<b>B</b>–<b>E</b>) HEL (<b>B</b>) and K562 (<b>C</b>) cells were treated with N2 at the indicated doses. The expression levels of p-JAK2, JAK2, p-STAT3, and STAT3 were analyzed by Western blotting. Densitometry analysis of p-JAK2, JAK2, p-STAT3, and STAT3 in HEL (<b>D</b>) and K562 (<b>E</b>) cells. All data are expressed as the mean ± SD, with GAPDH serving as the loading control. Each experiment was repeated in triplicate. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group.</p>
Full article ">Figure 9
<p>Nootkatone derivative N2 promotes megakaryocytic differentiation via activation of the JAK2/STAT3 signaling pathways. (<b>A</b>,<b>B</b>) JAK2/STAT3 pathway specific inhibitor WP1066 treatment inhibited N2-induced increases in cell size, multinucleation in HEL and K562 cells via Wright–Giemsa staining. Magnification: ×400. Scale bar: 50 µm. (<b>C</b>,<b>D</b>) HEL and K562 cells were treated with N2 (8 μM) either alone or in combination with JAK2/STAT3 inhibitor, WP1066 (1 μM), and the expression levels of CD41a and CD61 analyzed using flow cytometry. (<b>E</b>–<b>H</b>) Quantification of the percentage of CD41a<sup>+</sup> cells and CD61<sup>+</sup> cells in HEL (<b>E</b>,<b>F</b>) and K562 (<b>G</b>,<b>H</b>) cells. Data are expressed as the mean ± SD. Each experiment was repeated in triplicate. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group. <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. N2 group.</p>
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<p>Nootkatone derivative N2 promotes megakaryocytic differentiation via activation of the PKCδ/MAPK signaling pathways. (<b>A</b>,<b>B</b>) Treatment of HEL and K562 cells with N2 at a concentration of 8 μM, both independently and in conjunction with the PKCδ-specific inhibitor Rottlerin (1 μM). The cells were subjected to Wright–Giemsa staining for morphological assessment. Magnification: ×400. Scale bar: 50 µm. (<b>C</b>,<b>D</b>) HEL and K562 cells were treated with N2 (8 μM) in the absence or presence of Rottlerin (1 μM), and expression of CD41a and CD61 analyzed using flow cytometry. (<b>E</b>–<b>H</b>) Quantification of the percentage of CD41a<sup>+</sup> cells and CD61<sup>+</sup> cells in HEL (<b>E</b>,<b>F</b>) and K562 (<b>G</b>,<b>H</b>) cells. Data are presented as the mean ± SD. Each experiment was repeated in triplicate. *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. N2 group.</p>
Full article ">Figure 11
<p>WP1066 treatment significantly reduced N2-induced phosphorylation of JAK2, STAT3, PKCδ, MEK, and ERK, as well as the expression of GATA1. (<b>A</b>,<b>B</b>) HEL and K562 cells were treated with N2 (8 μM) and/or WP1066 (1 μM), and the protein expression levels of p-JAK2, JAK2, p-STAT3, STAT3, p-PKCδ, PKCδ, p-MEK, MEK, p-ERK, ERK, and GATA1 were detected using Western blotting. (<b>C</b>,<b>D</b>) Densitometry analysis of these proteins in HEL (<b>C</b>) and K562 (<b>D</b>) cells. Data are presented as the mean ± SD. GAPDH was used as loading control. Each experiment was repeated in triplicate. *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. N2 group.</p>
Full article ">Figure 12
<p>Rottlerin significantly diminished N2-induced PKCδ, STAT3, MEK and ERK phosphorylation. (<b>A</b>,<b>B</b>) HEL and K562 cells were treated with N2 (8 μM) in the absence or presence of Rottlerin (1 μM), and the proteins expression of p-JAK2, JAK2, p-STAT3, STAT3, p-PKCδ, PKCδ, p-MEK, MEK, p-ERK, ERK and GATA1 were detected using Western blotting. (<b>C</b>,<b>D</b>) Densitometry analysis of these proteins in HEL (<b>C</b>) and K562 (<b>D</b>) cells. Data are presented as the mean ± SD. GAPDH was used as loading control. Each experiment was repeated in triplicate. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001 vs. the DMSO group. <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. N2 group.</p>
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<p>Nootkatone derivative N2 binds to JAK2. (<b>A</b>) Molecular docking of N2 and JAK2 was conducted using AutoDock Vina 1.1.2. (<b>B</b>) CETSA was performed to assess the binding interactions between N2 and JAK2. (<b>C</b>) The stability of the JAK2 protein across varying temperatures was quantified using Western blotting analysis. (<b>D</b>) The DARTS experiments confirmed the binding of N2 to the JAK2 protein. (<b>E</b>) Densitometry analysis of JAK2. Data are presented as the mean ± SD. Each experiment was repeated in triplicate. <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. lysates group, *** <span class="html-italic">p</span> &lt; 0.001 vs. pronase alone group.</p>
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<p>Nootkatone derivative N2-mediated megakaryocytic differentiation in erythroleukemia cells is JAK2-dependent. (<b>A</b>) Morphological analysis was conducted using Wright–Giemsa staining on LV-NC and LV-sh-JAK2 HEL cells exposed to 8 μM N2. Magnification: ×400. Scale bar: 50 µm. (<b>B</b>) Flow cytometry was employed to assess the expression levels of CD41a and CD61 in LV-NC and LV-sh-JAK2 HEL cells treated with 8 μM N2. (<b>C</b>,<b>D</b>) Quantification of the percentage of CD41a<sup>+</sup> and CD61<sup>+</sup> cells. (<b>E</b>) The expression of p-JAK2, JAK2, p-PKCδ, PKCδ, p-STAT3, STAT3, p-MEK, and MEK in LV-NC and LV-sh-JAK2 HEL cells treated with 8 μM N2 were measured by Western blotting. (<b>F</b>) Densitometry analysis of these proteins. All data are presented as the mean ± SD. Each experiment was repeated in triplicate. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. LV-NC/DMSO group. <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. LV-NC/N2-8 µM group.</p>
Full article ">Figure 15
<p>Nootkatone derivative N2 accelerates megakaryocytic differentiation and suppresses erythroleukemia in vivo. (<b>A</b>) Spleen size of mice in different experimental groups. (<b>B</b>) Spleen weight presented as mean ± SD (<span class="html-italic">n</span> = 5). (<b>C</b>) Hematocrit values. (<b>D</b>) Platelet counts. (<b>E</b>) Flow cytometric analysis of CD41 and CD61 expression of spleen of each groups. (<b>F</b>,<b>G</b>) The histogram represents the percentage of CD41<sup>+</sup> and CD61<sup>+</sup> cells of spleen in each groups. (<b>H</b>) Representative H&amp;E stained images of spleen from each groups. The yellow arrow represents megakaryocytes. Magnification: ×400. Scale bar: 50 µm. Data represent the mean ± SD (<span class="html-italic">n</span> = 3). * <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 vs. model group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. normal group.</p>
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<p>Nootkatone derivative N2 activates JAK2/STAT3 and PKCδ/MAPK signaling pathways. (<b>A</b>) The expression of p-JAK2, JAK2, p-PKCδ, PKCδ, p-STAT3, STAT3, p-MEK, MEK, p-ERK, and ERK of spleen tissue from each groups were measured by Western blotting. (<b>B</b>) Densitometry analysis of these proteins. (<b>C</b>) The impact of N2 on the mRNA expression of nine transcription factors related to megakaryocytic differentiation in spleen tissue. Data are expressed as the mean ± SD (<span class="html-italic">n</span> = 3). * <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 vs. model group. <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>##</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>###</sup> <span class="html-italic">p</span> &lt; 0.001 vs. normal group.</p>
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<p>Illustration of the role and mechanism of nootkatone derivative N2 in promoting megakaryocytic differentiation in erythroleukemia. The red arrow indicates up-regulation.</p>
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18 pages, 1354 KiB  
Article
Antibacterial and Mosquito Repellent Potential of Eight Citrus Cultivars and Their Chemical Composition
by Mehwish Nawaz, Bait Ullah, Muhammad Ghazanfar Abbas, Muhammad Binyameen, Violeta Apšegaitė, Raimondas Mozūraitis and Muhammad Azeem
Horticulturae 2025, 11(1), 9; https://doi.org/10.3390/horticulturae11010009 - 26 Dec 2024
Abstract
Citrus fruit peels are a rich source of essential oils (EOs), which contain biologically active compounds; however, they are often discarded as waste, which causes pollution. The fresh peels of eight citrus cultivars growing in Pakistan were used to extract EOs through steam [...] Read more.
Citrus fruit peels are a rich source of essential oils (EOs), which contain biologically active compounds; however, they are often discarded as waste, which causes pollution. The fresh peels of eight citrus cultivars growing in Pakistan were used to extract EOs through steam distillation. Gas chromatography-mass spectrometry (GC-MS) analysis of fresh peel EOs revealed that limonene was the most abundant compound, constituting 94.5%, 96.1%, 95.3%, 93.3%, 56.2%, 91.5%, 96.4%, and 96.7% of Citrus jambhiri, C. aurantium, C. sinensis var. Malta cv. Blood Malta, C. sinensis var. Malta cv. Shakri Malta, C. limon, C. pseudolimon, C. reticulata var. Mandarin cv. Feutrell’s Early, and C. reticulata var. Mandarin cv. Kinnow, respectively. The dried peel EO of C. reticulata var. Mandarin cv. Kinnow contained 95.2% limonene. C. limon peel EO exhibited the highest antibacterial activity among all citrus peel EOs with the minimum inhibitory concentration of 312 μg/mL against Staphylococcus aureus. The C. aurantium and C. sinensis var. Malta cv. Shakri Malta peel EOs exhibited the highest mosquito repellent activity against Ae. aegypti females, providing protection for 45 min when tested at a concentration of 166 µg/cm2. This study showed C. aurantium and Shaki Malta peel EOs could be used to formulate natural mosquito repellent. Full article
(This article belongs to the Section Processed Horticultural Products)
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<p>The chemical structures of components constitute over 2% of essential oils of citrus peels.</p>
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<p>Repellent persistence of nine citrus EO samples and DEET tested at 33.3 μg/cm<sup>2</sup> against <span class="html-italic">Ae. aegypti</span> females. RL—<span class="html-italic">Citrus jambhiri</span>, SO—<span class="html-italic">Citrus aurantium</span>; BM—<span class="html-italic">Citrus sinensis</span> var. Malta, cv. Blood Malta; SM—<span class="html-italic">Citrus sinensis</span> var. Malta, cv. Shakri Malta; DL—<span class="html-italic">Citrus limon</span>; GA—<span class="html-italic">Citrus pseudolimon</span>; FE—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Feutrell’s early; KF—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Kinnow (from fresh peel); KD—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Kinnow (from dried peel). Bars having different letters depict significant differences (<span class="html-italic">p</span> &lt; 0.05) among the repellency of test substances after different periods independently (ANOVA post-hoc Bonferroni test). Error bars denote the standard error (n = 5).</p>
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<p>Repellent persistence of nine citrus EO samples and DEET tested at 166 μg/cm<sup>2</sup> against <span class="html-italic">Ae. aegypti</span> females. RL—<span class="html-italic">Citrus jambhiri</span>, SO—<span class="html-italic">Citrus aurantium</span>; BM—<span class="html-italic">Citrus sinensis</span> var. Malta, cv. Blood Malta; SM—<span class="html-italic">Citrus sinensis</span> var. Malta, cv. Shakri Malta; DL—<span class="html-italic">Citrus limon</span>; GA—<span class="html-italic">Citrus pseudolimon</span>; FE—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Feutrell’s early; KF—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Kinnow (from fresh peel); KD—<span class="html-italic">Citrus reticulata</span> var. Mandarin cv. Kinnow (from dried peel). Bars having different letters depict significant differences (<span class="html-italic">p</span> &lt; 0.05) among the repellency of test substances after different time periods independently (ANOVA post-hoc Bonferroni test). Error bars denote the standard error (n = 5).</p>
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16 pages, 401 KiB  
Review
Potato Processing Waste as a Reservoir of Bioactive Hydroxycinnamates: A Critical Review
by Dimitris P. Makris
Biomass 2025, 5(1), 2; https://doi.org/10.3390/biomass5010002 - 25 Dec 2024
Abstract
Natural resources are currently overexploited to provide food supply for the ever-increasing world population, and because of the intensification of agricultural and food production, there is a growing rate of waste generation. This waste biomass is usually dumped into landfills, causing unprecedented damage [...] Read more.
Natural resources are currently overexploited to provide food supply for the ever-increasing world population, and because of the intensification of agricultural and food production, there is a growing rate of waste generation. This waste biomass is usually dumped into landfills, causing unprecedented damage to ecosystems. Nowadays, circular economy strategies are channeled towards waste harnessing, aiming at reducing the irrational use of resources and minimizing waste generation. Potatoes are the second largest food crop after cereals, and there is an overwhelming amount of waste derived from potato tuber processing, composed almost exclusively of peels. Potato peels (PPs) are considered a source of polyphenolic compounds, largely represented by chlorogenic acid and other structurally related hydroxycinnamates, which possess a spectrum of bioactivities; however, there is a lack of analytical data compilations that could be of assistance in pertinent studies. With this as the conceptual basis, the scope of this review focused on a particular class of polyphenols, the so-called hydroxycinnamates, to deliver compiled data associated with the occurrence, retrieval, and application of this group of compounds derived from potato waste with major emphasis being given to PPs. It is believed that the collection of data of this nature, due to their undisputed significance in studies pertaining to bioeconomy, biorefinery, and food waste valorization, would provide a highly useful contribution to the field. Full article
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<p>Some major hydroxycinnamates that are frequently encountered in plant foods and their processing residues.</p>
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22 pages, 20237 KiB  
Article
Essential Oils from Citrus Peels Promote Calcium Overload-Induced Calcicoptosis in U251 Cells
by Yurong Li, Juanjuan Wei, Zimao Ye, Chen Ji, Wenji Li, Li Xu and Zhiqin Zhou
Antioxidants 2025, 14(1), 11; https://doi.org/10.3390/antiox14010011 - 25 Dec 2024
Abstract
Citrus peel essential oils (CPEOs) have demonstrated substantial medicinal potential for glioblastoma treatment because of their extensive antitumor effects, low potential for drug resistance, and ability to cross the human blood–brain barrier. In this study, the chemical compositions of five CPEOs were analyzed [...] Read more.
Citrus peel essential oils (CPEOs) have demonstrated substantial medicinal potential for glioblastoma treatment because of their extensive antitumor effects, low potential for drug resistance, and ability to cross the human blood–brain barrier. In this study, the chemical compositions of five CPEOs were analyzed via gas chromatography–mass spectrometry (GC-MS). CCK8 assays were used to evaluate the ability of five CPEOs to inhibit U251 human glioblastoma cells, and XLB and RA were selected for further investigation. Through wound healing assays and cell cycle and apoptosis analyses via flow cytometry, it was revealed that these CPEOs inhibited cell migration, arrested the cell cycle at G1/G0, and induced apoptosis with similar levels of inhibition. After CPEOs treatment, the intracellular Ca2+ content and reactive oxygen species levels in U251 cells increased significantly, whereas the mitochondrial membrane potential decreased. Additionally, the antioxidant enzyme system (SOD, POD, CAT, and GR) and the nonenzymatic defense system (GSH) were inhibited, leading to an increase in lipid peroxidation. qRT–PCR indicated the significant upregulation of intracellular calcium ion signaling pathways and the upregulation of mitochondrial apoptosis-related genes. Additionally, the activation of calcicoptosis-related indicators induced by the CPEOs could be reversed by inhibitor treatment, confirming that both of the selected CPEOs inhibit tumors by activating calcicoptosis-related pathways. These findings highlight the immense potential of CPEOs in healthcare and pharmaceutical applications by not only providing a scientific basis for the potential application of CPEOs in the treatment of glioblastoma but also offering new insights for the development of novel antitumor drugs. Full article
(This article belongs to the Section Natural and Synthetic Antioxidants)
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<p>The relative content and composition of five CPEOs. (<b>A</b>) Phenotype of five citrus fruits. (<b>B</b>) The colors of the five CPEOs. (<b>C</b>) The differences in the relative content and composition of five EOs components. FJ: FengJieQiCheng peel essential oil; JC26: JinCheng26 peel essential oil; STJ: ShaTangJu peel essential oil; XLB: XingLuBiXiYou peel essential oil; and RA: RongAnJinDan fruit peel essential oil.</p>
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<p>Effect of five CPEOs on the growth of U251 cells. (<b>A</b>–<b>E</b>) U251 cells were treated with various concentrations of FJ, JC26, STJ, XLB, and RA EOs for 24 h. (<b>F</b>) The control was treated with 0.5% DMSO. The data represent the mean ± SD. The green dashed line indicated a cell viability rate of 50%.</p>
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<p>Effect of the CPEOs on proliferation and migration in U251 cells. (<b>A</b>) XLB and RA EOs can inhibit cell proliferation. Proliferating cells and cell nuclei were stained with BeyoClick™ EdU-555 kit and Hoechst 33342. (<b>B</b>) The cell migration ability of U251 cells was determined using the wound healing assay, where the cells were treated with XLB and RA EOs in serum-free medium for 24 h. (<b>C</b>) Statistical data of migration rate (%). The concentrations of XLB40 and RA40 were 40 µg/mL, while those of XLB80 and RA80 were 80 µg/mL. CK was treated with 0.5% DMSO. The data represent the mean ± SD. Values followed by different superscripts (a,b) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of the CPEOs on the U251 cells cycle. (<b>A</b>–<b>E</b>) Determination of cell cycle distribution by flow cytometry. (<b>F</b>) The proportions of cell populations in G0/G1, S, and G2/M phases after treatment with XLB and RA EOs. The concentrations of XLB40 and RA40 were 40 µg/mL, while those of XLB80 and RA80 were 80 µg/mL. CK was treated with 0.5% DMSO. The data are presented as mean ± SD. Values followed by different superscripts (a–d) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of the CPEOs on U251 cell apoptosis. (<b>A</b>–<b>E</b>) Apoptotic cells were assessed by flow cytometry after Annexin V-FITC and PI staining. Q1 represents necrotic cells; Q2 represents late apoptotic cells; Q3 represents early apoptotic cells; Q4 represents viable cells. (<b>F</b>) Living cells, early and late apoptotic cell rates. The concentration of XLB40 and RA40 was 40 µg/mL, while that of XLB80 and RA80 was 80 µg/mL. CK was treated with 0.5% DMSO. The data are presented as the mean ± SD. Values followed by different superscripts (a–e) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of the CPEOs on Ca<sup>2+</sup> levels, ROS generation, and the MMP in U251 cells. (<b>A</b>) The cell nuclei and intracellular Ca<sup>2+</sup> in U251 cells after CPEOs treatment were stained with DAPI (blue) and Fluo-4 AM (green), respectively. (<b>B</b>) Average fluorescence intensity of Ca<sup>2+</sup> in different treatment groups. (<b>C</b>) Using DCFH-DA (green) to stain ROS in U251 cells treated with CPEOs. (<b>D</b>) Fluorescence images of U251 incubated with JC-1 after treatment with XLB and RA EOs. (<b>E</b>) MMP quantified by measuring green fluorescence intensity and red fluorescence intensity. XLB80 = 80 µg/mL, RA80 = 80 µg/mL, XLB80 + A23187, XLB80 + NIP, RA80 + A23187, and XLB80 + NIP represents pretreatment with 10 µM of A23187 and NIP for 1.5 h before adding XLB and RA EOs. The data are presented as mean ± SD. Values followed by different superscripts (a–e) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of the CPEOs on MDA (<b>A</b>); GSH levels (<b>B</b>); and GR (<b>C</b>), POD (<b>D</b>), SOD (<b>E</b>), and CAT (<b>F</b>) activities in U251 cells. XLB80 = 80 µg/mL, RA80 = 80 µg/mL, XLB80 + A23187, XLB80 + NIP, RA80 + A23187, and XLB80 + NIP represents pretreatment with 10 µM of A23187 and NIP for 1.5 h before adding XLB and RA EOs. The data are presented as mean ± SD. Values followed by different superscripts (a–f) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of the CPEOs on the expression of the <span class="html-italic">CHRNA7</span> (<b>A</b>), <span class="html-italic">MICU1</span> (<b>B</b>), <span class="html-italic">MICU2</span> (<b>C</b>), <span class="html-italic">BAX</span> (<b>D</b>), <span class="html-italic">Caspase-9</span> (<b>E</b>), <span class="html-italic">Caspase-7</span> (<b>F</b>), and <span class="html-italic">Caspase-3</span> (<b>G</b>) in U251 cells. XLB80 = 80 µg/mL, RA80 = 80 µg/mL, XLB80 + A23187, XLB80 + NIP, RA80 + A23187, and XLB80 + NIP represents pretreatment with 10 µM of A23187 and NIP for 1.5 h before adding XLB and RA EOs. The data are presented as mean ± SD. Values followed by different superscripts (a–g) are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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14 pages, 1483 KiB  
Article
Exploring the Pharmacokinetics and Gut Microbiota Modulation of Hesperidin and Nobiletin from Mandarin Orange Peel in Experimental Dogs: A Pilot Study
by Jun Nakahigashi, Makoto Kurikami, Satomi Iwai, Sadahiko Iwamoto, Shou Kobayashi and Eiji Kobayashi
Metabolites 2025, 15(1), 3; https://doi.org/10.3390/metabo15010003 - 25 Dec 2024
Abstract
Background/Objectives: Mandarin orange peel (MOP) is recognized for its traditional medicinal properties due to its high flavonoid content. This study aimed to analyze MOP harvested in Japan for specific bioactive compounds and to explore its health applications in dogs, including effects on gut [...] Read more.
Background/Objectives: Mandarin orange peel (MOP) is recognized for its traditional medicinal properties due to its high flavonoid content. This study aimed to analyze MOP harvested in Japan for specific bioactive compounds and to explore its health applications in dogs, including effects on gut microbiota and cognitive symptoms. Methods: Flavonoid content (particularly hesperidin and nobiletin) of MOP was measured. High-flavonoid MOP was then incorporated into gelatin cubes. In the time–course blood concentration study, experimental beagle dogs received a single oral dose (4 g). For intestinal microbiota analysis and blood biochemical tests, beagle dogs were administered 1 g twice daily. For the Demonstration Test, older dogs (a 14-year-old female Shiba Inu, a 14-year-old female Miniature Dachshund, and a 19-year-old male Miniature Dachshund) were administered 1 g twice daily. Analysis included microbiota profiling via 16S rDNA sequencing and observational assessment of cognitive indicators in a pilot study involving senior dogs with Alzheimer’s disease. Results: The MOP powder contained 9.3% hesperidin in early-ripening varieties (October harvest) and 6.9% in ripe varieties (December harvest). Nobiletin content was 41 mg/100 g (0.041%) and 35 mg/100 g (0.035%) for the early and late harvests, respectively. Administration of MOP-enriched gelatin cubes reduced Fusobacteriaceae and increased Eggerthellaceae. Cognitive symptoms like howling and counterclockwise turning showed improvement in senior dogs (n = 3). Conclusions: This study provides preliminary support for the potential health benefits of MOP in canine dietary applications, particularly for gut health and cognitive function. Improvement in cognitive symptoms may be due to the anxiolytic effects of mandarin peel. Full article
(This article belongs to the Special Issue Food Additives in Gut Microbiota and Metabolic Health)
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<p><b>α-Diversity analysis.</b> Changes in the chao1 index before (vehicle_pre) and two weeks after (vehicle_2w) administration of cubes without mandarin orange peel (<b>left</b>), and changes before (orange_pre) and two weeks after (orange_2w) administration of cubes containing mandarin orange peel (<b>right</b>).</p>
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<p><b>LEfSe Analysis.</b> Cladogram of individuals as subclass variables before and after administration of cubes without mandarin orange peel (vehicle_pre, 2w) (<b>A</b>), before and after administration of cubes containing mandarin orange peel (orange_pre, 2w) (<b>B</b>), and LDA histogram (<b>C</b>). The pairwise Wilcoxon test indicates which bacterial species showed significant increases before and after administration, marked in green or red. Additionally, pairwise plots show the relative abundance of <span class="html-italic">Eggerthellaceae</span> and <span class="html-italic">Fusobacteriaceae,</span> which significantly changed before and after administration of cubes containing mandarin orange peel (<b>D</b>). LEfSe, Linear Discriminant Analysis Effect Size.</p>
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<p><b>Demonstration test on senior dogs</b>. Three senior dogs exhibiting symptoms of Alzheimer’s disease (such as loss of appetite, fear, nighttime crying, and decreased activity) were administered gelatin cubes containing mandarin orange peel (MOP). All three dogs showed improvement in their symptoms.</p>
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19 pages, 8353 KiB  
Article
Comparison of Ignition Process and Thermodynamic Conditions of TC4 and TC17 Alloys Under High-Speed Rubbing Ignition
by Yajun Li, Jianjun Li, Zichong Zu, Congzhen Wang, Yuqi Zhang, Lei Shao and Jinfeng Huang
Materials 2025, 18(1), 16; https://doi.org/10.3390/ma18010016 - 24 Dec 2024
Abstract
This study investigates the combustion characteristics and critical thermodynamic conditions for the ignition of TC4 and TC17 alloys under high-speed friction conditions. The results indicate that, under identical rubbing conditions, both the critical pressure and the ignition temperature of the TC17 alloy are [...] Read more.
This study investigates the combustion characteristics and critical thermodynamic conditions for the ignition of TC4 and TC17 alloys under high-speed friction conditions. The results indicate that, under identical rubbing conditions, both the critical pressure and the ignition temperature of the TC17 alloy are higher than those of the TC4 alloy. The critical ignition conditions for both alloys increase with thickness, while they decrease with increasing rotational speed, oxygen concentration, and oxygen pressure. The primary characteristics in the initial stage of friction ignition are abrasive and adhesive wear. As the duration of friction increases, material from the friction surface begins to peel away, creating favorable conditions for ignition. At the moment of ignition, significant peeling occurs, along with visible cracks and molten structures, resulting in the production of a substantial amount of titanium oxide on the friction surface. Based on the ignition theory proposed by Frank-Kamenetskii, the reaction order, adsorption coefficient, pre-exponential factor, and activation energy of the ignition criterion under high-speed friction conditions were determined by fitting and analyzing the experimental results. The ignition temperatures of the TC4 and TC17 alloys at different speeds were predicted with a relative error of less than 2.06%. This demonstrates that the Frank-Kamenetskii model can be utilized to explain the critical ignition conditions of titanium alloys under high-speed rubbing conditions. Full article
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<p>3D representation and schematic diagram of equipment.</p>
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<p>The combustion process of TC4 alloy samples: (<b>a</b>–<b>c</b>) ignition stage; (<b>d</b>,<b>e</b>) intense combustion stage; (<b>f</b>) combustion extinction phase.</p>
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<p>The combustion process of TC17 alloy samples: (<b>a</b>–<b>c</b>) ignition stage; (<b>d</b>,<b>e</b>) intense combustion stage; (<b>f</b>) combustion extinction phase.</p>
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<p>In situ thermal imaging of TC4 alloy during rubbing ignition process: (<b>a</b>–<b>d</b>) thermal imaging; (<b>e</b>) ignition temperature curve.</p>
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<p>In situ thermal imaging of TC17 alloy during rubbing ignition process: (<b>a</b>–<b>d</b>) thermal imaging; (<b>e</b>) ignition temperature curve.</p>
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<p>The friction coefficient during rubbing ignition process: (<b>a</b>) friction coefficient curve; (<b>b</b>) average friction coefficient.</p>
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<p>Microstructure of TC4 alloy during rubbing ignition process: (<b>a</b>,<b>b</b>) 0.5 s; (<b>c</b>,<b>d</b>) 1.5 s; (<b>e</b>,<b>f</b>) 0.5 s; (<b>g</b>,<b>h</b>) ignition moment.</p>
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<p>Microstructure of TC17 alloy during rubbing ignition process: (<b>a</b>,<b>b</b>) 0.5 s; (<b>c</b>,<b>d</b>) 1.5 s; (<b>e</b>,<b>f</b>) 2.5 s; (<b>g</b>,<b>h</b>) ignition moment.</p>
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<p>XRD analysis during rubbing ignition process: (<b>a</b>) TC4; (<b>b</b>) TC17.</p>
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<p>The combustion threshold temperatures and pressures of TC4 and TC17 alloys under the following conditions: (<b>a</b>,<b>b</b>) thickness; (<b>c</b>,<b>d</b>) rotational speed; (<b>e</b>) oxygen pressure; (<b>f</b>) oxygen concentration.</p>
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<p>(<b>a</b>) the determination of adsorption coefficient (<b>b</b>) plots of T versus lnP.</p>
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<p>The experimental and computed values of ignition temperature at different rotational speeds of TC4 and TC17 alloys.</p>
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14 pages, 4915 KiB  
Article
Development and Evaluation of Steel Component Coatings for Substations/Converter Stations with Both Fire and Corrosion Prevention Functions
by Yu Liu, Baohui Chen, Chuanping Wu, Tiannian Zhou and Bichen Pan
Fire 2025, 8(1), 1; https://doi.org/10.3390/fire8010001 - 24 Dec 2024
Abstract
There are a large number of steel components in substations/converter stations whose performance is seriously affected by being exposed to environmental corrosion and fire, endangering the operation of the substation/converter station. The current protective measures for steel components in substations/converter stations primarily involve [...] Read more.
There are a large number of steel components in substations/converter stations whose performance is seriously affected by being exposed to environmental corrosion and fire, endangering the operation of the substation/converter station. The current protective measures for steel components in substations/converter stations primarily involve the application of anti-corrosion and fireproof coatings. However, these coatings can easily peel off, resulting in a significant loss of their protective effectiveness. In response to this challenge, a new type of silicone-modified epoxy resin substrate has been synthesized by chemically grafting silicone resin onto epoxy resin segments, which retains the high adhesion of epoxy resin while enhancing its weather resistance. The use of synthesized nano zinc oxide-modified graphene oxide as a fireproof filler significantly improves the physical barrier effect and corrosion resistance of the coating. Additionally, the innovative addition of new metal anti-corrosion active pigments improves the adhesion and impermeability of the coating. Therefore, a steel structure coating for substations/converter stations with both fire and corrosion prevention functions has been developed. Standard tests conducted by national institutions have shown that the coating meets the performance requirements. Full article
(This article belongs to the Special Issue Fire Detection and Public Safety, 2nd Edition)
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<p>Product status of different modification methods and appearance of cured coatings.</p>
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<p>Infrared spectra of polyamide-cured silicone-modified epoxy resin.</p>
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<p>Changes in surface water contact angle after modification (<b>a</b>) and before modification (<b>b</b>).</p>
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<p>Salt-water corrosion resistance of modified (<b>a</b>) and pre modified (<b>b</b>) coatings.</p>
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<p>Process diagram of modified graphene oxide.</p>
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<p>XRD patterns and Raman spectrum of GO, ZnO, and GO/ZnO.</p>
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<p>Excellent expansion performance of modified graphene oxide at high temperatures.</p>
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<p>Expansion process of intumescent fireproof coatings.</p>
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<p>Expansion height map after coating burning.</p>
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<p>Time–temperature curve of steel plate back.</p>
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<p>Surface morphology of coating before and after salt-water resistance test.</p>
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<p>Changes in coating after adding film-forming agents. (<b>a</b>) After adding dispersants. (<b>b</b>) After adding rheological agents.</p>
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<p>Schematic diagram of the coating fire test device.</p>
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18 pages, 841 KiB  
Article
Factors Affecting Growth and Survival of Salmonella in Onion Extracts and Onion Bulbs
by Emmanuel Kiplagat, Moazzameh Ramezani, Subas Malla, Luis Cisneros-Zevallos, Vijay Joshi and Alejandro Castillo
Foods 2025, 14(1), 1; https://doi.org/10.3390/foods14010001 - 24 Dec 2024
Abstract
This study investigated the survival and growth of Salmonella in onion extracts and bulbs. The inhibition or retardation of Salmonella growth by extracts of red, white, and yellow onions was tested against the onion germplasm and exposure to different light spectra during curing. [...] Read more.
This study investigated the survival and growth of Salmonella in onion extracts and bulbs. The inhibition or retardation of Salmonella growth by extracts of red, white, and yellow onions was tested against the onion germplasm and exposure to different light spectra during curing. Separately, survival of Salmonella Newport was tested on red, white, and yellow onion bulbs on the external and internal onion layers with a syringe and needle. Onions exposed to blue, red, and white LED light during curing produced extracts with variable antimicrobial effects (p < 0.05), with those exposed to blue light showing the strongest inhibitory effect on red and white onions only. In survival studies, Salmonella inoculated on the outer scale was reduced by 1.2, >2.7, and >2.4 logs on red, white, and yellow onions, respectively, within 3 days, whereas it grew by 2.4, 2.6, and 2.8 logs inside red, white, and yellow onion bulbs, respectively, over 18 days. In separate trials, the outer layer again did not support the survival of Salmonella Newport. The aw increased significantly from 0.51 to 0.58 in the outer scales and 0.96 to 0.98 for the fourth inner scales. Despite being rich in antimicrobial polyphenols, tissue integrity and water content may still promote Salmonella growth in onions. Full article
(This article belongs to the Section Food Quality and Safety)
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Figure 1
<p>Growth and inhibition of <span class="html-italic">Salmonella</span> in extracts of red (<b>A</b>), white (<b>B</b>), and yellow (<b>C</b>) onions made from bulbs exposed to natural light (diamonds) or artificial blue (circles), red (triangles), white (squares) light during curing.</p>
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<p>Growth of <span class="html-italic">Salmonella</span> Newport cocktail on the outer papery skin layers (triangles) and in the inner layers (circles) of red (<b>A</b>), white (<b>B</b>), and yellow (<b>C</b>) bulb onions stored in containers and held at room temperature (25 °C). The lines crossing the chart show the limit of detection of the counting method (−1.2 log CFU/cm<sup>2</sup>). Each data point represents the mean of at least 9 tested samples and the error bars represent standard error (SE). There were no differences in counts between onion varieties (<span class="html-italic">p</span> ≥ 0.05).</p>
Full article ">Figure 3
<p>Reduction of <span class="html-italic">Salmonella</span> Newport on outer (triangles) and inner (circles) layers of red (<b>A</b>), white (<b>B</b>), and yellow (<b>C</b>) onions during storage at room temperature. The dotted lines crossing the chart show the limit of detection of the counting method (1.1 log CFU/cm<sup>2</sup>) and the error bars represent standard error (SE). Each data point represents the mean of at least 9 tested samples.</p>
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23 pages, 5065 KiB  
Article
Application of DS-DFT to the Fine Spectral Estimation of High-Noise Signals
by Lin Qin, Suihu Dang, Di Fu and Yutao Feng
Electronics 2024, 13(24), 5057; https://doi.org/10.3390/electronics13245057 - 23 Dec 2024
Abstract
This paper presented an extended double-subsegment discrete Fourier transform (DS-DFT) algorithm as a tool for the fine spectral estimation of high-noise environments, which was previously effective in low-noise scenarios, and as such, its application to the analysis of noisy signals observed by a [...] Read more.
This paper presented an extended double-subsegment discrete Fourier transform (DS-DFT) algorithm as a tool for the fine spectral estimation of high-noise environments, which was previously effective in low-noise scenarios, and as such, its application to the analysis of noisy signals observed by a satellite-based interferometer was investigated. The observation of satellite-borne Doppler asymmetric spatial heterodyne spectroscopy (DASH) was first simulated to obtain the signals of low- and high-noise levels; then, a practical criterion to classify noise levels in the interferograms based on the DS-DFT results was introduced and validated by calculating the SNR. For high-noise signals, DS-DFT remains robust by employing phase differences and amplitude ratios for fine frequency estimation. Full article
(This article belongs to the Topic Hyperspectral Imaging and Signal Processing)
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Figure 1
<p>Simulated DASH interferogram (in Rayleighs) for FOV1 (left) and FOV2 (right) with the instrumental noises. The horizontal direction of each FOV is the <math display="inline"><semantics> <mrow> <mi>x</mi> </mrow> </semantics></math> direction along the satellite orbit. The wavelength of atmospheric airglow emission is 557.7 nm. The integration is along the satellite limb-viewing LOS and covers altitudes of 80–120 km. The CCD of each FOV has 512 pixels in the horizontal and a 2 km resolution in the vertical.</p>
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<p>The noise-free bilateral (left) and unilateral (right) DASH interferograms (top), their amplitude spectra (middle), and phase spectra (bottom) for the 557.7 nm airglow emission observed by FOV1 at 111.9 km. Upper left: The simulated bilateral interferogram (black) and the bias-removed, Haming-window-apodized interferogram (red). Upper right: The real (black) and imaginary (red) parts of the unilateral interferogram.</p>
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<p>Same as <a href="#electronics-13-05057-f002" class="html-fig">Figure 2</a>, but contains readout noise, quantization noise, and dark current.</p>
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<p>The amplitude (left) and phase difference <math display="inline"><semantics> <mrow> <mi mathvariant="sans-serif">δ</mi> <msub> <mrow> <mi mathvariant="sans-serif">Φ</mi> </mrow> <mrow> <mi>t</mi> <mi>o</mi> <mi>t</mi> </mrow> </msub> <mfenced separators="|"> <mrow> <mi>x</mi> <mo>,</mo> <msub> <mrow> <mi>κ</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> </mrow> </mfenced> </mrow> </semantics></math> (right) for the noise-free unilateral interferogram in <a href="#electronics-13-05057-f002" class="html-fig">Figure 2</a> (upper-right panel). The phase difference is shown in black and its linear fitting in red.</p>
Full article ">Figure 5
<p>Same as <a href="#electronics-13-05057-f004" class="html-fig">Figure 4</a>, but for the unilateral interferogram with the measurement noises (<a href="#electronics-13-05057-f003" class="html-fig">Figure 3</a>, upper-right panel).</p>
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<p>From right to left: (1) The phase, and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">Φ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> (black), <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">Φ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> <mo> </mo> </mrow> </semantics></math> (red), and their difference <math display="inline"><semantics> <mrow> <msub> <mrow> <mi mathvariant="sans-serif">Δ</mi> <mi mathvariant="sans-serif">Φ</mi> <mo>=</mo> <mi mathvariant="sans-serif">Φ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> <mo>−</mo> <msub> <mrow> <mi mathvariant="sans-serif">Φ</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> (blue) at the DS-DFT spectral amplitude peaks; the solid and dotted lines denote the DS-DFT phases and their linear fitting, respectively. (2) The peak amplitudes of the DS-DFT spectra <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> (black), <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> (red), and their ratios <math display="inline"><semantics> <mrow> <mrow> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> <mo>/</mo> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </mrow> </mrow> </semantics></math> (blue), where <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> <mo> </mo> </mrow> </semantics></math>and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> are equal. (3) The frequency offsets <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>ε</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> (black) and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>ϵ</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> (red) and coefficients <math display="inline"><semantics> <mrow> <mrow> <mrow> <mi>a</mi> </mrow> <mo>/</mo> <mrow> <mn>2</mn> <mi>π</mi> </mrow> </mrow> </mrow> </semantics></math> (blue) and <math display="inline"><semantics> <mrow> <mrow> <mrow> <mfenced separators="|"> <mrow> <mrow> <mrow> <mi>b</mi> </mrow> <mo>/</mo> <mrow> <mi>a</mi> </mrow> </mrow> </mrow> </mfenced> </mrow> <mo>/</mo> <mrow> <mn>2</mn> <mi>π</mi> </mrow> </mrow> </mrow> </semantics></math> (green). (4) The Fizeau fringe frequencies <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>0</mn> </mrow> </msub> </mrow> </semantics></math> (blue), estimated from the entire sampling sequence, <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> (black), and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math> (red) from the DS-DFT, as well as the fine estimation <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mi>e</mi> <mi>s</mi> </mrow> </msub> </mrow> </semantics></math> (green) from both <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>, where <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> <mo> </mo> </mrow> </semantics></math>is the same as <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>. The spectra are derived from the DASH interferograms of the 557 nm airglow emission observed by FOV1 without instrumental measurement noise.</p>
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<p>Same as <a href="#electronics-13-05057-f006" class="html-fig">Figure 6</a>, but the DASH interferograms include the measurement noises (the left panel of <a href="#electronics-13-05057-f001" class="html-fig">Figure 1</a>).</p>
Full article ">Figure 8
<p>SNRs (in db) of each pixel bin (left) and the CCD-column-averaged SNR (in db) of each row (right) calculated from the simulated interferogram of 557 nm airglow emission observed by FOV1 (the left panel of <a href="#electronics-13-05057-f001" class="html-fig">Figure 1</a>). The high- (<math display="inline"><semantics> <mrow> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> <mo>≠</mo> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> </mrow> </semantics></math>), moderate- (<math display="inline"><semantics> <mrow> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> <mo>=</mo> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> </mrow> </semantics></math>, but <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> <mo>≠</mo> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>), and low- (<math display="inline"><semantics> <mrow> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>1</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> <mo>=</mo> <msubsup> <mrow> <mi>k</mi> </mrow> <mrow> <mn>2</mn> </mrow> <mrow> <mo>*</mo> </mrow> </msubsup> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>1</mn> </mrow> </msub> <mo>=</mo> <msub> <mrow> <mi>A</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msub> </mrow> </semantics></math>) noise levels determined by the DS-DFT criterion are indicated by the pink diamond, pink square, and green circle, respectively.</p>
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<p>The average signal-to-noise ratio (averaged by column of CCD) at each height (row of CCD) in the presence of random noises with magnitudes at 10% (left), 20% (middle), and 30% (right) of the simulated emission intensity.</p>
Full article ">Figure A1
<p>Flowchart of the SHS forward model and inversion algorithm.</p>
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18 pages, 1136 KiB  
Article
Economic and Environmental Impact Analysis of Innovative Peeling Methods in the Tomato Processing Industry
by Elham Eslami, Giovanni Landi, Miriam Benedetti and Gianpiero Pataro
Sustainability 2024, 16(24), 11272; https://doi.org/10.3390/su162411272 - 23 Dec 2024
Abstract
Peeling is a key step in the industrial production of canned peeled tomatoes, vital for optimizing efficiency, yield, product quality, waste reduction, and environmental impact. This study presents a comparative assessment of the economic and environmental impacts of adopting innovative peeling technologies, including [...] Read more.
Peeling is a key step in the industrial production of canned peeled tomatoes, vital for optimizing efficiency, yield, product quality, waste reduction, and environmental impact. This study presents a comparative assessment of the economic and environmental impacts of adopting innovative peeling technologies, including infrared (IR), ohmic heating-assisted lye (OH-lye), and ultrasound-assisted lye (US-lye) peeling, relative to conventional steam and lye peeling methods. Focusing on a medium-sized Italian tomato processor, the impacts of these methods on productivity, water and energy consumption, wastewater generation, and environmental footprint using Life Cycle Assessment (LCA) methodology, were evaluated. Findings indicated that adopting IR, OH-lye, and US-lye methods enhanced peelability (ease of peeling > 4.5) and increased production capacity by 2.6–9.2%, while reducing solid waste by 16–52% compared to conventional steam and lye methods. LCA results showed IR as the most environmentally favorable method, followed by steam, OH-lye, and US-lye, with conventional lye peeling being the least sustainable. OH-lye and IR methods also significantly reduce water and energy use, while US-lye shows higher demands in these areas. Additionally, OH-lye and IR methods require little or no NaOH, minimizing chemical consumption and wastewater production, which offers notable environmental and cost advantages. Overall, this preliminary study underscores economic and environmental potential for novel peeling technologies, encouraging industry consideration for adoption. Full article
(This article belongs to the Section Resources and Sustainable Utilization)
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<p>Current value stream map for a plant processing whole peeled tomatoes with a production capacity of 60,000 tons per season.</p>
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<p>The total wastewater generated by the tomato processing company, with an annual capacity of 60,000 tons, across the washing, sorting, and peeling stages, utilizing both conventional and innovative methods in the peeling phase.</p>
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<p>Environmental midpoint indicator impacts on the production of peeled tomatoes by different peeling methods. (<b>a</b>) Global warming potential (GWP100a), (<b>b</b>) ozone layer depletion (ODP), (<b>c</b>) human toxicity (HT), (<b>d</b>) abiotic depletion (fossil fuels) (AD), (<b>e</b>) acidification potential (AP), and (<b>f</b>) eutrophication potential (EP).</p>
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15 pages, 2977 KiB  
Article
Jeju Citrus (Citrus unshiu) Leaf Extract and Hesperidin Inhibit Small Intestinal α-Glucosidase Activities In Vitro and Postprandial Hyperglycemia in Animal Model
by Gi-Jung Kim, Yelim Jang, Kyoung-Tae Kwon, Jae-Won Kim, Seong-IL Kang, Hee-Chul Ko, Jung-Yun Lee, Emmanouil Apostolidis and Young-In Kwon
Int. J. Mol. Sci. 2024, 25(24), 13721; https://doi.org/10.3390/ijms252413721 - 23 Dec 2024
Abstract
Citrus fruits are widely distributed in East Asia, and tea made from citrus peels has demonstrated health benefits, such as a reduction in fever, inflammation, and high blood pressure. However, citrus leaves have not been evaluated extensively for their possible health benefits. In [...] Read more.
Citrus fruits are widely distributed in East Asia, and tea made from citrus peels has demonstrated health benefits, such as a reduction in fever, inflammation, and high blood pressure. However, citrus leaves have not been evaluated extensively for their possible health benefits. In this study, the α-glucosidase-inhibitory activity of Jeju citrus hot-water (CW) and ethyl alcohol (CE) extracts, along with hesperidin (HP) (a bioactive compound in citrus leaf extracts), was investigated, and furthermore, their effect on postprandial blood glucose reduction in an animal model was determined. The hesperidin contents of CW and CE were 15.80 ± 0.18 and 39.17 ± 0.07 mg/g-extract, respectively. Hesperidin inhibited α-glucosidase (IC50, 4.39), sucrase (0.50), and CE (2.62) and demonstrated higher α-glucosidase inhibitory activity when compared to CW (4.99 mg/mL). When using an SD rat model, during sucrose and starch loading tests with CE (p < 0.01) and HP (p < 0.01), a significant postprandial blood glucose reduction effect was observed when compared to the control. The maximum blood glucose levels (Cmax) of the CE administration group decreased by about 15% (from 229.3 ± 14.5 to 194.0 ± 7.4, p < 0.01) and 11% (from 225.1 ± 13.8 to 201.1 ± 7.2 hr·mg/dL, p < 0.05) in the sucrose and starch loading tests, respectively. Our findings suggest that citrus leaf extracts standardized to hesperidin may reduce postprandial blood glucose levels through the observed inhibitory effect against sucrase, which results in delayed carbohydrate absorption. Our findings provide a biochemical rationale for further evaluating the benefits of citrus leaves. Full article
(This article belongs to the Special Issue Bioactive Phenolics and Polyphenols 2024)
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<p>Chemical structure of hesperidin.</p>
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<p>HPLC profiles of citrus leaf extracts (standard solution (<b>a</b>), hot-water extract (<b>b</b>), and ethyl alcohol extract (<b>c</b>)). 1. Rutin; 2. Neoeriocitrin; 3. Narirutin; 4. Rhoifolin; 5. Naringin; 6. Hesperidin; 7. Neohesperidin; 8. Neoponcirin; 9. Poncirin; 10. Naringenin; 11. Hesperetin; 12. Isosinensetin; 13. Sinensetin; 14. 4,5,7-Trimethoxy flavon; 15. Nobiletin; 16. 4,5,6,7-Tetramethoxy flavon; 17. Tangeretin; 18. 5-Demethyl nobiletin; and 19. Gardenin B.</p>
Full article ">Figure 2 Cont.
<p>HPLC profiles of citrus leaf extracts (standard solution (<b>a</b>), hot-water extract (<b>b</b>), and ethyl alcohol extract (<b>c</b>)). 1. Rutin; 2. Neoeriocitrin; 3. Narirutin; 4. Rhoifolin; 5. Naringin; 6. Hesperidin; 7. Neohesperidin; 8. Neoponcirin; 9. Poncirin; 10. Naringenin; 11. Hesperetin; 12. Isosinensetin; 13. Sinensetin; 14. 4,5,7-Trimethoxy flavon; 15. Nobiletin; 16. 4,5,6,7-Tetramethoxy flavon; 17. Tangeretin; 18. 5-Demethyl nobiletin; and 19. Gardenin B.</p>
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<p>Dose-dependent changes in SD rat small intestinal α-glucosidase-inhibitory activity (% inhibition) of GO2KA1 (GO), Jeju citrus leaf hot-water extract (CW), Jeju citrus leaf ethyl alcohol extract (CE), and hesperidin (HP). Different corresponding letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05 by Duncan’s test. <sup>a–d</sup> First letter indicates differences among different samples, and <sup>A–C</sup> second one indicates differences among different concentrations of same samples.</p>
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<p>Dose-dependent changes in SD rat small intestinal sucrase-inhibitory activity (% inhibition) of GO2KA1 (GO), Jeju citrus leaf hot-water extract (CW), Jeju citrus leaf ethyl alcohol extract (CE), and hesperidin (HP). Different corresponding letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05 by Duncan’s test. <sup>a–c</sup> First letter indicates differences among different samples, and <sup>A–C</sup> second one indicates differences among different concentrations of same samples.</p>
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<p>Dose-dependent changes in SD rat small intestinal maltase-inhibitory activity (% inhibition) of GO2KA1 (GO), Jeju citrus leaf hot-water extract (CW), Jeju citrus leaf ethyl alcohol extract (CE), and hesperidin (HP). Different corresponding letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05 by Duncan’s test. <sup>a–c</sup> First letter indicates differences among different samples, and <sup>A–D</sup> second one indicates differences among different concentrations of same samples.</p>
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<p>Dose-dependent changes in SD rat small intestinal glucoamylase-inhibitory activity (% inhibition) of GO2KA1 (GO), Jeju citrus leaf hot-water extract (CW), Jeju citrus leaf ethyl alcohol extract (CE), and hesperidin (HP). Different corresponding letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05 by Duncan’s test. <sup>a–c</sup> First letter indicates differences among different samples, and <sup>A–D</sup> second one indicates differences among different concentrations of same samples.</p>
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<p>Dose-dependent anti-hyperglycemic effect of ethyl alcohol extracts of citrus leaves (CE) in sucrose loading test. After fasting for 24 h, 5-week-old male SD rats were orally administered sucrose solution (2.0 g/kg-body weight (b.w.)) with or without samples (CE 0.1 g/kg-b.w., CE 0.5 g/kg-b.w., and positive control: GO2KA1 0.5 g/kg-b.w.). Each point represents mean ± standard deviation (<span class="html-italic">n</span> = 10). ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 compared to different samples at the same concentration by unpaired Student’s <span class="html-italic">t</span>-test.</p>
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<p>The dose-dependent anti-hyperglycemic effect of hesperidin (HP) on sucrose loading test results. After fasting for 24 h, 5-week-old male SD rats were orally administered a sucrose solution (2.0 g/kg-body weight (b.w.)) with or without the test samples (HP 0.1 g/kg-b.w. and HP 0.5 g/kg-b.w.). Each point represents mean ± standard deviation (<span class="html-italic">n</span> = 10). <span class="html-italic">*** p</span> &lt; 0.001 compared to different samples at the same concentration by unpaired Student’s <span class="html-italic">t</span>-test.</p>
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<p>The dose-dependent anti-hyperglycemic effect of ethyl alcohol extracts of citrus leaves (CE) on starch loading test results. After fasting for 24 h, 5-week-old male SD rats were orally administered a starch solution (2.0 g/kg-body weight (b.w.)) with or without samples (CE 0.1 g/kg-b.w., CE 0.5 g/kg-b.w., and positive control: GO2KA1 0.5 g/kg-b.w.). Each point represents mean ± standard deviation (<span class="html-italic">n</span> = 10). <span class="html-italic">* p</span> &lt; 0.05 and <span class="html-italic">*** p</span> &lt; 0.001 compared to different samples at the same concentration by unpaired Student’s <span class="html-italic">t</span>-test.</p>
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<p>The dose-dependent anti-hyperglycemic effect of hesperidin (HP) on starch loading test results. After fasting for 24 h, 5-week-old male SD rats were orally administered a starch solution (2.0 g/kg-body weight (b.w.)) with or without samples (HP 0.1 g/kg-b.w. and HP 0.5 g/kg-b.w.). Each point represents mean ± standard deviation (<span class="html-italic">n</span> = 10). <span class="html-italic">*** p</span> &lt; 0.001 compared to different samples at the same concentration by unpaired Student’s <span class="html-italic">t</span>-test.</p>
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14 pages, 5045 KiB  
Article
Comparative Transcriptome Analysis of Eggplant (Solanum melongena L.) Peels with Different Glossiness
by Hong Wang, Zhixing Nie, Tonglin Wang, Shuhuan Yang and Jirong Zheng
Agronomy 2024, 14(12), 3063; https://doi.org/10.3390/agronomy14123063 - 22 Dec 2024
Viewed by 194
Abstract
Peel glossiness is an important commercial trait of eggplant (Solanum melongena L.). In this study, two eggplant-inbred lines with different levels of peel glossiness were used to identify genes related to peel glossiness. Paraffin section analysis showed that increased wax thickness and [...] Read more.
Peel glossiness is an important commercial trait of eggplant (Solanum melongena L.). In this study, two eggplant-inbred lines with different levels of peel glossiness were used to identify genes related to peel glossiness. Paraffin section analysis showed that increased wax thickness and wrinkles on the wax surface of eggplant peels decreased glossiness. Differential gene expression related to eggplant peel glossiness was analyzed by comparing the transcriptomes of eggplant peels with different gloss levels and at different developmental stages. The results identified 996 differentially expressed genes (DEGs), including 502 upregulated and 494 downregulated genes, possibly related to eggplant peel glossiness. GO enrichment and KEGG enrichment analyses revealed that the DNA replication pathway (GO:0003688, GO:0006270) and the photosynthesis pathway (map00195) were downregulated and thus may be associated with reduced eggplant peel glossiness. Expression level analysis of eggplant peels with different glossiness levels revealed that a C2H2 transcription factor gene, two ERF transcription factor genes, one long-chain acyl-CoA synthetase gene, and four wax- or cutin-related genes may be associated with the glossiness of eggplant fruit peels. These findings will help guide future genetic improvements in eggplant peel glossiness. Full article
(This article belongs to the Special Issue Advances in Crop Molecular Breeding and Genetics)
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Figure 1
<p>Morphological characteristics related to fruit peel glossiness in the inbred eggplant lines A21 and A32. Fruits of A21 7 d (<b>a</b>) and 21 d (<b>b</b>) and A32 7 d (<b>c</b>) and 21 d (<b>d</b>) after flowing. Paraffin sections of the fruit epidermis of A21 7 d (<b>e</b>) and 21 d (<b>f</b>) and A32 7 d (<b>g</b>) and 21 d (<b>h</b>) after flowing.</p>
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<p>Gene expression in eggplant peels from inbred lines A21 and A32. (<b>a</b>) Principal component analysis (PCA) of expressed genes in eggplant inbred lines A21 and A32. (<b>b</b>) Histogram of the differentially expressed genes (DEGs) in inbred eggplant lines A21 and A32. (<b>c</b>) Volcano plots of the DEGs in inbred eggplant lines A21 and A32. (<b>d</b>) Clustering heatmap of the DEGs in inbred eggplant lines A21 and A32. The horizontal coordinate represents the names of the samples and their clustering results, while the vertical coordinate indicates the differential genes and the clustering results of these genes. The different colors on the right represent different subclusters.</p>
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<p>Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis results for the differentially expressed genes in eggplant peel from inbred line A32. (<b>a</b>) GO enrichment analysis results. (<b>b</b>) Scatterplot of KEGG pathway enrichment analysis results.</p>
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<p>Expression levels for 12 candidate genes related to eggplant peel glossiness in three inbred lines with high glossiness and three inbreds without glossiness on their fruit peel by qRT-PCR. The data of columns are the mean + standard deviation. The bars mean standard deviation.</p>
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19 pages, 1965 KiB  
Article
Purple Yampee Derivatives and Byproduct Characterization for Food Applications
by Sandra V. Medina-López, Cristian Molina García, Maria Cristina Lizarazo-Aparicio, Maria Soledad Hernández-Gómez and Juan Pablo Fernández-Trujillo
Foods 2024, 13(24), 4148; https://doi.org/10.3390/foods13244148 - 21 Dec 2024
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Abstract
This study assessed the technological potential and bioactive compounds present in purple yampee (Dioscorea trifida L.f.) lyophilized powder, peeled and whole flour, as well as the tuber peel, starch residual fiber, and wastewater mucilage. Although most values approached neutrality, flour showed a [...] Read more.
This study assessed the technological potential and bioactive compounds present in purple yampee (Dioscorea trifida L.f.) lyophilized powder, peeled and whole flour, as well as the tuber peel, starch residual fiber, and wastewater mucilage. Although most values approached neutrality, flour showed a lower pH and high density, while greater acidity was observed in the mucilage. Color differed statistically and perceptibly between all samples, with similar values of °hue to purple flours from other sources, and the maximum chroma was found in lyophilized pulp and lightness in fiber. Average moisture levels around 7.2% and water activity levels of 0.303 (0.194 for whole flour) in fractions suggested favorable storability, while the interaction of the powders with water was similar to other root and tuber powdered derivatives. Yampee periderm had the highest swelling power, oil absorption capacity, water holding capacity, and absorption index and capacity. Mucilage had a higher solubility index and outstanding emulsion activity, greater than 90%. Twelve anthocyanins, with new reports of petunidin derivatives for the species, and more than 30 phytochemicals were identified through advanced liquid chromatography techniques. The greatest amounts of pinitol and myo-inositol were found in the mucilage, and sucrose, glucose, and fructose prevailed in the other powders. Successfully characterized yampee fractions showed high potential as functional food ingredients. Full article
(This article belongs to the Section Food Security and Sustainability)
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Graphical abstract

Graphical abstract
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<p>Photos of powdered fractions and simulated colors of (<b>a</b>) YSF, (<b>b</b>) YSM, (<b>c</b>) LYP, (<b>d</b>) YPF, (<b>e</b>) WTP, and (<b>f</b>) YPP.</p>
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<p>Amino acids in <span class="html-italic">D. trifida</span> mucilage (<b>upper</b> chromatogram) and lyophilized pulp (<b>under</b>) observed through HPLC-FLD.</p>
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<p>Amino acids in <span class="html-italic">D. trifida</span> mucilage (<b>upper</b> chromatogram) and lyophilized pulp (<b>under</b>) observed through HPLC-FLD.</p>
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<p>Main anthocyanin compounds identified at 520 nm through HPLC-DAD in <span class="html-italic">D. trifida</span> fractions after 20 days from their manufacture.</p>
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<p>Main anthocyanins quantified in <span class="html-italic">D. trifida</span> fractions mucilage YSM, lyophilized pulp LYP, starch fiber, flour, periderm, and whole flour from left to right, after 20-day storage. Main peonidin derivatives are depicted as follows: Peonidin 3-<span class="html-italic">O</span>-glucoside-5-<span class="html-italic">O</span>glucoside (Peonidin 1), Peonidin 3-O-feruloylglucoside-5-O-glucoside (Peonidin 2), and Peonidin 3-O-<span class="html-italic">p</span>-cumaroylglucoside-5-O-glucoside (Peonidin 3). The average concentration of the molecules (<span class="html-italic">n</span> = 3) is presented in milligrams per 100 g of sample, letters correspond to significant statistical differences among fractions (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The evolution of sugars in time (day 43 -darker color- and 180 of storage) for each fraction depicted by individually quantified sugars (<b>a</b>) Myo-inositol, (<b>b</b>) Pinitol, (<b>c</b>) Glucose, (<b>d</b>) Fructose, (<b>e</b>) Sucrose. Concentrations of each measure are depicted as mean values with standard deviation error bars (<span class="html-italic">n</span> = 3). Means in a column followed by different lowercase letters (a–f) are significantly different at the 5% level at the initial time of measure. Means in the columns followed by different capital letters (A–E) are significantly different at the 5% level.</p>
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