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Search Results (692)

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Keywords = Lactiplantibacillus plantarum

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17 pages, 2849 KiB  
Article
Orally Administered Lactobacilli Strains Modulate Alveolar Macrophages and Improve Protection Against Respiratory Superinfection
by Leonardo Albarracin, Stefania Dentice Maidana, Kohtaro Fukuyama, Mariano Elean, Julio Nicolás Argañaraz Aybar, Yoshihito Suda, Keita Nishiyama, Haruki Kitazawa and Julio Villena
Biomolecules 2024, 14(12), 1600; https://doi.org/10.3390/biom14121600 - 14 Dec 2024
Viewed by 353
Abstract
Orally administered immunomodulatory lactobacilli can stimulate respiratory immunity and enhance the resistance to primary infections with bacterial and viral pathogens. However, the potential beneficial effects of immunomodulatory lactobacilli against respiratory superinfection have not been evaluated. In this work, we showed that the feeding [...] Read more.
Orally administered immunomodulatory lactobacilli can stimulate respiratory immunity and enhance the resistance to primary infections with bacterial and viral pathogens. However, the potential beneficial effects of immunomodulatory lactobacilli against respiratory superinfection have not been evaluated. In this work, we showed that the feeding of infant mice with Lacticaseibacillus rhamnosus CRL1505 or Lactiplantibacillus plantarum MPL16 strains can reduce susceptibility to the secondary pneumococcal infection produced after the activation of TLR3 in the respiratory tract or after infection with RVS. The treatment of mice with CRL1505 or MPL16 strains by the oral route improved the production of interferons in the respiratory tract, differentially modulated the balance of pro- and anti-inflammatory cytokines, reduced bacterial replication, and diminished lung damage. Additionally, we demonstrated that orally administered lactobacilli confer longstanding protection against secondary Streptococcus pneumoniae infection and that this effect would be mediated by the stimulation of trained alveolar macrophages. This work contributes to revealing the mechanisms involved in the modulation of the gut–lung axis by beneficial microbes by demonstrating that specific lactobacilli strains, through the stimulation of the common mucosal immune system, would be able to support the development of trained alveolar macrophages that would confer longstanding protection against secondary bacterial challenges produced after a primary inflammatory event in the respiratory mucosa. Full article
(This article belongs to the Section Natural and Bio-derived Molecules)
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Figure 1

Figure 1
<p>Effect of <span class="html-italic">Lacticaseibacillus rhamnosus</span> CRL1505 and <span class="html-italic">Lactiplantibacillus plantarum</span> CRL1506 on respiratory superinfection. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505 or <span class="html-italic">L. plantarum</span> CRL1506 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 (<b>A</b>) or challenged with respiratory syncytial virus (RSV) on day 7 (<b>B</b>) via the nasal route. Five days later, mice were nasally infected with <span class="html-italic">Streptococcus pneumoniae</span>. The pneumococcal cell counts in lung and blood, the concentration of BAL albumin, and the activity of BAL LDH were determined 2 days after <span class="html-italic">S. pneumoniae</span> infection. The results are shown as mean ± SD. Significant differences are shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*) or <span class="html-italic">p</span> &lt; 0.01 (**).</p>
Full article ">Figure 2
<p>Effect of lactobacilli on respiratory superinfection. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505, IBL027, CRL489, <span class="html-italic">L. plantarum</span> CRL1506, or MPL16 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 via the nasal route. Five days later, mice were nasally infected with <span class="html-italic">Streptococcus pneumoniae</span>. The pneumococcal cell counts in lung and blood, the concentration of BAL albumin, the activity of BAL LDH (<b>A</b>), and the concentrations of BAL IFN-β, IFN-γ, and IL-10 (<b>B</b>) were determined 2 days after <span class="html-italic">S. pneumoniae</span> infection. The results are shown as mean ± SD. Significant differences are shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*) or <span class="html-italic">p</span> &lt; 0.01 (**).</p>
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<p>Effect of lactobacilli on AMphs cytokine production. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505, IBL027, CRL489, <span class="html-italic">L. plantarum</span> CRL1506, or MPL16 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 via the nasal route. Five days later, AMphs were isolated from BAL samples, cultured, and in vitro challenged with <span class="html-italic">Streptococcus pneumoniae</span>. The concentrations of IFN-β, IFN-γ, IL-6, IL-10, IL-12, and IL-27 were evaluated on AMph supernatants after 24 h. (<b>A</b>) Cytokine production of AMphs from <span class="html-italic">L. rhamnosus</span> CRL1505 and <span class="html-italic">L. plantarum</span> MPL16. The results are shown as mean ± SD. Significant differences were shown compared to the respective basal levels without pneumococcal challenge at <span class="html-italic">p</span> &lt; 0.05 (†). Significant differences were shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*). (<b>B</b>) Heatmap shows the variations in the concentration of cytokines of all experimental groups in relation to the control.</p>
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<p>Effect of lactobacilli on AMphs MHC-II expression. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505, IBL027, CRL489, <span class="html-italic">L. plantarum</span> CRL1506, or MPL16 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 via the nasal route. Five days later, mice were nasally infected with <span class="html-italic">Streptococcus pneumoniae</span>. The numbers of CD45<sup>+</sup>CD11c<sup>+</sup>SiglecF<sup>+</sup> and CD11c<sup>+</sup>SiglecF<sup>+</sup>MHC-II<sup>+</sup> cells in BAL were determined on the last day of lactobacilli treatment (basal) and 2 days after poly(I:C) stimulation and <span class="html-italic">S. pneumoniae</span> infection. The results are shown as mean ± SD. Significant differences are shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*).</p>
Full article ">Figure 5
<p>Effect of lactobacilli on respiratory superinfection. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505, IBL027, CRL489, <span class="html-italic">L. plantarum</span> CRL1506, or MPL16 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 via the nasal route. For the evaluation of long-term protection, 5, 10, 15, or 20 days after the last administration of poly(I:C), mice were nasally infected with <span class="html-italic">Streptococcus pneumoniae</span>. The pneumococcal cell counts in lung and blood, the concentration of BAL albumin, the activity of BAL LDH (<b>A</b>), and the concentrations of BAL IFN-β, IFN-γ and IL-10 (<b>B</b>) were determined 2 days after <span class="html-italic">S. pneumoniae</span> infection. The results are shown as mean ± SD. Significant differences are shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*) or <span class="html-italic">p</span> &lt; 0.01 (**). (<b>C</b>) Heatmap shows the variations in the parameters evaluated for all experimental groups in relation to the controls.</p>
Full article ">Figure 6
<p>Effect of lactobacilli on respiratory superinfection. Infant mice were fed <span class="html-italic">L. rhamnosus</span> CRL1505, IBL027, CRL489, <span class="html-italic">L. plantarum</span> CRL1506, or MPL16 for 5 days and stimulated with poly(I:C) on days 7, 8, and 9 via the nasal route. Twenty days after the last administration of poly(I:C), mice were nasally infected with <span class="html-italic">Streptococcus pneumoniae</span>. (<b>A</b>) The number of macrophages and neutrophils and the concentrations of TNF-α and CCL2 in BAL samples were determined 3, 6, 12, 24, 32, 48, and 54 h after <span class="html-italic">S. pneumoniae</span> infection. The results are shown as mean ± SD. Significant differences are shown compared to the control group at <span class="html-italic">p</span> &lt; 0.05 (*) (<b>B</b>) Heatmap shows the variations in the parameters evaluated at hours 24 and 48 of all experimental groups in relation to the control.</p>
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11 pages, 1208 KiB  
Article
Development of High-Glucosinolate-Retaining Lactic-Acid-Bacteria-Co-Fermented Cabbage Products
by Chen-Che Hsieh, Yuan-Heng Liu, Shin-Ping Lin, Shella Permatasari Santoso, Kaemwich Jantama, Tsung-Yu Tsai, Chang-Wei Hsieh and Kuan-Chen Cheng
Fermentation 2024, 10(12), 635; https://doi.org/10.3390/fermentation10120635 - 12 Dec 2024
Viewed by 302
Abstract
Cabbage (Brassica oleracea var. capitata) is rich in dietary fiber, vitamins, trace elements, and functional components like glucosinolates, which are essential for promoting health. This study aims to enhance the health benefits and nutritional content of cabbage through lactic acid fermentation [...] Read more.
Cabbage (Brassica oleracea var. capitata) is rich in dietary fiber, vitamins, trace elements, and functional components like glucosinolates, which are essential for promoting health. This study aims to enhance the health benefits and nutritional content of cabbage through lactic acid fermentation using a bioreactor, with a particular focus on glucosinolate retention. The fermentation utilized a consortium of Lactiplantibacillus plantarum, known for its robust acidifying capabilities, and antioxidant-rich strains Lactobacillus acidophilus and Bifidobacterium longum. A 5 L bioreactor facilitated the controlled fermentation process (35 °C, 24 h of fermentation at 5 rpm). The efficacy of glucosinolate retention was quantitatively assessed alongside the analysis of antioxidant properties via 1,1-diphenyl-2-picrylhydrazil (DPPH) and 2,2′-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assays. The results indicated a notable enhancement in antioxidant capacity with a 16.32% increase in the DPPH radical scavenging rate compared to non-fermented cabbage. Glucosinolate retention was impressively sustained at 82.02% in bioreactor conditions. Storage stability tests conducted at 4 °C revealed minimal degradation of glucosinolates, maintaining significant levels up to 14 days (from 90.34% to 66.49%). This study underscores the potential of bioreactor-facilitated lactic acid fermentation in preserving and enhancing the nutritional and functional qualities of cabbage, thereby extending its market value and promoting sustainable agricultural practices. Full article
(This article belongs to the Special Issue Application of Lactic Acid Bacteria in Fermented Food: 2nd Edition)
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<p>The antioxidant activity of fresh cabbage and LAB fermented cabbage. Each value is expressed as means (n = 3), and standard deviations are shown as error bars. Values marked by ** (<span class="html-italic">p</span> &lt; 0.01) are significantly different according to an independent sample <span class="html-italic">t</span>-test. Fresh: fresh cabbage, fermented: fermented cabbage.</p>
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<p>Phenolic contents of fresh cabbage and lactic-acid-fermented cabbage. Each value is expressed as means (n = 3), and standard deviations are shown as error bars. Values marked by * (<span class="html-italic">p</span> &lt; 0.05) and ** (<span class="html-italic">p</span> &lt; 0.01) are significantly different according to an independent sample <span class="html-italic">t</span>-test. Fresh: fresh cabbage, fermented: fermented cabbage.</p>
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<p>The total flavonoid contents of fresh cabbage and lactic-acid-fermented cabbage. Each value is expressed as means (n = 3), and standard deviations are shown as error bars. Fresh: fresh cabbage, fermented: fermented cabbage.</p>
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<p>The total glucosinolate retention of lactic-acid-fermented cabbage produced by different processes. Each value is expressed as means (n = 3), and standard deviations are shown as error bars. Values marked by different letters are significantly different according to Duncan’s multiple range test (<span class="html-italic">p</span> &lt; 0.05). Salted: dehydrated cabbage by salted; canned: lactic-acid-fermented cabbage produced via small-scale production; bioreactor-0.3%: lactic-acid-fermented cabbage produced via the 5 L bioreactor with a 0.3% microbial inoculation size; bioreactor-3.0%: lactic-acid-fermented cabbage produced via the 5 L bioreactor with a 3.0% microbial inoculation size.</p>
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14 pages, 3391 KiB  
Article
Comparative Study on Selenium and Volatile Compounds in Selenium-Enriched Cardamine violifolia Pickles Fermented by Three Distinct Methods
by Jue Gong, Shen Rao, Xiaomeng Liu, Shuiyuan Cheng, Xin Cong and Dingxiang Zhu
Fermentation 2024, 10(12), 632; https://doi.org/10.3390/fermentation10120632 - 11 Dec 2024
Viewed by 338
Abstract
Cardamine violifolia is a selenium (Se)-rich vegetable crop belonging to the Brassicaceae family. This study investigated the Se concentration and volatiles in the fresh (CK) C. violifolia, natural fermented (NF), Lactiplantibacillus plantarum (LP), and Leuconostoc mesenteroides (LM) fermented C. violifolia pickles. Results [...] Read more.
Cardamine violifolia is a selenium (Se)-rich vegetable crop belonging to the Brassicaceae family. This study investigated the Se concentration and volatiles in the fresh (CK) C. violifolia, natural fermented (NF), Lactiplantibacillus plantarum (LP), and Leuconostoc mesenteroides (LM) fermented C. violifolia pickles. Results showed that fermentation promoted the levels of selenocysteine, methyl selenocysteine, and selenate. A total of 648 volatile compounds were found, including 119 terpenoids, 105 heterocyclic compounds, 103 esters, and 65 hydrocarbons. Differential analysis of volatiles indicated that fermentation induced the release of volatiles when compared to CK, whereas volatile profiles in LM and NF pickles showed notable differences from LP pickles. SeCys2, MeSeCys, and selenate significantly correlated to several volatile compounds, implying that Se metabolism may affect the formation of volatiles. Conclusively, fermentation promoted the release of aroma and bioactive volatiles and the degradation of unpleasant and harmful substances in C. violifolia pickles. Full article
(This article belongs to the Section Fermentation for Food and Beverages)
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<p>Overview of the volatile compounds in fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) classification of the volatile compounds, (<b>B</b>) principal component analysis of the samples, and (<b>C</b>) concentration changes of the volatiles in each group. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
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<p>Comprehensive analysis of the DVCs in fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) statistics of the DVCs in each comparison group, (<b>B</b>) classification of the DVCs, and (<b>C</b>) cluster analysis of the concentrations of DVCs. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
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<p>Analysis of the DVCs between CK and fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) overlap of the three comparison groups; (<b>B</b>) classification of the 248 DVCs in the overlap; (<b>C</b>) overlap of the DVCs with a fold change greater than 10 in the three comparison groups; (<b>D</b>) K-means analysis of the 48 DVCs. Different color lines indicate different subclasses of compounds; (<b>E</b>) concentration changes of the nine DVCs in subclass 5 from the K-means analysis; and (<b>F</b>) concentration changes of the 13 top changed DVCs. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control.</p>
Full article ">Figure 4
<p>Analysis of DVCs between the fermented <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) overlap of the two comparison groups; (<b>B</b>) concentration changes of the 40 DVCs in three pickles; (<b>C</b>) top changed DVCs in NF vs. LP comparison group; and (<b>D</b>) top changed DVCs in LM vs. LP comparison group. NF: natural fermentation; LP: inoculated with <span class="html-italic">L. plantarum</span>; LM: inoculated with <span class="html-italic">L. mesenteroides</span>; CK: control. XMW1398: methyl 5-hydroxynicotinate; XMW0533: 3-methylbenzothiophene; KMW0359: 3-ethyl-phenol; XMW0300: 3,5-dimethyl-phenol; KMW0469: 4-ethyl-2-methoxy-phenol; NMW0066: 2,4-dimethyl-benzenamine; D276: umbellulon; XMW0212: 1,4-benzodioxan-6-amine; NMW0193: 4-hydroxy-benzeneethanol; w21: 6-pentyl-2H-pyran-2-one; XMW0549: naphthalene.</p>
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<p>Correlation analysis between Se and volatile compounds detected in <span class="html-italic">C. violifolia</span> pickles: (<b>A</b>) correlation between SeCys<sub>2</sub> and volatile compounds; (<b>B</b>) correlation between MeSeCys and selenate and volatile compounds; and (<b>C</b>) correlation between Se and the representative volatile compounds.</p>
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16 pages, 893 KiB  
Article
Effects of Lactic Acid Bacterial Fermentation on the Biochemical Properties and Antimicrobial Activity of Hemp Seeds
by Dalia Čižeikienė, Ieva Gaidė, Daiva Žadeikė and Loreta Bašinskienė
Appl. Sci. 2024, 14(23), 11469; https://doi.org/10.3390/app142311469 - 9 Dec 2024
Viewed by 620
Abstract
Recently, there has been an increase in the application of lactic acid bacteria (LAB) for seed fermentation because of the improved functional, technological, and nutritional properties of the fermented seeds. The purpose of this study was to evaluate the effects of selected LAB [...] Read more.
Recently, there has been an increase in the application of lactic acid bacteria (LAB) for seed fermentation because of the improved functional, technological, and nutritional properties of the fermented seeds. The purpose of this study was to evaluate the effects of selected LAB on the biochemical and antimicrobial features of fermented hemp seeds and their water-, salt-, and ethanol-soluble protein fractions. The results showed that hemp seed medium was suitable for Lactiplantibacillus plantarum, Levilactobacillus brevis, and Lactobacillus acidophilus multiplication (with a LAB count > 109 colony-forming units/g). The biochemical and antimicrobial properties of the fermented hemp seeds strictly depended on the LAB strain used for fermentation. The hemp seeds fermented with L. brevis, which was previously isolated from rye sourdough, presented the highest total phenolic content and phytase, amylase, protease, and antioxidant activities. The hemp seeds fermented with L. acidophilus showed the broadest spectrum of antimicrobial activity against foodborne pathogens. The ethanol-soluble protein fractions from the fermented hemp seeds inhibited the growth of Escherichia coli, Staphylococcus aureus, Salmonella typhimurium, Bacillus subtilis, and Bacillus cereus, while the ethanol-soluble protein fraction from unfermented hemp seeds did not have an antimicrobial effect. The results of ABTS·+ radical scavenging and antimicrobial activity assays by agar well diffusion method confirmed that the tested LAB strains for hemp seed fermentation influenced the antioxidant and antimicrobial activities of protein fractions. Full article
(This article belongs to the Special Issue Advances in Food Safety and Microbial Control)
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<p>A clear growth inhibition zone of <span class="html-italic">Salmonella typhimurium</span> on agar media is visible around the hemp seed products fermented with <span class="html-italic">L. acidophilus</span> DSM 20079.</p>
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<p>The antimicrobial effect of 70% ethanol-soluble hemp seed protein fractions obtained after fermentation with (<b>a</b>) <span class="html-italic">L. plantarum</span> MR24 on the growth of <span class="html-italic">E. coli</span> and (<b>b</b>) <span class="html-italic">L. acidophilus</span> on the growth of <span class="html-italic">B. subtilis</span>. A clear zone of inhibition around the ‘well’ indicates inhibition of the growth of food spoilage bacteria. Top: the effect of the non-hydrolysed protein fraction (left) and the control—blank sample (right). Bottom: the effect of two samples of hydrolysed protein fractions obtained after fermentation with LAB.</p>
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18 pages, 10357 KiB  
Article
Lactiplantibacillus plantarum 1008 Promotes Reproductive Function and Cognitive Activity in Aged Male Mice with High-Fat-Diet-Induced Obesity by Altering Metabolic Parameters and Alleviating Testicular Oxidative Damage, Inflammation and Apoptosis
by Chin-Yu Liu, Tsung-Yu Tsai, Te-Hua Liu, Ting-Chia Chang, Yi-Wen Chen and Chih-Wei Tsao
Antioxidants 2024, 13(12), 1498; https://doi.org/10.3390/antiox13121498 - 9 Dec 2024
Viewed by 427
Abstract
The effects of Lactiplantibacillus plantarum 1008 (LP1008) on age-related cognitive impairment and skeletal muscle atrophy have been reported previously. However, its role in obesity- and age-related hypogonadism has yet to be explored. This study investigates the therapeutic efficacy of low- and high-dose LP1008 [...] Read more.
The effects of Lactiplantibacillus plantarum 1008 (LP1008) on age-related cognitive impairment and skeletal muscle atrophy have been reported previously. However, its role in obesity- and age-related hypogonadism has yet to be explored. This study investigates the therapeutic efficacy of low- and high-dose LP1008 in a high-fat-diet-fed male mouse model. Mice at 37 weeks of age were fed a standard diet (n = 8) or a 45% high-fat diet for 28 weeks, and the high-fat-diet-fed mice were divided into vehicle, low-dose and high-dose LP1008 groups (n = 8 per group) on the basis of the treatment administered for an additional 8 weeks. We found that LP1008 suppressed the increases in total cholesterol levels and liver function parameters and alleviated histological changes in the brain, ileum, gastrocnemius muscle and testes. In terms of reproductive function, LP1008 attenuated the decreases in sperm quality, sperm maturity, testosterone levels and levels of enzymes involved in testosterone biosynthesis. Furthermore, LP1008 altered impairments in spatial learning and memory and induced slight alterations in the gut microbiota. Moreover, LP1008 exerted antioxidant, anti-inflammatory and anti-apoptotic effects in aged, obese male mice. LP1008 reversed diet-induced obesity, age-related reproductive dysfunction and pathological damage by increasing testosterone levels and altering the gut microbiome through the regulation of mediators involved in oxidative stress, apoptosis and inflammation. Full article
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<p>(<b>A</b>) Body and liver weights; (<b>B</b>) histopathological observations of the liver (arrows indicate hepatic steatosis) and percentages of hepatic lipid droplet areas; and (<b>C</b>) serum glucose, insulin, total cholesterol, (<b>D</b>) ALT and AST levels in aged and obese mice (<span class="html-italic">n</span> = 8 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group; <sup>+</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HPL group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008, HPH, high-dose LP1008; AST, aspartate transaminase; ALT, alanine transaminase.</p>
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<p>(<b>A</b>) Histopathological observations of the brain and spatial learning and memory, including (<b>B</b>) the mean escape latency in spatial acquisition training, (<b>C</b>) swimming pathways and percentage of time spent in the target quadrant, and (<b>D</b>) the mean escape latency in the working memory test in aged and obese mice (<span class="html-italic">n</span> = 8 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008.</p>
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<p>Histopathological observations of muscle and gastrocnemius muscle weights and mean cross-sectional areas in aged and obese mice (<span class="html-italic">n</span> = 8 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008.</p>
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<p>(<b>A</b>) Testis, epididymis and vas deferens weights; (<b>B</b>) sperm quality, including sperm motility, sperm count and normal morphology rate; and (<b>C</b>) histopathological observations of testes with related parameters, including MSTD and MTBS, in aged and obese mice (<span class="html-italic">n</span> = 8 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008; MSTD, mean seminiferous tubule diameter; MTBS, mean testicular biopsy score.</p>
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<p>(<b>A</b>) Serum testosterone levels; and (<b>B</b>) Western blotting and quantitative analysis of the relative protein expression of testicular StAR, CYP11A1, 3β-HSD, CYP17A1 and 17β-HSD in aged and obese mice (<b>A</b>: <span class="html-italic">n</span> = 8 in per group; <b>B</b>: <span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008. The whole Western blot is shown in <a href="#app1-antioxidants-13-01498" class="html-app">Figure S2</a>.</p>
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<p>(<b>A</b>) Histopathological observations of the ileum; (<b>B</b>) ileum weight and related parameters, including villus length and crypt depth (arrows indicated); (<b>C</b>) the characteristics of microbial communities, including Shannon, Simpson and species richness; (<b>D</b>) Good’s coverage; (<b>E</b>) rank abundance curve; (<b>F</b>) weighted UniFrac; (<b>G</b>) weighted UniFrac-based PCoA; and (<b>H</b>) Bray–Curtis dissimilarity-based PCoA in aged and obese mice (<b>A</b>,<b>B</b>: <span class="html-italic">n</span> = 8 per group; <b>C</b>–<b>H</b>: <span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008.</p>
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<p>Relative abundances of the microbial community at (<b>A</b>) the phylum level with the F/B ratio, (<b>B</b>) the family level and (<b>C</b>) the genus level. Dominant taxa based on LEFSe at LDA scores &gt;4 in comparisons of (<b>D</b>) the CON and HFD groups; (<b>E</b>) the HFD, HPL and HPH groups; and (<b>F</b>) the CON, HPL and HPH groups. LDA score &gt; 3 in comparisons of the (<b>G</b>) HFD, HPL and HPH groups and (<b>H</b>) the HPL and HPH groups (<span class="html-italic">n</span> = 4 per group). * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008; F/B, <span class="html-italic">Firmicutes/Bacteroidetes</span>.</p>
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<p>Fecal SCFA contents in aged and obese mice (<span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008.</p>
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<p>Testicular SOD, CAT and GPx activities and MDA levels in aged and obese mice (<span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, and <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group, and <sup>+</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HPL group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008; SOD, superoxide dismutase; CAT, catalase; GPx, glutathione peroxidase; MDA, malondialdehyde.</p>
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<p>(<b>A</b>) Serum LPS levels and (<b>B</b>) Western blotting and quantitative analysis of the relative protein expression of testicular NF-κB p105, NF-κB p50, TNF-α and IL-6 in aged and obese mice (<b>A</b>: <span class="html-italic">n</span> = 8 per group; <b>B</b>: <span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008; LPS, lipopolysaccharide. The whole Western blot is shown shown in <a href="#app1-antioxidants-13-01498" class="html-app">Figure S3</a>.</p>
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<p>(<b>A</b>,<b>B</b>) Western blotting and quantitative analysis of the relative protein expression levels of the testicular Bax:Bcl-xl ratio, Caspase 9, C-Caspase 9, Caspase 3, C-Caspase 3, PARP, C-PARP, Caspase 8 and C-Caspase 8 in aged and obese mice (<span class="html-italic">n</span> = 4 per group). All data are represented as mean  ±  SD. * <span class="html-italic">p</span> &lt; 0.05 vs. the CON group, <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 vs. the HFD group. CON, control; HFD, high-fat diet; HPL, low-dose LP1008; HPH, high-dose LP1008. The whole Western blot is shown in <a href="#app1-antioxidants-13-01498" class="html-app">Figure S4</a>.</p>
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14 pages, 1904 KiB  
Article
Mixed Strains of Bacillus velezensis PBS-17, Lactiplantibacillus plantarum J-135, and Saccharomyces cerevisiae DAE-4 Increase the Storage Capacity of Fermented Feed and Silage
by Eun-Jae Park, Moon Joo Kim, Bori Lee, Hyun-Jae Jang and Seung Woong Lee
Fermentation 2024, 10(12), 621; https://doi.org/10.3390/fermentation10120621 - 5 Dec 2024
Viewed by 474
Abstract
In this study, we investigated whether three microbial strains, Lactiplantibacillus plantarum J-135, Saccharomyces cerevisiae DAE-4, and Bacillus velezensis PBS-17, could be used to reduce mold growth and spoilage during the production of fermented feed. These microorganisms were isolated and characterized via an evaluation [...] Read more.
In this study, we investigated whether three microbial strains, Lactiplantibacillus plantarum J-135, Saccharomyces cerevisiae DAE-4, and Bacillus velezensis PBS-17, could be used to reduce mold growth and spoilage during the production of fermented feed. These microorganisms were isolated and characterized via an evaluation of their antibacterial activity, enzymatic activity, bile acid resistance, and acid tolerance. L. plantarum J-135 and S. cerevisiae DAE-4 demonstrated excellent acid tolerance and bile acid resistance, and L. plantarum J-135 exhibited antibacterial activity against Salmonella species. B. velezensis PBS-17 showed the greatest protease, cellulase, α-amylase, and phytase enzymatic activities, and displayed antibacterial activity against Fusarium solani, Aspergillus flavus, Penicillium sp., and Fusarium oxysporum. The three isolated strains were diluted to the same concentration (1:1:1) to create a culture solution, which was added to a standard feed (experimental group) to prepare fermented feed. This was compared with feed treated with a commercially available single probiotic preparation (control group 1) or a mixed microbial preparation that was composed of multiple strains, including B. subtilis. The feed treated with the single probiotic preparation spoiled after 21 days due to insufficient lactic acid bacteria growth, whereas the feed treated with the mixed microbial preparation exhibited mold growth after 14 days. The bacteria and fungi that cause spoilage during fermented feed production were effectively controlled in feed treated with L. plantarum J-135, S. cerevisiae DAE-4, and B. velezensis PBS-17. Therefore, the mixture of these three microbial strains may reduce the risk of spoilage during fermented silage and feed processing, thereby improving storage properties and stability. Full article
(This article belongs to the Section Industrial Fermentation)
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<p>Antifungal activities of the isolated Bacillus strains. The isolated Bacillus strains were cultured in LB media for 24 h, after which the culture broth was inoculated on PDA. After incubation for 7 days at 25 °C, the size of the antimicrobial inhibition zone was measured. (<b>A</b>): <span class="html-italic">Fusarium solani</span>, (<b>B</b>): <span class="html-italic">Aspergillus flavus</span>, (<b>C</b>): <span class="html-italic">Penicillium</span> sp., (<b>D</b>): <span class="html-italic">Fusarium oxysporum</span>.</p>
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<p>Phylogenetic tree of strain PBS-17 based on the 16sRNA gene sequence.</p>
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<p>Changes in silage following <span class="html-italic">B. velezensis</span> PBS-17 treatment and no treatment after 12 months.</p>
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<p>Phylogenetic trees of strains J-135 (<b>A</b>) and DAE-4 (<b>B</b>) based on the 16sRNA gene sequence.</p>
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<p>Changes in pH (<b>A</b>) and microbial count (<b>B</b>–<b>D</b>) during the fermentation of the formulated feed. The groups were divided into groups without strain treatment (untreated group, ▲), groups treated with a commercially available single strain (control group 1, ●), groups treated with a commercially available mixed strain solution (control group 2, ■), and groups treated with a 1% mixed microbial solution (experimental group, ×). The changes in pH and bacterial counts were investigated according to the experimental method over 21 days of storage. According to Duncan’s multiple range test, values with the same letter in the same column were not significantly different at <span class="html-italic">p</span> &lt; 0.05. (<b>A</b>): pH; (<b>B</b>): lactic acid bacteria; (<b>C</b>): total fungil; (<b>D</b>): total bacteria.</p>
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<p>Changes in fermented feed after 21 days of microbial treatment.</p>
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10 pages, 3394 KiB  
Article
The Metagenomic Properties of Uşak Tarhana Dough
by Naciye Afranur Mitaf, Dudu Simsek Kirca and Omer Simsek
Fermentation 2024, 10(12), 620; https://doi.org/10.3390/fermentation10120620 - 4 Dec 2024
Viewed by 690
Abstract
This study investigated the bacterial diversity of geographically indicated Uşak tarhana using metagenomics. Tarhana dough samples were collected from local producers in different regions of the Uşak province. The samples were analyzed for their chemical and microbiological properties. The microbiota was examined through [...] Read more.
This study investigated the bacterial diversity of geographically indicated Uşak tarhana using metagenomics. Tarhana dough samples were collected from local producers in different regions of the Uşak province. The samples were analyzed for their chemical and microbiological properties. The microbiota was examined through metagenomic analysis using high-throughput sequencing, followed by bioinformatic processing with QIIME2 and DADA2 tools. Taxonomic analyses revealed that Lactiplantibacillus plantarum and Fructilactobacillus sanfranciscensis were the dominant species in most samples. In Silico analysis confirmed the presence of Fructilactobacillus sanfranciscensis in the tarhana fermentation microbiota. Diversity analyses, including Shannon and Chao1 indices, indicated significant variation in microbial diversity and homogeneity among the samples. Differences in microbiota diversity were observed between tarhana produced in the northern and southern regions of Uşak. The bacterial diversity of the tarhana samples showed partial differences at the micro-local level, and these results suggested that the slight variation in bacterial diversity between the northern and southern regions might be related to mild climatic transition. Full article
(This article belongs to the Special Issue Microbiota and Metabolite Changes in Fermented Foods)
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<p>The bacterial diversity of Uşak tarhana samples at the genus taxonomic level in a stacked bar plot.</p>
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<p>The bacterial diversity of Uşak tarhana samples at the species taxonomic level in a stacked bar plot.</p>
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<p>The alfa diversity parameters of Uşak tarhana samples. (<b>A</b>) OTU numbers, (<b>B</b>) Shannon’s diversity, and (<b>C</b>) Chao1 index.</p>
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<p>PCoA plot of tarhana samples at the species level.</p>
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14 pages, 2584 KiB  
Article
The Effect of Lactiplantibacillus plantarum and Lacticaseiba-cillus Rhamnosus Strains on the Reduction of Hexachlorobenzene Residues in Fermented Goat Milk During Refrigerated Storage
by Agata Witczak, Izabela Dmytrów and Anna Mituniewicz-Małek
Molecules 2024, 29(23), 5686; https://doi.org/10.3390/molecules29235686 - 30 Nov 2024
Viewed by 461
Abstract
Hexachlorobenzene (HCB) is a persistent organic pollutant (POP) commonly detected in milk and dairy products. These compounds pose a serious threat to the health of consumers due to their considerable bioaccumulation potential, high stability, and toxicity. (2) Methods: The study evaluated the potential [...] Read more.
Hexachlorobenzene (HCB) is a persistent organic pollutant (POP) commonly detected in milk and dairy products. These compounds pose a serious threat to the health of consumers due to their considerable bioaccumulation potential, high stability, and toxicity. (2) Methods: The study evaluated the potential of Lactiplantibacillus plantarum and Lacticaseibacillus rhamnosus probiotic cultures to reduce HCB residues in fermented goat milk beverages during 21-day refrigerated storage. HCB content was determined by gas chromatography coupled with mass spectrometry (GC/MS). (3) Results: A strong negative correlation was found between HCB concentration in fermented milk and storage time. After 21 days, a 75–78% reduction in HCB content was observed, with L. plantarum showing greater efficiency in reducing hexachlorobenzene levels than L. rhamnosus. (4) Conclusions: The use of probiotic cultures contributed to a significant reduction in the HCB content of fermented goat milk. Our findings support the hypothesis that the lactic acid bacteria Lactiplantibacillus plantarum and Lacticaseibacillus rhamnosus can lower hexachlorobenzene levels in fermented products Full article
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<p>Concentration of HCB in unfortified (<b>A</b>) and in fortified (<b>B</b>) samples of fermented goat milk (FGM), depending on the culture. The bars: arithmetic means with standard deviations.</p>
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<p>Effect of storage period on changes in HCB (%) and pH of fermented goat milk (FGM), depending on the culture. The bars: arithmetic means with standard deviations.</p>
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<p>Correlation between refrigeration storage time and changes in %HCB content in fermented goat milk (FGM).</p>
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<p>The variants of fermented milk.</p>
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<p>Chromatographic separation conditions [<a href="#B39-molecules-29-05686" class="html-bibr">39</a>].</p>
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<p>Mass spectrum of HCB [<a href="#B39-molecules-29-05686" class="html-bibr">39</a>]. Yellow—confirmation ions, red—the molecular ion.</p>
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15 pages, 3970 KiB  
Article
Targeting Inflammation and Skin Aging via the Gut–Skin Axis: The Role of Lactiplantibacillus plantarum HY7714-Derived Extracellular Vesicles
by Hayera Lee, Yun-Ha Lee, Dong-Ki Hong, Sung-Jun Mo, Soomin Jeon, Soo-Dong Park, Jae-Jung Shim, Jeong-Lyoul Lee and Jae-Hwan Lee
Microorganisms 2024, 12(12), 2466; https://doi.org/10.3390/microorganisms12122466 - 30 Nov 2024
Viewed by 604
Abstract
Intestinal mucosal tissues are prone to infections, often leading to inflammation. Lactic acid bacteria in the gut can modulate these inflammatory responses, but the interaction between host cells and lactic acid bacteria remains unclear. This study examines how Lactiplantibacillus plantarum HY7714 alleviates intestinal [...] Read more.
Intestinal mucosal tissues are prone to infections, often leading to inflammation. Lactic acid bacteria in the gut can modulate these inflammatory responses, but the interaction between host cells and lactic acid bacteria remains unclear. This study examines how Lactiplantibacillus plantarum HY7714 alleviates intestinal inflammation using gut-on-a-chip technology and in vitro models. Inflammation was induced using a gut-on-a-chip, and changes in cell morphology and barrier function were analyzed. Extracellular vesicles (EVs) derived from HY7714-improved intestinal cell structure repaired damage and restored tight junction integrity. Additionally, they attenuated inflammatory cytokines by regulating the MyD88/mTOR/NF-κB signaling pathway. RNA sequencing revealed downregulation of vicinal oxygen chelate (VOC) family proteins and proline aminopeptidase, both linked to inflammation and extracellular matrix interactions in skin health. Therefore, we explored the effects of HY7714 EVs on skin cells. The findings showed that HY7714 EVs reduced cytotoxicity and downregulated metalloproteinase expression in skin cells exposed to UVB radiation, indicating their potential anti-aging and anti-photoaging properties. These findings suggest that HY7714-derived EVs enhance both intestinal and skin health by reducing inflammation and improving barrier function, with potential benefits for the gut–skin axis. Full article
(This article belongs to the Special Issue Probiotic and Postbiotic Properties of Lactobacillus)
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<p>The flowchart of the gut-on-a-chip.</p>
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<p>Characterization of extracellular vesicles (EVs). (<b>A</b>) Size distribution determined by intensity of <span class="html-italic">Lpb. plantarum</span> HY7714 EVs. (<b>B</b>) Cryo-EM images of HY7714 EVs. Cryo-EM image analyses of density-purified HY7714 EVs. The out-lined EV images are enlarged, and indicate the lipid bilayer. Scale bars, 50 nm. Red focus sign: Focusing of center is needed to stabilize the stage before recording are performed.</p>
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<p>Evaluation of intestinal barrier function of EVs applied to the gut-on-a-chip. Immunostaining of Caco-2 cells on the gut chip. The nuclei were stained blue with 4′,6-diamidino-2-phenylindole dihydrochloride. Tight junction and F-actin were colored green and red due to zonula occludens-1 (ZO-1) and rhodamine-phalloidin. CONT, control; TS, <span class="html-italic">Lpb. plantarum</span> type strain KCTC3108; TS EVs, TS extracellular vesicles; HY7714, <span class="html-italic">Lpb. plantarum</span> HY7714; HY7714EVs, HY7714 extracellular vesicles.</p>
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<p>Protective effects and improvement of intestinal inflammation by EVs on HT-29 cells. (<b>A</b>) The protective effect of <span class="html-italic">Lpb. plantarum</span> HY7714 EVs in LPS-induced HT-29 cells. (<b>B</b>) The protein levels of myeloid differentiation primary response 88 (MyD88), phospho-mammalian target of rapamycin (p-mTOR), mTOR, phospho-nuclear factor kappa-light-chain-enhancer of activated B cells (p-NF-κB), NF-κB, and β-actin. The mRNA levels of (<b>C</b>) tumor necrosis factor-α (TNF-α), (<b>D</b>) interleukin 8 (IL-8), (<b>E</b>) zonula occludens-1 (ZO-1), and (<b>F</b>) occludin (OCLN) were monitored using qPCR and normalized against glyceraldehyde 3-phosphate dehydrogenase (GAPDH). The data are presented as the mean ± SE. Significant differences are indicated by * <span class="html-italic">p</span> &lt; 0.05 and *** <span class="html-italic">p</span> &lt; 0.001 relative to the control group. Significant differences are indicated by # <span class="html-italic">p</span> &lt; 0.05 and ## <span class="html-italic">p</span> &lt; 0.01 relative to the TS group. SE, standard error; CONT, control; EVs, extracellular vesicles; TS EVs, <span class="html-italic">Lpb. plantarum</span> type strain KCTC3180 EVs; HY7714 EVs, <span class="html-italic">Lpb. plantarum</span> HY7714 EVs.</p>
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<p>Differential expression analysis of 3467 small RNAs from exosomes of <span class="html-italic">Lactiplantibacillus plantarum</span> KCTC3108 and HY7714. (<b>A</b>) Volcano plot showing differentially expressed genes identified using the criteria of <span class="html-italic">p</span>-value &lt; 0.05 and Log2 Fold Change &gt; |2| (red dots). (<b>B</b>) Heatmap displaying 44 upregulated and 322 downregulated genes in HY7714-derived EVs. EVs, extracellular vesicles; TS EVs, <span class="html-italic">Lpb. plantarum</span> type strain KCTC3180 EVs; HY7714 EVs, <span class="html-italic">Lpb. plantarum</span> HY7714 EVs.</p>
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<p>Protective effect of <span class="html-italic">Lpb. plantarum</span> HY7714 EVs on HS68 cells. (<b>A</b>) Effect of different concentrations (25, 50, and 100 μg/mL) of HY7714 EVs on viability. (<b>B</b>–<b>D</b>) Effect of HY7714 EVs on ECM-related gene expressions. Data are presented as the mean ± SE. Significant differences are indicated 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 relative to the control group. Significant differences are indicated by # <span class="html-italic">p</span> &lt; 0.05 and ### <span class="html-italic">p</span> &lt; 0.001 relative to the TS group. SE, standard error; CONT, control; EVs, extracellular vesicles; TS EVs, <span class="html-italic">Lpb. plantarum</span> type strain KCTC3180 EVs; HY7714 EVs, <span class="html-italic">Lpb. plantarum</span> HY7714 EVs.</p>
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16 pages, 1973 KiB  
Article
Lactiplantibacillus plantarum KABP051: Stability in Fruit Juices and Production of Bioactive Compounds During Their Fermentation
by Francesca Rizzi, Bibiana Juan, Jordi Espadaler-Mazo, Marta Capellas and Pol Huedo
Foods 2024, 13(23), 3851; https://doi.org/10.3390/foods13233851 - 28 Nov 2024
Viewed by 491
Abstract
The lactic fermentation of fruit and vegetable juices by well-characterised probiotics remains relatively underexplored. We have investigated the stability and impact of Lactiplantibacillus plantarum KABP051 fermentation on orange, apple, and peach juices by microbiological, physicochemical, and sensory evaluation means. For each fruit juice, [...] Read more.
The lactic fermentation of fruit and vegetable juices by well-characterised probiotics remains relatively underexplored. We have investigated the stability and impact of Lactiplantibacillus plantarum KABP051 fermentation on orange, apple, and peach juices by microbiological, physicochemical, and sensory evaluation means. For each fruit juice, three different samples were analysed: original fruit juice without probiotic as blank (B), fruit juice inoculated with 107 CFU/mL of probiotic without fermentation (P), and fruit juice inoculated with 107 CFU/mL of probiotic and fermented at 37 °C for 24 h (PF). P samples displayed good stability throughout the study, and PF samples showed an initial increase in CFUs accompanied by a change in pH, confirming the ability of the probiotic to ferment these juices. After 60 days of refrigeration, PF samples contained >107 CFU/mL. Total phenolic content and antioxidant capacity were equivalent in F, P, and PF. Remarkably, deep metabolomic analyses confirmed malolactic fermentation and revealed the production of several bioactive compounds including the antimicrobial substance phenyllactic acid, the immunomodulatory and anti-fatigue amino acid N-acetyl glutamine, the vitamin B3 form nicotinic acid, the monoterpene (−)-β-pinene, and the neurotransmitter acetylcholine, among others, during probiotic fermentation. Finally, a hedonic analysis involving 51 participants showed that probiotic fermented orange juice is well accepted by panellists, with scores comparable to those of the control juice. Overall, we here show that fruit juices are excellent carriers for the delivery of the probiotic L. plantarum KABP051 and its non-alcoholic fermentation can result in tasty functional fruit juices enriched with health-promoting compounds. Full article
(This article belongs to the Special Issue Lactic Acid Bacteria: The Functions and Applications in Foods)
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<p>Results of stability analysis (log CFU/mL, pH and total soluble solids (°Bx)) in orange, apple, and peach juices inoculated with Lactiplantibacillus plantarum KABPTM 051 and stored 60 days at 4 °C without fermentation (<b>A</b>) and after a fermentation of 24 h at 37 <span class="html-italic">°C</span> (<b>B</b>).</p>
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<p>Metabolomic analysis of SCFAs in fruit juices. (<b>A</b>) Score plot of PC2 over PC1 in the model calculated on the relative concentrations of SCFAs in the reduced dataset. Data have been autoscaled. (<b>B</b>) Loading plot from PCA model calculated on the relative concentrations of SCFAs in the reduced dataset. Data have been autoscaled, and overlapping labels were removed to improve readability. (<b>C</b>) Acetic acid concentration (mM) in blank (B), probiotic-supplemented (P), and probiotic-fermented (PF) fruit juices. * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Semi-polar metabolite profile. (<b>A</b>) Score plot of PC2 over PC1 in the model calculated on the relative concentrations of the variables annotated on levels 1 and 2a in the reduced dataset. (<b>B</b>) Loading plot from PCA model calculated on the relative concentrations of the variables annotated on levels 1 and 2a in the reduced dataset. Data have been autoscaled, and overlapping labels were removed to improve readability. (<b>C</b>) Relative abundances (Area Under the Curve) of compounds of interest detected in level 1 and 2a in blank (B), probiotic-supplemented (P), and probiotic-fermented (PF) fruit juices. * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Results of the sensory evaluation involving 51 untrained panellists. (<b>A</b>) Results of organoleptic parameters and (<b>B</b>) score of the purchase probability of blank juices (<b>B</b>) and probiotic-fermented (PF) orange juices. A nine-point scale was used for the evaluation of acceptability and intensity of aroma, colour, bitterness, sweetness, acidity, and strange flavours, with 1 = Dislike extremely/Extremely low intensity and 9 = Like extremely/Extremely intense. The parameter “Purchase probability” was evaluated with a five-point scale, with 1 = Definitely will not buy and 5 = Definitely will buy. * <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.</p>
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14 pages, 1402 KiB  
Article
Volatile Compounds of Sucuk, a Dry Fermented Sausage: The Effects of Ripening Rate, Autochthonous Starter Cultures and Fat Type
by Mükerrem Kaya and Güzin Kaban
Foods 2024, 13(23), 3839; https://doi.org/10.3390/foods13233839 - 28 Nov 2024
Viewed by 499
Abstract
The aim of this study was to determine the effects of ripening rate (slow or fast), usage autochthonous starter cultures (control—spontaneous fermentation, Lactiplantibacillus plantarum GM77, Staphylococcus xylosus GM92 or L. plantarum GM77 + S. xylosus GM92) and type of fat (beef fat-BF, sheep [...] Read more.
The aim of this study was to determine the effects of ripening rate (slow or fast), usage autochthonous starter cultures (control—spontaneous fermentation, Lactiplantibacillus plantarum GM77, Staphylococcus xylosus GM92 or L. plantarum GM77 + S. xylosus GM92) and type of fat (beef fat-BF, sheep tail fat-STF and BF+STF) on the volatile compounds of sucuk (a Turkish dry fermented sausage). A total of 74 volatile compounds were identified, including groups of aliphatic hydrocarbons, aldehydes, ketones, alcohols, sulfide compounds, esters, aromatic hydrocarbons, nitrogenous compounds, acids and terpenes in sucuk. Slow ripening resulted in significant increases in the abundance of ethanol, acetic acid, ethyl acetate, acetoin and diacetyl. A similar situation was determined for a mixed culture (L. plantarum + S. xylosus). Correlation analysis showed that the effects of slow ripening and mixed culture use were more pronounced in terms of volatile compound content. Although the effect of fat type on volatile compounds was quite limited compared to other factors, correlation analysis showed that STF had a different volatile compound profile. Full article
(This article belongs to the Special Issue Latest Research on Flavor Components and Sensory Properties of Food)
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<p>Cluster analysis of heat map showing relationship between ripening rate and volatile compounds (<b>a</b>) and between ripening rate and chemical groups of volatile compounds (<b>b</b>).</p>
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<p>Cluster analysis of heat map showing relationship between starter culture and volatile compounds (<b>a</b>) and between starter culture and chemical groups of volatile compounds (<b>b</b>).</p>
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<p>Cluster analysis of heat map showing the relationship between fat type and volatile compounds (<b>a</b>) and between fat type and chemical groups of volatile compounds (<b>b</b>).</p>
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20 pages, 3951 KiB  
Article
Lactiplantibacillus plantarum for the Preparation of Fermented Low-Bitter Enzymatic Skim Milk with Antioxidant Ability
by Yi Jiang, Longfei Zhang, Yushi Jin, Haiyan Xu, Yating Liang, Zihan Xia, Chenchen Zhang, Chengran Guan, Hengxian Qu, Yunchao Wa, Wenqiong Wang, Yujun Huang, Ruixia Gu and Dawei Chen
Foods 2024, 13(23), 3828; https://doi.org/10.3390/foods13233828 - 27 Nov 2024
Viewed by 471
Abstract
A high degree of hydrolysis can reduce the allergenicity of milk, while lactic acid bacteria (LAB) fermentation can further enhance the antioxidant ability of enzymatic milk. LAB with a strong antioxidant ability was screened, and the effects of LAB on the bitterness, taste [...] Read more.
A high degree of hydrolysis can reduce the allergenicity of milk, while lactic acid bacteria (LAB) fermentation can further enhance the antioxidant ability of enzymatic milk. LAB with a strong antioxidant ability was screened, and the effects of LAB on the bitterness, taste and flavor of enzymatic skim milk (ESM) with a high degree of hydrolysis were investigated in this paper, in addition to the response surface methodology optimized the conditions of the LAB fermentation of ESM. The results indicate that the skim milk hydrolyzed by Protamex has a higher degree of hydrolysis and lower bitterness. The scavenging rate of 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radical, the inhibition rate of hydroxyl radical (·OH) and the superoxide dismutase (SOD) activity of Lactiplantibacillus plantarum 16 and Lactococcus lactis subsp. lactis m16 are significantly higher than those of other strains (p < 0.05), while the improvement effect of L. plantarum 16 on the bitterness and flavor of ESM is better than that of L. lactis subsp. lactis m16. The fermented ESM has a strong antioxidant ability and low bitterness when the inoculum quantity of L. plantarum 16 is 5%, fermentation at 37 °C for 18 h and the pH of the ESM is 6.5, for which the DPPH free radical scavenging rate is 61.32%, the ·OH inhibition rate is 83.35%, the SOD activity rate is 14.58 and the sensory evaluation is 4.25. The contents of amino acids related to bitterness and antioxidants were reduced and increased, respectively. The ESM fermented by L. plantarum 16 has a good flavor, antioxidant ability and low bitterness. Full article
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<p>Hydrolysis degree of ESM (<span class="html-italic">n</span> = 3, x ± sd). Different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Bitter taste of ESM by three kinds of proteases (<span class="html-italic">n</span> = 10, x ± sd). Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The effect of quinine concentration on bitterness response value.</p>
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<p>Electronic tongue flavor analysis of ESM.</p>
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<p>The antioxidant ability of ESM fermented by LAB (<span class="html-italic">n</span> = 3, x ± sd). Different lowercase letters of the same indicator indicate significant difference (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Bitterness evaluation value of ESM fermented by LAB (<span class="html-italic">n</span> = 3, x ± sd). Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Electronic tongue taste profiles of ESM fermented by LAB.</p>
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<p>The antioxidant ability of ESM fermented by <span class="html-italic">L. plantarum</span> 16 at different fermentation temperatures. (<b>A</b>), DPPH free radical scavenging rate; (<b>B</b>), ·OH inhibition rate; (<b>C</b>), SOD activity. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The antioxidant ability of ESM fermented by <span class="html-italic">L. plantarum</span> 16 at different fermentation times. (<b>A</b>), DPPH free radical scavenging rate; (<b>B</b>), ·OH inhibition rate; (<b>C</b>), SOD activity. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The antioxidant ability of ESM fermented by <span class="html-italic">L. plantarum</span> 16 under different inoculum quantity. (<b>A</b>), DPPH free radical scavenging rate; (<b>B</b>), ·OH inhibition rate; (<b>C</b>), SOD activity. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The antioxidant ability of <span class="html-italic">L. plantarum</span> 16-fermented ESM under different enzyme release pH conditions. (<b>A</b>), DPPH free radical scavenging rate; (<b>B</b>), ·OH inhibition rate; (<b>C</b>), SOD activity. Different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Response surface and contour plots of the impact of interaction on comprehensive evaluation values. The lighter the color, the less the influence of the experimental factors on the fuzzy comprehensive evaluation in this response surface plot.</p>
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13 pages, 2876 KiB  
Article
Limosilactobacillus fermentum MG5368 and Lactiplantibacillus plantarum MG989 Regulates Skin Health in UVB-Induced HaCaT Cells and Hairless Mice Model
by Jeong-Yong Park, Ji Yeon Lee, Seonghwa Hong, Huijin Heo, Hana Lee, Yong Gyeong Kim, Byoung-Kook Kim, Soo-Im Choi and Junsoo Lee
Nutrients 2024, 16(23), 4083; https://doi.org/10.3390/nu16234083 - 27 Nov 2024
Viewed by 522
Abstract
Background: Photoaging, induced by chronic ultraviolet B (UVB) exposure, results in the degradation of extracellular matrix (ECM) components, leading to skin roughness, wrinkle formation, and reduced elasticity. Recent studies have explored probiotics as potential inhibitors of extrinsic aging, primarily through mechanisms that protect [...] Read more.
Background: Photoaging, induced by chronic ultraviolet B (UVB) exposure, results in the degradation of extracellular matrix (ECM) components, leading to skin roughness, wrinkle formation, and reduced elasticity. Recent studies have explored probiotics as potential inhibitors of extrinsic aging, primarily through mechanisms that protect the skin barrier and reduce collagen breakdown. Methods: This study investigates the anti-photoaging effects of Limosilactobacillus fermentum MG5368 (L. fermentum MG5368) and Lactiplantibacillus plantarum MG989 (L. plantarum MG989) in UVB-exposed keratinocytes and an SKH-1 hairless mice model. Results: Both strains demonstrated significant efficacy in preserving collagen through the inhibition of activating protein-1 (AP-1) and reducing the expression of matrix metalloproteinase (MMP)-1 and MMP-3. Additionally, both strains restored COL1A1 protein expressions, thereby enhancing collagen synthesis and ECM stability. Enhanced skin elasticity was observed, attributed to restored levels of hyaluronic acid and hyaluronan synthase 2 (HAS2) protein expressions. Conclusions: These findings suggest that L. fermentum MG5368 and L. plantarum MG989 may serve as promising probiotic-based agents for anti-photoaging applications. Full article
(This article belongs to the Special Issue Effects of Probiotics, Prebiotics, and Postbiotics on Human Health)
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Figure 1

Figure 1
<p>Animal experimental procedure of UVB-exposed SKH-1 hairless mice. The dorsal skin of the SKH-1 mice was exposed to UVB at 1 minimal erythema dose (MED) was 60 mJ/cm<sup>2</sup>.</p>
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<p>Effect on (<b>A</b>) cell viability, (<b>B</b>) MMP-3, (<b>C</b>) MMP-1, and (<b>D</b>) hyaluronic acid production of CFS in UVB-exposed HaCaT keratinocytes. The cells were pre-treated with CFS (3%) for 24 h and then exposed to UVB (20 mJ/cm<sup>2</sup>), followed by additional treatment with CFS (3%) for 24 h. Values are expressed as the mean ± SEM (<span class="html-italic">n</span> = 3). * <span class="html-italic">p &lt;</span> 0.05, ** <span class="html-italic">p &lt;</span> 0.01, and *** <span class="html-italic">p &lt;</span> 0.001, significant difference compared to UVB-exposed group. White bar, no-exposed group; black bar, UVB-exposed group.</p>
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<p>Effect of CFS on (<b>A</b>) AP-1 (p-c-fos, c-fos, p-c-jun, and c-jun) and (<b>B</b>) p-Smad 2/3, Smad 2/3, COL1A1, and HAS2 in UVB-exposed HaCaT keratinocytes. The cells were pre-treated with CFS (3%) for 24 h and then exposed to UVB (20 mJ/cm<sup>2</sup>), followed by additional treatment with CFS (3%) for 24 h. The representative blotting images and relative expression were evaluated by Western blotting. The β-actin was used as a loading control. Values are expressed as the mean ± SEM (<span class="html-italic">n</span> = 3). * <span class="html-italic">p &lt;</span> 0.05, ** <span class="html-italic">p &lt;</span> 0.01, and *** <span class="html-italic">p &lt;</span> 0.001, significant difference compared to the UVB-exposed group.</p>
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<p>Effect of <span class="html-italic">L. fermentum</span> MG5368 and <span class="html-italic">L. plantarum</span> MG989 on wrinkle formation, roughness, and elasticity in UVB-exposed SKH-1 hairless mice. HR-1 hairless mice were orally administrated with <span class="html-italic">L. fermentum</span> MG5368 and <span class="html-italic">L. plantarum</span> MG989 (1 × 10<sup>9</sup> CFU/day) and were irradiated with UVB for 12 weeks. (<b>A</b>) Representative photographs of the mouse dorsal skin. (<b>B</b>) Mean of wrinkle depth, (<b>C</b>) maximum of wrinkle depth, (<b>D</b>) skin roughness (Rz), and (<b>E</b>) skin elasticity (A.U.) were analyzed. Values are expressed as the mean ± SEM (<span class="html-italic">n</span> = 8). * <span class="html-italic">p &lt;</span> 0.05, and *** <span class="html-italic">p &lt;</span> 0.001, significant difference compared to UVB-exposed group.</p>
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<p>Histological observation and hyaluronic acid (HA) contents on SKH-1 hairless mice dorsal skin orally administrated with <span class="html-italic">L. fermentum</span> MG5368 and <span class="html-italic">L. plantarum</span> MG989 (1 × 10<sup>9</sup> CFU/day) and were exposed with UVB for 12 weeks. (<b>A</b>) Representative images of H&amp;E and Masson’s trichrome (MT) staining of the mouse dorsal skin. (<b>B</b>) Epidermis thickness by H&amp;E stain, (<b>C</b>) collagen density by Masson’s trichrome stain, and (<b>D</b>) HA analyzed by ELISA. Values are expressed as the mean ± SEM (<span class="html-italic">n</span> = 8). * <span class="html-italic">p &lt;</span> 0.05, ** <span class="html-italic">p &lt;</span> 0.01, and *** <span class="html-italic">p &lt;</span> 0.001, significant difference compared to UVB-exposed group.</p>
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<p>Effects of <span class="html-italic">L. fermentum</span> MG5368 and <span class="html-italic">L. plantarum</span> MG989 on the AP-1/Smad pathway in UVB-exposed SKH-1 hairless mice. HR-1 hairless mice were orally administrated with <span class="html-italic">L. fermentum</span> MG5368 and <span class="html-italic">L. plantarum</span> MG989 (1 × 10<sup>9</sup> CFU/day) and were irradiated with UVB for 12 weeks. The representative blotting images and relative expression of (<b>A</b>) AP-1 (p-c-fos, c-fos, p-c-jun, and c-jun) and (<b>B</b>) p-Smad 2/3, Smad 2/3, COL1A1, and HAS2 were evaluated by Western blotting. The β-actin was used as a loading control. Values are expressed as the mean ± SEM (<span class="html-italic">n</span> = 8). * <span class="html-italic">p &lt;</span> 0.05, ** <span class="html-italic">p &lt;</span> 0.01, and *** <span class="html-italic">p &lt;</span> 0.001, significant difference compared to UVB-exposed group.</p>
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16 pages, 1095 KiB  
Article
The Effect of Ultrasound and Lactic Acid Fermentation on the Selected Quality Parameters and Bioactive Compounds Content in Fermented Pumpkin (Cucurbita pepo L.)
by Elżbieta Radziejewska-Kubzdela, Marcin Kidoń, Angelika Kowiel, Katarzyna Waszkowiak, Krystyna Szymandera-Buszka, Marta Bednarek, Maciej Kuligowski, Joanna Kobus-Cisowska and Dominik Mierzwa
Molecules 2024, 29(23), 5586; https://doi.org/10.3390/molecules29235586 - 26 Nov 2024
Viewed by 401
Abstract
Increasing the consumption of fruit and vegetables can be achieved by creating new products. A promising method seems to be the directed fermentation of vegetables. The aim of this study was to investigate the effect of ultrasonic pretreatment (US; 25 kHz; 5 min) [...] Read more.
Increasing the consumption of fruit and vegetables can be achieved by creating new products. A promising method seems to be the directed fermentation of vegetables. The aim of this study was to investigate the effect of ultrasonic pretreatment (US; 25 kHz; 5 min) and the lactic acid bacteria strain (LAB; Lactiplantibacillus plantarum 299v and Lacticaseibacillus rhamnosus GG) on the quality of fermented pumpkin (Cucurbita pepo L.). The pumpkin was inoculated with 5 log CFU/g of specific LAB strain. Fermentation was carried out for 7 days at 35 °C. Some samples were US treated at the washing stage. During fermentation, there was an increase in the LAB count of 3 logarithmic cycles compared to the initial inoculum. For L. rhamnosus, preceding fermentation by US treatment contributed to an increased bacteria count of 4 logarithmic cycles. In the case of fermentation with L. rhamnosus, the lactic acid content was significantly higher than for L. plantarum. These samples are also characterized by higher sensory properties, desirability of taste, and overall desirability. Fermentation contributed to a decrease in carotenoid and phenolic compounds content and an increase in the antioxidant capacity of the pumpkins, regardless of the bacterial strain. Full article
(This article belongs to the Special Issue Molecular Level Changes in Food Processing: Invisible Treasures)
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Figure 1
<p>LAB count (CFU/g) in the raw and fermented pumpkin samples. a, b—the means indicated by the different letters above the columns differ significantly at the α ≤ 0.05 significance level; P <span class="html-italic">L. plantarum</span>—pumpkin fermented with <span class="html-italic">L. plantarum</span>; PUS <span class="html-italic">L. plantarum</span>—pumpkin treated with US and fermented with <span class="html-italic">L. plantarum</span>; P <span class="html-italic">L. rhamnosus</span>—pumpkin fermented with <span class="html-italic">L. rhamnosus</span>; PUS <span class="html-italic">L. rhamnosus</span>—pumpkin treated with US and fermented with <span class="html-italic">L. rhamnosus</span>.</p>
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<p>Physicochemical properties of the raw and fermented pumpkin samples: (<b>a</b>) pH value; (<b>b</b>) soluble solid content. a, b—the means indicated by the different letters above the columns differ significantly at the α ≤ 0.05 significance level; P <span class="html-italic">L. plantarum</span>—pumpkin fermented with <span class="html-italic">L. plantarum</span>; PUS <span class="html-italic">L. plantarum</span>—pumpkin treated with US and fermented with <span class="html-italic">L. plantarum</span>; P <span class="html-italic">L. rhamnosus</span>—pumpkin fermented with <span class="html-italic">L. rhamnosus</span>; PUS <span class="html-italic">L. rhamnosus</span>—pumpkin treated with US and fermented with <span class="html-italic">L. rhamnosus</span>.</p>
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<p>Sugar content (g/100 g f.w.) of the raw and fermented pumpkin samples. a, b—different letters above the columns of the same color indicate statistically significant differences at α ≤ 0.05 as determined by Tukey means comparison; P <span class="html-italic">L. plantarum</span>—pumpkin fermented with <span class="html-italic">L. plantarum</span>; PUS <span class="html-italic">L. plantarum</span>—pumpkin treated with US and fermented with <span class="html-italic">L. plantarum</span>; P <span class="html-italic">L. rhamnosum</span>—pumpkin fermented with <span class="html-italic">L. rhamnosus</span>; PUS <span class="html-italic">L. rhamnosum</span>—pumpkin treated with US and fermented with <span class="html-italic">L. rhamnosus</span>.</p>
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<p>Antioxidant activity of the raw and fermented pumpkin samples. a, b, c—the means indicated by the different letters above the columns differ significantly at the α ≤ 0.05 significance level; P <span class="html-italic">L. plantarum</span>—pumpkin fermented with <span class="html-italic">L. plantarum</span>; PUS <span class="html-italic">L. plantarum</span>—pumpkin treated with US and fermented with <span class="html-italic">L. plantarum</span>; P <span class="html-italic">L. rhamnosus</span>—pumpkin fermented with <span class="html-italic">L. rhamnosus</span>; PUS <span class="html-italic">L. rhamnosus</span>—pumpkin treated with US and fermented with <span class="html-italic">L. rhamnosus</span>.</p>
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28 pages, 2842 KiB  
Article
Evaluation of Probiotic Potential and Functional Properties of Lactobacillus Strains Isolated from Dhan, Traditional Algerian Goat Milk Butter
by Mohamed Cherif Bentahar, Djilali Benabdelmoumene, Véronique Robert, Said Dahmouni, Wasim S. M. Qadi, Zineb Bengharbi, Philippe Langella, Bouasria Benbouziane, Ebtesam Al-Olayan, Esraa Adnan Dawoud Dawoud and Ahmed Mediani
Foods 2024, 13(23), 3781; https://doi.org/10.3390/foods13233781 - 25 Nov 2024
Viewed by 565
Abstract
Goat milk butter, locally known as “Dhan”, from the Sfisfa region of Algeria, holds significant cultural and economic value. This study investigates the probiotic properties of lactic acid bacteria (LAB) present in Dhan, focusing particularly on Lactobacillus strains. Molecular identification using 16S rRNA [...] Read more.
Goat milk butter, locally known as “Dhan”, from the Sfisfa region of Algeria, holds significant cultural and economic value. This study investigates the probiotic properties of lactic acid bacteria (LAB) present in Dhan, focusing particularly on Lactobacillus strains. Molecular identification using 16S rRNA revealed a dominance of Levilactobacillus brevis and Lactiplantibacillus plantarum, forming a substantial part of the bacterial profile. Three LAB isolates (DC01-A, DC04, and DC06) were selected from fresh samples, and rigorous analyses were performed to evaluate their probiotic properties. Safety assessments confirmed the absence of gelatinase, DNase, and haemolytic activities in all isolates. The isolates demonstrated high tolerance to bile salts and acidic conditions, along with the ability to survive simulated gastrointestinal digestion. Notably, strain DC06 exhibited exceptional survival at low pH (1.5) and high bile salt concentrations (0.15–0.3%). All isolates showed substantial growth in MRS medium with 2% phenol, although growth was significantly decreased at 5% phenol. Furthermore, our strains exhibited high adhesion rates to various solvents, demonstrating their potential for strong interaction with cell membranes. Specifically, adhesion to chloroform was observed at 98.26% for DC01-A, 99.30% for DC04, and 99.20% for DC06. With xylene, the adhesion rates were 75.94% for DC01-A, 61.13% for DC04, and 76.52% for DC06. The LAB strains demonstrated impressive growth in ethanol concentrations up to 12%, but their tolerance did not exceed this concentration. They also exhibited robust growth across temperatures from 10 °C to 37 °C, with strains DC04 and DC06 able to proliferate at 45 °C, though none survived at 50 °C. Additionally, the isolates showed significant resistance to oxidative stress induced by hydrogen peroxide (H2O2) and displayed medium to high autolytic activity, with rates of 50.86%, 37.53%, and 33.42% for DC01-A, DC04, and DC06, respectively. The cell-free supernatant derived from strain DC04 exhibited significant antimicrobial activity against the tested pathogens, while strain DC06 demonstrated moderate antioxidant activity with the highest DPPH scavenging rate at 68.56%, compared to the probiotic reference strain LGG at 61.28%. These collective findings not only suggest the probiotic viability of LAB strains found in Dhan but also highlight the importance of traditional food practises in contributing to health and nutrition. Consequently, this study supports the potential of traditional Dhan butter as a functional food and encourages further exploration of its health benefits. Full article
(This article belongs to the Section Food Microbiology)
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<p>Biosafety evaluation of <span class="html-italic">Lactobacillus</span> strains. (<b>a</b>) DNase activity and (<b>b</b>) haemolytic activity.</p>
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<p>Antibiotic resistance of <span class="html-italic">Lactobacillus</span> strains to different antibiotics. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>. IMP; Imipenem, K; Kanamycin, LEV; Levromycin, VA; Vancomycin, OX; Oxacillin, CTX; Cefotaxim.</p>
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<p>Survival rate (%) of <span class="html-italic">Lactobacillus</span> strains at 0.15, 0.30, and 0.50% bile salt. <sup>a–c</sup>: different lowercase letters in superscript indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among bile salt concentration for same strains. <sup>A–D</sup>: different uppercase letters in superscript within indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among strains. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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<p>Auto-aggregation percentages of <span class="html-italic">Lactobacillus</span> strains. <span class="html-italic">Lactobacillus</span> LGG was used as a reference probiotic strain. Data are expressed as mean ± SD (n = 3). <sup>a–c</sup>: different superscript in lowercase letters represent significant differences (<span class="html-italic">p</span> &lt; 0.05) among time for the same strain. <sup>A–D</sup>: different uppercase letters in superscript indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among strains. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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<p>Hydrophobicity percentages of <span class="html-italic">Lactobacillus</span> strains. <span class="html-italic">L. rhamnosus</span> GG was used as a reference probiotic strain. Data are expressed as mean ± SD (n = 3). <sup>A–D</sup>: different superscript in uppercase letters represent significant differences (<span class="html-italic">p</span> &lt; 0.05) among strains for same solvent. <sup>a–c</sup>: different small letters in superscript indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among solvent for same strain. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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<p>Autolytic activity (%) of <span class="html-italic">Lactobacillus</span> strains. Data are expressed as mean ± SD (n = 3). <sup>a–d</sup>: different small letters in superscript indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among strains. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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<p>Antibacterial activity of lactic acid bacteria. (<b>A</b>) <span class="html-italic">Escherichia coli</span> ATCC10536, (<b>B</b>) <span class="html-italic">Pseudomonas aeruginosa</span> ATCC27853, and (<b>C</b>) <span class="html-italic">Staphylococcus aureus</span> ATCC25923. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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<p>Antioxidant activity of <span class="html-italic">Lactobacillus</span> strain cell-free supernatant evaluated using DPPH (%). <sup>a–d</sup>: different small letters in superscript indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among strains. DC01-A: <span class="html-italic">Levilactobacillus brevis</span>; DC04: <span class="html-italic">Lactiplantibacillus plantarum</span>; DC06: <span class="html-italic">Levilactobacillus brevis</span>.</p>
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