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30 pages, 3680 KiB  
Review
Formation and Applications of Typical Basic Protein-Based Heteroprotein Complex Coacervations
by Yufeng Xie, Qingchen Liu, Yubo Ge, Yongqi Liu and Rui Yang
Foods 2024, 13(20), 3281; https://doi.org/10.3390/foods13203281 - 16 Oct 2024
Abstract
Lactoferrin, lysozyme, and gelatin are three common basic proteins known for their ability to interact with acidic proteins (lactoglobulin, ovalbumin, casein, etc.) and form various supramolecular structures. Their basic nature makes them highly promising for interaction with other acidic proteins to form heteroprotein [...] Read more.
Lactoferrin, lysozyme, and gelatin are three common basic proteins known for their ability to interact with acidic proteins (lactoglobulin, ovalbumin, casein, etc.) and form various supramolecular structures. Their basic nature makes them highly promising for interaction with other acidic proteins to form heteroprotein complex coacervation (HPCC) with a wide range of applications. This review extensively examines the structure, properties, and preparation methods of these basic proteins and delves into the internal and external factors influencing the formation of HPCC, including pH, ionic strength, mixing ratio, total protein concentration, temperature, and inherent protein properties. The applications of different HPCCs based on these three basic proteins are discussed, including the encapsulation of bioactive molecules, emulsion stabilization, protein separation and extraction, nanogel formation, and the development of formulas for infants. Furthermore, the challenges and issues that are encountered in the formation of heteroprotein complexes are addressed and summarized, shedding light on the complexities and considerations involved in utilizing HPCC technology in practical applications. By harnessing the basic proteins to interact with other proteins and to form complex coacervates, new opportunities arise for the development of functional food products with enhanced nutritional profiles and functional attributes. Full article
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Figure 1
<p>Schematic diagram of preparing heteroprotein complex coacervations based on acidic protein and basic protein with opposite charges.</p>
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<p>The 3D structures of (<b>A</b>) lactoferrin (PDB: 4U9C) and (<b>B</b>) lysozyme (PDB: 1TEW). (<b>C</b>) Constitution and structure of gelatin. Space structure refers to the protein formed by the winding and folding of the peptide chain [<a href="#B61-foods-13-03281" class="html-bibr">61</a>]. RGD represents the arginine–glycine–aspartate sequence.</p>
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<p>Factors (including pH, mixing ratio, protein concentration, ionic strength, temperature, etc.) influencing the formation of heteroprotein complex coacervates, along with the enhanced properties of these complexes compared to individual proteins.</p>
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<p>SEM micrography of the OVA-LYS complexes at five pH values (pH 2.0/4.0/6.0/8.0/10.0). The OVA-LYS complex structures were critically dependent on environmental pH [<a href="#B80-foods-13-03281" class="html-bibr">80</a>]. (<b>A</b>–<b>E</b>) SEM micrography of sample at pH 2.0, 4.0, 6.0, 8.0, and 10.0, respectively.</p>
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<p>Phase boundaries of coassembly of LF with β-LG isoforms at pH 5.50 and pH 5.75. (<b>A</b>,<b>B</b>) LF/β-LG A; (<b>C</b>,<b>D</b>) LF/β-LG B; (<b>E</b>,<b>F</b>) LF/β-LG AB. Black zones: domains without detectable supramolecular structures; Gray zones: aggregation domains. Red, Blue, and Green zones: coacervation domains. Optical microscopy of aggregates (<b>G</b>) formed by mixing, for example, 40 mM LF and 900 mM β-LG B at pH 5.50 versus coacervates (<b>H</b>) formed by mixing, for example, LF 40 mM and β-LG B 500 mM at pH 5.50 [<a href="#B95-foods-13-03281" class="html-bibr">95</a>].</p>
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<p>Challenges and approaches in the formation of heteroprotein complexes based on lactoferrin. (<b>A</b>) Limitations in delivery. (<b>B</b>) Strict formation condition. (<b>C</b>) Limited types of complex coacervates.</p>
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14 pages, 276 KiB  
Viewpoint
Could Snacks Based on Lupin Be a Nutritious Treat? A Point of View
by Francisco E. Carvajal Larenas, Michael J. Koziol and Mario Caviedes
Foods 2024, 13(20), 3227; https://doi.org/10.3390/foods13203227 - 11 Oct 2024
Viewed by 499
Abstract
This viewpoint article presents an opinion about snacks made with lupin species. The nutritional quality of cereal-based snacks increased significantly when lupin was added. For instance, the protein and fibre content of lupin snacks could be as high as 55.7% and 8.3% respectively, [...] Read more.
This viewpoint article presents an opinion about snacks made with lupin species. The nutritional quality of cereal-based snacks increased significantly when lupin was added. For instance, the protein and fibre content of lupin snacks could be as high as 55.7% and 8.3% respectively, soluble fibre as high as 61.2% of total fibre, and protein digestibility close to that of casein. As for sensory evaluation, some lupin snacks were ranked even better than controls. Moreover, some lupin snacks had similar or improved rheological behaviour with respect to controls. For instance, expansion indices of 11 versus 3 for controls. In summary, by adjusting formula and processing conditions, it is possible to obtain, at the same time, a healthy and tasty snack with very good machinability and rheological behaviour. This could improve the image and concept of snacks by providing an excellent opportunity for improving the diet quality of habitual consumers of snacks. This point of view also provides suggestions for improving the nutritional, rheological, and sensory evaluation of lupin snacks. Full article
19 pages, 1828 KiB  
Article
A Comprehensive Analysis of CSN1S2 I and II Transcripts Reveals Significant Genetic Diversity and Allele-Specific Exon Skipping in Ragusana and Amiatina Donkeys
by Gianfranco Cosenza and Alfredo Pauciullo
Animals 2024, 14(20), 2918; https://doi.org/10.3390/ani14202918 - 10 Oct 2024
Viewed by 328
Abstract
The αs2-casein is a phosphoprotein secreted in the milk of most mammals, and it is the most hydrophilic of all caseins. Contrary to genes found in ruminants, in donkeys two different encoding genes for donkey αs2-casein (CSN1S2 I and CSN1S2 II) have [...] Read more.
The αs2-casein is a phosphoprotein secreted in the milk of most mammals, and it is the most hydrophilic of all caseins. Contrary to genes found in ruminants, in donkeys two different encoding genes for donkey αs2-casein (CSN1S2 I and CSN1S2 II) have been identified. However, unlike in ruminants, the variability at these loci has not been characterized in detail in donkeys until now. In this study, we analyze the transcript profile of the donkey CSN1S2 I and CSN1S2 II genes, and we identify and describe the variability of these loci in the Ragusana and Amiatina breeds reared in Italy. The analysis of the CSN1S2 I Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) products and subsequent sequencing showed, in addition to correctly spliced mRNA, seven other minor mRNAs resulting from differential splicing events involving, in various combinations, entire exons (4, 5, 6, and 11), parts of exons (5′ or 3′ end of exon 17), or the recognition of intronic sequences as an exon (exon 12′). Similarly, the transcription analysis of the CSN1S2 II gene revealed a remarkable variability in splicing events, mainly concerning the alternative insertion of an extra exon 7 (named 7′); the first 33 bp of exon 13; or the alternative skipping of exons 9, 10, 11, 12, and 15, and their combinations. At the mRNA level for CSN1S2 I, seven SNPs were observed, five of which led to amino acid changes: p.T73>A, p.I109>V, p.I130>V, p.I146>T, and p.D217>Y. Similarly, nine SNPs were observed at the CSN1S2 II locus, seven of which are non-synonymous: p.L63>F, p.H70>Q, p.D90>N, p.129A>T, p.H131>Y, p.E144>G, and p.F157>S. In addition, the DNA sequencing of exon 17 and flanking introns of the CSN1S2 I gene revealed a G>A transition at the splice acceptor site of CSN1S2 I exon 17 (FM946022.1:c.375-1G>A), resulting in an allele-specific skipping of the first 15 nucleotides of this exon, which encode the peptide 176NKINQ180, and the recognition of an in-frame cryptic splicing acceptor site: arAACAAAATCAACCAG. A genotyping method based on restriction fragment length polymorphism (XbaI PCR-RFLP) was set up for this SNP. In the total population studied (105 Ragusana and 14 Amiatina donkeys), the A allele had a frequency of 0.2437 with no evidence of deviation from the Hardy–Weinberg equilibrium. This study adds new knowledge regarding the genetic variability of αs2-caseins in donkeys and may contribute significantly to the genetic improvement of milk production for this species. Full article
(This article belongs to the Section Animal Genetics and Genomics)
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<p>Nucleotide sequences of cDNA clones coding for αs2-CN-I. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey <span class="html-italic">CSN1S2</span> I gene [<a href="#B12-animals-14-02918" class="html-bibr">12</a>]. Exon numbering (above the blocks) follows the method of Cosenza et al. [<a href="#B12-animals-14-02918" class="html-bibr">12</a>]. Exon 12′ is an additional exon compared to the donkey <span class="html-italic">CSN1S2</span> I cDNA sequence (FM946022.1); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 17 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).</p>
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<p>Nucleotide sequences of cDNA clones coding for αs2-CN-II. Dashes represent identical nucleotides to those in the upper lines. The deduced protein sequence is shown above each corresponding nucleotide sequence. The large arrows indicate exons of the mRNA as deduced from known splice junctions of the donkey <span class="html-italic">CSN1S2</span> II gene [<a href="#B12-animals-14-02918" class="html-bibr">12</a>]. Exon numbering (above the blocks) follows the method of Cosenza et al. [<a href="#B12-animals-14-02918" class="html-bibr">12</a>]. Ex 7′ is an additional exon compared to the donkey <span class="html-italic">CSN1S2</span> II cDNA sequence (FN298386.2); therefore, it is numbered with a prime (′). Gray boxes depict skipped exons or sequences absent from the sequenced cDNA clones. The stop codon is indicated by an asterisk (*). The exon 13 gt cryptic splice site is in bold. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).</p>
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<p>Comparison of deduced <span class="html-italic">Equus asinus</span> (present work) and <span class="html-italic">Bos taurus</span> (GenBank: AAI14774.1) amino acid sequences of mature αs2-casein. Major bovine IgE-binding regions (corresponding amino acid sequences: 83–100 and 165–188) are in bold. Donkey sequences <sup>92</sup>NKINQ<sup>96</sup> and <sup>176</sup>NKINQ<sup>180</sup> are shaded. Alignment was performed using DNAsis pro Software v2.0 (Hitachi).</p>
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<p>Observed genotypes after <span class="html-italic">Xba</span>I (T/CTA<span class="underline">G</span>A) digestion of PCR-amplified fragments spanning exon 17 and its flanking regions in donkeys carrying the FM946022.1: c.375-1G&gt;A mutation in the splice acceptor site of exon 17 in the <span class="html-italic">CSN1S2</span> I gene. Lane 1, AA homozygous sample; lane 2, heterozygous sample; lane 3, GG homozygous sample. The marker (M) used is the 1kb Opti-DNA Ladder (0.1–10 kb) (Applied Biological Materials, ABM, Vancouver, BC, Canada).</p>
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13 pages, 7041 KiB  
Article
Biological Characterization and Fungicide Sensitivity of Dactylobotrys graminicola Causing Oat Spikelet Rot in China
by Ruifang Jia, Na Wang, Zhengqiang Chen, Shengze Wang, Kejian Lin and Yuanyuan Zhang
Agronomy 2024, 14(10), 2314; https://doi.org/10.3390/agronomy14102314 - 9 Oct 2024
Viewed by 337
Abstract
Oat (Avena sativa) is a significant cereal crop that is extensively cultivated in temperate regions and is suitable for growth at higher elevations. The damage degree and epidemic area of oat spikelet rot caused by Dactylobotrys graminicola are generally increasing and [...] Read more.
Oat (Avena sativa) is a significant cereal crop that is extensively cultivated in temperate regions and is suitable for growth at higher elevations. The damage degree and epidemic area of oat spikelet rot caused by Dactylobotrys graminicola are generally increasing and spreading. Mycelium growth rate method was used to identify biological characteristics and in vitro fungicide screenings of D. graminicola. The results show that sorbitol and casein tryptone were the best carbon and nitrogen source for the D. graminicola, respectively. The optimal temperature for mycelium growth and conidia production of the D. graminicola was 20 °C; meanwhile, an acidic environment was shown to be conducive to mycelia growth, and alkaline facilitated conidia production. Among the ten tested fungicides, 20% Pydiflumetofen showed the best inhibition rate, with an EC50 (concentration for 50% of maximal effect) value of 0.005 mg/L; 30% Difenoconazole Propiconazole and 35% Metalaxyl-M Fludioxonil also showed sufficient inhibitory effects against D. graminicola, with EC50 value of 0.05 mg/L and 0.04 mg/L. Furthermore, we used artificial inoculation to determine the effectiveness of fungicide control in field, Trifloxystrobin 10%-Tebuconazole 20% with more than 90% control effectiveness, followed by 20% Pydiflumetofen. The results of this study not only revealed the biological characteristics of D. graminicola, but also provided effective candidate fungicides for the prevention and control of oat spikelet rot disease. Full article
(This article belongs to the Section Pest and Disease Management)
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<p>Determination of efficacy of different fungicides against spikelet rot of oat in the field using artificial inoculation methods. Diseased nursery oat experimental area of grassland research institute’s experimental base in agricultural and animal husbandry intertwined areas (<b>A</b>). Experimental plot (25 m × 1 m): the red color represents the position where 100 oats were inoculated in a row; the reds are spaced 1 m apart (<b>B</b>). Oat inoculation period (<b>C</b>).</p>
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<p>Effects of temperature, pH, carbon, and nitrogen resources on mycelium growth and sporulation capacity of <span class="html-italic">D. graminicola</span> GY-18. Colonial growth diameter and sporulation capacity at different temperatures (<b>A</b>). Colonial growth diameter and sporulation capacity with different pH (<b>B</b>). Colonial growth diameter and sporulation capacity with different carbon resources (<b>C</b>). Colonial growth diameter and sporulation capacity with different nitrogen resources (<b>D</b>). The bar means colony diameter; the dark spot means the number of conidia. Lowercase letters above the bar indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among colony diameter; lowercase letters to the right of the black bar indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among sporulation capacity. Data are mean ± SD (<span class="html-italic">n</span> = 3).</p>
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<p>Mycelial growth of <span class="html-italic">D. graminicola</span> GY-18 on PDA plates incubated for 7 days under different temperature and pH. ((<b>A1</b>): 5 °C, (<b>A2</b>): 10 °C, (<b>A3</b>): 15 °C, (<b>A4</b>): 20 °C, (<b>A5</b>): 25 °C, (<b>A6</b>): 30 °C, (<b>A7</b>): 35 °C, (<b>A8</b>): 40 °C; (<b>B1</b>): pH = 4, (<b>B2</b>): pH = 5, (<b>B3</b>): pH = 6, (<b>B4</b>): pH = 7, (<b>B5</b>): pH = 8, (<b>B6</b>): pH = 9, (<b>B7</b>): pH = 10, (<b>B8</b>): pH = 11).</p>
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<p>Mycelial growth of <span class="html-italic">D. graminicola</span> GY-18 on different carbon and nitrogen resource plates incubated for 7 days. ((<b>A1</b>): mannitol, (<b>A2</b>): xylose, (<b>A3</b>): sucrose, (<b>A4</b>): soluble starch, (<b>A5</b>): sorbitol, (<b>A6</b>): carboxymethylcellulose sodium, (<b>A7</b>): inositol, (<b>A8</b>): fructose, (<b>A9</b>): glucose, (<b>B1</b>): L-proline, (<b>B2</b>): ammonium chloride (<b>B3</b>): sodium nitrate, (<b>B4</b>): glycine, (<b>B5</b>): casein tryptone, (<b>B6</b>): ammonium sulfate, (<b>B7</b>): potassium nitrate).</p>
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<p>Mycelial growth of <span class="html-italic">D. graminicola</span> GY-18 on PDA plates incubated for 7 days in the absence (CK) or presence of different concentrations of antimicrobial agents (10 antimicrobial agents in order from (<b>A</b>–<b>J</b>): DA, DP, MAN, FLU, MMM, PYD, KM, MMF, TRI, and TT. The last column is CK, and 1–5 were different concentrations (see <a href="#agronomy-14-02314-t001" class="html-table">Table 1</a> for details of the antimicrobial agent concentrations).</p>
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18 pages, 6213 KiB  
Article
Preparation and Characterization Study of Zein–Sodium Caseinate Nanoparticle Delivery Systems Loaded with Allicin
by Ling Hu, Pengcheng Zhao, Yabo Wei, Yongdong Lei, Xin Guo, Xiaorong Deng and Jian Zhang
Foods 2024, 13(19), 3111; https://doi.org/10.3390/foods13193111 - 28 Sep 2024
Viewed by 663
Abstract
Allicin, as a natural antibacterial active substance from plants, has great medical and health care value. However, due to its poor stability, its application in the field of food and medicine is limited. So, in this paper, allicin–zein–sodium caseinate composite nanoparticles (zein–Ali–SC) were [...] Read more.
Allicin, as a natural antibacterial active substance from plants, has great medical and health care value. However, due to its poor stability, its application in the field of food and medicine is limited. So, in this paper, allicin–zein–sodium caseinate composite nanoparticles (zein–Ali–SC) were prepared by antisolvent precipitation and electrostatic deposition. Through the analysis of the particle size, ζ-potential, encapsulation efficiency (EE), loading rate (LC) and microstructure, the optimum preparation conditions for composite nanoparticles were obtained. The mechanism of its formation was studied by fluorescence spectrum, Fourier infrared spectrum (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The stability study results showed that the particle size of composite nanoparticles was less than 200 nm and its PDI was less than 0.3 under different NaCl concentrations and heating conditions, showing good stability. When stored at 4 °C for 21 days, the retention rate of allicin reached 61.67%, which was 52.9% higher than that of free allicin. After freeze-drying and reheating, the nanoparticles showed good redispersibility; meanwhile, antioxidant experiments showed that, compared with free allicin, the nanoparticles had stronger scavenging ability of free radicals, which provided a new idea for improving the stability technology and bioavailability of bioactive compounds. Full article
(This article belongs to the Section Food Security and Sustainability)
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<p>Molecular docking of allicin and zein.</p>
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<p>Changes in appearance (<b>A</b>), particle size, and PDI (<b>B</b>) of composite nanoparticles under different amounts of sodium caseinate addition. different lowercase letters denote significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Microscopic morphology of nanoparticles: (<b>a</b>) zein, (<b>b</b>) zein–Ali, (<b>c</b>) zein–SC, (<b>d</b>) zein–Ali–SC.</p>
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<p>Fluorescence spectrum analysis of zein–Ali–SC with different sodium caseinate addition levels.</p>
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<p>FTIR spectra of different components and nanoparticles.</p>
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<p>XRD analysis diagram.</p>
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<p>(<b>A</b>) TGA curve diagram; (<b>B</b>) DTG curve diagram.</p>
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<p>Changes in appearance, particle size and PDI of composite nanoparticles at different pH levels. different lowercase letters denote significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in appearance, particle size and PDI of composite nanoparticles at different concentrations of sodium chloride. different lowercase letters denote significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in particle size, PDI and ζ-potential of composite nanoparticles under different heating times.</p>
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<p>Changes of allicin content under different storage times.</p>
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<p>Particle size changes of freshly prepared composite nanoparticle dispersion and freeze-dried sample before and after heating.</p>
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<p>Scavenging activity of DPPH and ABTS free radicals.</p>
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18 pages, 1381 KiB  
Review
High-Pressure Processing of Milk and Dairy Products: Latest Update
by Nawal Ozaybi
Processes 2024, 12(10), 2073; https://doi.org/10.3390/pr12102073 - 25 Sep 2024
Viewed by 1098
Abstract
The growing global demand for minimally processed fresh foods has driven the development of innovative food processing methods. High-pressure processing (HPP), a leading non-thermal technique, has proven to be environmentally friendly, cost-effective, and versatile across various food types. Its ability to extend shelf [...] Read more.
The growing global demand for minimally processed fresh foods has driven the development of innovative food processing methods. High-pressure processing (HPP), a leading non-thermal technique, has proven to be environmentally friendly, cost-effective, and versatile across various food types. Its ability to extend shelf life and ensure microbial safety is well established, particularly in dairy products. However, further research is needed to fully understand HPP’s impact on improving the digestion of milk compounds and assessing potential safety risks. Recent studies, for example, demonstrate HPP’s efficacy in enhancing the microbial safety and nutritional value of products like cheese, yogurt, and whey protein isolate. This review explores these advancements and highlights HPP’s role in improving the physicochemical, organoleptic, and functional properties of milk and dairy products. Full article
(This article belongs to the Section Food Process Engineering)
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<p>World production of milk by region (source: [<a href="#B4-processes-12-02073" class="html-bibr">4</a>]).</p>
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<p>The principles of high-pressure processing (HHP).</p>
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<p>Schematic of high-pressure processing system.</p>
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<p>Microbe inactivation mechanisms using high-pressure processing.</p>
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26 pages, 1382 KiB  
Review
Exploring Dietary Interventions in Autism Spectrum Disorder
by Ingrid Daniela Pérez-Cabral, Ariadna Thalía Bernal-Mercado, Alma Rosa Islas-Rubio, Guadalupe Miroslava Suárez-Jiménez, Miguel Ángel Robles-García, Andrés Leobardo Puebla-Duarte and Carmen Lizette Del-Toro-Sánchez
Foods 2024, 13(18), 3010; https://doi.org/10.3390/foods13183010 - 23 Sep 2024
Viewed by 1685
Abstract
Autism spectrum disorder (ASD) involves social communication difficulties and repetitive behaviors, and it has a growing prevalence worldwide. Symptoms include cognitive impairments, gastrointestinal (GI) issues, feeding difficulties, and psychological problems. A significant concern in ASD is food selectivity, leading to nutrient deficiencies. Common [...] Read more.
Autism spectrum disorder (ASD) involves social communication difficulties and repetitive behaviors, and it has a growing prevalence worldwide. Symptoms include cognitive impairments, gastrointestinal (GI) issues, feeding difficulties, and psychological problems. A significant concern in ASD is food selectivity, leading to nutrient deficiencies. Common GI issues in ASD, such as constipation and irritable bowel syndrome, stem from abnormal gut flora and immune system dysregulation. Sensory sensitivities and behavioral challenges exacerbate these problems, correlating with neurological symptom severity. Children with ASD also exhibit higher oxidative stress due to low antioxidant levels like glutathione. Therapeutic diets, including ketogenic, high-antioxidant, gluten-free and casein-free, and probiotic-rich diets, show potential in managing ASD symptoms like behavior, communication, GI issues, and oxidative stress, though the evidence is limited. Various studies have focused on different populations, but there is increasing concern about the impact among children. This review aims to highlight the food preferences of the ASD population, analyze the effect of the physicochemical and nutritional properties of foods on the selectivity in its consumption, GI problems, and antioxidant deficiencies in individuals with ASD, and evaluate the effectiveness of therapeutic diets, including diets rich in antioxidants, gluten-free and casein-free, ketogenic and essential fatty acids, and probiotic-rich diets in managing these challenges. Full article
(This article belongs to the Section Food Nutrition)
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<p>Impact of gastrointestinal symptoms on autism spectrum disorder symptoms. Figure created by the authors. ↑ means increase; ↓ means decrease.</p>
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<p>Diagram of affected activities in increased oxidative stress in children with autism spectrum disorder. Figure created by the authors.</p>
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<p>Chemical structures of carotenoids, phenols, and main antioxidant vitamins. Figure created by the authors.</p>
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17 pages, 10342 KiB  
Article
Characterization and Analysis of the Main Factors of Brittleness of Shale Oil Reservoirs in the Liushagang Formation, X Depression, Beibuwan Basin
by Fuqiang Lai, Yuejiao Liu, Mingzheng Tang, Chengxiang Zeng and Ruyue Wang
Minerals 2024, 14(9), 958; https://doi.org/10.3390/min14090958 - 23 Sep 2024
Viewed by 388
Abstract
The analysis of the main factors of brittleness is an important basis for the selection of engineering desserts in shale oil reservoirs. In this study, with the shale oil reservoir of the Liushagang Formation in the X Depression of the Beibuwan Basin as [...] Read more.
The analysis of the main factors of brittleness is an important basis for the selection of engineering desserts in shale oil reservoirs. In this study, with the shale oil reservoir of the Liushagang Formation in the X Depression of the Beibuwan Basin as the research object, a characterization and analysis of the main factors of brittleness of the reservoir was performed in order to further reveal the brittleness of shale reservoirs in the study area. The brittleness of reservoirs in the study area was controlled by both internal and external factors, and the main factors of brittleness in the target section included the maturity of organic matter, horizontal stress difference, and brittle minerals. As the maturity of organic matter increased, the density, elastic modulus, and hardness of casein increased and the differentially hardened internal structure occurred and significantly affected brittleness. The mineral composition of the reservoir was characterized by complex mineral types and high contents of brittle minerals, and the minerals determining brittleness were mainly quartz, feldspar, calcite, and dolomite. The horizontal stress difference of the shale oil section was relatively small and contributed to fracturing and reforming. This study clarified the brittleness characteristics of E2l shale and its main factors, and provided a basis for the selection of shale formation geo-engineering dessert layers in the study area. Full article
(This article belongs to the Special Issue Distribution and Development of Faults and Fractures in Shales)
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<p>Tectonic position, section, and stratigraphic histogram of the X Depression: (<b>a</b>) Location of the study area. (<b>b</b>) Structure of the study area. (<b>c</b>) Stratigraphic column of the study area.</p>
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<p>Inversion process of the double-skeleton mineral model of the reservoir.</p>
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<p>Flow chart of extracting the linear density of laminations from electro-imaging logging images.</p>
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<p>Whole-rock mineral and clay mineral analysis.</p>
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<p>Comparison of mineral fractions identified in the shale in Well Wa.</p>
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<p>Lamination identification and parameter extraction in Well Wa.</p>
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<p>Calculation results of fracture development index of Well Wa.</p>
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<p>Comparison of logging curve regression analysis and model calculation: (<b>a</b>) Correlation analysis of <span class="html-italic">Ro-Measured</span> and <span class="html-italic">AC</span> (acoustic logging). (<b>b</b>) Correlation analysis of <span class="html-italic">Ro-Measured</span> and <span class="html-italic">DEN</span> (density logging). (<b>c</b>) Correlation analysis of <span class="html-italic">Ro-Measured</span> and <span class="html-italic">GR</span> (gamma logging). (<b>d</b>) Correlation analysis of <span class="html-italic">Ro-Measured</span> and <span class="html-italic">RT</span> (resistivity logging). (<b>e</b>) Correlation analysis of <span class="html-italic">Ro-Measured</span> and <span class="html-italic">CNL</span> (neutron logging). (<b>f</b>) Correlation analysis of <span class="html-italic">Ro-Calculated</span> values and <span class="html-italic">Ro-Measured</span> values.</p>
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<p>Plot of the calculation results of horizontal stress in Well Wa.</p>
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<p>Plot of rock brittleness with Young’s modulus and Poisson’s ratio [<a href="#B44-minerals-14-00958" class="html-bibr">44</a>].</p>
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<p>Matrix of the correlation coefficients between Young’s modulus and control factors of brittleness: (<b>a</b>) Distribution characteristics of parameter values. (<b>b</b>) Correlation matrix between parameters.</p>
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<p>Core casting thin sections. (<b>a</b>) Section at the depth of 2978 m mainly composed of mud mixed with chalky quartz and other detrital particles. Granular pyrite was scattered or aggregated along the laminations and the size of most of particles was small. (<b>b</b>) Section at the depth of 2986 m mainly composed of mud. Granular pyrite was widely distributed; (<b>c</b>) Section at the depth of 2992 m. Granular pyrite was widely distributed and the particle size was small. Rhombic crystals of iron dolomite were occasionally observed. (<b>d</b>) Section at the depth of 3010 m. Rhombic crystals of iron dolomite were observed and a small quantity of granular pyrite existed. (<b>e</b>) Section at the depth of 3028 m. Detrital particles were mainly silt as well as some fine sand, and bituminous organic matter filled the intergranular space. Mud rhodonite aggregates showed an uneven distribution and pyrite was not observed; (<b>f</b>) Section at the depth of 3058 m mainly composed of muddy rock. Siltstone clast was not observed. A widespread moldy granular rhodonitization was observed.</p>
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<p>Correlation analysis between the maturity of organic matter and Young’s modulus.</p>
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15 pages, 1398 KiB  
Article
Antineoplastic Activity of Sodium Caseinate in a Cytarabine-Resistant Mouse Acute Myeloid Leukemia Cell Line
by Itzen Aguiñiga-Sánchez, Edgar Ledesma-Martínez, Mariana Vázquez-Guerrero, David Hernández-Álvarez, Amanda Velasco-García, Katia Michell Rodríguez-Terán, Daniel Romero-Trejo, Víctor Manuel Mendoza-Núñez, Víctor Manuel Macías-Zaragoza and Edelmiro Santiago-Osorio
Nutrients 2024, 16(18), 3190; https://doi.org/10.3390/nu16183190 - 20 Sep 2024
Viewed by 709
Abstract
Background: Acute myeloid leukemia (AML) is a hematological neoplasm of rapid and progressive onset, and is the most common form of leukemia in adults. Chemoresistance to conventional treatments such as cytarabine (Ara-C) and daunorubicin is a main cause of relapse, recurrence, metastasis, and [...] Read more.
Background: Acute myeloid leukemia (AML) is a hematological neoplasm of rapid and progressive onset, and is the most common form of leukemia in adults. Chemoresistance to conventional treatments such as cytarabine (Ara-C) and daunorubicin is a main cause of relapse, recurrence, metastasis, and high mortality in AML patients. It is known that sodium caseinate (SC), a salt derived from casein, a milk protein, inhibits growth and induces apoptosis in acute myeloid leukemia cells but not in normal hematopoietic cells. However, it is unknown whether SC retains its antileukemic effect in cytarabine-resistant AML cell lines. Objective: To evaluate the antineoplastic effect of SC in cytarabine-resistant leukemia models. Methods: The SC inhibits the growth and induces apoptosis in parental WEHI-3 AML cells. Here, we generated two cytarabine-resistant sublines, WEHI-CR25 and WEHI-CR50, which exhibit 6- and 16-fold increased resistance to cytarabine, respectively, compared to the parental WEHI-3 cells. Thus, these sublines mimic a chemoresistant model. Results: We demonstrate that WEHI-CR25 and WEHI-CR50 cells retain sensitivity to SC, similar to parental WEHI-3 cells. This sensitivity results in inhibited cell proliferation, induced apoptosis, and increased expression of ENT1 and dCK, molecules involved in the entry and metabolism of Ara-C, while decreasing MDR1 expression. Additionally, we observed that SC prolonged the survival of WEHI-CR50 tumor-bearing mice, despite their resistance to Ara-C. Conclusion: This is the first evidence that SC, a milk protein, may inhibit proliferation and induce apoptosis in cytarabine-resistant cells. Full article
(This article belongs to the Section Proteins and Amino Acids)
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<p>Cytarabine (Ara-C) inhibits the proliferation of parental WEHI-3 cells in a dose-dependent manner. The proliferation of 2 × 10<sup>4</sup>/mL parental WEHI-3 cells, treated with different of cytarabine (Ara-C) for 72 h was evaluated using the MTS assay. Data are presented as means ± SDs from three independent experiments performed in quadruplicate. Statistical significance was determined using one-way ANOVA followed by Tukey’s post hoc test. Significance levels are indicated as * <span class="html-italic">p</span> &lt; 0.05, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Workflow for generating the WEHI-CR25 and WEHI-CR50 cell sublines resistant to Ara-C. This figure illustrates the process for developing cytarabine-resistant sublines, derived from the parental WEHI-3 cells.</p>
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<p>Effect of cytarabine on parental WEHI-3, WEHI-CR25 and WEHI-CR50 cells. (<b>A</b>) Photographs from a representative experiment showing parental WEHI-3, WEHI-CR25 and WEHI-CR50 cells in the absence or presence of cytarabine. (<b>B</b>) Number of cells in the parental and resistant sublines treated with PBS or cytarabine (Ara-C, 197 nM). The initial cellular density for all conditions was 2 × 10<sup>4</sup>/mL. Data are presented as means ± SDs from three independent experiments conducted in quadruplicate. Statistical significance was determined using one-way ANOVA followed by Tukey’s post hoc test, with * <span class="html-italic">p</span> &lt; 0.05 indicating significance.</p>
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<p>Expression of genes related to cytarabine resistance in the WEHI-CR25 and WEHI-CR50 cells. (<b>A</b>) Real-time RT-PCR expression analysis of ENT1. (<b>B</b>) dCK. (<b>C</b>) MDR1 and (<b>D</b>) MRP1 (all data represent the Fold-Change mean value of mRNA expression of three independent measurements). The results were analyzed using one-way ANOVA followed by Tukey’s post hoc test (* <span class="html-italic">p</span> &lt; 0.05). Abbreviations: ENT1, equilibrium nucleoside transporter 1; dCK, deoxycytidine kinase; MRP1, multidrug resistance protein 1; MDR1, multidrug resistance gene 1; ns, not significant.</p>
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<p>Antiproliferative effect of sodium caseinate on parental WEHI-3, WEHI-CR25, and WEHI-CR50 cells. Proliferation curves of parental WEHI-3 cells and cytarabine-resistant WEHI-CR25 and WEHI-CR50 cells exposed to increasing concentrations of sodium caseinate, as assessed by the crystal violet staining technique. Data are presented as means ± SDs from three independent experiments performed in quadruplicate. Statistical significance was determined using two-way ANOVA followed by Tukey’s post hoc test with respect to the control groups (* <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Expression levels of mRNAs related to cytarabine resistance in WEHI-CR50 cells treated with sodium caseinate. mRNA expression analysis of ENT1, dCK, MRP1, and MDR1 in WEHI-CR50 cells treated with sodium caseinate or phosphate-buffered saline (PBS) (negative control) for 72 h. β-actin was used as a housekeeping gene for quantification and normalization of the expression of resistance-associated genes, determined using the 2<sup>^ΔΔ</sup>Cq method. Data are presented as means ± SDs from three independent experiments. Statistical significance was assessed using Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05). Abbreviations: ENT1, equilibrium nucleoside transporter 1; dCK, deoxycytidine kinase; MRP1, multidrug resistance protein 1; MDR1, multidrug resistance gene 1.</p>
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<p>The treatment with SC regulates the expression of proteins related to cytarabine resistance. Representative images of confocal microscopy against ENT1 and dCK (<b>left panel</b>); nuclei stained with DAPI (<b>middle panel</b>); and merged images (<b>right panel</b>). Scale bar 50 µm. Abbreviations: ENT1, equilibrium nucleoside transporter 1; dCK, deoxycytidine kinase; DAPI, 4′,6-diamidino-2-phenylindole.</p>
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<p>Apoptosis assay in WEHI-CR50 cells treated with sodium caseinate. (<b>A</b>) The distribution of WEHI-CR50 cells into early- and late-apoptosis groups, as well as the number of viable cells, was determined using flow cytometry with Annexin V-Phycoerythrin (PE) and 7-aminoactinomycin D (7-AAD) staining. (<b>B</b>) The percentage of total apoptosis (including both early and late stages) in WEHI-CR50 cells treated with sodium caseinate (SC) or phosphate-buffered saline (PBS) for 72 h. Data are presented as means ± SDs from three independent experiments. Statistical significance was assessed using Student’s <span class="html-italic">t</span>-test (* <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of sodium caseinate on the survival of leukemic mice bearing parental WEHI-3 or WEHI-CR50 cells. Survival of BALB/c leukemic mice inoculated with either parental WEHI-3 or WEHI-CR50 cells and treated with 1 mL of vehicle (parental WEHI-3 + PBS) or SC at doses of 2 and 4 g/kg (parental WEHI-3 + SC 2 g/kg, WEHI-CR50 + SC 2 g/kg or WEHI-CR50 + SC 4 g/kg) administered every 48 h. Healthy mice (no WEHI cells), parental WEHI-3 mice (inoculated with WEHI-3), and WEHI-CR50 mice (inoculated with WEHI-CR50) served as controls. Survival curves were generated using Kaplan–Meier analysis. Statistical significance was assessed using the Wilcoxon test with comparisons with parental WEHI-3 + PBS and WEHI-CR50 + PBS.</p>
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10 pages, 250 KiB  
Review
Preventing Dental Caries with Calcium-Based Materials: A Concise Review
by Jieyi Chen, Yuqing Zhang, Iris Xiaoxue Yin, Ollie Yiru Yu, Alice Kit Ying Chan and Chun Hung Chu
Inorganics 2024, 12(9), 253; https://doi.org/10.3390/inorganics12090253 - 19 Sep 2024
Viewed by 982
Abstract
This concise review provides an update on the use of calcium-based materials for the prevention of dental caries. Some calcium-based materials promote remineralization and neutralize bacterial acids, disrupting cariogenic biofilms and inhibiting bacterial growth. Medical Subject Headings of [Dental Caries] and [Calcium] were [...] Read more.
This concise review provides an update on the use of calcium-based materials for the prevention of dental caries. Some calcium-based materials promote remineralization and neutralize bacterial acids, disrupting cariogenic biofilms and inhibiting bacterial growth. Medical Subject Headings of [Dental Caries] and [Calcium] were adopted to search publications. Information related to the aim of this review was extracted and summarized. Common calcium-based materials are calcium phosphate, hydroxyapatite, calcium carbonate, calcium fluoride and casein phosphopeptide–amorphous calcium phosphate (CPP-ACP). Calcium phosphate is commonly used in toothpaste. It provides calcium and phosphate ions, enhances the incorporation of fluoride into caries lesions and increases mineral density. Hydroxyapatite is a form of calcium phosphate that is chemically similar to the mineral found in teeth. It can be applied on teeth to prevent caries. Calcium carbonate can be found in toothpastes. It neutralizes bacterial acids and acts as a calcium reservoir during remineralization. Calcium fluoride is found in dental products and promotes remineralization as a source of fluoride, which can be incorporated into tooth enamel, forming fluorapatite and increasing resistance to caries. CPP-ACP is derived from milk proteins. It contains calcium and phosphate, which help to remineralize tooth enamel. CPP-ACP inhibits cariogenic bacteria. It also interacts with bacterial biofilms and disrupts their formation. These calcium-based materials can be used to boost the preventive effect of fluorides or, alternatively, as a therapy for caries prevention. Full article
(This article belongs to the Special Issue Recent Research and Application of Amorphous Materials)
11 pages, 1266 KiB  
Article
Study on Single Nucleotide Polymorphism of LAP3 Gene and Its Correlation with Dairy Quality Traits of Gannan Yak
by Tong Wang, Xiaoming Ma, Fen Feng, Fei Zheng, Qingbo Zheng, Juanxiang Zhang, Minghao Zhang, Chaofan Ma, Jingying Deng, Xian Guo, Min Chu, Yongfu La, Pengjia Bao, Heping Pan, Chunnian Liang and Ping Yan
Foods 2024, 13(18), 2953; https://doi.org/10.3390/foods13182953 - 18 Sep 2024
Viewed by 435
Abstract
This study explored the polymorphism of the leucine aminopeptidase (LAP3) gene and its relationship with milk quality characteristics in Gannan yak. A cohort of 162 Gannan yak was genotyped utilizing the Illumina Yak cGPS 7K BeadChip, and the identified single nucleotide [...] Read more.
This study explored the polymorphism of the leucine aminopeptidase (LAP3) gene and its relationship with milk quality characteristics in Gannan yak. A cohort of 162 Gannan yak was genotyped utilizing the Illumina Yak cGPS 7K BeadChip, and the identified single nucleotide polymorphisms (SNPs) were evaluated for their association with milk protein, casein, lactose, and fat concentrations. The results showed that four SNPs (g.4494G > A, g.5919A > G, g.8033G > C, and g.15,615A > G) in the LAP3 gene exhibited polymorphism with information content values of 0.267, 0.267, 0.293, and 0.114, respectively. All four SNPs were in Hardy–Weinberg equilibrium (p > 0.05). The g.4494G > A and g.5919A > G SNPs were significantly associated with protein content (p < 0.05), with homozygous genotypes showing significantly higher protein content than heterozygous genotypes (p < 0.05). The g.8033G > C SNP was significantly associated with casein content, protein content, non-fat solids, and acidity (p < 0.05), with the CC genotype having significantly higher casein, protein, and non-fat solids content than the GG and GC genotypes (p < 0.05). The g.15,615A > G SNP was significantly associated with average fat globule diameter (p < 0.05). In general, the mutations within the LAP3 gene demonstrated a positive impact on milk quality traits in Gannan yak, with mutated genotypes correlating with enhanced milk quality. These results indicate that the LAP3 gene could be a significant or candidate gene affecting milk quality traits in Gannan yak and offer potential genetic markers for molecular breeding programs in this species. Full article
(This article belongs to the Section Dairy)
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<p>Distribution of SNP genotypes. (<b>A</b>): g.4494G &gt; A; (<b>B</b>): g.5919A &gt; G; (<b>C</b>–<b>F</b>): g.8033G &gt; C. The three different colored dots in the figure represent the distribution of genotype data, and the red line indicates the average value of the milk quality trait associated with the genotype.</p>
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<p>Linkage disequilibrium analysis among the four SNPs of LAP3 gene.</p>
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17 pages, 2005 KiB  
Review
An Overview of Interactions between Goat Milk Casein and Other Food Components: Polysaccharides, Polyphenols, and Metal Ions
by Bohan Ma, Majida Al-Wraikat, Qin Shu, Xi Yang and Yongfeng Liu
Foods 2024, 13(18), 2903; https://doi.org/10.3390/foods13182903 - 13 Sep 2024
Viewed by 642
Abstract
Casein is among the most abundant proteins in milk and has high nutritional value. Casein’s interactions with polysaccharides, polyphenols, and metal ions are important for regulating the functional properties and textural quality of dairy foods. To improve the functional properties of casein-based foods, [...] Read more.
Casein is among the most abundant proteins in milk and has high nutritional value. Casein’s interactions with polysaccharides, polyphenols, and metal ions are important for regulating the functional properties and textural quality of dairy foods. To improve the functional properties of casein-based foods, a deep understanding of the interaction mechanisms and the influencing factors between casein and other food components is required. This review started by elucidating the interaction mechanism of casein with polysaccharides, polyphenols, and metal ions. Thermodynamic incompatibility and attraction are the fundamental factors in determining the interaction types between casein and polysaccharides, which leads to different phase behaviors and microstructural types in casein-based foods. Additionally, the interaction of casein with polyphenols primarily occurs through non-covalent (hydrogen bonding, hydrophobic interactions, van der Waals forces, and ionic bonding) or covalent interaction (primarily based on the oxidation of proteins or polyphenols by enzymatic or non-enzymatic (alkaline or free radical grafting) approaches). Moreover, the selectivity of casein to specific metal ions is also introduced. Factors affecting the binding of casein to the above three components, such as temperature, pH, the mixing ratio, and the fine structure of these components, are also summarized to provide a good foundation for casein-based food applications. Full article
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<p>Phase behaviors and network structure of mixed milk casein and polysaccharides. (<b>a</b>) The schematic diagram of the phase transition in mixed casein/polysaccharides; (<b>b</b>) “water in water emulsion” structure of mixed casein and methylcellulose (MC) gels (8.0% casein + 0.2% MC), cited from Li et al. [<a href="#B19-foods-13-02903" class="html-bibr">19</a>] with permission from Elsevier.</p>
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<p>Main categories and chemical structures of fruit and vegetable phenolics.</p>
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<p>Non-covalent conjugation of casein and polyphenol and protein cross-linking via (<b>a</b>) hydrogen bonding, (<b>b</b>) hydrophobic-hydrophobic interaction, and (<b>c</b>) ionic interaction adopted from Quan et al. [<a href="#B51-foods-13-02903" class="html-bibr">51</a>].</p>
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<p>Covalent conjugation of casein and polyphenol and protein cross-links via (<b>a</b>) alkaline, (<b>b</b>) enzymatic, and (<b>c</b>) free-radical grafting reactions adopted from Quan et al. [<a href="#B51-foods-13-02903" class="html-bibr">51</a>].</p>
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<p>The (<b>a</b>) multidentate and (<b>b</b>) monodentate mechanism of protein-polyphenol interaction adopted from Günal-Köroğlu et al. [<a href="#B42-foods-13-02903" class="html-bibr">42</a>].</p>
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12 pages, 279 KiB  
Article
Fortification of Goat Milk Yogurts with Encapsulated Postbiotic Active Lactococci
by Andrea Lauková, Marián Maďar, Natália Zábolyová, Aleksandra Troscianczyk and Monika Pogány Simonová
Life 2024, 14(9), 1147; https://doi.org/10.3390/life14091147 - 11 Sep 2024
Viewed by 484
Abstract
The species Lactococcus lactis is a bacterium extensively used in the dairy industry. This bacterium is Generally Recognized as Safe and was added to the European Food Safety Authority’s Qualified Presumption of Safety list. The major functions of this species in dairy fermentation [...] Read more.
The species Lactococcus lactis is a bacterium extensively used in the dairy industry. This bacterium is Generally Recognized as Safe and was added to the European Food Safety Authority’s Qualified Presumption of Safety list. The major functions of this species in dairy fermentation are the production of lactic acid from lactose, citric acid fermentation, and the hydrolysis of casein. But, the representatives of this species that produce bacteriocin substances can also exert an inhibitory effect against spoilage bacteria. The aims of this study were to test three lactococcal strains isolated from raw goat milk for their postbiotic activity and to test their stability in goat milk yogurts after their application in encapsulated form for their further application. To achieve these aims, validated methods were used. Three Lactococcus lactis strains (identified by Blastn 16S rRNA analysis) produced bacteriocin substances/postbiotics. These concentrated postbiotics inhibited the growth of enterococci and staphylococci (by up to 97.8%), reaching an inhibitory activity of up to 800 AU/mL. The encapsulated (freeze-dried) lactococci survived in the goat milk yogurts with sufficient stability. Strain MK2/8 fortified the yogurts in the highest amount (8.1 ± 0.0 cfu/g log 10). It did not influence the pH of the yogurt. Full article
(This article belongs to the Special Issue Food Microbiological Contamination)
16 pages, 5616 KiB  
Article
Evaluation of Different Formulations on the Viability of Phages for Use in Agriculture
by Marcela León, Jorge Araya, Mauricio Nuñez, Manuel Arce, Fanny Guzmán, Carolina Yáñez, Ximena Besoain and Roberto Bastías
Viruses 2024, 16(9), 1430; https://doi.org/10.3390/v16091430 - 7 Sep 2024
Viewed by 703
Abstract
Bacteriophages have been proposed as biological controllers to protect plants against different bacterial pathogens. In this scenario, one of the main challenges is the low viability of phages in plants and under adverse environmental conditions. This work explores the use of 12 compounds [...] Read more.
Bacteriophages have been proposed as biological controllers to protect plants against different bacterial pathogens. In this scenario, one of the main challenges is the low viability of phages in plants and under adverse environmental conditions. This work explores the use of 12 compounds and 14 different formulations to increase the viability of a phage mixture that demonstrated biocontrol capacity against Pseudomonas syringae pv. actinidiae (Psa) in kiwi plants. The results showed that the viability of the phage mixture decreases at 44 °C, at a pH lower than 4, and under UV radiation. However, using excipients such as skim milk, casein, and glutamic acid can prevent the viability loss of the phages under these conditions. Likewise, it was demonstrated that the use of these compounds prolongs the presence of phages in kiwi plants from 48 h to at least 96 h. In addition, it was observed that phages remained stable for seven weeks when stored in powder with skim milk, casein, or sucrose after lyophilization and at 4 °C. Finally, the phages with glutamic acid, sucrose, or skim milk maintained their antimicrobial activity against Psa on kiwi leaves and persisted within kiwi plants when added through roots. This study contributes to overcoming the challenges associated with the use of phages as biological controllers in agriculture. Full article
(This article belongs to the Special Issue Bacteriophage-Based Biocontrol in Agriculture, 2nd Edition)
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<p>Viability of phages at different temperatures, pH, and UV radiation. The phage mixture in distilled water was incubated under different environmental conditions. (<b>A</b>) The concentration of phages after 1 h incubation in distilled water at the corresponding temperature. (<b>B</b>) The concentration of phages after 1 h incubation in distilled water was adjusted at the corresponding pH at 25 °C. (<b>C</b>) The concentration of phages after incubation in distilled water under UV radiation in a laminar flow hood for 0, 15, 30, or 60 min at 25 °C. The experiments were performed in triplicate, and the standard deviation bars are shown. Statistical analysis was performed using a 2-way ANOVA. The different letters in the bars indicate statistical differences (<span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Viability of phages in different excipients under different environmental conditions. The mix of phages in the different excipients was incubated under different environmental conditions of temperature (<b>A</b>), pH (<b>B</b>), and exposition to UV radiation (<b>C</b>). The experiments were performed in triplicate, and the standard deviation is shown. The detection limit of the assay was 100 PFU/mL. Error bars represent the standard deviation. Statistical analysis was performed using a 2-way ANOVA. Symbols denote significant differences (*: <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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<p>Viability of phages with the different excipients in kiwi plants. (<b>A</b>) The concentration of phages with the different excipients recovered from kiwi leaves at the corresponding time. Samples were collected throughout the experiment, and the points where no phage was detected were not plotted. The experiment detection point was 100 PFU/mL. (<b>B</b>) Concentration of phages per gram of leaf 96 h post-application with the different excipients. Phages were applied manually by aspersion with four replicates per treatment. Kiwi plants that did not receive treatment were used as controls to discard the presence of native phages. The error bars represent the standard deviation.</p>
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<p>Impact of the lyophilization process on the viability of phages with the different excipients. The concentration of phages lyophilized and non-lyophilized with the different excipients was determined. The detection limit of the technique was 100 PFU/mL. The experiments were performed in triplicate, and the standard deviation is shown. Error bars represent the standard deviation. Statistical analysis was performed using a 2-way ANOVA. Symbols denote significant differences (ns: not significant; *: <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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<p>Viability of phages stored under different conditions after seven weeks. Phages were stored in liquid and solid conditions as a powder (lyophilized) at 4 °C and 25 °C for seven weeks with the different excipients evaluated. The titer of phages was normalized as a percentage of the initial titer. A segmented line represents 100%. Assays were performed in triplicate; error bars represent the standard deviation.</p>
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<p>Persistence of phages with different excipients in kiwi plants. (<b>A</b>) Quantification of phages from kiwi plant leaves after inoculation in soil roots with the corresponding excipients. The detection limit of this assay was 200 PFU/g. (<b>B</b>) Detection of phages with enrichment with Psa 889 in kiwi plants after inoculation in soil roots. All experiments were performed in triplicate. Error bars represent the standard deviation. Statistical differences are presented (*: <span class="html-italic">p</span> &lt; 0.05).</p>
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30 pages, 1045 KiB  
Review
Cow’s Milk Bioactive Molecules in the Regulation of Glucose Homeostasis in Human and Animal Studies
by Emad Yuzbashian, Emily Berg, Stepheny C. de Campos Zani and Catherine B. Chan
Foods 2024, 13(17), 2837; https://doi.org/10.3390/foods13172837 - 6 Sep 2024
Viewed by 1464
Abstract
Obesity disrupts glucose metabolism, leading to insulin resistance (IR) and cardiometabolic diseases. Consumption of cow’s milk and other dairy products may influence glucose metabolism. Within the complex matrix of cow’s milk, various carbohydrates, lipids, and peptides act as bioactive molecules to alter human [...] Read more.
Obesity disrupts glucose metabolism, leading to insulin resistance (IR) and cardiometabolic diseases. Consumption of cow’s milk and other dairy products may influence glucose metabolism. Within the complex matrix of cow’s milk, various carbohydrates, lipids, and peptides act as bioactive molecules to alter human metabolism. Here, we summarize data from human studies and rodent experiments illustrating how these bioactive molecules regulate insulin and glucose homeostasis, supplemented with in vitro studies of the mechanisms behind their effects. Bioactive carbohydrates, including lactose, galactose, and oligosaccharides, generally reduce hyperglycemia, possibly by preventing gut microbiota dysbiosis. Milk-derived lipids of the milk fat globular membrane improve activation of insulin signaling pathways in animal trials but seem to have little impact on glycemia in human studies. However, other lipids produced by ruminants, including polar lipids, odd-chain, trans-, and branched-chain fatty acids, produce neutral or contradictory effects on glucose metabolism. Bioactive peptides derived from whey and casein may exert their effects both directly through their insulinotropic effects or renin-angiotensin-aldosterone system inhibition and indirectly by the regulation of incretin hormones. Overall, the results bolster many observational studies in humans and suggest that cow’s milk intake reduces the risk of, and can perhaps be used in treating, metabolic disorders. However, the mechanisms of action for most bioactive compounds in milk are still largely undiscovered. Full article
(This article belongs to the Section Dairy)
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<p>A summary of the evidence that bioactive compounds from milk can regulate glucose homeostasis. Abbreviations: BW, body weight; GTT, glucose tolerance test; IR, insulin resistance; AKT, protein kinase B; FBG, fasting blood (plasma) glucose; FM, fat mass; GLUT4, glucose transporter-4. Created with BioRender.com (accessed on 30 August 2024).</p>
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