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Search Results (407)

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22 pages, 1503 KiB  
Article
Effect of Chickpea (Cicer arietinum L.) Flour Incorporation on Quality, Antioxidant Properties, and Bioactive Compounds of Shortbread Cookies
by Katarzyna Felisiak, Sylwia Przybylska, Grzegorz Tokarczyk, Małgorzata Tabaszewska, Jacek Słupski and Joanna Wydurska
Foods 2024, 13(15), 2356; https://doi.org/10.3390/foods13152356 - 26 Jul 2024
Viewed by 624
Abstract
High nutritional value and antioxidant properties make chickpea flour a valuable substitute for wheat flour, although its texture-forming abilities are different. The aim of this study was to investigate the possibility of increasing the content of bioactive compounds and antioxidant properties of shortbread [...] Read more.
High nutritional value and antioxidant properties make chickpea flour a valuable substitute for wheat flour, although its texture-forming abilities are different. The aim of this study was to investigate the possibility of increasing the content of bioactive compounds and antioxidant properties of shortbread cookies by simple partial or complete replacement of wheat flour with chickpea flour without considerable changes in texture, color, sensory properties, or acceptability. Shortbread cookies were made from wheat flour (0% of chickpea flour), wheat flour and chickpea flour (replacement of 25%, 50%, and 75%), and chickpea flour (100%). Generally, the increase in chickpea flour share resulted in an increase in protein, fat, and ash content, as well as antioxidant properties. Polyphenol content, flavonoid content, and antioxidant activities increased three- to sixfold in shortbread cookies containing chickpea flour in comparison to wheat cookies. The level of proteins increased about 50% and the antioxidant properties were three to six times higher than in wheat cookies. Cookies containing up to 75% chickpea flour were assessed as very good or good quality, while only cookies without wheat flour were assessed as sufficient quality. It could be concluded that part of the wheat flour content in shortbread cookies can be replaced by chickpea flour. Application of a 25% proportion of chickpea flour increases physicochemical properties without changes in sensory properties. Sensory quality was up to 75% lower, but antioxidant properties were increased. However, complete replacement of wheat flour in shortbread cookies without changing the recipe resulted in a product of slightly lower sensory quality. Full article
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Graphical abstract

Graphical abstract
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<p>Effect of chickpea flour on the appearance and color of shortbread cookies (share of chickpea flour: S0—0%, S25—25%, S50—50%, S75—75%, S100—100%). Photo J. Wydurska.</p>
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<p>Taste sensory profile of shortbread cookies without and with chickpea flour.</p>
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<p>Odor sensory profile of shortbread cookies without and with chickpea flour.</p>
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<p>PCA biplot of the first two principal components for antioxidant activity, sensory assessment, hardness, color parameters, and shortbread cookie components and component distribution. TPC—total phenolic compound; TFC—total flavonoid compound; TC—total carotenoids; TEAC—Trolox equivalent antioxidant capacity; FRAP—ferric reducing antioxidant power; RSA—radical scavenging ability; FCA—ferrous chelating ability; Sens. a.—sensory assessment; <span class="html-italic">L</span>*—lightness, BI—browning index. * additional variables.</p>
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12 pages, 1379 KiB  
Article
Coffee Silverskin as a Fat Replacer in Chicken Patty Formulation and Its Effect on Physicochemical, Textural, and Sensory Properties
by İzzet Özhamamcı
Appl. Sci. 2024, 14(15), 6442; https://doi.org/10.3390/app14156442 - 24 Jul 2024
Viewed by 357
Abstract
Coffee silverskin (CSS) is a by-product released as waste after roasting coffee beans. This by-product can be used as a functional food ingredient as it contains many valuable compounds such as fibers, sugars, phenolic acids, carotenoids, and flavonoids. In this research, the effects [...] Read more.
Coffee silverskin (CSS) is a by-product released as waste after roasting coffee beans. This by-product can be used as a functional food ingredient as it contains many valuable compounds such as fibers, sugars, phenolic acids, carotenoids, and flavonoids. In this research, the effects of the partial substitution of animal fat with CSS on physicochemical, textural, and sensory properties in chicken patty production were investigated. For this purpose, four different groups of chicken patties were produced in which animal fat was replaced with CSS at different rates (control: 12% fat, SS1: 10% fat + 2% silverskin, SS2: 8% fat + 4% silverskin, SS3: 6% fat + 6% silverskin). The substitution of animal fat with CSS resulted in decreases in pH, moisture content, water activity, and color values while increasing TBARS (Thiobarbituric acid-reactive substances) and moisture retention. The cooking process also significantly affected the physicochemical properties (p < 0.01). Textural parameters, apart from adhesiveness, were affected by the replacement of animal fat with CSS. While hardness increased compared to the control, resilience, and springiness decreased. On the other hand, cohesiveness was similar in control and SS1 but decreased in other ratios. The use of CSS affected all sensory characteristics, and the sensory evaluation scores closest to the control were determined in the group that used 2% CSS instead of animal fat. Full article
(This article belongs to the Section Food Science and Technology)
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<p>Ground and unground coffee silverskin.</p>
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<p>Cooked patty pamples physical appearance of cooked patties produced in different formulations (C: 12% animal fat, CSS1: 2% CSS+ 10% animal fat, CSS2: 4% CSS+ 8% animal fat, CSS3: 6% CSS+ 6% animal fat).</p>
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<p>Changes in pH values of chicken patties during the production stages (Control: 12% fat, SS1: 10% fat + 2% silverskin, SS2: 8% fat + 4% silverskin, SS3: 6% fat + 6% silverskin). a–c: Means marked with different letters in different formulations at the same production stage are statistically different from each other (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in moisture contents of chicken patties during the production stages (Control: 12% fat, SS1: 10% fat + 2% silverskin, SS2: 8% fat + 4% silverskin, SS3: 6% fat + 6% silverskin). a–c: Means marked with different letters in different formulations at the same production stage are statistically different from each other (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in color properties of chicken patties during the production stages (Control: 12% fat, SS1: 10% fat + 2% silverskin, SS2: 8% fat + 4% silverskin, SS3: 6% fat + 6% silverskin). a–d: Means marked with different letters in different formulations at the same production stage are statistically different from each other (<span class="html-italic">p</span> &lt; 0.05). (<b>a</b>) L*: represents the lightness values, (<b>b</b>) a*: represents the redness/greenness values, and (<b>c</b>) b*: represents the yellowness/blueness values.</p>
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23 pages, 21539 KiB  
Article
Fatty Acids and Volatile Flavor Components of Adipose Tissue from Local Tibetan Sheep in Qinghai with Dietary Supplementation of Palm Kernel Meal (PKM)
by Ying Ma, Lijuan Han, Shengzhen Hou, Linsheng Gui, Shengnan Sun, Zhenzhen Yuan, Chao Yang, Zhiyou Wang and Baochun Yang
Animals 2024, 14(14), 2113; https://doi.org/10.3390/ani14142113 - 20 Jul 2024
Viewed by 690
Abstract
Substituting traditional protein feed with palm kernel meal (PKM) in the diet of Tibetan sheep can be a cost-effective feeding strategy. To determine the impact of PKM on flavor development in different adipose tissues of Tibetan sheep, subjects were fed with 15% and [...] Read more.
Substituting traditional protein feed with palm kernel meal (PKM) in the diet of Tibetan sheep can be a cost-effective feeding strategy. To determine the impact of PKM on flavor development in different adipose tissues of Tibetan sheep, subjects were fed with 15% and 18% of PKM, while the control group received no PKM. The fatty acids and volatile compounds in the samples were then analyzed by GC-MS and HS-GC-IMS. Adding PKM to the diet significantly increased the C12:0, C14:0, C16:0 and C18:1N9 content in adipose tissues compared with the control, and most of these were associated with flavor formation (p < 0.05). The flavor compounds in the adipose tissues predominantly consisted of alcohols, ketones, acids and aldehydes. In particular, including PKM in the diet increased the proportion of ketones but decreased the proportion of alcohols, acids and aldehydes in subcutaneous and tail fat. Specifically, the proportion of acetone, acetoin monomer, 2,3-butanedione, 2-butanone monomer, 2-methyl-2-propanol, 2-methyl-2-propanol and methyl acetate increased significantly in the subcutaneous and tail fat (p < 0.05), while that of ethanol, 1-propanol monomer, butanol monomer, acetic acid monomer and acetic acid monomer decreased. Intermuscular fat exhibited variable results, mainly because the addition of PKM resulted in higher proportions of alcohols, including ethanol, 1-propanol and butanol monomer, especially at 15% PKM. In summary, the addition of PKM improved the flavor of Tibetan sheep fat and increased the amount of favorable volatile flavor compounds. This study can serve as reference for understanding the effects of dietary PKM on the adipose tissue flavor profile of Tibetan sheep. Full article
(This article belongs to the Special Issue Nutrients and Feed Additives in Ruminants)
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Figure 1
<p>FAs Composition and Content Comparison Box Plot ((<b>a</b>) subcutaneous fat, (<b>b</b>) tail fat, (<b>c</b>) intermuscular fat). * denotes significant difference between groups (<span class="html-italic">p</span> &lt; 0.05), ** denotes highly significant difference (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>FAs Composition and Content Comparison Box Plot ((<b>a</b>) 0% PKM, (<b>b</b>) 15% PKM, (<b>c</b>)18% PKM). * denotes significant difference between groups (<span class="html-italic">p</span> &lt; 0.05),** denotes highly significant difference (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>(<b>a</b>–<b>c</b>) graphs of PCA analysis of three adipose tissue samples, (<b>d</b>–<b>f</b>) fingerprints of VOCs substances; P: indicates subcutaneous fat, W: indicates tail fat, J: indicates intermuscular fat. Substances in the regions delineated by A, B and C in the figure have higher concentrations in their corresponding groups, e.g., substances in region A of the (<b>d</b>) figure have higher concentrations in the P0 group; each row of the graph represents all the signal peaks selected from one sample, and each column represents the signal peaks of the same VOCs in different samples; some substances are followed by -M and -D, which are the monomer and dimer of the same substance; the uncharacterizable substances are marked with arabic numerals (e.g., 1, 2, 3).</p>
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<p>Percentage composition of VOCs in adipose tissue for each group. (<b>a</b>) subcutaneous fat; (<b>b</b>) tail fat; (<b>c</b>) intermuscular fat. lowercase letters: Same lowercase letters indicate insignificant differences (<span class="html-italic">p</span> &gt; 0.05), different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). P: indicates subcutaneous fat, W: indicates tail fat, J: indicates intermuscular fat, the different colors of the bar graph represent different parts of adipose tissue under different levels of PKM.</p>
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<p>(<b>a</b>–<b>c</b>) graphs of PCA analysis of three adipose tissue samples, (<b>d</b>–<b>f</b>) fingerprints of VOCs substances; P: indicates subcutaneous fat, W: indicates tail fat, J: indicates intermuscular. Substances in the regions delineated by A, B and C in the figure have higher concentrations in their corresponding groups, e.g., substances in region A of the (<b>d</b>) figure have higher concentrations in the P0 group.</p>
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<p>Percentage composition of VOCs in adipose tissue for each group. (<b>a</b>) 0%; (<b>b</b>) 15%; (<b>c</b>) 18%. lowercase letters: Same lowercase letters indicate insignificant differences (<span class="html-italic">p</span> &gt; 0.05), different lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). P: indicates subcutaneous fat, W: indicates tail fat, J: indicates intermuscular fat, the different colors of the bar graph represent different parts of adipose tissue under the same level of PKM.</p>
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<p>Sample Hierarchical Cluster Analysis Plot. (<b>a</b>) 0% PKM; (<b>b</b>) 15% PKM; (<b>c</b>) 18% PKM; blue for intermuscular fat, green for subcutaneous fat, red for caudal fat.</p>
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<p>Correlation analysis chart of some fatty acids and VOCs substances, * represents significant correlation between FA and VOC (<span class="html-italic">p</span> &lt; 0.05); ** represents highly significant correlation between them (<span class="html-italic">p</span> &lt; 0.01).</p>
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19 pages, 1553 KiB  
Article
Chitosan-Based Oleogels: Emulsion Drying Kinetics and Physical, Rheological, and Textural Characteristics of Olive Oil Oleogels
by Mario Lama, Leticia Montes, Daniel Franco, Amaya Franco-Uría and Ramón Moreira
Mar. Drugs 2024, 22(7), 318; https://doi.org/10.3390/md22070318 - 17 Jul 2024
Viewed by 468
Abstract
Oleogels are of high interest as promising substitutes for trans fats in foods. An emulsion-templated method was used to trap olive oil in the chitosan crosslinked with vanillin matrix. Oil in water emulsions (50:50 w/w) with different chitosan content (0.7 [...] Read more.
Oleogels are of high interest as promising substitutes for trans fats in foods. An emulsion-templated method was used to trap olive oil in the chitosan crosslinked with vanillin matrix. Oil in water emulsions (50:50 w/w) with different chitosan content (0.7 and 0.8% w/w) with a constant vanillin/chitosan ratio (1.3) were air-dried at different temperatures (50, 60, 70, and 80 °C) and freeze-dried (−26 °C and 0.1 mbar) to produce oleogels. Only falling rate periods were determined during air-drying kinetics and were successfully modeled with empirical and diffusional models. At a drying temperature of 70 °C, the drying kinetics were the fastest. The viscoelasticity of oleogels showed that the elastic modulus significantly increased after drying at 60 and 70 °C, and those dried at 50 °C and freeze-dried were weaker. All oleogels showed high oil binding capacity (>91%), but the highest values (>97%) were obtained in oleogels with a threshold elastic modulus (50,000 Pa). The oleogels’ color depended on the drying temperature and chitosan content (independent of the drying method). Significant differences were observed between air-dried and freeze-dried oleogels with respect to oxidative stability. Oxidation increased with the air-drying time regardless of chitosan content. The found results indicated that drying conditions must be carefully selected to produce oleogels with specific features. Full article
(This article belongs to the Special Issue Marine Drugs Research in Spain 2nd Edition)
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<p>Drying kinetics (main plot) and specific drying rates (subplot) at different air temperatures (°C): 50 <span style="color:#002060">■</span>, 60 <span style="color:#00B050">♦</span>, 70 <span style="color:#ED7D31">▲</span>, 80 <span style="color:red">●</span> for 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content. Lines correspond to the Page model (main plot) and the diffusional model (subplot).</p>
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<p>Total color difference, Δ<span class="html-italic">E</span>, with moisture content, <span class="html-italic">X</span>, of emulsion at different air-drying temperatures (°C): 50 <span style="color:#002060">■</span>, 60 <span style="color:#00B050">♦</span>, 70 <span style="color:#ED7D31">▲</span>, 80 <span style="color:red">●</span> for chitosan content of (<b>a</b>) 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span>; (<b>b</b>) 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> (darker colors correspond to 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> and clearer ones to 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content).</p>
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<p>Elastic modulus, <span class="html-italic">G</span>′, trend with frequency, <span class="html-italic">f</span>, of oleogels formed from emulsion with 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan concentration, air-dried at several temperatures (°C): 50 ■, 60 <span style="color:#00B050">♦</span>, 70 <span style="color:#ED7D31">▲</span>, 80 <span style="color:red">●</span>, and freeze-dried: <span style="color:#7F7F7F">●</span>.</p>
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<p>Texture properties of tested oleogels. Dried samples at 50 °C (blue), 60 °C (green), 70 °C (orange), 80 °C (red), and freeze-dried (grey). Darker colors correspond to 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> and clearer ones to 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content. Different letters in error bars (a, b, c for 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content; A, B, C for 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among mean values at different temperatures according to Duncan’s test.</p>
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<p>Relationship between elastic modulus, <span class="html-italic">G</span>′, and oil binding capacity (<span class="html-italic">OBC</span>) of tested oleogels.</p>
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<p>Oxidation parameters for oleogels (conjugated dienes (<span class="html-italic">CD</span>, (<b>a</b>)) and trienes (<span class="html-italic">CT</span>, (<b>b</b>)), and peroxide index (<span class="html-italic">PI</span>, (<b>c</b>))). Dried samples at 50 °C (blue), 60 °C (green), 70 °C (orange), 80 °C (red), and freeze-dried (grey). Darker colors correspond to 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> and clearer ones to 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content. Different letters in error bars (a, b, c for 0.7% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content; A, B, C for 0.8% <span class="html-italic">w</span>/<span class="html-italic">w</span> chitosan content) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among mean values at different temperatures according to Duncan’s test.</p>
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18 pages, 4465 KiB  
Article
New Derivatives of Modified Starch for Food Technology
by Emilia Konował, Joanna Sulej-Chojnacka and Krystyna Prochaska
Molecules 2024, 29(14), 3292; https://doi.org/10.3390/molecules29143292 - 12 Jul 2024
Viewed by 405
Abstract
The food industry extensively uses chemically modified starches and their hydrolysates, which is mainly due to their emulsification ability. Therefore, it becomes inevitable to develop new starch derivatives, including modified starch hydrolysates, and effective preparation methods to meet the increasing demands of producers, [...] Read more.
The food industry extensively uses chemically modified starches and their hydrolysates, which is mainly due to their emulsification ability. Therefore, it becomes inevitable to develop new starch derivatives, including modified starch hydrolysates, and effective preparation methods to meet the increasing demands of producers, consumers, and technology. This study comprehensively researches the physical, chemical, and functional properties (such as the water-binding capacity, swelling power, solubility, and fat absorption capacity) of chemically modified biopolymers and their enzymatic hydrolysis products. We utilized oxidized and acetylated potato and waxy-corn starches with varying degrees of substitution by carboxyl and acetyl groups in our research. The process of enzymatic hydrolysis was performed in a recirculated membrane reactor (CRMR). Our findings indicated that the physicochemical properties of starch derivatives and their hydrolysates depended on the biological origin of the biopolymer and the type and degree of modification. However, the presence of carboxyl groups in the modified starch molecules is critical and affects the rheological properties and water-binding capacity of the starch preparations. For example, in the case of waxy-corn starch preparations with a lower content of carboxyl groups (i.e., derivatives with a low degree of oxidation), the water-binding capacity (WBC) increases when compared to native starch. The highest WBC value of 206.3% was noted for the doubly modified waxy-corn starch with an oxidation degree of 0.2% and an acetylation degree of 2.5%, while native waxy-corn starch shows a WBC of 161.4%. In contrast, it was observed that preparations with a higher content of carboxyl groups, i.e., derivatives with an oxidation degree of 2.5%, show a lower swelling power compared to native waxy starch. Full article
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<p>FT-IR spectra of acetylated starch and oxidized starch derived from (<b>A</b>) potato, (<b>B</b>) waxy-corn.</p>
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<p>Micrographs of starch granules (magnitude ×4000): (<b>A</b>) native waxy-corn starch, (<b>B</b>) C-0.2Ox-0.5Ac, (<b>C</b>) C-2.5Ox-0.5Ac, (<b>D</b>) C-0.2Ox-2.5Ac, (<b>E</b>) C-2.5Ox-2.5Ac and micrographs of starch granules (magnitude ×1000): (<b>F</b>) native potato starch, (<b>G</b>) P-0.2Ox-0.5Ac, (<b>H</b>) P-2.5Ox-0.5Ac.</p>
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<p>Flow curves of (<b>A</b>) native waxy-corn starch, (<b>B</b>) C-0.2Ox-0.5Ac, (<b>C</b>) C-2.5Ox-0.5Ac, (<b>D</b>) C-0.2Ox-2.5Ac, (<b>E</b>) C-2.5Ox-2.5Ac at temperature: ♦ 30, ■ 40, ▲ 60 and ● 75 °C.</p>
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<p>Change in the value of glucose equivalent (<b>A</b>) and dry substance content (<b>B</b>) over time for the hydrolysis products of waxy-corn starch derivatives.</p>
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<p>Change in the value of glucose equivalent (<b>A</b>,<b>C</b>) and dry matter content (<b>B</b>,<b>D</b>) over time for the hydrolysis products of potato starch derivatives.</p>
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<p>The fat absorption capacity of starch hydrolysates of potato starch and waxy-corn starch.</p>
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<p>The binding capacity of water of waxy-corn starch and modified starches.</p>
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<p>The swelling force of native waxy-corn starch and starch modified at various temperatures.</p>
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<p>The solubility of native waxy-corn starch and starch modified at various temperatures.</p>
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<p>(<b>A</b>) Recirculated membrane reactor: 1—reactor tank, 2—circulation pump, 3—power inverter, 4—UF module, 5—pipelines, 6—cooler, 7—manometer, 8—thermometer, 17—rotameter, 18—bypass, K1 ÷ K7—stubs, Z9 ÷ Z16—valves; (<b>B</b>) reaction of obtaining acetylated oxidized starch.</p>
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25 pages, 7878 KiB  
Review
Management of Metabolic-Associated Fatty Liver Disease/Metabolic Dysfunction-Associated Steatotic Liver Disease: From Medication Therapy to Nutritional Interventions
by Mohammad Beygi, Salma Ahi, Samaneh Zolghadri and Agata Stanek
Nutrients 2024, 16(14), 2220; https://doi.org/10.3390/nu16142220 - 11 Jul 2024
Viewed by 1108
Abstract
Non-alcoholic fatty liver disease (NAFLD) is a common long-lasting liver disease that affects millions of people around the world. It is best identified with a hepatic fat build-up that ultimately leads to inflammation and damage. The classification and nomenclature of NAFLD have long [...] Read more.
Non-alcoholic fatty liver disease (NAFLD) is a common long-lasting liver disease that affects millions of people around the world. It is best identified with a hepatic fat build-up that ultimately leads to inflammation and damage. The classification and nomenclature of NAFLD have long been a controversial topic, until 2020 when a group of international experts recommended substituting NAFLD with MAFLD (metabolic dysfunction-associated FLD). MAFLD was then terminologically complemented in 2023 by altering it to MASLD, i.e., metabolic dysfunction-associated steatotic liver disease (MASLD). Both the MAFLD and the MASLD terminologies comprise the metabolic element of the disorder, as they offer diagnostic benchmarks that are embedded in the metabolic risk factors that underlie the disease. MASLD (as a multisystemic disease) provides a comprehensive definition that includes a larger population of patients who are at risk of liver morbidity and mortality, as well as adverse cardiovascular and diabetes outcomes. MASLD highlights metabolic risks in lean or normal weight individuals, a factor that has not been accentuated or discussed in previous guidelines. Novel antihyperglycemic agents, anti-hyperlipidemic drugs, lifestyle modifications, nutritional interventions, and exercise therapies have not been extensively studied in MAFLD and MASLD. Nutrition plays a vital role in managing both conditions, where centralizing on a diet rich in whole vegetables, fruits, foods, healthy fats, lean proteins, and specific nutrients (e.g., omega-3 fatty acids and fibers) can improve insulin resistance and reduce inflammation. Thus, it is essential to understand the role of nutrition in managing these conditions and to work with patients to develop an individualized plan for optimal health. This review discusses prevention strategies for NAFLD/MAFLD/MASLD management, with particular attention to nutrition and lifestyle correction. Full article
(This article belongs to the Special Issue Diet, Oxidative Stress and Liver Metabolism)
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<p>Therapy plans for MAFLD/MASLD management.</p>
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<p>Effects of KD (i.e., consuming more fat and protein instead of carbohydrates) on the incidence and progression of hepatic conditions, compared to HFD and Chow. (<b>A</b>) Images taken from the liver sections (with scale bar = 100 μm), which are stained with H&amp;D, cleaved caspase 3, and Gom and mass (for fibrosis). As shown, marked hepatic inflammation, ballooning of hepatocytes, and fibrosis are visible in mice fed with KD, compared to other treatments. Further, apoptotic hepatocytes can be found in KD-fed mice, suggestive of “caspase 3” activation in hepatocytes. (<b>B</b>) Lipid profile (i.e., distribution of lipid species in the pool of upregulated lipids, compared to the total pool). Under various treatments (i.e., KD vs. HFD vs. Chow), it can be seen that triglycerides (TGs) are overrepresented (compared to other species), suggestive of marked effect of KD on TGs. (<b>C</b>) Liver sections (stained with oil red O or H&amp;S) (scale bar = 100 μm). As depicted, KD can potentially trigger IL-6 and JNK signaling pathway, which both are linked with glucose intolerance and HS. (KD: ketogenic diet; HFD: high-fat diet, IgG: immunoglobulin G; IL-6Ab: interleukin 6 antibody) [<a href="#B84-nutrients-16-02220" class="html-bibr">84</a>]. This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.</p>
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<p>Effects of KDR (ketogenic diet; with 89.5% F, 0.1% C, 10.4% P), NCR (fed control normal chow of KDR; with 10% F, 70% C, 20% P), KDH (ketogenic diet’ with 91.3% 1% C, 7.7% P), and NCH (fed control normal chow of KDH; with 15.5% F, 64.5% C, and 20% P) diets on hepatic parameters in male C57BL/6J mice. (<b>A</b>,<b>B</b>) KDR triggers insulin resistance and impaired glucose homeostasis, more severely than other diets. (<b>C</b>,<b>D</b>) Hematoxylin and eosin (H&amp;S) staining of the liver and epididymal adipose tissue (eAT) section and adipocyte area, implying higher scores of NAFLD and adipocyte size in mice fed with KDR and KDH (than NCH and NCR); these scores are higher in KDH than in KDR. F: Fat; C: Carbohydrates; P: Protein. (** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001) [<a href="#B86-nutrients-16-02220" class="html-bibr">86</a>]. This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.</p>
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<p>The HA diet (low fat + <span class="html-italic">A. muciniphila</span>) is supposed to alleviate HS, slow down weight loss, and relieve hepatic injury. It further mitigates “adiposity” and “alteration of adipokines”, both of which are contributors to MAFLD pathogenesis. Overall, the size of the total white adipose tissue (WAT) is reduced in HA-fed mice. Specifically, the size of the epididymal WAT tissue (eWAT) is reduced in the HA diet (compared to the HP diet = high fat) (<b>A</b>), while treatment with HA (compared to HP) reduces the size of adipocytes (<b>B</b>). Notably, one of the hallmarks of MAFLD is highly permeable intestinal barriers, which enhance the risk of systemic inflammation due to over transportation of bacteria (and bacterial products) and commensal metabolites. As shown in (<b>C</b>), the HA diet makes the “mucus layer and tight junctions” thicker (compared to the thinner layer in HP-fed mice). These suggest “<span class="html-italic">A. muciniphila</span>” as a potent probiotic that can bring beneficial outcomes and is worth exploring in future human clinical trials [<a href="#B100-nutrients-16-02220" class="html-bibr">100</a>]. HA (low fat + <span class="html-italic">A. muciniphila</span>), HP (high fat), LP (low fat), WAT, eWAT. This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.</p>
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<p>Mechanisms and enzymes involved in the development of HS, and therapy options which can avoid MAFLD (and subsequent NASH, cirrhosis, and HCC). Note that the content in this figure is only suggestions and needs to be approved in clinical trials [<a href="#B103-nutrients-16-02220" class="html-bibr">103</a>]. HS: hepatic steatosis; MAFLD: metabolic dysfunction–associated FLD; NASH: non–alcoholic steatotic hepatis; AST: aspartate transaminase alanine; ALT: alanine transaminase; DNL: de novo lipogenesis; FAS: fatty acid synthase; SCD1: stearoyl–CoA desaturase; PPAR–α: peroxisome proliferator-activated receptor–α; FAs: fatty acids; ROS: reactive oxygen species; BMI: body mass index; HCC: hepatocellular carcinoma. This content is distributed under the terms of the Creative Commons Attribution 4.0 International license.</p>
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<p>The Mediterranean diet (MD), its food components, and benefits for MAFLD patients. MD: Mediterranean diet; TRF: time-restricted feeding; BMI: body mass index; WC: waist circumference; T2DM: type 2 diabetes mellitus; MAFLD: metabolic dysfunction-associated fatty liver disease.</p>
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16 pages, 2314 KiB  
Article
Phenylalanine-Free Infant Formula in Patients with Phenylketonuria: A Retrospective Study
by Ozlem Yilmaz Nas, Catherine Ashmore, Sharon Evans, Alex Pinto, Anne Daly, Nurcan Yabancı Ayhan and Anita MacDonald
Nutrients 2024, 16(14), 2204; https://doi.org/10.3390/nu16142204 - 10 Jul 2024
Viewed by 807
Abstract
The long-term efficacy and use of phenylalanine-free infant amino acid formula (PFIF) is understudied. This retrospective, longitudinal study evaluated PFIF (PKU Start: Vitaflo International) in children with phenylketonuria, collecting data on metabolic control, growth, dietary intake, and symptoms and the child’s experience with [...] Read more.
The long-term efficacy and use of phenylalanine-free infant amino acid formula (PFIF) is understudied. This retrospective, longitudinal study evaluated PFIF (PKU Start: Vitaflo International) in children with phenylketonuria, collecting data on metabolic control, growth, dietary intake, and symptoms and the child’s experience with PFIF. Twenty-five children (12 males, 48%) with a median age of 3.6 years (2.0–6.2 years) were included. During 24 months follow-up, children maintained normal growth and satisfactory metabolic control. The protein intake from protein substitutes increased from 2.7 at 6 months to 2.8 g/kg/day at 24 months, while natural protein decreased from 0.6 to 0.4 g/kg/day. By 24 months, most children (n = 16, 64%) had stopped PFIF, while nine (36%) continued with a median intake of 450 mL/day (Q1:300 mL, Q3: 560 mL). Children who continued PFIF after 24 months of age had higher energy and fat intakes with higher weight/BMI z-scores compared with those who stopped earlier (p < 0.05). Constipation was reported in 44% of infants but improved with age. Initial difficulty with PFIF acceptance was reported in 20% of infants but also improved with time. Prolonged use of PFIF in pre-school children may contribute to poor feeding patterns and overweight; thus, replacing the majority of the protein equivalent provided by PFIF with a weaning protein substitute by 12 months and discontinuing PFIF before 2 years is recommended. Full article
(This article belongs to the Special Issue Nutritional Management of Patients with Inborn Errors of Metabolism)
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<p>Schematic diagram of the study design.</p>
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<p>Blood phenylalanine control by age groups. Blue lines represent the target therapeutic range of 120–360 µmol/L.</p>
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<p>Changes in median weight-for-age, length-for-age, and BMI-for-age z-scores by age groups.</p>
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<p>Viral infections and symptoms by age group.</p>
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15 pages, 1961 KiB  
Article
The Impact of Beeswax and Glycerol Monolaurate on Camellia Oil Oleogel’s Formulation and Application in Food Products
by Xingchen Wei, Ronghui Xia, Chenxi Wei, Longchen Shang, Jianhui An and Lingli Deng
Molecules 2024, 29(13), 3192; https://doi.org/10.3390/molecules29133192 - 4 Jul 2024
Viewed by 654
Abstract
This study assessed the nutritional profile of camellia oil through its fatty acid composition, highlighting its high oleic acid content (81.4%), followed by linoleic (7.99%) and palmitic acids (7.74%), demonstrating its excellence as an edible oil source. The impact of beeswax (BW) and [...] Read more.
This study assessed the nutritional profile of camellia oil through its fatty acid composition, highlighting its high oleic acid content (81.4%), followed by linoleic (7.99%) and palmitic acids (7.74%), demonstrating its excellence as an edible oil source. The impact of beeswax (BW) and glycerol monolaurate (GML) on camellia oil oleogels was investigated, revealing that increasing BW or GML concentrations enhanced hardness and springiness, with 10% BW oleogel exhibiting the highest hardness and springiness. FTIR results suggested that the structure of the oleogels was formed by interactions between molecules without altering the chemical composition. In biscuits, 10% BW oleogel provided superior crispness, expansion ratio, texture, and taste, whereas GML imparted a distinct odor. In sausages, no significant differences were observed in color, water retention, and pH between the control and replacement groups; however, the BW group scored higher than the GML group in the sensory evaluation. The findings suggest that the BW oleogel is an effective fat substitute in biscuits and sausages, promoting the application of camellia oil in food products. Full article
(This article belongs to the Section Food Chemistry)
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<p>Camellia oil oleogels with different concentrations of beeswax (BW) and glycerol monolaurate (GML): (<b>a</b>)-oleogels were formed by BW, (<b>b</b>)-oleogels were formed by GML.</p>
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<p>FTIR spectra of camellia oleogel prepared with different concentrations of BW (<b>A</b>) and GML (<b>B</b>).</p>
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<p>FTIR spectra of camellia oleogel prepared with different concentrations of BW (<b>A</b>) and GML (<b>B</b>).</p>
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<p>Sensory evaluation analysis of biscuits prepared with different fats.</p>
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<p>Water holding capacity analysis of sausages made with different types of fats. Note: Lard: each formulation contains 36 g of lard. Butter: each formulation contains 18 g lard + 18 g butter. BW: each formulation contains 18 g lard + 18 g 10% BW camellia oleogel. GML: each formulation contains 18 g lard + 18 g 10% GML camellia oleogel. Letters in the same row indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Sensory evaluation analysis of sausages prepared with different fats.</p>
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12 pages, 1771 KiB  
Article
Effect of Replacing Fishmeal with Algal Meal on Growth Parameters and Meat Composition in Rainbow Trout (Oncorhynchus mykiss W.)
by Katya Velichkova, Ivaylo Sirakov, Stefka Stoyanova, Apostol Simitchiev, David Yovchev and Kamelia Stamatova-Yovcheva
Fishes 2024, 9(7), 249; https://doi.org/10.3390/fishes9070249 - 26 Jun 2024
Viewed by 2854
Abstract
Aquafarms should reduce the use of fishmeal and fish oil in nutritional feed. One such accessible and relatively inexpensive food component that could successfully meet the challenge posed by aquaculture is algae. The objective of the present study was to evaluate the algae [...] Read more.
Aquafarms should reduce the use of fishmeal and fish oil in nutritional feed. One such accessible and relatively inexpensive food component that could successfully meet the challenge posed by aquaculture is algae. The objective of the present study was to evaluate the algae meal inclusion of Chlorella and Spirulina sp. in a diet for rainbow trout, evaluating its effects on fish growth, histological parameters and fillet quality. Experiments were carried out to replace 50% and 100% of fishmeal with Spirulina sp. and Chlorella vulgaris in feed for rainbow trout (Oncorhynchus mykiss W.) cultured in a recirculation system. At the end of the experimental period, the highest mean live weight was measured in rainbow trout fed a feed containing 50% algal meal in the feed. The absorptive vacuolization of cells was increased the most and lamina propria was average thickened when fed 50% algae diets. Fat droplets in the hepatocytes were larger in the 50% algae meal fed group, and their nuclei were replaced in the peripheral zone of the cells. Substitution of fishmeal with 50% algal meal in fish feed resulted in a 36.44% reduction in the lipid content of rainbow trout fillets compared to control fish. Full article
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<p>Recirculation aquaculture system: 1. Tanks; 2. Mechanical filter; 3. Biological filter; 4. Tank with pump; 5. Incoming water; 6. Outgoing water.</p>
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<p>Single screw laboratory extruder—BRABENDER 20 DN: 1—feeding device; 2—working screw; 3—cylinder; 4—die with nozzle and heater; 5—heating devices; by Cherpokov et al. [<a href="#B39-fishes-09-00249" class="html-bibr">39</a>].</p>
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<p>Microphotograph of the intestine of rainbow trout (<span class="html-italic">Oncorhynchus mykiss</span>) fed with control diet (<b>A</b>), 50% algae meal (<b>B</b>), 100% algae meal (<b>C</b>).</p>
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<p>Microphotograph of the liver of rainbow trout (<span class="html-italic">Oncorhynchus mykiss</span>) fed with control diet (<b>A</b>), 50% algae meal (<b>B</b>), 100% algae meal (<b>C</b>).</p>
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14 pages, 2261 KiB  
Article
Dried Rice for Alternative Feed as a Waste Management Product for Sustainable Bioeconomy in Rice-Producing Countries
by Rusli Tonda, Roy Hendroko Setyobudi, Zane Vincevica-Gaile, Lili Zalizar, Dyah Roeswitawati, Ida Ekawati, Ivar Zekker, Juris Burlakovs, Iswahyudi Iswahyudi and Vita Rudovica
Sustainability 2024, 16(13), 5372; https://doi.org/10.3390/su16135372 - 24 Jun 2024
Viewed by 1125
Abstract
Dried rice, an organic waste recycling product, is made from dried rice leftovers. With a carbohydrate content nearly equivalent to corn but at a lower price, it has potential as an energy-generating feed, especially in poultry farming. The nutrient content and price of [...] Read more.
Dried rice, an organic waste recycling product, is made from dried rice leftovers. With a carbohydrate content nearly equivalent to corn but at a lower price, it has potential as an energy-generating feed, especially in poultry farming. The nutrient content and price of dried rice were evaluated to assess its efficiency for animal feed use. Dried rice samples from three areas in East Java, Indonesia, were analyzed for moisture, ash, crude protein, crude fat, and crude fiber content. Additionally, this research assesses the effectiveness of dried rice as a corn substitute in broiler feed by observing its impact on feed intake, average daily gain, feed conversion ratio, and broiler performance index. Proximate analysis showed insignificant differences among treatments, with moisture content ranging 12.45–12.71%, ash content 0.55–1.31%, crude protein 10.34–10.64%, crude fat 0.12–2.48%, and crude fiber from 0.81 to 1.55%. Although all samples were assessed as efficient, products from Lumajang and Pasuruan were preferred for feed production due to their similarity to corn nutrient content. Dried rice costs approximately USD 213–228 per ton, significantly lower than corn. Dried rice production reduces both organic waste and poultry production costs concurrently, serving as a sustainable waste management model in Indonesia and other rice-producing countries, shifting towards a bioeconomy from a linear economy. Full article
(This article belongs to the Section Environmental Sustainability and Applications)
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<p>Image of dried rice obtained in Lumajang (<b>A</b>), Pasuruan (<b>B</b>), and Malang (<b>C</b>).</p>
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<p>The moisture content of dried rice samples.</p>
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<p>The ash content of dried rice.</p>
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<p>The crude protein content of dried rice.</p>
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<p>The crude fat contents of dried rice.</p>
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<p>The crude fiber content of dried rice.</p>
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<p>Dried rice price (USD per t).</p>
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23 pages, 3027 KiB  
Article
The Potential of Using Bisr Date Powder as a Novel Ingredient in Biscuits Made of Wheat Flour Only or Mixed with Barley
by Haiam O. Elkatry, Sukainah E. H. Almubarak, Heba I. Mohamed, Khaled M. A. Ramadan and Abdelrahman R. Ahmed
Foods 2024, 13(12), 1940; https://doi.org/10.3390/foods13121940 - 19 Jun 2024
Cited by 1 | Viewed by 966
Abstract
An overproducing date fruit with limited industrial utilization leads to significant waste and losses, especially in the early stage of date maturity known as bisr. This study aimed to investigate the potential use of bisr date powder (BDP) at different concentrations (25%, 50%, [...] Read more.
An overproducing date fruit with limited industrial utilization leads to significant waste and losses, especially in the early stage of date maturity known as bisr. This study aimed to investigate the potential use of bisr date powder (BDP) at different concentrations (25%, 50%, and 100%) as a natural sweetener instead of sugar and barley flour as a source of dietary fiber, vitamins, and minerals instead of wheat flour (50%) in biscuit production over storage periods of 7, 14, and 21 days. The analysis revealed that the bisr Al-Khalas powder sample had a moisture content of 11.84%, ash content of 2.30%, and crude fiber content of 10.20%. Additionally, it had a low protein (2.50%) and fat (0.77%) content, with total carbohydrates at 82.59%. The gradual substitution of bisr Al-Khalas in biscuit production resulted in an increased moisture, ash, fat, protein, crude fiber, and iron content, as well as a decrease in total carbohydrate percentage. A chemical analysis of bisr Al-Khalas powder demonstrated high levels of antioxidants, with 248.49 mg gallic acid/g of phenolic compounds, 31.03 mg quercetin/g of flavonoids, and an antioxidant activity ranging from 42.30%, as shown by the DPPH test. The peroxide content was 0.009 mg equivalent/kg. Biscuit samples with different proportions of bisr Al-Khalas showed an improved resistance to oxidation compared to samples without bisr Al-Khalas, with increased resistance as the percentage of replacement increased during storage. Physical properties such as the diameter, height, and spread percentage, as well as organoleptic properties like color, flavor, aroma, and taste, were significantly enhanced with higher levels of bisr Al-Khalas in the mixture. Biscuit samples fortified with 100% pure bisr Al-Khalas powder were found to be less acceptable, while samples with a 25% substitution did not negatively impact sensory properties. In addition, acrylamide and hydroxymethylfurfural (HMF) were not detected in bisr powder and biscuit samples prepared at different concentrations (25%, 50%, and 100%). In conclusion, the study suggests that bisr Al-Khalas powder, an underutilized waste product, has the potential to add value to commercial biscuit production due to its high nutritional value and extended storage period resulting from its potent antioxidant activity. Full article
(This article belongs to the Special Issue Novel Technologies to Improve the Nutritional Properties of Food)
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<p>Growth stages of date fruits [<a href="#B16-foods-13-01940" class="html-bibr">16</a>]: Bisr (Khalal) stage.</p>
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<p>Total flavonoid content (mg quercetin acid/g) of biscuit samples made from wheat flour alone or mixed with barley flour and fortified with bisr date powder in different concentrations. The mean ± SD of three replicates is used to represent the data. Duncan’s test at <span class="html-italic">p</span> &lt; 0.05 indicates that the various letters denote the significance within each bar. *** Highly significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The antioxidant activity (DPPH%) of biscuit samples made from wheat flour alone or mixed with barley flour and fortified with bisr date powder (BDP) in different proportions. The mean ± SD of three replicates is used to represent the data. Duncan’s test at <span class="html-italic">p</span> &lt; 0.05 indicates that the various letters denote the significance within each bar. *** Highly significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Peroxide content (mEq/kg) of samples of biscuits made from wheat or barley flour using bisr date powder (BDP) in different proportions during the storage period. The data are represented as the mean ± SD of three replicates.</p>
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<p>The biscuits prepared by addition of bisr date powder.</p>
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<p>LC-MS TIC of detection of acrylamide in bisr powder and biscuit samples prepared with wheat flour and sugar replaced by different concentrations of bisr date powder (25, 50, 75, and 100%).</p>
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<p>LC-MS TIC of detection of HMF in bisr powder and biscuit samples prepared with wheat flour and sugar replaced by different concentrations of bisr date powder (25, 50, 75, and 100%).</p>
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14 pages, 2784 KiB  
Article
2α-Substituted Vitamin D Derivatives Effectively Enhance the Osteoblast Differentiation of Dedifferentiated Fat Cells
by Michiyasu Ishizawa, Masashi Takano, Atsushi Kittaka, Taro Matsumoto and Makoto Makishima
Biomolecules 2024, 14(6), 706; https://doi.org/10.3390/biom14060706 - 15 Jun 2024
Viewed by 543
Abstract
The active form of vitamin D3, 1α,25-dihydroxyvitamin D3 [1,25(OH)2D3], is a principal regulator of calcium homeostasis through activation of the vitamin D receptor (VDR). Previous studies have shown that 2α-(3-hydroxypropyl)-1,25D3 (O1C3) and 2α-(3-hydroxypropoxy)-1,25D3 (O2C3), [...] Read more.
The active form of vitamin D3, 1α,25-dihydroxyvitamin D3 [1,25(OH)2D3], is a principal regulator of calcium homeostasis through activation of the vitamin D receptor (VDR). Previous studies have shown that 2α-(3-hydroxypropyl)-1,25D3 (O1C3) and 2α-(3-hydroxypropoxy)-1,25D3 (O2C3), vitamin D derivatives resistant to inactivation enzymes, can activate VDR, induce leukemic cell differentiation, and increase blood calcium levels in rats more effectively than 1,25(OH)2D3. In this study, to further investigate the usefulness of 2α-substituted vitamin D derivatives, we examined the effects of O2C3, O1C3, and their derivatives on VDR activity in cells and mouse tissues and on osteoblast differentiation of dedifferentiated fat (DFAT) cells, a cell type with potential therapeutic application in regenerative medicine. In cell culture experiments using kidney-derived HEK293 cells, intestinal mucosa-derived CaCO2 cells, and osteoblast-derived MG63 cells, and in mouse experiments, O2C2, O2C3, O1C3, and O1C4 had a weaker effect than or equivalent effect to 1,25(OH)2D3 in VDR transactivation and induction of the VDR target gene CYP24A1, but they enhanced osteoblast differentiation in DFAT cells equally to or more effectively than 1,25(OH)2D3. In long-term treatment with the compound without the medium change (7 days), the derivatives enhanced osteoblast differentiation more effectively than 1,25(OH)2D3. O2C3 and O1C3 were more stable than 1,25(OH)2D3 in DFAT cell culture. These results indicate that 2α-substituted vitamin D derivatives, such as inactivation-resistant O2C3 and O1C3, are more effective than 1,25(OH)2D3 in osteoblast differentiation of DFAT cells, suggesting potential roles in regenerative medicine with DFAT cells and other multipotent cells. Full article
(This article belongs to the Special Issue Biochemistry and Molecular Biology of Vitamin D and Its Analog II)
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<p>Chemical structures of 2α-substituted vitamin D derivatives. (<b>A</b>) 2α-Hydroxyalkoxylated derivatives, O2C2, O2C3, and O2C4. (<b>B</b>) 2α-Hydroxyalkylated derivatives, O1C1, O1C2, O1C3, and O1C4. The details about the compounds were reported previously [<a href="#B10-biomolecules-14-00706" class="html-bibr">10</a>,<a href="#B11-biomolecules-14-00706" class="html-bibr">11</a>].</p>
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<p>Effects of 1,25(OH)<sub>2</sub>D<sub>3</sub> and vitamin D derivatives on VDR transactivation activity and interactions of VDR with RXR and SRC-1. The effects of O2C2, O2C3, and O2C4 on VDR transactivation (<b>A</b>), VDR–RXR interaction (<b>B</b>), and VDR–SRC1 interaction (<b>C</b>), and those of O1C1, O1C2, O1C3, and O1C4 on VDR transactivation (<b>D</b>), VDR–RXR interaction (<b>E</b>), and VDR–SRC1 interaction were compared to those of 1,25(OH)<sub>2</sub>D<sub>3</sub>. HEK293 cells were transfected with pCMX−VDR and TK-Spp × 3-LUC reporter plasmid, CMX-VP16-VDR, CMX-GAL4-RXRα, and MH100(UAS) × 4-tk-LUC reporter plasmid, and CMX-VP16-VDR, CMX-GAL4-SRC-1, and MH100(UAS) × 4-tk-LUC reporter plasmid for VDR transactivation activity (<b>A</b>,<b>D</b>), interaction of VDR with RXRα (<b>B</b>,<b>E</b>), and that with SRC-1 (<b>C</b>,<b>F</b>), respectively. Cells were treated with a range of concentrations of each compound (0–10 nM). Luciferase activity values are expressed relative to those of 10 nM 1,25(OH)<sub>2</sub>D<sub>3</sub>, which are set at 100%.</p>
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<p>Effects of 1,25(OH)<sub>2</sub>D<sub>3</sub> and vitamin D derivatives on mRNA expression of the VDR target genes in human cells. The effects of O2C2, O2C3, and O2C4 (<b>A</b>,<b>C</b>,<b>E</b>,<b>G</b>) and those of O1C1, O1C2, O1C3, and O1C4 (<b>B</b>,<b>D</b>,<b>F</b>,<b>H</b>) were compared to those of 1,25(OH)<sub>2</sub>D<sub>3</sub>. Human kidney-derived HEK293 cells (<b>A</b>,<b>B</b>), intestinal mucosa-derived CaCO<sub>2</sub> cells (<b>C</b>,<b>D</b>), and osteoblast-derived MG63 cells (<b>E</b>–<b>H</b>) were treated with a vehicle (ethanol) control (CNT), 1,25(OH)<sub>2</sub>D<sub>3</sub> or vitamin D derivative (10 nM) for 24 h, and mRNA expression of <span class="html-italic">CYP24A1</span> (<b>A</b>–<b>F</b>) and <span class="html-italic">BGLAP</span> (<b>G</b>,<b>H</b>) was determined with reverse transcription and quantitative real-time PCR analysis. mRNA levels were normalized to the level of 18S rRNA and expressed relative to those of cells treated with 1,25(OH)<sub>2</sub>D<sub>3</sub>, which are set at 100%. One-way ANOVA followed by Dunnett’s multiple comparisons. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 versus CNT; # <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 versus 1,25(OH)<sub>2</sub>D<sub>3</sub>.</p>
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<p>Effects of vitamin D derivatives on <span class="html-italic">Cyp24a1</span> expression in the kidney and small intestine, and plasma calcium and phosphorus levels in mice. (<b>A</b>) Effects of O2C2 and O2C3 on <span class="html-italic">Cyp24a1</span> mRNA expression in the kidney, duodenum, jejunum, and ileum were compared to those of 1,25(OH)<sub>2</sub>D<sub>3</sub>. (<b>B</b>) Effects of O2C2 and O2C3 on plasma calcium and phosphorus levels were compared to those of 1,25(OH)<sub>2</sub>D<sub>3</sub>. Effects of O1C3 on <span class="html-italic">Cyp24a1</span> mRNA expression (<b>C</b>) and plasma calcium and phosphorus levels (<b>D</b>) were also examined. Mice were administered vehicle (ethanol) control (CNT), 12.5 nmol/kg 1,25(OH)<sub>2</sub>D<sub>3</sub>, O2C2, O2C3, or O1C3 via intraperitoneal injection, and blood and tissue samples were collected 6 h after injection. mRNA levels were normalized to the level of <span class="html-italic">GAPDH</span> mRNA and expressed relative to those of 1,25(OH)<sub>2</sub>D<sub>3</sub>-treated mice, which are set at 100%. Data are presented as means ± S.D. One-way ANOVA followed by Dunnett’s multiple comparisons. * <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 versus CNT; # <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 versus 1,25(OH)<sub>2</sub>D<sub>3</sub>.</p>
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<p>Effects of vitamin D derivatives on the expression of the VDR target gene <span class="html-italic">CYP24A1</span> (<b>A</b>), the osteoblast marker genes <span class="html-italic">SPP1</span> (<b>B</b>), <span class="html-italic">BGLAP</span> (<b>C</b>), and <span class="html-italic">RUNX2</span> (<b>D</b>), and the adipocyte marker gene <span class="html-italic">PPARG</span> (<b>E</b>) in human DFAT cells. Cells were treated with vehicle (ethanol) control (CNT), 10 nM 1,25(OH)<sub>2</sub>D<sub>3</sub>, or vitamin D derivative for 24 h, and the expression of each gene was determined via reverse transcription and quantitative real-time PCR analysis. mRNA levels were normalized to the level of 18S rRNA and expressed relative to those of cells treated with 1,25(OH)<sub>2</sub>D<sub>3</sub>, which are set at 100%. One-way ANOVA followed by Dunnett’s multiple comparisons. * <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 versus CNT; ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 versus 1,25(OH)<sub>2</sub>D<sub>3</sub>.</p>
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<p>Effects of vitamin D derivatives on osteoblast differentiation in human DFAT cells. Cells were treated without or with OM in the presence of vehicle (ethanol) control (CNT), 10 nM 1,25(OH)<sub>2</sub>D<sub>3</sub>, or vitamin D derivative. OM plus test compound was changed on day 4 (<b>A</b>) or left unchanged (<b>B</b>). ALP activity was evaluated on day 7. ALP activity was determined in cell lysates and normalized to protein content and expressed relative to those of cells treated with OM plus 1,25(OH)<sub>2</sub>D<sub>3</sub>, which are set at 100%. One-way ANOVA followed by Dunnett’s multiple comparisons. * <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 versus OM + CNT (<span class="html-italic">p</span> = 0.07, OM + 1,25(OH)<sub>2</sub>D<sub>3</sub> versus OM + CNT in (<b>A</b>) right panel); # <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 versus OM + 1,25(OH)<sub>2</sub>D<sub>3</sub>.</p>
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<p>Stability of 1,25(OH)<sub>2</sub>D<sub>3</sub>, O2C3, and O1C3 in human DFAT cells. Cells were treated with OM plus 1 μM 1,25(OH)<sub>2</sub>D3, O2C3, or O1C3 for 3 days (“with cells”). Each compound was also incubated with OM in the absence of cells for 3 days (“without cells”). Compounds were extracted from medium +/− cells and analyzed with HPLC. Peak areas for compounds in HPLC were expressed relative to those without cells, which are set at 100%. Unpaired two-group Student’s <span class="html-italic">t</span> test: * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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11 pages, 611 KiB  
Article
Modelling Food Substitution Using the Ofcom Nutrient Profiling Model on Population Intakes from the Canadian Community Health Survey–Nutrition 2015
by Qiuyu (Julia) Chen, Misa Gillis, Jodi T. Bernstein, Adelia Jacobs, Conor L. Morrison and Mahsa Jessri
Nutrients 2024, 16(12), 1874; https://doi.org/10.3390/nu16121874 - 14 Jun 2024
Viewed by 630
Abstract
This study aimed to model how substituting foods consumed by Canadians for alternatives with more favourable nutrient profiling (NP) scores would impact dietary intakes. The Ofcom NP system, developed to help the UK Office of Communication differentiate foods that can be advertised to [...] Read more.
This study aimed to model how substituting foods consumed by Canadians for alternatives with more favourable nutrient profiling (NP) scores would impact dietary intakes. The Ofcom NP system, developed to help the UK Office of Communication differentiate foods that can be advertised to children, was applied to foods consumed by Canadians aged 2 years and older in the 2015 Canadian Community Health Survey (CCHS) (n = 19,447). Foods were substituted for similar options from the Euromonitor branded food composition database (Scenario 1) or from the primarily aggregated food profiles in the CCHS survey food composition database (Scenario 2) with either the most favourable (optimistic; 1A and 2A) or a more favourable Ofcom score (realistic; 1B and 2B). Mean intakes of Ofcom scores, calories, saturated fat, sugars, and sodium from these scenarios were compared to baseline. Only 2.9% of foods consumed had a similar Euromonitor option with a lower Ofcom score. Scenarios 1A, 1B, and 2A had lower Ofcom scores, calorie, sodium, saturated fat, and sugar intakes compared to baseline. Scenario 2B had lower levels of all outcome measures, except for an increase in calories compared to baseline. Selection of foods with more favourable NP scores has the potential to decrease the Canadian intake of nutrients of concern. Full article
(This article belongs to the Section Nutritional Policies and Education for Health Promotion)
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<p>Process flow diagram and overview of study design.</p>
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17 pages, 1060 KiB  
Article
Candelilla Wax and Glycerol Monostearate-Based Oleogels as Animal Fat Substitutes in Bologna Sausages
by Anda Elena Tanislav, Anca Alexandra Cornea, Eugen Dan Radu, Dorin Țibulcă, Vlad Mureșan and Elena Mudura
Gels 2024, 10(6), 399; https://doi.org/10.3390/gels10060399 - 13 Jun 2024
Viewed by 867
Abstract
The aim of this study was to produce Bologna sausages rich in unsaturated fatty acids and to evaluate this replacement on the structural characteristics. For the purpose of a comparative analysis, three different types of sausages were produced, distinct only in the type [...] Read more.
The aim of this study was to produce Bologna sausages rich in unsaturated fatty acids and to evaluate this replacement on the structural characteristics. For the purpose of a comparative analysis, three different types of sausages were produced, distinct only in the type of fat used: I. sausages obtained with pork backfat (PBF), II. sausages produced with oleogel formed from refined sunflower oil and glycerol monostearate (GM_OG), and III. with candelilla wax oleogel (CW_OG). The meat composition was also analyzed to better understand the process in the dynamics and the finished products were analyzed both uncooked and cooked. The enhanced oil-binding capacity of oleogels suggests their potential value as substitutes for saturated fats (>99%). In terms of meat composition textural analysis, the highest hardness value was registered for PBF_C of 25.23 N, followed by a CW_OG_C of 13.08 N and a GM_OG_C of 12.27 N. However, adhesiveness, cohesiveness, springiness index, and gumminess showed similar values between samples. Reformulation of products with oleogels as a fat source abundant in mono- and polyunsaturated fatty acids resulted in uncooked products exhibiting reduced hardness values of 49.01 N (CW_OG_US) and 40.51 N (GM_OG_US), compared to 65.03 N (PBF_US). Color results of the cross-section color can indicate the potential for consumer acceptance due to the reduced color differences between the conventional and oleogel samples. Full article
(This article belongs to the Special Issue Recent Advances in Oil Structuring)
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<p>Storage modulus G′ (<b>A</b>) and loss modulus G″ (<b>B</b>) curves for meat compositions during the frequency test. PBF_C—meat composition with pork backfat; GM_OG_C—meat composition with glycerol monostearate oleogel; CW_OG_C—meat composition with candelilla wax oleogel.</p>
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<p>Storage modulus G′ (<b>A</b>) and loss modulus G″ (<b>B</b>) curves for meat compositions during the frequency test. PBF_C—meat composition with pork backfat; GM_OG_C—meat composition with glycerol monostearate oleogel; CW_OG_C—meat composition with candelilla wax oleogel.</p>
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<p>Hardness for uncooked and cooked Bologna sausages. Values are expressed as mean ± standard deviation. PBF_US—uncooked sausages with pork backfat; GM_OG_US—uncooked sausages with glycerol monostearate oleogel; CW_OG_US—uncooked sausages with candelilla wax oleogel; PBF_CS—cooked sausages with pork backfat; GM_OG_CS—cooked sausages with glycerol monostearate oleo-gel; CW_OG_CS—cooked sausages with candelilla wax oleogel. For each characteristic, identically superscript capital letters indicate no significant differences (<span class="html-italic">p</span> &gt; 0.05) between samples (PBF_US vs. GM_OG_US vs. CW_OG_US; PBF_CS vs. _GM_OG_CS vs. CW_OG_CS). Identically superscript lowercase letters indicate no significant differences (p &gt;0.05) between uncooked and cooked samples (PBF_US vs. PBF_CS; GM_OG_US vs. GM_OG_CS; CW_OG_US vs. CW_OG_CS).</p>
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<p>Process flow diagram of Bologna sausages.</p>
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16 pages, 1645 KiB  
Article
Effect of Inoculation with Autochthonous Lactic Acid Bacteria on Flavor, Texture, and Color Formation of Dry Sausages with NaCl Partly Substituted by KCl
by Jiawang Wang, Jiasheng Lu, Xin Zhang, Baohua Kong, Yongjie Li, Qian Chen and Rongxin Wen
Foods 2024, 13(11), 1747; https://doi.org/10.3390/foods13111747 - 2 Jun 2024
Viewed by 442
Abstract
The effects of inoculating lactic acid bacteria (LAB), specifically Lactiplantibacillus plantarum, Latilactobacillus sakei, Latilactobacillus curvatus, and Weissella hellenica on the flavor, texture, and color formation of dry sausages in which NaCl was partially substituted by 40% KCl, were explored in [...] Read more.
The effects of inoculating lactic acid bacteria (LAB), specifically Lactiplantibacillus plantarum, Latilactobacillus sakei, Latilactobacillus curvatus, and Weissella hellenica on the flavor, texture, and color formation of dry sausages in which NaCl was partially substituted by 40% KCl, were explored in this study. It was found that LAB inoculation increased the presence of ketones, alcohols, acids, esters, and terpenes. It also reduced the pH, moisture, protein, and fat content, improving the b*-value, flavor, and texture of the sausages. Notably, L. sakei inoculation showed the most significant improvement in dry sausages with NaCl substitutes, especially on the reduction of bitterness. Meanwhile, there was a close positive correlation between the LAB count with the alcohols and esters formation of dry sausage with NaCl substitution (p < 0.05). These findings offer insight into improving the product characteristics of dry sausages using NaCl substitutes. Full article
(This article belongs to the Special Issue Meat Quality and Microbial Analysis II)
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<p>Effects of various lactic acid bacteria on lactic acid bacteria count (<b>A</b>), pH (<b>B</b>), moisture (<b>C</b>), protein (<b>D</b>), and fat content (<b>E</b>) of dry sausages with NaCl substitutes during fermentation. Different lowercase letters (a–d) denote variations between treatments at the same time, while different uppercase letters (A–D) show variations within same treatments over different times (<span class="html-italic">p</span> &lt; 0.05). CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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<p>Effects of various lactic acid bacteria on lactic acid bacteria count (<b>A</b>), pH (<b>B</b>), moisture (<b>C</b>), protein (<b>D</b>), and fat content (<b>E</b>) of dry sausages with NaCl substitutes during fermentation. Different lowercase letters (a–d) denote variations between treatments at the same time, while different uppercase letters (A–D) show variations within same treatments over different times (<span class="html-italic">p</span> &lt; 0.05). CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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<p>Sensor response (<b>A</b>) and principal component analysis (<b>B</b>) of the electronic nose for dry sausages with NaCl substitutes inoculated with different lactic acid bacteria on day 9. W1C: aromatic; W5S: broad range; W3C: aromatic; W6S: hydrogen; W5C: arom-aliph; W1S: broad-methane; W1W: sulfur-organic; W2S: broad-alcohol; W2W: sulf-chlor; W3S: methane-aliph. CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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<p>Classification (<b>A</b>) and principal component analysis (<b>B</b>) of volatile compounds in dry sausages with NaCl substitutes inoculated with various lactic acid bacteria on day 9. CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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<p>Classification (<b>A</b>) and principal component analysis (<b>B</b>) of volatile compounds in dry sausages with NaCl substitutes inoculated with various lactic acid bacteria on day 9. CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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<p>Sensory evaluation (<b>A</b>) and Spearman rank correlation between physicochemical characteristics, flavor, and quality (<b>B</b>) of dry sausages with NaCl substitutes inoculated with various lactic acid bacteria. W1C: aromatic; W5S: broad range; W3C: aromatic; W6S: hydrogen; W5C: arom-aliph; W1S: broad-methane; W1W: sulfur-organic; W2S: broad-alcohol; W2W: sulf-chlor; W3S: methane-aliph. The color scale denotes the nature of the correlation, with 1 indicating a positive correlation (red) and −1 indicating a negative correlation (blue). “*” represents significance at <span class="html-italic">p</span> &lt; 0.05. CT: 100% NaCl; CS: 60% NaCl + 40% KCl; LC: 60% NaCl + 40% KCl + <span class="html-italic">L. curcatus</span>; LS: 60% NaCl + 40% KCl + <span class="html-italic">L. sakei</span>; WH: 60% NaCl + 40% KCl + <span class="html-italic">W. hellenica</span>; LP: 60% NaCl + 40% KCl + <span class="html-italic">L. plantarum</span>.</p>
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