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Search Results (3,623)

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5 pages, 190 KiB  
Editorial
Fermented Foods and Food Microorganisms: Antioxidant Benefits and Biotechnological Advancements
by Myung-Ji Seo
Antioxidants 2024, 13(9), 1120; https://doi.org/10.3390/antiox13091120 - 16 Sep 2024
Abstract
Fermented foods have been a part of human civilization since ancient times, offering enhanced flavors, extended shelf-life, and improved nutritional value through the action of microorganisms [...] Full article
(This article belongs to the Special Issue Antioxidant Activity of Fermented Foods and Food Microorganisms)
21 pages, 3419 KiB  
Article
Novel Bioplastic Based on PVA Functionalized with Anthocyanins: Synthesis, Biochemical Properties and Food Applications
by Giuseppe Tancredi Patanè, Antonella Calderaro, Stefano Putaggio, Giovanna Ginestra, Giuseppina Mandalari, Santa Cirmi, Davide Barreca, Annamaria Russo, Teresa Gervasi, Giovanni Neri, Meryam Chelly, Annamaria Visco, Cristina Scolaro, Francesca Mancuso, Silvana Ficarra, Ester Tellone and Giuseppina Laganà
Int. J. Mol. Sci. 2024, 25(18), 9929; https://doi.org/10.3390/ijms25189929 (registering DOI) - 14 Sep 2024
Viewed by 268
Abstract
Over the last ten years, researchers’ efforts have aimed to replace the classic linear economy model with the circular economy model, favoring green chemical and industrial processes. From this point of view, biologically active molecules, coming from plants, flowers and biomass, are gaining [...] Read more.
Over the last ten years, researchers’ efforts have aimed to replace the classic linear economy model with the circular economy model, favoring green chemical and industrial processes. From this point of view, biologically active molecules, coming from plants, flowers and biomass, are gaining considerable value. In this study, firstly we focus on the development of a green protocol to obtain the purification of anthocyanins from the flower of Callistemon citrinus, based on simulation and on response surface optimization methodology. After that, we utilize them to manufacture and add new properties to bioplastics belonging to class 3, based on modified polyvinyl alcohol (PVA) with increasing amounts from 0.10 to 1.00%. The new polymers are analyzed to monitor morphological changes, optical properties, mechanical properties and antioxidant and antimicrobial activities. Fourier transform infrared spectroscopy (FTIR) spectra of the new materials show the characteristic bands of the PVA alone and a modification of the band at around 1138 cm−1 and 1083 cm−1, showing an influence of the anthocyanins’ addition on the sequence with crystalline and amorphous structures of the starting materials, as also shown by the results of the mechanical tests. These last showed an increase in thickening (from 29.92 μm to approx. 37 μm) and hydrophobicity with the concomitant increase in the added anthocyanins (change in wettability with water from 14° to 31°), decreasing the poor water/moisture resistance of PVA that decreases its strength and limits its application in food packaging, which makes the new materials ideal candidates for biodegradable packaging to extend the shelf-life of food. The functionalization also determines an increase in the opacity, from 2.46 to 3.42 T%/mm, the acquisition of antioxidant activity against 2,2-diphenyl-1-picrylhdrazyl and 2,2′-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) radicals and, in the ferric reducing power assay, the antimicrobial (bactericidal) activity against different Staphylococcus aureus strains at the maximum tested concentration (1.00% of anthocyanins). On the whole, functionalization with anthocyanins results in the acquisition of new properties, making it suitable for food packaging purposes, as highlighted by a food fresh-keeping test. Full article
(This article belongs to the Section Materials Science)
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Figure 1

Figure 1
<p>Representative pictogram for the green index of the extraction of anthocyanin from <span class="html-italic">Callistemon citrinus</span> using two different methods. (<b>A</b>) The index for the extraction with accelerated solvent extraction using methanol solution; (<b>B</b>) The index for the extraction with MAE using the new ethanol (EtOH) solution. In both pictograms, the colour scale (red-yellow-green) indicates the performance at each stage of the procedure. The less chemically ‘green’ the process, the more red it appears.</p>
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<p>Pareto chart diagram for the extraction of total anthocyanin content (TAC) from <span class="html-italic">Callistemon citrinus</span>. A = microwave power (W); B = extraction time (min); C = EtOH% in the extraction solution.</p>
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<p>Response surface plots analysis for the total anthocyanin content yield (TAC) from <span class="html-italic">Callistemon citrinus</span> powder with microwave assisted extraction (MAE) with the same solid-liquid ratio, 1:10 (<span class="html-italic">w</span>/<span class="html-italic">v</span>). (<b>A</b>) microwave power and EtOH % in the reaction mix; (<b>B</b>) microwave power and minutes; (<b>C</b>) EtOH % in the reaction mix and minutes.</p>
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<p>Representative FTIR spectra of the new PVA-based bioplastics produced by the addition of increasing amount of anthocyanins (0.0–1.0%). (<b><span style="color:lime">―</span></b>) Anthocyanins powder; (<b>―</b>) PVA alone; (<b><span style="color:red">―</span></b>) PVA plus 0.1% anthocyanins; (<b><span style="color:#2E74B5">―</span></b>) PVA plus 0.25% anthocyanins; (<b><span style="color:#FF66FF">―</span></b>) PVA plus 0.5% anthocyanins; (<b><span style="color:#66FFFF">―</span></b>) PVA plus 1.0% anthocyanins.</p>
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<p>Release for short- and long-term migration of anthocyanins from PVA films in different food simulants. (<b>A</b>) PVA plus 0.10% of anthocyanins; (<b>B</b>) PVA plus 0.25% of anthocyanins; (<b>C</b>) PVA plus 0.50% of anthocyanins; (<b>D</b>) PVA plus 1.00% of anthocyanins. (<span style="color:#3366CC">⬤</span>) H<sub>2</sub>O; (<span style="color:red">■</span>) ethanol 10%; (<span style="color:green">▲</span>) ethanol 50%; (<span style="color:#7100E2">▼</span>) acetic acid 3%.</p>
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<p>Evaluation of antioxidant activity of PVA-based bioplastics with different % of anthocyanins (0.10, 0.25, 0.50, 1%) in the most common antioxidant assays. (<b>A</b>) ABTS assay; (<b>B</b>) DPPH assay; (<b>C</b>) ferric reducing power (FRAP) assay. The letters in the different graph indicate: a, control sample; b, PVA alone; c, PVA plus 0.10% of anthocyanins; d, PVA plus 0.25% of anthocyanins; e, PVA plus 0.50% of anthocyanins; f, PVA plus 1.00% of anthocyanins. *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Preparation of bags for food packaging produced with PVA plus 1.0% of anthocyanins and its utilization for apple samples.</p>
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<p>Analysis of the changes in apple samples packed or not packed after different intervals of time (0 and 72 h). (<b>A</b>) Changes in the browning of the samples monitored at 420 nm. The letters in the graph indicate: a, apple samples not packed after 0 h; b, apple samples not packed after 72 h; c, apple sample packed with PVA film alone after 72 h; d, apple samples packed with PVA plus 1.00% of anthocyanins after 72 h. (<b>B</b>) Changes in the antioxidant potential monitored by DPPH assay. The letters in the graph indicate: a, control without samples; b, apple samples not packed after 0 h; c, apple samples not packed after 72 h; d, apple sample packed with PVA film alone after 72 h; e, apple samples packed with PVA plus 1.00% of anthocyanins after 72 h. The ** indicates significant changes with respect to the control at <span class="html-italic">p</span> &gt; 0.05.</p>
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15 pages, 2100 KiB  
Article
Quality Changes on Cod Fish (Gadus morhua) during Desalting Process and Subsequent High-Pressure Pasteurization
by Liliana G. Fidalgo, Maria J. Mota, Juliana D’Amil, Rui P. Queirós, Carlos A. Pinto, Ivonne Delgadillo and Jorge A. Saraiva
Appl. Sci. 2024, 14(18), 8260; https://doi.org/10.3390/app14188260 - 13 Sep 2024
Viewed by 257
Abstract
During the desalting of salted cod, significant textural, histological, and biochemical changes occur. Understanding these changes is crucial for enhancing the preservation and extending the shelf life of desalted cod. This study aimed to investigate the physicochemical quality parameters and enzymatic activities during [...] Read more.
During the desalting of salted cod, significant textural, histological, and biochemical changes occur. Understanding these changes is crucial for enhancing the preservation and extending the shelf life of desalted cod. This study aimed to investigate the physicochemical quality parameters and enzymatic activities during the desalting process of cod (16 h at 4 and 20 °C) and to extend the shelf life of desalted cod through high-pressure processing (HPP) at 400 and 550 MPa for 5 min. During desalting, a correlation was noted between the pH and trimethylamine content in samples desalted at 20 °C, with both parameters increasing in the initial 4 h and stabilizing thereafter. The soluble protein in cod muscle decreased over desalting time, as it dissolved into the desalting water. Enzymatic activity showed a decline in cathepsins (B and D) and acid phosphatase throughout desalting, whereas lipase activity increased, particularly at 20 °C. HPP effectively extended the shelf life of desalted cod by controlling endogenous microbial growth, enabling an extension to 14–21 days compared to the 7 days observed in untreated control samples. This study highlights quality changes during desalting, with lesser effects at lower temperatures. Subsequent HPP improved the microbiological quality of desalted cod during refrigerated storage. Full article
(This article belongs to the Special Issue Novel Food Technologies and Applications)
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Figure 1
<p>Water ((<b>A</b>), g H<sub>2</sub>O/g IS) and salt content ((<b>B</b>), g NaCl/g IS) in cod fish during desalting. Different letters (a–e) denote significant differences (<span class="html-italic">p</span> &lt; 0.05) between desalting times.</p>
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<p>pH (<b>A</b>), trimethylamine content ((<b>B</b>), mg TMA/g IS), and soluble protein ((<b>C</b>), mg albumin/g IS) in cod fish during the desalting time (hours). Different letters (a–d) denote significant differences (<span class="html-italic">p</span> &lt; 0.05) between desalting times. The symbol * denotes significant differences between desalting temperatures.</p>
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<p>Cathepsin B ((<b>A</b>), FU/min/g IS) and cathepsin D ((<b>B</b>), µg tyrosine/min/g IS) activities in cod fish during desalting. Different letters (a–d) denote significant differences (<span class="html-italic">p</span> &lt; 0.05) between desalting times. The symbol * denotes significant differences between desalting temperatures.</p>
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<p>Acid phosphatase ((<b>A</b>), nmol p-NP/min/g IS) and lipase ((<b>B</b>), ×10<sup>2</sup> µmol FFA/min/g SI) activities in cod fish during desalting. Different letters (a–d) denote significant differences (<span class="html-italic">p</span> &lt; 0.05) between desalting times. The symbol * denotes significant differences between desalting temperatures.</p>
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<p>Microbial evolution ((<b>A</b>) Total aerobic mesophiles; (<b>B</b>) Total aerobic psychrophiles; (<b>C</b>) Enterobacteriaceae; and (<b>D</b>) Yeast and moulds) in control (<span style="color:#C00000">■</span>) and high-pressure processed desalted cod samples at 400 MPa (<span style="color:#70AD47">▲</span>) and 550 MPa (<span style="color:#7030A0">●</span>), with a pressure holding time of 5 min for 28 days of storage at 4 °C. Empty dots meant values lower than 1 log units (or 1.7 log units for yeast and moulds), which corresponded to the detection limit. Different letters denote significant differences (<span class="html-italic">p</span> &lt; 0.05) during storage times (a–d) and between conditions (A–C).</p>
Full article ">
28 pages, 4255 KiB  
Review
Bacterial Cellulose in Food Packaging: A Bibliometric Analysis and Review of Sustainable Innovations and Prospects
by Aida Aguilera Infante-Neta, Alan Portal D’Almeida and Tiago Lima de Albuquerque
Processes 2024, 12(9), 1975; https://doi.org/10.3390/pr12091975 - 13 Sep 2024
Viewed by 256
Abstract
The scientific community has explored new packaging materials owing to environmental challenges and pollution from plastic waste. Bacterial cellulose (BC), produced by bacteria like Gluconacetobacter xylinus, shows high potential for food preservation owing to its exceptional mechanical strength, high crystallinity, and effective [...] Read more.
The scientific community has explored new packaging materials owing to environmental challenges and pollution from plastic waste. Bacterial cellulose (BC), produced by bacteria like Gluconacetobacter xylinus, shows high potential for food preservation owing to its exceptional mechanical strength, high crystallinity, and effective barrier properties against gases and moisture, making it a promising alternative to conventional plastics. This review highlights recent advances in BC production, particularly agro-industrial residues, which reduce costs and enhance environmental sustainability. Incorporating antimicrobial agents into BC matrices has also led to active packaging solutions that extend food shelf-life and improve safety. A bibliometric analysis reveals a significant increase in research on BC over the last decade, reflecting growing global interest. Key research themes include the development of BC-based composites and the exploration of their antimicrobial properties. Critical areas for future research include improving BC production’s scalability and economic viability and the integration of BC with other biopolymers. These developments emphasize BC’s potential as a sustainable packaging material and its role in the circular economy through waste valorization. Full article
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Figure 1
<p>Scientific production over the past 10 years (2014–2024) about (■) “bacterial cellulose” and (●) “bacterial cellulose in food”.</p>
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<p>Three-field plot representing the correlation between the title, keywords, and source of the published papers.</p>
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<p>Top countries by number of publications on “bacterial cellulose in food applications”, highlighting the leading 10 nations.</p>
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<p>Thematic map of “bacterial cellulose in food”.</p>
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<p>(<b>A</b>) Factorial analysis and (<b>B</b>) dendrogram of “bacterial cellulose in food” applications.</p>
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<p>(<b>A</b>) Factorial analysis and (<b>B</b>) dendrogram of “bacterial cellulose in food” applications.</p>
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<p>Keyword cluster map for bacterial cellulose food applications.</p>
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17 pages, 3759 KiB  
Article
Strigolactone Preserves Fresh-Cut Apple Quality during Shelf Life
by Zunchun Liu, Xinyu Zhang, Shuhua Zhu and Dandan Huang
Agriculture 2024, 14(9), 1588; https://doi.org/10.3390/agriculture14091588 - 12 Sep 2024
Viewed by 315
Abstract
Strigolactone (SL) is a signal factor that plays a vital role in plants. The application of SL for the storability of horticultural products has recently received attention. In this experiment, fresh-cut apples were treated with SL at diverse concentrations and stored at 4 [...] Read more.
Strigolactone (SL) is a signal factor that plays a vital role in plants. The application of SL for the storability of horticultural products has recently received attention. In this experiment, fresh-cut apples were treated with SL at diverse concentrations and stored at 4 °C for 10 days, and the changes in quality characteristics, antioxidant system, hydrogen sulfide metabolism, and nitric oxide metabolism were determined. Compared with other treatments, the results showed that SL treatment at 0.50 µmol L−1 had excellent effects on maintaining fruit surface color, weight, firmness, reduced respiration rate, soluble solids content, and electrolyte leakage. SL treatment increased antioxidant enzyme activities, reduced reactive oxygen species (ROS) accumulation, altered the nitric oxide synthase (NOS)-like pathway to promote endogenous NO production in the fruit, and facilitated the L-cysteine-catalyzed process to increase the endogenous hydrogen sulfide (H2S) content. In addition, SL treatment affected the mRNA transcription levels of several genes related to the antioxidant system, H2S metabolism, and NO synthesis, including MdSOD, MdCAT, MdPOD, and MdSAT. Taken together, the results indicated that 0.50 µmol L−1 SL treatment improves the endogenous synthesis of NO and H2S, enhances the antioxidative system, and maintains the quality of fresh-cut apples during their shelf life. Therefore, the present study opens up the possibility of using the exogenous application of strigolactone in the fresh-cut processing industry. Full article
(This article belongs to the Section Agricultural Product Quality and Safety)
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Figure 1
<p>Changes in the basal quality index of fresh-cut apple during storage. (<b>a</b>) Photos of fresh-cut apples on day 10; (<b>b</b>) weight loss; (<b>c</b>) firmness; (<b>d</b>) electrolyte leakage; (<b>e</b>) browning index; (<b>f</b>) respiration rate; and (<b>g</b>) soluble solids content. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of SL on the reactive oxygen species content and activities of antioxidative enzymes in fresh-cut apples. (<b>a</b>) H<sub>2</sub>O<sub>2</sub>; (<b>b</b>) O<sub>2</sub><sup>−</sup>; (<b>c</b>) OH; (<b>d</b>) SOD activity; (<b>e</b>) CAT activity; and (<b>f</b>) POD activity. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effect of SL on the ASA-GSH cycle in fresh-cut apples. (<b>a</b>) DHAR activity; (<b>b</b>) MDHAR activity; (<b>c</b>) APX activity; (<b>d</b>) GR activity; (<b>e</b>) GSH content; (<b>f</b>) GSSG content; (<b>g</b>) AsA content; and (<b>h</b>) DHA content. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p &lt;</span> 0.05).</p>
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<p>Effect of SL on NO metabolism in fresh-cut apples. (<b>a</b>) NO content; (<b>b</b>) NOS-like activity; (<b>c</b>) nitrite content; (<b>d</b>) L-arginine content; and (<b>e</b>) NR activity. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in H<sub>2</sub>S metabolism during the storage of fresh-cut apple. (<b>a</b>) H<sub>2</sub>S content; (<b>b</b>) L-CD activity; (<b>c</b>) OAS-TL activity; and (<b>d</b>) SAT activity. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in the relative gene expression of essential enzymes of fresh-cut apple during storage. (<b>a</b>) <span class="html-italic">MdCAT</span>; (<b>b</b>) <span class="html-italic">MdPOD</span>; (<b>c</b>) <span class="html-italic">MdSOD</span>; (<b>d</b>) <span class="html-italic">MdDHAR</span>; (<b>e</b>) <span class="html-italic">MdMDHAR</span>; (<b>f</b>) <span class="html-italic">MdGR</span>; (<b>g</b>) <span class="html-italic">MdAPX</span>; (<b>h</b>) <span class="html-italic">MdL-CD</span>; and (<b>i</b>) <span class="html-italic">MdSAT</span>. Vertical bars in the graph represent the standard error of three replications (n = 3), and different lower letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Modulation of the antioxidant system, H<sub>2</sub>S, and NO metabolism in fresh-cut apples by SL. Abbreviations: strigolactone, SL; hydrogen sulfide, H<sub>2</sub>S; L-cysteine desulfhydrase, L-CD; serine acetyltransferase, SAT; <span class="html-italic">O</span>-acetyl-1-serine (thiol) lyase, OAS-TL; nitric oxide, NO; nitrate reductase, NR; nitric oxide synthase, NOS-like; catalase, CAT; peroxidase, POD; superoxide dismutase, SOD; monodehydroascorbic acid reductase, MDHAR; dehydroascorbic acid reductase, DHAR; ascorbic acid peroxidase, APX; glutathione reductase, GR; reduced glutathione, GSH; oxidized glutathione, GSSG; reduced ascorbate, AsA; and dehydroascorbate, DHA.</p>
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23 pages, 4200 KiB  
Article
A Novel Approach to Protect Brazil Nuts from Lipid Oxidation: Efficacy of Nanocellulose–Tocopherol Edible Coatings
by Debora Ribeiro Nascimento, Juliana Mesquita, Thayanne da Silva, Thais Hernandes, Elaine Cristina Lengowski and Katiuchia Takeuchi
Coatings 2024, 14(9), 1182; https://doi.org/10.3390/coatings14091182 - 12 Sep 2024
Viewed by 301
Abstract
High levels of unsaturated fatty acids in Brazil nuts compromise their sensory quality through lipid oxidation. To mitigate this reaction, it is crucial to package nuts under a vacuum and in aluminate packaging. An alternative method is the application of an edible coating [...] Read more.
High levels of unsaturated fatty acids in Brazil nuts compromise their sensory quality through lipid oxidation. To mitigate this reaction, it is crucial to package nuts under a vacuum and in aluminate packaging. An alternative method is the application of an edible coating with antioxidant properties. This study aimed to develop an edible coating composed of carboxymethylcellulose and sorbitol, physically reinforced with nanocellulose, and chemically fortified with tocopherol. The edible coating was characterized based on its physical properties, mechanical strength, biodegradability, optical light transmission properties, color parameters, and water vapor permeability. Formulations CC5 (Carboxymethyl cellulose (CMC) + sorbitol + 5% nanocellulose) and CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% nanocellulose) showed enhanced mechanical strength. The combination of nanocellulose with tocopherol in formulations CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% nanocellulose) and CCT5 developed superior barriers to visible and ultraviolet light, a desired characteristic for coatings intended to increase the shelf life of Brazil nuts. The nuts coated with CC5 and CCT3 showed the lowest PV values at the end of the accelerated oxidation test conducted at 60 °C. Full article
(This article belongs to the Special Issue Edible Films and Coatings: Fundamentals and Applications, 2nd Edition)
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Figure 1
<p>CNF produced with pulp of <span class="html-italic">Eucalyptus</span> sp. Bleached. (<b>a</b>) 5 kx; (<b>b</b>) 10 kx magnification.</p>
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<p>X-ray diffraction pattern of bleached fibrillated nanocellulose.</p>
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<p>Solutions of film-forming edible coatings of formulations C01, CC1, CC3, and CC5, after the 7th day of the creaming test. CC1 (CMC + sorbitol + 1% de CNF); CC3 (CMC + sorbitol + 3% de CNF); CC5 (CMC + sorbitol + 5% de CNF). Source: Author (2023).</p>
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<p>Film-forming solutions of edible coatings of formulations C02, CCT1, CCT3, and CCT5, after the 7th day of the creaming test. CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF). Source: Author (2023).</p>
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<p>Results of analyses of (<b>a</b>) water content (%); (<b>b</b>) thickness (mm). C01 (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF).</p>
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<p>The visual appearance of transparency and opacity of prepared edible films. C01 (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF).</p>
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<p>Results of water vapor permeability analysis (g h<sup>−1</sup> m<sup>−2</sup> kPa<sup>−1</sup>). C01 (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF). Different capital letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) by the Kruskal–Wallis test.</p>
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<p>Result of analysis of mechanical properties for puncture deformation. (<b>a</b>) Puncture deformation (<b>b</b>) Puncture Force. (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF). Different lowercase letters indicate significant difference (<span class="html-italic">p</span> &lt; 0.05) by Tukey test.</p>
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<p>(<b>a</b>) Day 1 of biodegradability analysis. (<b>b</b>) Day 7 of biodegradability analysis.</p>
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<p>(<b>a</b>) Biplots of the eigenvectors and eigenvalues of two main components according to the variables of mechanical properties, such as a barrier against visible light, ultraviolet light, and water vapor. (<b>b</b>) Hierarchical cluster analysis. TS: Tensile strength; EB: Elongation at Break; VLT: Visible Light Transmission Value; URV: Ultraviolet Light Rejection Rate; IRR: Infrared Light Rejection Rate; WVP: Water vapor permeability.</p>
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<p>Evolution of the acidity index of oils extracted from coated Brazil nuts subjected to accelerated oxidation. (<b>a</b>) Formulations with reinforced physical barriers; (<b>b</b>) formulations with reinforced physical and chemical barriers. SR (uncoated); C01 (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF. Different lowercase letters indicate significant difference (<span class="html-italic">p</span> &lt; 0.05) by Tukey test.</p>
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<p>Evolution of the peroxide value of oils extracted from coated Brazil nuts subjected to accelerated oxidation. (<b>a</b>) Formulations with reinforced physical barrier; (<b>b</b>) formulations with reinforced physical and chemical barriers. SR (without coating); C01 (CMC + sorbitol); CC1 (CMC + sorbitol + 1% CNF); CC3 (CMC + sorbitol + 3% CNF); CC5 (CMC + sorbitol + 5% CNF); C02 (CMC + sorbitol + tocopherol + soy lecithin); CCT1 (CMC + sorbitol + tocopherol + soy lecithin + 1% CNF); CCT3 (CMC + sorbitol + tocopherol + soy lecithin + 3% CNF); CCT5 (CMC + sorbitol + tocopherol + soy lecithin + 5% CNF). Different capital letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) using the Kruskal–Wallis test.</p>
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27 pages, 3426 KiB  
Article
Combination of a Natural Bioactive Compound and High-Hydrostatic-Pressure Treatment to Increase the Shelf-Life and Quality of Pork Meat
by Tamás Csurka, Zoltán Fekete, Anna Visy, Karina Ilona Hidas, István Dalmadi, Ferenc Horváth, László Ferenc Friedrich and Gábor Jónás
Appl. Sci. 2024, 14(18), 8212; https://doi.org/10.3390/app14188212 - 12 Sep 2024
Viewed by 257
Abstract
Currently, there is a growing demand for ready-to-eat, prepared, high-quality, preservative-free products. However, the shelf-life of these products is often so short that a relatively high percentage of these products cannot be sold and end up as food waste. In this study, pork [...] Read more.
Currently, there is a growing demand for ready-to-eat, prepared, high-quality, preservative-free products. However, the shelf-life of these products is often so short that a relatively high percentage of these products cannot be sold and end up as food waste. In this study, pork loin with different marinades (paprika and herbs) was treated with different high hydrostatic pressures (0 MPa, 300 MPa, 450 MPa and 600 MPa) and a bioactive component (piperine) and then the quality of the meat was examined after 0, 4, 8, 12 and 14 days of cold storage. Changes were monitored using color, pH, texture and microbiological analyses. Both pressure, piperine enrichment, storage time and the interactions of different factors had a significant effect on the quality of the loin samples with different marinades. Due to the denaturation of myoglobin, meat slices were less red and lighter after HHP treatment. The addition of piperine reduced this lightness. The pH increased with increasing pressure and decreased with storage time. HHP treatment significantly increased meat hardness, with samples treated at 600 MPa being 19% harder than those treated at 450 MPa. Microbiological results indicated that HHP at 450 MPa and 600 MPa effectively reduced anaerobic total live plate counts, ensuring satisfactory sensory and microbiological quality throughout storage. Piperine fortification also resulted in a more favorable microbiological status during storage without any perceptible change in quality properties during storage. These findings underscore the effectiveness of HHP and piperine enrichment in enhancing the safety and quality of marinated meats. Full article
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<p>Anaerobic total live plate count [lg (CFU g<sup>−1</sup>)] results of paprika-marinated BA− meat sample groups.</p>
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<p>Anaerobic total live plate count [lg (CFU g<sup>−1</sup>)] results of paprika-marinated BA+ meat sample groups.</p>
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<p>Anaerobic total live plate count [lg (CFU g<sup>−1</sup>)] results of herb-marinated BA− meat sample groups.</p>
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<p>Anaerobic total live plate count [lg (CFU g<sup>−1</sup>)] results of herb-marinated BA+ meat sample groups.</p>
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17 pages, 2594 KiB  
Article
Fluorescence of Intrinsic Milk Chromophores as a Novel Verification Method of UV-C Treatment of Milk
by Kallis Souroullas, Andreas Manoli, Grigorios Itskos, Theofylaktos Apostolou and Photis Papademas
Foods 2024, 13(18), 2887; https://doi.org/10.3390/foods13182887 - 12 Sep 2024
Viewed by 326
Abstract
The European Food Safety Authority (EFSA) has approved the use of a 1045 J/L UV-C dose as an adjunct to pasteurization to increase the shelf life and vitamin D3 content of milk. However, there are no verification methods analogous to the alkaline phosphatase [...] Read more.
The European Food Safety Authority (EFSA) has approved the use of a 1045 J/L UV-C dose as an adjunct to pasteurization to increase the shelf life and vitamin D3 content of milk. However, there are no verification methods analogous to the alkaline phosphatase test for pasteurized milk to ensure that the desired UV-C dose has been correctly applied. The aim is to develop a real-time in-line detector based on fluorescence spectroscopy. In this study, 22 different UV-C doses (ranging from 0 to 2000 J/L) were applied to milk to assess the impact of photooxidation on intrinsic photosensitive chromophores. Fluorescence spectroscopy (90°-angle) was employed as the method of analysis for monitoring the changes in the fluorescence spectra of chromophores in milk without sample pretreatment. Three important chromophore areas (CAs) were identified: CA 1 (riboflavin), CA 3 (vitamin A and dityrosine) and CA 4 (tryptophan), with statistically significant changes at around 1045 J/L and 1500 J/L. The findings of our preliminary study support our hypothesis that the fluorescence of intrinsic chromophores can be used as verification of the applied UV-C dose. Full article
(This article belongs to the Section Dairy)
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<p>Scatter plot of the various photooxidation modifications in dairy products (excitation/emission nm) [<a href="#B8-foods-13-02887" class="html-bibr">8</a>,<a href="#B9-foods-13-02887" class="html-bibr">9</a>,<a href="#B10-foods-13-02887" class="html-bibr">10</a>,<a href="#B11-foods-13-02887" class="html-bibr">11</a>,<a href="#B12-foods-13-02887" class="html-bibr">12</a>,<a href="#B13-foods-13-02887" class="html-bibr">13</a>,<a href="#B14-foods-13-02887" class="html-bibr">14</a>,<a href="#B15-foods-13-02887" class="html-bibr">15</a>,<a href="#B16-foods-13-02887" class="html-bibr">16</a>,<a href="#B17-foods-13-02887" class="html-bibr">17</a>,<a href="#B18-foods-13-02887" class="html-bibr">18</a>,<a href="#B19-foods-13-02887" class="html-bibr">19</a>,<a href="#B20-foods-13-02887" class="html-bibr">20</a>,<a href="#B21-foods-13-02887" class="html-bibr">21</a>,<a href="#B22-foods-13-02887" class="html-bibr">22</a>,<a href="#B23-foods-13-02887" class="html-bibr">23</a>,<a href="#B24-foods-13-02887" class="html-bibr">24</a>,<a href="#B25-foods-13-02887" class="html-bibr">25</a>,<a href="#B26-foods-13-02887" class="html-bibr">26</a>,<a href="#B27-foods-13-02887" class="html-bibr">27</a>,<a href="#B28-foods-13-02887" class="html-bibr">28</a>].</p>
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<p>(<b>A</b>,<b>B</b>) Averaged fluorescence spectra (FLS) of CA 1 and 2. Vertical lines indicate emission peak. (<b>C</b>,<b>D</b>) Averaged fluorescence spectra (FLS) of CA 3 and 4. Vertical lines indicate emission peak.</p>
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<p>(<b>A</b>–<b>D</b>) Plots of the integrated fluorescence quantified by the area under the curve (AUC) at each UV-C dose with standard deviation error bars and a red-colored smoothed curve (percentile filter 50) for easier presentation. <span class="html-italic">Y</span>-axis is the AUC intensity and <span class="html-italic">X</span>-axis is the UV-C dose applied. The shadowed areas indicate the areas where the major, statistically significant changes occurred.</p>
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<p>(<b>A</b>–<b>D</b>) Contour maps for chromophores at the excitation–emission parameters described in <a href="#foods-13-02887-t002" class="html-table">Table 2</a>. <span class="html-italic">Y</span>-axis is the UV-C dose applied and <span class="html-italic">X</span>-axis is the emission. These contour maps were developed using the same dataset as for <a href="#foods-13-02887-f002" class="html-fig">Figure 2</a>A–D.</p>
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17 pages, 2648 KiB  
Article
Production of Long Fermentation Bread with Jabuticaba Peel Flour Added: Technological and Functional Aspects and Impact on Glycemic and Insulinemic Responses
by Miriam Regina Canesin Takemura, Juliana Silva da Graça, Marianna Miranda Furtado, Marcella Camargo Marques, Anderson S. Sant’Ana, Mário Roberto Maróstica Junior, Lilian Regina Barros Mariutti, Bruno Geloneze and Cinthia Baú Betim Cazarin
Foods 2024, 13(18), 2878; https://doi.org/10.3390/foods13182878 - 11 Sep 2024
Viewed by 355
Abstract
The consumption of jabuticaba (Plinia cauliflora), a native Brazilian fruit, has shown promising results concerning some metabolic disorders. Therefore, studying it may aid in the development of products capable of preventing or delaying pathological conditions. The objective of the present study [...] Read more.
The consumption of jabuticaba (Plinia cauliflora), a native Brazilian fruit, has shown promising results concerning some metabolic disorders. Therefore, studying it may aid in the development of products capable of preventing or delaying pathological conditions. The objective of the present study was to formulate a functional sourdough bread with the inclusion of jabuticaba peel flour (JPF) and to evaluate the effect on the postprandial response. The proximate composition of the JPF and bread, the stability of the antioxidant compounds after baking, and the functional activity in a clinical trial were carried out to develop the product and guarantee its quality. JPF increased the fiber content of the bread in comparison to the control from 1.0 g/100 g to 2.3–2.9 g/100 g. Also, the antioxidant capacity increased 1.35 to 3.53 times by adding JPF to the bread, as well as the total reducing capacity (1.56 to 2.67 times). The bread’s shelf life was guaranteed for seven days. In the clinical trial, the consumption of control bread resulted in a glycemia peak at 30 min, remaining high until 45 min; for the JPF bread, we noticed a less prominent peak at 45 min and a decrease with less inflection until 180 min. The serum antioxidant capacity of the individuals increased after the 3 h. Although no statistical difference was observed between the groups in the satiety profile, JPF bread presented higher scores after 60 min. Furthermore, a lessened desire to eat other foods and hunger was observed after consuming JPF bread. The inclusion of JPF in the bread manufacturing process promoted a longer shelf life and increased nutritional quality. Full article
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<p>Flowchart for preparing and manufacturing slow fermentation artisanal bread—adapted type II sourdough method.</p>
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<p>A representative image of bread produced without and with the addition of jabuticaba peel flour (JPF1 = 5%; JPF2 = 7.5%; JPF3 = 10%).</p>
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<p>Glycemic (<b>A</b>) and insulinemic (<b>B</b>) responses after consumption of bread with jabuticaba peel flour (JBF) or control by healthy individuals. NS = not significant; IAUC = incremental area over the curve. * Indicates statistical differences when analyzed by two-way ANOVA and Bonferroni post-test (<b>A</b>,<b>B</b>) and Student’s <span class="html-italic">t</span> test (<b>C</b>,<b>D</b>), considering <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Oxygen radical absorbance capacity (ORAC) postprandial concentration in healthy individuals after consumption of JPF bread. * Indicates statistical differences when analyzed by two-way ANOVA and Bonferroni post-test, considering <span class="html-italic">p</span> &lt; 0.05.</p>
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13 pages, 4911 KiB  
Article
Effect of Near-Freezing Storage Combined with High-Voltage Electric Fields on the Freshness of Large Yellow Croaker
by Hui Zhang, Qizhang Yang, Songyi Lin, Zhaobin Yan, Xuancheng Wu, Wenqiang Wei and Guibing Pang
Foods 2024, 13(18), 2877; https://doi.org/10.3390/foods13182877 - 11 Sep 2024
Viewed by 278
Abstract
Seafood is highly perishable after being caught, making effective preservation technology essential. A few studies have explored the mechanisms of near-freezing storage combined with high-voltage electric fields for seafood preservation. This study uses near-freezing storage at −1 °C in conjunction with three high-voltage [...] Read more.
Seafood is highly perishable after being caught, making effective preservation technology essential. A few studies have explored the mechanisms of near-freezing storage combined with high-voltage electric fields for seafood preservation. This study uses near-freezing storage at −1 °C in conjunction with three high-voltage electric fields (5 kV/m, 8 kV/m, and 16 kV/m) to store large yellow croakers for 21 days and assesses their quality through sensory evaluation, pH values, malondialdehyde, total volatile basic nitrogen, and total viable counts. The results indicate that high-voltage electric fields effectively inhibit endogenous enzyme activity and microbial growth while reducing lipid oxidation in large yellow croakers. The preservation effect is optimal at an electric field strength of 16 kV/m, extending their shelf life by 9 days. These findings offer valuable theoretical and data-driven insights for applying near-freezing storage and electric field preservation technology in cross-regional fish transportation. Full article
(This article belongs to the Section Food Engineering and Technology)
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<p>High-voltage electric field generator and monitoring unit.</p>
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<p>Sensory scores of large yellow croakers subjected to high-voltage electric fields during storage at −1 °C. (<b>a1</b>) Gill brightness; (<b>a2</b>) muscle elasticity; (<b>a3</b>) volatile odor; (<b>a4</b>) eye appearance; (<b>a5</b>) comprehensive sensory scores.</p>
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<p>Eye appearance of high-voltage electric fields on large yellow croakers during storage at −1 °C.</p>
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<p>Changes in pH values of large yellow croakers when stored at −1 °C under different high-voltage electric fields. Note 1: Lowercase letters represent significant differences between groups (<span class="html-italic">p</span> &lt; 0.05), while capital letters indicate significant differences within the same treatment groups (<span class="html-italic">p</span> &lt; 0.05). Data are presented as means ± standard deviations (n = 5).</p>
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<p>Effects of high-voltage electric fields on MDA levels of large yellow croakers during storage at −1 °C. Note 2: The different letters convey the same meaning as in Note 1. Data are presented as means ± standard deviations (n = 5).</p>
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<p>Changes in TVB-N values of large yellow croakers treated with high-voltage electric fields during storage at −1 °C. Note 3: The different letters convey the same meaning as in Note 1. Data are presented as means ± standard deviations (n = 5).</p>
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<p>Changes in the TVC of large yellow croakers when stored at −1 °C under high-voltage electric fields.</p>
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<p>Mechanism of storage and preservation of large yellow croakers using storage at −1 °C combined with high-voltage electric fields.</p>
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13 pages, 2632 KiB  
Article
Effects of Cultivar Factors on Fermentation Characteristics and Volatile Organic Components of Strawberry Wine
by Wei Lan, Mei Zhang, Xinyu Xie, Ruilong Li, Wei Cheng, Tingting Ma and Yibin Zhou
Foods 2024, 13(18), 2874; https://doi.org/10.3390/foods13182874 - 11 Sep 2024
Viewed by 362
Abstract
Strawberry wine production is a considerable approach to solve the problem of the Chinese concentrated harvesting period and the short shelf life of strawberries, but the appropriative strawberry cultivars for fermentation are still undecided. In this study, the strawberry juice and wines of [...] Read more.
Strawberry wine production is a considerable approach to solve the problem of the Chinese concentrated harvesting period and the short shelf life of strawberries, but the appropriative strawberry cultivars for fermentation are still undecided. In this study, the strawberry juice and wines of four typical strawberry cultivars named Akihime (ZJ), Sweet Charlie (TCL), Snow White (BX), and Tongzhougongzhu (TZ) were thoroughly characterized for their physicochemical indicators, bioactive compounds, and volatile organic components (VOCs) to determine the optimal strawberry cultivars for winemaking. The results showed that there were significant differences in the total sugar content, pH, total acid, and other physicochemical indexes in the strawberry juice of different cultivars, which further affected the physicochemical indexes of fermented strawberry wine. Moreover, the content of polyphenols, total flavonoids, vitamin C, and color varied among the four strawberry cultivars. A total of 42 VOCs were detected in the strawberry juice and wines using headspace solid-phase microextraction coupled with gas chromatography–mass spectrometry (HS-SPME-GC-MS), and 3-methyl-1-butanol, linalool, trans-2-pinanol, hexanoic acid, and hexanoic acid ethyl ester were the differential VOCs to identify the strawberry wine samples of different cultivars. Overall, strawberry cultivar ZJ had a relatively high VOC and bioactive compound content, indicating that it is the most suitable cultivar for strawberry wine fermentation. In addition to determining the relatively superior fermentation characteristics of cultivar ZJ, the results may provide a theoretical basis for the raw material quality control and quality improvement of strawberry wine. Full article
(This article belongs to the Section Food Engineering and Technology)
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<p>Fermentation kinetics analysis of different cultivars of strawberry wine. (<b>A</b>) Brix; (<b>B</b>) residual sugar content; (<b>C</b>) ethanol content; (<b>D</b>) glucose content; (<b>E</b>) fructose content; BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime.</p>
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<p>Ethanol and residual sugar content of different cultivars of strawberry wine. (<b>A</b>) Ethanol content; (<b>B</b>) residual sugar content; BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime. Means with the same letter are not significantly different from each other (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total acid content and pH of different cultivars of strawberry juice and wines. (<b>A</b>) pH; (<b>B</b>) total acid content; BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime. Means with the same letter are not significantly different from each other (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total polyphenol, total flavonoid, and ascorbic acid content of different cultivars of strawberry juice and wines. (<b>A</b>) Total polyphenol content; (<b>B</b>) total flavonoid content; (<b>C</b>) ascorbic acid content; BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime. Means with the same letter are not significantly different from each other (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Coordinate analysis and variable importance in the projection (VIP) analysis of VOCs in strawberry juice and wines of different cultivars. (<b>A</b>) PCA; (<b>B</b>) OPLS-DA; (<b>C</b>) VIP value. BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime. Juice (m) samples, BXm: Snow White; TCLm: Sweet Charlie; TZm: Tongzhougongzhu; ZJm: Akihime.</p>
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<p>Cluster heatmap analysis based on differential VOCs in strawberry juice and wine samples. Wine samples, BX: Snow White; TCL: Sweet Charlie; TZ: Tongzhougongzhu; ZJ: Akihime. Juice (m) samples, BXm: Snow White; TCLm: Sweet Charlie; TZm: Tongzhougongzhu; ZJm: Akihime.</p>
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24 pages, 5237 KiB  
Article
Effect of the Bioprotective Properties of Lactic Acid Bacteria Strains on Quality and Safety of Feta Cheese Stored under Different Conditions
by Angeliki Doukaki, Olga S. Papadopoulou, Antonia Baraki, Marina Siapka, Ioannis Ntalakas, Ioannis Tzoumkas, Konstantinos Papadimitriou, Chrysoula Tassou, Panagiotis Skandamis, George-John Nychas and Nikos Chorianopoulos
Microorganisms 2024, 12(9), 1870; https://doi.org/10.3390/microorganisms12091870 - 10 Sep 2024
Viewed by 432
Abstract
Lately, the inclusion of additional lactic acid bacteria (LAB) strains to cheeses is becoming more popular since they can affect cheese’s nutritional, technological, and sensory properties, as well as increase the product’s safety. This work studied the effect of Lactiplantibacillus pentosus L33 and [...] Read more.
Lately, the inclusion of additional lactic acid bacteria (LAB) strains to cheeses is becoming more popular since they can affect cheese’s nutritional, technological, and sensory properties, as well as increase the product’s safety. This work studied the effect of Lactiplantibacillus pentosus L33 and Lactiplantibacillus plantarum L125 free cells and supernatants on feta cheese quality and Listeria monocytogenes fate. In addition, rapid and non-invasive techniques such as Fourier transform infrared (FTIR) and multispectral imaging (MSI) analysis were used to classify the cheese samples based on their sensory attributes. Slices of feta cheese were contaminated with 3 log CFU/g of L. monocytogenes, and then the cheese slices were sprayed with (i) free cells of the two strains of the lactic acid bacteria (LAB) in co-culture (F, ~5 log CFU/g), (ii) supernatant of the LAB co-culture (S) and control (C, UHT milk) or wrapped with Na-alginate edible films containing the pellet (cells, FF) or the supernatant (SF) of the LAB strains. Subsequently, samples were stored in air, in brine, or in vacuum at 4 and 10 °C. During storage, microbiological counts, pH, and water activity (aw) were monitored while sensory assessment was conducted. Also, in every sampling point, spectral data were acquired by means of FTIR and MSI techniques. Results showed that the initial microbial population of Feta was ca. 7.6 log CFU/g and consisted of LAB (>7 log CFU/g) and yeast molds in lower levels, while no Enterobacteriaceae were detected. During aerobic, brine, and vacuum storage for both temperatures, pathogen population was slightly postponed for S and F samples and reached lower levels compared to the C ones. The yeast mold population was slightly delayed in brine and vacuum packaging. For aerobic storage at 4 °C, an elongation in the shelf life of F samples by 4 days was observed compared to C and S samples. At 10 °C, the shelf life of both F and S samples was extended by 13 days compared to C samples. FTIR and MSI analyses provided reliable estimations of feta quality using the PLS-DA method, with total accuracy (%) ranging from 65.26 to 84.31 and 60.43 to 89.12, respectively. In conclusion, the application of bioprotective LAB strains can result in the extension of feta’s shelf life and provide a mild antimicrobial action against L. monocytogenes and spoilage microbiota. Furthermore, the findings of this study validate the effectiveness of FTIR and MSI techniques, in tandem with data analytics, for the rapid assessment of the quality of feta samples. Full article
(This article belongs to the Section Food Microbiology)
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<p>Population of the examined microorganisms and pH values in aerobic storage of non-inoculated feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) Total viable counts, (<b><span style="color:#5B9BD5">•</span></b>) cocci/streptococci, (<b><span style="color:#ED7D31">•</span></b>) lactic acid bacteria, (<b><span style="color:#2F5496">•</span></b>) yeasts and molds are represented by a continuous line (-). pH values (<b><span style="color:#000000">•</span></b>) are indicated in the secondary axis and are represented with a dotted line (…). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Population of total viable counts (TVC) and <span class="html-italic">Listeria monocytogenes</span> in aerobic storage of inoculated feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) TVC is represented by a continuous line (-), and <span class="html-italic">Listeria monocytogenes</span> (<b><span style="color:red">•</span></b>) is represented in dashed lines (---). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Population of the examined microorganisms and pH values in brine storage of non-inoculated Feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) Total viable counts, (<b><span style="color:#5B9BD5">•</span></b>) cocci/streptococci, (<b><span style="color:#ED7D31">•</span></b>) lactic acid bacteria, (<b><span style="color:#2F5496">•</span></b>) yeasts and molds are represented by a continuous line (-). pH values (<b><span style="color:#000000">•</span></b>) are indicated in the secondary axis and are represented with a dotted line (…). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05), except from TVC between C and both F and S samples and cocci/streptococci at 10 °C between C and S samples.</p>
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<p>Population of total viable counts (TVC) and <span class="html-italic">Listeria monocytogenes</span> in brine storage of inoculated feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) TVC is represented by a continuous line (-) and <span class="html-italic">Listeria monocytogenes</span> (<b><span style="color:red">•</span></b>) is represented in dashed lines (---). Statistically important differences (<span class="html-italic">p</span> &lt; 0.05) were observed for TVC between C and both F and S samples.</p>
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<p>Population of the examined microorganisms and pH values in vacuum storage of non-inoculated feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) Total viable counts, (<b><span style="color:#5B9BD5">•</span></b>) cocci/streptococci, (<b><span style="color:#ED7D31">•</span></b>) lactic acid bacteria, (<b><span style="color:#2F5496">•</span></b>) yeasts and molds are represented by a continuous line (-). pH values (<b><span style="color:#000000">•</span></b>) are indicated in the secondary axis and are represented with a dotted line (…). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05) except from cocci/streptococci at 10 °C.</p>
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<p>Population of total viable counts (TVC) and <span class="html-italic">Listeria monocytogenes</span> in vacuum storage of inoculated feta cheese samples (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): F samples stored at 4 °C, (<b>c</b>): S samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): F samples stored at 10 °C, (<b>f</b>): S samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) TVC is represented by a continuous line (-) and <span class="html-italic">Listeria monocytogenes</span> (<b><span style="color:red">•</span></b>) is represented in dashed lines (---). Statistically important differences (<span class="html-italic">p</span> &lt; 0.05) were observed for <span class="html-italic">L. monocytogenes</span> between C and S samples.</p>
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<p>Population of the examined microorganisms and pH values in vacuum storage of non-inoculated feta cheese samples with edible film (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): FF samples stored at 4 °C, (<b>c</b>): SF samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): FF samples stored at 10 °C, (<b>f</b>): SF samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) Total viable counts, (<b><span style="color:#5B9BD5">•</span></b>) cocci/streptococci, (<b><span style="color:#ED7D31">•</span></b>) lactic acid bacteria, (<b><span style="color:#2F5496">•</span></b>) yeasts and molds are represented by a continuous line (-). pH values (<b><span style="color:#000000">•</span></b>) are indicated in the secondary axis and are represented with a dotted line (…). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05) except from cocci/streptococci at 4 °C for C and FF samples.</p>
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<p>Population of total viable counts (TVC) and <span class="html-italic">Listeria monocytogenes</span> in vacuum storage of inoculated feta cheese samples with edible film (mean values ± standard deviations) for (<b>a</b>): C samples stored at 4 °C, (<b>b</b>): FF samples stored at 4 °C, (<b>c</b>): SF samples stored at 4 °C, (<b>d</b>): C samples stored at 10 °C, (<b>e</b>): FF samples stored at 10 °C, (<b>f</b>): SF samples stored at 10 °C. (<b><span style="color:#3DF729">•</span></b>) TVC is represented by a continuous line (-) and <span class="html-italic">Listeria monocytogenes</span> (<b><span style="color:red">•</span></b>) is represented in dashed lines (---). No statistically important differences were observed (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Sensory scores of aerobic (<b>a</b>), brine (<b>b</b>), vacuum (<b>c</b>), vacuum with edible films (<b>d</b>), storage of feta cheese samples during storage at 4 and 10 °C for appearance (Ap), texture (Te), aroma (Ar), taste (Ts), and total score (T). Dashed lines represent the end of shelf life.</p>
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<p>Raw Fourier transform infrared (FTIR) spectra, in the selected wavenumber range 1800–900 cm<sup>−1</sup>, corresponding to feta cheese samples stored under aerobic conditions (<b>a</b>), brine (<b>b</b>), vacuum packaging (<b>c</b>), and with edible film under vacuum packaging (<b>d</b>). Fresh samples (Day 0) are represented in black solid line (──), spoiled samples at 4 °C in green dashed line (<span style="color:#00B050">----</span>), and spoiled samples at 10 °C in red dashed line (<span style="color:red">----</span>).</p>
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<p>Indicative multispectral imaging (MSI) reflectance spectra (mean ± standard deviation) from the benchtop-MSI instrument, corresponding to feta cheese samples stored in aerobic conditions (<b>a</b>), brine (<b>b</b>), vacuum (<b>c</b>), and vacuum with edible film (<b>d</b>). Fresh samples (Day 0) are represented in black solid line (──), spoiled samples at 4 °C in green dashed line (<span style="color:#00B050">----</span>), and spoiled samples at 10 °C in red dashed line (<span style="color:red">----</span>).</p>
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<p>Indicative multispectral imaging (MSI) reflectance spectra (mean ± standard deviation) from the portable-MSI instrument, corresponding to feta cheese samples stored in aerobic conditions (<b>a</b>), brine (<b>b</b>), vacuum (<b>c</b>), and vacuum with edible film (<b>d</b>). Fresh samples (Day 0) are represented in black solid line (──), spoiled samples at 4 °C in green dashed line (<span style="color:#00B050">----</span>), and spoiled samples at 10 °C in red dashed line (<span style="color:red">----</span>).</p>
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12 pages, 1271 KiB  
Review
Novel Insights in the Application of Probiotic Yeast Saccharomyces boulardii in Dairy Products and Health Promotion
by Zorica Tomičić, Ljubiša Šarić and Ružica Tomičić
Foods 2024, 13(18), 2866; https://doi.org/10.3390/foods13182866 - 10 Sep 2024
Viewed by 518
Abstract
Probiotic organisms are increasingly being incorporated into foods in order to develop products to prevent and reduce many diseases. Saccharomyces boulardii, a probiotic yeast with unique properties, such as viability over a wide pH range, antibiotic resistance, and the ability to reach [...] Read more.
Probiotic organisms are increasingly being incorporated into foods in order to develop products to prevent and reduce many diseases. Saccharomyces boulardii, a probiotic yeast with unique properties, such as viability over a wide pH range, antibiotic resistance, and the ability to reach a steady state, has an advantage over bacterial probiotics. The present review highlights the potential application of S. boulardii in functional fermented dairy products and the genetic engineering of this probiotic microorganism as a therapeutic agent for the treatment of various infectious diseases. It was found that probiotic yeast stimulates the growth of lactic acid bacteria in dairy products, creating favorable conditions and positively affecting the product’s sensory characteristics. Moreover, its viability of more than 106 cfu/mL at the end of the yogurt shelf life confirms its probiotic effect. On the other hand, there is a growing interest in the design of probiotic strains to improve their characteristics and fill existing gaps in their spectrum of action such as the inhibition of some bacterial toxins, as well as anti-inflammatory and immunomodulatory effects. The strengthening of immune functions and effective therapies against various diseases by S. boulardii was confirmed. However, considering this yeast species’ potential, further research is necessary to accurately determine the functional properties in terms of incorporation into food matrices and from the aspect of health and well-being claims. Full article
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<p>Image of <span class="html-italic">S. boulardii</span> cells taken using a microscope with a camera (Leica DFC290, Wetzlar, Germany) at a magnification of ×100.</p>
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<p>Current taxonomic position of <span class="html-italic">S. boulardii</span>.</p>
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<p>Health advantages of probiotic yeast <span class="html-italic">S. boulardii</span>.</p>
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11 pages, 692 KiB  
Article
Composite Coatings of Gellan Gum and Inulin with Lactobacillus casei: Enhancing the Post-Harvest Quality of Guava
by Rafael Emilio González-Cuello, Leidy Mendoza-Nova, Virginia Consuelo Rodriguez-Rodriguez, Joaquín Hernández-Fernández and Rodrigo Ortega-Toro
J. Compos. Sci. 2024, 8(9), 353; https://doi.org/10.3390/jcs8090353 - 9 Sep 2024
Viewed by 314
Abstract
Guava is a highly sought-after tropical fruit in the market due to its high content of vitamins, minerals, antioxidants, and other phenolic compounds. However, due to its climacteric nature, it has a short post-harvest shelf life. The aim of this study was to [...] Read more.
Guava is a highly sought-after tropical fruit in the market due to its high content of vitamins, minerals, antioxidants, and other phenolic compounds. However, due to its climacteric nature, it has a short post-harvest shelf life. The aim of this study was to develop coatings based on gellan gum (GG) and inulin (IN) incorporating Lactobacillus casei, which were tested for their potential ability to extend the post-harvest shelf life of whole guava fruit. The coatings were prepared using the following formulations: 0.5 GG/1.0 IN (w/v), 0.8 GG/5.0 IN (w/v), 0.5 GG/1.0 IN(w/v), and 0.8 GG/5.0 IN (w/v). The coated and uncoated (control) fruits were stored at 25 °C for 12 days, and various quality attributes were evaluated (including respiration rate, soluble solids, titratable acidity, weight loss, total phenol content, and color). The results indicated that the application of the coatings reduced weight loss, color change, and respiration rate in the fruits. However, the 0.8 GG/5.0 IN (w/v) formulation provided the best maintenance of post-harvest quality for the fruit evaluated. The coatings with a higher inulin content showed the highest growth of L. casei, which could enhance the antimicrobial effect of the coating. Therefore, the combined application of L. casei and inulin in coatings based on gellan gum can be considered an effective treatment to extend the shelf life and preserve the quality of guava fruits. Full article
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<p>Physicochemical characteristics of guava fruits coated with gellan gum and inulin. (<b>a</b>) Respiration rate values; (<b>b</b>) soluble solids; (<b>c</b>) acidity; and (<b>d</b>) weight loss. (** significant difference in <span class="html-italic">p</span> &lt; 0.05 according to LSD test for end of the storage time; <span class="html-italic">NS</span>: there was no significant difference in <span class="html-italic">p</span> &lt; 0.05). Vertical bars indicate standard error of the means.</p>
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<p>Phenolic content of guava fruits coated with gellan gum and inulin. (** significant difference in <span class="html-italic">p</span> &lt; 0.05 according to LSD test for end of the storage time. Vertical bars indicate standard error of the means. Vertical bars indicate standard error of the means.</p>
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20 pages, 2658 KiB  
Article
Impact of Ultrasound Pre-Treatment on the Drying Kinetics and Quality of Chicken Breast—A Comparative Study of Convective and Freeze-Drying Methods
by Iwona Szymanska, Aleksandra Matys, Katarzyna Rybak, Magdalena Karwacka, Dorota Witrowa-Rajchert and Malgorzata Nowacka
Foods 2024, 13(17), 2850; https://doi.org/10.3390/foods13172850 - 8 Sep 2024
Viewed by 616
Abstract
Fresh meat has a limited shelf life and is prone to spoilage. Drying serves as a common method for food preservation. Non-thermal techniques such as ultrasound treatment (US) can positively affect the drying processes and alter the final product. The study aimed to [...] Read more.
Fresh meat has a limited shelf life and is prone to spoilage. Drying serves as a common method for food preservation. Non-thermal techniques such as ultrasound treatment (US) can positively affect the drying processes and alter the final product. The study aimed to evaluate the impact of US pre-treatment on the hot air (HA) and freeze-drying (FD) of chicken breast meat and the quality of the dried products. US pre-treatment had a varied impact depending on the drying method used. The contact US method extended the HA drying time (about 50%) but improved water removal during FD (about 30%) compared to the untreated samples. Both methods resulted in low water content (<8.3%) and low water activity (<0.44). While rehydration properties (RR) and hygroscopicity (H) were not significantly affected by US pre-treatment in HA drying (about 1.35% and about 1.1, respectively), FD noticed differences due to shrinkage and porosity variations (RR: 2.4–3.2%, H: 1.19–1.25). The HA-dried samples exhibited notably greater tissue shrinkage and a darker surface color than the FD meat. Ultrasonic processing holds substantial potential in creating dried meat products with tailored characteristics. Hence, meticulous consideration of processing methods and parameters is of utmost importance. Full article
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<p>Drying kinetics (dimensionless moisture content—MR) in non-treated and US-treated chicken breast meat dried with (<b>a</b>) hot-air (HA) and (<b>b</b>) freeze-drying (FD) methods; green line marked on graphs indicates the critical moisture content required for dried meat-based snacks, such as beef jerky, which was established at 0.2.</p>
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<p>(<b>a</b>) Rehydration Ratio (RR), and (<b>b</b>) Soluble Solids Loss (SSL) in untreated and US-pretreated hot-air-dried (HA) and freeze-dried (FD) chicken breast meat.</p>
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<p>Hygroscopic properties (H) of untreated and US-pretreated hot-air-dried (HA) and freeze-dried (FD) chicken breast meat.</p>
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<p>Scanning electron microscope images of untreated and US-pretreated hot-air-dried (HA) and freeze-dried (FD) chicken breast meat, magnification 100×.</p>
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<p>Macroscopic photographs of untreated and US-pretreated hot-air-dried (HA) and freeze-dried (FD) chicken breast meat.</p>
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<p>(<b>a</b>) Projection of the quality parameters (variables) and the sample types (cases) on the plane of two first principal components and (<b>b</b>) a tree diagram derived from Hierarchical Cluster Analysis. For the denomination of the samples, see <a href="#foods-13-02850-t002" class="html-table">Table 2</a>. DT0.2—drying time to MR = 0.2 (min), DT0.04—drying time to MR = 0.04 (min), <span class="html-italic">Wc</span>%—water content (%), <span class="html-italic">a<sub>w</sub></span>—water activity (─), <span class="html-italic">L</span>*—lightness (─), <span class="html-italic">a</span>*—redness (─), <span class="html-italic">b</span>*—yellowness (─), <span class="html-italic">BI</span>—browning index (─), RR—rehydration rate (─), SSL—soluble solid loss (─), H1—hygroscopicity after 1 h (─), H24—hygroscopicity after 24 h (─). The numbers (1–6) presented on graphs shows the separate groups of samples.</p>
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