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Topic Editors

College of Food Science and Engineering, Ocean University of China, Qingdao 266100, China
Prof. Dr. Yanbo Wang
School of Food and Health, Beijing Technology and Business University, Beijing 100048, China
National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, China

Future Foods from the Sea

Abstract submission deadline
closed (5 June 2024)
Manuscript submission deadline
closed (5 September 2024)
Viewed by
33570

Topic Information

Dear Colleagues,

It is a big challenge for our world to feed ten billion people healthily in the near future without increasing the environmental impact of this process. Land-based and/or emission-intensive expansion of food production is prohibited to avoid the compromise of ecosystem services. We are expecting the ocean to fill the food gap sustainably in the future. Increases in the main seafood sectors—finfish capture and mariculture—are likely, but we should also look elsewhere on the incorporation of marine invertebrates, fish processing byproducts, seaweeds, and microalgae in routine diet to feed people high-quality protein and fat, as well as vitamins and minerals. This Topic will host diverse contributions ranging from research papers to up-to-date reviews dealing with edible sea products from farm to fork as part of dietary transition toward a sustainable and healthy future. It attempts to highlight the development of innovative food products or ingredients from the sea, as well as green and emerging technologies in seafood processing. It includes but is not limited to the following relevant themes:

  • Meat and dairy analogues
  • 3D food printing
  • Food nanotechnology
  • New food ingredients
  • Designer foods
  • Consumers’ behavior
  • Fish byproducts
  • Jellyfish
  • Macroalgal and microalgal biomass
  • Seafood allergens
  • Seafood safety

Prof. Dr. Haohao Wu
Prof. Dr. Yanbo Wang
Prof. Dr. Na Sun
Topic Editors

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Aquaculture Journal
aquacj
- - 2021 29.3 Days CHF 1000
Fishes
fishes
2.1 1.9 2016 17.4 Days CHF 2600
Foods
foods
4.7 7.4 2012 14.5 Days CHF 2900
Nutrients
nutrients
4.8 9.2 2009 13.5 Days CHF 2900
Oceans
oceans
1.5 3.1 2020 23.3 Days CHF 1600

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Published Papers (11 papers)

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10 pages, 252 KiB  
Article
A Sustainable Approach to Managing Invasive Macroalgae: Assessment of the Nutritional Profile and the Potential for Enteric Methane Mitigation of Rugulopteryx okamurae
by Helder P. B. Nunes, Cristiana Maduro-Dias, Joana Carvalho and Alfredo Borba
Oceans 2024, 5(3), 662-671; https://doi.org/10.3390/oceans5030038 - 10 Sep 2024
Viewed by 1062
Abstract
The expansion of the invasive Asian macroalgae Rugulopteryx okamurae along the coasts of the Azores represents a significant challenge for local marine biodiversity. A promising approach to managing the biomass produced by this alien alga is to valorize it in the context of [...] Read more.
The expansion of the invasive Asian macroalgae Rugulopteryx okamurae along the coasts of the Azores represents a significant challenge for local marine biodiversity. A promising approach to managing the biomass produced by this alien alga is to valorize it in the context of the blue economy. This study characterizes and evaluates the potential of R. okamurae biomass for incorporation into cattle feed, with a focus on mitigating enteric methane production. The nutritional value of R. okamurae, its digestibility, and its potential as a mitigating agent for enteric methane production were analyzed in vitro. The results indicate that the inclusion of 5% R. okamurae in the diet significantly (p < 0.05) reduced accumulated methane production by 98% after 24 h of incubation. The addition of 1% algae over the same period resulted in a 38% reduction in methane production. However, a significant decrease (p < 0.05) in gas production of 57.02% and 73.5% was also observed in relation to control, with the inclusion of 1% and 5%, respectively, during 96 h. Nutritionally, R. okamurae was found to have a crude protein content of 18.68% and fiber (NDF) of 55.71% of DM. It is also worth highlighting the high content of ash (31.86%) that was identified in these brown macroalgae. In conclusion, the fresh biomass of R. okamurae could serve as a functional ingredient in cattle feed to mitigate enteric methane production, provided it is used in low percentages. However, it is important to emphasize that high concentrations in the first 12 h did not produce methane, which is also not recommended for enteric fermentation. However, before including it in animal feed, in vivo tests are needed to assess its toxicity. Full article
(This article belongs to the Topic Future Foods from the Sea)
20 pages, 6724 KiB  
Article
Comprehensive Nutritional and Functional Characterization of Novel Mycoprotein Derived from the Bioconversion of Durvillaea spp.
by Catalina Landeta-Salgado, Nicolás Salas-Wallach, Javiera Munizaga, María Paz González-Troncoso, César Burgos-Díaz, Lhaís Araújo-Caldas, Patricia Sartorelli, Irene Martínez and María Elena Lienqueo
Foods 2024, 13(15), 2376; https://doi.org/10.3390/foods13152376 - 27 Jul 2024
Viewed by 1511
Abstract
This study aimed, for the first time, to determine the nutritional composition, beta-glucan and ergosterol contents, phenolic compound composition, and biological and functional activities of a novel mycoprotein produced through a bioconversion process of Durvillaea spp., a brown seaweed. An untargeted metabolomics approach [...] Read more.
This study aimed, for the first time, to determine the nutritional composition, beta-glucan and ergosterol contents, phenolic compound composition, and biological and functional activities of a novel mycoprotein produced through a bioconversion process of Durvillaea spp., a brown seaweed. An untargeted metabolomics approach was employed to screen metabolites and annotate molecules with nutraceutical properties. Two products, each representing a distinct consortia of co-cultured fungi, named Myco 1 and Myco 2, were analysed in this study. These consortia demonstrated superior properties compared to those of Durvillaea spp., showing significant increases in total protein (~238%), amino acids (~219%), and β-D-glucans (~112%). The protein contains all essential amino acids, a low fatty acid content, and exhibits high antioxidant activity (21.5–25.5 µmol TE/g). Additionally, Myco 2 exhibited the highest anti-alpha-glucosidase activity (IC50 = 16.5 mg/mL), and Myco 1 exhibited notable anti-lipase activity (IC50 = 10.5 mg/mL). Among the 69 top differentially abundant metabolites screened, 8 nutraceutical compounds were present in relatively high concentrations among the identified mycoproteins. The proteins and polysaccharides in the mycoprotein may play a crucial role in the formation and stabilization of emulsions, identifying it as a potent bioemulsifier. In conclusion, the bioconversion of Durvillaea spp. results in a mycoprotein with high-quality protein, significant nutritional and functional value, and prebiotic and nutraceutical potential due to the production of unique bioactive compounds. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Beta-glucan content (<b>a</b>) and ergosterol content (<b>b</b>) in Myco 1, Myco 2, and <span class="html-italic">Durvillaea</span> spp. samples. Values are presented as mean ± SD. Bars with different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). All values are based on dry weight (dw) analysis. The different bar colours are used solely for visual distinction between the data for Myco and <span class="html-italic">Durvillaea</span> spp. and do not represent any additional variable.</p>
Full article ">Figure 2
<p>Images of the O/W emulsions stabilized by Myco 1 and Myco 2 at different concentrations (1–5%, <span class="html-italic">w</span>/<span class="html-italic">w</span>).</p>
Full article ">Figure 3
<p>Optical micrographs of the O/W Pickering emulsions stabilized at different Myco 1 concentrations (1.0–5.0%, <span class="html-italic">w</span>/<span class="html-italic">w</span>). The images were acquired at 40× magnification.</p>
Full article ">Figure 4
<p>Optical micrographs of the O/W Pickering emulsions stabilized at different Myco 2 concentrations (1.0–5.0%, <span class="html-italic">w</span>/<span class="html-italic">w</span>). The images were acquired at 40× magnification.</p>
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16 pages, 8576 KiB  
Article
Impact of Corn Starch Molecular Structures on Texture, Water Dynamics, Microstructure, and Protein Structure in Silver Carp (Hypophthalmichthys molitrix) Surimi Gel
by Congyun Jiang, Xin Yang, Songyi Lin, Yumeng Yang, Jinzhi Yu, Xinqi Du and Yue Tang
Foods 2024, 13(5), 675; https://doi.org/10.3390/foods13050675 - 23 Feb 2024
Cited by 2 | Viewed by 1697
Abstract
This study systematically investigates the impact of corn starch molecular structures on the quality attributes of surimi gel products. Employing molecular analyses to characterize corn starch, three amylopectin fractions (A, B1, and B2), categorized by the degree of polymerization [...] Read more.
This study systematically investigates the impact of corn starch molecular structures on the quality attributes of surimi gel products. Employing molecular analyses to characterize corn starch, three amylopectin fractions (A, B1, and B2), categorized by the degree of polymerization ranges (6 < X ≤ 12, 12 < X ≤ 24, and 24 < X ≤ 36, respectively) were specifically focused on. The surimi gel quality was comprehensively assessed through texture profile analysis, nuclear magnetic resonance, scanning electron microscopy, stained section analysis, and Fourier transform infrared spectroscopy. Results indicated the substantial volume expansion of corn amylopectin upon water absorption, effectively occupying the surimi gel matrix and fostering the development of a more densely packed protein network. Starch gels with higher proportions of A, B1, and B2 exhibited improved hardness, chewiness, and bound water content in the resultant surimi gels. The weight-average molecular weight and peak molecular weight of corn starch showed a strong positive correlation with surimi gel hardness and chewiness. Notably, the secondary structure of proteins within the surimi gel was found to be independent of corn starch’s molecular structure. This study provides valuable insights for optimizing formulations in surimi gel products, emphasizing the significance of elevated A, B1, and B2 content in corn starch as an optimal choice for crafting dense, chewy, water-retaining surimi gels. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>SEC molecular mass distribution and molar mass of whole starch samples. The red dotted line (LS) represents the multi-angle laser light scattering signal, reflecting the molecular size of samples, while the blue dotted line (RI) indicates the differential signal, reflecting sample concentration. NG010, NG28, NG46, NG64, NG82, and NG100 denote the mixed starch samples with mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
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<p>Gel-permeation chromatography results of the chain-length distribution (CLDs) in whole starch samples. NG010, NG28, NG46, NG64, NG82, and NG100 represent the mixed starch samples with mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
Full article ">Figure 3
<p>The G’ (<b>a</b>) and G’’ (<b>b</b>) against angular frequency profiles of surimi/starch composites. NG010, NG28, NG46, NG64, NG82, and NG100 denote surimi/starch composite gels with added mixed starch at mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
Full article ">Figure 4
<p>Distribution curves of T<sub>2</sub> relaxation time for different surimi/starch composite gels. NG010, NG28, NG46, NG64, NG82, and NG100 represent surimi/starch composite gels with added mixed starch at mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
Full article ">Figure 5
<p>Light microscopy images (10×) with periodic acid-Schiff/naphthol yellow S double-staining of surimi/starch composite gels. NG010, NG28, NG46, NG64, NG82, and NG100 represent surimi/starch composite gels with added mixed starch at mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
Full article ">Figure 6
<p>Cryo-SEM (3× and 10×) images of different surimi/starch composite gels. NG010, NG28, NG46, NG64, NG82, and NG100 denote surimi/starch composite gels with added mixed starch at mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively.</p>
Full article ">Figure 7
<p>FT-IR (<b>a</b>) and relative content (%) of protein secondary structures (<b>b</b>) of different surimi/starch composite gels. NG010, NG28, NG46, NG64, NG82, and NG100 represent surimi/starch composite gels with added mixed starch at mass ratios of LACCS and HACCS at 0:10, 2:8, 4:6, 6:4, 8:2, and 10:0, respectively. Different lowercase letters represent the significant difference of surimi/starch composite gels with protein secondary structure content (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 8
<p>Heat map of the distribution of correlation coefficients between starch molecular structure and properties of different surimi/starch composite gels.</p>
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18 pages, 6123 KiB  
Article
Iron Complexes with Antarctic Krill–Derived Peptides Show Superior Effectiveness to Their Original Protein–Iron Complexes in Mice with Iron Deficiency Anemia
by Shengjie Hu, Songyi Lin, Qi Feng, Xueqing He, Haowei Xu, Lei Chen and Na Sun
Nutrients 2023, 15(11), 2510; https://doi.org/10.3390/nu15112510 - 28 May 2023
Cited by 2 | Viewed by 2282
Abstract
Antarctic krill protein–iron complex and peptide–iron complex were acquired to investigate their iron bioavailability, expression of iron-regulated genes, and in vivo antioxidant capacity. Results indicated that the Antarctic krill peptide–iron complex significantly increased the hemoglobin (Hb), serum iron (SI), and iron contents in [...] Read more.
Antarctic krill protein–iron complex and peptide–iron complex were acquired to investigate their iron bioavailability, expression of iron-regulated genes, and in vivo antioxidant capacity. Results indicated that the Antarctic krill peptide–iron complex significantly increased the hemoglobin (Hb), serum iron (SI), and iron contents in the liver and spleen in iron-deficiency anemia (IDA) mice (p < 0.05) compared with those of the Antarctic krill protein–iron complex. Despite the gene expressions of the divalent metal transporter 1(DMT1), the transferrin (Tf), and the transferrin receptor (TfR) being better regulated by both Antarctic krill peptide–iron complex and protein–iron complex, the relative iron bioavailability of the Antarctic krill peptide–iron complex group (152.53 ± 21.05%) was significantly higher than that of the protein–iron complex group (112.75 ± 9.60%) (p < 0.05). Moreover, Antarctic krill peptide–iron complex could enhance the antioxidant enzyme activities of superoxidase dismutase (SOD) and glutathione peroxidase (GSH-Px), reduce the malondialdehyde (MDA) level in IDA mice compared with the protein–iron complex, and reduce the cell damage caused by IDA. Therefore, these results indicated that Antarctic krill peptide–iron complex could be used as a highly efficient and multifunctional iron supplement. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Figure 1

Figure 1
<p>Mice experimental protocol and body weight changes in mice. (<b>A</b>) Mice experimental protocol: an iron−deficient diet was used for 8 weeks to establish an IDA mice model and mice were treated for 3 weeks with Antarctic krill peptide−iron complex, protein–iron complex or FeSO<sub>4</sub>; body weight and collected serum were regularly measured; at the end of the experiment, serum, stomach, duodenum, liver and spleen were collected; (<b>B</b>) the body weight changes after iron supplementation for different groups (control, model, Antarctic krill protein−iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). SEM error bars are present. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 2
<p>Hb, SI, and TIBC levels of the mice in different groups. (<b>A</b>) The changes in Hb concentration before and after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes in SI concentration after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes in TIBC levels after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 2 Cont.
<p>Hb, SI, and TIBC levels of the mice in different groups. (<b>A</b>) The changes in Hb concentration before and after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes in SI concentration after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes in TIBC levels after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 3
<p>The changes of iron contents of mice in the liver and spleen after iron supplementation for different groups. (<b>A</b>) the changes of iron contents of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes of iron contents of mice in the spleen after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 4
<p>Hemoglobin regeneration efficiency and relative biological value of iron-supplement groups. (<b>A</b>) effects of different iron supplements (Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub>) on hemoglobin concentration after iron supplementation; (<b>B</b>) analysis of the relative biological value of the iron-supplemented group (Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups) using the Hb regeneration efficiency of FeSO<sub>4</sub> as a reference (100%). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 5
<p>Effects of in the iron-supplemented group on expression of iron-regulated genes in the liver. (<b>A</b>) The changes of gene expression level of DMT1 of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes of gene expression level of Tf of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes of gene expression level of TfR of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 5 Cont.
<p>Effects of in the iron-supplemented group on expression of iron-regulated genes in the liver. (<b>A</b>) The changes of gene expression level of DMT1 of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes of gene expression level of Tf of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes of gene expression level of TfR of mice in the liver after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 6
<p>Effects of iron-supplemented group on in vivo antioxidant enzymes activity and level of mice. (<b>A</b>) The changes of SOD activity of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes of GSH-Px activity of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes of MDA concentration of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 6 Cont.
<p>Effects of iron-supplemented group on in vivo antioxidant enzymes activity and level of mice. (<b>A</b>) The changes of SOD activity of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>B</b>) the changes of GSH-Px activity of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups); (<b>C</b>) the changes of MDA concentration of mice in the gastric tissue after iron supplementation for different groups (control, model, Antarctic krill protein–iron complex, peptide–iron complex, and FeSO<sub>4</sub> groups). Data are presented as mean ± SD. Significant differences are indicated by asterisks (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 7
<p>Histopathological examination of liver and spleen of mice after iron supplementation for different groups. (<b>A</b>) Representative images of liver and spleen in control group stained with H&amp;E and photographed 40× magnifications; (<b>B</b>) representative images of liver and spleen in model group stained with H&amp;E and photographed 40× magnifications; (<b>C</b>) representative images of liver and spleen in Antarctic krill protein–iron group stained with H&amp;E and photographed 40× magnifications; (<b>D</b>) representative images of liver and spleen in Antarctic krill peptide–iron group stained with H&amp;E and photographed 40× magnifications; (<b>E</b>) representative images of liver and spleen in FeSO<sub>4</sub> group stained with H&amp;E and photographed 40× magnifications. Black arrows showing monocyte infiltration in the portal area and fine hemosiderin pigment deposited in individual macrophages in the liver, and the obvious appearance of tangible body macrophages and inflammatory cells in the spleen.</p>
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15 pages, 2234 KiB  
Article
Chemical-Structural Identification of Crude Gelatin from Jellyfish (Stomolophus meleagris) and Evaluation of Its Potential Biological Activity
by Dania Marisol Esparza-Espinoza, Hisila del Carmen Santacruz-Ortega, Maribel Plascencia-Jatomea, Santiago P. Aubourg, Jesús Aarón Salazar-Leyva, Francisco Rodríguez-Felix and Josafat Marina Ezquerra-Brauer
Fishes 2023, 8(5), 246; https://doi.org/10.3390/fishes8050246 - 8 May 2023
Cited by 6 | Viewed by 2605
Abstract
The demand for jellyfish is growing worldwide, especially due to their high nutraceutical value. In this study, the extraction and characterization of crude gelatin from the brown cannonball jellyfish (Stomolophus meleagris), which is periodically found in large volumes on the American [...] Read more.
The demand for jellyfish is growing worldwide, especially due to their high nutraceutical value. In this study, the extraction and characterization of crude gelatin from the brown cannonball jellyfish (Stomolophus meleagris), which is periodically found in large volumes on the American Pacific coasts, were carried out. The crude gelatin obtained by alkaline treatment, with subsequent heat and dialysis treatment, showed an ability to quench free radicals (via ABTS and ORAC methods), and protect human cells against oxidative damage (through inhibition of hemolysis by AAPH), and they protected against mutations caused by aflatoxin B1 in the Salmonella enterica Typhimurium TA100 strain. Furthermore, it was established that these extracts were innocuous for eukaryotic cells (genotoxicity assay). The amino acid profiles indicate a high concentration of glycine and proline, as well as charged amino acids. Electrophoretic, FT-IR, and 1H-NMR studies indicated that one of the main proteins present in this crude gelatin is collagen. The presence of collagen and other proteins was identified by proteomic studies. Alkaline crude gelatin from brown jellyfish could be considered as potential candidates to be evaluated as antioxidant agents in foods in future research. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Graphical abstract

Graphical abstract
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<p>Effect of the gelatinous extract obtained from the cannonball jellyfish on mutagenicity induced by AFB<sub>1</sub>, based on the <span class="html-italic">Salmonella enterica</span> Typhimurium TA100 assay.</p>
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<p>Phases of normal and abnormal mitoses exposed to water and sodium azide. Chromosomal aberrations observed in <span class="html-italic">Allium cepa</span> root tip cells: (<b>A</b>) normal prophase; (<b>B</b>) normal metaphase; (<b>C</b>) normal anaphase; (<b>D</b>) normal late anaphase; (<b>E</b>) normal telophase; (<b>F</b>) abnormal metaphase; (<b>G</b>) abnormal metaphase; (<b>H</b>) abnormal anaphase with lagging; (<b>I</b>) abnormal anaphase with lag; and (<b>J</b>) abnormal telophase.</p>
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<p>SDS–polyacrylamide protein pattern of the jellyfish (<span class="html-italic">Stomolophus meleagris</span>) crude gelatin sample. (<b>A</b>): molecular weight marker; (<b>B</b>): jellyfish crude gelatin sample.</p>
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<p>FT-IR spectra of the jellyfish crude gelatin sample.</p>
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<p><sup>1</sup>H-NMR spectra of the jellyfish crude gelatin sample. Amino acids are indicated by their corresponding peaks.</p>
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17 pages, 508 KiB  
Review
The Prevalence of Viruses Related to the Production of Mussels and Oysters in Saldanha Bay: A Systematic Review
by Likentso Sylvia Shuping, Izanne Susan Human, Jan Frederik Rykers Lues and Arnelia Natalie Paulse
Aquac. J. 2023, 3(2), 90-106; https://doi.org/10.3390/aquacj3020009 - 13 Apr 2023
Cited by 3 | Viewed by 3226
Abstract
The disposal of treated and untreated sewage near shellfish harvesting areas is a global concern. Discharged sewage may be contaminated with enteric viruses present in human faeces. Bivalve molluscs, in turn, act as vectors for enteric viruses through bioaccumulation and retention of these [...] Read more.
The disposal of treated and untreated sewage near shellfish harvesting areas is a global concern. Discharged sewage may be contaminated with enteric viruses present in human faeces. Bivalve molluscs, in turn, act as vectors for enteric viruses through bioaccumulation and retention of these viruses during the filter-feeding process, resulting in outbreaks of infections due to the consumption of contaminated shellfish. This review was conducted using peer-reviewed articles published from 2012 until September 2022, obtained from online databases such as Google Scholar, Scopus, and Science Direct, highlighting the challenges that the shellfish industry is faced with concerning pollutants ending up in the shellfish production areas. Developed countries have made some advancements by upgrading sewage infrastructures, which reduced viral loads in sewage. However, it is difficult to measure the significance of these improvements, as there are no regulations in place which stipulate the permissible limits for viruses. In most developing countries, including South Africa, there is a lack of effective management plans for virus monitoring in shellfish harvesting areas. The findings of this study indicated a need for extensive research on the origin of viruses, their interactions with other organisms within the marine ecosystem, the quantification of viruses within the Saldanha Bay harbour, and the development of virus management plans which currently are non-existent. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Figure 1
<p>PRISMA methodology of literature search (available from: <uri>http://www.prisma-statement.org</uri>, accessed on 6 September 2022).</p>
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28 pages, 3485 KiB  
Article
Combination of Solid State and Submerged Fermentation Strategies to Produce a New Jellyfish-Based Food
by Francesca Anna Ramires, Gianluca Bleve, Stefania De Domenico and Antonella Leone
Foods 2022, 11(24), 3974; https://doi.org/10.3390/foods11243974 - 8 Dec 2022
Cited by 10 | Viewed by 3525
Abstract
This study describes the set-up and optimization of a fermentation strategy applied to a composite raw material containing jellyfish biomass as the principal ingredient. New fermented food was developed by combining fresh jellyfish Rhizostoma pulmo and the sequential solid-state submerged liquid fermentation method [...] Read more.
This study describes the set-up and optimization of a fermentation strategy applied to a composite raw material containing jellyfish biomass as the principal ingredient. New fermented food was developed by combining fresh jellyfish Rhizostoma pulmo and the sequential solid-state submerged liquid fermentation method used in Asian countries for processing a high-salt-containing raw material. Aspergillus oryzae was used to drive the first fermentation, conducted in solid-state conditions, of a jellyfish-based product, here named Jelly paste. The second fermentation was performed by inoculating the Jelly paste with different selected bacteria and yeasts, leading to a final product named fermented Jellyfish paste. For the first time, a set of safety parameters necessary for monitoring and describing a jellyfish-based fermented food was established. The new fermented products obtained by the use of Debaryomyces hansenii BC T3-23 yeast strain and the Bacillus amyloliquefaciens MS3 bacterial strain revealed desirable nutritional traits in terms of protein, lipids and total phenolic content, as well as valuable total antioxidant activity. The obtained final products also showed a complex enzyme profile rich in amylase, protease and lipase activities, thus making them characterized by unique composite sensory odor descriptors (umami, smoked, dried fruit, spices). Full article
(This article belongs to the Topic Future Foods from the Sea)
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Graphical abstract

Graphical abstract
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<p>Diagram illustrating the procedure of the new proposed fermentation method for jellyfish-based food production. See also <a href="#app1-foods-11-03974" class="html-app">Figure S1</a>.</p>
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<p>Evolution of microbial counts over 20 days of fermentation of Jellyfish-based food products inoculated with selected yeast strains. Jelly paste (<span class="html-italic">Aspergillus oryzae</span>): product obtained by the first fermentation step (solid-state fermentation) performed by inoculating the Koji starter (<span class="html-italic">A. oryzae</span>) into Jellyfish puree (consisting of jellyfish, starch and wheat bran). SF: spontaneous fermentation of uninoculated Jelly paste, as control. Y1D: <span class="html-italic">Metschnikowia</span> sp., YB51: <span class="html-italic">Candida parapsilosis</span>; BC T3-23: <span class="html-italic">Debaryomyces hansenii</span>; LI 180-7: <span class="html-italic">Saccharomyces cerevisiae</span>. The initial inoculum of the four yeast starter strains (LI 180-7, YB51, BC T3-23, Y1D) was about 10<sup>7</sup> CFU/g. Microbial parameters: TBC (total bacterial count, accounting for aerobic colony count), BAC (<span class="html-italic">Bacillus</span> spp.), CPS (presumptive coagulase-positive staphylococci), PTS (presumptive total staphylococci), YDRBC (total yeast count), MDRBC (total mold count), MGS (MRS glucose seawater salts), MSS (MRS sucrose seawater salts), NAS (nutrient agar seawater salts). Media where microbial counts were equal to zero were not reported. For each fermented sample, microbial parameters were individually submitted to one-way analysis of variance (ANOVA), and Tukey’s post hoc method was applied to determine significant differences (<span class="html-italic">p</span> &lt; 0.05) among the microbial counts at different time points (as showed in the graph legends).</p>
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<p>Evolution of microbial counts over 20 days of fermentation of Jellyfish-based food products (Jelly paste) inoculated with selected bacterial strains. SB26: <span class="html-italic">Staphylococcus pasteuri</span>; MS3: <span class="html-italic">Bacillus amyloliquefaciens</span>; C 180-11: <span class="html-italic">Lactiplantibacillus plantarum</span>; KT 5-1: <span class="html-italic">Leuconostoc mesenteroides</span>. Commercial microbial starter preparations provided by Sacco srl, SBM-11: <span class="html-italic">Lactobacillus sakei</span>, <span class="html-italic">Staphylococcus carnosus</span> and <span class="html-italic">S. xylosus</span>; PROMIX-1: <span class="html-italic">S. xylosus</span>. The initial inoculum of the four bacterial starter strains (C 180-11, KT-5-1, MS3, SB26) and of two commercial bacterial starter preparations (SBM-11, PROMIX-1, Sacco Srl, Cadorago, Italy) was about 10<sup>8</sup> CFU/g. Microbial parameters: TBC (total bacterial count, accounting for aerobic colony count), BAC (<span class="html-italic">Bacillus</span> spp.), CPS (presumptive coagulase-positive staphylococci), PTS (presumptive total staphylococci), YDRBC (total yeast count), MDRBC (total mold count), MGS (MRS glucose seawater salts), MSS (MRS sucrose seawater salts), NAS (nutrient agar seawater salts). Media where microbial counts were equal to zero were not reported. For each fermented sample, microbial parameters were individually submitted to one-way analysis of variance (ANOVA), and Tukey’s post hoc method was applied to determine significant differences (<span class="html-italic">p</span> &lt; 0.05) among the microbial counts at different time points (as showed in the graph legends).</p>
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<p>(<b>a</b>) Total phenolic contents and (<b>b</b>) antioxidant activity in fermented Jellyfish paste samples. Total phenolic content is expressed as mg gallic acid equivalents per g of fresh weight (GAE/ g FW); antioxidant activity is expressed as nmol of TE per g fresh weight (nmol TE/g FW). SF: spontaneous fermentation of uninoculated Jelly paste, as control. Jelly paste inoculated with yeast strains: Y1D, <span class="html-italic">Metschnikowia</span> sp.; YB51, <span class="html-italic">Candida parapsilosis</span>; BC T3-23, <span class="html-italic">Debaryomyces hansenii</span>; LI 180-7, <span class="html-italic">Saccharomyces cerevisiae</span>. Jelly paste inoculated with bacterial strains: SB26, <span class="html-italic">Staphylococcus pasteuri</span>; MS3, <span class="html-italic">Bacillus amyloliquefaciens</span>; C 180-11, <span class="html-italic">Lactiplantibacillus plantarum</span>, KT 5-1, <span class="html-italic">Leuconostoc mesenteroides</span>; SBM-11, <span class="html-italic">Lactobacillus sakei</span>, <span class="html-italic">Staphylococcus carnosus</span> and <span class="html-italic">Staphylococcus xylosus</span>; PROMIX-1, <span class="html-italic">Staphylococcus xylosus</span>. Data were submitted to one-way analysis of variance (ANOVA), Tukey’s post hoc method was applied to determine significant differences among samples (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>(<b>a</b>) Effects of fermentation by yeast starter cultures on odor characteristics of jellyfish-based food products. Jelly paste (<span class="html-italic">A. oryzae</span>): product obtained by the first fermentation step (solid-state fermentation) performed by inoculating the Koji starter (<span class="html-italic">A. oryzae</span>) into Jellyfish puree (consisting of Jellyfish, starch, and wheat bran). SF: spontaneous fermentation of uninoculated Jelly paste, as control; LI 180-7: <span class="html-italic">Saccharomyces cerevisiae</span>; Y1D: <span class="html-italic">Metschnikowia</span> sp.; YB51: <span class="html-italic">Candida parapsilosis</span>; BC T3-23: <span class="html-italic">Debaryomyces hansenii</span>. (<b>b</b>) Effects of fermentation by bacterial starter cultures on odor characteristics of jellyfish-based food products. MS3: <span class="html-italic">Bacillus amyloliquefaciens</span>; SB26: <span class="html-italic">Staphylococcus pasteuri</span>; C 180-11: <span class="html-italic">Lactiplantibacillus plantarum</span>, KT 5-1: <span class="html-italic">Leuconostoc mesenteroides</span>. SBM-11: <span class="html-italic">Lactobacillus sakei</span>, <span class="html-italic">Staphylococcus carnosus</span> and <span class="html-italic">S. xylosus</span>; PROMIX-1: <span class="html-italic">S. xylosus</span>.</p>
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<p>(<b>a</b>) Effects of fermentation by yeast starter cultures on odor characteristics of jellyfish-based food products. Jelly paste (<span class="html-italic">A. oryzae</span>): product obtained by the first fermentation step (solid-state fermentation) performed by inoculating the Koji starter (<span class="html-italic">A. oryzae</span>) into Jellyfish puree (consisting of Jellyfish, starch, and wheat bran). SF: spontaneous fermentation of uninoculated Jelly paste, as control; LI 180-7: <span class="html-italic">Saccharomyces cerevisiae</span>; Y1D: <span class="html-italic">Metschnikowia</span> sp.; YB51: <span class="html-italic">Candida parapsilosis</span>; BC T3-23: <span class="html-italic">Debaryomyces hansenii</span>. (<b>b</b>) Effects of fermentation by bacterial starter cultures on odor characteristics of jellyfish-based food products. MS3: <span class="html-italic">Bacillus amyloliquefaciens</span>; SB26: <span class="html-italic">Staphylococcus pasteuri</span>; C 180-11: <span class="html-italic">Lactiplantibacillus plantarum</span>, KT 5-1: <span class="html-italic">Leuconostoc mesenteroides</span>. SBM-11: <span class="html-italic">Lactobacillus sakei</span>, <span class="html-italic">Staphylococcus carnosus</span> and <span class="html-italic">S. xylosus</span>; PROMIX-1: <span class="html-italic">S. xylosus</span>.</p>
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<p>Score scatter plot of PCA model performed on parameters associated with all jellyfish-based fermented samples. PCA variables were the data obtained from the analysis of values of microbiological data, chemical composition, nutritional traits, enzyme-associated activities and odor descriptors at the end of the process.</p>
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12 pages, 2926 KiB  
Article
Three-Dimensional Printing Properties of Polysaccharide Hydrocolloids–Unrinsed Sturgeon Surimi Complex Hydrogels
by Kang Liu, Nana Zhao, Chenxi Xiang, Yujin Li, Xiaoming Jiang, Mingyong Zeng, He Xu, Haiyan Wang, Haohao Wu, Xiaoqing Yu and Yuanhui Zhao
Foods 2022, 11(19), 2947; https://doi.org/10.3390/foods11192947 - 21 Sep 2022
Cited by 14 | Viewed by 2786
Abstract
Herein, the microstructure and mechanical properties of hydrogels consisting of unrinsed sturgeon surimi (URSS) and plant-derived polysaccharides such as κ-carrageenan (KC), konjac gum (KG), xanthan gum (XG), guar gum (GG) and sodium alginate (SA), were studied by texture analysis, rheological measurement and scanning [...] Read more.
Herein, the microstructure and mechanical properties of hydrogels consisting of unrinsed sturgeon surimi (URSS) and plant-derived polysaccharides such as κ-carrageenan (KC), konjac gum (KG), xanthan gum (XG), guar gum (GG) and sodium alginate (SA), were studied by texture analysis, rheological measurement and scanning electron microscopy (SEM). Rheological results showed that the apparent viscosity, storage modulus (G′) and loss modulus (G″) of URSS increased by addition of KC, KG, GG and SA. The gel strength of resultant surimi products fabricated with KG/URSS mixture was significantly higher than that of other groups. KG could significantly improve the hardness (44.14 ± 1.14 N), chewiness (160.34 ± 8.33 mJ) and cohesiveness (0.56 ± 0.02) of the unrinsed surimi gel. Adding SA and KC had no significant effect on the textural characteristics of printed gels. However, an apparent decrease in the relevant mechanical properties of printed hydrogels was observed when XG and GG were added into surimi. SEM indicated that the incorporation of KG and KC could further integrate the gel structure of URSS as compared to hindering the cross-linking of surimi protein by XG and GG, which were in accordance with gel strength and water-holding capacity. These results provided useful information to regulate the 3D printing performance in functionalized surimi-based material. Full article
(This article belongs to the Topic Future Foods from the Sea)
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<p>The general process of 3D printing.</p>
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<p>Effects of different polysaccharides on apparent viscosity of unwashed surimi gel. KC: κ-carrageenan; KG: konjac gum; XG: xanthan gum; GG: guar gum; SA: sodium alginate.</p>
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<p>Effect of different polysaccharides on the dynamic rheological characteristics of unwashed surimi gel. (<b>A</b>) Storage modulus (G′); (<b>B</b>) loss modulus (G″); (<b>C</b>) loss tangent (tanδ). KC: κ-carrageenan; KG: konjac gum; XG: xanthan gum; GG: guar gum; SA: sodium alginate.</p>
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<p>Three-dimensional printing effect of unwashed surimi with different polysaccharides. KC: κ-carrageenan; KG: konjac gum; XG: xanthan gum; GG: guar gum; SA: sodium alginate.</p>
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<p>Electron microscope pictures of raw surimi paste and cooked surimi with different polysaccharides. Raw surimi paste: (<b>A</b>–<b>F</b>) at magnification 1000×, cooked surimi: (<b>G</b>–<b>L</b>) at magnification 2000×. AG: control; BH: κ-carrageenan (KC); CI: konjac gum (KG); DJ: xanthan gum (XG); EK: guar gum (GG); FL: sodium alginate (SA).</p>
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<p>Gel strength of printed cylindrical surimi with different polysaccharides after cooking. KC: κ-carrageenan; KG: konjac gum; XG: xanthan gum; GG: guar gum; SA: sodium alginate. Bars indicate the standard deviation (n = 5). Lowercase letters on the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Water-holding capacity (WHC) of 3D-printed unwashed surimi gel after cooking. KC: κ-carrageenan; KG: konjac gum; XG: xanthan gum; GG: guar gum; SA: sodium alginate. Bars indicate the standard deviation (n = 5). Lowercase letters on the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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26 pages, 3681 KiB  
Article
Screening of a Novel Lactiplantibacillus plantarum MMB-05 and Lacticaseibacillus casei Fermented Sandwich Seaweed Scraps: Chemical Composition, In Vitro Antioxidant, and Volatile Compounds Analysis by GC-IMS
by Tengqi Gao, Jinling Chen, Jie Xu, Han Gu, Pengpeng Zhao, Wenbin Wang, Saikun Pan, Yang Tao, Hongli Wang and Jie Yang
Foods 2022, 11(18), 2875; https://doi.org/10.3390/foods11182875 - 16 Sep 2022
Cited by 11 | Viewed by 2553
Abstract
Lactic acid fermentation is a promising method for developing sandwich seaweed scraps. The objectives of this study were to investigate the effect of fermentation with Lactiplantibacillus plantarum MMB-05, Lactiplantibacillus casei FJAT-7928, mixed bacteria (1:1, v/v) and control on the physicochemical indexes, in [...] Read more.
Lactic acid fermentation is a promising method for developing sandwich seaweed scraps. The objectives of this study were to investigate the effect of fermentation with Lactiplantibacillus plantarum MMB-05, Lactiplantibacillus casei FJAT-7928, mixed bacteria (1:1, v/v) and control on the physicochemical indexes, in vitro antioxidant activity, and volatile compounds of Porphyra yezoensis sauce. Sensory evaluation was also performed. The results indicated that all lactic acid bacteria strains grew well in P. yezoensis sauce after 72 h of fermentation, with the viable cell counts of L. plantarum MMB-05 exceeding 10.0 log CFU/mL, the total phenolic content increasing by 16.54%, and the lactic acid content increasing from 0 to 44.38 ± 0.11 mg/mL. Moreover, the metabolism of these strains significantly increased the content of umami, sweet and sour free amino acids in P. yezoensis sauce. The total antioxidant capacity of L. plantarum MMB-05, L. casei FJAT-7928, mix and control groups increased by 594.59%, 386.49%, 410.27%, and 287.62%, respectively. Gas chromatography-ion mobility spectrometry (GC-IMS) analysis suggested that aldehydes and ketones accounted for the largest proportion, and the relative contents of acids and alcohols in P. yezoensis sauce increased significantly after lactic acid bacteria fermentation. In addition, the analysis of dynamic principal component analysis (PCA) and fingerprinting showed that the volatile components of the four treatment methods could be significantly distinguished. Overall, the L. plantarum MMB-05 could be recommended as an appropriate starter for fermentation of sandwich seaweed scraps, which provides a fundamental knowledge for the utilization of sandwiched seaweed scraps. Full article
(This article belongs to the Topic Future Foods from the Sea)
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<p>Growth and pH changes in <span class="html-italic">L. plantarum</span> MMB-05.</p>
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<p>Salt tolerance (<b>A</b>) and antibacterial activity (<b>B</b>) of <span class="html-italic">L. plantarum</span> MMB-05.</p>
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<p>Salt tolerance (<b>A</b>) and antibacterial activity (<b>B</b>) of <span class="html-italic">L. plantarum</span> MMB-05.</p>
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<p>Sensory evaluation radars of <span class="html-italic">Porphyra yezoensis</span> sauce fermented for 24 (<b>A</b>), 48 (<b>B</b>) and 72 (<b>C</b>) h, respectively.</p>
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<p>Sensory evaluation radars of <span class="html-italic">Porphyra yezoensis</span> sauce fermented for 24 (<b>A</b>), 48 (<b>B</b>) and 72 (<b>C</b>) h, respectively.</p>
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<p>Changes in viable cell counts (<b>A</b>), pH value (<b>B</b>), and total sugar content (<b>C</b>), during 3 days LAB stains fermentation of <span class="html-italic">P. yezoensis</span> sauce.</p>
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<p>Changes in viable cell counts (<b>A</b>), pH value (<b>B</b>), and total sugar content (<b>C</b>), during 3 days LAB stains fermentation of <span class="html-italic">P. yezoensis</span> sauce.</p>
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<p>Changes in total phenol (<b>A</b>) and total flavonoids (<b>B</b>) contents during LAB stains fermentation of <span class="html-italic">P. yezoensis</span> sauce. Note: abcd represents the significant difference between groups (different fermentation time in the same group). ABCD represents the significant difference between the same fermentation time of different groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changes in organic acid contents during LAB stains fermentation of <span class="html-italic">P. yezoensis</span> sauce.</p>
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<p>ABTS<sup>+</sup> radical scavenging (<b>A</b>), FRAP (<b>B</b>) and total antioxidant capacity (<b>C</b>), in <span class="html-italic">P. yezoensis</span> sauce fermented by LAB stains. Note: abcd represents the significant difference between groups (different fermentation time in the same group). ABC represents the significant difference between the same fermentation time of different groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Principal component diagram of free amino acid content changes during LAB stains fermentation of <span class="html-italic">P. yezoensis</span> sauce. score plot (<b>A</b>); loading plot (<b>B</b>).</p>
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<p>The volatile organic compounds analysis of 72 h fermented <span class="html-italic">P. yezoensis</span> sauce by GC-IMS. 3D-topographic top view plot (<b>A</b>); difference map of 3D-topographic top view plot (<b>B</b>); PCA score chart (<b>C</b>); fingerprint spectrum of some of the volatile organic compounds (<b>D</b>).</p>
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<p>The volatile organic compounds analysis of 72 h fermented <span class="html-italic">P. yezoensis</span> sauce by GC-IMS. 3D-topographic top view plot (<b>A</b>); difference map of 3D-topographic top view plot (<b>B</b>); PCA score chart (<b>C</b>); fingerprint spectrum of some of the volatile organic compounds (<b>D</b>).</p>
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17 pages, 2260 KiB  
Article
Insight into the Gel Properties of Antarctic Krill and Pacific White Shrimp Surimi Gels and the Feasibility of Polysaccharides as Texture Enhancers of Antarctic Krill Surimi Gels
by Shuang Li, Songyi Lin, Pengfei Jiang, Zhijie Bao, Sibo Li and Na Sun
Foods 2022, 11(16), 2517; https://doi.org/10.3390/foods11162517 - 20 Aug 2022
Cited by 18 | Viewed by 2926
Abstract
Antarctic krill is a potential and attractive resource for consumption. However, most Antarctic krill meat is used to produce primary products with low commercial value, with few highly processed products. This study aimed to evaluate and improve the gelling properties of Antarctic krill [...] Read more.
Antarctic krill is a potential and attractive resource for consumption. However, most Antarctic krill meat is used to produce primary products with low commercial value, with few highly processed products. This study aimed to evaluate and improve the gelling properties of Antarctic krill surimi, with Pacific white shrimp surimi as control. Compared with Pacific white shrimp surimi, the lower β-sheet content and protein aggregation degree had a severe impact on the formation of the gel network of Antarctic krill surimi, which resulted in weaker breaking force, gel strength, and viscoelasticity (p < 0.05). Moreover, water retention capacity and molecular forces had a positive effect on the stability of the gel matrix of shrimp surimi. Thus, the high α-helix/β-sheet ratio, weak intermolecular interactions, and low level of protein network cross-linkage were the main reasons for the poor quality of Antarctic krill surimi. On this basis, the effects of six polysaccharides on the texture properties of Antarctic krill surimi were studied. Chitosan, konjac glucomannan, sodium carboxyl methyl cellulose, and waxy maize starch resulted in no significant improvement in the texture properties of Antarctic krill surimi (p > 0.05). However, the addition of ι-carrageenan (2%) or κ-carrageenan (1~2%) is an effective way to improve the texture properties of Antarctic krill surimi (p < 0.05). These findings will contribute to the development of reconstituted Antarctic krill surimi products with high nutritional quality and the promotion of deep-processing products of Antarctic krill meat. Full article
(This article belongs to the Topic Future Foods from the Sea)
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Graphical abstract

Graphical abstract
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<p>Gel strength and water-holding capacity of Antarctic krill and Pacific white shrimp surimi gels: (<b>a</b>) Breaking force, (<b>b</b>) deformation, (<b>c</b>) gel strength, and (<b>d</b>) water-holding capacity. Different letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi.</p>
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<p>Viscoelastic properties of Antarctic krill and Pacific white shrimp surimi during the heat-induced gelation process: (<b>a</b>) Frequency sweep, (<b>b</b>) temperature sweep, and (<b>c</b>) tan δ. PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi.</p>
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<p>Nuclear magnetic resonance spin–spin relaxation (T<sub>2</sub>) of Antarctic krill and Pacific white shrimp surimi gels: (<b>a</b>) The curve of T<sub>2</sub> relaxation time, and (<b>b</b>) the percentage of T<sub>21</sub>, T<sub>22</sub>, and T<sub>23</sub>. PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi. Different letters (a, b) within the same sample indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Cryo-SEM images of Antarctic krill and Pacific white shrimp surimi gels: (<b>a</b>) PWSS (2000×), (<b>b</b>) PWSS (5000×), (<b>c</b>) PWSS (10,000×), (<b>d</b>) AKS (2000×), (<b>e</b>) AKS (5000×), and (<b>f</b>) AKS (10,000×). PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi.</p>
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<p>Protein patterns and gray value of Antarctic krill and Pacific white shrimp surimi (gels): (<b>a</b>) SDS-PAGE pattern, (<b>b</b>) grayscale map; (<b>c</b>) gray value of the top of the lane, (<b>d</b>) gray value of myosin heavy chain, (<b>e</b>) gray value of paramyosin, (<b>f</b>) gray value of actin, (<b>g</b>) gray value of troponin T, and (<b>h</b>) gray value of myosin light chain. AK, Antarctic krill; AKS, Antarctic krill surimi; PWS, Pacific white shrimp; and PWSS, Pacific white shrimp surimi. Different letters (a–d) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>FTIR of Antarctic krill and Pacific white shrimp surimi gels: (<b>a</b>) FTIR spectra curve, and (<b>b</b>) the change of secondary structure. PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi. Different letters (a, b) within the same protein structure tested indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The correlation analysis and principal component analysis (PCA): (<b>a</b>) Correlation analysis; (<b>b</b>) the score scatter and loading plot of PCA. PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi.</p>
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<p>Texture properties of shrimp surimi gels: (<b>a</b>) Hardness, (<b>b</b>) springiness, (<b>c</b>) cohesiveness, and (<b>d</b>) chewiness. PWSS, Pacific white shrimp surimi; and AKS, Antarctic krill surimi; CS, chitosan; KG, konjac glucomannan; CMC-Na, sodium carboxyl methyl cellulose; WMS, waxy maize starch; ιCG, ι-carrageenan; and κCG, κ-carrageenan. Different letters within the same polysaccharide used indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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13 pages, 276 KiB  
Article
Consumer Knowledge and Acceptance of “Algae” as a Protein Alternative: A UK-Based Qualitative Study
by Chloe Mellor, Rochelle Embling, Louise Neilson, Tennessee Randall, Chloe Wakeham, Michelle D. Lee and Laura L. Wilkinson
Foods 2022, 11(12), 1703; https://doi.org/10.3390/foods11121703 - 10 Jun 2022
Cited by 18 | Viewed by 5503
Abstract
Overconsumption of meat has been recognised as a key contributing factor to the climate emergency. Algae (including macroalgae and microalgae) are a nutritious and sustainable food source that may be utilised as an alternative to animal-based proteins. However, little is known about the [...] Read more.
Overconsumption of meat has been recognised as a key contributing factor to the climate emergency. Algae (including macroalgae and microalgae) are a nutritious and sustainable food source that may be utilised as an alternative to animal-based proteins. However, little is known about the consumer awareness and acceptance of algae as a protein alternative. The aim of this qualitative study was to develop a rich and contextualised understanding of consumer beliefs about the use of algae in novel and innovative food products. A total of 34 participants from the UK assisted with our study. Each participant engaged in one focus group, with six focus groups conducted in total. Existing consumer knowledge of algae was discussed before participants explored the idea of algae-based food products. Reflexive (inductive) thematic analysis was used to analyse these data. Results showed that consumers have limited pre-existing knowledge of algae as a food source; however, participants were open to the idea of trying to consume algae. This anticipated acceptance of algae was influenced by several product attributes, including perceived novelty, edibility, healthiness, sustainability, and affordability. These findings highlight algae as a promising protein alternative to support plant-forward diets in the UK and identify key attributes to consider in future product development and marketing strategies. Full article
(This article belongs to the Topic Future Foods from the Sea)
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