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21 pages, 6332 KiB  
Article
Unveiling the Potential of Silymarin, Spirulina platensis, and Chlorella vulgaris towards Cardiotoxicity via Modulating Antioxidant Activity, Inflammation, and Apoptosis in Rats
by Hanem F. El-Gendy, Hanem K. Khalifa, Ahmed Omran, Reda M. S. Korany, Shaimaa Selim, Eman Hussein, Rashed A. Alhotan, Anam Ayyoub and Shimaa R. Masoud
Life 2024, 14(10), 1289; https://doi.org/10.3390/life14101289 - 11 Oct 2024
Viewed by 446
Abstract
This study assessed the possible pharmacological effects of Chlorella vulgaris (Cg), Spirulina platensis (St), and silymarin (Sl) against thioacetamide (TA)-induced cardiotoxicity in rats, with a focus on their antioxidant, cardioprotective, and anti-inflammatory properties. The following is the random grouping of sixty male rats [...] Read more.
This study assessed the possible pharmacological effects of Chlorella vulgaris (Cg), Spirulina platensis (St), and silymarin (Sl) against thioacetamide (TA)-induced cardiotoxicity in rats, with a focus on their antioxidant, cardioprotective, and anti-inflammatory properties. The following is the random grouping of sixty male rats into six groups of ten animals each: the control (negative control), TA-intoxicated group (positive control; 300 mg/kg body weight (BW)), Sl + TA group (100 mg Sl/kg BW + TA), St + TA group (400 mg St/kg BW + TA), Cg + TA (400 mg Cg/kg BW + TA), and St + Cg + TA group (400 St + 400 Cg mg/kg BW + TA) were all administered for 30 days. At the start of the study, groups 2 through 6 were administered TA intraperitoneally at a dosage of 300 mg/kg BW for two consecutive days, with a 24 h gap between each dose, to induce cardiac damage. Blood samples were obtained to measure hematological parameters and perform biochemical assays, including lipid profiles and cardiac enzymes. For histopathology and immunohistochemistry determination, tissue samples were acquired. The current findings showed that TA injection caused hematological alterations and cardiac injury, as evidenced by greater serum levels of troponin I, creatine kinase-MB, and total creatine kinase (p < 0.05), as well as significantly elevated serum malondialdehyde and decreased serum total antioxidant capacity (p < 0.05) concentrations. Moreover, an increase in blood low-density lipoprotein and total cholesterol concentration (p < 0.05) was recorded in the TA group. There were alterations in the heart tissue’s histological structure of the TA group compared to the control ones. These alterations were characterized by vacuolar degeneration of myocytes, loss of cross striation, coagulative necrosis, and fibrosis of interstitial tissue, which was ameliorated by the supplementation of SI, St, and Cg. The TA-intoxicated group showed weak expression of B-cell lymphoma protein 2 (p < 0.05) and strong immunoreactivity of tumor necrosis factor-α and B-cell lymphoma protein 2-associated X (p < 0.05). However, the groups receiving Sl, St, and Cg experienced the opposite. The administration of Sl, St, Cg, and St + Cg along with TA significantly improved and restored (p < 0.05) erythrogram indices, including RBCs, hemoglobin, total leukocytic count, lymphocytes, and monocyte, to the normal control values. The administration of Sl, St, and Cg alleviated the cardiotoxicity caused by TA via reducing oxidative stress, inflammatory markers, and apoptosis in heart tissue. In summary, the current findings suggest that the treatment with Sl, St, and Cg was beneficial in ameliorating and reducing the cardiotoxicity induced by TA in rats. Full article
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Figure 1
<p>Effect of TA, Sl, St, and Cg on final body weight (g) of the experimental rats. Values are represented as means ± SE, <span class="html-italic">n</span> = 10. Different letters (a, b, c) indicate statistical significance at <span class="html-italic">p</span> &lt; 0.05. TA, thoiacetamide; Sl, silymarin; St, <span class="html-italic">Spirulina platensis</span>; Cg, <span class="html-italic">Chlorella vulgaris</span>.</p>
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<p>Effect of TA, Sl, St, and Cg on body weight gain (g) of the experimental rats. Values are represented as means ± SE, <span class="html-italic">n</span> = 10. Different letters (a, b, c) indicate statistical significance at <span class="html-italic">p</span> &lt; 0.05. TA, thoiacetamide; Sl, silymarin; St, <span class="html-italic">Spirulina platensis</span>; Cg, <span class="html-italic">Chlorella vulgaris</span>.</p>
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<p>Photomicrograph of rat heart (H&amp;E-stained sections, scale bar 50 µm): (<b>a</b>) the control group showed normal histological structure of myocytes (arrow). (<b>b</b>) The group treated with TA showed vacuolar degeneration of myocytes (arrow). (<b>c</b>) The group treated with TA showed loss of cross striation and sarcoplasm was more eosinophilic (arrow). (<b>d</b>) The group treated with TA showed fibrosis of interstitial tissue (arrow). (<b>e</b>) The group treated with TA showed perivascular fibrosis and inflammatory cell infiltration. (<b>f</b>) The group treated with TA showed hypertrophy of the tunica media of blood vessels. (<b>g</b>) The SI + TA group showing necrosis of few myocytes (arrow); (<b>h</b>) the SI + TA group showing mild fibrosis and inflammatory cells infiltration (arrow); (<b>i</b>) the SI + TA group showing normal interstitial blood vessel (arrow).</p>
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<p>Photomicrograph of rat heart (H&amp;E-stained sections, scale bar 50 µm): (<b>a</b>) the St + TA group had vacuolar degeneration of myocytes (arrow). (<b>b</b>) The St + TA group showed necrosis of myocytes (arrow). (<b>c</b>) The St + TA group showed perivascular fibrosis and inflammatory cell infiltration (arrow). (<b>d</b>) The St + TA group showed a mild thickness of interstitial blood vessels (arrow). (<b>e</b>) The Cg + TA group had a necrosis of a few myocytes (arrow). (<b>f</b>) The Cg + TA group had normal blood vessel thickness (arrow). (<b>g</b>) The St + Cg + TA group had mild vacuolar degeneration (arrow); (<b>h</b>) the St + Cg + TA group showed mild necrosis (arrow); (<b>i</b>) the St + Cg + TA group showed normal vascular thickness (arrow).</p>
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<p>(<b>a</b>) Immunostaining area expression % of BAX protein in the heart of different groups. (<b>b</b>) Immunostaining area expression % of Bcl-2 protein in the heart of different groups. (<b>c</b>) Immunostaining area expression % of TNF-α in the heart of different groups. (<b>d</b>) BAX/Bcl-2 ratio in experimental groups. Data were expressed as mean ±SE, with different letters indicating significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Photomicrograph of rat heart (Bax-, Bcl-2-, and TNF-α-stained sections, scale bar 50 µm): (<b>a</b>) the control group showed weak immune expression of Bax and TNF-α and strong expression of Bcl-2. (<b>b</b>) The TA group showed strong immunoreactivity of Bax and TNF-α and weak expression of Bcl-2. (<b>c</b>) The SI + TA group showed weak expression of Bax and TNF-α and strong expression of Bcl-2. (<b>d</b>) The St + TA group showed moderate expression of Bax, Bcl-2, and TNF-α. (<b>e</b>) The Cg + TA had mild expression of Bax and TNF-α and strong expression of Bcl-2. (<b>f</b>) The St + Cg + TA group had mild expression of Bax and TNF-α and strong expression of Bcl-2.</p>
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24 pages, 1586 KiB  
Review
The Neuroprotective Role of Cyanobacteria with Focus on the Anti-Inflammatory and Antioxidant Potential: Current Status and Perspectives
by Flávia Rodrigues, Mariana Reis, Leonor Ferreira, Clara Grosso, Ricardo Ferraz, Mónica Vieira, Vitor Vasconcelos and Rosário Martins
Molecules 2024, 29(20), 4799; https://doi.org/10.3390/molecules29204799 - 10 Oct 2024
Viewed by 501
Abstract
Neurodegenerative diseases are linked to the process of neurodegeneration. This can be caused by several mechanisms, including inflammation and accumulation of reactive oxygen species. Despite their high incidence, there is still no effective treatment or cure for these diseases. Cyanobacteria have been seen [...] Read more.
Neurodegenerative diseases are linked to the process of neurodegeneration. This can be caused by several mechanisms, including inflammation and accumulation of reactive oxygen species. Despite their high incidence, there is still no effective treatment or cure for these diseases. Cyanobacteria have been seen as a possible source for new compounds with anti-inflammatory and antioxidant potential, such as polysaccharides (sacran), phycobiliproteins (phycocyanin) and lipopeptides (honaucins and malyngamides), which can be interesting to combat neurodegeneration. As a promising case of success, Arthrospira (formerly Spirulina) has revealed a high potential for preventing neurodegeneration. Additionally, advantageous culture conditions and sustainable production of cyanobacteria, which are allied to the development of genetic, metabolic, and biochemical engineering, are promising. The aim of this review is to compile and highlight research on the anti-inflammatory and antioxidant potential of cyanobacteria with focus on the application as neuroprotective agents. Also, a major goal is to address essential features that brand cyanobacteria as an ecoefficient and economically viable option, linking health to sustainability. Full article
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<p>General mechanisms of neurodegeneration and the most promising cyanobacterial natural products for the prevention of neurological disorders include those with well-documented anti-inflammatory and antioxidant properties.</p>
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<p>Structure of Malyngamide 2 (<b>1</b>), a lipopeptide that inhibits NO production.</p>
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<p>Structure of aeruginosin-865 (<b>2</b>) is a nonribosomal linear tetrapeptide that inhibits interleukin-8 (IL-8).</p>
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<p>Structure of mycosporine-2-glycine (<b>3</b>) a Mycosporine-like amino acid able to inhibit iNOS and suppress the NF-κB pathway.</p>
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<p>The structure of scytonemin (<b>4</b>) is an indole-alkaloid able to inhibit iNOS and suppress the NF-κB pathway.</p>
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17 pages, 4894 KiB  
Article
Eco-Friendly Photocatalytic Treatment of Dyes with Ag Nanoparticles Obtained through Sustainable Process Involving Spirulina platensis
by Agnieszka Sidorowicz, Giacomo Fais, Francesco Desogus, Francesco Loy, Roberta Licheri, Nicola Lai, Giacomo Cao and Alessandro Concas
Sustainability 2024, 16(20), 8758; https://doi.org/10.3390/su16208758 - 10 Oct 2024
Viewed by 422
Abstract
The development of efficient photocatalysts is crucial in addressing water pollution concerns, specifically in the removal of organic dyes from wastewater. In this context, the use of silver nanoparticles (Ag NPs) might represent a method to achieve high dye degradation efficiencies. On the [...] Read more.
The development of efficient photocatalysts is crucial in addressing water pollution concerns, specifically in the removal of organic dyes from wastewater. In this context, the use of silver nanoparticles (Ag NPs) might represent a method to achieve high dye degradation efficiencies. On the other hand, the classical Ag NP production process involves several reactants and operating conditions, which make it poorly sustainable. In the present work, Ag NPs were synthesized according to a new sustainable process involving the use of natural extracts of Spirulina platensis and milder operating conditions. The material was also calcined to determine the influence of organic content on the properties of Ag NPs. The X-ray diffraction (XRD) analysis displayed the AgCl and Ag phases with a crystalline size of 11.79 nm before calcination. After calcination, only the Ag phase was present with an increased crystalline size of 24.60 nm. Fourier Transform Infrared Spectroscopy (FTIR) confirmed the capping role of the metabolites from the extract. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) revealed the spherical or quasi-spherical morphologies with agglomeration due to the calcination. Energy-dispersive X-ray spectroscopy (EDX) and Thermogravimetric (TGA) analyses further confirmed the involvement of metabolites in the synthesis of Ag NPs. The optical changes in the products were observed in a UV-Vis analysis. The Ag NPs were tested for their photocatalytic activity against the laboratory dye brilliant blue r in visible light in various conditions. The highest degradation efficiency of 81.9%, with a kapp value of 0.00595 min−1, was observed in alkaline medium after 90 min of light irradiation. Full article
(This article belongs to the Section Sustainable Water Management)
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<p>Emission spectrum of the light source provided by the manufacturer.</p>
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<p>Crystallographic and spectroscopic analyses (<b>A</b>) XRD, (<b>B</b>) FTIR, BC—before calcination, and AC—after calcination.</p>
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<p>Microscopy analysis: (<b>A</b>) SEM of Ag NPs BC, (<b>B</b>) EDX spectrum of Ag NPs BC, (<b>C</b>) EDX mappings of Ag NPs BC, (<b>D</b>) TEM of Ag NPs BC, (<b>E</b>) SEM of Ag NPs AC, (<b>F</b>) EDX spectrum of Ag NPs AC, (<b>G</b>) EDX mappings of Ag NPs AC, and (<b>H</b>) TEM of Ag NPs AC.</p>
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<p>Thermal and optical properties of Ag NPs: (<b>A</b>) TG and DTG of Ag NPs BC, (<b>B</b>) TG and DTG of Ag NPs AC, (<b>C</b>) DTA of Ag NPs BC and Ag NPs AC, (<b>D</b>) UV-Vis spectrum of Ag NPs BC, (<b>E</b>) UV-Vis spectrum of Ag NPs AC, and (<b>F</b>) Tauc plot of Ag NPs BC.</p>
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<p>Degradation of BBR dye in the dark: (<b>A</b>) UV-Vis spectral changes for the degradation of dye, (<b>B</b>) changes in dye concentration, (<b>C</b>) pseudo-first-order kinetic plot, and (<b>D</b>) percentage degradation efficiency. Reaction conditions: dye concentration: 21 mg/L, Ag NPs BC concentration: 1000 mg/L, and pH: 7.</p>
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<p>Percentage degradation efficiencies at different operating conditions: (<b>A</b>) light intensities, (<b>B</b>) dye concentration, (<b>C</b>) catalyst concentration, (<b>D</b>) pH, and (<b>E</b>) calcination.</p>
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<p>Mechanism of BBR dye degradation, adapted from [<a href="#B50-sustainability-16-08758" class="html-bibr">50</a>].</p>
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24 pages, 9408 KiB  
Article
Combined Dietary Spirulina platensis and Citrus limon Essential Oil Enhances the Growth, Immunity, Antioxidant Capacity and Intestinal Health of Nile Tilapia
by Safaa E. Abdo, Abeer F. El-Nahas, Rabab E. Abdellatif, Radi Mohamed, Mohamed A. Helal, Mahmoud M. Azzam, Alessandro Di Cerbo and Seham El-Kassas
Vet. Sci. 2024, 11(10), 474; https://doi.org/10.3390/vetsci11100474 - 4 Oct 2024
Viewed by 496
Abstract
The dietary presence of feed additives is crucial for boosting fish growth and immunity. Accordingly, this feeding trial aimed to investigate the effects of the separate and concurrent dietary supplementation of Spirulina platensis (SP) and bitter lemon (Citrus limon) peel essential [...] Read more.
The dietary presence of feed additives is crucial for boosting fish growth and immunity. Accordingly, this feeding trial aimed to investigate the effects of the separate and concurrent dietary supplementation of Spirulina platensis (SP) and bitter lemon (Citrus limon) peel essential oil (LEO) on the growth, immunity, antioxidant capacity, and intestinal health of Nile tilapia (Oreochromis niloticus). Four groups of male Nile tilapia were employed. The first group (control) was given the basal diet, while the second and third groups received the basal diet supplemented with LEO extract (1%) and SP (1 g/kg diet), respectively. The fourth group received the basal diet supplemented with a mix of LEO (1%) and SP at 1 g/kg. After two months of feeding, using LEO or/and SP improved the overall growth and immunological parameters, with their combination yielding the best outcomes. The supplementation of LEO or/and SP improved the Nile tilapia’s growth metrics and transcriptomic levels of growth-regulating genes such as (oligo-peptide transporter 1 (Pep1), growth hormone receptors 1 (GHR1), and insulin-like growth factor (IGF1). The improved growth performance was linked to significant increases in the expression levels of mucin and fat metabolism-related genes. Moreover, fish supplemented with LEO, SP, or their combination showed enhanced non-specific immunological measures, including phagocytic and lysozyme activities and the mRNA copies of its regulating genes. Additionally, remarkable increases in the antioxidant enzyme activities and the mRNA levels of their related genes were detected. The complement (C3) gene’s transcriptomic level was also significantly increased. Furthermore, the dietary supplementation of LEO, SP, or their combination improved the histological structures of the spleen, hepatopancreas, and intestine. The enhanced effects of LEO, SP, or their combination on fish immunity and growth are suggested to be due to their contents of bioactive compounds with anti-inflammatory, antioxidant, and antimicrobial properties. Thus, using the LOE and SP blends as feed additives is recommended for better growth and immunity of Nile tilapia. Full article
(This article belongs to the Special Issue Epidemiology, Biosecurity and Aquatic Animals Health)
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<p>Histological features of the intestinal wall (mucosa, propria sub-mucosa, muscularis, and serosa) and intestinal villi of Nile tilapia supplemented with LEO, SP, and their combination. LEO: lemon essential oil, SP: <span class="html-italic">Spirulina platensis</span>. Arrow: lining enterocytes with goblet cells. V: intestinal villi. M: intestinal wall.</p>
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<p>Histological features of hepatopancreas of Nile tilapia supplemented with LEO, SP, and their combination. LEO: lemon essential oil. SP: <span class="html-italic">Spirulina platensis</span>. H: hepatocytes. P: pancreatic acini. Arrow: glycogen deposition.</p>
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<p>Histological features of the spleen of Nile tilapia supplemented with LEO, SP, and their combination. LEO: lemon essential oil. SP: <span class="html-italic">Spirulina platensis</span>. Arrow: lymphocytic aggregation in the white pulp.</p>
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<p>The effects of dietary supplementation of LEO, SP, and their combination on the expression levels of growth-related genes. (<b>A</b>) <span class="html-italic">Ghr1</span>: growth hormone receptor 1, (<b>B</b>) <span class="html-italic">Igf-1</span>: insulin-like growth factor 1, (<b>C</b>) <span class="html-italic">Muc</span>: mucin-like protein, (<b>D</b>) <span class="html-italic">Pept1</span>: oligo-peptide transporter 1. LEO: lemon essential oil, SP: <span class="html-italic">Spirulina platensis</span>. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, respectively.</p>
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<p>The effects of dietary supplementation of LEO, SP, and their combination on the expression levels of immune and antioxidant genes. (<b>A</b>) <span class="html-italic">C3</span>: complement, (<b>B</b>) <span class="html-italic">LZM</span>: lysozyme, (<b>C</b>) <span class="html-italic">CAT</span>: catalase, (<b>D</b>) <span class="html-italic">GPX</span>: glutathione peroxidase. LEO: lemon essential oil, SP: <span class="html-italic">Spirulina platensis</span>. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, respectively.</p>
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<p>The effects of dietary supplementation of LEO, SP, and their combination on the expression levels of fat metabolism-regulating genes. (<b>A</b>) <span class="html-italic">FAS</span>: fatty acid synthesis, (<b>B</b>) <span class="html-italic">LPL</span>: lipoprotein lipase, (<b>C</b>) <span class="html-italic">FABP3</span>: fatty acid binding protein 3, (<b>D</b>) <span class="html-italic">CD36:</span> cluster of differentiation 36. LEO: lemon essential oil, SP: <span class="html-italic">Spirulina platensis</span>. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, respectively.</p>
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38 pages, 2438 KiB  
Review
Comprehensive Review of the Latest Investigations of the Health-Enhancing Effects of Selected Properties of Arthrospira and Spirulina Microalgae on Skin
by Mirosława Chwil, Rok Mihelič, Renata Matraszek-Gawron, Paulina Terlecka, Michał M. Skoczylas and Karol Terlecki
Pharmaceuticals 2024, 17(10), 1321; https://doi.org/10.3390/ph17101321 - 3 Oct 2024
Viewed by 428
Abstract
Arthospira platensis and Spirulina platensis microalgae are a rich source of pro-health metabolites (% d.m.): proteins (50.0–71.3/46.0–63.0), carbohydrates (16.0–20.0/12.0–17.0), fats (0.9–14.2/6.4–14.3), polyphenolic compounds and phenols (7.3–33.2/7.8–44.5 and 4.2/0.3 mg GAE/g), and flavonoids (1.9/0.2 QUE/g) used in pharmaceutical and cosmetic formulations. This review summarises [...] Read more.
Arthospira platensis and Spirulina platensis microalgae are a rich source of pro-health metabolites (% d.m.): proteins (50.0–71.3/46.0–63.0), carbohydrates (16.0–20.0/12.0–17.0), fats (0.9–14.2/6.4–14.3), polyphenolic compounds and phenols (7.3–33.2/7.8–44.5 and 4.2/0.3 mg GAE/g), and flavonoids (1.9/0.2 QUE/g) used in pharmaceutical and cosmetic formulations. This review summarises the research on the chemical profile, therapeutic effects in dermatological problems, application of Arthrospira and Spirulina microalgae, and contraindications to their use. The pro-health properties of these microalgae were analysed based on the relevant literature from 2019 to 2024. The antiviral mechanism of microalgal activity involves the inhibition of viral replication and enhancement of immunity. The anti-acne activity is attributed to alkaloids, alkanes, phenols, alkenes, phycocyanins, phthalates, tannins, carboxylic and phthalic acids, saponins, and steroids. The antibacterial activity generally depends on the components and structure of the bacterial cell wall. Their healing effect results from the inhibition of inflammatory and apoptotic processes, reduction of pro-inflammatory cytokines, stimulation of angiogenesis, and proliferation of fibroblasts and keratinocytes. The photoprotective action is regulated by amino acids, phlorotannins, carotenoids, mycosporins, and polyphenols inhibiting the production of tyrosinase, pro-inflammatory cytokines, and free oxygen radicals in fibroblasts and the stimulation of collagen production. Microalgae are promising molecular ingredients in innovative formulations of parapharmaceuticals and cosmetics used in the prophylaxis and therapy of dermatological problems. This review shows the application of spirulina-based commercial skin-care products as well as the safety and contraindications of spirulina use. Furthermore, the main directions for future studies of the pro-health suitability of microalgae exerting multidirectional effects on human skin are presented. Full article
(This article belongs to the Section Natural Products)
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<p>Pro-health properties of <span class="html-italic">Arthrospira platensis</span> and <span class="html-italic">Spirulina platensis</span>.</p>
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<p>Antiviral effects of <span class="html-italic">A. platensis</span> and <span class="html-italic">S. platensis</span>.</p>
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<p>Selected mechanisms of the healing action of <span class="html-italic">A. platensis</span> and <span class="html-italic">S. platensis</span>.</p>
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<p>Photoprotective action of <span class="html-italic">Arthrospira platensis</span> and <span class="html-italic">Spirulina platensis</span>.</p>
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<p>Application of <span class="html-italic">A. platensis</span> and <span class="html-italic">S. platensis</span> in selected pharmaceutical and cosmetic products.</p>
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<p>Companies using spirulina as an ingredient of various cosmetic products.</p>
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11 pages, 813 KiB  
Article
Extraction and Concentration of Spirulina Water-Soluble Metabolites by Ultrafiltration
by Claudia Salazar-González, Carolina Mendoza Ramos, Hugo A. Martínez-Correa and Hugo Fabián Lobatón García
Plants 2024, 13(19), 2770; https://doi.org/10.3390/plants13192770 - 3 Oct 2024
Viewed by 564
Abstract
Spirulina (Arthospira platensis) is known for its rich content of natural compounds like phycocyanin, chlorophylls, carotenoids, and high protein levels, making it a nutrient-dense food. Over the past decade, research has aimed to optimize the extraction, separation, and purification of these [...] Read more.
Spirulina (Arthospira platensis) is known for its rich content of natural compounds like phycocyanin, chlorophylls, carotenoids, and high protein levels, making it a nutrient-dense food. Over the past decade, research has aimed to optimize the extraction, separation, and purification of these valuable metabolites, focusing on technologies such as high-pressure processing, ultrasound-assisted extraction, and microwave-assisted extraction as well as enzymatic treatments, chromatographic precipitation, and membrane separation. In this study, various extraction methods (conventional vs. ultrasound-assisted), solvents (water vs. phosphate buffer), solvent-to-biomass ratios (1:5 vs. 1:10), and ultrafiltration (PES membrane of MWCO 3 kDa, 2 bar) were evaluated. The quantities of total protein, phycocyanin (PC), chlorophyll a (Cla), and total carotenoids (TCC) were measured. The results showed that ultrasound-assisted extraction (UAE) with phosphate buffer at a 1:10 ratio yielded a metabolite-rich retentate (MRR) with 37.0 ± 1.9 mg/g of PC, 617 ± 15 mg/g of protein, 0.4 ± 0.2 mg/g of Cla, and 0.15 ± 0.14 mg/g of TCC. Water extraction in the concentration process achieved the highest concentrations in MRR, with approximately 76% PC, 92% total protein, 62% Cla, and 41% TCC. These findings highlight the effective extraction and concentration processes to obtain a metabolite-rich retentate from Spirulina biomass, reducing the volume tenfold and showing potential as a functional ingredient for the food, cosmetic, and pharmaceutical industries. Full article
(This article belongs to the Special Issue Microalgae Photobiology, Biotechnology, and Bioproduction)
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<p>Permeate flux during the ultrafiltration of crude extract.</p>
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<p>Lyophilized retentates (<b>a</b>) from buffer extraction and (<b>b</b>) from water extraction.</p>
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21 pages, 5173 KiB  
Article
Phycocyanin-Loaded Alginate-Based Hydrogel Synthesis and Characterization
by Diana-Ioana Buliga, Alexandra Mocanu, Edina Rusen, Aurel Diacon, Gabriela Toader, Oana Brincoveanu, Ioan Călinescu and Aurelian Cristian Boscornea
Mar. Drugs 2024, 22(10), 434; https://doi.org/10.3390/md22100434 - 25 Sep 2024
Viewed by 774
Abstract
Phycocyanin was extracted from Spirulina platensis using conventional extraction (CE), direct ultrasonic-assisted extraction (direct UAE), indirect ultrasonic-assisted extraction (indirect UAE), and microwave-assisted extraction (MAE) methods at different temperatures, extraction intervals, stirring rate, and power intensities while maintaining the same algae to solvent ratio [...] Read more.
Phycocyanin was extracted from Spirulina platensis using conventional extraction (CE), direct ultrasonic-assisted extraction (direct UAE), indirect ultrasonic-assisted extraction (indirect UAE), and microwave-assisted extraction (MAE) methods at different temperatures, extraction intervals, stirring rate, and power intensities while maintaining the same algae to solvent ratio (1:15 w/v). The optimization of the extraction parameters indicated that the direct UAE yielded the highest phycocyanin concentration (29.31 ± 0.33 mg/mL) and antioxidant activity (23.6 ± 0.56 mg TE/g algae), while MAE achieved the highest purity (Rp = 0.5 ± 0.002). Based on the RP value, phycocyanin extract obtained by MAE (1:15 w/v algae to solvent ratio, 40 min, 40 °C, and 900 rpm) was selected as active compound in an alginate-based hydrogel formulation designed as potential wound dressings. Phycocyanin extracts and loaded hydrogels were characterized by FT-IR analysis. SEM analysis confirmed a porous structure for both blank and phycocyanin loaded hydrogels, while the mechanical properties remained approximately unchanged in the presence of phycocyanin. Phycocyanin release kinetics was investigated at two pH values using Zero-order, First-order, Higuchi, and Korsmeyer-Peppas kinetics models. The Higuchi model best fitted the experimental results. The R2 value at higher pH was nearly 1, indicating a superior fit compared with lower pH values. Full article
(This article belongs to the Special Issue Recent Advances in Marine-Derived Pigments)
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<p>Influence of time, temperature and rotation speed on the extracted phycocyanin content using MAE and on the antioxidant activity.</p>
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<p>Influence of time, temperature and power input on the extracted phycocyanin content and on the antioxidant activity (expressed as mg TE/g alga) using an ultrasonic probe in continuous mode.</p>
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<p>Influence of time, temperature and power input on the extracted phycocyanin content and on the antioxidant activity (expressed as mg TE/g alga) using an ultrasonic bath.</p>
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<p>Influence of time and temperature on the extracted phycocyanin content using CE methods and comparison with the unconventional equivalents.</p>
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<p>FT-IR spectra of the extracts (conv—conventional, MW—MAE, US-sd—1 s ON 1 s OFF direct sonication, US-b—indirect sonication, US-sc—continuous direct sonication).</p>
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<p>FT-IR analysis of the blank, phycocyanin loaded hydrogels and MW extracted phycocyanin.</p>
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<p>SEM images of polymer-alginate-based structure at a magnification of 5000× (<b>a</b>), 10000× (<b>b</b>), and 20000× (<b>c</b>).</p>
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<p>Stress-strain plots for equilibrium swelled hydrogels submitted to compression tests.</p>
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<p>Graphical representation of zero-order kinetics (<b>a</b>), first-order kinetics (<b>b</b>), Higuchi kinetics (<b>c</b>), and Korsmeyer-Peppas kinetics (<b>d</b>) for the phycocyanin release at pH = 7.45.</p>
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<p>Graphical representation of zero-order kinetics (<b>a</b>), first-order kinetics (<b>b</b>), Higuchi kinetics (<b>c</b>), and Korsmeyer-Peppas kinetics (<b>d</b>) for the phycocyanin release at pH = 6.5.</p>
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<p>Calibration curve for phycocyanin in phosphate buffer solution.</p>
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<p>Rubber-like behavior of the polymer-based hydrogel loaded with phycocyanin.</p>
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11 pages, 5759 KiB  
Article
Upcycling of Expanded Polystyrene Waste-Impregnated PVP Using Wet-Phase Inversion for Effective Microalgae Harvesting
by Tutik Sriani, Muslim Mahardika, Shofa Aulia Aldhama, Chandrawati Putri Wulandari and Gunawan Setia Prihandana
Polymers 2024, 16(19), 2703; https://doi.org/10.3390/polym16192703 - 25 Sep 2024
Viewed by 438
Abstract
The aim of this study was to investigate the potential of upcycling Expanded Polystyrene (EPS) waste collected from food packaging into a membrane for microalgae harvesting, in which membrane filtration often challenges fouling and pore blocking. The target species is Spirulina platensis, [...] Read more.
The aim of this study was to investigate the potential of upcycling Expanded Polystyrene (EPS) waste collected from food packaging into a membrane for microalgae harvesting, in which membrane filtration often challenges fouling and pore blocking. The target species is Spirulina platensis, with Chlorella vulgaris as a comparison agent. The membrane was fabricated from used Styrofoam, which typically ends up as single-use food packaging waste. In this study, PVP was used as an additive at varying concentrations, from 2 wt.% to 8 wt.%. The experimental results indicated that despite varying PVP concentrations, all EPS waste membranes exhibited near-complete recovery of Spirulina platensis biomass extraction. Despite the similar harvesting efficiency, EPS/PVP-8 exhibited the largest flux of 970.5 LMH/Bar, which is twice the value of the pristine EPS waste membrane. All membranes were hydrophilic; however, hydrophobicity increased with PVP concentration. SEM micrographs revealed that PVP enlarged the membrane surface pores and improved connectivity within the membrane’s structure, ensuring efficient flow. The EPS waste membrane offers promising insights for sustainable materials and wastewater treatment. The upcycling of EPS waste into flat sheet membranes not only addresses the problem of Styrofoam waste accumulation but also paves the way to transform waste into valuable products. Full article
(This article belongs to the Special Issue Advances in Sustainable Polymeric Materials, 3rd Edition)
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<p>Simplified flow diagram of EPS waste membrane preparation.</p>
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<p>Experimental setup of the water flux test using a dead-end cell unit.</p>
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<p>SEM micrographs on top surfaces of 20 wt.% EPS/PVP waste membranes: (<b>a</b>) pristine EPS, (<b>b</b>) EPS/PVP-2, (<b>c</b>) EPS/PVP-4, (<b>d</b>) EPS/PVP-6, and (<b>e</b>) EPS/PVP-8.</p>
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<p>Cross-sectional SEM micrographs of 20 wt.% EPS/PVP waste membranes: (<b>a</b>) pristine EPS membrane, (<b>b</b>) EPS/PVP-2, (<b>c</b>) EPS/PVP-4, (<b>d</b>) EPS/PVP-6, and (<b>e</b>) EPS/PVP-8.</p>
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<p>Microalgae harvesting using WEPS membranes with varied PVP concentrations.</p>
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<p>Pure water flux of EPS waste membranes with varied PVP concentrations.</p>
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<p>Water contact angle of EPS waste membranes with varied PVP concentrations.</p>
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17 pages, 1708 KiB  
Article
The Impact of Silver Nanoparticles Functionalized with Spirulina Protein Extract on Rats
by Ludmila Rudi, Inga Zinicovscaia, Liliana Cepoi, Tatiana Chiriac, Dmitrii Grozdov and Alexandra Kravtsova
Pharmaceuticals 2024, 17(9), 1247; https://doi.org/10.3390/ph17091247 - 22 Sep 2024
Viewed by 614
Abstract
Background/Objectives: This study investigates the biocompatibility and physiological impacts of silver nanoparticles (AgNPs) functionalized with Spirulina protein extract (SPE) on laboratory rats. The objective was to assess and compare the systemic distribution, organ accumulation, and changes in hematological and biochemical parameters between [...] Read more.
Background/Objectives: This study investigates the biocompatibility and physiological impacts of silver nanoparticles (AgNPs) functionalized with Spirulina protein extract (SPE) on laboratory rats. The objective was to assess and compare the systemic distribution, organ accumulation, and changes in hematological and biochemical parameters between biofunctionalized and non-functionalized silver nanoparticles. Methods: AgNPs were functionalized with SPE. Adult Wistar rats were administered these nanoparticles to assess their distribution across various organs using ICP-MS analysis. Hematological and biochemical markers were measured to evaluate systemic effects. Results: Functionalized silver nanoparticles demonstrated preferential accumulation in the brain, liver, and testicles, with significant clearance observed post-administration. The persistence of AgNPs SPE in reproductive organs was established. Hematological analysis revealed moderate changes, suggesting mild immune activation. Biochemical tests indicated transient increases in liver enzymes, signaling reversible hepatic stress. Conclusions: The biofunctionalization of AgNPs with Spirulina protein extract modifies the nanoparticles’ systemic behavior and organ distribution, enhancing their biocompatibility while inducing minimal physiological stress. These findings support the potential of Spirulina-based coatings to mitigate the toxicity and enhance the therapeutic efficacy of nanomedical agents. Full article
(This article belongs to the Special Issue Therapeutic Potential of Silver Nanoparticles (AgNPs))
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<p>FTIR spectra of (A) Spirulina protein extract (SPE) and (B) the functional mixture AgNPs-SPE.</p>
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<p>UV-Vis absorption spectra of (A) Spirulina protein extract (SPE) and (B) functional mixture AgNPs-SPE.</p>
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<p>Antioxidant activity (DPPH, % inhibition) of Spirulina protein extract (SPE) and functional mixture (AgNPs-SPE) monitored over 30 days. * <span class="html-italic">p</span> ˂ 0.05 and ** <span class="html-italic">p</span> ˂ 0.01 indicate a significant difference between adjacent groups.</p>
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<p>The content of silver in rats’ organs: (<b>A</b>) animals administered AgNPs and AgNPs-SPE for 28 days, measured immediately after the end of the experiment; (<b>B</b>) animals administered AgNPs for 28 days with measurements taken after a clearance expiration time (CET, 28 days); (<b>C</b>) animals administered AgNPs-SPE for 28 days with measurements taken after a clearance expiration time (CET, 28 days). * <span class="html-italic">p</span> ˂ 0.05 and ** <span class="html-italic">p</span> ˂ 0.01 indicate a significant difference between adjacent groups.</p>
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11 pages, 578 KiB  
Article
Physico-Chemical Properties and Chemical Analysis of Wildflower Honey Before and After the Addition of Spirulina (Arthrospira platensis)
by Cosimo Taiti, Lara Costantini, Diego Comparini, Nicolò Merendino and Stefania Garzoli
Molecules 2024, 29(18), 4373; https://doi.org/10.3390/molecules29184373 - 14 Sep 2024
Viewed by 611
Abstract
In this study, in order to verify the effects due to the addition of spirulina (Arthrospira platensis) in a food product, a wildflower honey was analyzed in terms of chemical composition, physicochemical properties and antioxidant activity before and after the addition [...] Read more.
In this study, in order to verify the effects due to the addition of spirulina (Arthrospira platensis) in a food product, a wildflower honey was analyzed in terms of chemical composition, physicochemical properties and antioxidant activity before and after the addition of the spirulina. HS-SPME/GC–MS and HPLC/UV were applied to carry out the chemical analyses. The obtained results demonstrated that the volatile profile and also the sugar content were significantly influenced by the addition of spirulina, showing significant qualitative and quantitative differences compared to honey without spirulina. The increase in HMF in honey added with spirulina was significant, demonstrating that its presence could accelerate the Maillard reaction. Electrical conductivity measured by using a conductometer was also increased while the moisture content was reduced in honey enriched with spirulina. Instead, the pH value was similar between the two samples. On the other hand, honey fortification with spirulina determined a significant increase of 12.5% in the total phenolic content (TPC), and a 56.25% increase in protein content. Further, the total antioxidant capacity (TAC) was also evaluated and a significant increase was determined as a result of the addition of spirulina. In conclusion, honey enriched with A. platensis was found to be characterized by a high pool of bioactive metabolites as well as significant changes in almost all the measurements performed. Full article
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<p>Calibration curve of HMF.</p>
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14 pages, 14978 KiB  
Article
Serum-Free Media Formulation Using Marine Microalgae Extracts and Growth Factor Cocktails for Madin-Darby Canine Kidney and Vero Cell Cultures
by Areumi Park, Yeon-Ji Lee, Eunyoung Jo, Gun-Hoo Park, Seong-Yeong Heo, Eun-Jeong Koh, Seung-Hong Lee, Seon-Heui Cha and Soo-Jin Heo
Int. J. Mol. Sci. 2024, 25(18), 9881; https://doi.org/10.3390/ijms25189881 - 12 Sep 2024
Viewed by 587
Abstract
The development of serum-free media (SFM) is critical to advance cell culture techniques used in viral vaccine production and address the ethical concerns and contamination risks associated with fetal bovine serum (FBS). This study evaluated the effects of marine microalgal extracts and growth [...] Read more.
The development of serum-free media (SFM) is critical to advance cell culture techniques used in viral vaccine production and address the ethical concerns and contamination risks associated with fetal bovine serum (FBS). This study evaluated the effects of marine microalgal extracts and growth factor cocktails on the activity of Madin-Darby canine kidney (MDCK) and Vero cells. Five marine microalgal species were used: Spirulina platensis (SP), Dunaliella salina (DS), Haematococcus pluvialis (HP), Nannochloropsis salina (NS), and Tetraselmis sp. (TS). DS and SP extracts significantly increased the proliferation rate of both MDCK and Vero cells. DS had a proliferation rate of 149.56% and 195.50% in MDCK and Vero cells, respectively, compared with that in serum-free medium (SFM). Notably, DS and SP extracts significantly increased superoxide dismutase (SOD) activity, which was 118.61% in MDCK cells and 130.08% in Vero cells for DS, and 108.72% in MDCK cells and 125.63% in Vero cells for SP, indicating a reduction in intracellular oxidative stress. Marine microalgal extracts, especially DS and SP, are feasible alternatives to FBS in cell culture as they promote cell proliferation, ensure safety, and supply essential nutrients while reducing oxidative stress. Full article
(This article belongs to the Special Issue Recent Research of Natural Products from Microalgae and Cyanobacteria)
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<p>Contamination detection in the microalgae extraction. (<b>A</b>) Mycoplasma, (<b>B</b>) bacteria, and (<b>C</b>) endotoxin. P: positive, N: negative, M: marker, SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, and TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Microalgae extract (50 and 100 µg/mL) cytotoxicity in Madin-Darby canine kidney (MDCK) and Vero cells. (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, and TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Growth factor cocktail (1 and 10 ng/mL) cytotoxicity in Madin-Darby canine kidney (MDCK) and Vero cells. (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. ** <span class="html-italic">p</span> &lt; 0.01 indicate values compared to serum-free medium (SFM).</p>
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<p>Madin-Darby canine kidney (MDCK) and Vero cell growth with microalgae extract (50 µg/mL) and growth factor cocktail. (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, and TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Madin-Darby canine kidney (MDCK) and Vero cell growth with microalgae extract (100 µg/mL) and growth factor cocktail. (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, and TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Madin-Darby canine kidney (MDCK) and Vero cell growth with microalgae extract (50 µg/mL) and growth factor cocktail. Scale bar = 50 µm. (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Madin-Darby canine kidney (MDCK) and Vero apoptosis assay cultured in microalgae extract (50 µg/mL) and growth factor cocktail (10 ng/mL). (<b>A</b>) MDCK and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. *** <span class="html-italic">p</span> &lt; 0.001 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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<p>Superoxide dismutase (SOD) activity of microalgae extract and growth factor cocktail. (<b>A</b>) Madin-Darby canine kidney (MDCK) and (<b>B</b>) Vero cells. Values are expressed as mean ± standard deviation (SD) from three replications. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 indicate values compared to serum-free medium (SFM). SP: <span class="html-italic">Spirulina plantensis</span>, DS: <span class="html-italic">Dunaliella salina</span>, HP: <span class="html-italic">Haematococcus pluvialis</span>, NS: <span class="html-italic">Nannochloropsis salina</span>, TS: <span class="html-italic">Tetraselmis</span> sp.</p>
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13 pages, 6023 KiB  
Article
Assessing the Efficacy of Cyanobacterial Strains as Oryza sativa Growth Biostimulants in Saline Environments
by Meruyert O. Bauenova, Fariza K. Sarsekeyeva, Asemgul K. Sadvakasova, Bekzhan D. Kossalbayev, Ramazan Mammadov, Aziza I. Token, Huma Balouch, Pavel Pashkovskiy, Yoong Kit Leong, Jo-Shu Chang and Suleyman I. Allakhverdiev
Plants 2024, 13(17), 2504; https://doi.org/10.3390/plants13172504 - 6 Sep 2024
Viewed by 528
Abstract
Soil salinity, which affects plant photosynthesis mechanisms, significantly limits plant productivity. Soil microorganisms, including cyanobacteria, can synthesize various exometabolites that contribute to plant growth and development in several ways. These microorganisms can increase plant tolerance to salt stress by secreting various phytoprotectants; therefore, [...] Read more.
Soil salinity, which affects plant photosynthesis mechanisms, significantly limits plant productivity. Soil microorganisms, including cyanobacteria, can synthesize various exometabolites that contribute to plant growth and development in several ways. These microorganisms can increase plant tolerance to salt stress by secreting various phytoprotectants; therefore, it is highly relevant to study soil microorganisms adapted to high salinity and investigate their potential to increase plant resistance to salt stress. This study evaluated the antioxidant activity of four cyanobacterial strains: Spirulina platensis Calu-532, Nostoc sp. J-14, Trichormus variabilis K-31, and Oscillatoria brevis SH-12. Among these, Nostoc sp. J-14 presented the highest antioxidant activity. Their growth-stimulating effects under saline conditions were also assessed under laboratory conditions. These results indicate that Nostoc sp. J-14 and T. variabilis K-31 show significant promise in mitigating the harmful effects of salinity on plant size and weight. Both strains notably enhanced the growth of Oryza sativa plants under saline conditions, suggesting their potential as biostimulants to improve crop productivity in saline environments. This research underscores the importance of understanding the mechanisms by which cyanobacteria increase plant tolerance to salt stress, paving the way for sustainable agricultural practices in saline areas. Full article
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<p>Total flavonoid contents of cyanobacterial extracts. Different asterisks indicate the levels of statistical significance: * <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 5. QE = quercetin equivalents; DE = dried extract.</p>
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<p>Dry biomass cyanobacterial cultures at different NaCl concentrations. The mean values ± SDs are shown. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 5.</p>
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<p>The impact of the combined action of cyanobacteria utilized in the experiment and NaCl treatment on the growth of 16-day-old <span class="html-italic">O. sativa</span> plants. The scale bar in the figure is 10 cm.</p>
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<p>The impact of the combination of cyanobacteria and NaCl on the shoot length of 16-day-old <span class="html-italic">O. sativa</span> plants. The mean values ± SDs are shown. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 5.</p>
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<p>The impact of the combination of cyanobacteria and NaCl on the shoot dry weight of 16-day-old <span class="html-italic">O. sativa</span> plants. Different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 5.</p>
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27 pages, 8736 KiB  
Article
Ameliorative Effect of Chitosan/Spirulina platensis Ethanolic Extract Nanoformulation against Cyclophosphamide-Induced Ovarian Toxicity: Role of PPAR-γ/Nrf-2/HO-1 and NF-kB/TNF-α Signaling Pathways
by May Almukainzi, Thanaa A. El-Masry, Hanaa A. Ibrahim, Hebatallah M. Saad, Enas I. El Zahaby, Asmaa Saleh and Maysa M. F. El-Nagar
Mar. Drugs 2024, 22(9), 395; https://doi.org/10.3390/md22090395 - 30 Aug 2024
Viewed by 2511
Abstract
Cyclophosphamide (CP) is an anticancer drug that causes infertility disorders. This study was designed to evaluate a nanoformulation of chitosan with an ethanolic extract from Spirulina platensis in terms of its protection against cyclophosphamide-induced ovarian toxicity. Nine groups of female Wistar rats were [...] Read more.
Cyclophosphamide (CP) is an anticancer drug that causes infertility disorders. This study was designed to evaluate a nanoformulation of chitosan with an ethanolic extract from Spirulina platensis in terms of its protection against cyclophosphamide-induced ovarian toxicity. Nine groups of female Wistar rats were randomly assigned as follows: 1: control vehicle, 2: chitosan polymer, 3: telmisartan, 4: Spirulina platensis extract, 5: nanoformulation of the Spirulina platensis, and 6: single injection of CP; groups 7, 8, and 9 received the same treatments as those used in groups 3, 4, and 5, respectively, with a single dose of CP (200 mg/kg, I.P). The results displayed that the CP treatment decreased estradiol, progesterone, anti-mullerian hormone, and GSH content, and it downregulated PPAR-γ, Nrf-2, and HO-1 gene expression. In addition, the CP treatment caused an increase in the FSH, LH, and MDA levels. In the same manner, the protein expression of caspase-3, NF-kB, and TNF-α was upregulated in response to the CP treatment, while PPAR-γ was downregulated in comparison with the control. The rats treated with SPNPs exhibited a substantial reduction in the detrimental effects of oxidative stress and inflammation of the ovarian tissue. This study’s conclusions showed that SPNPs counteracted the effects of CP, preventing the death of ovarian follicles and restoring the gonadotropin hormone balance and normal ovarian histological appearance. Full article
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<p>HPLC chromatogram of phenolic compounds in the SP ethanolic extract.</p>
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<p>HPLC chromatogram of the flavonoid compounds in the SP ethanolic extract.</p>
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<p>GC-MS chromatogram of the SP ethanolic extract.</p>
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<p>Particle size distribution (<b>A</b>) and zeta potential (<b>B</b>) of the SPNPs.</p>
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<p>SEM of Free SP particles (<b>A</b>) and SPNPs (<b>B</b>,<b>C</b>).</p>
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<p>DSC analysis of Free SP particles (<b>A</b>), SPNPs (<b>B</b>), and a polymer (Cs) (<b>C</b>).</p>
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<p>DSC analysis of Free SP particles (<b>A</b>), SPNPs (<b>B</b>), and a polymer (Cs) (<b>C</b>).</p>
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<p>XRD analysis of Free SP particles and SPNP.</p>
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<p>Effects of free SP extract and the nanoformulation on serum levels of estradiol, progesterone, and AMH. (<b>A</b>) Estradiol concentration; (<b>B</b>) progesterone concentration; (<b>C</b>) anti-mullerian hormone concentration. Data are presented as the mean ± SD (n = 6). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group. CP: Cyclophosphamide, SP: <span class="html-italic">Spirulina platenesis</span> extract, SPNPs: <span class="html-italic">Spirulina platenesis</span> extract nanoformulation.</p>
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<p>Effect of free and nanoformulation of SP on serum levels of FSH and LH. (<b>A</b>) FSH concentration (<b>B</b>) LH concentration. Data presented as mean ± SD (n = 6). Each group differed significantly from the others at <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group. CP: Cyclophosphamide, SP: <span class="html-italic">Spirulina platenesis</span> extract, SPNPs: <span class="html-italic">Spirulina platenesis</span> extract nanoformulation.</p>
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<p>Effects of free SP extract and the nanoformulation on oxidative stress biomarkers in ovarian tissues. (<b>A</b>) MDA content; (<b>B</b>) GSH content. Data are expressed as the mean ± SD (n = 6/group). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group. CP: Cyclophosphamide, SP: <span class="html-italic">Spirulina platenesis</span> extract, SPNPs: <span class="html-italic">Spirulina platenesis</span> extract nanoformulation.</p>
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<p>Effects of the free SP extract and the nanoformulation on the PPAR-γ, Nrf-2, and HO-1 signaling pathways in ovarian tissues. (<b>A</b>) PPAR-γ expression; (<b>B</b>) Nrf2 expression; (<b>C</b>) HO-1 expression. Data are presented as mean ± SD (n = 6). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group. CP: Cyclophosphamide, SP: <span class="html-italic">Spirulina platenesis</span> extract, SPNPs: <span class="html-italic">Spirulina platenesis</span> extract nanoformulation.</p>
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<p>Representative light photomicrographs of rats’ ovarian tissue stained with hematoxylin and eosin (H and E). (<b>A</b>,<b>B</b>) The control vehicle, (<b>C</b>,<b>D</b>) control polymer, (<b>E</b>,<b>F</b>) telmisartan (Tel), (<b>G</b>,<b>H</b>) free <span class="html-italic">Spirulina platensis</span> extract (FreeSP), and (<b>I</b>,<b>J</b>) nanoformulation of <span class="html-italic">Spirulina platensis</span> extract (SPNPs) showed normal ovarian histoarchitecture and follicular developmental stages, including the primordial follicle (PrF), primary follicle (PF), secondary follicle (SF), and antral follicle (AF). (<b>K</b>–<b>N</b>) The cyclophosphamide (CP)-intoxicated group showed marked vascular congestion and multiple atretic follicles with the sloughing of granulosa cells into the lumen (arrows). (<b>O</b>,<b>P</b>) Tel+CP. (<b>Q</b>,<b>R</b>) Free SP+CP. (<b>S</b>,<b>T</b>) SPNPs+CP. (<b>U</b>) Ovarian lesion histological score; (<b>V</b>) number of atretic follicles. Scale bar (<b>A</b>,<b>C</b>,<b>E</b>,<b>G</b>,<b>I</b>,<b>K</b>,<b>M</b>,<b>O</b>,<b>Q</b>,<b>S</b>): 200 µm. Scale bar (<b>B</b>,<b>D</b>,<b>F</b>,<b>H</b>,<b>J</b>,<b>L</b>,<b>N</b>,<b>P</b>,<b>R</b>,<b>T</b>): 50 µm. Data are presented as the mean ± SD (n = 6). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group.</p>
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<p>Representative light photomicrographs of rats’ ovarian tissue immunostained with peroxisome-proliferator-activated receptor gamma (PPAR-γ). (<b>A</b>) The control vehicle, (<b>B</b>) control polymer, (<b>C</b>) telmisertan (Tel), (<b>D</b>) free <span class="html-italic">Spirulina platensis</span> extract (Free SP), (<b>E</b>) nanoformulation of <span class="html-italic">Spirulina platensis</span> extract (SPNPs) showed marked PPAR-γ immunoexpression. (<b>F</b>) cyclophosphamide (CP) showed mild PPAR-γ immunoexpression. (<b>G</b>) Tel+CP showed moderate to marked PPAR-γ immunoexpression. (<b>H</b>) Free SP+CP showed moderate PPAR-γ immunoexpression, and (<b>I</b>) SPNPs+CP showed intense PPAR-γ immunoexpression. (<b>J</b>) The area % of PPAR-γ immunoexpression. Scale bar: 50 µm. Data presented as the mean ± SD (n = 6). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group.</p>
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<p>Representative light photomicrographs of rats’ ovarian tissue immunostained with nuclear factor kappa B (NF-κB). (<b>A</b>) The control vehicle, (<b>B</b>) control polymer, (<b>C</b>) telmisertan (Tel), (<b>D</b>) free <span class="html-italic">Spirulina platensis</span> extract (Free SP), and (<b>E</b>) nanoformulation of <span class="html-italic">Spirulina platensis</span> extract (SPNPs) showed negative NF-κB immunoexpression. (<b>F</b>) Cyclophosphamide (CP) showed intense NF-κB immunoexpression. (<b>G</b>) Tel+CP showed mild NF-κB immunoexpression. (<b>H</b>) Free SP+CP showed moderate NF-κB immunoexpression. (<b>I</b>) SPNPs+CP showed weak NF-κB immunoexpression. (<b>J</b>) The area % of NF-κB immunoexpression. Scale bar: 50 µm. Data are presented as the mean ± SD (n = 6). Each group differed significantly from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group.</p>
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<p>Representative light photomicrographs of rats’ ovarian tissue immunostained with tumor necrosis factor-alpha (TNF-α). (<b>A</b>) The control vehicle, (<b>B</b>) control polymer, (<b>C</b>) telmisertan (Tel), (<b>D</b>) free <span class="html-italic">Spirulina platensis</span> extract (Free SP), and (<b>E</b>) nanoformulation of the <span class="html-italic">Spirulina platensis</span> extract (SPNPs) showed negative TNF-α immunoexpression. (<b>F</b>) Cyclophosphamide (CP) showed intense TNF-α immunoexpression. (<b>G</b>) Tel+CP showed mild TNF-α immunoexpression. (<b>H</b>) Free SP+CP showed moderate TNF-α immunoexpression. (<b>I</b>) SPNPs+CP showed weak TNF-α immunoexpression. (<b>J</b>) The area % of TNF-α immunoexpression. Scale bar: 50 µm. Data are presented as the mean ± SD (n = 6). Each group significantly differed from the others at a <span class="html-italic">p</span>-value ≤ 0.05. * versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group.</p>
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<p>Representative light photomicrographs of rats’ ovarian tissue immunostained with caspase-3. (<b>A</b>) The control vehicle, (<b>B</b>) control polymer, (<b>C</b>) telmisertan (Tel), (<b>D</b>) free <span class="html-italic">Spirulina platensis</span> extract (Free SP), and (<b>E</b>) nanoformulation of the <span class="html-italic">Spirulina platensis</span> extract (SPNPs) showed mild caspase-3 immunoexpression. (<b>F</b>) Cyclophosphamide (CP) showed marked caspase-3 immunoexpression. (<b>G</b>) Tel+CP showed mild caspase-3 immunoexpression. (<b>H</b>) Free SP+CP showed moderate caspase-3 immunoexpression. (<b>I</b>) SPNPs+CP showed weak caspase-3 immunoexpression. (<b>J</b>) The area % of caspase-3 immunoexpression. Scale bar: 50 µm. Data are presented as the mean ± SD (n = 6). Each group significantly differed from the others at a <span class="html-italic">p</span>-value ≤ 0.05. *: versus the control group, <sup>a</sup> versus the CP group, <sup>b</sup> versus the Tel+CP group, and <sup>c</sup> versus the Free SP+CP group.</p>
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22 pages, 1699 KiB  
Review
Bioactive Compounds from Spirulina spp.—Nutritional Value, Extraction, and Application in Food Industry
by Blaženko Marjanović, Maja Benković, Tamara Jurina, Tea Sokač Cvetnić, Davor Valinger, Jasenka Gajdoš Kljusurić and Ana Jurinjak Tušek
Separations 2024, 11(9), 257; https://doi.org/10.3390/separations11090257 - 30 Aug 2024
Viewed by 1514
Abstract
The surging popularity of plant-based diets and the growing emphasis on clean-label products have intensified interest in Spirulina within the food industry. As more people adopt vegetarian, vegan, or flexitarian lifestyles, demand for plant-based protein sources has escalated. Spirulina’s high protein content [...] Read more.
The surging popularity of plant-based diets and the growing emphasis on clean-label products have intensified interest in Spirulina within the food industry. As more people adopt vegetarian, vegan, or flexitarian lifestyles, demand for plant-based protein sources has escalated. Spirulina’s high protein content and complete amino acid profile make it an ideal candidate to meet this demand. However, incorporating Spirulina into food products is not without its challenges. Its strong, earthy, or fishy taste can be off-putting to consumers and difficult to mask in food formulations. Furthermore, isolating Spirulina’s bioactive compounds while preserving their integrity is complex, especially considering the heat sensitivity of many of these components. Traditional extraction methods often employ high temperatures, which can degrade these valuable compounds. Consequently, there is a growing preference for non-thermal extraction techniques. This paper provides an overview of recent advancements in Spirulina cultivation, bioactive extraction, and their application in food products. Full article
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Figure 1
<p>(<b>a</b>) The average amounts of the most important groups of nutrients in <span class="html-italic">Spirulina</span>. (<b>b</b>) Differences in nutrient status among the various species of <span class="html-italic">Spirulina</span>, including <span class="html-italic">Spirulina platensis</span>, <span class="html-italic">Spirulina maxima</span>, <span class="html-italic">Spirulina pacifica</span>, and <span class="html-italic">Spirulina fusiformis</span> [<a href="#B7-separations-11-00257" class="html-bibr">7</a>,<a href="#B37-separations-11-00257" class="html-bibr">37</a>,<a href="#B56-separations-11-00257" class="html-bibr">56</a>,<a href="#B57-separations-11-00257" class="html-bibr">57</a>,<a href="#B58-separations-11-00257" class="html-bibr">58</a>,<a href="#B59-separations-11-00257" class="html-bibr">59</a>,<a href="#B60-separations-11-00257" class="html-bibr">60</a>,<a href="#B61-separations-11-00257" class="html-bibr">61</a>].</p>
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<p>Advantages of using the most-used non-thermal extraction methods for extracting the bioactive form of <span class="html-italic">Spirulina</span>.</p>
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24 pages, 1305 KiB  
Review
Spirulina/Arthrospira/Limnospira—Three Names of the Single Organism
by Maria A. Sinetova, Elena V. Kupriyanova and Dmitry A. Los
Foods 2024, 13(17), 2762; https://doi.org/10.3390/foods13172762 - 30 Aug 2024
Cited by 1 | Viewed by 1829
Abstract
Recent advances in research techniques have enabled rapid progress in the study of spirulina, an ancient edible cyanobacteria. Nowadays, spirulina species are classified into three genera: Spirulina, Arthrospira, and Limnospira. The latter now refers to industrially manufactured spirulina strains. Whole-genome [...] Read more.
Recent advances in research techniques have enabled rapid progress in the study of spirulina, an ancient edible cyanobacteria. Nowadays, spirulina species are classified into three genera: Spirulina, Arthrospira, and Limnospira. The latter now refers to industrially manufactured spirulina strains. Whole-genome sequencing revealed gene clusters involved in metabolite production, and the physiology of spirulina. Omics technologies demonstrated the absence of hazardous compounds in spirulina cells, confirming the safety of this biomass as a food product. Spirulina is a good source of different chemicals used in food manufacturing, food supplements, and pharmaceuticals. Spirulina’s enrichment with inherent biologically active substances makes it a potential supplier of natural products for dietary and pharmaceutical applications. Spirulina is also a prospective component of both terrestrial and space-based life support systems. Here, we review current breakthroughs in spirulina research and clarify fallacies that can be found in both professional literature and public media. Full article
(This article belongs to the Special Issue Bioactive Compounds in Food: From Molecule to Biological Function)
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<p>Microscopic visualization of spirulina. Spiral <span class="html-italic">Limnospira</span> sp. IPPAS B-1526 (<b>a</b>) and linear <span class="html-italic">Limnospira</span> sp. IPPAS B-287 (<b>b</b>) from the collection of microalgae and cyanobacteria of K.A. Timiryazev Institute of Plant Physiology, Russian Academy of Sciences (IPPAS, Moscow, Russia).</p>
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<p>A simplified scheme of taxonomic positioning of <span class="html-italic">Spirulina</span>, <span class="html-italic">Arthrospira</span>, and <span class="html-italic">Limnospira</span> families according to Algabase (<a href="https://www.algaebase.org/search/species/" target="_blank">https://www.algaebase.org/search/species/</a> (accessed on 14 August 2024 [<a href="#B29-foods-13-02762" class="html-bibr">29</a>])). * According to NCBI taxonomy browser, all <span class="html-italic">Limnospira</span> substrains belong to Sirenicapillariaceae family [<a href="#B30-foods-13-02762" class="html-bibr">30</a>].</p>
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<p>A scheme of fatty acid (FA) synthesis and desaturation in <span class="html-italic">Spirulina subsalsa</span> and <span class="html-italic">Arthrospira</span>/<span class="html-italic">Limnospira</span> species. One complex FA synthase is responsible for cyclic elongation of malonyl-CoA (C2) to palmitoleate (C16:0) and stearate (C18:0). These two FAs undergo desaturation (the formation of double bonds). Palmitic acid, C16:0, is desaturated into monoenoic palmitoleic acid C16:1∆<sup>9</sup> by ∆<sup>9</sup>-FAD. Stearic acid, C18:0, is desaturated into monoenoic oleic acid, C18:1∆<sup>9</sup>, by the same ∆<sup>9</sup>-FAD. Oleic acid is further desaturated into dienoic linoleic acid, C18:1∆<sup>9,12</sup>, by ∆<sup>12</sup>-FAD, and to trienoic γ-linolenic acid, C18:1∆<sup>6,9,12</sup>, by ∆<sup>6</sup>-FAD. The chromosome of spirulina contains three genes for FADs mentioned above, each only in one copy. No FA elongases exist in spirulina for building FA chains longer that C18.</p>
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