Exploring Rhamnus alaternus Polysaccharides: Extraction, Characterization, and Analysis of Antioxidant and Antimicrobial Properties

In the present study, polysaccharides were isolated from the leaves (WSPRaL) and stems (WSPRaS) of <i>Rhamnus alaternus</i> with yields of 3% and 3.25% for WSPRaS and WSPRaL, respectively. Crude WSPRaL was composed of proteins (260.740 ± 0.98 µg/mg), lipids (53.34 ± 2.38 µg/mg), total sugars (482.716 ± 3.02 µg/mg), and reducing sugars (420.240 ± 1.68 µg/mg). In contrast, WSPRaS contained proteins (269.629 ± 1.48 µg/mg), lipids (13.33 ± 0.28 µg/mg), total sugars (569.135 ± 3.82 µg/mg), and reducing sugars (531.732 ± 2.59 µg/mg). FTIR, TLC, and HPLC analyses revealed that the carbohydrate fraction of WSPRaS consisted mainly of glucuronic acid, glucose, galactose, xylose, mannose, and arabinose, whereas WSPRaL consisted of galacturonic acid, sucrose, glucose, rhamnose, xylose, mannose, and arabinose. Scanning electron microscopy (SEM) analysis was used to determine the microstructure of the water-soluble polysaccharides. The physicochemical properties were evaluated using Fourier transform infrared (FT-IR) spectroscopy and ultraviolet‒visible (UV‒visible) absorption spectroscopy. The total antioxidant activities of the crude polysaccharides were evaluated using various assays: DPPH radical scavenging (IC<sub>50</sub> WSPRaL = 615 ± 2.05 µg/mL, IC<sub>50</sub> WSPRaS = 628 ± 2.38 µg/mL), ABTS radical scavenging (470 ± 5.78 µg/mL and 559 ± 4.32 µg/mL for WSPRaL and WSPRaS, respectively), reducing power (IC<sub>50</sub> WSPRaS = 141.76 ± 3.16 µg/mL, IC<sub>50</sub> WSPRaL = 203.89 ± 1.07 µg/mL), and chelating capacity (IC<sub>50</sub> WSPRaS = 225 ± 1.75 µg/mL, IC<sub>50</sub> WSPRaL = 219 ± 2.51 µg/mL). In addition, the antibacterial and biofilm inhibitory activities of both polysaccharides were tested against pathogenic strains, and the polysaccharides significantly inhibited plant growth. Overall, the results indicate that the crude polysaccharides extracted from <i>R. alaternus</i> are promising for use as functional and bioactive ingredients in the food and nutraceutical industries. These results highlight the potential of both polysaccharides as natural products in various sectors, including food, cosmetics, pharmaceuticals, and medicine, due to their significant biological properties.

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Publication Details

Journal
Polymers
Published
2024-11-15
DOI
https://doi.org/10.3390/polym16223180
Citations
9
Primary Topic
Polysaccharides and Plant Cell Walls
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article
Field-Weighted Citation Impact
5.40
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article

Exploring Rhamnus alaternus Polysaccharides: Extraction, Characterization, and Analysis of Antioxidant and Antimicrobial Properties

Ali Ellafi, Sami Mnif, Eduardo Alberto López‐Maldonado, Ahmed Slaheddine Masmoudi et al.
9 citations
Polymers
Polysaccharides and Plant Cell Walls
5.40
article

Exploring Rhamnus alaternus Polysaccharides: Extraction, Characterization, and Analysis of Antioxidant and Antimicrobial Properties

Ali Ellafi, Sami Mnif, Eduardo Alberto López‐Maldonado, Ahmed Slaheddine Masmoudi, Sonia Ben Younes, Souha Chokri
article en
9 citations

Abstract

In the present study, polysaccharides were isolated from the leaves (WSPRaL) and stems (WSPRaS) of <i>Rhamnus alaternus</i> with yields of 3% and 3.25% for WSPRaS and WSPRaL, respectively. Crude WSPRaL was composed of proteins (260.740 ± 0.98 µg/mg), lipids (53.34 ± 2.38 µg/mg), total sugars (482.716 ± 3.02 µg/mg), and reducing sugars (420.240 ± 1.68 µg/mg). In contrast, WSPRaS contained proteins (269.629 ± 1.48 µg/mg), lipids (13.33 ± 0.28 µg/mg), total sugars (569.135 ± 3.82 µg/mg), and reducing sugars (531.732 ± 2.59 µg/mg). FTIR, TLC, and HPLC analyses revealed that the carbohydrate fraction of WSPRaS consisted mainly of glucuronic acid, glucose, galactose, xylose, mannose, and arabinose, whereas WSPRaL consisted of galacturonic acid, sucrose, glucose, rhamnose, xylose, mannose, and arabinose. Scanning electron microscopy (SEM) analysis was used to determine the microstructure of the water-soluble polysaccharides. The physicochemical properties were evaluated using Fourier transform infrared (FT-IR) spectroscopy and ultraviolet‒visible (UV‒visible) absorption spectroscopy. The total antioxidant activities of the crude polysaccharides were evaluated using various assays: DPPH radical scavenging (IC<sub>50</sub> WSPRaL = 615 ± 2.05 µg/mL, IC<sub>50</sub> WSPRaS = 628 ± 2.38 µg/mL), ABTS radical scavenging (470 ± 5.78 µg/mL and 559 ± 4.32 µg/mL for WSPRaL and WSPRaS, respectively), reducing power (IC<sub>50</sub> WSPRaS = 141.76 ± 3.16 µg/mL, IC<sub>50</sub> WSPRaL = 203.89 ± 1.07 µg/mL), and chelating capacity (IC<sub>50</sub> WSPRaS = 225 ± 1.75 µg/mL, IC<sub>50</sub> WSPRaL = 219 ± 2.51 µg/mL). In addition, the antibacterial and biofilm inhibitory activities of both polysaccharides were tested against pathogenic strains, and the polysaccharides significantly inhibited plant growth. Overall, the results indicate that the crude polysaccharides extracted from <i>R. alaternus</i> are promising for use as functional and bioactive ingredients in the food and nutraceutical industries. These results highlight the potential of both polysaccharides as natural products in various sectors, including food, cosmetics, pharmaceuticals, and medicine, due to their significant biological properties.

PolymersVol. 16(22)
Tunis University (TN), University of Monastir (TN), Universidad Autónoma de Baja California (MX), University of Gafsa (TN), Institut Supérieur de Biotechnologie de Sfax (TN), Centre of Biotechnology of Sfax (TN), Faculté de médecine de Tunis, Tunis El Manar University (TN)
Clean water and sanitation
Openalex Percentile: Top 5%
Polysaccharides and Plant Cell Walls
5.40
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