4.6 Article

Biosynthesis of Selenium Nanoparticles (via Bacillus subtilis BSN313), and Their Isolation, Characterization, and Bioactivities

Journal

MOLECULES
Volume 26, Issue 18, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26185559

Keywords

selenium; SeNPs; probiotic; Bacillus subtilis BSN313; antioxidant; antibacterial

Funding

  1. Beijing Municipal Education Commission, Beijing Natural Science Foundations [KM201910011005, PXM2019_014213_000007]
  2. National Natural Science Foundation of China [21808005]
  3. Central Public-interest Scientific Institution Basal Research Fund [ZX1945]

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Selenium nanoparticles have minor toxicity, superior reactivity, and excellent bioavailability compared to other forms, and can be produced using a biosynthetic approach. These nanoparticles showed good antioxidant and antibacterial activity, making them potential candidates for biomedical and nutritional applications.
Among the trace elements, selenium (Se) has great demand as a health supplement. Compared to its other forms, selenium nanoparticles have minor toxicity, superior reactivity, and excellent bioavailability. The present study was conducted to produce selenium nanoparticles (SeNPs) via a biosynthetic approach using probiotic Bacillus subtilis BSN313 in an economical and easy manner. The BSN313 exhibited a gradual increase in Se reduction and production of SeNPs up to 5-200 mu g/mL of its environmental Se. However, the capability was decreased beyond that concentration. The capacity for extracellular SeNP production was evidenced by the emergence of red color, then confirmed by a microscopic approach. Produced SeNPs were purified, freeze-dried, and subsequently characterized systematically using UV-Vis spectroscopy, FTIR, Zetasizer, SEM-EDS, and TEM techniques. SEM-EDS analysis proved the presence of selenium as the foremost constituent of SeNPs. With an average particle size of 530 nm, SeNPs were shown to have a -26.9 (mV) zeta potential and -2.11 mu m cm/Vs electrophoretic mobility in water. SeNPs produced during both the 24 and 48 h incubation periods showed good antioxidant activity in terms of DPPH and ABST scavenging action at a concentration of 150 mu g/mL with no significant differences (p > 0.05). Moreover, 200 mu g/mL of SeNPs showed antibacterial reactivity against Escherichia coli ATCC 8739, Staphylococcus aureus ATCC 9027, and Pseudomonas aeruginosa ATCC 25923. In the future, this work will be helpful to produce biogenic SeNPs using probiotic Bacillus subtilis BSN313 as biofactories, with the potential for safe use in biomedical and nutritional applications.

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