Abstract
Sustainable biosynthesis of metal oxide nanoparticles using an eco-friendly approach is a growing research area owing to their promising environmental and biomedical applications. This work aims to biosynthesize and characterize magnesium oxide nanoparticles (MgONPS@Aj) for possible application in dye biosorption and antibacterial activity. For the first time, MgONPS@Aj was successfully synthesized by harnessing exometabolites of Aspergillus japonicus. Various parameters were statistically optimized to maximize the production of MgONPS@Aj using Plackett Burman's design and central composite design. The analysis of variance (ANOVA) revealed that pH was the most significant variable, affecting the bioproduction process followed by biomass quantity and Mg(2+) precursor concentration. The suggested model (quadratic) was greatly significant and acceptable due to the nonsignificant lack of fit (15.10), and P-value (0.001). The optimized nanoparticles were characterized using X-ray powder diffraction, Fourier-transform infrared (FTIR) spectroscopy, transmission electron microscope (TEM), and Scanning electron microscopy. A high biosorption capacity (204.08 mg/g) of reactive black 5 dye was achieved within 40 min using a 5 mg biosorbent dose (MgONPS@Aj), 100 mg/l initial dye concentration, and pH 6.0. The biosorption process followed a pseudo-second-order (R(2) of 0.9842) and Langmuir isotherm (R(2) of 0.9422) models with a dimensionless separation factor (R(L)) of 8 × 10(4), hinting favorable and effective biosorption of dye molecules. A biosorption capacity of 81.97 mg/g after five successive cycles hints that the nanomaterial is suitable for several time utilization. Biogenic MgONPS@Aj displayed dramatic concentration-dependent antibacterial activity with the largest inhibition zones for P. aeruginosa (24.1 ± 0.8 mm, MIC: 3.125 µg/ml), followed by E. coli (22.3 ± 0.7 mm, MIC 6.25), B. subtilis (14.7 ± 0.4 mm, MIC: 12.5 µg/ml) and S. aureus (19.2 ± 0.6 mm, MIC: 6.25 µg/ml). The antibacterial activity was further interpreted using molecular simulation analysis. The lowest binding affinity was determined between MgONPS@Aj and target bacterial proteins (chloramphenicol acetyltransferase E. coli, and S. aureus MurE). The ligand (MgONPS@Aj) can bind to the active site's residues (Tyr(172) and SER(224)), indicating a possible antibacterial mechanism. This study recommends MgONPS@Aj as an eco-friendly, and reusable alternative to traditional anionic dye sorbents and a uniquely promising candidate for antimicrobial applications.