Fungal xylanases‐mediated synthesis of silver nanoparticles for catalytic and biomedical applications

Green synthesis of nanoparticles has fuelled the use of biomaterials to synthesise a variety of metallic nanoparticles. The current study investigates the use of xylanases of Aspergillus niger L3 (NEA) and Trichoderma longibrachiatum L2 (TEA) to synthesise silver nanoparticles (AgNPs). Characterisation of AgNPs was carried out using UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy, while their effectiveness as antimicrobial, antioxidant, catalytic, anticoagulant, and thrombolytic agents were determined. The colloidal AgNPs was brownish with surface plasmon resonance at 402.5 and 410 nm for NEA‐AgNPs and TEA‐AgNPs, respectively; while FTIR indicated that protein molecules were responsible for the capping and stabilisation of the nanoparticles. The spherical nanoparticles had size of 15.21–77.49 nm. The nanoparticles significantly inhibited the growth of tested bacteria (63.20–88.10%) and fungi (82.20–86.10%), and also scavenged DPPH (37.48–79.42%) and hydrogen peroxide (20.50–96.50%). In addition, the AgNPs degraded malachite green (78.97%) and methylene blue (25.30%). Furthermore, the AgNPs displayed excellent anticoagulant and thrombolytic activities using human blood. This study has demonstrated the potential of xylanases to synthesise AgNPs which is to the best of our knowledge the first record of such. The present study underscores the relevance of xylanases in nanobiotechnology.Inspec keywords: visible spectra, catalysis, ultraviolet spectra, silver, microorganisms, antibacterial activity, transmission electron microscopy, surface plasmon resonance, nanoparticles, nanofabrication, colloids, blood, Fourier transform infrared spectra, particle sizeOther keywords: Ag, fungal xylanases‐mediated synthesis, silver nanoparticles, catalytic applications, biomedical applications, green synthesis, metallic nanoparticles, Trichoderma longibrachiatum L2, transmission electron microscopy, antimicrobial agents, antioxidant agents, catalytic agents, thrombolytic agents, surface plasmon resonance, spherical nanoparticles, FTIR spectra, anticoagulant agents, colloidal nanoparticles, biomaterials, Aspergillus niger L3, UV‐vis spectroscopy, Fourier transform infrared spectroscopy, protein molecules, DPPH, hydrogen peroxide, malachite green, methylene blue, human blood, nanobiotechnology