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. 2021 Apr;28(4):2229-2235.
doi: 10.1016/j.sjbs.2021.01.012. Epub 2021 Jan 26.

Biosynthesis of silver nanoparticles using Malva parviflora and their antifungal activity

Affiliations

Biosynthesis of silver nanoparticles using Malva parviflora and their antifungal activity

Fatimah Al-Otibi et al. Saudi J Biol Sci. 2021 Apr.

Abstract

Cheeseweed mallow (Malva parviflora L.) was used to biosynthesize silver nanoparticles. The biosynthesized silver nanoparticles were classified by UV-vis Spectroscopy and Fourier-Transform Infrared Spectroscopy (FT-IR). The shape and size distribution were visualized by Transmission Electron Microscopy (TEM), Field Emission Scanning Electron Microscopy (FE-SEM), and Zeta potential analysis. The chemical composition of M. parviflora leaf extract was identified by Gas Chromatography and Mass Spectroscopy (GC/MS). Finally, in vitro antifungal assay was done to assess the potential of biosynthesized silver nanoparticles and crude leaf extract of M. parviflora for inhibiting the mycelial growth of phytopathogenic fungi. The UV-vis analysis manifests the formation of silver nanoparticles. FTIR analysis established that chemicals of the leaf extract stabilized the biosynthesized silver nanoparticles by binding with the free silver ions. The TEM, FE-SEM and zeta potential analyzer confirmed that the biosynthesized silver nanoparticles were mostly spherical with an average diameter of 50.6 nm. The biosynthesized silver nanoparticles and leaf extract of M. parviflora effectively mitigate the mycelial growth of Helminthosporium rostratum, Fusarium solani, Fusarium oxysporum, and Alternaria alternata. The maximum reduction in mycelial growth by biosynthesized nanoparticles was observed against H. rostratum (88.6%). Whereas, the leaf extract of M. parviflora was most effective against F. solani (65.3%). Thus, the biosynthesis of nanoparticle assisted by M. parviflora is a feasible and eco-friendly method for the synthesis of silver nanoparticles. Further the silver nanoparticles and leaf extract of M. parviflora could be explored for the development of the fungicide.

Keywords: AgNPs, silver nanoparticles; Antifungal activity; DLS, Dynamic Light Scattering; FE-SEM; FE-SEM, Field Emission Scanning Electron Microscopy; FT-IR; FT-IR, Fourier-Transform Infrared Spectroscopy; GC/MS, Gas Chromatography/Mass Spectrometry; Helminthosporium rostratum; LEMP, leaf extract of M. parviflora; Malva parviflora; PDI, Polydispersity Index; SPR, Surface Plasmon Resonance; Silver nanoparticles.

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Conflict of interest statement

The authors declare that they have no conflict of interest

Figures

Fig. 1
Fig. 1
UV–vis absorbance spectra of biosynthesized AgNPs assisted by aqueous extract of M. parviflora.
Fig. 2
Fig. 2
FT-IR absorbance spectra of biosynthesized AgNPs assisted by aqueous extract of M. parviflora.
Fig. 3
Fig. 3
DLS analysis to determine size of biosynthesized AgNPs assisted by aqueous extract of M. parviflora.
Fig. 4
Fig. 4
TEM (a) and FE-SEM (b) image of biosynthesized AgNPs assisted by aqueous extract of M. parviflora.
Fig. 5
Fig. 5
In vitro Antifungal activity of biosynthesized AgNPs assisted by aqueous extract of M. parviflora against H. rostratum, F. solani, F. oxysporum and A. alternate. The vertical bars represent ± standard error (n = 3).
Fig. 6
Fig. 6
Mycelial growth of F. solani (a), H. rostratum (b), F. oxysporum (c) and A. alternaria (d) treated with 5% AgNPs (2.2a-d); LEMP (2.3a-d) and untreated (2.1a-d).

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