Abstract:
Nanotechnology is one of the developing areas with wide applications and iron (Fe)
is a very common and easily accessible option for manufacturing nanoparticles
(NPs). Iron nanoparticles (FeNPs) can be produced through physical, chemical, or
biological processes. Therefore, the objective of this study was to synthesize iron
nanoparticles by Escherichia coli. The state of microorganisms and their
morphological characteristics were investigated prior to the synthesis of
nanoparticles. Escherichia coli bacterium (ATCC 25922) was selected for
synthesized FeNPs using extra cellular method. Escherichia coli was cultured and
incubated on a shaking water bath and on an orbital shaker at room temperature to
identify the suitable way for the growth of Escherichia coli. The biomass of
Escherichia coli was harvested and centrifuged. Then, the pellet was collected for
the further reaction to the synthesis of nanoparticles. The Ferric Chloride (FeCl3)
solution of different concentration was used for synthesized iron nanoparticles.
Nanoparticle formation was confirmed by UV- visible spectroscopy, Fourier-Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy
(SEM) analysis methods. According to the results, the UV spectrum of FeNPs
synthesized by Escherichia coli exhibited broad absorption peaks between 220 and
250 nm; the interaction of extracts with the nanoparticle was explained by FTIR
spectroscopy. Accordingly, scanning the FeNP sample between the range of 1000
and 4000 cm-1 was used to get FTIR spectra for FeNPs produced by Escherichia
coli, and (SEM) examination of iron nanoparticles revealed the presence of the
FeNPs. Extracellular enzymes in microorganisms have the ability to reduce metallic
ions on their surfaces and the synthesis of iron nanoparticles using E.coli plays a
vital role in the reduction of metal ions in the microbial synthesis method.
