A Novel Biological Synthesis of Gold Nanoparticle by Enterobacteriaceae Family
Purpose: To demonstrate eco-friendly biosynthesis of gold nanoparticles by Enterobacteriaceae . Methods: Pure colonies of nine different bacteria from the Enterobacteriaceae family were separated from water and cultured in Luria Bertani broth medium. Their respective supernatants were examined for a...
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Veröffentlicht in: | Tropical journal of pharmaceutical research 2012-12, Vol.11 (6) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose: To demonstrate eco-friendly biosynthesis of gold nanoparticles
by Enterobacteriaceae . Methods: Pure colonies of nine different
bacteria from the Enterobacteriaceae family were separated from water
and cultured in Luria Bertani broth medium. Their respective
supernatants were examined for ability to produce gold nanoparticles.
In this step, 1 mM solution of Gold(III) chloride trihydrate H(AuCl4)
added to reaction matrices (supernatant) separately. The reaction was
performed in a dark environment at 37 °C. After 24 h, it was
observed that the color of the solutions turned to dark purple from
light yellow. The gold nanoparticles were characterized by UV-Visible
spectroscopy, dynamic light scattering, scanning electron microscopy
and Fourier transform infrared spectroscopy (FTIR) for yield, particle
size, shape and presence of different functional groups, respectively.
The nanoparticles were centrifuged and re-dispersed in double distilled
water thrice to purify them for FTIR studies. Results: The gold
nanoparticles were fairly uniform in size, spherical in shape and with
Z-average diameter ranging from 11.8 to 459 nm depending on the
bacteria used. FTIR spectra revealed the presence of various functional
groups in the gold nanoparticles which were also present in the
bacterial extract. Conclusion: The current approach suggests that rapid
synthesis of nanoparticles would be feasible in developing a biological
process for mass scale production of gold nanoparticles. |
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ISSN: | 1596-5996 1596-9827 |
DOI: | 10.4314/tjpr.v11i6.3 |