Extracellular synthesis of silver nanoparticles using culture supernatant of Pseudomonas aeruginosa

被引:180
作者
Kumar, C. Ganesh [1 ]
Mamidyala, Suman Kumar [1 ]
机构
[1] Indian Inst Chem Technol, Biol Chem Lab, Hyderabad 500607, Andhra Pradesh, India
关键词
Pseudomonas; Silver nanoparticles; Capping rhamnolipids; Antimicrobial; Nanobiotechnology; REDUCTASE-MEDIATED SYNTHESIS; METAL NANOPARTICLES; PLASMON RESONANCE; PARTICLES; BIOSYNTHESIS; MATRIX; AGNO3; CELLS; AG;
D O I
10.1016/j.colsurfb.2011.01.042
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Bio-directed synthesis of metal nanoparticles is gaining importance due to their biocompatibility, low toxicity and eco-friendly nature. We used culture supernatant of Pseudomonas aeruginosa strain BS-161R for the simple and cost effective green synthesis of silver nanoparticles. The reduction of silver ions occurred when silver nitrate solution was treated with the Pseudomonas aeruginosa culture supernatant at room temperature. The nanoparticles were characterized by UV-visible, TEM, EDAX, FTIR and XRD spectroscopy. The nanoparticles exhibited an absorption peak around 430 nm, a characteristic surface plasmon resonance band of silver nanoparticles. They were mono-dispersed and spherical in shape with an average particle size of 13 nm. The EDAX analysis showed the presence of elemental silver signal in the synthesized nanoparticles. The FT-IR analysis revealed that the protein component in the form of enzyme nitrate reductase and the rhamnolipids produced by the isolate in the culture supernatant may be responsible for reduction and as a capping material. The XRD spectrum showed the characteristic Bragg peaks of 111,200,220 and 3 11 facets of the face centered cubic silver nanoparticles and confirms that these nanoparticles are crystalline in nature. The prepared silver nanoparticles exhibited strong antimicrobial activity against Gram-positive, Gram-negative and different Candida species at concentrations ranging between 4 and 32 mu g ml(-1). 0 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:462 / 466
页数:5
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