Extracellular biosynthesis, characterization, optimization of silver nanoparticles (AgNPs) using Bacillus mojavensis BTCB15 and its antimicrobial activity against multidrug resistant pathogens

被引:36
作者
Iqtedar, Mehwish [1 ]
Aslam, Mehral [1 ]
Akhyar, Muhammad [2 ]
Shehzaad, Asma [1 ]
Abdullah, Roheena [1 ]
Kaleem, Afshan [1 ]
机构
[1] Lahore Coll Women Univ, Dept Biotechnol, Lahore 54000, Pakistan
[2] Govt Coll Univ, Dept Chem, Nanolab, Lahore, Pakistan
关键词
AgNPs biosynthesis; Bacillus mojavensis; extracellular nanoparticles; MEDIATED SYNTHESIS; IMMOBILIZATION;
D O I
10.1080/10826068.2018.1550654
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biosynthesis of metal nanoparticles is an area of interest among researchers because of its eco-friendly approach. Current study focuses at biosynthesis of silver nanoparticles (AgNPs) and optimization of physico-chemical conditions to obtain mono-dispersed and stable AgNPs having antimicrobial activity. Initially Bacillus mojavensis BTCB15 produced silver nanoparticles (AgNPs) of 105nm. Silver nanoparticles (AgNPs) were characterized by particle size analyzer, UV-Vis Spectroscopy, Fourier transforms infrared spectroscopy (FTIR), Atomic force microscopy (AFM), and X-ray diffraction (XRD). Whereas, under optimal conditions of temperature 55 degrees C, pH 8, addition of surfactant Tween 20, and metal ion K2SO4, about 104% size reduction was achieved with average size of 2.3nm. Molecular characterization revealed 98% sequence homology with Bacillus mojavensis. AgNPs exhibited antibacterial activity at concentrations ranging from 0.5 to 2.5 mu g/mu l against Escherichia coli BTCB03, Klebsiella pneumonia BTCB04, Acinetobacter sp. BTCB05, and Pseudomonas aeruginosa BTCB01 but none against Staphylococcus aureus BTCB02. Highest antibacterial activity was observed at 0.27 mu g/mu l and lowest at 0.05 mu g/mu l of AgNPs indicated by zone of inhibition. Conclusively, under optimum conditions, Bacillus mojavensis BTCB15 was able to produce AgNPs of 2.3nm size and had antibacterial activity against multi drug resistant pathogens.
引用
收藏
页码:136 / 142
页数:7
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