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首页> 外文期刊>Journal of Applied Life Sciences International >Green Synthesis of Silver Nanoparticles Using Supernatant from Lactobacillus casei LPW2 Cultured in Modified Exopolysaccharides Selection Medium
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Green Synthesis of Silver Nanoparticles Using Supernatant from Lactobacillus casei LPW2 Cultured in Modified Exopolysaccharides Selection Medium

机译:用改良的胞外多糖选择培养基培养干酪乳杆菌LPW2上清液绿色合成银纳米颗粒。

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Aim: Biosynthesis of silver nanoparticle using supernatant from L. casei cultured in modified exopolysaccharide selection medium. Study Design: To bio-reduced AgNO3 using supernatant from L. casei cultured in modified exoploysaccharides selection medium and to evaluate the antibacterial potential of the biosynthesized SNPs. Place and Duration of Study: Department of Microbiology, University of Ibadan, Ibadan, Oyo State, Nigeria between Jan to December 2016. Methodology: Production and characterization of SNPs using supernatant from L. casei cultured in modified Exopolysaccharides selection medium and to evaluate the antibacterial activity of the SNPs. Results: Nanotechnology has to do with the manufacture of materials at the nanometer level.Clusters of atoms in the size range of 1 – 100 nm are known as nanoparticles. Biosynthesis of silver nanoparticles (SNPs) using supernatant of lactic acid bacteria (LAB) culture in modified Exopolysaccharides selection medium (mESM) was investigated. The supernatant obtained from L. casei LPW2 cultured in modified exopolysaccharides selection medium was used in the bio-reduction of AgNO3. The reaction mixture turned deep brown after 24 hrs of incubation indicating the formation of SNPs. The SNPs was characterized with UV-Visible spectrophotometer and it had a broad band between 400 – 600 nm with strong surface plasmon resonance at 500 nm. The FTIR analysis revealed the presence of carboxylic acids, hydroxyl group, amino acids and protein as the possible functional groups responsible for the bioreduction of silver to its nanoparticles. The antibacterial potential of the SNPs was evaluated and the zone of inhibition ranged from 13 – 24 mm with Bacillus species being the most susceptible. The minimum inhibitory concentration (MIC) of the biosynthesized SNPs was investigated and an MIC of 3.125% was observed on the tested pathogens. Conclusion: In conclusion, supernatant from LAB cultured using mESM can be used for the production of SNPs with potent antibacterial activity on Gram positive bacteria.
机译:目的:利用在改良的胞外多糖选择培养基中培养的干酪乳杆菌的上清液生物合成银纳米颗粒。研究设计:使用改良的胞外多糖选择培养基中培养的干酪乳杆菌的上清液生物还原AgNO 3 ,并评估其生物合成的SNP的抗菌潜力。研究地点和时间:2016年1月至2016年12月,尼日利亚,奥约州,伊巴丹,伊巴丹大学微生物学系。方法:采用改良的胞外多糖选择培养基中培养的干酪乳杆菌上清液生产和表征SNP,并评估其抗菌性SNP的活性。结果:纳米技术与纳米级材料的制造有关。1-100nm范围内的原子簇被称为纳米颗粒。研究了在改良的胞外多糖选择培养基(mESM)中使用乳酸菌(LAB)培养物的上清液对银纳米颗粒(SNP)的生物合成。在改良的胞外多糖选择培养基中培养的干酪乳杆菌LPW2获得的上清液用于AgNO 3 的生物还原。温育24小时后,反应混合物变成深褐色,表明SNP的形成。 SNPs用紫外可见分光光度计进行表征,它具有400至600 nm之间的宽带,在500 nm处具有很强的表面等离子体共振。 FTIR分析表明,羧酸,羟基,氨基酸和蛋白质的存在是可能导致银生物还原成纳米颗粒的可能官能团。对SNPs的抗菌潜力进行了评估,其抑制区域范围为13 – 24 mm,其中最容易感染芽孢杆菌。研究了生物合成的SNP的最小抑菌浓度(MIC),观察到的病原体的MIC为3.125%。结论:总之,使用mESM培养的LAB上清液可用于生产对革兰氏阳性细菌具有有效抗菌活性的SNP。

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