Sambalova Olga, Thorwarth Kerstin, Heeb Norbert Victor, Bleiner Davide, Zhang Yucheng, Borgschulte Andreas, Kroll Alexandra
Laboratory for Advanced Analytical Technologies, Coating Competence Center, and Electron Microscopy Centre, Empa, Ueberlandstrasse 129, 8600 Dübendorf, Switzerland.
Department of Chemistry, University Zürich, Winterthurerstrasse 190, 8057 Zürich, Switzerland.
ACS Omega. 2018 Jan 31;3(1):724-733. doi: 10.1021/acsomega.7b00982. Epub 2018 Jan 22.
Biofilms causing medical conditions or interfering with technical applications can prove undesirably resistant to silver nanoparticle (AgNP)-based antimicrobial treatment, whereas beneficial biofilms may be adversely affected by the released silver nanoparticles. Isolated biofilm matrices can induce reduction of silver ions and stabilization of the formed nanosilver, thus altering the exposure conditions. We thus study the reduction of silver nitrate solution in model experiments under chemically defined conditions as well as in stream biofilms. Formed silver nanoparticles are characterized by state-of-the art methods. We find that isolated biopolymer fractions of biofilm organic matrix are capable of reducing ionic Ag, whereas other isolated fractions are not, meaning that biopolymer fractions contain both reducing agent and nucleation seed sites. In all of the investigated systems, we find that silver nanoparticle-biopolymer interface is dominated by carboxylate functional groups. This suggests that the mechanism of nanoparticle formation is of general nature. Moreover, we find that glucose concentration within the biofilm organic matrix correlates strongly with the nanoparticle formation rate. We propose a simple mechanistic explanation based on earlier literature and the experimental findings. The observed generality of the extracellular polymeric substance/AgNP system could be used to improve the understanding of impact of Ag on aqueous ecosystems, and consequently, to develop biofilm-specific medicines and bio-inspired water decontaminants.
导致医疗状况或干扰技术应用的生物膜可能对基于银纳米颗粒(AgNP)的抗菌治疗具有不良抗性,而有益生物膜可能会受到释放的银纳米颗粒的不利影响。分离出的生物膜基质可诱导银离子还原并使形成的纳米银稳定,从而改变暴露条件。因此,我们在化学定义的条件下以及在河流生物膜中的模型实验中研究硝酸银溶液的还原情况。通过先进方法对形成的银纳米颗粒进行表征。我们发现生物膜有机基质的分离生物聚合物组分能够还原离子态银,而其他分离组分则不能,这意味着生物聚合物组分既含有还原剂又含有成核位点。在所有研究的系统中,我们发现银纳米颗粒 - 生物聚合物界面以羧基官能团为主。这表明纳米颗粒形成的机制具有普遍性。此外,我们发现生物膜有机基质中的葡萄糖浓度与纳米颗粒形成速率密切相关。我们基于早期文献和实验结果提出了一个简单的机理解释。观察到的细胞外聚合物/AgNP系统的普遍性可用于增进对银对水生生态系统影响的理解,进而开发针对生物膜的药物和受生物启发的水净化剂。