利用肽功能化sers活性底物检测炭疽芽孢杆菌孢子

Atanu Sengupta, C. Shende, S. Farquharson, Frank Inscore
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引用次数: 9

摘要

正如2011年《生物武器公约》所表达的那样,对能够在现场快速识别生物战剂(BWAs)的便携式技术的需求仍然是国际优先事项。近年来,表面增强拉曼光谱(SERS)在极低浓度下快速检测各种BWAs的能力已经得到证实。然而,在炭疽芽孢杆菌的具体情况下,需要在物种水平上进行区分,因为其他杆菌在环境中很常见,代表潜在的假阳性反应。为了克服这一限制,我们描述了使用附着在sers活性金属上的肽,选择性地结合炭疽芽孢杆菌作为目标分析物。采用这种方法,109 B。炭疽芽孢杆菌孢子/mL在添加乙酸时产生强烈的二吡啶酸谱,而相同浓度和处理的蜡样芽孢杆菌和枯草芽孢杆菌则没有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Bacillus anthracis Spores Using Peptide Functionalized SERS-Active Substrates
The need for portable technologies that can rapidly identify biological warfare agents (BWAs) in the field remains an international priority as expressed at the 2011 Biological Weapons Convention. In recent years, the ability of surface-enhanced Raman spectroscopy (SERS) to rapidly detect various BWAs at very low concentrations has been demonstrated. However, in the specific case of Bacillus anthracis, differentiation at the species level is required since other bacilli are common in the environment, representing potential false-positive responses. To overcome this limitation, we describe the use of a peptide attached to the SERS-active metal that selectively binds Bacillus anthracis-Sterne as the target analyte. Using this approach, 109  B. anthracis-Sterne spores/mL produced an intense dipicolinic acid spectrum upon the addition of acetic acid, while the same concentration and treatment of B. cereus and B. subtilis did not.
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