适体
蜡样芽孢杆菌
蜡样体
孢子
化学
离解常数
食品科学
表面等离子共振
色谱法
微生物学
生物
生物化学
纳米技术
纳米颗粒
细菌
分子生物学
材料科学
受体
遗传学
作者
Christin Fischer,Tim Hünniger,Jan-Hinnerk Jarck,Esther Frohnmeyer,Constanze Kallinich,Ilka Haase,Ulrich Hahn,Markus Fischer
标识
DOI:10.1021/acs.jafc.5b03738
摘要
Aerobic spores pose serious problems for both food product manufacturers and consumers. Milk is particularly at risk and thus an important issue of preventive consumer protection and quality assurance. The spore-former Bacillus cereus is a food poisoning Gram-positive pathogen which mainly produces two different types of toxins, the diarrhea inducing and the emetic toxins. Reliable and rapid analytical assays for the detection of B. cereus spores are required, which could be achieved by combining in vitro generated aptamers with highly specific molecular biological techniques. For the development of routine bioanalytical approaches, already existing aptamers with high affinity to B. cereus spores have been characterized by surface plasmon resonance (SPR) spectroscopy and fluorescence microscopy in terms of their dissociation constants and selectivity. Dissociation constants in the low nanomolar range (from 5.2 to 52.4 nM) were determined. Subsequently, the characterized aptamers were utilized for the establishment and validation of an aptamer-based trapping technique in both milk simulating buffer and milk with fat contents between 0.3 and 3.5%. Thereby, enrichment factors of up to 6-fold could be achieved. It could be observed that trapping protocol and characterized aptamers were fully adaptable to the application in milk. Due to the fact that aptamer selectivity is limited, a highly specific real time PCR assay was utilized following trapping to gain a higher degree of selectivity.
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