林淑凤,徐珍霞,吴仁蔚.适配体结合聚酰胺-胺修饰的磁性纳米粒子富集单增李斯特菌[J].食品安全质量检测学报,2020,11(9):2904-2910
适配体结合聚酰胺-胺修饰的磁性纳米粒子富集单增李斯特菌
Enrichment of Listeria monocytogenes by aptamer-conjugated polyamide-amine polymer-magnetic nanoparticles
投稿时间:2020-01-15  修订日期:2020-05-08
DOI:
中文关键词:  单增李斯特菌  磁性纳米粒子  适配体  聚酰胺-胺树枝状聚合物  细菌富集
英文关键词:Listeria monocytogenes  magnetic nanoparticles  aptamer  poly(amidomine)dendrimers  bacterial enrichment
基金项目:国家自然科学基金项目(31201374)、中央高校基本科研业务费专项资金项目(2662015PY152)
作者单位
林淑凤 华中农业大学食品科学与技术学院 
徐珍霞 中国农业科学院油料作物研究所 
吴仁蔚 华中农业大学食品科学与技术学院 
AuthorInstitution
LIN Shu-Feng College of Food Science and Technology, Huazhong Agricultural University 
XU Zhen-Xia Oil Crops Research Institute of Chinese Academy of Agricultural Sciences 
WU Ren-Wei College of Food Science and Technology, Huazhong Agricultural University 
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中文摘要:
      目的 制备聚酰胺-胺聚合物修饰的磁性纳米粒子, 增加连接适配体的数量, 提高富集单增李斯特菌的效率。方法 通过迈克尔加成和酰胺化的级联反应, 在Fe3O4磁性纳米粒子表面接枝3.0代聚酰胺-胺树枝状聚合物(poly(amidoamine)dendrimers, PAMAM), 制得聚酰胺-胺磁性纳米粒子(G3-MNPs), 并对其进行表征。G3-MNPs偶联生物素标记的单增李斯特菌特异性适配体, 获得适配体磁性纳米粒子(AP-G3-MNPs)。然后对AP-G3-MNPs富集单增李斯特菌的工作条件和捕获率进行测定。结果 傅里叶变换红外光谱(Fourier transform infrared spectroscopy, FT-IR)分析、Zeta电位测定以及碳、氮元素分析结果表明, PAMAM已接枝在MNPs表面, G3-MNPs偶联适配体的效率为1.412 nmol/mg。AP-G3-MNPs(200 μg)对浓度为2×102~2×108 CFU/mL的单增李斯特菌的捕获率均大于90%。结论 接枝PAMAM提高了MNPs的负载能力, 增强了其富集单增李斯特菌的能力。
英文摘要:
      Objective To prepare magnetic nanoparticles modified by polyamide-amine polymer to increase the number of joint aptamers and improve the efficiency of enrichment of Listeria monocytogenes. Methods The surface of Fe3O4 magnetic nanoparticles were grafted with three gaps of poly(amidoamine)dendrimers (PAMAM) (G3-MNPs) by michael addition and amidation cascade reaction. Then G3-MNPs were characterized. G3-MNPs were conjugated with biotined aptamers against L. monocytogenes to get AP-G3-MNPs. The enrichment conditions of AP-G3-MNPs and capture efficiency for L. monocytogenes were determined. Results PAMAM was successfully grafted on MNPs based on FT-IR spectra, zeta potential determination and element analysis of carbon and nitrogen. The loading rate of G3-MNPs for biotined aptamers was 1.412 nmol/mg. The specific capture rate of AP-G3-MNPs (200 μg) was higher than 90% for Listeria monocytogenes with concentration of 2×102?2×108 CFU/mL. Conclusion Grafting PAMAM on MNPs increased its loading rate for aptamers and the capture efficiency for L. monocytogenes.
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