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Vancomycin modified PEGylated-magnetic nanoparticles combined with PCR for efficient enrichment and detection of Listeria monocytogenes

Sensors and Actuators B: Chemical. 2017; 
XiangyuMengFulaiLiFanLiYonghuaXiongHengyiXu
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Gene Synthesis The specificity primer pairs used in this study are listed in Table 2. The L. monocytogenes specific primers were designed to amplify a 268 bp segment from the hly gene [31] that was used to encoding the virulence factor listeriolysin O. The sequences designed to amplify 475 bp segment from 16S rRNA gene [32]. The hlyprimers were designed using Oligo 6.0 software (http://www.oligo.net/). The specificity of the sequences was tested by searched against NCBI’s non-redundant database using the BLASTN algorithm [33]. All primers were synthesized by GenScript (Nanjing) Co., Ltd. (Nanjing, China). Get A Quote

摘要

In this study, vancomycin (Van) functionalized PEGylated-magnetic nanoparticles(Van-PMs) combined with polymerase chain reaction (PCR) showed great potential for highly efficient detection of L. monocytogenes at low infectious dose. Herein, Van-PMs played as universal molecular probes for targeting bacterial cells, while PEG was used to help Van close to D-alanyl-d-alanine (D-Ala-d-Ala) moieties on surface of L. monocytogenes. Under optimum conditions, the developed Van-PMs complexes exhibited extremely high capture efficiency (CE) in a 10 mL bacterium suspension with the value was higher than 90% and 83% in the phosphate-buffered saline (PBS) solution and lettuce samples, respectively. Meanwhil... More

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