大肠杆菌
噬菌体
沙门氏菌
检出限
微生物学
细菌
操纵子
酶
受污染的食物
基质(水族馆)
生物
化学
生物化学
色谱法
基因
遗传学
生态学
作者
Anqi Chen,Danhui Wang,Sam R. Nugen,Juhong Chen
出处
期刊:Microorganisms
[Multidisciplinary Digital Publishing Institute]
日期:2021-02-19
卷期号:9 (2): 436-436
被引量:16
标识
DOI:10.3390/microorganisms9020436
摘要
Despite enhanced sanitation implementations, foodborne bacterial pathogens still remain a major threat to public health and generate high costs for the food industry. Reporter bacteriophage (phage) systems have been regarded as a powerful technology for diagnostic assays for their extraordinary specificity to target cells and cost-effectiveness. Our study introduced an enzyme-based fluorescent assay for detecting the presence of E. coli using the T7 phage engineered with the lacZ operon which encodes beta-galactosidase (β-gal). Both endogenous and overexpressed β-gal expression was monitored using a fluorescent-based method with 4-methylumbelliferyl β-d-galactopyranoside (MUG) as the substrate. The infection of E. coli with engineered phages resulted in a detection limit of 10 CFU/mL in ground beef juice after 7 h of incubation. In this study, we demonstrated that the overexpression of β-gal coupled with a fluorogenic substrate can provide a straightforward and sensitive approach to detect the potential biological contamination in food samples. The results also suggested that this system can be applied to detect E. coli strains isolated from environmental samples, indicating a broader range of bacterial detection.
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