Starbuck M A, Hill P J, Stewart G S
University of Nottingham, Faculty of Agriculture and Food Sciences, Department of Applied Biochemistry and Food Science, Loughborough, Leics, UK.
Lett Appl Microbiol. 1992 Dec;15(6):248-52. doi: 10.1111/j.1472-765x.1992.tb00775.x.
The polymerase chain reaction (PCR) has been used to detect Listeria monocytogenes in whole milk at a level of 0.1 cfu per 30 ml. This high degree of sensitivity has been achieved following enzymatic digestion, polysulphonone membrane filtration and amplification of a nucleotide sequence within the promoter region of hlyA. Key elements of the procedure are the absence of enrichment culture and a complete solubilization of the membrane filter, ensuring total nucleic acid recovery. The simplicity of the protocol coupled with high sample volumes and exquisite sensitivity extends the relevance of PCR within food and environmental microbiology.
聚合酶链反应(PCR)已用于检测全脂牛奶中的单核细胞增生李斯特菌,检测水平为每30毫升0.1个菌落形成单位(cfu)。在经过酶消化、聚砜膜过滤以及对hlyA启动子区域内的核苷酸序列进行扩增之后,实现了如此高的灵敏度。该方法的关键要素包括不进行富集培养以及使膜滤器完全溶解,以确保核酸的完全回收。该方案的简便性、高样本量和极高的灵敏度扩展了PCR在食品和环境微生物学中的应用范围。