Koupal A, Deibel R H
Appl Environ Microbiol. 1978 Jun;35(6):1193-7. doi: 10.1128/aem.35.6.1193-1197.1978.
A rapid method for the detection of heat-stable staphylococcal nuclease in foods is described. The procedure consists of an acid precipitation, boiling, and centrifugation followed by enzyme detection in an agar plate containing deoxyribonucleic acid. To test the efficacy of the procedure, purified Staphylococcus aureus nuclease was added to various foods and recovery experiments were performed. Additionally, foods were inoculated and incubated with S. aureus, and the staphylococcal counts were compared with nuclease activity. The results indicate that the procedure possesses merit for a rapid method that can be incorporated into quality control programs. The procedure requires approximately 2.5 h, and it will detect nuclease levels as low as 10 ng/g of food.
本文描述了一种快速检测食品中热稳定葡萄球菌核酸酶的方法。该程序包括酸沉淀、煮沸和离心,然后在含有脱氧核糖核酸的琼脂平板中进行酶检测。为了测试该程序的有效性,将纯化的金黄色葡萄球菌核酸酶添加到各种食品中并进行回收率实验。此外,将食品接种金黄色葡萄球菌并进行培养,然后将葡萄球菌计数与核酸酶活性进行比较。结果表明,该程序作为一种可纳入质量控制程序的快速方法具有优点。该程序大约需要2.5小时,并且能够检测低至10 ng/g食品的核酸酶水平。