Niskanen A, Nurmi E
Appl Environ Microbiol. 1976 Jan;31(1):11-20. doi: 10.1128/aem.31.1.11-20.1976.
Different amounts of enterotoxin A-, B-, and C1-producing staphylococci were added to dry sausage prepared by normal processes, either alone or in conjunction with a starter culture (micrococci and lactobacilli). The sausage was examined after 0, 3, 7, 14, and 30 days for staphylococci, micrococci, and lactobacilli, and measurements were made of water activity, pH, enterotoxin, and thermostable nuclease. The results showed that in the absence of starter culture measurable amounts of enterotoxin A were formed in a 200-g sample of dry sausage in 3 days, the level of Staphylococcus aureus infection being over 10(6) cells/g. Enterotoxin B was not found, although the total number of staphylococci was over 10(8) cells/g. Enterotoxin C1 was observed when the Staphylococcus count was about 8 X 10(7) cells/g, but was no longer detectable after 7 days. The starter culture prevented the production of enterotoxin A in all cases investigated. By contrast, a very high-level inoculation of an enterotoxin C1-producing strain gave a positive result after 3 days of incubation even in the presence of a starter culture. Heat-stable nuclease was observed in all sausages to which enterotoxin-producing staphylococci were added. The cell count determined in a sample of sausage had no definite correlation with the thermonuclease activity of the sample.
将不同数量的产肠毒素A、B和C1的葡萄球菌添加到通过常规工艺制备的干香肠中,这些葡萄球菌可以单独添加,也可以与发酵剂培养物(微球菌和乳酸菌)一起添加。在0、3、7、14和30天后检查香肠中的葡萄球菌、微球菌和乳酸菌,并测量水分活度、pH值、肠毒素和热稳定核酸酶。结果表明,在没有发酵剂培养物的情况下,200克干香肠样品在3天内形成了可测量的肠毒素A,金黄色葡萄球菌感染水平超过10⁶个细胞/克。尽管葡萄球菌总数超过10⁸个细胞/克,但未发现肠毒素B。当葡萄球菌计数约为8×10⁷个细胞/克时观察到肠毒素C1,但7天后不再可检测到。在所有研究的情况下,发酵剂培养物都能阻止肠毒素A的产生。相比之下,即使在有发酵剂培养物存在的情况下,对产肠毒素C1菌株进行非常高剂量的接种,在培养3天后也得到了阳性结果。在所有添加了产肠毒素葡萄球菌的香肠中都观察到了热稳定核酸酶。香肠样品中测定的细胞计数与样品的热核酸酶活性没有明确的相关性。