Calicioglu M, Faith N G, Buege D R, Luchansky J B
Meat Science and Muscle Biology Laboratory, The University of Wisconsin-Madison, USA.
J Food Prot. 2001 Aug;64(8):1156-61. doi: 10.4315/0362-028x-64.8.1156.
Two soudjouk batters were prepared from ground beef (20% fat) and nonmeat ingredients and inoculated with a five-strain mixture of Escherichia coli O157:H7 to yield an initial inoculum of 7.65 log10 CFU/g. One batter contained a commercial-starter culture mixture (approximately 8.0 log10 CFU/g) and dextrose (1.5%), while the other batter relied upon a natural fermentation with no added carbohydrate. Following mixing, sausage batters were held at 4 degrees C for 24 h prior to stuffing into natural beef round casings. Stuffed soudjouk sticks were fermented and dried at 24 degrees C with 90 to 95% relative humidity (RH) for 3 days and then at 22 degrees C with 80 to 85% RH until achieving a product moisture level of approximately 40%. After fermentation and drying with an airflow of 1 to 1.5 m/s, the sticks were either not cooked or cooked to an instantaneous internal temperature of 54.4 degrees C (130 degrees F) and held for 0, 30, or 60 min. The sticks were then vacuum packaged and stored at either 4 or 21 degrees C. For each of three trials, three sticks for each treatment/batter were analyzed for numbers of E. coli O157:H7 after inoculation, after fermentation, after cooking, and after storage for 7, 14, 21, and 28 days. Reductions in numbers of E. coli O157:H7 after fermentation and drying for sticks fermented by the starter culture (pH 4.6) and for sticks naturally fermented (pH 5.5) were 1.96 and 0.28 log10 CFU/g, respectively. However, cooking soudjouk sticks produced with a starter culture and holding at 54.4 degrees C for 0, 30, or 60 min reduced pathogen numbers from an initial level after fermentation and drying of 5.69 log10 CFU/g to below a detectable level by either direct plating (<1.0 log10 CFU/g) or by enrichment. In contrast, cooking soudjouk sticks produced without an added starter culture decreased pathogen numbers from an initial level after fermentation and drying of 7.37 to 5.65 log10 CFU/g (54.4 degrees C, no hold), 5.04 log10 CFU/g (54.4 degrees C, 30 min hold), and 4.67 log10 CFU/g (54.4 degrees C, 60 min hold). In general, numbers of E. coli O157:H7 within both groups of soudjouk sticks decreased faster during storage at 21 degrees C compared to 4 degrees C. After 28 days of storage, total reductions in pathogen numbers in soudjouk sticks produced using a starter culture but that were not subsequently cooked were 7.65 and 3.93 log10 CFU/g at 21 and 4 degrees C, respectively. For naturally fermented soudjouk, total reductions varied from 4.47 to 0.45 log10 CFU/g, depending on the cooking time and storage temperature. These data provide guidelines for manufacturers of dry sausage of ethnic origin, including soudjouk, to assess the safety of their processes for control of E. coli O157:H7.
用含20%脂肪的绞碎牛肉和非肉类成分制备了两种苏久克香肠面糊,并接种了由5种大肠杆菌O157:H7菌株组成的混合物,使初始接种量达到7.65 log10 CFU/g。一种面糊含有商业发酵剂培养物混合物(约8.0 log10 CFU/g)和葡萄糖(1.5%),而另一种面糊依靠自然发酵,不添加碳水化合物。混合后,将香肠面糊在4℃下保存24小时,然后填入天然牛肉圆肠衣中。填充好的苏久克香肠棒在24℃、相对湿度90%至95%的条件下发酵和干燥3天,然后在22℃、相对湿度80%至85%的条件下干燥,直至产品水分含量达到约40%。在1至1.5 m/s的气流中进行发酵和干燥后,香肠棒要么不烹饪,要么烹饪至内部瞬时温度达到54.4℃(130℉)并保持0、30或60分钟。然后将香肠棒真空包装并储存在4℃或21℃下。在三项试验中的每一项中,对每种处理/面糊的三根香肠棒在接种后、发酵后、烹饪后以及储存7、14、21和28天后分析大肠杆菌O157:H7的数量。对于用发酵剂培养物发酵的香肠棒(pH 4.6)和自然发酵的香肠棒(pH 5.5),发酵和干燥后大肠杆菌O157:H7数量的减少分别为1.96和0.28 log10 CFU/g。然而,用发酵剂培养物生产的苏久克香肠棒在54.4℃下烹饪并保持0、30或60分钟后,病原体数量从发酵和干燥后的初始水平5.69 log10 CFU/g降至通过直接平板计数(<1.0 log10 CFU/g)或富集法检测不到的水平。相比之下,未添加发酵剂培养物生产的苏久克香肠棒烹饪后,病原体数量从发酵和干燥后的初始水平7.37 log10 CFU/g降至5.65 log10 CFU/g(54.4℃,不保持)、5.04 log10 CFU/g(54.4℃,保持30分钟)和4.67 log10 CFU/g(54.4℃,保持60分钟)。一般来说,与4℃相比,两组苏久克香肠棒中的大肠杆菌O157:H7数量在21℃储存期间下降得更快。储存28天后,使用发酵剂培养物生产但随后未烹饪的苏久克香肠棒中病原体数量的总减少量在21℃和4℃下分别为7.65和3.93 log10 CFU/g。对于自然发酵的苏久克香肠,总减少量根据烹饪时间和储存温度在4.47至0.45 log10 CFU/g之间变化。这些数据为包括苏久克在内的民族特色干香肠制造商评估其控制大肠杆菌O157:H7的工艺安全性提供了指导。