Department of Food Science, Louisiana State University Agricultural Center, Baton Rouge, Louisiana 70803, USA.
J Food Prot. 2013 Jan;76(1):59-64. doi: 10.4315/0362-028X.JFP-12-141.
The purpose of this study was to determine whether the current consumer method of boiling shrimp until floating and pink in color is adequate for destroying Listeria and Salmonella. Shrimp samples were submerged in bacterial suspensions of Listeria and Salmonella for 30 min and allowed to air dry for 1 h under a biosafety cabinet. Color parameters were then measured with a spectrophotometer programmed with the CIELAB system. Twenty-four shrimp samples were divided into groups (days 0, 1, or 2) and stored at 4°C. The samples were treated by placing them in boiling water (100°C) on days 0, 1, and 2. The shrimp were immediately removed from the boiling water once they floated to the surface, and color parameters were measured. Bacterial counts were determined, and the log CFU per gram was calculated. The effect of sodium tripolyphosphate on the color change of cooked shrimp also was determined. Initial bacterial counts on shrimp after air drying were 5.31 ± 0.14 log CFU/g for Salmonella Enteritidis, 5.24 ± 0.31 log CFU/g for Salmonella Infantis, 5.40 ± 0.16 log CFU/g for Salmonella Typhimurium, 3.91 + 0.11 log CFU/g for Listeria innocua, 4.45 ± 0.11 log CFU/g for Listeria monocytogenes (1/2a), and 3.70 ± 0.22 log CFU/g for Listeria welshimeri. On days 0, 1, and 2, all bacterial counts were reduced to nondetectable levels for shrimp samples that floated. The average time for shrimp to float was 96 ± 8 s. The bacterial counts remained at nondetectable levels (<10 log CFU/g) during refrigerated (4°C) storage of cooked shrimp for 2 days. The redness, yellowness, and lightness were significantly higher (P < 0.0001) for the cooked shrimp than for the uncooked shrimp on all days tested. The standard deviation for redness in the cooked shrimp was large, indicating a wide range of pink coloration on all days tested. The results suggest that boiling shrimp until they float will significantly reduce Listeria and Salmonella contamination, but color change is not a good indication of reduction of these pathogens because of the wide natural color variation.
本研究旨在确定当前消费者将虾煮沸至漂浮和粉红色的方法是否足以破坏李斯特菌和沙门氏菌。将虾样本浸入李斯特菌和沙门氏菌的细菌悬浮液中 30 分钟,然后在生物安全柜下风干 1 小时。然后使用分光光度计通过 CIELAB 系统测量颜色参数。将 24 个虾样本分为几组(第 0、1 或 2 天)并在 4°C 下储存。在第 0、1 和 2 天,将样品置于沸水中(100°C)进行处理。一旦虾漂浮到表面,就立即将它们从沸水中取出,并测量颜色参数。测量细菌计数,并计算每克 log CFU。还确定了三聚磷酸钠对熟虾颜色变化的影响。风干后虾的初始细菌计数为:肠炎沙门氏菌 5.31 ± 0.14 log CFU/g,婴儿沙门氏菌 5.24 ± 0.31 log CFU/g,鼠伤寒沙门氏菌 5.40 ± 0.16 log CFU/g,无害李斯特菌 3.91 + 0.11 log CFU/g,单核细胞增生李斯特菌(1/2a)4.45 ± 0.11 log CFU/g,威尔斯李斯特菌 3.70 ± 0.22 log CFU/g。在第 0、1 和 2 天,所有细菌计数均降低至漂浮的虾样本不可检测水平。虾平均漂浮时间为 96 ± 8 s。在 4°C 冷藏(4°C)储存熟虾 2 天期间,细菌计数保持在不可检测水平(<10 log CFU/g)。与所有测试日的未煮虾相比,煮熟的虾的红色、黄色和亮度明显更高(P <0.0001)。在所有测试日,煮熟的虾的红色标准差都很大,表明所有测试日的粉红色范围都很广。结果表明,将虾煮沸至漂浮状态将显著减少李斯特菌和沙门氏菌的污染,但颜色变化并不能很好地表明这些病原体的减少,因为天然颜色变化范围很广。