Koseki Shigenobu, Yamamoto Kazutaka
Food Piezotechnology Laboratory, National Food Research Institute, 2-1-12, Kannondai, Tsukuba, Ibaraki 305-8642, Japan.
Int J Food Microbiol. 2006 Jul 1;110(1):108-11. doi: 10.1016/j.ijfoodmicro.2006.01.039. Epub 2006 May 8.
Escherichia coli ATCC 25922 in phosphate buffered saline solution (PBS, pH 7.1, 10(8) CFU/ml) was inactivated by high hydrostatic pressure (HHP, 400 to 600 MPa) treatment at 25 degrees C for 10 min. Colonies of E. coli were not detected on non-selective plate count agar immediately after a HHP-treatment of at least 550 MPa. E. coli subjected to at least 500 MPa in PBS were incubated at 4, 25, and 37 degrees C for 120 h. No colonies were detected on plate count agar throughout the 120-h incubation period at 4 or 37 degrees C. In contrast, the number of E. coli during storage at 25 degrees C increased from an undetectable level (< 1 CFU/ml) to the level of initial cell counts regardless of the treatment pressure level. The recovery in PBS required a maximum time of 48 h, while the period during which cell numbers remained at an undetectable level increased from 24 to 72 h as the treatment pressure increased. E. coli treated at 550 and 600 MPa in PBS were inoculated into trypticase soy broth (TSB) and stored at 4, 25, and 37 degrees C for 120 h. No recovery was recorded in TSB during the 120-h storage at 37 degrees C. In contrast, the number of E.coli during storage at 25 degrees C in TSB increased beyond the level of initial cell counts regardless of the treatment pressure level. The recovery of cell numbers observed in TSB was faster than that in PBS samples, as bacterial growth in TSB assisted faster recovery. When the incubation temperature in PBS was shifted to 25 degrees C after 120-h at 4 or 37 degrees C, recovery of E. coli was observed in samples shifted from 4 to 25 degrees C regardless of the treatment pressure. However, the time during which cell numbers remained at an undetectable level was extended by increasing the level of treatment pressure, and recovery required a maximum time of 48 h. On the other hand, no recovery was observed with HHP-treated E. coli subjected to an incubation temperature shift from 37 to 25 degrees C. This study indicates that an appropriate incubation temperature after HHP-treatment is needed to optimize the recovery of HHP-injured bacteria and thus prevent overestimation of the lethal effect of HHP-treatment.
将处于磷酸盐缓冲盐溶液(PBS,pH 7.1,10⁸CFU/ml)中的大肠杆菌ATCC 25922在25℃下通过400至600兆帕的高静水压(HHP)处理10分钟使其失活。在至少550兆帕的HHP处理后,立即在非选择性平板计数琼脂上未检测到大肠杆菌菌落。将在PBS中经受至少500兆帕的大肠杆菌在4℃、25℃和37℃下孵育120小时。在4℃或37℃的整个120小时孵育期内,平板计数琼脂上均未检测到菌落。相比之下,无论处理压力水平如何,在25℃储存期间大肠杆菌的数量从不可检测水平(<1 CFU/ml)增加到初始细胞计数水平。在PBS中的恢复最长需要48小时,而细胞数量保持在不可检测水平的时间随着处理压力的增加从24小时增加到72小时。将在PBS中经550和600兆帕处理的大肠杆菌接种到胰蛋白酶大豆肉汤(TSB)中,并在4℃、25℃和37℃下储存120小时。在37℃下储存120小时期间,TSB中未记录到恢复情况。相比之下,无论处理压力水平如何,在TSB中25℃储存期间大肠杆菌的数量增加超过初始细胞计数水平。在TSB中观察到的细胞数量恢复比在PBS样品中更快,因为TSB中的细菌生长有助于更快恢复。当在4℃或37℃下120小时后将PBS中的孵育温度转移到25℃时,无论处理压力如何,从4℃转移到25℃的样品中均观察到大肠杆菌的恢复。然而,细胞数量保持在不可检测水平的时间通过增加处理压力水平而延长,恢复最长需要48小时。另一方面,对于从37℃转移到25℃孵育温度的经HHP处理的大肠杆菌,未观察到恢复。这项研究表明,HHP处理后需要适当的孵育温度来优化HHP损伤细菌的恢复,从而防止高估HHP处理的致死效果。