Department of Physics, East Carolina University, Greenville, NC 27858-4353, USA.
Appl Environ Microbiol. 2010 Mar;76(6):1796-805. doi: 10.1128/AEM.02851-09. Epub 2010 Jan 22.
Dual-trap laser tweezers Raman spectroscopy (LTRS) and elastic light scattering (ELS) were used to investigate dynamic processes during high-temperature treatment of individual spores of Bacillus cereus, Bacillus megaterium, and Bacillus subtilis in water. Major conclusions from these studies included the following. (i) After spores of all three species were added to water at 80 to 90 degrees C, the level of the 1:1 complex of Ca(2+) and dipicolinic acid (CaDPA; approximately 25% of the dry weight of the spore core) in individual spores remained relatively constant during a highly variable lag time (T(lag)), and then CaDPA was released within 1 to 2 min. (ii) The T(lag) values prior to rapid CaDPA release and thus the times for wet-heat killing of individual spores of all three species were very heterogeneous. (iii) The heterogeneity in kinetics of wet-heat killing of individual spores was not due to differences in the microscopic physical environments during heat treatment. (iv) During the wet-heat treatment of spores of all three species, spore protein denaturation largely but not completely accompanied rapid CaDPA release, as some changes in protein structure preceded rapid CaDPA release. (v) Changes in the ELS from individual spores of all three species were strongly correlated with the release of CaDPA. The ELS intensities of B. cereus and B. megaterium spores decreased gradually and reached minima at T(1) when approximately 80% of spore CaDPA was released, then increased rapidly until T(2) when full CaDPA release was complete, and then remained nearly constant. The ELS intensity of B. subtilis spores showed similar features, although the intensity changed minimally, if at all, prior to T(1). (vi) Carotenoids in B. megaterium spores' inner membranes exhibited two changes during heat treatment. First, the carotenoid's two Raman bands at 1,155 and 1,516 cm(-1) decreased rapidly to a low value and to zero, respectively, well before T(lag), and then the residual 1,155-cm(-1) band disappeared, in parallel with the rapid CaDPA release beginning at T(lag).
双捕获激光镊子拉曼光谱(LTRS)和弹性光散射(ELS)用于研究在 80 至 90°C 下高温处理单个蜡样芽孢杆菌、巨大芽孢杆菌和枯草芽孢杆菌孢子时的动态过程。这些研究的主要结论包括以下几点。(i) 在将这三种细菌的孢子加入 80 至 90°C 的水中后,在高度变化的滞后时间(T(lag))内,单个孢子中钙(Ca)与二吡啶羧酸(CaDPA;占孢子核心干重的约 25%)的 1:1 复合物的水平相对保持恒定,然后在 1 至 2 分钟内释放 CaDPA。(ii) 所有三种细菌的单个孢子快速释放 CaDPA 之前的 T(lag)值,以及所有三种细菌的单个孢子湿热致死的时间差异很大。(iii) 单个孢子湿热致死动力学的异质性不是由于热处理过程中微观物理环境的差异造成的。(iv) 在所有三种细菌的孢子湿热处理过程中,孢子蛋白变性在很大程度上但不完全伴随着 CaDPA 的快速释放,因为一些蛋白质结构的变化先于 CaDPA 的快速释放。(v) 所有三种细菌的单个孢子的 ELS 变化与 CaDPA 的释放密切相关。蜡样芽孢杆菌和巨大芽孢杆菌孢子的 ELS 强度逐渐降低,在 T(1)时达到最小值,此时大约 80%的孢子 CaDPA 被释放,然后迅速增加,直到 T(2)时 CaDPA 完全释放,然后几乎保持不变。枯草芽孢杆菌孢子的 ELS 强度也具有类似的特征,尽管在 T(1)之前,强度可能没有变化,也可能有微小变化。(vi) 巨大芽孢杆菌孢子内膜中的类胡萝卜素在热处理过程中发生了两次变化。首先,在 T(lag)之前,类胡萝卜素在 1155 和 1516 cm(-1)处的两个拉曼带迅速降低到低值和零值,然后残留的 1155-cm(-1)带消失,与 T(lag)开始时快速释放 CaDPA平行。