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Characterization of Wet-Heat Inactivation of Single Spores of Bacillus Species by Dual-Trap Raman Spectroscopy and Elastic Light Scattering

机译:双陷阱拉曼光谱和弹性光散射表征芽孢杆菌单孢子的湿热失活

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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°C, the level of the 1:1 complex of Ca2+ and dipicolinic acid (CaDPA; ~25% of the dry weight of the spore core) in individual spores remained relatively constant during a highly variable lag time (Tlag), and then CaDPA was released within 1 to 2 min. (ii) The Tlag 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 T1 when ~80% of spore CaDPA was released, then increased rapidly until T2 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 T1. (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 Tlag, and then the residual 1,155-cm?1 band disappeared, in parallel with the rapid CaDPA release beginning at Tlag.
机译:使用双阱激光镊子拉曼光谱(LTRS)和弹性光散射(ELS)来研究高温处理水中蜡状芽孢杆菌,巨大芽孢杆菌和枯草芽孢杆菌的单个孢子的动态过程。这些研究的主要结论包括以下内容。 (i)将这三种菌种的孢子在80至90°C的水中加入后,Ca2 +与二吡啶甲酸的1:1配合物(CaDPA;孢子核干重的约25%)的水平在高度可变的滞后时间(Tlag)中,单个孢子保持相对恒定,然后CaDPA在1-2分钟内释放。 (ii)快速释放CaDPA之前的Tlag值,因此湿热杀死所有三种物种的单个孢子的时间非常不同。 (iii)湿热杀死单个孢子的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。 (iv)在湿热处理所有三种孢子的过程中,孢子蛋白质变性很大程度上但不完全伴随CaDPA的快速释放,因为CaDPA的快速释放之前蛋白质结构发生了一些变化。 (v)来自所有三个物种的单个孢子的ELS的变化与CaDPA的释放密切相关。蜡状芽孢杆菌和巨大芽孢杆菌孢子的ELS强度在孢子CaDPA释放约80%时在T1逐渐降低并达到极小值,然后在CaDPA完全释放完全之前迅速增加直到T2,然后保持几乎恒定。枯草芽孢杆菌孢子的ELS强度显示出相似的特征,尽管强度在T1之前变化很小,即使有变化。 (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表现出两个变化。首先,类胡萝卜素的两个拉曼谱带分别在1,155和1,516 cm?1处迅速下降到低值,并在Tlag之前就迅速降至零,然后剩余的1,155-cm?1谱带消失了,与此同时CaDPA迅速释放开始在Tlag。

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