Department of Food Science, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
Department of Food Science, University of Otago, PO Box 56, Dunedin 9054, New Zealand; Riddet Institute, Palmerston North, New Zealand.
Food Res Int. 2019 May;119:462-468. doi: 10.1016/j.foodres.2018.12.041. Epub 2018 Dec 24.
Differential gene expression was used to explore the mechanisms underpinning the differences in the impact of heat activation (70 °C for 30 min) on the germination of Bacillus cereus spores in the presence and absence of a germinant (L-alanine). The number of germinated cells, after heat activation plus L-alanine (3.5 ± 0.02 log CFU/ml) in the spore only initial population was found to be higher than that in only heat activated spores (2.01 ± 0.02 log CFU/ml). The concentration of DPA released by heat activated spores in the presence of L-alanine was 68.3 ± 0.1 and 112.1 ± 0.02 μg/ml after 30 and 60 min, compared to 96.5 and 166.2 ± 0.01 μg/ml after 30 and 90 min, respectively released by spores subjected only to heat activation. Gene (BC0784) encoding for the spore germination protein, gerA operon was up-regulated with a log-transformed fold change value of 1.2 due to heat activation in the presence of L-alanine. The GerA operon located in the inner membrane is known to be involved in the uptake of L-alanine by B. cereus and has been reported to be involved in L-alanine mediated germination. In addition the up-regulation of genes involved in the uptake of L-alanine is proposed to provide the answer to the synergistic effect of heat and L-alanine in inducing germination in B. cereus spores. In short, heat activation increases the ability of L-alanine to penetrate into the spore's inner membrane, where it can be recognized by the receptors for initiation of the germination pathway. In the current study, the majority of the ribosomal proteins were down-regulated (when spores were heat treated in presence of germinants) this process also appeared to slow down protein synthesis by restricting the protein translation machinery. Differential gene expression revealed the genes responsible for the pathways related to transport and recognition of L-alanine into the spore that could have led to the accelerated germination process along with partial shutting down of protein synthesis pathway and ABC transporters. Knowledge of gene regulation in spores during heat activation will help in the development of approaches to prevent spore germination, which could provide an additional safeguard against bacterial growth and toxin production in improperly cooled heat treated foods.
差异基因表达被用来探索热激活(70°C 30 分钟)对有和没有发芽剂(L-丙氨酸)存在时蜡状芽孢杆菌孢子发芽影响差异的机制。在仅存在热激活的孢子中,发现经热激活加 L-丙氨酸(3.5±0.02 log CFU/ml)处理的发芽细胞数量高于仅热激活的孢子(2.01±0.02 log CFU/ml)。在存在 L-丙氨酸的情况下,经热激活的孢子释放的 DPA 浓度在 30 分钟和 60 分钟时分别为 68.3±0.1 和 112.1±0.02μg/ml,而仅经热激活的孢子在 30 分钟和 90 分钟时分别为 96.5 和 166.2±0.01μg/ml。编码孢子发芽蛋白 gerA 操纵子的基因(BC0784)在有 L-丙氨酸存在的情况下因热激活而上调,对数转化倍数为 1.2。位于内膜中的 GerA 操纵子已知参与蜡状芽孢杆菌对 L-丙氨酸的摄取,并且据报道它参与 L-丙氨酸介导的发芽。此外,L-丙氨酸摄取相关基因的上调被认为是解释热和 L-丙氨酸协同诱导蜡状芽孢杆菌孢子发芽的原因。简而言之,热激活增加了 L-丙氨酸穿透孢子内膜的能力,在那里它可以被发芽途径的受体识别。在本研究中,大多数核糖体蛋白(当孢子在有发芽剂的情况下受热处理时)下调,这一过程似乎通过限制蛋白质翻译机制来减缓蛋白质合成。差异基因表达揭示了与 L-丙氨酸进入孢子的运输和识别相关的途径相关的基因,这些基因可能导致加速的发芽过程,同时部分关闭蛋白质合成途径和 ABC 转运体。了解热激活过程中孢子中的基因调控将有助于开发防止孢子发芽的方法,这可能为防止不当冷却热处理食品中的细菌生长和毒素产生提供额外的保障。