热超声波与山梨酸钾结合对膜葡萄孢的抗菌机制

Jingya Qian , Zixuan Zhang , Di Chen , Feng Zhao , Shuhao Huo , Haile Ma , Feng Wang
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摘要

本研究探讨了超声波(US)结合加热(T)和山梨酸钾(PS)处理对膜衣壳菌(P. membranifaciens)的抗菌机制的影响。研究发现,超声波结合加热(热超声波 [TS])具有协同灭活效率,而 US、T 和 TS 与 PS 的组合也提高了灭活效率,使用 US + PS、T + PS 和 TS + PS 可使膜衣壳菌的灭活效率分别降低 0.32 ± 0.02 log、0.73 ± 0.04 log 和 4.50 ± 0.04 log。此外,使用 TS + PS 处理会导致细胞质渗漏、脱氢酶活性降低以及细胞膜通透性显著增加,从而引起膜去极化和细胞外钙离子内流。此外,通过红外光谱检测细胞膜成分,证明 TS + PS 处理会导致细胞膜中脂质和蛋白质含量减少,磷脂含量增加。扫描和透射电子显微镜显示,TS + PS 处理后细胞结构变形,细胞膜完整性受损。此外,与 T 和 T + PS 处理组相比,TS 和 TS + PS 处理后热休克蛋白(Hsp82 和 Hsp70)基因的表达量减少,这表明细胞平衡已被打破,细胞正通过激活保护性基因表达程序来应对损伤。
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Antibacterial mechanism of thermoultrasound combined with potassium sorbate against Pichia membranifaciens

The effect of the antimicrobial mechanism of ultrasound (US) in combination with heat (T) and potassium sorbate (PS) treatment on Pichia membranifaciens (P. membranifaciens) is investigated in this study. It is found that ultrasound combined with heat (thermoultrasound [TS]) exhibits a synergistic inactivation efficiency, and the combinations of US, T, and TS with PS also improve inactivation efficacy through reductions of 0.32 ± 0.02 log, 0.73 ± 0.04 log, and 4.50 ± 0.04 log in P. membranifaciens achieved using US + PS, T + PS, and TS + PS, respectively. Further, use of the TS + PS treatment leads to cytoplasmic leakage and a decrease in dehydrogenase activity, as well as a significant increase in cell membrane permeability, causing membrane depolarization and the inward flow of extracellular calcium ions. In addition, the cell membrane composition is detected by infrared spectroscopy, demonstrating that TS + PS treatment results in a decrease in lipid and protein content and an increase in phospholipid content in the cell membrane. Scanning and transmission electron microscopy reveals a deformed cell structure and damage to cell membrane integrity after TS + PS treatment. In addition, the expression of heat shock protein (Hsp82 and Hsp70) genes is shown to decrease after TS and TS + PS treatment compared to the T and T + PS treatment groups, indicating cellular homeostasis has been broken and cells are responding to the damage by activating the protective gene expression program.

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