Middelbeek E J, Crützen Q H, Vogels G D
Antimicrob Agents Chemother. 1980 Oct;18(4):519-24. doi: 10.1128/AAC.18.4.519.
Loss of viability of toxin-treated cells of Saccharomyces cerevisiae SCF 1717 could be prevented in the period before they altered physiologically if cells were incubated in media with a suitable concentration of potassium (0.08 to 0.13 M) and hydrogen ions (pH 6.2 to 6.7). Incorporation of higher amounts of potassium chloride in the media had a pronounced negative effect on cell survival, particularly when the pH of the medium was lowered. Replacement of KCl by NaCl in the plate media was even more deleterious to toxin-treated cells and, in contrast with potassium, low concentrations of sodium ions could not sustain recovery of cells. Complete recovery of a toxin-treated cell suspension required an incubation of 3 h in a suitable medium. The recovery process was blocked by cycloheximide.
如果将酿酒酵母SCF 1717的毒素处理细胞在生理改变之前置于含有适宜浓度钾离子(0.08至0.13 M)和氢离子(pH 6.2至6.7)的培养基中培养,其活力丧失是可以预防的。培养基中加入更高量的氯化钾对细胞存活有显著的负面影响,尤其是当培养基pH降低时。平板培养基中用氯化钠替代氯化钾对毒素处理细胞更具毒害作用,并且与钾离子不同,低浓度的钠离子无法维持细胞的恢复。毒素处理的细胞悬液完全恢复需要在适宜培养基中培养3小时。恢复过程被环己酰亚胺阻断。