MOSS C W, SPECK M L
Appl Microbiol. 1963 Jul;11(4):326-9. doi: 10.1128/am.11.4.326-329.1963.
Cells of Streptococcus lactis were harvested in the early stationary phase, washed, and resuspended in either skim milk (10% nonfat milk) or buffered distilled water (0.0003 m dipotassium phosphate, pH 7.2). Samples of each suspension were frozen and stored at -20 C for intervals up to 28 days. Colony counts of the frozen culture were made using lactic agar and a "restricted" lactic agar medium (Tryptone reduced to 0.5%) to determine injury and death. Death was determined by the difference in plate counts on lactic agar before and after freezing. Injured cells were determined by the difference in plate counts on the two plating media. Greatest injury of the cells occurred during early stages of frozen storage and decreased with time, and death continuously increased. Injury and death were more pronounced when cells were frozen in water than when frozen in 10% nonfat milk solids. Certain cultures survived better when frozen rapidly, whereas with others survival was greater when freezing was slow. Successive freezing, thawing, and propagation of the culture gradually eliminated cells which showed injury by freezing.
乳酸链球菌细胞在稳定期早期收获,洗涤后重悬于脱脂乳(10%脱脂乳)或缓冲蒸馏水(0.0003m磷酸氢二钾,pH 7.2)中。每种悬浮液的样品冷冻并在-20℃下保存长达28天。使用乳酸琼脂和“改良”乳酸琼脂培养基(胰蛋白胨降至0.5%)对冷冻培养物进行菌落计数,以确定损伤和死亡情况。通过冷冻前后乳酸琼脂平板计数的差异来确定死亡情况。通过两种平板培养基上的平板计数差异来确定受损细胞。细胞的最大损伤发生在冷冻储存的早期阶段,并随时间减少,而死亡则持续增加。细胞在水中冷冻时的损伤和死亡比在10%脱脂乳固体中冷冻时更明显。某些培养物快速冷冻时存活得更好,而其他培养物缓慢冷冻时存活率更高。培养物的连续冷冻、解冻和传代逐渐消除了因冷冻而受损的细胞。