Komatsu Y, Kaul S C, Iwahashi H, Obuchi K
Fermentation Research Institute, Ibaraki, Japan.
FEMS Microbiol Lett. 1990 Oct;60(1-2):159-62. doi: 10.1016/0378-1097(90)90364-v.
Yeast cells were frozen by plunging directly into liquid nitrogen (LN2) after exposure at 43 degrees C. Both the cells frozen without prior exposure to heat shock and those treated with cycloheximide showed almost 100% loss of viability during freezing and thawing. Heat exposure prior to freezing and thawing significantly increased the cell viability. This increase in cell viability was associated with the induction of heat shock protein synthesis, which was detected by gel electrophoresis. This protein may act by stabilizing the macromolecules and by increasing the hydrophobic interactions.
酵母细胞在43摄氏度暴露后直接投入液氮(LN₂)中冷冻。未经热休克预处理而冷冻的细胞以及用环己酰亚胺处理的细胞在冻融过程中几乎100%丧失活力。冻融前的热暴露显著提高了细胞活力。这种细胞活力的提高与热休克蛋白合成的诱导有关,这通过凝胶电泳检测到。这种蛋白质可能通过稳定大分子和增加疏水相互作用来发挥作用。