Levin R L, Ushiyama M, Cravalho E G
J Membr Biol. 1979 Apr 20;46(2):91-124. doi: 10.1007/BF01961376.
A combined cryomicroscopic-multiple nonlinear regression analysis technique has been used to determine the water permeability of the yeast cell Saccharomyces cerevisiae during freezing. The time rate of change in volume of "supercooled" yeast cells was photographically monitored using a "cryomicroscope" which is capable of controlling in a programmable manner both the temperature and the time rate of change in temperature of the cell suspension being studied. Multiple nonlinear regression analysis together with a thermodynamic model of cell water transport during freezing was then used to statistically deduce the subzero temperature dependence of the cell water permeability. The water permeability process for S. cerevisiae being cooled at subzero temperatures was found to be rate-limited by the passage of water through either the plasmalemma, the cell wall, or a combination of these two permeability barriers. The hydraulic water permeability coefficient for yeast at 20 degrees C is approximately 1--2 x 10(-13) cm3/dyne sec, if extrapolation from subzero temperatures to room temperature is permissible, while the apparent activation energy governing the permeability process at subzero temperatures is approximately 45--68 kJ/mol (11--16 kcal/mol).
一种结合低温显微镜 - 多重非线性回归分析的技术已被用于测定酿酒酵母细胞在冷冻过程中的水渗透性。使用“低温显微镜”通过摄影监测“过冷”酵母细胞体积的时间变化率,该显微镜能够以可编程的方式控制所研究细胞悬浮液的温度以及温度的时间变化率。然后,将多重非线性回归分析与冷冻过程中细胞水运输的热力学模型相结合,以统计推导细胞水渗透性对零下温度的依赖性。发现酿酒酵母在零下温度冷却时的水渗透过程受水通过质膜、细胞壁或这两种渗透屏障组合的速率限制。如果允许从零下温度外推至室温,酵母在20摄氏度时的水力水渗透系数约为1 - 2×10⁻¹³立方厘米/达因·秒,而在零下温度下控制渗透过程的表观活化能约为45 - 68千焦/摩尔(11 - 16千卡/摩尔)。