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冷冻过程中单个细胞的渗透反应。II. 膜通透性分析。

Osmotic response of individual cells during freezing. II. Membrane permeability analysis.

作者信息

Schwartz G J, Diller K R

出版信息

Cryobiology. 1983 Oct;20(5):542-52. doi: 10.1016/0011-2240(83)90042-1.

Abstract

An analytical model is presented to simulate the freezing of individual yeast cells. In addition the model is solved numerically on a digital computer to obtain values for cell volume as a function of temperature, based on the thermal protocol during freezing, and the transport parameters of the cell membrane. The numerical procedure was modified to enable values for the membrane hydraulic permeability reference coefficient, Lpg, and activation energy, ELp, to be deduced by nonlinear analysis of complementary experimental data (10). It was observed that the apparent values of both Lpg and ELp increase with cooling rate, from Lpg = 0.0116 micrometer 3 micrometers-2 atm-1 min-1 and ELp = 19.4 kJ mol-1 for 9 degrees K/min to Lpg = 2.11 micrometers 3 micrometer-2 atm-1 min-1 and ELp = 101 kJ mol-1 for 35 degrees K/min. The deduced permeabilities fall within the range of values determined in a prior study by Levin (6). Analysis with the model also indicates that the turgor pressure exerts a negligible effect on yeast exposed to freezing stress.

摘要

提出了一个分析模型来模拟单个酵母细胞的冷冻过程。此外,基于冷冻过程中的热协议和细胞膜的传输参数,在数字计算机上对该模型进行了数值求解,以获得细胞体积随温度变化的值。对数值程序进行了修改,以便通过对补充实验数据的非线性分析来推导膜水力渗透参考系数Lpg和活化能ELp的值(10)。观察到Lpg和ELp的表观值均随冷却速率的增加而增加,从9 K/min时的Lpg = 0.0116立方微米·微米-2·大气压-1·分钟-1和ELp = 19.4 kJ/mol增加到35 K/min时的Lpg = 2.11立方微米·微米-2·大气压-1·分钟-1和ELp = 101 kJ/mol。推导得到的渗透率落在Levin先前研究(6)确定的值范围内。该模型的分析还表明,膨压对遭受冷冻胁迫的酵母的影响可忽略不计。

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