Abstract
When cooled at rapid rates to temperatures between −10 and −30°C, the incidence of intracellular ice formation was less in protoplasts enzymically isolated from cold acclimated leaves of rye (Secale cereale L. cv Puma) than that observed in protoplasts isolated from nonacclimated leaves. The extent of supercooling of the intracellular solution at any given temperature increased in both nonacclimated and acclimated protoplasts as the rate of cooling increased. There was no unique relationship between the extent of supercooling and the incidence of intracellular ice formation in either nonacclimated or acclimated protoplasts. In both nonacclimated and acclimated protoplasts, the extent of intracellular supercooling was similar under conditions that resulted in the greatest difference in the incidence of intracellular ice formation—cooling to −15 or −20°C at rates of 10 or 16°C/minute. Further, the hydraulic conductivity determined during freeze-induced dehydration at −5°C was similar for both nonacclimated and acclimated protoplasts. A major distinction between nonacclimated and acclimated protoplasts was the temperature at which nucleation occurred. In nonacclimated protoplasts, nucleation occurred over a relatively narrow temperature range with a median nucleation temperature of −15°C, whereas in acclimated protoplasts, nucleation occurred over a broader temperature range with a median nucleation temperature of −42°C. We conclude that the decreased incidence of intracellular ice formation in acclimated protoplasts is attributable to an increase in the stability of the plasma membrane which precludes nucleation of the supercooled intracellular solution and is not attributable to an increase in hydraulic conductivity of the plasma membrane which purportedly precludes supercooling of the intracellular solution.
Full text
PDF










Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ASAHINA E. Intracellular freezing and frost resistance in egg-cells of the sea urchin. Nature. 1961 Sep 23;191:1263–1265. doi: 10.1038/1911263a0. [DOI] [PubMed] [Google Scholar]
- Leibo S. P., McGrath J. J., Cravalho E. G. Microscopic observation of intracellular ice formation in unfertilized mouse ova as a function of cooling rate. Cryobiology. 1978 Jun;15(3):257–271. doi: 10.1016/0011-2240(78)90036-6. [DOI] [PubMed] [Google Scholar]
- Levin R. L., Cravalho E. G., Huggins C. E. A membrane model describing the effect of temperature on the water conductivity of erythrocyte membranes at subzero temperatures. Cryobiology. 1976 Aug;13(4):415–429. doi: 10.1016/0011-2240(76)90097-3. [DOI] [PubMed] [Google Scholar]
- Lilley R. M. Isolation of Functionally Intact Rhodoplasts from Griffithsia monilis (Ceramiaceae, Rhodophyta). Plant Physiol. 1981 Jan;67(1):5–8. doi: 10.1104/pp.67.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lyman G. H., Preisler H. D., Papahadjopoulos D. Membrane action of DMSO and other chemical inducers of Friend leukaemic cell differentiation. Nature. 1976 Jul 29;262(5567):361–363. doi: 10.1038/262360a0. [DOI] [PubMed] [Google Scholar]
- MAZUR P. KINETICS OF WATER LOSS FROM CELLS AT SUBZERO TEMPERATURES AND THE LIKELIHOOD OF INTRACELLULAR FREEZING. J Gen Physiol. 1963 Nov;47:347–369. doi: 10.1085/jgp.47.2.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MAZUR P. Physical and temporal factors involved in the death of yeast at subzero temperatures. Biophys J. 1961 Jan;1:247–264. doi: 10.1016/s0006-3495(61)86887-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MAZUR P. Studies on rapidly frozen suspensions of yeast cells by differential thermal analysis and conductometry. Biophys J. 1963 Jul;3:323–353. doi: 10.1016/s0006-3495(63)86824-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mazur P. Cryobiology: the freezing of biological systems. Science. 1970 May 22;168(3934):939–949. doi: 10.1126/science.168.3934.939. [DOI] [PubMed] [Google Scholar]
- Mazur P. The role of cell membranes in the freezing of yeast and other single cells. Ann N Y Acad Sci. 1965 Oct 13;125(2):658–676. doi: 10.1111/j.1749-6632.1965.tb45420.x. [DOI] [PubMed] [Google Scholar]
- Mazur P. The role of intracellular freezing in the death of cells cooled at supraoptimal rates. Cryobiology. 1977 Jun;14(3):251–272. doi: 10.1016/0011-2240(77)90175-4. [DOI] [PubMed] [Google Scholar]
- McKenzie J. S., Weiser C. J., Stadelmann E. J., Burke M. J. Water Permeability and Cold Hardiness of Cortex Cells in Cornus stolonifera Michx.-A Preliminary Report. Plant Physiol. 1974 Aug;54(2):173–176. doi: 10.1104/pp.54.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rasmussen D. H., Macaulay M. N., MacKenzie A. P. Supercooling and nucleation of ice in single cells. Cryobiology. 1975 Aug;12(4):328–339. doi: 10.1016/0011-2240(75)90006-1. [DOI] [PubMed] [Google Scholar]
- Stout D. G., Steponkus P. L. Quantitative study of the importance of water permeability in plant cold hardiness. Plant Physiol. 1977 Sep;60(3):374–378. doi: 10.1104/pp.60.3.374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sukumaran N. P., Weiser C. J. Freezing injury in potato leaves. Plant Physiol. 1972 Nov;50(5):564–567. doi: 10.1104/pp.50.5.564. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiest S. C., Steponkus P. L. Freeze-thaw injury to isolated spinach protoplasts and its simulation at above freezing temperatures. Plant Physiol. 1978 Nov;62(5):699–705. doi: 10.1104/pp.62.5.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
