Journal
CRYOBIOLOGY
Volume 52, Issue 1, Pages 48-61Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cryobiol.2005.09.004
Keywords
cryopreservation; Allium sativum; garlic; Mentha; mint; shoot tip; differential scanning calorimetry
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Plant shoot tips do not survive exposure to liquid nitrogen temperatures without cryoprotective treatments. Some cryoprotectant solutions, such as plant vitrification solution 2 (PVS2), dehydrate cells and decrease lethal ice formation, but the extent of dehydration and the effect on water freezing properties are not known. We examined the effect of a PVS2 cryoprotection protocol on the water content and phase behavior of mint and garlic shoot tips using differential scanning calorimetry. The temperature and enthalpy of water melting transitions in unprotected and recovering shoot tips were comparable to dilute aqueous solutions. Exposure to PVS2 changed the behavior of water in shoot tips: enthalpy of melting transitions decreased to about 40 J g H2O-1 (compared to 333 J g H2O-1 for pure H2O), amount of unfrozen water increased to similar to 0.7 g H2O g dry mass(-1) (compared to similar to 0.4 g H2O g dry mass(-1) for unprotected shoot tips), and a glass transition (T-g) at - 115 degrees C was apparent. Evaporative drying at room temperature was slower in PVS2-treated shoot tips compared to shoot tips receiving no cryoprotection treatments. We quantified the extent that ethylene glycol and dimethyl sulfoxide components permeate into shoot tips and replace some of the water. Since T-g in PVS2-treated shoot tips occurs at - 115 degrees C, mechanisms other than glass formation prevent freezing at temperatures between 0 and - 115 degrees C. Protection is likely a result of controlled dehydration or altered thermal properties of intracellular water. A comparison of thermodynamic measurements for cryoprotection solutions in diverse plant systems will identify efficacy among cryopreservation protocols. Published by Elsevier Inc.
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