Because water is essential in the formation and maintenance of the bilayer
structure, dehydration has a major impact on the conformation of membranes.
Dehydration leads to increases in the gel-to-liquid crystalline transition
temperature (T-m) and, depending on the phospholipid species involved, to
the formation of nonbilayer phases. Di- and oligosaccharides, which are abu
ndant in desiccation-tolerant organisms, are particularly effective at supp
ressing the dehydration-induced increase in T-m, by interacting with the po
lar headgroups. Moreover, they prevent membrane fusion by the timely format
ion of a glassy matrix. Both properties are crucial in the protection of li
posomes from dehydration stress. Dry, desiccation-tolerant organisms lack n
on-bilayer phases, but gel phase has been encountered. T-m of membranes in
dried organisms is fewer than that of dried isolated membranes, probably as
a result of the interaction of the sugars with the headgroups and the part
itioning of amphiphilic (fluidizing) compounds into the membranes in situ.
Depression of T-m in situ may be beneficial in postponing or preventing a p
hase change with drying and the associated loss of solutes. It may also be
beneficial in preventing lateral phase separations when the interacting sug
ars partake in a glassy matrix at a low moisture content. Injury can ensue
when dry cells having gel phase phospholipids are plunged into (cold) water
. Melting the gel phase lipid before imbibition, e.g., by exposure to humid
air or heating, reduces leakage and preserves viability. We suggest that d
epression of T-m, the interaction of sugars with the polar headgroups, as w
ell as the formation of a glassy matrix, are required for the irt situ pres
ervation of membranes in a dry state.