Numerous chemical additives lower the freezing point of water, but life at sub-zero temperatures is
sustained by a limited number of biological cryoprotectants. Antifreeze proteins in fish, plants, and insects provide
protection to a few degrees below freezing. Microbes have been found to survive at even lower temperatures, and
with a few exceptions, antifreeze proteins are missing. Survival has been attributed to external factors, such as the
high salt concentration of brine veins and adhesion to particulates or ice crystal defects. We have discovered an
endogenous cryoprotectant in the cell wall of bacteria, lipoteichoic acid biopolymers. Adding 1% LTA to bacteria
cultures immediately prior to freezing provides 50% survival rate, similar to the results obtained with 1% glycerol.
In the absence of an additive, bacterial survival is negligible as measured with the resazurin cell viability assay. The
mode of action for LTA cryoprotection is unknown. With a molecular weight of 3-5 kDa, it is unlikely to enter the
cell cytoplasm. Our observations suggest that teichoic acids could provide a shell of liquid water around biofilms
and planktonic bacteria, removing the need for brine veins to prevent bacterial freezing.
The bacterial spore is a formidable container of life, protecting the vital contents from chemical attack, antimicrobial
agents, heat damage, UV light degradation, and water dehydration. The exact role of the spore components remains in
dispute. Nevertheless, water molecules are important in each of these processes. The physical state of water within the
bacterial spore has been investigated since the early 1930's. The water is found two states, free or bound, in two different
areas, core and non-core. It is established that free water is accessible to diffuse and exchange with deuterated water and
that the diffusible water can access all areas of the spore. The presence of bound water has come under recent scrutiny
and has been suggested the water within the core is mobile, rather than bound, based on the analysis of deuterium
relaxation rates. Using an alternate method, deuterium quadrupole-echo spectroscopy, we are able to distinguish between
mobile and immobile water molecules. In the absence of rapid motion, the deuterium spectrum of D2O is dominated by a
broad line, whose line shape is used as a characteristic descriptor of molecular motion. The deuterium spectrum of
bacterial spores reveals three distinct features: the broad peak of immobilized water, a narrow line of water in rapid
motion, and a signal of intermediate width. This third signal is assigned this peak from partially deuterated proteins with
the spore in which N-H groups have undergone exchange with water deuterons to form N-D species. As a result of these
observations, the nature of water within the spore requires additional explanation to understand how the spore and its
water preserve life.
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