Lipids were labeled with 3P during frost hardening of two varieties of winter wheat (Triticumn aestivum), hardy Kharkov and much less hardy Champlein. The main labeled compounds were phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, and phosphatidylglycerol. With time of incorporation the proportion of the radioactivity incorporated into the lipids increased in phosphatidylcholine, especially in Kharkov and at 1 C. During hardening, phospholipid synthesis was greatly stimulated in Kharkov, but much less in Champlein. The proportion of the phospholipids synthesized changed only little with hardening, with a trend towards an increase in phosphatidylcholine. Increased phospholipid synthesis does not seem to be a prerequisite to hardening in winter wheat. However, a high rate of phospholipid synthesis may be required to maintain frost resistance.An increase in phospholipids has generally been observed during hardening of plants (4,5,7,8,11,12, 14). It is not known whether this increase is a result of low temperature or whether it is part of the frost-hardening process. In an attempt to dissociate the two effects, phospholipid biosynthesis was measured at two temperatures during controlled hardening of a hardy and a less hardy variety of winter wheat.
MATERIALS AND METHODSGrowth and Hardening of Plants. Two varieties of winter wheat (Triticuin aestivum), hardy Kharkov, and less hardy Champlein, were grown in 10-cm pots containing a 1: 1 mixture of sand and vermiculite in a growth cabinet (Controlled Environment, Winnipeg) at a 20 C day and 15 C night temperature, a 16-hr photoperiod, a relative humidity of 60%, and a light intensity of 18,000 lux. The plants were watered with Hoagland No. 1 solution (9). After 12 days they were transferred to a hardening cabinet at a constant temperature of 1 C, an 8-hr photoperiod, and a light intensity of 8,000 lux. Before and during hardening the frost resistance of the plants was tested by controlled freezing (7,13) in the pots at several temperatures. The temperature at which 50% of the plants were killed (killing temperature) was determined after 3 weeks of recovery.'Contribution No. 50 from the Canada Department of Agriculture Research Station, Ste-Foy.Labeling with "'P. The roots of triplicate samples of two plants were covered with 2 ml of a radioactive solution containing 0.05 M citrate buffer pH 5 and 3 to 8 /,Ci of 'P (H333PO4, 50 mCi/mmole, New England Nuclear) in 10-ml beakers for varying times at either 20 C or 1 C under continuous light at an intensity of 8,000 lux. During hardening experiments, feeding times were either 24 hr at 1 C or 12 hr at 20 C. At the end of the incorporation, the roots and crowns were rinsed, boiled for 3 min, covered with 6 ml of chloro-