Radlioactive amiino aci(ds have been utilized in the stu(ly of protein synthesis in both detached plant tissues and plant mitochondria. When a plant tissue is incubated in the presence of a radioactive amino acid, the radioactivity is rapidly accumulated in the cells (1,7,8,11,12,13,14 tioIns per minute in a water bath nmaintained at 25°. At the end of the incubation period, tissue sections were removed from the medium and washed thoroughly under running water, blotted dry, and weighed. The tissues were immediately frozen and stored in a dry ice cabinet until further work could be carried out. The frozen tissues were first pulverized in a mortar and then finely ground with water. The total homogenate was made up to 10 ml and filtered through a glass fiber filter paper disc. After thoroughly washing this residue witlh water, followed with a smlall amount of ethyl alcohol, the residue was dried under an infrared lamp before submitted to the measurement of radioactivity. The activity aifter correction for background and self-absorption factor, was designated as the amount of incorporation into water insoluble residue. The activity of water soluble fractioni was determined by plating 0.5 ml aliquots of the filtrate in 2.5 cim stainless steel cuppedI planchets. PLANT PHYSIOLOGY Shoot Sections. Data in table I shows that the C14 from labeled glycine incorporated readily into the protein of pea shoot sections. This incorporation was linearly increased with time of incubation during the first 16 hours, with the exception of a slight initial lag. After that, the incorporation of C14 activity in the protein started to decline indicating that the rate of degradation of C14-protein was greater than the rate of incorporation. Despite the uptakes of glycine by 2,4-D and IAA treated tissues were 25 % and 35 % less respectively, approximately an equal amount of C14 from labeled glycine was incorporated into the pea shoot protein from both the control and the treated sections. At 1 X 10-4 M of 2,4-D or IAA, no significant differences in C'4 incorporation were evident during the first 10 hours. The average radioactivity in the protein found between sixteenth and fortieth hours seemed to indicate a slight increase of glycine incorporation from auxin-treated tissues. Only a small fraction (less than 10 %) of the absorbed glycine was incorporated into the protein while the major portion of the activity was not recovered and was presumably lost as respiratory CO2. Parthier (8) in his study of amino acid incorporation into tobacco leaf protein observed that from 60 to 80 % of glycine-1-C'4 was lost as CO2. In short-term experiments, approximately 17 % of glycine-1-C14 absorbed by excised roots was incorporated in the respired CO2 (14). The average rate of C14 incorporation calculated from the specific activity of protein at sixteenth hour was 0.14 ,umoles per g protein per hour for pea shoot tissues. This value is considerably less than the incorporation of C'4-glutamate in pea seedlings as reported by Webster (11,12). This difference...