
A study of the metabolic pathways of H3-thymidine utilization in buds of Lilium longiflorum and root tips of Vicia faba was undertaken in order to obtain information that might explain the binding of H3 from H3-thymidine in the cytoplasm of these plants. H3-thymidine was administered for various periods of time, the tissues were fixed and processed in the manner routinely used in preparation for sectioning and autoradiography, and the radioactivity removed in this way from the tissues was determined. It was found that the ethanol/acetic acid fixative contained the major portion of the radioactivity. Analysis of this extract by paper chromatography showed that the radioactivity was distributed among various degradation products of thymidine, principally ß-ureidoisobutyric acid and ß-aminoisobutyric acid. Time course experiments with Vicia showed that these degradation products rapidly appeared in the tissue during incubation with H3-thymidine, while H3-thymine appeared in the incubation medium. Preliminary studies indicated that Vicia root tips incubated with H3-dihydrothymine for 24 hours would bind a small amount of H3 non-specifically in the cells. It seems unlikely that utilization of degradation products of H3-thymidine is sufficient to explain labeling which is concentrated in the cytoplasm.
Cytoplasm, Aminoisobutyric Acids, Autoradiography, Urea, Plants, Thymidine
Cytoplasm, Aminoisobutyric Acids, Autoradiography, Urea, Plants, Thymidine
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