Abstract
A comparative study of the metabolism of radiolabeled gibberellin (GA) 1, 19, and 20 in isolated vegetative tissues of isogenic Le and le pea (Pisum sativum) plants incubated in vitro with the appropriate GA substrate is described. The results of this study provide evidence that the enzymes involved in the latter stages of GA biosynthesis are spatially separated within the growing pea plant. Apical buds were not apparently involved in the production of bioactive GA1 or its immediate precursors. The primary site of synthesis of GA20 from GA19 was immature leaflets and tendrils, and the synthesis of bioactive GA1 and its inactive catabolite GA8 occurred predominantly in stem tissue. GA29, the inactive catabolite of GA20, was produced to varying extents in all the tissues examined. Little or no difference was observed in the ability of corresponding Le and le tissues to metabolize radiolabeled GA1, GA19, or even GA20. During a fixed period of 24 hours, stems of plants carrying the le mutation produced slightly more [3H]GA1 (and [3H]GA29) than those of Le plants. It has been concluded that the le mutation does not lie within the gene encoding the GA20 3β-hydroxylase protein.