Terminal buds of dark-grown pea (Pisum sativum) seedlings have an indole-3-acetic acid oxidase which does not require Mn2+ and 2,4-dichlorophenol as cofactors. Oxidase activity is at least 50 times higher in buds of tall peas than in dwarf seedlings. Administration of gibberellic acid to dwarf peas stimulates both growth and indoleacetic acid oxidase activity to the same levels as in tall seedlings. By contrast, indoleacetic acid oxidation assayed in the presence of Mn2+ and 2,4-dichlorophenol proceeds at similar rates regardless of gibberellin application. Treatment of tall peas with the growth retardant AMO-1618 reduces growth and oxidase activity. Such treated seedlings are indistinguishably dwarf. The enzyme does not appear to be polyphenol oxidase, nor do the results suggest that reduced activity in dwarf buds is due to higher levels of a dialyzable inhibitor. The peroxidative nature of the oxidase is probable.The presence of IAA oxidase in plant tissues has been firmly established (23). The loss of added IAA from tissue extracts has been attributed in part to this enzyme. There is evidence that IAA oxidase is a peroxidase-based enzyme (5,24) and studies in vitro with horseradish peroxidase revealed that IAA is oxidized via a multiplicity of intermediates to oxindole-3-carbinol, which is converted to methyleneoxindole in a postenzymatic step (8,15). In view of the inverse correlation between the levels of this enzyme and ability of pea tissue to respond to IAA, Galston and Dalberg (6) proposed that TAA oxidase is a growth-regulatory system. Thus, the enzyme is thought to inactivate IAA, thereby controlling the endogenous auxin level.In