Abstract
Experiments with sterile grown maize coleoptiles were carried out to decide whether or not a biosynthetic path for β-indolyl-acetic acid (IAA) from indole exists without tryptophan occurring as an intermediate. β-Indolyl-acrylic acid as a tryptophan synthetase inhibitor significantly reduces the yield of [3H]tryptophan obtained from [3H]indole while the reduction in the [3H]IAA yield is considerably less pronounced. This, however, indicates only a non-linear relationship between the tryptophan concentration and the IAA yield and not the sought path. Moreover, double labelling combined with isotope competition methods in experiments with [3H]indole and L-[14C]serin show that all IAA synthesized from [3H]indole is produced on a path involving the synthesis of tryptophan as an intermediate.

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