Steric course and rearrangements in the biosynthesis of phenylalanine, tyrosine, and 3-(3-carboxyphenyl)ala nine from shikimic acid in higher plants

Abstract
Incorporation of stereospecifically labelled shikimic acid into Reseda lutea L. demonstrates the same steric course and rearrangement in the biosynthesis of phenylalanine and tyrosine as that known from bacteria, whereas the biosynthesis of 3-(3-carboxyphenyl)alanine involves a different rearrangement reaction.

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