Biosynthesis of vitamin E and of the plastoquinones in chloroplasts: Steric course of the decarboxylation

Abstract

Samples of (3 R)- and (3 S)-4′hydroxyphenyl[3- 2H 1, 3- 3H]pyruvate were prepared by taking advantage of the known stereospecificity of phenylpyruvate keto-enol isomerase (tautomerase). 4′-Hydroxyphenyl[3- 14C]pyruvate was obtained by the action of l-amino acid oxidase on dl-[3- 14C]tyrosine, whereas a simple base-catalyzed exchange procedure yielded samples of 4′-hydroxyphenyl[3- 3H]- and 4′-hydroxyphenyl[3- 2H 2]pyruvate. All labeled samples were converted in situ into the corresponding homogentisic acids on 4′-hydroxyphenyl-pyruvate dioxygenase that is known to catalyze the migration of the acetate side chain with retention of configuration. The isolated doubly labeled homogentisic acids were incubated with chloroplasts from Raphanus sativus cv. saxa Treib, and from the lipophilic products a fraction containing inter alia tocopherol, tocoquinone, and plastoquinone was obtained by chromatographic procedures. The incorporation of radioactivity was between 0.5 and 11% based on homogentisate. Reductive acetylation of the quinones yielded crystalline diacetylhydroquinones, which were submitted to Kuhn-Roth degradation. The radioactive acetate samples thus obtained were analyzed for chirality by an enzymatic procedure previously published. (2 R)-[2- 2H 1, 2- 3H]Homogentisate gave mainly ( S)-acetate, whereas (2 S)-[2- 2H 1, 2- 3H]homogentisate was converted mainly into ( R)-acetate. It is concluded that the decarboxylation of the side chain occurred with stereochemical retention during the biosynthetic process.