Stereochemistry of Ornithine Decarboxylase Reaction

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Abstract
To determine the steric course of the reaction of bacterial ornithine decarboxylase [EC 4.1.1.17], we have carried out the decarboxylation of L-ornithine in 2 H 2 O, and that of DL-[2- 2 H]ornithine in H 2 O, and obtained putrescine bearing a single deuterium atom in the C-1 position. The stereochemistry of [1–2H]putrescine was established by conversion to 1-(2-pyrrolidinyl)-2-propanone with acetoacetate and the pro-S hydrogen-specific diamine oxidase from pea seedlings. Analysis of deuterium content by gas chromatography-mass spectrometry showed that the deuterium label was fully retained during the conversion of [1- 2 H]putrescine produced by the decarboxylation of L-ornithine in 2 H 2 O to 1-(2-pyrrolidinyl)-2-propanone, in contrast with the considerable loss of label from [1- 2 H]putrescine which was produced by the decarboxylation of DL-[2- 2 H]ornithine in H 2 O. The extent of loss of the deuterium label was in good agreement with the estimated value based on the isotope effect in the diamine oxidase reaction. These results indicate that the introduced deuterium (or hydrogen) is in the pro-R position at C-1 of putrescine, and consequently the ornithine decarboxylase reaction proceeds with retention of configuration.