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Updated: Jul 23, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Studies on the biosynthesis of asperparaline A: origin of the spirosuccinimde ring system
Chandele R Gray1, Juan F Sanz-Cervera, Louis A Silks
1Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Abstract:
The primary amino acid building blocks that constitute asperparaline A have been determined through feeding and incorporation of 13C-labeled intermediates. The beta-methyl proline residue is constituted from (S)-isoleucine, the novel spiro-succinime moiety is derived from the oxidative degradation of (S)-tryptophan, and (S)-adenosylmethionine contributes the two N-methyl residues. In addition, it was found that the incorporation of 13C-labeled acetate into the single isoprene unit clearly demonstrates that the isoprene moiety is derived from the mevalonate pathway.
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