抄録
Prenylation is a key post-translational reaction to increase the structural diversity and bioactivity of peptides and proteins. Until now, only one post-translational modification enzyme, ComQ, has been identified to mediate the prenylation of a tryptophan residue in ribosomally synthesized peptides. Here, we report the in vitro characterization of KgpF, a novel prenyltransferase which transfers dimethylallyl moieties to tryptophan residues during kawaguchipeptin A biosynthesis. The stereospecific prenylation by KgpF was determined by a combination of in vitro dimethylallylation of Fmoc-tryptophan by KgpF and chemical synthesis of dimethylallylated Fmoc-tryptophan diastereomers. KgpF modified the tryptophan derivative with a dimethylallyl group at the 3 position of its indole ring, resulting in the formation of a tricyclic structure with the same scaffold as prenylation by ComQ, but with the opposite stereochemistry.
本文言語 | 英語 |
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ページ(範囲) | 9639-9644 |
ページ数 | 6 |
ジャーナル | Organic and Biomolecular Chemistry |
巻 | 14 |
号 | 40 |
DOI | |
出版ステータス | 出版済み - 2016 |
ASJC Scopus 主題領域
- 生化学
- 物理化学および理論化学
- 有機化学