Issue 37, 2016

A ThDP-dependent enzymatic carboligation reaction involved in Neocarazostatin A tricyclic carbazole formation

Abstract

Although the biosynthetic pathway of Neocarazostatin A (1) has been identified, the detailed enzymatic reactions underlying the assembly of the carbazole ring still remain largely unknown. We demonstrate here that NzsH, a putative thiamine diphosphate dependent enzyme, can catalyze an acyloin coupling reaction between indole-3-pyruvate and pyruvate to generate a β-ketoacid intermediate. Our findings thus shed light on further characterization of the unusual biosynthetic pathway of the bacterial tricyclic carbazole alkaloids.

Graphical abstract: A ThDP-dependent enzymatic carboligation reaction involved in Neocarazostatin A tricyclic carbazole formation

Supplementary files

Article information

Article type
Communication
Submitted
01 Aug 2016
Accepted
31 Aug 2016
First published
01 Sep 2016
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2016,14, 8679-8684

A ThDP-dependent enzymatic carboligation reaction involved in Neocarazostatin A tricyclic carbazole formation

L. Su, M. Lv, K. Kyeremeh, Z. Deng, H. Deng and Y. Yu, Org. Biomol. Chem., 2016, 14, 8679 DOI: 10.1039/C6OB01651K

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