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.
Cite
CITATION STYLE
Su, L., Lv, M., Kyeremeh, K., Deng, Z., Deng, H., & Yu, Y. (2016). A ThDP-dependent enzymatic carboligation reaction involved in Neocarazostatin A tricyclic carbazole formation. Organic and Biomolecular Chemistry, 14(37), 8679–8684. https://doi.org/10.1039/c6ob01651k
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.