Details

Autor(en) / Beteiligte

• Wang, Zhiyan
• Yang, Feng-Xian
• Liu, Chongxi
• Wang, Li
• Qi, Yuxin
• Cao, Minghang
• Guo, Xiaowei
• Li, Jie
• Huang, Xueshuang
• Yang, Jing
• Huang, Sheng-Xiong

Titel

Isolation and Biosynthesis of Phenazine–Polyketide Hybrids from Streptomyces sp. KIB-H483

Ist Teil von

• Journal of natural products (Washington, D.C.), 2022-05, Vol.85 (5), p.1324-1331

Ort / Verlag

United States: American Chemical Society and American Society of Pharmacognosy

Erscheinungsjahr

2022

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• A phenazine–polyketide hybrid compound, nexphenazine A (1), was isolated from Streptomyces sp. KIB-H483. The bioinformatic analysis of the draft genome of the producing strain and gene inactivation experiments revealed that the biosynthesis of 1 involves a phenazine–polyketide hybrid gene cluster. The abolished production of 1 as well as the accumulation of shunt metabolites 4–7 in mutant strain ΔnpzI revealed the key role of the npzI gene, which encodes an NAD­(P)­H-dependent ketoreductase, in nexphenazine biosynthesis. The structures and absolute configurations of the isolated intermediates were established on the basis of spectroscopic data analysis, single-crystal X-ray diffraction, chiral chromatography, and chemical conversion experiments. NpzI exhibited stereochemical selectivity in reducing the carbonyl group of 4. Nexphenazine biosynthesis is proposed to involve a condensation of the carboxyl group of phenazine with one molecule of methylmalonyl-CoA by a type I PKS, followed by a ketone reduction by NpzI and an unknown methylation reaction.