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在巴西酰胺生物合成中,由单个模块 NRPS 形成哌嗪环,并由 α-KG 依赖性非血红素铁双加氧酶切割。

Piperazine ring formation by a single-module NRPS and cleavage by an α-KG-dependent nonheme iron dioxygenase in brasiliamide biosynthesis.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, People's Republic of China.

Technical Innovation Center for Utilization of Marine Biological Resources, Third Institute of Oceanography, MNR, Xiamen, 361005, People's Republic of China.

出版信息

Appl Microbiol Biotechnol. 2020 Jul;104(14):6149-6159. doi: 10.1007/s00253-020-10678-w. Epub 2020 May 21.

Abstract

Brasiliamides are a class of piperazine-containing alkaloids produced by Penicillium brasilianum with a range of pharmaceutical activities. The mechanism of brasiliamide biosynthesis, including piperazine ring formation and multiple tailoring modifications, still remains unclear. In this study, the biosynthetic gene cluster of brasiliamides, brs, was identified from the marine-derived fungal strain Penicillium brasilianum WZXY-M122-9. Deletion of a histone deacetylase-encoding gene using a CRISPR/Cas9 gene editing system led to the production of a new compound, namely brasiliamide I (1). The brs-encoded single-module nonribosomal peptide synthetase (NRPS) BrsA is involved in the formation of the piperazine skeleton of brasiliamides. Full-length BrsA protein (113.6 kDa) was purified, and reconstitution of enzymatic activity in vitro confirmed that BrsA stereoselectively accepts L-phenylalanine as the substrate. Multiple deletion of tailoring genes and analysis of purified proteins in vitro enabled us to propose a brasiliamide biosynthetic pathway. In the tailoring steps, an α-ketoglutarate (KG)-dependent nonheme iron dioxygenase, BrsJ, was identified to catalyze piperazine ring cleavage during biosynthesis of brasiliamide A (2). KEY POINTS: The gene cluster encoding brasiliamide biosynthesis, brs, is identified. Deletion of a histone deacetylase-encoding gene produces brasiliamide I. BrsA catalyzes brasiliamide piperazine skeleton formation. BrsJ catalyzes piperazine ring cleavage to produce brasiliamide A. Graphical abstract.

摘要

巴西利酰胺是一类含哌嗪的生物碱,由 Penicillium brasilianum 产生,具有多种药物活性。巴西利酰胺生物合成的机制,包括哌嗪环的形成和多种修饰修饰,仍然不清楚。在这项研究中,从海洋来源的真菌菌株 Penicillium brasilianum WZXY-M122-9 中鉴定出巴西利酰胺的生物合成基因簇 brs。使用 CRISPR/Cas9 基因编辑系统删除组蛋白去乙酰化酶编码基因导致产生了一种新化合物,即巴西利酰胺 I(1)。brs 编码的单模块非核糖体肽合酶(NRPS)BrsA 参与巴西利酰胺哌嗪骨架的形成。全长 BrsA 蛋白(113.6 kDa)被纯化,并在体外重建酶活性证实 BrsA 立体选择性地接受 L-苯丙氨酸作为底物。多个修饰基因的缺失和体外纯化蛋白的分析使我们能够提出巴西利酰胺的生物合成途径。在修饰步骤中,鉴定出 α-酮戊二酸(KG)依赖性非血红素铁双加氧酶 BrsJ 在巴西利酰胺 A(2)的生物合成过程中催化哌嗪环裂解。要点:鉴定出编码巴西利酰胺生物合成的基因簇 brs。缺失一个组蛋白去乙酰化酶编码基因产生巴西利酰胺 I。BrsA 催化巴西利酰胺哌嗪骨架形成。BrsJ 催化哌嗪环裂解生成巴西利酰胺 A。

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