Identification of a lichen depside polyketide synthase gene by heterologous expression in Saccharomyces cerevisiae

IF 3.7 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
James T. Kealey, James P. Craig, Philip J. Barr
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引用次数: 18

Abstract

Lichen-forming fungi produce a variety of secondary metabolites including bioactive polyketides. Advances in DNA and RNA sequencing have led to a growing database of new lichen gene clusters encoding polyketide synthases (PKS) and associated ancillary activities. Definitive assignment of a PKS gene to a metabolic product has been challenging in the lichen field due to a lack of established gene knockout or heterologous gene expression systems. Here, we report the reconstitution of a non-reducing PKS gene from the lichen Pseudevernia furfuracea and successful heterologous expression of the synthetic lichen PKS gene in engineered Saccharomyces cerevisiae. We show that P. furfuracea PFUR17_02294 produces lecanoric acid, the depside dimer of orsellinic acid, at 360 mg/L in small-scale yeast cultures. Our results unequivocally identify PFUR17_02294 as a lecanoric acid synthase and establish that a single lichen PKS synthesizes two phenolic rings and joins them by an ester linkage to form the depside product.

Abstract Image

Abstract Image

Abstract Image

一个地衣苷多酮合成酶基因在酿酒酵母中的异种表达鉴定
地衣形成真菌产生多种次生代谢物,包括生物活性聚酮。随着DNA和RNA测序技术的进步,编码聚酮合成酶(PKS)和相关辅助活性的新地衣基因簇的数据库越来越多。由于缺乏已建立的基因敲除或异源基因表达系统,在地衣领域将PKS基因确定为代谢产物一直具有挑战性。本文报道了一种非还原性PKS基因的重组,并成功地将合成的PKS基因在工程酿酒酵母中异源表达。我们发现,在小规模酵母培养中,P. furacea PFUR17_02294以360 mg/L的速度产生油籽酸(orsellinic acid的深层二聚体)。我们的研究结果明确地确定了PFUR17_02294是一种lecanoric acid合成酶,并建立了一个单一的地衣PKS合成两个酚环,并通过酯链连接它们形成深苷产物。
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来源期刊
Metabolic Engineering Communications
Metabolic Engineering Communications Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
13.30
自引率
1.90%
发文量
22
审稿时长
18 weeks
期刊介绍: Metabolic Engineering Communications, a companion title to Metabolic Engineering (MBE), is devoted to publishing original research in the areas of metabolic engineering, synthetic biology, computational biology and systems biology for problems related to metabolism and the engineering of metabolism for the production of fuels, chemicals, and pharmaceuticals. The journal will carry articles on the design, construction, and analysis of biological systems ranging from pathway components to biological complexes and genomes (including genomic, analytical and bioinformatics methods) in suitable host cells to allow them to produce novel compounds of industrial and medical interest. Demonstrations of regulatory designs and synthetic circuits that alter the performance of biochemical pathways and cellular processes will also be presented. Metabolic Engineering Communications complements MBE by publishing articles that are either shorter than those published in the full journal, or which describe key elements of larger metabolic engineering efforts.
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