重组芦花菌从几种糖类来源生产白藜芦醇的研究

IF 3.7 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yuma Kobayashi , Kentaro Inokuma , Mami Matsuda , Akihiko Kondo , Tomohisa Hasunuma
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引用次数: 12

摘要

白藜芦醇是一种植物衍生的芳香族化合物,具有广泛的有益特性,包括抗氧化和抗衰老作用。目前市场上的白藜芦醇主要是从某些植物中提取的,如葡萄和日本虎杖。由于这些植物的收获不稳定,获得的白藜芦醇纯度低,有必要开发一种稳定的从廉价原料中生产高纯度白藜芦醇的工艺。在这里,我们试图利用具有广泛糖利用能力的基因工程酵母Scheffersomyces stipitis(以前称为Pichia stipitis)从多种糖作为碳源生产白藜芦醇。首先,我们通过引入编码白藜芦醇生物合成必需酶的基因,构建了白藜芦醇生产菌株[来自Herpetosiphon aurantiacus的酪氨酸解氨酶1 (HaTAL1),来自拟南芥的4-香豆酸:辅酶a连接酶2 (At4CL2)和来自葡萄的二苯乙烯合成酶1 (VvVST1)]。随后,在构建的菌株中过度表达一个反馈不敏感的choris酸突变酶等位基因,以提高白藜芦醇的产量。所构建的菌株在摇瓶培养中成功地从多种生物质衍生糖(葡萄糖、果糖、木糖、n -乙酰氨基葡萄糖(GlcNAc)、半乳糖、纤维素二糖、麦芽糖和蔗糖)中生产白藜芦醇。在纤维素二糖和蔗糖发酵中检测到显著的白藜芦醇滴度(发酵120 h后分别为529.8和668.6 mg/L),是葡萄糖(237.6 mg/L)的两倍。代谢组学分析显示,糖酵解和莽草酸途径的代谢物,以及能量代谢的辅助因子和代谢物的变化,取决于所使用的底物。白藜芦醇前体如l -酪氨酸的水平在纤维二糖和蔗糖生长的细胞中增加。结果表明,刺孢酵母是一种有吸引力的微生物平台,可以从多种生物质来源的糖中生产白藜芦醇,选择合适的底物对于提高该酵母的白藜芦醇产量至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Resveratrol production from several types of saccharide sources by a recombinant Scheffersomyces stipitis strain

Resveratrol production from several types of saccharide sources by a recombinant Scheffersomyces stipitis strain

Resveratrol is a plant-derived aromatic compound with a wide range of beneficial properties including antioxidant and anti-aging effects. The resveratrol currently available on the market is predominantly extracted from certain plants such as grape and the Japanese knotweed Polygonum cuspidatum. Due to the unstable harvest of these plants and the low resveratrol purity obtained, it is necessary to develop a stable production process of high-purity resveratrol from inexpensive feedstocks. Here, we attempted to produce resveratrol from a wide range of sugars as carbon sources by a using the genetically-engineered yeast Scheffersomyces stipitis (formerly known as Pichia stipitis), which possesses a broad sugar utilization capacity. First, we constructed the resveratrol producing strain by introducing genes coding the essential enzymes for resveratrol biosynthesis [tyrosine ammonia-lyase 1 derived from Herpetosiphon aurantiacus (HaTAL1), 4-coumarate: CoA ligase 2 derived from Arabidopsis thaliana (At4CL2), and stilbene synthase 1 derived from Vitis vinifera (VvVST1)]. Subsequently, a feedback-insensitive allele of chorismate mutase was overexpressed in the constructed strain to improve resveratrol production. The constructed strain successfully produced resveratrol from a broad range of biomass-derived sugars [glucose, fructose, xylose, N-acetyl glucosamine (GlcNAc), galactose, cellobiose, maltose, and sucrose] in shake flask cultivation. Significant resveratrol titers were detected in cellobiose and sucrose fermentation (529.8 and 668.6 mg/L after 120 h fermentation, respectively), twice above the amount obtained with glucose (237.6 mg/L). Metabolomic analysis revealed an altered profile of the metabolites involved in the glycolysis and shikimate pathways, and also of cofactors and metabolites of energy metabolisms, depending on the substrate used. The levels of resveratrol precursors such as L-tyrosine increased in cellobiose and sucrose-grown cells. The results indicate that S. stipitis is an attractive microbial platform for resveratrol production from broad types of biomass-derived sugars and the selection of suitable substrates is crucial for improving resveratrol productivity of this yeast.

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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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