姜黄素在酿酒酵母中的新生物合成。

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2024-05-24 DOI:10.1021/acssynbio.4c00059
João Rainha, Joana L. Rodrigues* and Lígia R. Rodrigues, 
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引用次数: 0

摘要

姜黄素是从姜黄中提取的一种天然多酚,因其具有多种药理特性而备受关注。从姜黄植物中提取姜黄素的传统方法存在局限性,无法满足人们对这种生物活性化合物日益增长的需求,因此通过转基因微生物生产姜黄素显得尤为重要。在此,我们开发了一种工程化的酿酒酵母,可从葡萄糖中生产姜黄素。我们将铜绿假单胞菌和肠炎沙门氏菌的 4-hydroxyphenylacetate 3-monooxygenase oxygenase complex、拟南芥的咖啡酸 O-甲基转移酶、白假单胞菌的阿魏酰-CoA 合成酶、龙胆草的二酮苷-CoA 合成酶和姜黄素合成酶组成的途径引入到一个过量生产对香豆酸的酿酒酵母菌株中。该菌株产生了 240.1 ± 15.1 μg/L 的姜黄素。在对苯丙氨酸转化进行优化后,获得了一株能够生产 4.2 ± 0.6 mg/L 姜黄素的菌株。本研究首次报道了在 S. cerevisiae 中成功地从头生产姜黄素。
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De Novo Biosynthesis of Curcumin in Saccharomyces cerevisiae

Curcumin, a natural polyphenol derived from turmeric, has attracted immense interest due to its diverse pharmacological properties. Traditional extraction methods from Curcuma longa plants present limitations in meeting the growing demand for this bioactive compound, giving significance to its production by genetically modified microorganisms. Herein, we have developed an engineered Saccharomyces cerevisiae to produce curcumin from glucose. A pathway composed of the 4-hydroxyphenylacetate 3-monooxygenase oxygenase complex from Pseudomonas aeruginosa and Salmonella enterica, caffeic acid O-methyltransferase from Arabidopsis thaliana, feruloyl-CoA synthetase from Pseudomonas paucimobilis, and diketide-CoA synthase and curcumin synthase from C. longa was introduced in a p-coumaric acid overproducing S. cerevisiae strain. This strain produced 240.1 ± 15.1 μg/L of curcumin. Following optimization of phenylpropanoids conversion, a strain capable of producing 4.2 ± 0.6 mg/L was obtained. This study reports for the first time the successful de novo production of curcumin in S. cerevisiae.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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