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利用工程化酿酒酵母合成大豆皂醇 B。

Biosynthesis of Soyasapogenol B by Engineered Saccharomyces cerevisiae.

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.

Key Laboratory of System Bioengineering (Tianjin University), Ministry of Education, Tianjin, People's Republic of China.

出版信息

Appl Biochem Biotechnol. 2021 Oct;193(10):3202-3213. doi: 10.1007/s12010-021-03599-5. Epub 2021 Jun 7.

Abstract

Soyasapogenol B is an oleanane-type pentacyclic triterpene that has various applications in food and healthcare and has a higher biological activity than soyasaponin. Saccharomyces cerevisiae is a potential platform for terpenoid production with mature genetic tools for metabolic pathway manipulation. In this study, we developed a biosynthesis method to produce soyasapogenol B. First, we expressed β-amyrin synthase derived from Glycyrrhiza glabra in S. cerevisiae to generate β-amyrin, as the precursor of soyasapogenol B. Several different types of promoters were then used to regulate the expression of key genes in the mevalonate pathway (MVA), and this subsequently increased the yield of β-amyrin to 17.6 mg/L, 25-fold more than that produced in the original strain L01 (0.68 mg/L). Then, using the β-amyrin-producing strain, we expressed soyasapogenol B synthases from Medicago truncatula (CYP93E2 and CYP72A61V2) and from G. glabra (CYP93E3 and CYP72A566). Soyasapogenol B yields were then optimized by using soyasapogenol B synthases and cytochrome P450 reductase from G. glabra. The most effective soyasapogenol B production strain was used for fermentation, and the yield of soyasapogenol B reached 2.9 mg/L in flask and 8.36 mg/L in a 5-L bioreactor with fed glucose and ethanol. This study demonstrated the heterologous synthesis of soyasapogenol B in S. cerevisiae using the combined expression of CYP93E3 and CYP72A566 in the synthesis pathway, which significantly increased the production of soyasapogenol B and provides a reference method for the biosynthesis of other triterpenes.

摘要

大豆皂苷元 B 是一种齐墩果烷型五环三萜,在食品和医疗保健领域有多种应用,其生物活性高于大豆皂苷。酿酒酵母是萜类化合物生产的潜在平台,具有成熟的代谢途径操作遗传工具。在这项研究中,我们开发了一种生产大豆皂苷元 B 的生物合成方法。首先,我们在酿酒酵母中表达了来源于甘草的β-香树脂醇合酶,以生成大豆皂苷元 B 的前体β-香树脂醇。然后,使用几种不同类型的启动子来调节甲羟戊酸途径(MVA)中的关键基因的表达,这随后将β-香树脂醇的产量提高到 17.6mg/L,比原始菌株 L01(0.68mg/L)提高了 25 倍。然后,使用产生β-香树脂醇的菌株,我们表达了来自 Medicago truncatula(CYP93E2 和 CYP72A61V2)和甘草(CYP93E3 和 CYP72A566)的大豆皂苷元 B 合酶。然后通过使用甘草的大豆皂苷元 B 合酶和细胞色素 P450 还原酶来优化大豆皂苷元 B 的产量。最有效的大豆皂苷元 B 生产菌株用于发酵,在摇瓶和 5L 生物反应器中分别以葡萄糖和乙醇为碳源进行补料分批发酵时,大豆皂苷元 B 的产量达到 2.9mg/L 和 8.36mg/L。本研究通过在合成途径中联合表达 CYP93E3 和 CYP72A566,在酿酒酵母中异源合成了大豆皂苷元 B,显著提高了大豆皂苷元 B 的产量,为其他三萜类化合物的生物合成提供了参考方法。

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