利用具有更强 GPP 积累能力的 Erg20 突变体,在酿酒酵母中高效生产 (S)- 柠檬烯和香叶醇

IF 6.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Metabolic engineering Pub Date : 2024-04-15 DOI:10.1016/j.ymben.2024.04.003
Armand Bernard , Seungwoo Cha , Hyesoo Shin , Daeyeol Lee , Ji-Sook Hahn
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引用次数: 0

摘要

(S)-柠檬烯和香叶醇等单萜烯和单萜化合物是有价值的化学物质,用途广泛,包括化妆品、药品和生物燃料。事实证明,酿酒酵母是生产各种萜烯和萜类化合物的有效宿主。(S)-柠檬烯和香叶醇分别通过柠檬烯合成酶(LS)和香叶醇合成酶(GES)的酶促作用从焦磷酸香叶酯(GPP)中生成。然而,产生这些物质的一个主要障碍是负责产生 GPP 的 Erg20(一种焦磷酸法呢酰(FPP)合成酶)具有双重功能。Erg20 不仅通过将焦磷酸异戊烯酯(IPP)与焦磷酸二甲基烯丙基酯缩合合成 GPP,而且还催化 IPP 与 GPP 进一步缩合生成 FPP。在本研究中,我们利用之前开发的 Erg20 突变体 Erg20K197G(Erg20G)和 Erg20F96W、N127W(Erg20WW)解决了这一问题。通过这些突变体的组合,我们产生了一种新型的 Erg20WWG 突变体,其 GPP 积累能力比 Erg20WW 高四倍以上,这可以通过香叶醇的生产水平观察到。将 Erg20WWG 突变体与薄荷的 LS 或石竹的 GES 融合,可分别将 GPP 高效转化为(S)-柠檬烯和香叶醇。通过将整个甲羟戊酸途径和与 Erg20WWG 融合的酶定位在过氧物酶体中,同时利用葡萄糖感应 HXT1 启动子下调重要的 ERG20 基因,进一步改进了这种方法。在生产(S)-柠檬烯的情况下,在细胞质中表达了额外的 Erg20WWG-LS。因此,通过喂食乙醇的分批双相发酵,最终菌株产生了 1063 毫克/升的(S)-柠檬烯和 1234 毫克/升的香叶醇。新发现的 Erg20WWG 突变体为高效生产其他各种 GPP 衍生化学品(包括单萜衍生物和大麻素)打开了大门。
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Efficient production of (S)-limonene and geraniol in Saccharomyces cerevisiae through the utilization of an Erg20 mutant with enhanced GPP accumulation capability

Monoterpenes and monoterpenoids such as (S)-limonene and geraniol are valuable chemicals with a wide range of applications, including cosmetics, pharmaceuticals, and biofuels. Saccharomyces cerevisiae has proven to be an effective host to produce various terpenes and terpenoids. (S)-limonene and geraniol are produced from geranyl pyrophosphate (GPP) through the enzymatic actions of limonene synthase (LS) and geraniol synthase (GES), respectively. However, a major hurdle in their production arises from the dual functionality of the Erg20, a farnesyl pyrophosphate (FPP) synthase, responsible for generating GPP. Erg20 not only synthesizes GPP by condensing isopentenyl pyrophosphate (IPP) with dimethylallyl pyrophosphate but also catalyzes further condensation of IPP with GPP to produce FPP. In this study, we have tackled this issue by harnessing previously developed Erg20 mutants, Erg20K197G (Erg20G) and Erg20F96W, N127W (Erg20WW), which enhance GPP accumulation. Through a combination of these mutants, we generated a novel Erg20WWG mutant with over four times higher GPP accumulating capability than Erg20WW, as observed through geraniol production levels. The Erg20WWG mutant was fused to the LS from Mentha spicata or the GES from Catharanthus roseus for efficient conversion of GPP to (S)-limonene and geraniol, respectively. Further improvements were achieved by localizing the entire mevalonate pathway and the Erg20WWG-fused enzymes in peroxisomes, while simultaneously downregulating the essential ERG20 gene using the glucose-sensing HXT1 promoter. In the case of (S)-limonene production, additional Erg20WWG-LS was expressed in the cytosol. As a result, the final strains produced 1063 mg/L of (S)-limonene and 1234 mg/L of geraniol by fed-batch biphasic fermentations with ethanol feeding. The newly identified Erg20WWG mutant opens doors for the efficient production of various other GPP-derived chemicals including monoterpene derivatives and cannabinoids.

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来源期刊
Metabolic engineering
Metabolic engineering 工程技术-生物工程与应用微生物
CiteScore
15.60
自引率
6.00%
发文量
140
审稿时长
44 days
期刊介绍: Metabolic Engineering (MBE) is a journal that focuses on publishing original research papers on the directed modulation of metabolic pathways for metabolite overproduction or the enhancement of cellular properties. It welcomes papers that describe the engineering of native pathways and the synthesis of heterologous pathways to convert microorganisms into microbial cell factories. The journal covers experimental, computational, and modeling approaches for understanding metabolic pathways and manipulating them through genetic, media, or environmental means. Effective exploration of metabolic pathways necessitates the use of molecular biology and biochemistry methods, as well as engineering techniques for modeling and data analysis. MBE serves as a platform for interdisciplinary research in fields such as biochemistry, molecular biology, applied microbiology, cellular physiology, cellular nutrition in health and disease, and biochemical engineering. The journal publishes various types of papers, including original research papers and review papers. It is indexed and abstracted in databases such as Scopus, Embase, EMBiology, Current Contents - Life Sciences and Clinical Medicine, Science Citation Index, PubMed/Medline, CAS and Biotechnology Citation Index.
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