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通过引入异戊烯醇利用途径工程化大肠杆菌,有效地生产香叶基芳樟醇。

Engineering Escherichia coli via introduction of the isopentenol utilization pathway to effectively produce geranyllinalool.

机构信息

Laboratory of Biotransformation and Biocatalysis, School of Tobacco Science and Engineering, Zhengzhou University of Light Industry, No.136 Ke Xue Avenue, Zhengzhou, Henan, 450002, People's Republic of China.

Laboratory of Synthetic Biology, Shandong Binzhou Animal Science and Veterinary Medicine Academy, Research Institution of Veterinarian, No.777 Chang Jiang 5th Road, Binzhou, Shandong Province, 256600, China.

出版信息

Microb Cell Fact. 2024 Oct 24;23(1):292. doi: 10.1186/s12934-024-02563-2.

Abstract

BACKGROUND

Geranyllinalool, a natural diterpenoid found in plants, has a floral and woody aroma, making it valuable in flavors and fragrances. Currently, its synthesis primarily depends on chemical methods, which are environmentally harmful and economically unsustainable. Microbial synthesis through metabolic engineering has shown potential for producing geranyllinalool. However, achieving efficient synthesis remains challenging owing to the limited availability of terpenoid precursors in microorganisms. Thus, an artificial isopentenol utilization pathway (IUP) was constructed and introduced in Escherichia coli to enhance precursor availability and further improve terpenoid synthesis.

RESULTS

We first constructed an artificial IUP in E. coli to enhance the supply of precursor geranylgeranyl diphosphate (GGPP) and then screened geranyllinalool synthases from plants to achieve efficient synthesis of geranyllinalool (274.78 ± 2.48 mg/L). To further improve geranyllinalool synthesis, we optimized various cultivation factors, including carbon source, IPTG concentration, and prenol addition and obtained 447.51 ± 6.92 mg/L of geranyllinalool after 72 h of shaken flask fermentation. Moreover, a scaled-up production in a 5-L fermenter was investigated to give 2.06 g/L of geranyllinalool through fed-batch fermentation. To the best of our knowledge, this is the highest reported titer so far.

CONCLUSIONS

Efficient synthesis of geranyllinalool in E. coli can be achieved through a two-step pathway and optimization of culture conditions. The findings of this study provide valuable insights into the production of other terpenoids in E. coli.

摘要

背景

香叶基芳樟醇是一种天然二萜,存在于植物中,具有花香和木香,在香料和香精中很有价值。目前,其合成主要依赖于化学方法,但这种方法对环境有害且经济上不可持续。通过代谢工程的微生物合成显示出生产香叶基芳樟醇的潜力。然而,由于微生物中萜烯前体的有限可用性,实现高效合成仍然具有挑战性。因此,构建了人工异戊烯醇利用途径(IUP)并引入大肠杆菌中,以提高前体的可用性,并进一步提高萜烯合成。

结果

我们首先在大肠杆菌中构建了一个人工 IUP 以增强前体香叶基香叶基二磷酸(GGPP)的供应,然后筛选植物中的香叶基芳樟醇合酶以实现香叶基芳樟醇的高效合成(274.78±2.48 mg/L)。为了进一步提高香叶基芳樟醇的合成,我们优化了各种培养因素,包括碳源、IPTG 浓度和 prenol 添加,并在摇瓶发酵 72 小时后获得 447.51±6.92 mg/L 的香叶基芳樟醇。此外,还研究了在 5-L 发酵罐中的放大生产,通过分批补料发酵得到 2.06 g/L 的香叶基芳樟醇。据我们所知,这是迄今为止报道的最高产量。

结论

通过两步途径和培养条件的优化,可以在大肠杆菌中实现香叶基芳樟醇的高效合成。本研究的结果为在大肠杆菌中生产其他萜烯提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8339/11515624/d448cc6856f1/12934_2024_2563_Fig1_HTML.jpg

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