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内生菌 Priestia megaterium PH3 通过苯丙烷途径生物合成白藜芦醇。

Biosynthesis of resveratrol by an endophytic Priestia megaterium PH3 via the phenylpropane pathway.

机构信息

School of Food Science and Technology, Dalian Polytechnic University, Dalian, 116034, China.

State Key Laboratory of Marine Food Processing and Safety Control, Dalian Polytechnic University, Dalian, China.

出版信息

Appl Microbiol Biotechnol. 2023 Dec;107(24):7581-7599. doi: 10.1007/s00253-023-12768-x. Epub 2023 Oct 6.

Abstract

Resveratrol (RES) is a secondary metabolite synthesized by plants in response to environmental stress and pathogen infection, which is of great significance for the industrial production of RES by fermentation culture. In this study, we aimed to explore the biosynthesis pathway of RES and its key enzymes in the Priestia megaterium PH3, which was isolated and screened from peanut fruit. Through Liquid Chromatography-Mass Spectrometry (LC-MS) analysis, we quantified the RES content and distribution in the culture medium and determined that Priestia megaterium PH3 mainly secreted RES extracellularly. Furthermore, the highest production of RES was observed in YPD, yielding an impressive 127.46 ± 6.11 μg/L. By optimizing the fermentation conditions, we achieved a remarkable RES yield of 946.82 ± 24.74 μg/L within just 2 days, which represents the highest reported yield for a natural isolate produced in such a short time frame. Our investigation revealed that the phenylpropane pathway is responsible for RES synthesis in this bacterium, with cinnamate 4-hydroxylase (C4H) identified as the main rate-limiting enzyme. Overall, our findings highlight the robust RES production capabilities of Priestia megaterium PH3, offering novel insights and potential applications for bacterial fermentation in RES production. KEY POINTS: • RES synthesized by the bacterium was confirmed through the phenylpropane pathway. • The key rate-limiting enzyme for biosynthesis-RES is C4H. • RES reached 946.82 ± 24.74 μg/L after fermentation for 2 days.

摘要

白藜芦醇(RES)是植物响应环境胁迫和病原体感染而合成的一种次生代谢物,这对于通过发酵培养生产 RES 具有重要意义。在本研究中,我们旨在探索 Priestia megaterium PH3 中 RES 的生物合成途径及其关键酶,该菌是从落花生果实中分离和筛选出来的。通过液相色谱-质谱(LC-MS)分析,我们定量了 RES 在培养基中的含量和分布,并确定 Priestia megaterium PH3 主要将 RES 分泌到细胞外。此外,在 YPD 中观察到 RES 的最高产量,达到 127.46±6.11μg/L。通过优化发酵条件,我们在短短 2 天内实现了令人瞩目的 RES 产量 946.82±24.74μg/L,这是在如此短的时间内从天然分离物中获得的最高产量。我们的研究表明,该细菌中 RES 的合成途径是通过苯丙烷途径进行的,肉桂酸 4-羟化酶(C4H)被鉴定为主要的限速酶。总的来说,我们的研究结果突出了 Priestia megaterium PH3 具有强大的 RES 生产能力,为细菌发酵生产 RES 提供了新的见解和潜在的应用。研究亮点:• 通过苯丙烷途径证实了细菌合成的 RES。• 生物合成-RES 的关键限速酶是 C4H。• 发酵 2 天后 RES 达到 946.82±24.74μg/L。

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