Xu Tao, Duan Jun-Lu, Ntakirutimana Samuel, Wang Li, Liu Zhi-Hua, Li Chun, Li Bing-Zhi
Frontiers Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.
Frontiers Research Institute for Synthetic Biology, Tianjin University, Tianjin, 300072, People's Republic of China.
Curr Microbiol. 2025 May 30;82(7):315. doi: 10.1007/s00284-025-04286-y.
Rosmarinic acid (RA) is a natural polyphenolic compound with various biological and pharmaceutical activities. Due to the limited availability in plant sources and the complexity of its chemical synthesis, the biosynthesis of RA shows great potential. However, few studies have investigated RA biosynthesis in S. cerevisiae, and inhibitory effects from its biosynthesis on intrinsic metabolic pathways remain unclear. In this study, RNA-seq technology was employed to investigate the stress response of S. cerevisiae to RA and its precursors (caffeic acid, CA and salvianic acid, SAA). The results revealed an increased inhibitory effect with a variation number of differentially expressed genes (DEGs): 338 for 200-mg/L SAA, 510 for 200-mg/L CA, and 934 for 200-mg/L RA. Furthermore, trends analysis of DEGs expression level uncovered similar stress response patterns of S. cerevisiae under RA and SAA, indicating a shared inhibition mechanism. Common response pathways, including ribosome biogenesis, RNA polymerase biosynthesis, and purine and pyrimidine metabolism, were elucidated. Additionally, common regulated genes (HSP12, PAU4, TIR3) and different regulated genes (UTP6, NAN1, IMP4) in aforementioned pathways were identified. Unique genes and pathways were also mapped to reveal the special response mechanism to different polyphenolic acids, such as oxidative phosphorylation for RA and amino acid metabolism for CA. Overall, this work provides a foundation for understanding transcriptomic response of yeast to RA and RA biosynthesis.
迷迭香酸(RA)是一种具有多种生物和药学活性的天然多酚化合物。由于其在植物来源中的可用性有限以及化学合成的复杂性,RA的生物合成具有巨大潜力。然而,很少有研究调查酿酒酵母中RA的生物合成,其生物合成对内在代谢途径的抑制作用仍不清楚。在本研究中,采用RNA测序技术研究酿酒酵母对RA及其前体(咖啡酸,CA和丹酚酸,SAA)的应激反应。结果显示,随着差异表达基因(DEG)数量的变化,抑制作用增强:200 mg/L SAA为338个,200 mg/L CA为510个,200 mg/L RA为934个。此外,对DEG表达水平的趋势分析揭示了酿酒酵母在RA和SAA下类似的应激反应模式,表明存在共同的抑制机制。阐明了包括核糖体生物发生、RNA聚合酶生物合成以及嘌呤和嘧啶代谢在内的共同反应途径。此外,还鉴定了上述途径中的共同调控基因(HSP12、PAU4、TIR3)和不同调控基因(UTP6、NAN1、IMP4)。还绘制了独特的基因和途径,以揭示对不同多酚酸的特殊反应机制,例如RA的氧化磷酸化和CA的氨基酸代谢。总体而言,这项工作为理解酵母对RA和RA生物合成的转录组反应提供了基础。