Zhou Zhe, Hatzios Stavroula K
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, 06520, USA; Microbial Sciences Institute, Yale University, West Haven, CT, 06516, USA.
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, 06520, USA; Microbial Sciences Institute, Yale University, West Haven, CT, 06516, USA; Department of Chemistry, Yale University, New Haven, CT, 06520, USA.
Curr Opin Chem Biol. 2025 Feb;84:102565. doi: 10.1016/j.cbpa.2024.102565. Epub 2024 Dec 24.
Humans are exposed to a wide variety of small molecules with antioxidant properties that are poorly metabolized by mammalian cells. However, gastrointestinal microbes encode enzymes that convert these redox-active molecules into nutrient sources and electron acceptors to support bacterial growth in the gut. Here, we describe recent studies highlighting how microbial metabolism of host-derived antioxidants modulates interspecies interactions and provide an overview of the interdisciplinary approaches being used to map these metabolic pathways in vivo. Uncovering microbe-driven biotransformations of redox-active small molecules could create new opportunities to improve human health by modulating redox reactions at the host-microbe interface.
人类会接触到各种各样具有抗氧化特性的小分子,而哺乳动物细胞对这些小分子的代谢能力较差。然而,胃肠道微生物编码的酶可将这些具有氧化还原活性的分子转化为营养源和电子受体,以支持肠道内细菌的生长。在此,我们描述了近期的研究,这些研究突出了宿主衍生抗氧化剂的微生物代谢如何调节种间相互作用,并概述了用于在体内绘制这些代谢途径的跨学科方法。揭示微生物驱动的具有氧化还原活性的小分子生物转化,可能会通过调节宿主-微生物界面的氧化还原反应,为改善人类健康创造新机会。