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分层糖酵解途径控制人类肠道中的碳水化合物利用调节因子。

Hierarchical glycolytic pathways control the carbohydrate utilization regulator in human gut .

作者信息

Kabonick Seth G, Verma Kamalesh, Modesto Jennifer L, Pearce Victoria H, Winokur Kailyn M, Groisman Eduardo A, Townsend Guy E

机构信息

Penn State College of Medicine, Hershey, PA, USA.

Penn State One Health Microbiome Center, Pennsylvania State University, State College, PA, USA.

出版信息

bioRxiv. 2025 Apr 2:2024.11.13.623061. doi: 10.1101/2024.11.13.623061.

Abstract

Human dietary choices control the gut microbiome. Industrialized populations consume abundant amounts of glucose and fructose, resulting in microbe-dependent intestinal disorders. Simple sugars inhibit the carbohydrate utilization regulator (Cur), a transcription factor in members of the prominent gut bacterial phylum, . Cur controls products necessary for carbohydrate utilization, host immunomodulation, and intestinal colonization. Here, we demonstrate how simple sugars decrease Cur activity in the mammalian gut. Our findings in two species show that ATP-dependent fructose-1,6-bisphosphate (FBP) synthesis is necessary for glucose or fructose to inhibit Cur, but dispensable for growth because of an essential pyrophosphate (PPi)-dependent enzyme. Furthermore, we show that ATP-dependent FBP synthesis is required to regulate Cur in the gut but does not contribute to fitness when is absent, indicating PPi is sufficient to drive glycolysis in these bacteria. Our findings reveal how sugar-rich diets inhibit Cur, thereby disrupting fitness and diminishing products that are beneficial to the host.

摘要

人类的饮食选择控制着肠道微生物群。工业化人群摄入大量葡萄糖和果糖,导致微生物依赖性肠道疾病。单糖抑制碳水化合物利用调节因子(Cur),这是一种在主要肠道细菌门类成员中的转录因子。Cur控制碳水化合物利用、宿主免疫调节和肠道定植所必需的产物。在这里,我们展示了单糖如何降低哺乳动物肠道中Cur的活性。我们在两个物种中的发现表明,ATP依赖性果糖-1,6-二磷酸(FBP)合成对于葡萄糖或果糖抑制Cur是必要的,但由于一种必需的焦磷酸(PPi)依赖性酶,它对于生长是可有可无的。此外,我们表明ATP依赖性FBP合成是调节肠道中Cur所必需的,但当不存在时对适应性没有贡献,这表明PPi足以驱动这些细菌中的糖酵解。我们的发现揭示了富含糖的饮食如何抑制Cur,从而破坏适应性并减少对宿主有益的产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef8/11967576/69106b33f174/nihpp-2024.11.13.623061v2-f0001.jpg

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