酮甾体
孕烯醇酮
还原酶
生物
类固醇
异构酶
激素
类固醇激素
背景(考古学)
脱氢酶
生物化学
酶
古生物学
作者
Gabriela Arp,Angela Jiang,Keith Dufault‐Thompson,Sophia Levy,Aoshu Zhong,Jyotsna Talreja Wassan,Maggie Grant,Yue Li,Brantley Hall,Xiaofang Jiang
标识
DOI:10.1101/2024.10.04.616736
摘要
Abstract The metabolism of steroids by the gut microbiome affects hormone homeostasis, impacting host development, mental health, and reproductive functions. In this study, we identify the Δ 4 -3-ketosteroid 5β-reductase, 3β-hydroxysteroid dehydrogenase/Δ 5-4 isomerase, and Δ 6 -3-ketosteroid reductase enzyme families encoded by common human gut bacteria. Through phylogenetic reconstruction and mutagenesis, We show that 5β-reductase and Δ 6 -3-ketosteroid reductase have evolved to specialize in converting diverse 3-keto steroid hormones into their 5β- and Δ 6 -reduced derivatives. We also find that the novel 3β-hydroxysteroid dehydrogenase/Δ 5-4 isomerase is fused with 5β-reductase in multiple species, streamlining the multi-step conversion of pregnenolone, a steroid hormone precursor, into epipregnanolone. Through metagenomic analysis, we reveal that these enzymes are prevalent in healthy populations, being enriched in females over males. These findings provide the molecular basis for studying microbial steroid metabolism in the gut, offering insights into its potential impact on hormonal health in hosts, especially in the context of women’s health.
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