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肠菌中黄酮和黄酮醇分解代谢起始的烯还原酶的发现。

Discovery of an ene-reductase for initiating flavone and flavonol catabolism in gut bacteria.

机构信息

CAS-Key Laboratory of Synthetic Biology, CAS Center for Excellence in Molecular Plant Sciences, Shanghai Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, 200032, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

Nat Commun. 2021 Feb 4;12(1):790. doi: 10.1038/s41467-021-20974-2.

Abstract

Gut microbial transformations of flavonoids, an enormous class of polyphenolic compounds abundant in plant-based diets, are closely associated with human health. However, the enzymes that initiate the gut microbial metabolism of flavones and flavonols, the two most abundant groups of flavonoids, as well as their underlying molecular mechanisms of action remain unclear. Here, we discovered a flavone reductase (FLR) from the gut bacterium, Flavonifractor plautii ATCC 49531 (originally assigned as Clostridium orbiscindens DSM 6740), which specifically catalyses the hydrogenation of the C2-C3 double bond of flavones/flavonols and initiates their metabolism as a key step. Crystal structure analysis revealed the molecular basis for the distinct catalytic property of FLR. Notably, FLR and its widespread homologues represent a class of ene-reductases that has not been previously identified. Genetic and biochemical analyses further indicated the importance of FLR in gut microbial consumption of dietary and medicinal flavonoids, providing broader insight into gut microbial xenobiotic transformations and possible guidance for personalized nutrition and medicine.

摘要

肠道微生物对类黄酮(大量存在于植物性饮食中的一类多酚化合物)的转化与人类健康密切相关。然而,肠道微生物代谢黄酮和黄酮醇(类黄酮中最丰富的两个群组)的起始酶以及其潜在的作用机制仍不清楚。在这里,我们从肠道细菌 Flavonifractor plautii ATCC 49531(最初被归类为 Clostridium orbiscindens DSM 6740)中发现了一种黄酮还原酶(FLR),它可以特异性地催化黄酮/黄酮醇的 C2-C3 双键加氢,并作为关键步骤启动其代谢。晶体结构分析揭示了 FLR 独特催化特性的分子基础。值得注意的是,FLR 及其广泛存在的同源物代表了一类以前未被识别的烯还原酶。遗传和生化分析进一步表明了 FLR 在肠道微生物消耗饮食和药用类黄酮中的重要性,为肠道微生物对外源化合物的转化提供了更广泛的认识,并为个性化营养和医学提供了可能的指导。

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