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甘油/二醇脱水酶活性调控对肠道微生物群落生态和代谢的影响。

Impact of manipulation of glycerol/diol dehydratase activity on intestinal microbiota ecology and metabolism.

机构信息

Laboratory of Food Biotechnology, Department of Health Sciences and Technology, ETH Zürich, Zürich, Switzerland.

Laboratory of Toxicology, Department of Health Sciences and Technology, ETH Zürich, Zürich, Switzerland.

出版信息

Environ Microbiol. 2021 Mar;23(3):1765-1779. doi: 10.1111/1462-2920.15431. Epub 2021 Mar 15.

Abstract

Glycerol/diol dehydratases (GDH) are enzymes that catalyse the production of propionate from 1,2-propanediol, and acrolein from glycerol. Acrolein reacts with dietary carcinogenic heterocyclic amines (HCA), reducing HCA mutagenicity, but is itself also an antimicrobial agent and toxicant. Gut microbial GDH activity has been suggested as an endogenous acrolein source; however, there is limited information on the potential of the intestinal microbiota to have GDH activity, and what impact it can have on the intestinal ecosystem and host health. We hypothesized that GDH activity of gut microbiota is determined by the abundance and distribution of GDH-active taxa and can be enhanced by supplementation of the GDH active Anaerobutyricum hallii, and tested this hypothesis combining quantitative profiling of gdh, model batch fermentations, microbiota manipulation, and kinetic modelling of acrolein formation. Our results suggest that GDH activity is a common trait of intestinal microbiota shared by a few taxa, which was dependent on overall gdh abundance. Anaerobutyricum hallii was identified as a key taxon in GDH metabolism, and its supplementation increased the rate of GDH activity and acrolein release, which enhanced the transformation of HCA and reduced fermentation activity. The findings of this first systematic study on acrolein release by intestinal microbiota indicate that dietary and microbial modulation might impact GDH activity, which may influence host health.

摘要

甘油/二醇脱水酶(GDH)是一种能够催化 1,2-丙二醇生成丙酸和甘油生成丙烯醛的酶。丙烯醛与膳食中致癌的杂环胺(HCA)反应,降低 HCA 的致突变性,但它本身也是一种抗菌剂和有毒物质。肠道微生物群的 GDH 活性被认为是内源性丙烯醛的来源;然而,关于肠道微生物群具有 GDH 活性的潜力以及它对肠道生态系统和宿主健康的影响的信息有限。我们假设肠道微生物群的 GDH 活性由 GDH 活性分类群的丰度和分布决定,并可以通过补充 GDH 活性 Anaerobutyricum hallii 来增强,并通过定量分析 gdh、模型批量发酵、微生物群操作和丙烯醛形成的动力学模型来验证这一假设。我们的研究结果表明,GDH 活性是肠道微生物群的一个共同特征,由少数几个分类群共享,这取决于 gdh 的总体丰度。Anaerobutyricum hallii 被鉴定为 GDH 代谢中的关键分类群,其补充增加了 GDH 活性和丙烯醛释放的速度,从而增强了 HCA 的转化并降低了发酵活性。这是第一项关于肠道微生物群释放丙烯醛的系统研究,表明饮食和微生物调节可能会影响 GDH 活性,从而可能影响宿主健康。

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