功能宏基因组学揭示了人类肠道细菌对益生元分解的新途径。

Functional metagenomics reveals novel pathways of prebiotic breakdown by human gut bacteria.

机构信息

Université de Toulouse, Institut National des Sciences Appliquées, Université Paul Sabatier, Institut National Polytechnique, Ingénierie des Systèmes Biologiques et des Procédés, Toulouse, France ; UMR5504, UMR792 Ingénierie des Systèmes Biologiques et des Procédés, Centre National de la Recherche Scientifique, Institut National de la Recherche Agronomique, Toulouse, France.

出版信息

PLoS One. 2013 Sep 16;8(9):e72766. doi: 10.1371/journal.pone.0072766. eCollection 2013.

Abstract

The human intestine hosts a complex bacterial community that plays a major role in nutrition and in maintaining human health. A functional metagenomic approach was used to explore the prebiotic breakdown potential of human gut bacteria, including non-cultivated ones. Two metagenomic libraries, constructed from ileum mucosa and fecal microbiota, were screened for hydrolytic activities on the prebiotic carbohydrates inulin, fructo-oligosaccharides, xylo-oligosaccharides, galacto-oligosaccharides and lactulose. The DNA inserts of 17 clones, selected from the 167 hits that were identified, were pyrosequenced in-depth, yielding in total 407, 420 bp of metagenomic DNA. From these sequences, we discovered novel prebiotic degradation pathways containing carbohydrate transporters and hydrolysing enzymes, for which we provided the first experimental proof of function. Twenty of these proteins are encoded by genes that are also present in the gut metagenome of at least 100 subjects, whatever are their ages or their geographical origin. The sequence taxonomic assignment indicated that still unknown bacteria, for which neither culture conditions nor genome sequence are available, possess the enzymatic machinery to hydrolyse the prebiotic carbohydrates tested. The results expand the vision on how prebiotics are metabolized along the intestine, and open new perspectives for the design of functional foods.

摘要

人类肠道中栖息着复杂的细菌群落,这些细菌在营养吸收和维持人体健康方面发挥着重要作用。本研究采用功能宏基因组学方法来探索人类肠道细菌(包括未培养细菌)对益生元的潜在分解能力。我们构建了来自回肠黏膜和粪便微生物群的两个宏基因组文库,并对其进行了益生元碳水化合物菊粉、低聚果糖、木低聚糖、半乳低聚糖和乳果糖的水解活性筛选。从 167 个鉴定的阳性克隆中选择了 17 个克隆进行深度焦磷酸测序,总共获得了 407,420bp 的宏基因组 DNA。从这些序列中,我们发现了包含碳水化合物转运蛋白和水解酶的新型益生元降解途径,并首次提供了功能实验证据。这 20 种蛋白由至少 100 名个体的肠道宏基因组中存在的基因编码,无论其年龄或地理位置如何。序列分类学分析表明,仍有未知细菌拥有可水解测试用益生元碳水化合物的酶机制,但这些细菌目前既无法培养,其基因组序列也无法获得。研究结果拓展了我们对益生元在肠道内代谢方式的认识,并为功能性食品的设计开辟了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/302c/3774763/8d4d51218bbd/pone.0072766.g001.jpg

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