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人类肠道微生物群中的聚糖利用系统:结构发现的金矿。

Glycan utilization systems in the human gut microbiota: a gold mine for structural discoveries.

机构信息

Michael Smith Laboratories, University of British Columbia, 2185 East Mall, Vancouver, BC, V6T 1Z4, Canada; Department of Biochemistry and Molecular Biology, University of British Columbia, 2350 Health Sciences Mall, Vancouver, BC, V6T 1Z3, Canada.

Michael Smith Laboratories, University of British Columbia, 2185 East Mall, Vancouver, BC, V6T 1Z4, Canada; Department of Biochemistry and Molecular Biology, University of British Columbia, 2350 Health Sciences Mall, Vancouver, BC, V6T 1Z3, Canada; Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada.

出版信息

Curr Opin Struct Biol. 2021 Jun;68:26-40. doi: 10.1016/j.sbi.2020.11.001. Epub 2020 Dec 4.

Abstract

The complex glycans comprising 'dietary fiber' evade the limited repertoire of human digestive enzymes and hence feed the vast community of microbes in the lower gastrointestinal tract. As such, complex glycans drive the composition of the human gut microbiota and, in turn, influence diverse facets of our nutrition and health. To access these otherwise recalcitrant carbohydrates, gut bacteria produce coordinated, substrate-specific arsenals of carbohydrate-active enzymes, glycan-binding proteins, oligosaccharide transporters, and transcriptional regulators. A recent explosion of biochemical and enzymological studies of these systems has led to the discovery of manifold new carbohydrate-active enzyme (CAZyme) families. Crucially underpinned by structural biology, these studies have also provided unprecedented molecular insight into the exquisite specificity of glycan recognition in the diverse CAZymes and non-catalytic proteins from the HGM. The revelation of a multitude of new three-dimensional structures and substrate complexes constitutes a 'gold rush' in the structural biology of the human gut microbiota.

摘要

膳食纤维所包含的复杂聚糖逃避了人类有限的消化酶,从而为下消化道的大量微生物提供了养分。因此,复杂聚糖驱动着人类肠道微生物群的组成,并反过来影响我们营养和健康的多个方面。为了获取这些难以消化的碳水化合物,肠道细菌产生了协调的、底物特异性的碳水化合物活性酶、聚糖结合蛋白、寡糖转运蛋白和转录调节剂的组合。最近对这些系统的生物化学和酶学研究的爆炸式增长,导致了多种新型碳水化合物活性酶(CAZyme)家族的发现。这些研究在结构生物学的支持下,为 HGM 中不同 CAZymes 和非催化蛋白的聚糖识别的精细特异性提供了前所未有的分子见解。大量新的三维结构和底物复合物的揭示,构成了人类肠道微生物群结构生物学的“淘金热”。

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