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

被引:27
|
作者
Tamura, Kazune [1 ,2 ]
Brumer, Harry [1 ,2 ,3 ]
机构
[1] Univ British Columbia, Michael Smith Labs, 2185 East Mall, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Dept Biochem & Mol Biol, 2350 Hlth Sci Mall, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Chem, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ALPHA-N-ACETYLGALACTOSAMINIDASE; GLYCOSIDE HYDROLASE FAMILY; CARBOHYDRATE-ACTIVE ENZYMES; BACTEROIDES-THETAIOTAOMICRON; CRYSTAL-STRUCTURE; BINDING PROTEIN; DIETARY FIBER; BIFIDOBACTERIUM; RECOGNITION; METABOLISM;
D O I
10.1016/j.sbi.2020.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, glycanbinding 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.
引用
收藏
页码:26 / 40
页数:15
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