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Nature ; 544(7648): 65-70, 2017 04 06.
Artículo en Inglés | MEDLINE | ID: mdl-28329766

RESUMEN

The metabolism of carbohydrate polymers drives microbial diversity in the human gut microbiota. It is unclear, however, whether bacterial consortia or single organisms are required to depolymerize highly complex glycans. Here we show that the gut bacterium Bacteroides thetaiotaomicron uses the most structurally complex glycan known: the plant pectic polysaccharide rhamnogalacturonan-II, cleaving all but 1 of its 21 distinct glycosidic linkages. The deconstruction of rhamnogalacturonan-II side chains and backbone are coordinated to overcome steric constraints, and the degradation involves previously undiscovered enzyme families and catalytic activities. The degradation system informs revision of the current structural model of rhamnogalacturonan-II and highlights how individual gut bacteria orchestrate manifold enzymes to metabolize the most challenging glycan in the human diet.


Asunto(s)
Bacteroides thetaiotaomicron/enzimología , Bacteroides thetaiotaomicron/metabolismo , Biocatálisis , Tracto Gastrointestinal/microbiología , Glicósido Hidrolasas/metabolismo , Pectinas/química , Pectinas/metabolismo , Bacteroides thetaiotaomicron/crecimiento & desarrollo , Boratos/química , Boratos/metabolismo , Dominio Catalítico , Microbioma Gastrointestinal , Glicósido Hidrolasas/química , Glicósido Hidrolasas/clasificación , Humanos , Modelos Moleculares , Especificidad por Sustrato
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