Molecular basis of an agarose metabolic pathway acquired by a human intestinal symbiont.
Molecular basis of an agarose metabolic pathway acquired by a human intestinal symbiont.
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DOI:
10.1038/s41467-018-03366-x
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发表时间:
2018-03-13
影响因子:
16.6
通讯作者:
Abbott DW
中科院分区:
文献类型:
--
作者:
Pluvinage B;Grondin JM;Amundsen C;Klassen L;Moote PE;Xiao Y;Thomas D;Pudlo NA;Anele A;Martens EC;Inglis GD;Uwiera RER;Boraston AB;Abbott DW
In red algae, the most abundant principal cell wall polysaccharides are mixed galactan agars, of which agarose is a common component. While bioconversion of agarose is predominantly catalyzed by bacteria that live in the oceans, agarases have been discovered in microorganisms that inhabit diverse terrestrial ecosystems, including human intestines. Here we comprehensively define the structure–function relationship of the agarolytic pathway from the human intestinal bacterium Bacteroides uniformis (Bu) NP1. Using recombinant agarases from Bu NP1 to completely depolymerize agarose, we demonstrate that a non-agarolytic Bu strain can grow on GAL released from agarose. This relationship underscores that rare nutrient utilization by intestinal bacteria is facilitated by the acquisition of highly specific enzymes that unlock inaccessible carbohydrate resources contained within unusual polysaccharides. Intriguingly, the agarolytic pathway is differentially distributed throughout geographically distinct human microbiomes, reflecting a complex historical context for agarose consumption by human beings. Polysaccharides are the primary structural cell wall and energy storage molecules of seaweed. Here, the authors show how the geographically restricted dietary polysaccharide agarose is selectively utilized by the human intestinal bacterium Bacteroides uniformis, providing insight into how carbohydrate metabolism evolves within the human microbiome.
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影响因子:
5.4
作者:
Fu XT;Kim SM
通讯作者:
Kim SM
DOI:
10.1107/s0907444904019158
发表时间:
2004-12-01
影响因子:
2.2
作者:
Emsley, P;Cowtan, K
通讯作者:
Cowtan, K
DOI:
10.1007/s00018-016-2242-x
发表时间:
2016-07
期刊:
Cellular and molecular life sciences : CMLS
影响因子:
--
作者:
Foley MH;Cockburn DW;Koropatkin NM
通讯作者:
Koropatkin NM
影响因子:
14.9
作者:
Davis IW;Leaver-Fay A;Chen VB;Block JN;Kapral GJ;Wang X;Murray LW;Arendall WB 3rd;Snoeyink J;Richardson JS;Richardson DC
通讯作者:
Richardson DC
影响因子:
3.4
作者:
Baos, S. C.;Phillips, D. B.;Berry, M.
通讯作者:
Berry, M.