首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes
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Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes

机译:人类肠道微生物组的细菌利用来自外部微生物的糖活性酶更新来分解红藻藻聚糖

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摘要

Humans host an intestinal population of microbes—collectively referred to as the gut microbiome—which encode the carbohydrate active enzymes, or CAZymes, that are absent from the human genome. These CAZymes help to extract energy from recalcitrant polysaccharides. The question then arises as to if and how the microbiome adapts to new carbohydrate sources when modern humans change eating habits. Recent metagenome analysis of microbiomes from healthy American, Japanese, and Spanish populations identified putative CAZymes obtained by horizontal gene transfer from marine bacteria, which suggested that human gut bacteria evolved to degrade algal carbohydrates—for example, consumed in form of sushi. We approached this hypothesis by studying such a polysaccharide utilization locus (PUL) obtained by horizontal gene transfer by the gut bacterium Bacteroides plebeius. Transcriptomic and growth experiments revealed that the PUL responds to the polysaccharide porphyran from red algae, enabling growth on this carbohydrate but not related substrates like agarose and carrageenan. The X-ray crystallographic and biochemical analysis of two proteins encoded by this PUL, BACPLE_01689 and BACPLE_01693, showed that they are β-porphyranases belonging to glycoside hydrolase families 16 and 86, respectively. The product complex of the GH86 at 1.3 Å resolution highlights the molecular details of porphyran hydrolysis by this new porphyranase. Combined, these data establish experimental support for the argument that CAZymes and associated genes obtained from extrinsic microbes add new catabolic functions to the human gut microbiome.
机译:人类拥有一个肠道菌群(统称肠道微生物群),该菌群编码人类基因组中不存在的碳水化合物活性酶或CAZymes。这些酶有助于从顽固性多糖中提取能量。然后出现的问题是,当现代人改变饮食习惯时,微生物组是否以及如何适应新的碳水化合物来源。最近对来自美国,日本和西班牙健康人群的微生物组进行的元基因组分析发现,通过从海洋细菌中进行水平基因转移获得了假定的酶,这表明人类肠道细菌会进化为降解藻类碳水化合物,例如以寿司形式食用。我们通过研究这种由肠道细菌Bacteroides plebeius的水平基因转移获得的多糖利用位点(PUL)来接近这个假设。转录组学和生长实验表明,PUL对红藻中的多糖卟啉有反应,从而使其能够在这种碳水化合物上生长,但不能在相关底物(如琼脂糖和角叉菜胶)上生长。 X-射线晶体学和生化分析此PUL编码的两个蛋白质BACPLE_01689和BACPLE_01693,表明它们分别是属于糖苷水解酶家族16和86的β-卟啉酶。 GH86的产物复合物分辨率为1.3Å,突出了这种新型卟啉酶水解卟啉的分子细节。结合起来,这些数据为从外部微生物获得的CAZymes和相关基因为人类肠道微生物组增加了新的分解代谢功能提供了实验依据。

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