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人类肠道细菌中一种用于降解膳食纤维中C5糖的替代戊糖磷酸途径。

An alternative pentose phosphate pathway in human gut bacteria for the degradation of C5 sugars in dietary fibers.

作者信息

Garschagen Laura S, Franke Thomas, Deppenmeier Uwe

机构信息

Institute of Microbiology and Biotechnology, University of Bonn, Bonn, Germany.

出版信息

FEBS J. 2021 Mar;288(6):1839-1858. doi: 10.1111/febs.15511. Epub 2020 Sep 2.

Abstract

The microbial degradation of pentoses in the human gut is a crucial factor for the utilization of plant-based dietary fibers. A vast majority of gut microbes are able to use these C5-sugars as a carbon and energy source. However, the underlying metabolic pathways are not fully understood. Bioinformatic analysis showed that a large number of abundant gut bacteria lack genes encoding a transaldolase as a key enzyme of the pentose phosphate pathway. Among them was the important human gut microbe Prevotella copri, which was able to grow in minimal media containing xylose or hemicelluloses as the sole carbon source. Therefore, we looked for an alternative pathway for pentose conversion in P. copri using bioinformatics, enzyme activity assays, and the detection of intermediates of pentose metabolism. It became evident that the organism converted C5-sugars via the sedoheptulose-1,7-bisphosphate pathway (SBPP) to connect pentose metabolism with glycolysis. To circumvent the transaldolase reaction, P. copri uses the combined catalysis of a pyrophosphate-dependent phosphofructokinase and a fructose-bisphosphate aldolase. Furthermore, we present strong evidence that the SBPP is widely distributed in important gut bacteria, including members of the phyla Bacteroides, Firmicutes, Proteobacteria, Verrucomicrobia, and Lentisphaerae.

摘要

人类肠道中戊糖的微生物降解是利用植物性膳食纤维的关键因素。绝大多数肠道微生物能够利用这些C5糖作为碳源和能源。然而,其潜在的代谢途径尚未完全清楚。生物信息学分析表明,大量丰富的肠道细菌缺乏编码转醛醇酶(戊糖磷酸途径的关键酶)的基因。其中包括重要的人类肠道微生物柯氏普雷沃菌,它能够在以木糖或半纤维素作为唯一碳源的基本培养基中生长。因此,我们利用生物信息学、酶活性测定以及戊糖代谢中间产物的检测,寻找柯氏普雷沃菌中戊糖转化的替代途径。很明显,该生物体通过景天庚酮糖-1,7-二磷酸途径(SBPP)将C5糖转化,从而将戊糖代谢与糖酵解联系起来。为了规避转醛醇酶反应,柯氏普雷沃菌利用焦磷酸依赖性磷酸果糖激酶和果糖-1,6-二磷酸醛缩酶的联合催化作用。此外,我们提供了强有力的证据表明,SBPP广泛分布于重要的肠道细菌中,包括拟杆菌门、厚壁菌门、变形菌门、疣微菌门和浮霉菌门的成员。

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