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肠道和自然界中的 C-糖苷代谢:C-C 键裂解酶的鉴定、特性、结构分析和分布。

C-Glycoside metabolism in the gut and in nature: Identification, characterization, structural analyses and distribution of C-C bond-cleaving enzymes.

机构信息

Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.

Collaborative Research Institute for Innovative Microbiology, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo, 113-8657, Japan.

出版信息

Nat Commun. 2021 Nov 2;12(1):6294. doi: 10.1038/s41467-021-26585-1.

Abstract

C-Glycosides, in which a sugar moiety is linked via a carbon-carbon (C-C) bond to a non-sugar moiety (aglycone), are found in our food and medicine. The C-C bond is cleaved by intestinal microbes and the resulting aglycones exert various bioactivities. Although the enzymes responsible for the reactions have been identified, their catalytic mechanisms and the generality of the reactions in nature remain to be explored. Here, we present the identification and structural basis for the activation of xenobiotic C-glycosides by heterocomplex C-deglycosylation enzymes from intestinal and soil bacteria. They are found to be metal-dependent enzymes exhibiting broad substrate specificity toward C-glycosides. X-ray crystallographic and cryo-electron microscopic analyses, as well as structure-based mutagenesis, reveal the structural details of these enzymes and the detailed catalytic mechanisms of their remarkable C-C bond cleavage reactions. Furthermore, bioinformatic and biochemical analyses suggest that the C-deglycosylation enzymes are widely distributed in the gut, soil, and marine bacteria.

摘要

C-糖苷是一类糖苷化合物,其中糖部分通过碳-碳(C-C)键与非糖部分(糖苷配基)相连,存在于我们的食物和药物中。C-C 键被肠道微生物裂解,生成的糖苷配基发挥各种生物活性。尽管已经鉴定出负责这些反应的酶,但它们的催化机制以及自然界中反应的普遍性仍有待探索。在这里,我们介绍了肠道和土壤细菌中异源杂合 C-去糖基化酶对异生物质 C-糖苷的激活作用及其结构基础。这些酶是金属依赖性酶,对 C-糖苷表现出广泛的底物特异性。X 射线晶体学和低温电子显微镜分析以及基于结构的突变分析揭示了这些酶的结构细节以及它们显著的 C-C 键裂解反应的详细催化机制。此外,生物信息学和生化分析表明,C-去糖基化酶广泛分布于肠道、土壤和海洋细菌中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3305/8563793/4248a4d0f247/41467_2021_26585_Fig1_HTML.jpg

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