Discovery and mechanism of intestinal bacteria in enzymatic cleavage of C–C glycosidic bonds
C-Glycosides, a special type of glycoside, are frequently distributed in many kinds of medicinal plants, such as puerarin and mangiferin, showing various and significant bioactivities. C-Glycosides are usually characterized by the C–C bond that forms between the anomeric carbon of sugar moieties and...
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Published in | Applied microbiology and biotechnology Vol. 104; no. 5; pp. 1883 - 1890 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Berlin/Heidelberg
Springer Berlin Heidelberg
01.03.2020
Springer Springer Nature B.V |
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Abstract | C-Glycosides, a special type of glycoside, are frequently distributed in many kinds of medicinal plants, such as puerarin and mangiferin, showing various and significant bioactivities. C-Glycosides are usually characterized by the C–C bond that forms between the anomeric carbon of sugar moieties and the carbon atom of aglycon, which is usually resistant against acidic hydrolysis and enzymatic treatments. Interestingly, C-glycosides could be cleaved by several intestinal bacteria, but whether the enzymatic cleavage of C–C glycosidic bond is reduction or hydrolysis has been controversial; furthermore, whether existence of a “C-glycosidase” directly catalyzing the cleavage is not clear. Here we review research advances about the discovery and mechanism of intestinal bacteria in enzymatic cleavage of C–C glycosidic bond with an emphasis on the identification of enzymes manipulation the deglycosylation. Finally, we give a brief conclusion about the mechanism of C-glycoside deglycosylation and perspectives for future study in this field. |
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AbstractList | C-Glycosides, a special type of glycoside, are frequently distributed in many kinds of medicinal plants, such as puerarin and mangiferin, showing various and significant bioactivities. C-Glycosides are usually characterized by the C–C bond that forms between the anomeric carbon of sugar moieties and the carbon atom of aglycon, which is usually resistant against acidic hydrolysis and enzymatic treatments. Interestingly, C-glycosides could be cleaved by several intestinal bacteria, but whether the enzymatic cleavage of C–C glycosidic bond is reduction or hydrolysis has been controversial; furthermore, whether existence of a “C-glycosidase” directly catalyzing the cleavage is not clear. Here we review research advances about the discovery and mechanism of intestinal bacteria in enzymatic cleavage of C–C glycosidic bond with an emphasis on the identification of enzymes manipulation the deglycosylation. Finally, we give a brief conclusion about the mechanism of C-glycoside deglycosylation and perspectives for future study in this field. C-Glycosides, a special type of glycoside, are frequently distributed in many kinds of medicinal plants, such as puerarin and mangiferin, showing various and significant bioactivities. C-Glycosides are usually characterized by the C-C bond that forms between the anomeric carbon of sugar moieties and the carbon atom of aglycon, which is usually resistant against acidic hydrolysis and enzymatic treatments. Interestingly, C-glycosides could be cleaved by several intestinal bacteria, but whether the enzymatic cleavage of C-C glycosidic bond is reduction or hydrolysis has been controversial; furthermore, whether existence of a "C-glycosidase" directly catalyzing the cleavage is not clear. Here we review research advances about the discovery and mechanism of intestinal bacteria in enzymatic cleavage of C-C glycosidic bond with an emphasis on the identification of enzymes manipulation the deglycosylation. Finally, we give a brief conclusion about the mechanism of C-glycoside deglycosylation and perspectives for future study in this field.C-Glycosides, a special type of glycoside, are frequently distributed in many kinds of medicinal plants, such as puerarin and mangiferin, showing various and significant bioactivities. C-Glycosides are usually characterized by the C-C bond that forms between the anomeric carbon of sugar moieties and the carbon atom of aglycon, which is usually resistant against acidic hydrolysis and enzymatic treatments. Interestingly, C-glycosides could be cleaved by several intestinal bacteria, but whether the enzymatic cleavage of C-C glycosidic bond is reduction or hydrolysis has been controversial; furthermore, whether existence of a "C-glycosidase" directly catalyzing the cleavage is not clear. Here we review research advances about the discovery and mechanism of intestinal bacteria in enzymatic cleavage of C-C glycosidic bond with an emphasis on the identification of enzymes manipulation the deglycosylation. Finally, we give a brief conclusion about the mechanism of C-glycoside deglycosylation and perspectives for future study in this field. |
Audience | Academic |
Author | Xu, Xue-Wei Wang, Ya-Kun Wang, Hong Qiu, Wen-Hui Wang, Si-Jia Wei, Bin Wu, Yue-Hong |
Author_xml | – sequence: 1 givenname: Bin surname: Wei fullname: Wei, Bin organization: Key Laboratory of Marine Ecosystem and Biogeochemistry, State Oceanic Administration & Second Institute of Oceanography, Ministry of Natural Resources, College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology – sequence: 2 givenname: Ya-Kun surname: Wang fullname: Wang, Ya-Kun organization: College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology – sequence: 3 givenname: Wen-Hui surname: Qiu fullname: Qiu, Wen-Hui organization: College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology – sequence: 4 givenname: Si-Jia surname: Wang fullname: Wang, Si-Jia organization: College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Center for Human Nutrition, David Geffen School of Medicine, University of California – sequence: 5 givenname: Yue-Hong surname: Wu fullname: Wu, Yue-Hong organization: Key Laboratory of Marine Ecosystem and Biogeochemistry, State Oceanic Administration & Second Institute of Oceanography, Ministry of Natural Resources – sequence: 6 givenname: Xue-Wei surname: Xu fullname: Xu, Xue-Wei email: xuxw@sio.org.cn organization: Key Laboratory of Marine Ecosystem and Biogeochemistry, State Oceanic Administration & Second Institute of Oceanography, Ministry of Natural Resources – sequence: 7 givenname: Hong orcidid: 0000-0003-0058-060X surname: Wang fullname: Wang, Hong email: hongw@zjut.edu.cn organization: College of Pharmaceutical Science & Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31932892$$D View this record in MEDLINE/PubMed |
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Keywords | Deglycosylation Intestinal bacteria C–C glycosidic bond Puerarin C-glycosides |
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SubjectTerms | acid hydrolysis Animals Bacteria Bacteria - enzymology Bacteria - isolation & purification Bacteria - metabolism Bacterial Proteins - genetics Bacterial Proteins - metabolism bioactive properties Biomedical and Life Sciences Biotechnology Biotransformation Carbon chemical bonding Cleavage Covalent bonds Deglycosylation enzymatic treatment Enzymes Feces Glycosidases Glycoside Hydrolases - genetics Glycoside Hydrolases - metabolism Glycosides Glycosides - chemistry Glycosides - metabolism glycosidic linkages Glycosylation Herbal medicine Humans Hydrolysis intestinal microorganisms Intestine Intestines - microbiology Life Sciences Medicinal plants Medicine, Botanic Medicine, Herbal Microbial Genetics and Genomics Microbiology Mini-Review moieties Molecular Structure Natural products sugars |
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Title | Discovery and mechanism of intestinal bacteria in enzymatic cleavage of C–C glycosidic bonds |
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