Literature DB >> 31875448

[Research progress on carbohydrate active enzymes of human microbiome].

Zhi-Yan Zhou1, Xin Xu1, Yuan Zhou2.   

Abstract

A massive variety of microorganisms live in and on the human body, especially at oral, skin, vaginal, gastroin-testinal, and respiratory sites. The complicated metabolic activities of microorganisms assist human digestive function and participate in a series of physiological and pathogenetic processes. Carbohydrate-active enzymes (CAZymes) are a series of enzymes that function in degradation, modification, and formation of glycoside bonds. Microbes regulate the physiological and pathogenetic processes of human body by producing various CAZymes to degrade and modify complex carbohydrates and generate signal molecules for further utilization in human cells. Here, we reviewed the mechanisms of complex carbohy-drate metabolism and related microbial CAZymes, especially in digestive tract and oral cavity. We also summarized the rela-tionship between microbial CAZymes and human health, and proposed potential applications.

Entities:  

Keywords:  carbohydrate active enzymes; glycoside hydrolases; gut microbiome; oral microbiome

Mesh:

Substances:

Year:  2019        PMID: 31875448      PMCID: PMC7030758          DOI: 10.7518/hxkq.2019.06.017

Source DB:  PubMed          Journal:  Hua Xi Kou Qiang Yi Xue Za Zhi        ISSN: 1000-1182


  35 in total

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Review 2.  Glycosyltransferase-mediated Sweet Modification in Oral Streptococci.

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3.  The Human Microbiome Project: lessons from human genomics.

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4.  Characterizing a model human gut microbiota composed of members of its two dominant bacterial phyla.

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Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-24       Impact factor: 11.205

5.  Role of sialidase in glycoprotein utilization by Tannerella forsythia.

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6.  Milk sialyllactose influences colitis in mice through selective intestinal bacterial colonization.

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7.  Complex carbohydrate utilization by the healthy human microbiome.

Authors:  Brandi L Cantarel; Vincent Lombard; Bernard Henrissat
Journal:  PLoS One       Date:  2012-06-13       Impact factor: 3.240

8.  Utilisation of mucin glycans by the human gut symbiont Ruminococcus gnavus is strain-dependent.

Authors:  Emmanuelle H Crost; Louise E Tailford; Gwenaelle Le Gall; Michel Fons; Bernard Henrissat; Nathalie Juge
Journal:  PLoS One       Date:  2013-10-25       Impact factor: 3.240

9.  An evolutionarily distinct family of polysaccharide lyases removes rhamnose capping of complex arabinogalactan proteins.

Authors:  José Munoz-Munoz; Alan Cartmell; Nicolas Terrapon; Arnaud Baslé; Bernard Henrissat; Harry J Gilbert
Journal:  J Biol Chem       Date:  2017-06-21       Impact factor: 5.157

10.  Functional consequences of microbial shifts in the human gastrointestinal tract linked to antibiotic treatment and obesity.

Authors:  Ester Hernández; Rafael Bargiela; María Suárez Diez; Anette Friedrichs; Ana Elena Pérez-Cobas; María José Gosalbes; Henrik Knecht; Mónica Martínez-Martínez; Jana Seifert; Martin von Bergen; Alejandro Artacho; Alicia Ruiz; Cristina Campoy; Amparo Latorre; Stephan J Ott; Andrés Moya; Antonio Suárez; Vitor A P Martins dos Santos; Manuel Ferrer
Journal:  Gut Microbes       Date:  2013-06-12
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Journal:  Front Cell Infect Microbiol       Date:  2022-08-26       Impact factor: 6.073

  1 in total

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