β-N-Acetylhexosaminidases-the wizards of glycosylation.

Carbohydrate Enzymatic synthesis Glycosidase Glycosylation Modified substrate N-acetylgalactosamine N-acetylglucosamine Oligosaccharide β-N-acetylhexosaminidase

Journal

Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 18 06 2019
accepted: 24 07 2019
revised: 23 07 2019
pubmed: 12 8 2019
medline: 29 1 2020
entrez: 12 8 2019
Statut: ppublish

Résumé

β-N-Acetylhexosaminidases (EC 3.2.1.52) are a unique family of glycoside hydrolases with dual substrate specificity and a particular reaction mechanism. Though hydrolytic enzymes per se, their good stability, easy recombinant production, absolute stereoselectivity, and a broad substrate specificity predestine these enzymes for challenging applications in carbohydrate synthesis. This mini-review aims to demonstrate the catalytic potential of β-N-acetylhexosaminidases in a range of unusual reactions, processing of unnatural substrates, formation of unexpected products, and demanding reaction designs. The use of unconventional media can considerably alter the progress of transglycosylation reactions. By means of site-directed mutagenesis, novel catalytic machineries can be constructed. Glycosylation of difficult substrates such as sugar nucleotides was accomplished, and the range of afforded glycosidic bonds comprises unique non-reducing sugars. Specific functional groups may be tolerated in the substrate molecule, which makes β-N-acetylhexosaminidases invaluable allies in difficult synthetic problems.

Identifiants

pubmed: 31401752
doi: 10.1007/s00253-019-10065-0
pii: 10.1007/s00253-019-10065-0
doi:

Substances chimiques

Mutant Proteins 0
beta-N-Acetylhexosaminidases EC 3.2.1.52

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

7869-7881

Subventions

Organisme : Ministerstvo Školství, Mládeže a Tělovýchovy
ID : LTC17005
Organisme : Ministerstvo Školství, Mládeže a Tělovýchovy
ID : LTC18041

Auteurs

Pavla Bojarová (P)

Laboratory of Biotransformation, Institute of Microbiology, Czech Academy of Sciences, Vídeňská 1083, CZ-14220, Praha 4, Czech Republic.
Department of Health Care Disciplines and Population Protection, Faculty of Biomedical Engineering, Czech Technical University in Prague, Nám. Sítná 3105, CZ-272 01, Kladno, Czech Republic.

Jan Bruthans (J)

Department of Biomedical Technology, Faculty of Biomedical Engineering, Czech Technical University in Prague, Nám. Sítná 3105, CZ-272 01, Kladno, Czech Republic.

Vladimír Křen (V)

Laboratory of Biotransformation, Institute of Microbiology, Czech Academy of Sciences, Vídeňská 1083, CZ-14220, Praha 4, Czech Republic. kren@biomed.cas.cz.

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Classifications MeSH