β-N-Acetylhexosaminidases-the wizards of glycosylation

被引:26
作者
Bojarova, Pavla [1 ,2 ]
Bruthans, Jan [3 ]
Kren, Vladimir [1 ]
机构
[1] Czech Acad Sci, Inst Microbiol, Lab Biotransformat, Videnska 1083, CZ-14220 Prague 4, Czech Republic
[2] Czech Tech Univ, Fac Biomed Engn, Dept Hlth Care Disciplines & Populat Protect, Nam Sitna 3105, CZ-27201 Kladno, Czech Republic
[3] Czech Tech Univ, Fac Biomed Engn, Dept Biomed Technol, Nam Sitna 3105, CZ-27201 Kladno, Czech Republic
关键词
beta-N-acetylhexosaminidase; Carbohydrate; Enzymatic synthesis; N-acetylglucosamine; N-acetylgalactosamine; Glycosidase; Glycosylation; Modified substrate; Oligosaccharide; SUBSTRATE-ASSISTED CATALYSIS; D-GLUCOSAMINIDASE; ENZYMATIC GLYCOSYLATION; CHEMOENZYMATIC SYNTHESIS; GLYCOSIDE HYDROLASE; ASPERGILLUS-ORYZAE; REVERSE HYDROLYSIS; PROVIDES INSIGHT; ACTIVE ENZYMES; GLASS PHASES;
D O I
10.1007/s00253-019-10065-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
beta-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 beta-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 beta-N-acetylhexosaminidases invaluable allies in difficult synthetic problems.
引用
收藏
页码:7869 / 7881
页数:13
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