Cofactor-Driven Cascade Reactions Enable the Efficient Preparation of Sugar Nucleotides

被引:18
作者
Zheng, Yuan [1 ]
Zhang, Jiabin [1 ,3 ]
Meisner, Jeffrey [4 ]
Li, Wanjin [1 ]
Luo, Yawen [1 ,2 ]
Wei, Fangyu [1 ,2 ]
Wen, Liuqing [1 ,2 ]
机构
[1] Chinese Acad Sci, Carbohydrate Based Drug Res Ctr, Shanghai Inst Mat Media, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Media, Zhongshan 528400, Guangdong, Peoples R China
[4] Kaleido Biosci, Lexington, MA 02421 USA
基金
中国国家自然科学基金;
关键词
Biocatalysis; Cascade Reactions; One-Pot Reactions; Sugar Nucleotides; LARGE-SCALE PRODUCTION; DEHYDROGENASE-CATALYZED REGENERATION; UDP-N-ACETYLGLUCOSAMINE; O-ANTIGEN BIOSYNTHESIS; IN-VITRO BIOSYNTHESIS; ENZYMATIC-SYNTHESIS; NAD(P)-DEPENDENT OXIDOREDUCTASES; CHEMOENZYMATIC SYNTHESIS; GLUCOSE-DEHYDROGENASE; GLYCAN BIOSYNTHESIS;
D O I
10.1002/anie.202115696
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Glycosylation is catalyzed by glycosyltransferases using sugar nucleotides or occasionally lipid-linked phosphosugars as donors. However, only very few common sugar nucleotides that occur in humans can be obtained readily, while the majority of sugar nucleotides that exist in bacteria, plants, archaea, or viruses cannot be synthesized in sufficient quantities by either enzymatic or chemical synthesis. The limited availability of such rare sugar nucleotides is one of the major obstacles that has greatly hampered progress in glycoscience. Herein we describe a general cofactor-driven cascade conversion strategy for the efficient synthesis of sugar nucleotides. The described strategy allows the large-scale preparation of rare sugar nucleotides from common sugars in high yields and without the need for tedious purification processes.
引用
收藏
页数:8
相关论文
共 104 条
[11]   Cloning, expression and characterization of a glucose dehydrogenase from Bacillus sp G3 in Escherichia coli [J].
Chen, Xuejiao ;
Ding, Haitao ;
Du, Yiqing ;
Lin, Hui ;
Li, Zeli ;
Zhao, Yuhua .
AFRICAN JOURNAL OF MICROBIOLOGY RESEARCH, 2011, 5 (32) :5882-5888
[12]   One-pot three-enzyme synthesis of UDP-GlcNAc derivatives [J].
Chen, Yi ;
Thon, Vireak ;
Li, Yanhong ;
Yu, Hai ;
Ding, Li ;
Lau, Kam ;
Qu, Jingyao ;
Hie, Liana ;
Chen, Xi .
CHEMICAL COMMUNICATIONS, 2011, 47 (38) :10815-10817
[13]  
Chenault H K, 1988, Biotechnol Genet Eng Rev, V6, P221
[14]  
CHENAULT HK, 1989, BIOORG CHEM, V17, P400
[15]   Reconstitution and optimisation of the biosynthesis of bacterial sugar pseudaminic acid (Pse5Ac7Ac) enables preparative enzymatic synthesis of CMP-Pse5Ac7Ac [J].
Chidwick, Harriet S. ;
Flack, Emily K. P. ;
Keenan, Tessa ;
Walton, Julia ;
Thomas, Gavin H. ;
Fascione, Martin A. .
SCIENTIFIC REPORTS, 2021, 11 (01)
[16]   Bacterial glycans: Key mediators of diverse host immune responses [J].
Comstock, Laurie E. ;
Kasper, Dennis L. .
CELL, 2006, 126 (05) :847-850
[17]   Characterization of CJ1293, a new UDP-GIcNAc C6 dehydratase from Campylobacter jejuni [J].
Creuzenet, C .
FEBS LETTERS, 2004, 559 (1-3) :136-140
[18]   Potential applications of NAD(P)-dependent oxidoreductases in synthesis: A survey [J].
DevauxBasseguy, R ;
Bergel, A ;
Comtat, M .
ENZYME AND MICROBIAL TECHNOLOGY, 1997, 20 (04) :248-258
[19]   NTP Regeneration and its Application in the Biosynthesis of Nucleotides and their Derivatives [J].
Ding, Qingbao ;
Ou, Ling .
CURRENT PHARMACEUTICAL DESIGN, 2017, 23 (45) :6936-6947
[20]   Enzymatic Redox Cascade for One-Pot Synthesis of Uridine 5′-Diphosphate Xylose from Uridine 5′-Diphosphate Glucose [J].
Eixelsberger, Thomas ;
Nidetzky, Bernd .
ADVANCED SYNTHESIS & CATALYSIS, 2014, 356 (17) :3575-3584