Production of α-galactosyl epitopes via combined use of two recombinant whole cells harboring UDP-galactose 4-epimerase and α-1,3-galactosyltransferase

被引:25
作者
Chen, X [1 ]
Zhang, W [1 ]
Wang, JQ [1 ]
Fang, JW [1 ]
Wang, PG [1 ]
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
关键词
D O I
10.1021/bp000052s
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
alpha-Galactosyl epitopes (or alpha-Gal, oligosaccharides with a terminal Gal alpha 1,3Gal sequence) are a class of biologically important oligosaccharides in great demand in bulk quantities for basic and clinical studies on preventing hyperacute rejection in pig-to-primate organ xenotransplantaion. A truncated bovine alpha-1,3-galactosyltransferase, the key enzyme responsible for the biosynthesis of the terminal structure of alpha-Gal, was cloned and overexpressed previously. The acceptor specificity was further studied in the present paper, and lactose and galactose derivatives were found to be good accepters. To develop a more proficient reaction process, we report herein an example of an efficient enzymatic synthesis of alpha-Gal oligosaccharides catalyzed by the combination of two recombinant Escherichia coli whole cells harboring the genes of a UDP-galactose 4-epimerase and the alpha-1,3-galactosyltransferase, respectively. Using lactosyl azide (LacN(3)) as the acceptor for the glycosyltransferase, the combined use of the two recombinant cells efficiently produced alpha-Gal epitope Gal alpha 1,3LacN(3) in 60-68% yield.
引用
收藏
页码:595 / 599
页数:5
相关论文
共 20 条
[1]  
BLANKEN WM, 1985, J BIOL CHEM, V260, P2927
[2]   Cloning, expression and characterization of a UDP-galactose 4-epimerase from Escherichia coli [J].
Chen, X ;
Kowal, P ;
Hamad, S ;
Fan, HN ;
Wang, PG .
BIOTECHNOLOGY LETTERS, 1999, 21 (12) :1131-1135
[3]   Large-scale production of CMP-NeuAc and sialylated oligosaccharides through bacterial coupling [J].
Endo, T ;
Koizumi, S ;
Tabata, K ;
Ozaki, A .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2000, 53 (03) :257-261
[4]   Large-scale production of N-acetyllactosamine through bacterial coupling [J].
Endo, T ;
Koizumi, S ;
Tabata, K ;
Kakita, S ;
Ozaki, A .
CARBOHYDRATE RESEARCH, 1999, 316 (1-4) :179-183
[5]   Highly efficient chemoenzymatic synthesis of α-galactosyl epitopes with a recombinant α(1→3)-galactosyltransferase [J].
Fang, JW ;
Li, J ;
Chen, X ;
Zhang, YN ;
Wang, JQ ;
Guo, ZM ;
Zhang, W ;
Yu, LB ;
Brew, K ;
Wang, PG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (27) :6635-6638
[6]   GENE-SEQUENCES SUGGEST INACTIVATION OF ALPHA-1,3-GALACTOSYLTRANSFERASE IN CATARRHINES AFTER THE DIVERGENCE OF APES FROM MONKEYS [J].
GALILI, U ;
SWANSON, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7401-7404
[7]   INTERACTION OF THE NATURAL ANTI-GAL ANTIBODY WITH ALPHA-GALACTOSYL EPITOPES - A MAJOR OBSTACLE FOR XENOTRANSPLANTATION IN HUMANS [J].
GALILI, U .
IMMUNOLOGY TODAY, 1993, 14 (10) :480-482
[8]   RECOMBINANT WHOLE CELLS AS CATALYSTS FOR THE ENZYMATIC-SYNTHESIS OF OLIGOSACCHARIDES AND GLYCOPEPTIDES [J].
HERRMANN, GF ;
WANG, P ;
SHEN, GJ ;
WONG, CH .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1994, 33 (12) :1241-1242
[9]   Large-scale production of UDP-galactose and globotriose by coupling metabolically engineered bacteria [J].
Koizumi, S ;
Endo, T ;
Tabata, K ;
Ozaki, A .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :847-850
[10]  
Martina JA, 1996, J NEUROSCI RES, V46, P485, DOI 10.1002/(SICI)1097-4547(19961115)46:4<485::AID-JNR10>3.0.CO