INVESTIGATION OF SUCROSE SYNTHASE FROM RICE FOR THE SYNTHESIS OF VARIOUS NUCLEOTIDE SUGARS AND SACCHARIDES

被引:48
作者
ELLING, L
GROTHUS, M
KULA, MR
机构
[1] Institut fur Enzymtechnologie, Heinrich-Heine-Universitat Dusseldorf, Forschungszentrum Julich, D-5170 Julich
关键词
N-ACETYLLACTOSAMINE; NUCLEOTIDE SUGARS; SACCHARIDES; SUCROSE SYNTHASE;
D O I
10.1093/glycob/3.4.349
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The unique character of the plant glucosyltransferase sucrose synthase, to catalyse in vitro the synthesis and cleavage of sucrose under appropriate conditions, can be exploited for the enzymatic synthesis of carbohydrates. The present paper describes the potential utilization of sucrose synthase from rice for the enzymatic synthesis of activated sugars and saccharides. In the cleavage reaction of sucrose, the nucleoside diphosphates can be used in the order UDP > TDP > ADP > CDP > GDP to obtain the corresponding activated glucoses. In batch reactions, > 90% conversion of UDP and TDP could be achieved. Substituting different di- and trisaccharides for sucrose in the cleavage reaction with UDP 2-deoxysucrose was the most promising substrate. Sucrose synthase was combined with UDP-galactose 4'-epimerase and beta1-4 galactosyltransferase to synthesize N-acetyllactosamine with in situ regeneration of UDP-glucose. In the synthesis reaction of sucrose synthase, different donor (UDP-sugars) and acceptor substrates were investigated. UDP-N-acetytglucosamine and UDP-xylose could be used in combination with fructose as acceptor. D-Xylulose, D-tagatose, D-lyxose, D-psicose, L-sorbose, D-mannose, L-arabinose, 1,6 anhydroglucose, lactulose, raffinose and isomaltulose can serve as acceptors for UDP-glucose.
引用
收藏
页码:349 / 355
页数:7
相关论文
共 25 条
[1]  
AVIGAD G, 1982, ENCY PLANT PHYSL A, V13, P217
[2]  
AVIGAD G, 1966, METHOD ENZYMOL, V8, P341
[3]   SYNTHESIS OF DISACCHARIDES WITH PEA PREPARATIONS [J].
BEAN, RC ;
HASSID, WZ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (21) :5737-5738
[4]  
BOUCHU A, 1992, 16TH INT CARB S PAR, P681
[5]  
CARDINI C. E., 1955, JOUR BIOL CHEM, V214, P149
[6]  
CARDINI CE, 1962, PLANT CELL PHYSIOL, V3, P313
[7]  
Collins P. M., 1987, CARBOHYDRATES
[8]  
Copeland L., 1990, METHODS PLANT BIOCH, V3, P73
[9]   ENZYMATIC METHODS IN PREPARATIVE CARBOHYDRATE-CHEMISTRY [J].
DAVID, S ;
AUGE, C ;
GAUTHERON, C .
ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY, 1991, 49 :175-237
[10]  
DELMER DP, 1972, J BIOL CHEM, V247, P3822