TY - JOUR
T1 - Constructing an Intensified UDP Recycling System for the Glycosylation of Natural Products by Phosphorylation of Byproduct Fructose
AU - Wang, Yingying
AU - Sun, Qiuyan
AU - Chi, Yanfei
AU - Liu, Zhiqiang
AU - Liu, Hu
AU - Li, Chun
AU - Feng, Xudong
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/6/21
Y1 - 2023/6/21
N2 - UDP-glucosyltransferase can be coupled with sucrose synthase to construct a two-enzyme UDP (UDP-2E) recycling system for glucosylation of natural products with inexpensive sucrose as the consumed substrate. However, sucrose hydrolysis leads to the accumulation of fructose as a byproduct, which decreases the atom economy of sucrose and suppresses in situ UDP recycling. In this study, a polyphosphate-dependent glucokinase was demonstrated to convert fructose to fructose-6-phosphate independent of expensive ATP for the first time. Then the glucokinase was introduced into the UDP-2E recycling system to construct a modified three-enzyme UDP (UDP-3E) recycling system, which showed enhanced glucosylation efficiency of triterpenoids by fructose phosphorylation to accelerate sucrose hydrolysis and UDP recycling. Finally, by further introducing a phosphofructokinase into the UDP-3E recycling system, we transformed fructose-6-phosphate into fructose-1,6-diphosphate, demonstrating that the UDP-3E recycling system can be coupled with extra enzymes to obtain final products with high added-value without compromising the glycosylation efficiency.
AB - UDP-glucosyltransferase can be coupled with sucrose synthase to construct a two-enzyme UDP (UDP-2E) recycling system for glucosylation of natural products with inexpensive sucrose as the consumed substrate. However, sucrose hydrolysis leads to the accumulation of fructose as a byproduct, which decreases the atom economy of sucrose and suppresses in situ UDP recycling. In this study, a polyphosphate-dependent glucokinase was demonstrated to convert fructose to fructose-6-phosphate independent of expensive ATP for the first time. Then the glucokinase was introduced into the UDP-2E recycling system to construct a modified three-enzyme UDP (UDP-3E) recycling system, which showed enhanced glucosylation efficiency of triterpenoids by fructose phosphorylation to accelerate sucrose hydrolysis and UDP recycling. Finally, by further introducing a phosphofructokinase into the UDP-3E recycling system, we transformed fructose-6-phosphate into fructose-1,6-diphosphate, demonstrating that the UDP-3E recycling system can be coupled with extra enzymes to obtain final products with high added-value without compromising the glycosylation efficiency.
KW - UDP recycling
KW - UDP-glucosyltransferase
KW - fructose phosphorylation
KW - glycosylation
KW - sucrose hydrolysis
UR - http://www.scopus.com/inward/record.url?scp=85163752923&partnerID=8YFLogxK
U2 - 10.1021/acs.jafc.3c01077
DO - 10.1021/acs.jafc.3c01077
M3 - Article
C2 - 37289015
AN - SCOPUS:85163752923
SN - 0021-8561
VL - 71
SP - 9441
EP - 9450
JO - Journal of Agricultural and Food Chemistry
JF - Journal of Agricultural and Food Chemistry
IS - 24
ER -