TY - JOUR
T1 - Biotransformation of ginsenoside Rb1 and Rd to four rare ginsenosides and evaluation of their anti-melanogenic effects
AU - Zhang, Le
AU - Wang, Liwei
AU - Chen, Yufei
AU - Yang, Yaya
AU - Xia, Guohua
AU - Guo, Yuao
AU - Yang, Huan
AU - Shen, Yuping
AU - Meyer, Anne S.
PY - 2023
Y1 - 2023
N2 - Improving physiological activity of primary ginsenosides through biotransformation is of great significance for food applications. In this study, gynostapenoside XVII, gynostapenoside LXXV, ginsenoside F2, and ginsenoside CK were obtained by enzymolysis of an accessible extract composed of ginsenoside Rb1 and Rd. Their effects on melanin content and tyrosinase activity were compared in vitro, and molecular docking simulation was employed to elucidate the interaction between tyrosinase and individual saponin. The results indicated that four rare ginsenosides decreased tyrosinase activity, melanin content and microphthalmia-associated transcription factor (MITF) expression level, more greatly than their primary ginsenosides, and they were more readily to bind with ASP10 and GLY68 at active site of tyrosinase to inhibit tyrosinase activity as well. These findings suggested that the rare ginsenosides obtained by enzymolysis had excellent anti-melanogenic effect, which could expand the application of ginsenosides in the field of functional foods and health supplements.
AB - Improving physiological activity of primary ginsenosides through biotransformation is of great significance for food applications. In this study, gynostapenoside XVII, gynostapenoside LXXV, ginsenoside F2, and ginsenoside CK were obtained by enzymolysis of an accessible extract composed of ginsenoside Rb1 and Rd. Their effects on melanin content and tyrosinase activity were compared in vitro, and molecular docking simulation was employed to elucidate the interaction between tyrosinase and individual saponin. The results indicated that four rare ginsenosides decreased tyrosinase activity, melanin content and microphthalmia-associated transcription factor (MITF) expression level, more greatly than their primary ginsenosides, and they were more readily to bind with ASP10 and GLY68 at active site of tyrosinase to inhibit tyrosinase activity as well. These findings suggested that the rare ginsenosides obtained by enzymolysis had excellent anti-melanogenic effect, which could expand the application of ginsenosides in the field of functional foods and health supplements.
KW - Ginsenoside
KW - Biotransformation
KW - Melanin
KW - Gynostapenoside XVII
KW - Gynostapenoside LXXV
KW - Skin whitening
U2 - 10.1007/s11418-023-01719-5
DO - 10.1007/s11418-023-01719-5
M3 - Journal article
C2 - 37329418
SN - 1861-0293
VL - 77
SP - 939
EP - 952
JO - Journal of Natural Medicines
JF - Journal of Natural Medicines
ER -