Unknown

Dataset Information

0

Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102.


ABSTRACT: Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30?. Under optimal conditions, ginsenoside Rb1 was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb1? gypenoside XVII and ginsenoside Rd?ginsenoside F2?compound K.

SUBMITTER: Quan LH 

PROVIDER: S-EPMC3659545 | biostudies-literature | 2011 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Biotransformation of Ginsenoside Rb1 to Prosapogenins, Gypenoside XVII, Ginsenoside Rd, Ginsenoside F2, and Compound K by Leuconostoc mesenteroides DC102.

Quan Lin-Hu LH   Piao Jin-Ying JY   Min Jin-Woo JW   Kim Ho-Bin HB   Kim Sang-Rae SR   Yang Dong-Uk DU   Yang Deok Chun DC  

Journal of ginseng research 20110901 3


Ginsenoside Rb1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb1 was decomposed  ...[more]

Similar Datasets

| S-EPMC3659600 | biostudies-literature
| S-EPMC4175505 | biostudies-literature
| S-EPMC8803428 | biostudies-literature
| S-EPMC5519667 | biostudies-literature
| S-EPMC2600284 | biostudies-literature
| S-EPMC5686332 | biostudies-literature
| S-EPMC3349346 | biostudies-literature
| S-EPMC3264068 | biostudies-literature
| S-EPMC6113708 | biostudies-literature
| S-EPMC5628084 | biostudies-literature