
AbstractMicrobial transformation of one oleane‐type pentacyclic triterpene aglycone, phytolaccagenin (2β,3β,23‐trihydroxy‐olean‐12‐ene‐28,30‐dioic acid 30‐methyl ester) by Streptomyces griseus ATCC 13273 was investigated for developing new bioactive derivatives. A new oxidized metabolite, through the regio‐specific hydroxylation on the C‐29 methyl group, was obtained from the preparative‐scale biotransformation with a standard two‐stage fermentation protocol. The metabolite was identified as 2β,3β,23,29‐tetrahydroxy‐olean‐12‐ene‐28,30‐dioic acid 30‐methyl ester by mass and 2D‐NMR spectra.
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