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Isolation and biosynthesis of 3 alpha-hydroxy-3,5-dihydromonacolin L
T Nakamura1, D Komagata, S Murakawa
1Department of Applied Biological Sciences, Tokyo Noko University, Japan.
The Journal of Antibiotics
|December 1, 1990
Abstract:
3 alpha-Hydroxy-3,5-dihydromonacolin L acid (acid form), a new compound related to monacolin K (mevinolin), was isolated from the culture broth of a strain of Monascus ruber. The structure of the compound was determined by a combination of physical techniques. 4a,5-Dihydromonacolin L was converted to 3 alpha-hydroxy-3,5-dihydromonacolin L by a cell-free extract of M. ruber in the presence of molecular oxygen. The results demonstrate that the former is the direct precursor in the biosynthesis of the latter.