Enzymic formation of a tricyclic sesterterpene alcohol from mevalonic acid and all-trans-geranylfarnesyl pyrophosphate
- 1 January 1969
- journal article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society D: Chemical Communications
- No. 22,p. 1319-1320
- https://doi.org/10.1039/c29690001319
Abstract
Mevalonic acid lactone and the chemically synthesized all-trans-geranylfarnesyl pyrophosphate are converted into a tricyclic sesterterpene alcohol, ophiobolin F, by incubation with 100,000 ×g supernatant fraction from cell-free system of Chochlibolus heterostrophus.Keywords
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