Abstract

A system for the production of [ 14C]taxol in vitro has been devised. The aseptic system utilized an appropriate 14C-labeled precursor, a reducing environment (dithiothreitol) and aseptically prepared pieces of the inner bark of Taxus brevifolia (Pacific yew). [ 14C]Phenylalanine and [ 14C]leucine are the best precursors, of the compounds tested, for [ 14C]taxol production. However, in the standard assay sodium [1- 14C]acetate is used because of its relatively low price and its ability to label taxol uniformly. Chlorocholine chloride, an inhibitor of plant steroid metabolism, was an effective stimulator of [ 14C]taxol production, as were certain fungal elicitors. Taxol biosynthetic activity is greatest in the bark from lower portions of the main stem (trunk: 1 m from ground level).

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