A new triterpene synthase from Arabidopsis thaliana produces a tricyclic triterpene with two hydroxyl groups |
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Authors: | Xiang Ting Shibuya Masaaki Katsube Yuji Tsutsumi Takehiko Otsuka Miyuki Zhang Hong Masuda Kazuo Ebizuka Yutaka |
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Affiliation: | Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo-ku, Japan. |
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Abstract: | ![]() [structure: see text] Thirteen oxidosqualene cyclase homologues exist in the genome of Arabidopsis thaliana. One of these genes, At4g15340, was amplified by PCR and expressed in yeast. The yeast transformant accumulated tricyclic triterpene, (3S,13R)-malabarica-17,21-dien-3,14-diol (arabidiol), whose structure was determined by NMR and MS analyses. Its epoxide analogue, (3S,13R,21S)-malabarica-17-en-20,21-epoxy-3,14-diol (arabidiol 20,21-epoxide), was also isolated from the transformed yeast. This is the first example of a triterpene synthase that yields a tricyclic triterpene with two hydroxyl groups. |
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