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Biosynthesis of Indole Diterpene Lolitrems: Radical-Induced Cyclization of an Epoxyalcohol Affording a Characteristic Lolitremane Skeleton |
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| Authors: | Yulu Jiang Dr Taro Ozaki Mei Harada Tadachika Miyasaka Dr Hajime Sato Dr Kazunori Miyamoto Dr Junichiro Kanazawa Dr Chengwei Liu Prof?Dr Jun-ichi Maruyama Dr Masaatsu Adachi Dr Atsuo Nakazaki Prof?Dr Toshio Nishikawa Prof?Dr Masanobu Uchiyama Dr Atsushi Minami Prof?Dr Hideaki Oikawa |
| Institution: | 1. Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, 060-0810 Japan;2. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan
Cluster for Pioneering Research (CPR), Advanced Elements Chemistry Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama, 351-0198 Japan;3. Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya, 464-8601 Japan;4. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan;5. Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, 060-0810 Japan Present address: College of Life Sciences, Northeast Forestry University, Harbin, 150040 China;6. Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, 113-8657 Japan;7. Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3. Aoba, Aramaki, Aoba-ku, Sendai, 980-8578 Japan |
| Abstract: | Lolitrems are tremorgenic indole diterpenes that exhibit a unique 5/6 bicyclic system of the indole moiety. Although genetic analysis has indicated that the prenyltransferase LtmE and the cytochrome P450 LtmJ are involved in the construction of this unique structure, the detailed mechanism remains to be elucidated. Herein, we report the reconstitution of the biosynthetic pathway for lolitrems employing a recently established genome-editing technique for the expression host Aspergillus oryzae. Heterologous expression and bioconversion of the various intermediates revealed that LtmJ catalyzes multistep oxidation to furnish the lolitrem core. We also isolated the key reaction intermediate with an epoxyalcohol moiety. This observation allowed us to establish the mechanism of radical-induced cyclization, which was firmly supported by density functional theory calculations and a model experiment with a synthetic analogue. |
| Keywords: | cyclization cytochrome P450 lolitrem natural products radical reactions |