Arabidopsis det2 is defective in the conversion of (24R)-24-methylcholest-4-En-3-One to (24R)-24-methyl-5α-cholestan-3-one in brassinosteroid biosynthesis

被引:135
作者
Noguchi, T
Fujioka, S [1 ]
Takatsuto, S
Sakurai, A
Yoshida, S
Li, JM
Chory, J
机构
[1] RIKEN, Inst Phys & Chem Res, Wako, Saitama 3510198, Japan
[2] Tama Biochem Co Ltd, Shinjuku Ku, Tokyo 1630704, Japan
[3] Joetsu Univ Educ, Dept Chem, Joetsu, Niigata 9438512, Japan
[4] Salk Inst Biol Studies, Plant Biol Lab, La Jolla, CA 92037 USA
关键词
D O I
10.1104/pp.120.3.833
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Previously, we have shown that the Arabidopsis det2 (deetiolated2) mutant is defective in the biosynthesis of brassinosteroids (BR) and that DET2 (a steroid 5 alpha-reductase) acts early in the proposed BR biosynthetic pathway. In this paper we present further biochemical characterization of det2. We have undertaken metabolic experiments with H-2-labeled substrates of intermediates involved in the formation of campestanol from campesterol, and quantitative analysis of intermediates in Arabidopsis wild type and det2. The results of these studies indicate the early operating steps of BR biosynthesis as: campesterol --> 4-en-3 beta-ol --> 4-en-3-one --> 3-one --> campestanol in Arabidopsis, with det2 deficient in the conversion of 4-en-3-one to 3-one. We have also detected these intermediates in the formation of campestanol from campesterol and their metabolic conversions using cultured cells of Catharanthus roseus. These studies confirmed the biosynthetic sequence of events from campesterol to campestanol as was found in Arabidopsis. As such, the originally proposed biosynthetic pathway should be modified.
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页码:833 / 839
页数:7
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