The tomato DWARF enzyme catalyses C-6 oxidation in brassinosteroid biosynthesis

被引:256
作者
Bishop, GJ [1 ]
Nomura, T
Yokota, T
Harrison, K
Noguchi, T
Fujioka, S
Takatsuto, S
Jones, JDG
Kamiya, Y
机构
[1] RIKEN, Inst Phys & Chem Res, Frontier Res Program, Wako, Saitama 3510198, Japan
[2] Tokyo Univ Agr & Technol, Tokyo 1838509, Japan
[3] Teikyo Univ, Utsunomiya, Tochigi 3208551, Japan
[4] Joetsu Univ Educ, Dept Chem, Joetsu, Niigata 9438512, Japan
[5] Sainsbury Lab, Norwich NR4 7UH, Norfolk, England
关键词
D O I
10.1073/pnas.96.4.1761
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Brassinosteroids (BRs) are steroidal plant hormones essential for normal plant growth and development. Mutants in the biosynthesis or perception of BRs are usually dwarf, The tomato Dwarf gene (D), which was predicted to encode a cytochrome P450 enzyme (P450) with homology to other P450s involved in BR biosynthesis, was cloned previously. Here, we show that DWARF catalyses the C-6 oxidation of 6-deoxocastasterone (6-deoxoCS) to castasterone (CS), the immediate precursor of brassinolide. To do this, we first confirmed that the D cDNA complemented the mutant light- and dark-grown phenotypes of the extreme dwarf (d(x)) allele of tomato. To identify a substrate for the DWARF enzyme, exogenous application of BR intermediates to d(x) plants was carried out. C-6 oxoBR intermediates enhanced hypocotyl elongation whereas the C-6 deoxoBR, 6-deoxoCS, had little effect. Quantitative analysis of endogenous BR levels in tomato showed mainly the presence of 6-deoxoBRs. Furthermore, d(x) plants were found to lack CS and had a high level of 6-deoxoCS in comparison to D plants that had CS and a lower level of 6-deoxoCS. Confirmation that DWARF catalyzed the C-6 oxidation of 6-deoxoCS to CS was obtained by functional expression of DWARF in yeast. In these experiments, the intermediate 6 alpha-hydroxycastasterone was identified, indicating that DWARF catalyzes two steps in BR biosynthesis. These data show that DWARF is involved in the C-6 oxidation in BR biosynthesis.
引用
收藏
页码:1761 / 1766
页数:6
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