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Published on September 6, 2002; 10.1104/pp.008722


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Received May 18, 2002
Returned for revision June 11, 2002
Accepted June 18, 2002

An Early C-22 Oxidation Branch in the Brassinosteroid Biosynthetic Pathway

Shozo Fujioka *, Suguru Takatsuto , and Shigeo Yoshida

RIKEN (The Institute of Physical and Chemical Research), Wako-shi, Saitama 351-0198, Japan (S.F., S.Y.); and Department of Chemistry, Joetsu University of Education, Joetsu-shi, Niigata 943-8512, Japan (S.T.)

* Corresponding author; email: sfujioka{at}postman.riken.go.jp.

The natural occurrence of 22-hydroxylated steroids in cultured Catharanthus roseus cells and in Arabidopsis seedlings was investigated. Using full-scan gas chromatography-mass spectrometry analysis, (22S)-22-hydroxycampesterol (22-OHCR), (22S,24R)-22-hydroxyergost-4-en-3-one (22-OH-4-en-3-one), (22S,24R)-22-hydroxy-5{alpha}-ergostan-3-one (22-OH-3-one), 6-deoxocathasterone (6-deoxoCT), 3-epi-6-deoxoCT, 28-nor-22-OHCR, 28-nor-22-OH-4-en-3-one, 28-nor-22-OH-3-one, 28-nor-6-deoxoCT, and 3-epi-28-nor-6-deoxoCT were identified. Metabolic experiments with deuterium-labeled 22-OHCR were performed in cultured C. roseus cells and Arabidopsis seedlings (wild type and det2), and the metabolites were analyzed by gas chromatography-mass spectrometry. In both C. roseus cells and wild-type Arabidopsis seedlings, [2H6]22-OH-4-en-3-one, [2H6]22-OH-3-one, [2H6]6-deoxoCT, and [2H6]3-epi-6-deoxoCT were identified as metabolites of [2H6]22-OHCR, whereas the major metabolite in det2 seedlings was [2H6]22-OH-4-en-3-one. Analysis of endogenous levels of these brassinosteroids revealed that det2 accumulates 22-OH-4-en-3-one. The levels of downstream compounds were remarkably reduced compared with the wild type. Exogenously applied 22-OH-3-one and 6-deoxoCT were found to rescue det2 mutant phenotypes, whereas 22-OHCR and 22-OH-4-en-3-one did not. These results substantiate the existence of a new subpathway (22-OHCR -> 22-OH-4-en-3-one -> 22-OH-3-one -> 6-deoxoCT) and reveal that the det2 mutant is defective in the conversion of 22-OH-4-en-3-one to 22-OH-3-one, which leads to brassinolide biosynthesis.




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