Literature DB >> 9178548

Studies on biosynthesis of brassinosteroids.

A Sakurai1, S Fujioka.   

Abstract

Biosynthesis of steroidal plant hormones, brassinosteroids, was studied using the cell culture system of Catharanthus roseus. Feeding labeled compounds of possible intermediates to the cultured cells, followed by analyzing the metabolites by gas chromatography-mass spectrometry disclosed the pathways from a plant sterol, campesterol, to brassinolide. There are two pathways, named the early C6-oxidation pathway and late C6-oxidation pathway, both of which would be operating in a wide variety of plants. Recent findings of brassinosteroid-deficient mutants of Arabidopsis and the garden pea by several groups, and the possible blocked steps of the mutants in the biosynthetic pathways are also introduced.

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Year:  1997        PMID: 9178548     DOI: 10.1271/bbb.61.757

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  16 in total

Review 1.  Genetic regulation of embryonic pattern formation.

Authors:  Thomas Laux; Tobias Würschum; Holger Breuninger
Journal:  Plant Cell       Date:  2004-04-20       Impact factor: 11.277

2.  Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor.

Authors:  T Asami; Y K Min; N Nagata; K Yamagishi; S Takatsuto; S Fujioka; N Murofushi; I Yamaguchi; S Yoshida
Journal:  Plant Physiol       Date:  2000-05       Impact factor: 8.340

3.  FACKEL is a sterol C-14 reductase required for organized cell division and expansion in Arabidopsis embryogenesis.

Authors:  K Schrick; U Mayer; A Horrichs; C Kuhnt; C Bellini; J Dangl; J Schmidt; G Jürgens
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

4.  In vitro and in vivo evidence for the inhibition of brassinosteroid synthesis by propiconazole through interference with side chain hydroxylation.

Authors:  Keimei Oh; Tadashi Matsumoto; Tomoki Hoshi; Yuko Yoshizawa
Journal:  Plant Signal Behav       Date:  2016-05-03

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

Authors:  T Noguchi; S Fujioka; S Takatsuto; A Sakurai; S Yoshida; J Li; J Chory
Journal:  Plant Physiol       Date:  1999-07       Impact factor: 8.340

6.  Changes in the shapes of leaves and flowers upon overexpression of cytochrome P450 in Arabidopsis.

Authors:  G T Kim; H Tsukaya; Y Saito; H Uchimiya
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

7.  Brassinosteroid-insensitive dwarf mutants of Arabidopsis accumulate brassinosteroids.

Authors:  T Noguchi; S Fujioka; S Choe; S Takatsuto; S Yoshida; H Yuan; K A Feldmann; F E Tax
Journal:  Plant Physiol       Date:  1999-11       Impact factor: 8.340

8.  Biosynthetic pathways of brassinolide in Arabidopsis.

Authors:  T Noguchi; S Fujioka; S Choe; S Takatsuto; F E Tax; S Yoshida; K A Feldmann
Journal:  Plant Physiol       Date:  2000-09       Impact factor: 8.340

9.  The Arabidopsis deetiolated2 mutant is blocked early in brassinosteroid biosynthesis.

Authors:  S Fujioka; J Li; Y H Choi; H Seto; S Takatsuto; T Noguchi; T Watanabe; H Kuriyama; T Yokota; J Chory; A Sakurai
Journal:  Plant Cell       Date:  1997-11       Impact factor: 11.277

Review 10.  Control of cell elongation and stress responses by steroid hormones and carbon catabolic repression in plants.

Authors:  K Salchert; R Bhalerao; Z Koncz-Kálmán; C Koncz
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1998-09-29       Impact factor: 6.237

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