KEGG   PATHWAY: zof00905
Entry
zof00905                    Pathway                                
Name
Brassinosteroid biosynthesis - Zingiber officinale (ginger)
Description
Brassinosteroids are a group of plant steroid hormones that regulate growth and development. More than fifty naturally occurring brassinosteroids have been identified in a wide range of plant species. The most abundant and widely occurring brassinosteroids are C28 steroids, and among them brassinolide (BL) is the most biologically active. Plants have multiple pathways for biosynthesis of BL, which are derived from the steroid biosynthetic pathway. Two pathways from campestanol to castasterone (CS), C6 oxidation and the late-C6 oxidation pathways, operate in many plants. Another branching pathway, the early-C22 oxidation pathway, was demonstrated using a brassinosteroid-deficient mutant of Arabidopsis thaliana. Recently, a new shortcut pathway from campesterol to 6-deoxotyphasterol was demonstrated by a functional analysis of cytochrome P450 monooxygenases responsible for brassinosteroid biosynthesis. Thus, at least four pathways are involved in the biosynthesis of CS, and CS is further metabolized to BL by lactonization of the B ring.
Class
Metabolism; Metabolism of terpenoids and polyketides
Pathway map
zof00905  Brassinosteroid biosynthesis
zof00905

Module
zof_M00371  Castasterone biosynthesis, campesterol => castasterone [PATH:zof00905]
Other DBs
GO: 0016132
Organism
Zingiber officinale (ginger) [GN:zof]
Gene
122026256  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122026454  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122027838  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122028682  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122030413  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122030415  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122008713  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122032511  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122011363  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122034945  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122013395  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122014363  cytochrome P450 90B2-like isoform X1 [KO:K09587] [EC:1.14.14.178]
122015895  cytochrome P450 90B2-like [KO:K09587] [EC:1.14.14.178]
122045268  cytochrome P450 724B1-like [KO:K12639] [EC:1.14.14.178]
122027304  cytochrome P450 90A3-like [KO:K09588] [EC:1.14.19.79]
122028724  cytochrome P450 90A3-like [KO:K09588] [EC:1.14.19.79]
122036630  cytochrome P450 90A3-like [KO:K09588] [EC:1.14.19.79]
122037555  cytochrome P450 90A4-like [KO:K09588] [EC:1.14.19.79]
122017271  steroid 5-alpha-reductase DET2-like [KO:K09591] [EC:1.3.1.22]
122008808  steroid 5-alpha-reductase DET2-like [KO:K09591] [EC:1.3.1.22]
121972536  steroid 5-alpha-reductase DET2-like [KO:K09591] [EC:1.3.1.22]
122044032  3-epi-6-deoxocathasterone 23-monooxygenase CYP90C1-like [KO:K12637] [EC:1.14.14.147]
121976062  cytochrome P450 90D2-like [KO:K12638] [EC:1.14.14.147]
122017716  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
121975689  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
122049062  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
122034502  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
122012212  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
122039599  cytochrome P450 85A1-like [KO:K09590] [EC:1.14.14.179]
121988825  cytochrome P450 90D2-like [KO:K09589] [EC:1.14.-.-]
122004838  cytochrome P450 90D2-like [KO:K09589] [EC:1.14.-.-]
121997768  cytochrome P450 90D2-like isoform X1 [KO:K09589] [EC:1.14.-.-]
122035986  cytochrome P450 90D2-like [KO:K09589] [EC:1.14.-.-]
121971591  cytochrome P450 90D2-like [KO:K09589] [EC:1.14.-.-]
122043939  trimethyltridecatetraene synthase-like [KO:K20623]
122029259  trimethyltridecatetraene synthase-like [KO:K20623]
122048512  dimethylnonatriene synthase-like [KO:K20623]
122049368  trimethyltridecatetraene synthase-like [KO:K20623]
122012681  trimethyltridecatetraene synthase-like [KO:K20623]
121983816  trimethyltridecatetraene synthase-like [KO:K20623]
122015188  trimethyltridecatetraene synthase-like [KO:K20623]
122038289  trimethyltridecatetraene synthase-like [KO:K20623]
122038290  trimethyltridecatetraene synthase-like [KO:K20623]
122039949  trimethyltridecatetraene synthase-like [KO:K20623]
121988860  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
121988888  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
122005602  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
122008125  cytochrome P450 734A6-like isoform X1 [KO:K15639] [EC:1.14.-.-]
122049602  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
121997814  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
122001310  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
122015402  cytochrome P450 734A6-like isoform X1 [KO:K15639] [EC:1.14.-.-]
122038767  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
122040224  cytochrome P450 734A6-like [KO:K15639] [EC:1.14.-.-]
Compound
C01789  Campesterol
C08814  Brassinolide
C15784  Campest-4-en-3beta-ol
C15785  Campest-4-en-3-one
C15786  5alpha-Campestan-3-one
C15787  Campestanol
C15788  6alpha-Hydroxycampestanol
C15789  6-Oxocampestanol
C15790  Cathasterone
C15791  Teasterone
C15792  3-Dehydroteasterone
C15793  Typhasterol
C15794  Castasterone
C15795  22alpha-Hydroxy-campesterol
C15796  (22S)-22-Hydroxycampest-4-en-3-one
C15797  22alpha-Hydroxy-5alpha-campestan-3-one
C15798  6-Deoxocathasterone
C15799  6-Deoxoteasterone
C15800  3-Dehydro-6-deoxoteasterone
C15801  6-Deoxotyphasterol
C15802  6-Deoxocastasterone
C15803  6alpha-Hydroxycastasterone
C16251  3-epi-6-Deoxocathasterone
C16252  (22R,23R)-22,23-Dihydroxycampesterol
C16253  (22R,23R)-22,23-Dihydroxy-campest-4-en-3-one
C17733  7-Oxateasterone
C17735  7-Oxatyphasterol
C19873  26-Hydroxycastasterone
C19874  26-Hydroxybrassinolide
Reference
  Authors
Koshiba K, Kamiya Y.
  Title
[Atarasii Syokubutuhorumon no Kagaku] (In Japanese)
  Journal
Koudansya saientific:199-138 (2002)
Reference
  Authors
Fukuda H, Matida Y, Kamiya Y, Kakimoto T.
  Title
[Shinpan Syokubutuhorumon no Sigunarudentatu] (In Japanese)
  Journal
Syujyunsya:165-186 (2004)
Reference
  Authors
Shimada Y, Goda H, Nakamura A, Takatsuto S, Fujioka S, Yoshida S.
  Title
Organ-specific expression of brassinosteroid-biosynthetic genes and distribution of endogenous brassinosteroids in Arabidopsis.
  Journal
Plant Physiol 131:287-97 (2003)
DOI:10.1104/pp.013029
Reference
  Authors
Choe, S.
  Title
Brassinosteroid biosynthesis and inactivation.
  Journal
Physiol Plant 126:539-548 (2006)
DOI:10.1111/j.1399-3054.2006.00681.x
Reference
  Authors
Ohnishi T, Szatmari AM, Watanabe B, Fujita S, Bancos S, Koncz C, Lafos M, Shibata K, Yokota T, Sakata K, Szekeres M, Mizutani M
  Title
C-23 hydroxylation by Arabidopsis CYP90C1 and CYP90D1 reveals a novel shortcut in brassinosteroid biosynthesis.
  Journal
Plant Cell 18:3275-88 (2006)
DOI:10.1105/tpc.106.045443
Reference
  Authors
Bishop GJ
  Title
Refining the plant steroid hormone biosynthesis pathway.
  Journal
Trends Plant Sci 12:377-80 (2007)
DOI:10.1016/j.tplants.2007.07.001
Reference
  Authors
Nomura T, Kushiro T, Yokota T, Kamiya Y, Bishop GJ, Yamaguchi S
  Title
The last reaction producing brassinolide is catalyzed by cytochrome P-450s, CYP85A3 in tomato and CYP85A2 in Arabidopsis.
  Journal
J Biol Chem 280:17873-9 (2005)
DOI:10.1074/jbc.M414592200
Reference
  Authors
Katsumata T, Hasegawa A, Fujiwara T, Komatsu T, Notomi M, Abe H, Natsume M, Kawaide H
  Title
Arabidopsis CYP85A2 catalyzes lactonization reactions in the biosynthesis of 2-deoxy-7-oxalactone brassinosteroids.
  Journal
Biosci Biotechnol Biochem 72:2110-7 (2008)
DOI:10.1271/bbb.80192
Reference
  Authors
Tanabe S, Ashikari M, Fujioka S, Takatsuto S, Yoshida S, Yano M, Yoshimura A, Kitano H, Matsuoka M, Fujisawa Y, Kato H, Iwasaki Y
  Title
A novel cytochrome P450 is implicated in brassinosteroid biosynthesis via the characterization of a rice dwarf mutant, dwarf11, with reduced seed length.
  Journal
Plant Cell 17:776-90 (2005)
DOI:10.1105/tpc.104.024950
Reference
  Authors
Hong Z, Ueguchi-Tanaka M, Umemura K, Uozu S, Fujioka S, Takatsuto S, Yoshida S, Ashikari M, Kitano H, Matsuoka M
  Title
A rice brassinosteroid-deficient mutant, ebisu dwarf (d2), is caused by a loss of function of a new member of cytochrome P450.
  Journal
Plant Cell 15:2900-10 (2003)
DOI:10.1105/tpc.014712
Related
pathway
zof00100  Steroid biosynthesis
KO pathway
ko00905   
LinkDB

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