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Pathway Description
Gibberellin Biosynthesis II (Early C-13 Hydroxylation)
Arabidopsis thaliana
Category:
Metabolite Pathway
Sub-Category:
Metabolic
Created: 2017-03-02
Last Updated: 2025-02-08
Gibberellins (GAs) are a large class of tetracyclic diterpenoid plant hormones that regulate numerous growth and developmental processes, such as seed germination, organ elongation, and flowering induction. All known gibberellins share an ent-gibberellane skeleton and follow the same synthesis pathway. Biosynthesis begins in the plasmids via the terpenoid pathway and finishes in the endoplasmic reticulum and cytosol where they undergo modification until a biologically-active form is reached (GA1, GA3, GA4, or GA7). Gibberellin biosynthesis via early C-13 hydroxylation occurs in the cytosol and converts the inactive GA12 to the active GA1. First, the predicted enzyme gibberellin 13-hydroxylase (coloured orange in the image) is theorized to catalyze the conversion of gibberellin A12 into gibberellin A53. Second, gibberellin 20-oxidase catalyzes the conversion of gibberellin A53 into gibberellin A44 open lactone, requiring Fe2+ and L-ascorbate as cofactors. The main fate of gibberellin A44 open lactone is conversion into gibberellin A19 which is catalyzed by the not yet elucidated enzyme gibberellin-44 dioxygenase, requiring Fe3+ as a cofactor. The secondary fate of gibberellin A44 open lactone is conversion into gibberellin A38 which is catalyzed by gibberellin 3-oxidase, requiring Fe2+ and L-ascorbate as cofactors. The main fate of gibberellin A19 is conversion into gibberellin A20 and its secondary fate is conversion into gibberellin A17. These reactions' enzymes have not yet been elucidated and are referred to as simply gibberellin oxidase for reference purposes. Last, gibberellin 3-oxidase converts gibberellin A20 into the active gibberellin A1. It requires Fe2+ and L-ascorbate as cofactors.
References
Gibberellin Biosynthesis II (Early C-13 Hydroxylation) References
Yamaguchi S: Gibberellin metabolism and its regulation. Annu Rev Plant Biol. 2008;59:225-51. doi: 10.1146/annurev.arplant.59.032607.092804.
Pubmed: 18173378
Phillips AL, Ward DA, Uknes S, Appleford NE, Lange T, Huttly AK, Gaskin P, Graebe JE, Hedden P: Isolation and expression of three gibberellin 20-oxidase cDNA clones from Arabidopsis. Plant Physiol. 1995 Jul;108(3):1049-57. doi: 10.1104/pp.108.3.1049.
Pubmed: 7630935
Xu YL, Li L, Wu K, Peeters AJ, Gage DA, Zeevaart JA: The GA5 locus of Arabidopsis thaliana encodes a multifunctional gibberellin 20-oxidase: molecular cloning and functional expression. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6640-4. doi: 10.1073/pnas.92.14.6640.
Pubmed: 7604047
Hisamatsu T, King RW, Helliwell CA, Koshioka M: The involvement of gibberellin 20-oxidase genes in phytochrome-regulated petiole elongation of Arabidopsis. Plant Physiol. 2005 Jun;138(2):1106-16. doi: 10.1104/pp.104.059055. Epub 2005 May 27.
Pubmed: 15923331
Mitchum MG, Yamaguchi S, Hanada A, Kuwahara A, Yoshioka Y, Kato T, Tabata S, Kamiya Y, Sun TP: Distinct and overlapping roles of two gibberellin 3-oxidases in Arabidopsis development. Plant J. 2006 Mar;45(5):804-18. doi: 10.1111/j.1365-313X.2005.02642.x.
Pubmed: 16460513
Matsushita A, Furumoto T, Ishida S, Takahashi Y: AGF1, an AT-hook protein, is necessary for the negative feedback of AtGA3ox1 encoding GA 3-oxidase. Plant Physiol. 2007 Mar;143(3):1152-62. doi: 10.1104/pp.106.093542. Epub 2007 Feb 2.
Pubmed: 17277098
Chiang HH, Hwang I, Goodman HM: Isolation of the Arabidopsis GA4 locus. Plant Cell. 1995 Feb;7(2):195-201. doi: 10.1105/tpc.7.2.195.
Pubmed: 7756830
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