Kaurenolides and fujenoic acids are side products of the gibberellin P450-1 monooxygenase in Gibberella fujikuroi
- PMID: 15081281
- DOI: 10.1016/j.phytochem.2004.02.007
Kaurenolides and fujenoic acids are side products of the gibberellin P450-1 monooxygenase in Gibberella fujikuroi
Abstract
The steps involved in kaurenolide and fujenoic acids biosynthesis, from ent-kauradienoic acid and ent-6alpha,7alpha-dihydroxykaurenoic acid, respectively, are demonstrated in the gibberellin (GA)-deficient Gibberella fujikuroi mutant SG139, which lacks the entire GA-biosynthesis gene cluster, complemented with the P450-1 gene of GA biosynthesis (SG139-P450-1). ent-[2H]Kauradienoic acid was efficiently converted into 7beta-hydroxy[2H]kaurenolide and 7beta,18-dihydroxy[2H]kaurenolide by the cultures while 7beta-hydroxy[2H]kaurenolide was transformed into 7beta,18-dihydroxy[2H]kaurenolide. The limiting step was found to be hydroxylation at C-18. In addition, SG139-P450-1 transformed ent-6alpha,7alpha-dihydroxy[14C4]kaurenoic acid into [14C4]fujenoic acid and [14C4]fujenoic triacid. Fujenal was also converted into the same products but was demonstrated not to be an intermediate in this sequence. All the above reactions were absent in the mutant SG139 and were suppressed in the wild-type strain ACC917 by disruption of the P450-1 gene. Kaurenolide and fujenoic acids synthesis were associated with the microsomal fraction and showed an absolute requirement for NADPH or NADH, all properties of cytochrome P450 monooxygenases. Only 7beta-hydroxy[14C4]kaurenolide synthesis and not further 18-hydroxylation was detected in the microsomal fraction. The substrates for the P450-1 monooxygenase, ent-kaurenoic acid and [2H]GA12, efficiently inhibited kaurenolide synthesis with I50 values of 3 and 6 microM, respectively. Both substrates also inhibited ent-6alpha,7alpha-dihydroxy[14C4]kaurenoic acid metabolism by SG139-P450-1. Conversely, [14C4]GA14 synthesis from [14C4]GA12-aldehyde was inhibited by ent-[2H]kauradienoic acid and fujenal with I50 values of 10 and 30 microM, respectively. These results demonstrate that kaurenolides and seco-ring B kaurenoids are formed by the P450-1 monooxygenase (GA14 synthase) of G. fujikuroi and are thus side products that probably result from stabilization of radical intermediates involved in GA14 synthesis.
Similar articles
-
The P450-1 gene of Gibberella fujikuroi encodes a multifunctional enzyme in gibberellin biosynthesis.Proc Natl Acad Sci U S A. 2001 May 8;98(10):5838-43. doi: 10.1073/pnas.091096298. Epub 2001 Apr 24. Proc Natl Acad Sci U S A. 2001. PMID: 11320210 Free PMC article.
-
The microbiological transformation of 7alpha-hydroxy-ent-kaur-16-ene derivatives by Gibberella fujikuroi.Phytochemistry. 2007 Jun;68(11):1557-63. doi: 10.1016/j.phytochem.2007.03.024. Epub 2007 Apr 30. Phytochemistry. 2007. PMID: 17467750
-
The P450-4 gene of Gibberella fujikuroi encodes ent-kaurene oxidase in the gibberellin biosynthesis pathway.Appl Environ Microbiol. 2001 Aug;67(8):3514-22. doi: 10.1128/AEM.67.8.3514-3522.2001. Appl Environ Microbiol. 2001. PMID: 11472927 Free PMC article.
-
Biochemical and molecular analyses of gibberellin biosynthesis in fungi.Biosci Biotechnol Biochem. 2006 Mar;70(3):583-90. doi: 10.1271/bbb.70.583. Biosci Biotechnol Biochem. 2006. PMID: 16556972 Review.
-
Biosynthesis of gibberellins in Gibberella fujikuroi: biomolecular aspects.Appl Microbiol Biotechnol. 1999 Sep;52(3):298-310. doi: 10.1007/s002530051524. Appl Microbiol Biotechnol. 1999. PMID: 10531641 Review.
Cited by
-
The remarkable structural diversity achieved in ent-Kaurane Diterpenes by fungal biotransformations.Molecules. 2014 Feb 10;19(2):1856-86. doi: 10.3390/molecules19021856. Molecules. 2014. PMID: 24518806 Free PMC article. Review.
-
Isolation and characterization of the gibberellin biosynthetic gene cluster in Sphaceloma manihoticola.Appl Environ Microbiol. 2008 Sep;74(17):5325-39. doi: 10.1128/AEM.00694-08. Epub 2008 Jun 20. Appl Environ Microbiol. 2008. PMID: 18567680 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
Miscellaneous