The Peroxidative Cleavage of Kaempferol Contributes to the Biosynthesis of the Benzenoid Moiety of Ubiquinone in Plants. Issue 12 (14th November 2018)
- Record Type:
- Journal Article
- Title:
- The Peroxidative Cleavage of Kaempferol Contributes to the Biosynthesis of the Benzenoid Moiety of Ubiquinone in Plants. Issue 12 (14th November 2018)
- Main Title:
- The Peroxidative Cleavage of Kaempferol Contributes to the Biosynthesis of the Benzenoid Moiety of Ubiquinone in Plants
- Authors:
- Soubeyrand, Eric
Johnson, Timothy S.
Latimer, Scott
Block, Anna
Kim, Jeongim
Colquhoun, Thomas A.
Butelli, Eugenio
Martin, Cathie
Wilson, Mark A.
Basset, Gilles J. - Abstract:
- Abstract : Genetic and biochemical evidence shows that Arabidopsis and tomato can derive the ubiquinone precursor 4-hydroxybenzoate from the B-ring of kaempferol. Abstract: Land plants possess the unique capacity to derive the benzenoid moiety of the vital respiratory cofactor, ubiquinone (coenzyme Q), from phenylpropanoid metabolism via β-oxidation of p -coumarate to form 4-hydroxybenzoate. Approximately half of the ubiquinone in plants comes from this pathway; the origin of the rest remains enigmatic. In this study, Phe-[ Ring - 13 C6 ] feeding assays and gene network reconstructions uncovered a connection between the biosynthesis of ubiquinone and that of flavonoids in Arabidopsis ( Arabidopsis thaliana ). Quantification of ubiquinone in Arabidopsis and tomato ( Solanum lycopersicum ) mutants in flavonoid biosynthesis pinpointed the corresponding metabolic branch-point as lying between flavanone-3-hydroxylase and flavonoid-3′-hydroxylase. Further isotopic labeling and chemical rescue experiments demonstrated that the B-ring of kaempferol is incorporated into ubiquinone. Moreover, heme-dependent peroxidase activities were shown to be responsible for the cleavage of B-ring of kaempferol to form 4-hydroxybenzoate. By contrast, kaempferol 3-β-d -glucopyranoside, dihydrokaempferol, and naringenin were refractory to peroxidative cleavage. Collectively, these data indicate that kaempferol contributes to the biosynthesis of a vital respiratory cofactor, resulting in anAbstract : Genetic and biochemical evidence shows that Arabidopsis and tomato can derive the ubiquinone precursor 4-hydroxybenzoate from the B-ring of kaempferol. Abstract: Land plants possess the unique capacity to derive the benzenoid moiety of the vital respiratory cofactor, ubiquinone (coenzyme Q), from phenylpropanoid metabolism via β-oxidation of p -coumarate to form 4-hydroxybenzoate. Approximately half of the ubiquinone in plants comes from this pathway; the origin of the rest remains enigmatic. In this study, Phe-[ Ring - 13 C6 ] feeding assays and gene network reconstructions uncovered a connection between the biosynthesis of ubiquinone and that of flavonoids in Arabidopsis ( Arabidopsis thaliana ). Quantification of ubiquinone in Arabidopsis and tomato ( Solanum lycopersicum ) mutants in flavonoid biosynthesis pinpointed the corresponding metabolic branch-point as lying between flavanone-3-hydroxylase and flavonoid-3′-hydroxylase. Further isotopic labeling and chemical rescue experiments demonstrated that the B-ring of kaempferol is incorporated into ubiquinone. Moreover, heme-dependent peroxidase activities were shown to be responsible for the cleavage of B-ring of kaempferol to form 4-hydroxybenzoate. By contrast, kaempferol 3-β-d -glucopyranoside, dihydrokaempferol, and naringenin were refractory to peroxidative cleavage. Collectively, these data indicate that kaempferol contributes to the biosynthesis of a vital respiratory cofactor, resulting in an extraordinary metabolic arrangement where a specialized metabolite serves as a precursor for a primary metabolite. Evidence is also provided that the ubiquinone content of tomato fruits can be manipulated via deregulation of flavonoid biosynthesis. … (more)
- Is Part Of:
- The Plant Cell. Volume 30:Issue 12(2018)
- Journal:
- The Plant Cell
- Issue:
- Volume 30:Issue 12(2018)
- Issue Display:
- Volume 30, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 30
- Issue:
- 12
- Issue Sort Value:
- 2018-0030-0012-0000
- Page Start:
- 2910
- Page End:
- 2921
- Publication Date:
- 2018-11-14
- Journal URLs:
- http://www.oxfordjournals.org/ ↗
- DOI:
- 10.1105/tpc.18.00688 ↗
- Languages:
- English
- ISSNs:
- 1040-4651
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16317.xml