Completion of Tricin Biosynthesis Pathway in Rice: Cytochrome P450 75B4 Is a Unique Chrysoeriol 5′-Hydroxylase. Issue 4 (16th June 2015)
- Record Type:
- Journal Article
- Title:
- Completion of Tricin Biosynthesis Pathway in Rice: Cytochrome P450 75B4 Is a Unique Chrysoeriol 5′-Hydroxylase. Issue 4 (16th June 2015)
- Main Title:
- Completion of Tricin Biosynthesis Pathway in Rice: Cytochrome P450 75B4 Is a Unique Chrysoeriol 5′-Hydroxylase
- Authors:
- Lam, Pui Ying
Liu, Hongjia
Lo, Clive - Abstract:
- Abstract : Biosynthesis of tricin requires specific hydroxylation catalyzed by a phylogenetically distinct hydroxylase. Abstract: Flavones are ubiquitously accumulated in land plants, but their biosynthesis in monocots remained largely elusive until recent years. Recently, we demonstrated that the rice ( Oryza sativa ) cytochrome P450 enzymes CYP93G1 and CYP93G2 channel flavanones en route to flavone O -linked conjugates and C -glycosides, respectively. In tricin, the 3′, 5′-dimethoxyflavone nucleus is formed before O -linked conjugations. Previously, flavonoid 3′, 5′-hydroxylases belonging to the CYP75A subfamily were believed to generate tricetin from apigenin for 3′, 5′- O -methylation to form tricin. However, we report here that CYP75B4 a unique flavonoid B-ring hydroxylase indispensable for tricin formation in rice. A CYP75B4 knockout mutant is tricin deficient, with unusual accumulation of chrysoeriol (a 3′-methoxylated flavone). CYP75B4 functions as a bona fide flavonoid 3′-hydroxylase by restoring the accumulation of 3′-hydroxylated flavonoids in Arabidopsis ( Arabidopsis thaliana ) transparent testa7 mutants and catalyzing in vitro 3′-hydroxylation of different flavonoids. In addition, overexpression of both CYP75B4 and CYP93G1 (a flavone synthase II) in Arabidopsis resulted in tricin accumulation. Specific 5′-hydroxylation of chrysoeriol to selgin by CYP75B4 was further demonstrated in vitro. The reaction steps leading to tricin biosynthesis are then reconstructedAbstract : Biosynthesis of tricin requires specific hydroxylation catalyzed by a phylogenetically distinct hydroxylase. Abstract: Flavones are ubiquitously accumulated in land plants, but their biosynthesis in monocots remained largely elusive until recent years. Recently, we demonstrated that the rice ( Oryza sativa ) cytochrome P450 enzymes CYP93G1 and CYP93G2 channel flavanones en route to flavone O -linked conjugates and C -glycosides, respectively. In tricin, the 3′, 5′-dimethoxyflavone nucleus is formed before O -linked conjugations. Previously, flavonoid 3′, 5′-hydroxylases belonging to the CYP75A subfamily were believed to generate tricetin from apigenin for 3′, 5′- O -methylation to form tricin. However, we report here that CYP75B4 a unique flavonoid B-ring hydroxylase indispensable for tricin formation in rice. A CYP75B4 knockout mutant is tricin deficient, with unusual accumulation of chrysoeriol (a 3′-methoxylated flavone). CYP75B4 functions as a bona fide flavonoid 3′-hydroxylase by restoring the accumulation of 3′-hydroxylated flavonoids in Arabidopsis ( Arabidopsis thaliana ) transparent testa7 mutants and catalyzing in vitro 3′-hydroxylation of different flavonoids. In addition, overexpression of both CYP75B4 and CYP93G1 (a flavone synthase II) in Arabidopsis resulted in tricin accumulation. Specific 5′-hydroxylation of chrysoeriol to selgin by CYP75B4 was further demonstrated in vitro. The reaction steps leading to tricin biosynthesis are then reconstructed as naringenin → apigenin → luteolin → chrysoeriol → selgin → tricin. Hence, chrysoeriol, instead of tricetin, is an intermediate in tricin biosynthesis. CYP75B4 homologous sequences are highly conserved in Poaceae, and they are phylogenetically distinct from the canonical CYP75B flavonoid 3′-hydroxylase sequences. Recruitment of chrysoeriol-specific 5′-hydroxylase activity by an ancestral CYP75B sequence may represent a key event leading to the prevalence of tricin-derived metabolites in grasses and other monocots today. … (more)
- Is Part Of:
- Plant physiology. Volume 168:Issue 4(2015)
- Journal:
- Plant physiology
- Issue:
- Volume 168:Issue 4(2015)
- Issue Display:
- Volume 168, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 168
- Issue:
- 4
- Issue Sort Value:
- 2015-0168-0004-0000
- Page Start:
- 1527
- Page End:
- 1536
- Publication Date:
- 2015-06-16
- Subjects:
- Plant physiology -- Periodicals
Botany -- Periodicals
Periodicals
Electronic journals
571.2 - Journal URLs:
- https://academic.oup.com/plphys/issue ↗
http://www.plantphysiol.org/ ↗
http://www.jstor.org/journals/00320889.html ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=69 ↗
http://www-us.ebsco.com/online/direct.asp?JournalID=101725 ↗
http://www.oxfordjournals.org/ ↗ - DOI:
- 10.1104/pp.15.00566 ↗
- Languages:
- English
- ISSNs:
- 0032-0889
- 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:
- 22698.xml