Metabolomic and genetic analyses of flavonol synthesis in Arabidopsis thaliana support the in vivo involvement of leucoanthocyanidin dioxygenase

被引:107
作者
Stracke, Ralf [4 ]
De Vos, Ric C. H. [1 ,2 ]
Bartelniewoehner, Lutz [4 ]
Ishihara, Hirofumi [4 ]
Sagasser, Martin [4 ]
Martens, Stefan [3 ]
Weisshaar, Bernd [4 ]
机构
[1] Plant Res Int, NL-6700 AA Wageningen, Netherlands
[2] Ctr Biosyst Genom, NL-6700 AB Wageningen, Netherlands
[3] Univ Marburg, Inst Pharmaceut Biol, D-35037 Marburg, Germany
[4] Univ Bielefeld, Chair Genome Res, D-33594 Bielefeld, Germany
关键词
Arabidopsis; Dihydroflavonol; Flavonoid biosynthesis; Flavonol synthase; Leucoanthocyanidin dioxygenase; PHENYLPROPANOID BIOSYNTHESIS; ANTHOCYANIDIN SYNTHASE; FUNCTIONAL EXPRESSION; TRANSCRIPTION FACTOR; PETUNIA-HYBRIDA; FLAVANONE; 3-BETA-HYDROXYLASE; DIFFERENTIAL REGULATION; CONSERVED HISTIDINE; MASS-SPECTROMETRY; ESCHERICHIA-COLI;
D O I
10.1007/s00425-008-0841-y
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Flavonol synthase (FLS) (EC-number 1.14.11.23), the enzyme that catalyses the conversion of flavonols into dihydroflavonols, is part of the flavonoid biosynthesis pathway. In Arabidopsis thaliana, this activity is thought to be encoded by several loci. In addition to the FLAVONOL SYNTHASE1 (FLS1) locus that has been confirmed by enzyme activity assays, loci displaying similarity of the deduced amino acid sequences to FLS1 have been identified. We studied the putative A. thaliana FLS gene family using a combination of genetic and metabolite analysis approaches. Although several of the FLS gene family members are expressed, only FLS1 appeared to influence flavonoid biosynthesis. Seedlings of an A. thaliana fls1 null mutant (fls1-2) show enhanced anthocyanin levels, drastic reduction in flavonol glycoside content and concomitant accumulation of glycosylated forms of dihydroflavonols, the substrate of the FLS reaction. By using a leucoanthocyanidin dioxygenase (ldox) fls1-2 double mutant, we present evidence that the remaining flavonol glycosides found in the fls1-2 mutant are synthesized in planta by the FLS-like side activity of the LDOX enzyme.
引用
收藏
页码:427 / 445
页数:19
相关论文
共 63 条
[1]   BANYULS, a novel negative regulator of flavonoid biosynthesis in the Arabidopsis seed coat [J].
Albert, S ;
Delseny, M ;
Devic, M .
PLANT JOURNAL, 1997, 11 (02) :289-299
[2]  
[Anonymous], 2006, The science of flavonoids
[3]   Altering expression of cinnamic acid 4-hydroxylase in transgenic plants provides evidence for a feedback loop at the entry point into the phenylpropanoid pathway [J].
Blount, JW ;
Korth, KL ;
Masoud, SA ;
Rasmussen, S ;
Lamb, C ;
Dixon, RA .
PLANT PHYSIOLOGY, 2000, 122 (01) :107-116
[4]   L-PHENYLALANINE AMMONIA-LYASE FROM PHASEOLUS-VULGARIS - MODULATION OF THE LEVELS OF ACTIVE ENZYME BY TRANS-CINNAMIC ACID [J].
BOLWELL, GP ;
CRAMER, CL ;
LAMB, CJ ;
SCHUCH, W ;
DIXON, RA .
PLANTA, 1986, 169 (01) :97-107
[5]   High-flavonol tomatoes resulting from the heterologous expression of the maize transcription factor genes LC and C1 [J].
Bovy, A ;
de Vos, R ;
Kemper, M ;
Schijlen, E ;
Pertejo, MA ;
Muir, S ;
Collins, G ;
Robinson, S ;
Verhoeyen, M ;
Hughes, S ;
Santos-Buelga, C ;
van Tunen, A .
PLANT CELL, 2002, 14 (10) :2509-2526
[6]  
BRITSCH L, 1981, Z NATURFORSCH C, V36, P742
[7]   MOLECULAR CHARACTERIZATION OF FLAVANONE 3-BETA-HYDROXYLASES - CONSENSUS SEQUENCE, COMPARISON WITH RELATED ENZYMES AND THE ROLE OF CONSERVED HISTIDINE-RESIDUES [J].
BRITSCH, L ;
DEDIO, J ;
SAEDLER, H ;
FORKMANN, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 217 (02) :745-754
[8]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[9]   Elucidation of active site residues of Arabidopsis thaliana flavonol synthase provides a molecular platform for engineering flavonols [J].
Chua, Chun Song ;
Biermann, Damela ;
Goo, Kian Sim ;
Sim, Tiow-Suan .
PHYTOCHEMISTRY, 2008, 69 (01) :66-75
[10]   Structural studies on 2-oxoglutarate oxygenases and related double-stranded β-helix fold proteins [J].
Clifton, Ian J. ;
McDonough, Michael A. ;
Ehrismann, Dominic ;
Kershaw, Nadia J. ;
Granatino, Nicolas ;
Schofield, Christopher J. .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2006, 100 (04) :644-669