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- Name help_outline (S)-eriodictyol Identifier CHEBI:28412 (Beilstein: 92358; CAS: 552-58-9) help_outline Charge 0 Formula C15H12O6 InChIKeyhelp_outline SBHXYTNGIZCORC-ZDUSSCGKSA-N SMILEShelp_outline Oc1cc(O)c2C(=O)C[C@H](Oc2c1)c1ccc(O)c(O)c1 2D coordinates Mol file for the small molecule Search links Involved in 6 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 2-oxoglutarate Identifier CHEBI:16810 (Beilstein: 3664503; CAS: 64-15-3) help_outline Charge -2 Formula C5H4O5 InChIKeyhelp_outline KPGXRSRHYNQIFN-UHFFFAOYSA-L SMILEShelp_outline [O-]C(=O)CCC(=O)C([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 418 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline O2 Identifier CHEBI:15379 (CAS: 7782-44-7) help_outline Charge 0 Formula O2 InChIKeyhelp_outline MYMOFIZGZYHOMD-UHFFFAOYSA-N SMILEShelp_outline O=O 2D coordinates Mol file for the small molecule Search links Involved in 2,648 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline (2R,3R)-dihydroquercetin Identifier CHEBI:17948 (Beilstein: 93548; CAS: 480-18-2) help_outline Charge 0 Formula C15H12O7 InChIKeyhelp_outline CXQWRCVTCMQVQX-LSDHHAIUSA-N SMILEShelp_outline O[C@@H]1[C@H](Oc2cc(O)cc(O)c2C1=O)c1ccc(O)c(O)c1 2D coordinates Mol file for the small molecule Search links Involved in 6 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline CO2 Identifier CHEBI:16526 (Beilstein: 1900390; CAS: 124-38-9) help_outline Charge 0 Formula CO2 InChIKeyhelp_outline CURLTUGMZLYLDI-UHFFFAOYSA-N SMILEShelp_outline O=C=O 2D coordinates Mol file for the small molecule Search links Involved in 980 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline succinate Identifier CHEBI:30031 (Beilstein: 1863859; CAS: 56-14-4) help_outline Charge -2 Formula C4H4O4 InChIKeyhelp_outline KDYFGRWQOYBRFD-UHFFFAOYSA-L SMILEShelp_outline [O-]C(=O)CCC([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 325 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:61088 | RHEA:61089 | RHEA:61090 | RHEA:61091 | |
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| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
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Related reactions help_outline
More general form(s) of this reaction
Publications
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Functional Analysis of Two Flavanone-3-Hydroxylase Genes from Camellia sinensis: A Critical Role in Flavonoid Accumulation.
Han Y., Huang K., Liu Y., Jiao T., Ma G., Qian Y., Wang P., Dai X., Gao L., Xia T.
Flavonoids are major secondary metabolites in <i>Camellia sinensis</i>. Flavanone-3-hydroxylase (F3H) is a key enzyme in flavonoid biosynthesis in plants. However, its role in the flavonoid metabolism in <i>C. sinensis</i> has not been well studied. In this study, we cloned two <i>F3H</i>s from <i ... >> More
Flavonoids are major secondary metabolites in <i>Camellia sinensis</i>. Flavanone-3-hydroxylase (F3H) is a key enzyme in flavonoid biosynthesis in plants. However, its role in the flavonoid metabolism in <i>C. sinensis</i> has not been well studied. In this study, we cloned two <i>F3H</i>s from <i>C. sinensis</i>, named <i>CsF3Ha</i> and <i>CsF3Hb</i>, where <i>CsF3Ha</i> containing 1107 bases encoded 368 amino acids, and <i>CsF3Hb</i> containing 1071 bases encoded 357 amino acids. Enzymatic activity analysis showed both recombinant CsF3H enzymes in <i>Escherichia coli</i> could convert naringenin and eriodictyol into dihydrokaempferol (DHK) and dihydroquercetin (DHQ), respectively. The expression profiles showed that <i>CsF3Ha</i> and <i>CsF3Hb</i> were highly expressed in the tender leaves of tea plants. Under different abiotic stresses, the two <i>CsF3H</i>s were induced remarkably by ultraviolet (UV) radiation, sucrose, and abscisic acid (ABA). In the seeds of <i>CsF3H</i>s transgenic <i>Arabidopsis thaliana</i>, the concentration of most flavonol glycosides and oligomeric proanthocyanidins increased significantly, while the content of monocatechin derivatives decreased. The present study revealed that <i>CsF3H</i>s played critical roles in flavonoid biosynthesis in tea plants. << Less
Genes (Basel) 8:E300-E300(2017) [PubMed] [EuropePMC]
This publication is cited by 1 other entry.
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Flavonol biosynthesis genes and their use in engineering the plant antidiabetic metabolite montbretin A.
Irmisch S., Ruebsam H., Jancsik S., Man Saint Yuen M., Madilao L.L., Bohlmann J.
The plant metabolite montbretin A (MbA) and its precursor mini-MbA are potential new drugs for treating type 2 diabetes. These complex acylated flavonol glycosides only occur in small amounts in the corms of the ornamental plant montbretia (<i>Crocosmia</i> × <i>crocosmiiflora</i>). Our goal is to ... >> More
The plant metabolite montbretin A (MbA) and its precursor mini-MbA are potential new drugs for treating type 2 diabetes. These complex acylated flavonol glycosides only occur in small amounts in the corms of the ornamental plant montbretia (<i>Crocosmia</i> × <i>crocosmiiflora</i>). Our goal is to metabolically engineer <i>Nicotiana benthamiana</i> using montbretia genes to achieve increased production of mini-MbA and MbA. Two montbretia UDP-dependent glycosyltransferases (UGTs), CcUGT1 and CcUGT2, catalyze the formation of the first two pathway-specific intermediates in MbA biosynthesis, myricetin 3-<i>O</i>-rhamnoside and myricetin 3-<i>O</i>-glucosyl rhamnoside. In previous work, expression of these UGTs in <i>N. benthamiana</i> resulted in small amounts of kaempferol glycosides but not myricetin glycosides, suggesting that myricetin was limiting. Here, we investigated montbretia genes and enzymes of flavonol biosynthesis to enhance myricetin formation in <i>N. benthamiana</i> We characterized two flavanone hydroxylases, a flavonol synthase, a flavonoid 3'-hydroxylase (F3'H), and a flavonoid 3'5'-hydroxylase (F3'5'H). Montbretia flavonol synthase converted dihydromyricetin into myricetin. Unexpectedly, montbretia F3'5'H shared higher sequence relatedness with F3'Hs in the CYP75B subfamily of cytochromes P450 than with those with known F3'5'H activity. Transient expression of combinations of montbretia flavonol biosynthesis genes and a montbretia MYB transcription factor in <i>N. benthamiana</i> resulted in availability of myricetin for MbA biosynthesis. Transient coexpression of montbretia flavonol biosynthesis genes combined with <i>CcUGT1</i> and <i>CcUGT2</i> in <i>N. benthamiana</i> resulted in 2 mg g<sup>-1</sup> fresh weight of the MbA pathway-specific compound myricetin 3-<i>O</i>-glucosyl rhamnoside. Additional expression of the montbretia acyltransferase <i>CcAT1</i> led to detectable levels of mini-MbA in <i>N. benthamiana</i>. << Less
Plant Physiol. 180:1277-1290(2019) [PubMed] [EuropePMC]
This publication is cited by 13 other entries.