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Quarantine ΔMass ✓ Oxidation

FLS

Arabidopsis thaliana

Brassicaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping
Substrate
dihydrokaempferol
PubChem ↗ C1=CC(=CC=C1[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O)O
FLS
ΔMass: -2.0157 Da ketone_formation(-2.0157)
Product
kaempferol
PubChem ↗ C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O

Evidence trail

Excerpts are machine-extracted plain text for biochemical provenance. Follow DOI / PubMed links for the primary literature; publisher figures and PDF images are not displayed here.

Source text excerpt ation; ation; FLS from Arabidopsis thaliana (AT5G08640) expressed in Yarrowia lipolytica; conversion of dihydrokaempferol to kaempferol confirmed by HPLC and LC-MS.

Reaction & quality gates

Mechanism
Ketone formation (-2.02 Da)
Evidence type
In vivo
Confidence
High
Data tier
Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class
Phenylpropanoids
Product class
Phenylpropanoids

Literature & public identifiers

PubMed
PMID:39841399 ↗
DOI
10.1186/s40643-024-00825-w ↗
UniProt
Q9XHG2 ↗
GenBank
NCBI TaxID
3702 ↗

De novo biosynthesis of quercetin in Yarrowia Lipolytica through systematic metabolic engineering for enhanced yield.