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Isoflavonoid synthase

From Wikipedia, the free encyclopedia
Isoflavonoid synthase
Identifiers
EC no.1.14.14.87
Databases
BRENDAenzyme data
ExPASyNiceZyme view
KEGGenzyme entry
MetaCycmetabolic pathway
Rheareactions
PDB structuresRCSB PDB PDBe PDBsum
Search
PMCarticles
PubMedarticles
NCBIproteins

2-hydroxyisoflavanone synthase (EC 1.14.14.87, CYT93C, IFS, isoflavonoid synthase) is an enzyme with systematic name liquiritigenin,NADPH:oxygen oxidoreductase (hydroxylating, aryl migration).[1][2] It catalyses a rearrangement reaction which converts flavonoids into isoflavones, for example:

+ NADPH + H+
 
 
O2
H2O
Rightward reaction arrow with minor substrate(s) from top left and minor product(s) to top right
 
 
 
2D representation of the chemical structure of Q27123131.
2,4',7-trihydroxyisoflavanone
 

The product 2,4',7-trihydroxyisoflavanone is unstable and loses water, either spontaneously or by the action of 2-hydroxyisoflavanone dehydratase, giving daidzein.[3]

2D representation of the chemical structure of Q27123131.
2,4',7-trihydroxyisoflavanone
 
 
H2O
Rightward reaction arrow with minor product(s) to top right
 
 
 

The enzyme can also act on naringenin, leading to the isoflavone genistein.{[4]

 
 
 
Rightward reaction arrow
 
 
 
2,4',5,7-tetrahydroxyisoflavanone
 
 
 
 
Rightward reaction arrow
 
 
 

Isoflavonoid synthase is a cytochrome P450 protein containing heme. It requires a partner cytochrome P450 reductase for functional expression. This uses nicotinamide adenine dinucleotide phosphate (NADPH).[5]

References

[edit]
  1. Hashim MF, Hakamatsuka T, Ebizuka Y, Sankawa U (October 1990). "Reaction mechanism of oxidative rearrangement of flavanone in isoflavone biosynthesis". FEBS Letters. 271 (1–2): 219–22. Bibcode:1990FEBSL.271..219H. doi:10.1016/0014-5793(90)80410-k. PMID 2226805.
  2. Sawada Y, Ayabe S (May 2005). "Multiple mutagenesis of P450 isoflavonoid synthase reveals a key active-site residue". Biochemical and Biophysical Research Communications. 330 (3): 907–13. Bibcode:2005BBRC..330..907S. doi:10.1016/j.bbrc.2005.03.053. PMID 15809082.
  3. Hakamatsuka, Takashi; Mori, Kazumi; Ishida, Shinichi; Ebizuka, Yutaka; Sankawa, Ushio (1998). "Purification of 2-Hydroxyisoflavanone Dehydratase from the Cell Cultures of Pueraria Lobata". Phytochemistry. 49 (2): 497–505. doi:10.1016/S0031-9422(98)00266-0.
  4. Enzyme 1.14.14.87 at KEGG Pathway Database.
  5. Sawada Y, Kinoshita K, Akashi T, Aoki T, Ayabe S (September 2002). "Key amino acid residues required for aryl migration catalysed by the cytochrome P450 2-hydroxyisoflavanone synthase". The Plant Journal. 31 (5): 555–64. doi:10.1046/j.1365-313x.2002.01378.x. PMID 12207646.
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