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Isoeugenol synthase
Identifiers
EC no. 1.1.1.319
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins

Isoeugenol synthase ( EC 1.1.1.319, IGS1, t-anol/isoeugenol synthase 1) is an enzyme with systematic name eugenol:NADP+ oxidoreductase (coniferyl acetate reducing). [1] [2] [3] This enzyme catalyses the following chemical reaction. [4]

isoeugenol + acetate + NADP+ coniferyl acetate + NADPH + H+

The enzyme acts in the reverse direction.

Dexter et al., 2007 finds that the substrate is coniferyl acetate. [5]

References

  1. ^ Koeduka T, Fridman E, Gang DR, Vassão DG, Jackson BL, Kish CM, Orlova I, Spassova SM, Lewis NG, Noel JP, Baiga TJ, Dudareva N, Pichersky E (June 2006). "Eugenol and isoeugenol, characteristic aromatic constituents of spices, are biosynthesized via reduction of a coniferyl alcohol ester". Proceedings of the National Academy of Sciences of the United States of America. 103 (26): 10128–33. doi: 10.1073/pnas.0603732103. PMC  1502517. PMID  16782809.
  2. ^ Koeduka T, Louie GV, Orlova I, Kish CM, Ibdah M, Wilkerson CG, Bowman ME, Baiga TJ, Noel JP, Dudareva N, Pichersky E (May 2008). "The multiple phenylpropene synthases in both Clarkia breweri and Petunia hybrida represent two distinct protein lineages". The Plant Journal. 54 (3): 362–74. doi: 10.1111/j.1365-313X.2008.03412.x. PMC  2741023. PMID  18208524.
  3. ^ Koeduka T, Baiga TJ, Noel JP, Pichersky E (January 2009). "Biosynthesis of t-anethole in anise: characterization of t-anol/isoeugenol synthase and an O-methyltransferase specific for a C7-C8 propenyl side chain". Plant Physiology. 149 (1): 384–94. doi: 10.1104/pp.108.128066. PMC  2613694. PMID  18987218.
  4. ^ Gupta AK, Schauvinhold I, Pichersky E, Schiestl FP (December 2014). "Eugenol synthase genes in floral scent variation in Gymnadenia species" (PDF). Functional & Integrative Genomics. 14 (4): 779–88. doi: 10.1007/s10142-014-0397-9. hdl: 20.500.11850/91540. PMID  25239559. S2CID  17207240.
  5. ^
    Vogt, Thomas (2010). "Phenylpropanoid Biosynthesis". Molecular Plant. 3 (1): 2–20. doi: 10.1093/mp/ssp106. PMID  20035037. S2CID  39503278.
    This review cites this research.
    Dexter, Richard; Qualley, Anthony; Kish, Christine M.; Ma, Choong Je; Koeduka, Takao; Nagegowda, Dinesh A.; Dudareva, Natalia; Pichersky, Eran; Clark, David (2006-12-07). "Characterization of a petunia acetyltransferase involved in the biosynthesis of the floral volatile isoeugenol". The Plant Journal. 49 (2): 265–275. doi: 10.1111/j.1365-313x.2006.02954.x. hdl: 2027.42/74478. PMID  17241449. S2CID  6714361.

External links