Category:FLI

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[[FLIA1AGS0001|Daidzin]] is its glycosylated form in soy beans. Daidzein (aglycon) is contained in fermented beans.
 
[[FLIA1AGS0001|Daidzin]] is its glycosylated form in soy beans. Daidzein (aglycon) is contained in fermented beans.
Medicarpin is the major phytoalexin in alfalfa ([[Species:Medicago|''Medicago sativa'']]), synthesized by bacterial infection.
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Medicarpin is the major phytoalexin in alfalfa ([[Species:Medicago|''Medicago sativa'']]) and clover ([[Species:Trifolium|Trifolium spp.]]), synthesized by bacterial infection<ref>Guo L, Dixon RA, Paiva NL (1994) Conversion of vestitone to medicarpin in alfalfa (Medicago sativa L.) is catalyzed by two independent enzymes. Identification, purification, and characterization of vestitone reductase and 7,2'-dihydroxy-4'-methoxyisoflavanol dehydratase. ''J Biol Chem'' 269:22372-22378</ref>.
 
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大豆に含まれるのは、[[FLIA1AGS0001|ダイジン]]というダイゼインの配糖体。豆を醗酵させるとアグリコンであるダイゼインになる。
 
大豆に含まれるのは、[[FLIA1AGS0001|ダイジン]]というダイゼインの配糖体。豆を醗酵させるとアグリコンであるダイゼインになる。
メディカルパンはアルファルファ([[Species:Medicago|''Medicago sativa'']])が微生物の感染に対抗して生産する防御物質として知られる。
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メディカルパンはアルファルファ([[Species:Medicago|''Medicago sativa'']])やクローバー([[Species:Trifolium|Trifolium spp.]])が微生物の感染に対抗して生産する防御物質として知られる。
 
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<references/>
 
<references/>

Revision as of 13:50, 19 August 2010

Isoflavonoid


Flavonoid Top Molecule Index Author Index Journals Structure Search Food New Input

Upper classes : FL Flavonoid

Contents

Overview

2nd Class
FLIA Isoflavone
Flia.png
FLIB Isoflavanone
Flib.png
FLIC Isoflavan
Flic.png
FLID Pterocarpane
Flid.png
FLIE Coumestan
Flie.png
FLIF Rotenoid
Flif.png
FLIG Coumaranochromone
Flig.png
FLIH 3-Arylcoumarin
Flih.png
FLII 2-Arylbenzofuran
Flii.png
FLIJ alpha-Methoxynbenzoin
Flij.png

The discovery of isoflavonoid was in 1842, when Reinsch and Hlasiwetz obtained ononin from the roots of spiny restharrow (Ononis spinosa L.)[1]. Its structure was later determined by Baker et al. as Formononetin 7-O-glucoside (1933). Since then, most isoflavonoids have been found in Fabaceae (bean family).
First isoflavonoid found in non-bean family was iridin from the rhizomes of Iris florentina (Iridaceae)[2]. The first structural identification was Prunetin from Prunus species in 1910 by Finnemore. Major isoflavonoids in iris are isoflavones and their O-glycosides. In iris, isoflavonoids are produced only in the rhizomes except for a trace of coumaranochromones in leaves [3].

  1. Reinsch H, Repert. Pharm. 26:12-31, 1842; Reinsch H, Repert. Pharm. 28:18-25, 1842; Hlasiwetz H, J. Prakt. Chem. 65:419-450, 1855; Hlasiwetz H, Sitzungsber. Kais. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 15:142-168, 1855
  2. de Laire G and Tiemann F, Chem. Ber., 26:2010, 1893
  3. Iwashita T, Ootani S: Flavonoids of the genus Iris: structures, distribution and function (review). Ann. Tsukuba Bot. Gard. 17:147-183 (in Japanese)

Representative Names

daidzein
FLIA1ANS0002.png
genistein
FLIAAANS0001.png
coumestrol
FLIE1ANS0001.png
Medicarpin
FLID1ANS0001.png

Daidzin is its glycosylated form in soy beans. Daidzein (aglycon) is contained in fermented beans. Medicarpin is the major phytoalexin in alfalfa (Medicago sativa) and clover (Trifolium spp.), synthesized by bacterial infection[1].

  1. Guo L, Dixon RA, Paiva NL (1994) Conversion of vestitone to medicarpin in alfalfa (Medicago sativa L.) is catalyzed by two independent enzymes. Identification, purification, and characterization of vestitone reductase and 7,2'-dihydroxy-4'-methoxyisoflavanol dehydratase. J Biol Chem 269:22372-22378

Biosynthesis

This pathway is said to exist as an enzyme complex at ER membrane. [1]

liquiritigenin
FL2F1ANS0001.png

Arrow00r35.png
IFS
daidzein
FLIA1ANS0002.png

Arrow00r35.png
IOMT
formononetin
FLIA1ANS0001.png

Arrow00r35.png
I2'H + IFR
vestitone
FLIB1LNS0002.png

Arrow00r35.png
VR + DMID
medicarpin
FLID1ANS0001.png


Structural Genes (continued from Flavonoid)
Abbrev. Name Origin Information
IFS isoflavone synthase cytochrome P450 oxygenase family [2]

[3] [4]

Use both liquiritigenin and naringenin as substrates to produce genistein and daidzein, respectively.
IOMT isoflavone O-methyltransferase
I2'H isoflavone 2'-hydroxylase cytochrome P450 oxygenase family[5]
IFR isoflavone reductase
VR vestitone reductase
DMID 7,2'-dihydroxy,4'-methyxyisoflavanol dehydratase
  1. Hrazdina G: Compartmentation in aromatic metabolism. In HA Stafford, RK Ibrahim, eds, Recent Advances in Phytochemistry. Plenum Press, New York, 1992 pp 1–23
  2. Akashi T, Aoki T, Ayabe S: Cloning and functional expression of a cytochrome P450 cDNA encoding 2-hydroxyisoflavanone synthase involved in biosynthesis of the isoflavonoid skeleton in licorice. Plant Physiol 1999 121:821-828
  3. Steele CL, Gijzen M, Qutob D, Dixon RA: Molecular characterization of the enzyme catalyzing the aryl migration reaction of isoflavonoid biosynthesis in soybean. Arch Biochem Biophys 1999 367: 146–150
  4. Jung W, Yu O, Sze-Mei CL, O’Keefe DP, Odell J, Fader G, McGonigle B: Identification and expression of isoflavone synthase, the key enzyme for biosynthesis of isoflavones in legumes. Nat Biotechnol 2000 18: 208–213
  5. Akashi T, Aoki T, Ayabe S: CYP81E1, a cytochrome P450 cDNA of licorice (Glycyrrhiza echinata L.), encodes isoflavone 29-hydroxylase. 1998 Biochem Biophys Res Comm 251: 67–70

Database statistics

Major Plant Families

The number in each family is counted as the number of genera (not species) listed in our registered references. Each reference record is accessible by clicking the link in compound pages. The taxonomy follows the APG-II classification. For details (or if the figure is broken), visit this page.

各科のカウントは種名でなく文献に記載された属名の数です。文献は代謝物ページのリンクからたどれ、分類はAPG-IIです。左の図が表示されない場合はここをクリックしてください。

Subcategories

This category has the following 10 subcategories, out of 10 total.

F

  • [×] FLIA(empty)
  • [×] FLIB(empty)
  • [×] FLIC(empty)
  • [×] FLID(empty)

F cont.

  • [×] FLIE(empty)
  • [×] FLIF(empty)
  • [×] FLIG(empty)
  • [×] FLIH(empty)

F cont.

  • [×] FLII(empty)
  • [×] FLIJ(empty)
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