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. 1990 Nov;94(3):1444–1448. doi: 10.1104/pp.94.3.1444

Biosynthesis of the Phytoalexin Pisatin 1

Isoflavone Reduction and Further Metabolism of the Product Sophorol by Extracts of Pisum sativum

Carol L Preisig 1,2,2, John N Bell 1,2,3, Yuejin Sun 1,2, Geza Hrazdina 1,2, David E Matthews 1,2,4, Hans D VanEtten 1,2,5
PMCID: PMC1077396  PMID: 16667851

Abstract

NADPH-dependent reduction of 2′,7-dihydroxy-4′,5′-methylenedioxyisoflavone to the isoflavanone sophorol, a proposed intermediate step in pisatin biosynthesis, was detected in extracts of Pisum sativum. This isoflavone reductase activity was inducible by treatment of pea seedlings with CuCl2. The timing of induction coincided with that of the 6a-hydroxymaackiain 3-O-methyltransferase, which catalyzes the terminal biosynthetic step. Neither enzyme was light inducible. Further NADPH-dependent metabolism of sophorol by extracts of Cucl2-treated seedlings was also observed; three products were radiolabeled when [3H]sophorol was the substrate, one of which is tentatively identified as maackiain.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
  2. Hagmann M. L., Heller W., Grisebach H. Induction of phytoalexin synthesis in soybean. Stereospecific 3,9-dihydroxypterocarpan 6a-hydroxylase from elicitor-induced soybean cell cultures. Eur J Biochem. 1984 Jul 2;142(1):127–131. doi: 10.1111/j.1432-1033.1984.tb08259.x. [DOI] [PubMed] [Google Scholar]
  3. Lamb C. J., Lawton M. A., Dron M., Dixon R. A. Signals and transduction mechanisms for activation of plant defenses against microbial attack. Cell. 1989 Jan 27;56(2):215–224. doi: 10.1016/0092-8674(89)90894-5. [DOI] [PubMed] [Google Scholar]
  4. Matthews D. E., Weiner E. J., Matthews P. S., Vanetten H. D. Role of oxygenases in pisatin biosynthesis and in the fungal degradation of maackiain. Plant Physiol. 1987 Feb;83(2):365–370. doi: 10.1104/pp.83.2.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Osbert I. M., Hammond K. B. Letter: Avoidance of errors in the automated determination of serum enzyme activities by use of a strip-chart recorder. Clin Chem. 1976 Aug;22(8):1411–1412. [PubMed] [Google Scholar]
  6. Preisig C. L., Matthews D. E., Vanetten H. D. Purification and Characterization of S-Adenosyl-l-methionine:6a-Hydroxymaackiain 3-O-Methyltransferase from Pisum sativum. Plant Physiol. 1989 Oct;91(2):559–566. doi: 10.1104/pp.91.2.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Stoessl A. Inermin associated with pisatin in peas inoculated with the fungus Monilinia fructicola. Can J Biochem. 1972 Jan;50(1):107–108. doi: 10.1139/o72-011. [DOI] [PubMed] [Google Scholar]

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