Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1978 Feb;61(2):226–230. doi: 10.1104/pp.61.2.226

Regulation of Phytoalexin Synthesis in Jackbean Callus Cultures

Stimulation of Phenylalanine Ammonia-Lyase and o-Methyltransferase 1

David L Gustine 1, Robert T Sherwood 1, Carroll P Vance 2
PMCID: PMC1091837  PMID: 16660265

Abstract

Jackbean, Canavalia ensiformis (L.), callus tissues synthesized the phytoalexin, medicarpin (3-hydroxy-9-methoxypterocarpan), when treated with spore suspensions of Pithomyces chartarum (Berk. and Curt.) M. B. Ellis, a nonpathogen of jackbean. Medicarpin was isolated from treated callus tissue and identified by its ultraviolet and mass spectra. The minimum spore concentration found to elicit medicarpin synthesis after 26 hours was 1 × 105 spores/ml; levels of medicarpin in callus tissue increased linearly up to 1 × 107 spores/ml, indicating that the recognition sites for presumed elicitors were not saturated. Medicarpin was first detected in callus treated with 1 × 107 spores/ml, 6 to 12 hours after application, and the concentration reached a maximum at 48 hours, slowly declining thereafter to 72 hours. In callus treated with 3.15 mm HgCl2, medicarpin concentrations were also maximum by 48 hours. Phenylalanine ammonia-lyase (EC 4.3.1.5) activity increased 2-fold in spore-treated callus after 36 hours. Isoliquiritigenin, daidzein, and genistein o-methyltransferase (EC 2.1.1.6) activities were increased 3- to 4-fold in treated callus. Caffeic acid and naringenin were more efficient substrates for o-methyltransferase activity than the other flavonoids or apigenin, but there was no increase in these o-methyltransferase activities in spore-treated callus. The phytoalexin response in this callus tissue culture system compares well with natural plant systems and should be an excellent system for investigating regulation of phytoalexin synthesis.

Full text

PDF
226

Selected References

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

  1. Ebel J., Ayers A. R., Albersheim P. Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans. Plant Physiol. 1976 May;57(5):775–779. doi: 10.1104/pp.57.5.775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Keen N. T. Specific elicitors of plant phytoalexin production: detenninants of race specificity in pathogens? Science. 1975 Jan 10;187(4171):74–75. doi: 10.1126/science.187.4171.74. [DOI] [PubMed] [Google Scholar]
  3. Krasnuk M., Witham F. H., Tegley J. R. Cytokinins extracted from pinto bean fruit. Plant Physiol. 1971 Sep;48(3):320–324. doi: 10.1104/pp.48.3.320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  5. Poulton J., Grisebach H., Ebel J., Schaller-Hekeler B., Hahlbrock K. Two distinct S-adenosyl-L-methionine:3,4-dithydric phenol 3-O-methyltransferases of phenylpropanoid metabolism in soybean cell suspension cultures. Arch Biochem Biophys. 1976 Mar;173(1):301–305. doi: 10.1016/0003-9861(76)90263-0. [DOI] [PubMed] [Google Scholar]
  6. Vance C. P., Sherwood R. T. Regulation of lignin formation in reed canarygrass in relation to disease resistance. Plant Physiol. 1976 Jun;57(6):915–919. doi: 10.1104/pp.57.6.915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Wengenmayer H., Ebel J., Grisebach H. Purification and properties of a S-adenosylmethionine: isoflavone 4'-O-methyltransferase from cell suspension cultures of Cicer arietinum L. Eur J Biochem. 1974 Dec 16;50(1):135–143. doi: 10.1111/j.1432-1033.1974.tb03881.x. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES