Plant Physiol. Drug Metab Dispos
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 77:591-601 (1985)
© 1985 American Society of Plant Biologists

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (109)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hahn, M. G.
Right arrow Articles by Grisebach, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hahn, M. G.
Right arrow Articles by Grisebach, H.
Agricola
Right arrow Articles by Hahn, M. G.
Right arrow Articles by Grisebach, H.
Articles

Quantitative Localization of the Phytoalexin Glyceollin I in Relation to Fungal Hyphae in Soybean Roots Infected with Phytophthora megasperma f. sp. glycinea 1

Michael G. Hahn2, Anne Bonhoff and Hans Grisebach

Lehrstuhl für Biochemie der Pflanzen, Biologisches Institut II der Universität Freiburg, Schänzlestrasse 1, D-7800 Freiburg im Breisgau, Federal Republic of Germany

A radioimmunoassay specific for glyceollin I was used to quantitate this phytoalexin in roots of soybean (Glycine max [L.] Merr. cv Harosoy 63) after infection with zoospores of either race 1 (incompatible) or race 3 (compatible) of Phytophthora megasperma Drechs. f. sp. glycinea Kuan and Erwin. The sensitivity of the radioimmunoassay and an inmmunofluorescent stain for hyphae permitted quantitation of phytoalexin and localization of the fungus in alternate serial cryotome sections from the same root. The incompatible interaction was characterized by extensive fungal colonization of the root cortex which was limited to the immediate vicinity of the inoculation site. Glyceollin I was first detected in extracts of whole roots 2 hours after infection, and phytoalexin content rose rapidly thereafter. Significant concentrations of glyceollin I were present at the infection site in cross-sections (42 micrometers thick) of such roots by 5 hours, and exceeded 0.6 micromoles per milliliter (EC90in vitro for glyceollin I) by 8 hours after infection. Longitudinal sectioning (14 micrometers thick) showed that glyceollin I accumulated particularly in the epidermal cell layers, but also was present in the root cortex at inhibitory concentrations. No hyphae were observed in advance of detectable levels of the phytoalexin and, in most roots, glyceollin I concentrations dropped sharply at the leading edge of the infection. In contrast, the compatible interaction was characterized by extensive unchecked fungal colonization of the root stele, with lesser growth in the rest of the root. Only small amounts of glyceollin I were detected in whole root extracts during the first 14 hours after infection. Measurable amounts of glyceollin I were detected only in occasional cross-sections of such roots 11 and 14 hours after infection. The phytoalexin was present at inhibitory concentrations in the epidermal cell layers, but the inhibitory zone did not extend appreciably into the cortex. Altogether, these data support the hypothesis that the accumulation of glyceollin I is an important early response of soybean roots to infection by P. megasperma, but may not be solely responsible for inhibition of fungal growth in the resistant response.


2 Current address: Plant Biology Laboratory, The Salk Institute for Biological Studies, P.O. Box 85800, San Diego, CA 92138-9216. Supported by a Research Fellowship from the Alexander von Humboldt-Stiftung.

1 Supported by the Deutsche Forschungsgemeinschaft (SFB 46) and the Badische Anilin and Sodafabrik (Ludwigshafen, F.R.G.).




This article has been cited by other articles:


Home page
Plant Physiol.Home page
K. Sasaki, K. Mito, K. Ohara, H. Yamamoto, and K. Yazaki
Cloning and Characterization of Naringenin 8-Prenyltransferase, a Flavonoid-Specific Prenyltransferase of Sophora flavescens
Plant Physiology, March 1, 2008; 146(3): 1075 - 1084.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
T. L. Graham, M. Y. Graham, S. Subramanian, and O. Yu
RNAi Silencing of Genes for Elicitation or Biosynthesis of 5-Deoxyisoflavonoids Suppresses Race-Specific Resistance and Hypersensitive Cell Death in Phytophthora sojae Infected Tissues
Plant Physiology, June 1, 2007; 144(2): 728 - 740.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
J. K. C. Rose, K.-S. Ham, A. G. Darvill, and P. Albersheim
Molecular Cloning and Characterization of Glucanase Inhibitor Proteins: Coevolution of a Counterdefense Mechanism by Plant Pathogens
PLANT CELL, June 1, 2002; 14(6): 1329 - 1345.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
J. P. Morrissey and A. E. Osbourn
Fungal Resistance to Plant Antibiotics as a Mechanism of Pathogenesis
Microbiol. Mol. Biol. Rev., September 1, 1999; 63(3): 708 - 724.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1985 by the American Society of Plant Biologists