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


     


Plant Physiology 86:619-622 (1988)
© 1988 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 (124)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Matringe, M.
Right arrow Articles by Scalla, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Matringe, M.
Right arrow Articles by Scalla, R.
Agricola
Right arrow Articles by Matringe, M.
Right arrow Articles by Scalla, R.
Environmental and Stress Physiology

Studies on the Mode of Action of Acifluorfen-Methyl in Nonchlorophyllous Soybean Cells 1

Accumulation of Tetrapyrroles

M. Matringe and R. Scalla

Laboratoire des Herbicides, Institut National de la Recherche Agronomique, BV 1540, 21034 Dijon, France

Phytotoxic effects of the herbicide acifluorfen-methyl on nonchlorophyllous soybean cells were estimated by 86Rb leakage. An action spectrum study showed maximum injury at 350 to 450 nanometers, with lesser activity between 450 and 700 nanometers. Cells treated in the dark with acifluorfen-methyl accumulated fluorescent pigments with the spectral characteristics of protoporphyrin IX. The action spectrum of acifluorfen-methyl matched the absorption spectrum of this tetrapyrrole, and the extent of cellular damage in the light was related to the degree of fluorescent pigment accumulation. We propose that the phytotoxicity of diphenyl ether herbicides could be explained by their ability to cause abnormal accumulations of tetrapyrroles, which in turn induce lethal photooxidative reactions.


1 Supported by a grant from Institut National de la Recherche Agronomique (AIP 4483).




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
J. M. Jez, R. E. Cahoon, and S. Chen
Arabidopsis thaliana Glutamate-Cysteine Ligase: FUNCTIONAL PROPERTIES, KINETIC MECHANISM, AND REGULATION OF ACTIVITY
J. Biol. Chem., August 6, 2004; 279(32): 33463 - 33470.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
J. Papenbrock, H.-P. Mock, R. Tanaka, E. Kruse, and B. Grimm
Role of Magnesium Chelatase Activity in the Early Steps of the Tetrapyrrole Biosynthetic Pathway
Plant Physiology, April 1, 2000; 122(4): 1161 - 1170.
[Abstract] [Full Text]


Home page
Plant Physiol.Home page
I. Lermontova and B. Grimm
Overexpression of Plastidic Protoporphyrinogen IX Oxidase Leads to Resistance to the Diphenyl-Ether Herbicide Acifluorfen
Plant Physiology, January 1, 2000; 122(1): 75 - 84.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J.-M. Camadro and P. Labbe
Cloning and Characterization of the Yeast HEM14 Gene Coding for Protoporphyrinogen Oxidase, the Molecular Target of Diphenyl Ether-type Herbicides
J. Biol. Chem., April 12, 1996; 271(15): 9120 - 9128.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1988 by the American Society of Plant Biologists