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


     


Plant Physiology 90:1267-1270 (1989)
© 1989 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 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 Google Scholar
Google Scholar
Right arrow Articles by Babbs, C. F.
Right arrow Articles by Coolbaugh, R. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Babbs, C. F.
Right arrow Articles by Coolbaugh, R. C.
Agricola
Right arrow Articles by Babbs, C. F.
Right arrow Articles by Coolbaugh, R. C.
Environmental and Stress Physiology

Lethal Hydroxyl Radical Production in Paraquat-Treated Plants 1

Charles F. Babbs, Jo Ann Pham and Ronald C. Coolbaugh

Biomedical Engineering Center, Purdue University, West Lafayette, Indiana 47907, Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907

Bipyridinium herbicides, including paraquat and diquat, are believed to act by generating highly reactive, oxygen-centered free radicals within chloroplasts when treated plants are exposed to sunlight. This hypothesis has not yet been confirmed by direct chemical measurements of specific free radicals. We studied paraquat-treated plants using a new method able to detect and quantify formation of highly reactive and deleterious hydroxyl radicals (HO*), in which dimethyl sulfoxide (DMSO) is used as a molecular probe. DMSO is oxidized by HO* to form the stable, nonradical compound, methane sulfinic acid, which can be easily extracted from plant tissue and measured spectrophotometrically. Initial experiments revealed formation of extraordinary numbers of hydroxyl radicals in light-exposed, paraquat + DMSO-treated plants, equivalent at least to the cumulative number of HO* radicals per gram of fresh tissue that would be produced by 10,000 rads of gamma irradiation. This appears to be the greatest production of hydroxyl radicals yet observed in a biological system and is quite sufficient to explain the rapid death of top growth in paraquat-treated plants.


1 This work was supported by a Focused Giving Grant from Johnson & Johnson, and by grant HL-35996 from the National Heart, Lung, and Blood Institute, U.S. Public health Service, Bethesda, MD.




This article has been cited by other articles:


Home page
Mol PlantHome page
D. Qiu, J. Xiao, W. Xie, H. Liu, X. Li, L. Xiong, and S. Wang
Rice Gene Network Inferred from Expression Profiling of Plants Overexpressing OsWRKY13, a Positive Regulator of Disease Resistance
Mol Plant, May 1, 2008; 1(3): 538 - 551.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
R. E. Rodriguez, A. Lodeyro, H. O. Poli, M. Zurbriggen, M. Peisker, J. F. Palatnik, V. B. Tognetti, H. Tschiersch, M.-R. Hajirezaei, E. M. Valle, et al.
Transgenic Tobacco Plants Overexpressing Chloroplastic Ferredoxin-NADP(H) Reductase Display Normal Rates of Photosynthesis and Increased Tolerance to Oxidative Stress
Plant Physiology, February 1, 2007; 143(2): 639 - 649.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Laloi, M. Stachowiak, E. Pers-Kamczyc, E. Warzych, I. Murgia, and K. Apel
Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana
PNAS, January 9, 2007; 104(2): 672 - 677.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
C. Miyake, Y. Shinzaki, M. Nishioka, S. Horiguchi, and K.-I. Tomizawa
Photoinactivation of Ascorbate Peroxidase in Isolated Tobacco Chloroplasts: Galdieria partita APX Maintains the Electron Flux through the Water-Water Cycle in Transplastomic Tobacco Plants
Plant Cell Physiol., February 1, 2006; 47(2): 200 - 210.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. J. Serrato, J. M. Perez-Ruiz, M. C. Spinola, and F. J. Cejudo
A Novel NADPH Thioredoxin Reductase, Localized in the Chloroplast, Which Deficiency Causes Hypersensitivity to Abiotic Stress in Arabidopsis thaliana
J. Biol. Chem., October 15, 2004; 279(42): 43821 - 43827.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. A. Belinky, N. Flikshtein, S. Lechenko, S. Gepstein, and C. G. Dosoretz
Reactive Oxygen Species and Induction of Lignin Peroxidase in Phanerochaete chrysosporium
Appl. Envir. Microbiol., November 1, 2003; 69(11): 6500 - 6506.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
M. Broin and P. Rey
Potato Plants Lacking the CDSP32 Plastidic Thioredoxin Exhibit Overoxidation of the BAS1 2-Cysteine Peroxiredoxin and Increased Lipid Peroxidation in Thylakoids under Photooxidative Stress
Plant Physiology, July 1, 2003; 132(3): 1335 - 1343.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
M. Jiang and J. Zhang
Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves
J. Exp. Bot., December 1, 2002; 53(379): 2401 - 2410.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
M. Broin, S. Cuine, F. Eymery, and P. Rey
The Plastidic 2-Cysteine Peroxiredoxin Is a Target for a Thioredoxin Involved in the Protection of the Photosynthetic Apparatus against Oxidative Damage
PLANT CELL, June 1, 2002; 14(6): 1417 - 1432.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
G. Langenkamper, N. Manac'h, M. Broin, S. Cuine, N. Becuwe, M. Kuntz, and P. Rey
Accumulation of plastid lipid-associated proteins (fibrillin/CDSP34) upon oxidative stress, ageing and biotic stress in Solanaceae and in response to drought in other species
J. Exp. Bot., July 1, 2001; 52(360): 1545 - 1554.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
P. Schopfer, C. Plachy, and G. Frahry
Release of Reactive Oxygen Intermediates (Superoxide Radicals, Hydrogen Peroxide, and Hydroxyl Radicals) and Peroxidase in Germinating Radish Seeds Controlled by Light, Gibberellin, and Abscisic Acid
Plant Physiology, April 1, 2001; 125(4): 1591 - 1602.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
F. Bouvier, R. A. Backhaus, and B. Camara
Induction and Control of Chromoplast-specific Carotenoid Genes by Oxidative Stress
J. Biol. Chem., November 13, 1998; 273(46): 30651 - 30659.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
I. Iturbe-Ormaetxe, P. R. Escuredo, C. Arrese-Igor, and M. Becana
Oxidative Damage in Pea Plants Exposed to Water Deficit or Paraquat
Plant Physiology, January 1, 1998; 116(1): 173 - 181.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1989 by the American Society of Plant Biologists