Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 85:928-933 (1987)
© 1987 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 Pfanz, H.
Right arrow Articles by Heber, U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pfanz, H.
Right arrow Articles by Heber, U.
Agricola
Right arrow Articles by Pfanz, H.
Right arrow Articles by Heber, U.
Environmental and Stress Physiology

Flux of SO2 into Leaf Cells and Cellular Acidification by SO21

Hardy Pfanz, Enrico Martinoia, Otto-Ludwig Lange and Ulrich Heber

Institute of Botany and Pharmaceutical Biology, University of Würzburg, Mittlerer Dallenbergweg 64, 8700 Würzburg, Federal Republic of Germany

A comparison of fluxes of SO2 from the atmosphere into leaves with fluxes across biomembranes revealed that, apart from the cuticle, the main barrier to SO2 entry into leaves are the stomates. SO2 fluxes into leaves can be calculated with an accuracy sufficient for many purposes on the assumption that the intracellular SO2 concentration is zero. SO2 entering green leaf cells is trapped in the cytoplasm. In the light, the products formed in its reaction with water are processed particularly in the chloroplasts. Flux of SO2 to the acidic central vacuole of leaf cells is insignificant. Intracellular acidification of barley mesophyll protoplasts by SO2 was measured by the uptake of 14C-labeled 5,5-dimethyl-oxazolidine-2,4-dione. The measured acidification was similar to the acidification calculated from known buffer capacities and the rate of SO2 influx when the H+/SO2 ratio was assumed to be 2. A comparison of photosynthesis inhibition by SO2 with calculated acidification revealed different mechanisms of inhibition at low and at high concentrations of SO2. At very low concentrations, inhibition by SO2 was even smaller than expected from calculated acidification. The data suggest that, if acidification cannot be compensated by pH-stabilizing cellular mechanisms, it is a main factor of SO2 toxicity at low SO2 levels. At high levels of SO2, anion toxicity and/or radical formation during oxidation of SO2 to sulfate may play a large role in inhibition.


1 Supported by a grant from the Bayerische Forschungsgruppe Forsttoxikologie and from the Projektgruppe Bayern zur Erforschung der Wirkung von Umweltschadstoffen (PBWU). It was performed within the research program of the Forschergruppe Ökophysiologie of the University of Würzburg.




This article has been cited by other articles:


Home page
Plant Physiol.Home page
S. Youssefian, M. Nakamura, E. Orudgev, and N. Kondo
Increased Cysteine Biosynthesis Capacity of Transgenic Tobacco Overexpressing an O-Acetylserine(thiol) Lyase Modifies Plant Responses to Oxidative Stress
Plant Physiology, July 1, 2001; 126(3): 1001 - 1011.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1987 by the American Society of Plant Biologists