Access the full text.
Sign up today, get DeepDyve free for 14 days.
J. Gilder, J. Cronshaw (1974)
A BIOCHEMICAL AND CYTOCHEMICAL STUDY OF ADENOSINE TRIPHOSPHATASE ACTIVITY IN THE PHLOEM OF NICOTIAN A TABACUMThe Journal of Cell Biology, 60
(1988)
Phloem transport - with emphasis on loading and unloading
R. Serrano (1989)
Structure and Function of Plasma Membrane ATPase, 40
K. Esau (1960)
Anatomy of seed plants
(1989)
Molecular cloning and sequence of a cDNA encoding the plasma membrane proton pump ( H - ATPase ) ofArabidopsis thaliana
J. Langdale, M. Metzler, T. Nelson (1987)
The argentia mutation delays normal development of photosynthetic cell-types in Zea mays.Developmental biology, 122 1
(1988)
Movements of ions across roots
L. Williams, J. Hall (1987)
ATPase and Proton Pumping Activities in Cotyledons and other Phloem-Containing Tissues2Ricinus communisJournal of Experimental Botany, 38
D. Baker, J. Hall (1988)
Solute transport in plant cells and tissues.
M. Weisenseel, A. Dorn, L. Jaffe (1979)
Natural H Currents Traverse Growing Roots and Root Hairs of Barley (Hordeum vulgare L.).Plant physiology, 64 3
J. Hanson (1978)
Application of the chemiosmotic hypothesis to ion transport across the root.Plant physiology, 62 3
E. Winter-Sluiter, A. Läuchli, D. Kramer (1977)
Cytochemical Localization of K-stimulated Adenosine Triphosphatase Activity in Xylem Parenchyma Cells of Barley Roots.Plant physiology, 60 6
Jeffrey Harper, Terry Surowy, Michael Sussman (1989)
Molecular cloning and sequence of cDNA encoding the plasma membrane proton pump (H+-ATPase) of Arabidopsis thaliana.Proceedings of the National Academy of Sciences of the United States of America, 86 4
K. Stanley, J. Luzio (1984)
Construction of a new family of high efficiency bacterial expression vectors: identification of cDNA clones coding for human liver proteins.The EMBO Journal, 3
R. Serrano (1988)
H+-ATPase from plasma membranes of Saccharomyces cerevisiae and Avena sativa roots: purification and reconstitution.Methods in enzymology, 157
(1988)
Subcellular localization of macromolecules by microscopy
G. Griffiths, K. Simons, G. Warren, K. Tokuyasu (1983)
Immunoelectron microscopy using thin, frozen sections: application to studies of the intracellular transport of Semliki Forest virus spike glycoproteins.Methods in enzymology, 96
J. Pardo, R. Serrano (1989)
Structure of a plasma membrane H+-ATPase gene from the plant Arabidopsis thaliana.The Journal of biological chemistry, 264 15
D. Clarkson, J. Hanson (1986)
Proton Fluxes and the Activity of a Stelar Proton Pump in Onion RootsJournal of Experimental Botany, 37
D. Katz, Michael Sussman, R. Mierzwa, Ray Evert (1988)
Cytochemical localization of ATPase activity in oat roots localizes a plasma membrane-associated soluble phosphatase, not the proton pump.Plant physiology, 86 3
S. BlakeMilan, K. Johnston, G. Russell-Jones, E. Gotschlich (1984)
A rapid, sensitive method for detection of alkaline phosphatase-conjugated anti-antibody on Western blots.Analytical biochemistry, 136 1
U. Lüttge, N. Higinbotham (1979)
Transport in Plants
(1977)
Ion transport in the xylem
M. Boutry, B. Michelet, A. Goffeau (1989)
Molecular cloning of a family of plant genes encoding a protein homologous to plasma membrane H+-translocating ATPases.Biochemical and biophysical research communications, 162 2
Abstract The localization of plasma membrane H+-ATPase has been studied at the optical microscope level utilizing frozen and paraffin sections of Avena sativa and Pisum sativum, specific anti-ATPase polyclonal antibody, and second antibody coupled to alkaline phosphatase. In leaves and stems the ATPase is concentrated at the phloem, supporting the notion that it generates the driving force for phloem loading. In roots the ATPase is concentrated at both the periphery (rootcap and epidermis) and at the central cylinder, including endodermis and vascular cells. This supports a `two-pump' mechanism for ion absorption, involving active uptake at the epidermis, symplast transport across the cortex, and active efflux at the xylem. The low ATPase content of root meristem and elongation zone may explain the observed transorgan H+ currents, which leave nongrowing parts and enter growing tips. 1 Present address: Instituto de Recursos Naturales y Agrobiologia, Avda. Reina Mercedes s/n, 41080 Sevilla, Spain. This content is only available as a PDF. © 1990 American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
Plant Physiology – Oxford University Press
Published: Aug 1, 1990
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.