spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


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 Google Scholar
Google Scholar
Right arrow Articles by HENRY, E. W.
Right arrow Articles by JENSEN, T. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by HENRY, E. W.
Right arrow Articles by JENSEN, T. E.

Journal of Cell Science, Vol 13, 591-601, Copyright © 1973 by Company of Biologists

Submitted on December 5, 1972

Peroxidases in Tobacco Abscission Zone Tissue

I. Fine-Structural Localization in Cell Walls During Ethylene-Induced Abscission

E. W. HENRY 1 and T. E. JENSEN 1

1 Department of Biological Sciences, Herbert H. Lehman College of the City University of New York, Bronx, New York 10468, U.S.A.

The fine-structural localization of peroxidases during ethylene-induced abscission of flower pedicels of Nicotiana tabacum L. cv. ‘Little Turkish’ has been investigated. Peroxidase activity has been localized in both the cell walls and intercellular spaces of ethylene-treated flower pedicels which were fixed in glutaraldehyde, incubated in diaminobenzidine (DAB) medium with postfixation in 2% osmium tetroxide. Peroxidase staining is present in the cell walls and intercellular spaces of control tissue but is not as intense as in ethylene-treated tissue. Increased peroxidase staining is evident in the intercellular spaces and cell walls after 2 h of exposure to ethylene and increases in intensity between 2 and 5 h. At 5 h, ethylene-induced abscission occurs. Fine-structural investigations revealed prominent staining in the middle-lamellar and peripheral areas of the cell walls in ethylene-treated tissue. The peroxidase staining appears to be due to peroxidase as prior incubation with potassium cyanide gives a marked reduction in the staining reaction. Incubation of the ethylene-exposed tissue in aminotriazole, a specific inhibitor of catalase, does not reduce peroxidase staining, except in the microbodies, which reportedly contain catalase.

Submitted on December 5, 1972







© The Company of Biologists Ltd 1973