Plant Physiol. Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 74:681-686 (1984)
© 1984 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 CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Servaites, J. C.
Right arrow Articles by Torisky, R. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Servaites, J. C.
Right arrow Articles by Torisky, R. S.
Agricola
Right arrow Articles by Servaites, J. C.
Right arrow Articles by Torisky, R. S.
Articles

Activation State of Ribulose Bisphosphate Carboxylase in Soybean Leaves 1

Jerome C. Servaites and Rebecca S. Torisky

Department of Biology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061

Conditions for extraction and assay of ribulose-1,5-bisphophate carboxylase present in an in vivo active form (initial activity) and an inactive form able to be activated by Mg2+ and CO2 (total activity) were examined in leaves of soybean, Glycine max (L.) Merr. cv Will. Total activity was highest after extracts had preincubated in NaHCO3 (5 millimolar saturating) and Mg2+ (5 millimolar optimal) for 5 minutes at 25°C or 30 minutes at 0°C before assay. Initial activity was about 70% of total activity. Kact (Mg2+) and Kact (CO2) were approximately 0.3 millimolar and 36 micromolar, respectively. The carry-over of endogenous Mg2+ in the leaf extract was sufficient to support considerable catalytic activity. While Mg2+ was essential for both activation and catalysis, Mg2+ levels greater than 5 millimolar were increasingly inhibitory of catalysis. Similar inhibition by high Mg2+ was also observed in filtered, centrifuged, or desalted extracts and partially purified enzyme. Activities did not change upon storage of leaves for up to 4 hours in ice water or liquid nitrogen before homogenization, but were about 20% higher in the latter. Activities were also stable for up to 2 hours in leaf extracts stored at 0°C. Initial activity quickly deactivated at 25°C in the absence of high CO2. Total activity slowly declined irreversibly upon storage of leaf homogenate at 25°C.


1 Supported by the Science and Education Administration of the United States Department of Agriculture under Grant 59-2511-0-1-520-0 from the Competitive Research Grants Office and the Virginia Agricultural Experiment Station, Hatch Project 612459.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1984 by the American Society of Plant Biologists