Plant Physiol. Bio-Rad Microplate Reader
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 63:908-915 (1979)
© 1979 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 Freyssinet, G.
Right arrow Articles by Schiff, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Freyssinet, G.
Right arrow Articles by Schiff, J. A.
Agricola
Right arrow Articles by Freyssinet, G.
Right arrow Articles by Schiff, J. A.
Articles

Events Surrounding the Early Development of Euglena Chloroplasts

14. Biosynthesis of Cytochrome c-552 in Wild Type and Mutant Cells 1

Georges Freyssinet2, Gary C. Harris3, Maimon Nasatir4 and Jerome A. Schiff5

a Institute for Photobiology of Cells and Organelles, Brandeis University, Waltham, Massachusetts 02154

Lack of a suitable assay has thwarted attempts to measure cytochrome c-552 in dark-grown wild type cells of Euglena gracilis var. bacillaris in mutants and in other situations where the concentrations are low. Purification methods are described based on electrofocusing which provide a cytochrome c-552 preparation homogeneous enough to elicit a single reactive antibody in rabbits; this antibody is then used as a specific and sensitive assay for cytochrome c-552. Dark-grown cells of wild type and of mutants O1BS, O2BX, G1BU and P1BXL (which make normal sized chloroplasts with abnormal internal structure in the light) have 0.02 to 0.1 x 10–11 micromoles of cytochrome c-552 per cell, 10 to 150 times less than light-grown cells. Light-grown cells of these mutants and of wild type show a ratio of chlorophyll to cytochrome of about 300 (mole to mole). Cytochrome c-552 is undetectable in dark-grown Y1BXD, Y3BUD, and W34ZUD which cannot carry plastid development beyond the proplastid in light; the light-grown cells of these mutants have levels of cytochrome similar to or lower than dark-grown wild type cells. Cytochrome c-552 is undetectable in light- and dark-grown mutants in which plastid DNA is undetectable (such as Y2BUL, W3BUL, W8BHL, and W10BSmL) consistent with the view, but not proving, that this molecule may be coded, at least in part, in plastid DNA. During light-induced chloroplast development in resting cells, cytochrome c-552 formation behaves in all respects like chlorophyll except that the dark-grown cells contain low amounts of the cytochrome c-552 but lack chlorophyll. Thus, both cytochrome c-552 and chlorophyll show the same lag period even when the length is changed by nutritional manipulation; preillumination largely eliminates the lag in the formation of both molecules, cycloheximide and streptomycin both inhibit the biosynthesis of chlorophyll and cytochrome c-552 in the same manner, and the formation of both during chloroplast development is strictly light-dependent. It is shown that chloroplasts isolated from Euglena by methods thought to give intact organelles, lack 95% of the cytochrome c-552; this and the loss of similar molecules may explain why these isolated chloroplasts are not photosynthetically active.


2 Supported in part by the European Molecular Biology Organization and by the French Foreign Office. Present address: Département de Biologie Générale et Appliquée, Université Lyon I, 69621 Villeurbanne, France.

3 Present address: Department of Biology, Wellesley College, Wellesley, Mass. 02181.

Part of this work was carried out under the auspices of the Experimental Marine Botany Program, Marine Biological Laboratory, Woods Hole, Mass. where G. C. H. was a summer postdoctoral research associate of the steps toward independence program.

4 Present address: Department of Biology, University of Toledo, Toledo, Ohio 43601.

5 Abraham and Etta Goodman Professor of Biology; to whom reprint requests should be directed.

1 Supported by Grants GM14595 from the National Institutes of Health and PCM76-21486 from the National Science Foundation.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY THE PLANT CELL
Copyright © 1979 by the American Society of Plant Biologists