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Open AccessJournal ArticleDOI

CHLOROPLAST STRUCTURE AND FUNCTION IN ac-20, A MUTANT STRAIN OF CHLAMYDOMONAS REINHARDI : III. Chloroplast Ribosomes and Membrane Organization

Ursula Goodenough, +1 more
- 01 Mar 1970 - 
- Vol. 44, Iss: 3, pp 547-562
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TLDR
These results, combined with earlier studies of the photosynthetic properties of the mutant strain, suggest that proper membrane organization, Photosystem II activity, and ribulose-1,5-diphosphate carboxylase formation are dependent on the presence of chloroplast ribosomes.
Abstract
The fine structure of the ac-20 strain of Chlamydomonas reinhardi is described. Cells grown mixotrophically in the presence of acetate have a highly disordered chloroplast membrane organization and usually lack pyrenoids. Chloroplast ribosome levels are only 5–10% of wild-type levels. Cells grown phototrophically without acetate possess more chloroplast ribosomes and have more normal membrane and pyrenoid organization. Chloroplast ribosome levels rise rapidly when cells are transferred from acetate to minimal medium, whereas membrane reorganization occurs only after a lag. These results, combined with earlier studies of the photosynthetic properties of the mutant strain, suggest that proper membrane organization, Photosystem II activity, and ribulose-1,5-diphosphate carboxylase formation are dependent on the presence of chloroplast ribosomes. Other chloroplast components tested are unaffected by a 10-fold reduction in levels of chloroplast ribosomes.

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Book ChapterDOI

The Green Flagellate Chlamydomonas

K. V. Kvitko
TL;DR: Green flagellates belonging to the genus Chlamydomonas are widely used as a model in experimental studies and are one of the more suitable unicellular eukaryotic organisms for studying cell differentiation with modern techniques.
Book ChapterDOI

Chloroplast Messenger RNA from Etiolated Pea Seedlings

TL;DR: Recent evidence shows that chloroplasts contain their own DNA with physicochemical properties different from those of the nuclear DNA.
Book ChapterDOI

Biogenesis of chloroplast membranes in Chlamydomonas reinhardi: Chloroplast-controlled transfer of cytoplasmic proteins to the developing chloroplast membranes as visualized by quantitative radioautography.

TL;DR: The results indicate that transport of some of the proteins of cytoplasmic origin to their final location within the chloroplast is at least partially controlled by concomitant synthesis of proteins by thechloroplast ribosomes.
References
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Journal ArticleDOI

The fractionation of high-molecular-weight ribonucleic acid by polyacrylamide-gel electrophoresis.

UE Loening
- 01 Jan 1967 - 
TL;DR: Electrophoresis in 2.2-2.6% gels gives a fractionation similar to density-gradient centrifugation, and the resolution is greater and more detailed than by centrifugations, and many samples can be analysed simultaneously and rapidly.
Journal ArticleDOI

FINE STRUCTURE OF CELL DIVISION IN CHLAMYDOMONAS REINHARDI : Basal Bodies and Microtubules

TL;DR: It is proposed that microtubules participate in the formation of the cleavage furrow in C. reinhardi and related to cell division in other organisms.
Journal ArticleDOI

BIOGENESIS OF CHLOROPLAST MEMBRANES : I. Plastid Dedifferentiation in a Dark-Grown Algal Mutant (Chlamydomonas reinhardi)

TL;DR: It was observed that during growth in the dark the chloroplast lamellar system is gradually disorganized and drastically decreased in extent, while other subchloroplast components are either unaffected (pyrenoid and its tubular system, matrix) or much less affected (eyespot, ribosomes).
Journal ArticleDOI

Structure and development of the chloroplast in Chlamydomonas. I. The normal green cell.

TL;DR: The cytoplasmic organization of a normal green strain of the alga Chlamydomonas reinhardi has been investigated with the electron microscope using thin sections of OsO4 fixed material, identified on the basis of morphological comparability with structures seen in animal cells.
Journal ArticleDOI

Identification of cytoplasmic basophilia (ribonucleic acid) by fluorescence microscopy

TL;DR: The applicability to living or supravital tissues of the fluorochrome technique decreases errors due to fixation, dehydration, embedding and related procedures, and the low concentrations applied in fluorochroma staining further safeguard against histochemical artifacts.
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