Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1977 Apr;73(1):139-48.
doi: 10.1083/jcb.73.1.139.

Characterization of mitochondrial and cytoplasmic ribosomes from Paramecium aurelia

Comparative Study

Characterization of mitochondrial and cytoplasmic ribosomes from Paramecium aurelia

A Tait et al. J Cell Biol. 1977 Apr.

Abstract

The ribosomes extracted from the mitochondria of the ciliate, Paramecium aurelia, have been shown to sediment at 80S in sucrose gradients. The cytoplasmic ribosomes also sediment at 80S but can be distinguished from their mitochondrial counterparts by a number of criteria. Lowering of the Mg++ concentration, addition of EDTA, or high KCl concentrations results in the dissociation of the cytoplasmic ribosomes into 60S and 40S subunits, whereas the mitochondrial ribosomes dissociate into a single sedimentation class at 55S. Furthermore, the relative sensitivity of the two types of ribosome to dissociating conditions can be distinguished. Electron microscopy of negatively stained 80S particles from both sources has also shown that the two types can be differentiated. The cytoplasmic particles show dimensions of 270 X 220 A whereas the mitochondrial particles are larger (330 X 240 A). In addition, there are several distinctive morphological features. The incorporation of [14C]leucine into nascent polypeptides associated with both mitochondrial and cytoplasmic ribosomes has been shown: the incorporation into cytoplasmic 80S particles is resistant to erythromycin and chloramphenicol but sensitive to cycloheximide, whereas incorporation into the mitochondrial particles is sensitive to erythromycin and chloramphenicol but resistant to cycloheximide.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochem J. 1961 Jul;80:9-21 - PubMed
    1. Symp Soc Exp Biol. 1970;24:449-96 - PubMed
    1. Int Rev Cytol. 1973;35:135-88 - PubMed
    1. J Cell Biol. 1974 Sep;62(3):860-75 - PubMed
    1. J Cell Biol. 1974 Mar;60(3):628-40 - PubMed

Publication types