The distribution in liver cell fractions of UDPG-glycogen transferase has been studied. In fasting animals which have been refed 6 hours before sacrifice, the distribution of the enzyme in the various cell fractions can be correlated with the glycogen content of each fraction. A purified glycogen fraction has been prepared by differential centrifugation in sucrose gradients. This glycogen fraction contains vesicular structures which resemble those seen in association with glycogen deposits in the intact liver cell. In addition, the glycogen pellet contains UDPG-glycogen transferase in high specific activity. Subfractionation of the glycogen pellet separates the majority of vesicular elements from the bulk of transferase activity and glycogen. The evidence presented suggests that the presence of UPDG-glycogen transferase in the glycogen pellet is to be attributed to its binding to glycogen rather than to its association with the structural elements found in the glycogen fraction.
Skip Nav Destination
Article navigation
1 June 1961
Content prior to 1962 was published under the journal name
The Journal of Biophysical and Biochemical Cytology
Article|
June 01 1961
GLYCOGEN SYNTHESIS FROM URIDINE DIPHOSPHATE GLUCOSE : The Distribution of the Enzyme in Liver Cell Fractions
David J. L. Luck
David J. L. Luck
From The Rockefeller Institute
Search for other works by this author on:
David J. L. Luck
From The Rockefeller Institute
Received:
March 29 1961
Copyright, 1961, by The Rockefeller Institute Press
1961
J Biophys and Biochem Cytol (1961) 10 (2): 195–209.
Article history
Received:
March 29 1961
Citation
David J. L. Luck; GLYCOGEN SYNTHESIS FROM URIDINE DIPHOSPHATE GLUCOSE : The Distribution of the Enzyme in Liver Cell Fractions . J Biophys and Biochem Cytol 1 June 1961; 10 (2): 195–209. doi: https://doi.org/10.1083/jcb.10.2.195
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement