carnitine palmitoyltransferase activity
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2008 ◽  
Vol 283 (11) ◽  
pp. 6878-6885 ◽  
Author(s):  
Adriana Y. Sierra ◽  
Esther Gratacós ◽  
Patricia Carrasco ◽  
Josep Clotet ◽  
Jesús Ureña ◽  
...  


1997 ◽  
Vol 59 (11) ◽  
pp. 1067-1069 ◽  
Author(s):  
Hisashi MIZUTANI ◽  
Toshinori SAKO ◽  
Naoyuki TAKEMURA ◽  
Hidekazu KOYAMA ◽  
Mamoru YAMAGUCHI ◽  
...  




1993 ◽  
Vol 55 (4) ◽  
pp. 357-363 ◽  
Author(s):  
Yoshikazu Noguchi ◽  
Nadarajen A. Vydelingum ◽  
Murray F. Brennan




1993 ◽  
Vol 264 (5) ◽  
pp. R1004-R1009 ◽  
Author(s):  
E. L. Crockett ◽  
B. D. Sidell

Hepatic beta-oxidation is characterized in a marine teleost, Myoxocephalus octodecimspinosus, to determine mitochondrial and peroxisomal substrate selectivity as well as metabolic partitioning. Substrate selectivity is broad for peroxisomal beta-oxidation. Acyl CoA oxidase activities, with all unsaturated substrates measured, are at least 35% of activity with palmitoyl CoA (16:0), a saturated substrate. Mitochondrial selectivities are more pronounced. Carnitine palmitoyltransferase activity with a monounsaturate, palmitoleoyl CoA (16:1), is nearly 40% greater than activity with palmitoyl CoA, whereas activities with two polyunsaturates are < 10% of activity with the saturate. The presence of polyunsaturated acyl CoA esters inhibits up to 70% the oxidation of palmitoyl CoA by intact peroxisomes. Acyl CoA hydrolase activity is localized to peroxisomal fractions prepared by density-gradient centrifugation. Hydrolytic activity in these fractions is nearly twofold the activity of beta-oxidation. Estimates for metabolic partitioning suggest that at least 50% of hepatic beta-oxidation may be initiated by the peroxisomal compartment.



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