TY - JOUR
T1 - Acyl CoA and lipid synthesis from ketone bodies by the extramitochondrial fraction of hepatoma tissue
AU - Hildebrandt, Leslie
AU - Spennetta, Terry
AU - Ackerman, Ronald
AU - Elson, Charles
AU - Shrago, Earl
N1 - Funding Information:
Research supported by the College of Agriculture and Life Sciences, University of Wisconsin, Madison, Wisconsin.
PY - 1996/8/5
Y1 - 1996/8/5
N2 - The compartmentation of the pathway for the synthesis of lipids from ketone bodies was examined in a cell free, post-mitochondrial supernatant fraction of malignant Morris hepatoma 7777 tissue. A fortified supernatant system effectively incorporated radioactive D(-)-3-hydroxybulyrate and acetoacetate into cholesterol and fatty acids, and both ketone bodies were directly converted to their CoA thioesters. Furthermore, a microsome-free (100,000 x g) cytosolic fraction was also able to acylate 3-hydroxybutyrate to 3-hydroxy-butyryl CoA. No previous identification of this enzyme activity has been described. These results which characterize a distinct extramitochondrial pathway for conversion of 3-hydroxybutyrate as well as acetoacetate into lipids also suggest the possibility of a previously undetected enzymatic activity for utilization of this ketone body.
AB - The compartmentation of the pathway for the synthesis of lipids from ketone bodies was examined in a cell free, post-mitochondrial supernatant fraction of malignant Morris hepatoma 7777 tissue. A fortified supernatant system effectively incorporated radioactive D(-)-3-hydroxybulyrate and acetoacetate into cholesterol and fatty acids, and both ketone bodies were directly converted to their CoA thioesters. Furthermore, a microsome-free (100,000 x g) cytosolic fraction was also able to acylate 3-hydroxybutyrate to 3-hydroxy-butyryl CoA. No previous identification of this enzyme activity has been described. These results which characterize a distinct extramitochondrial pathway for conversion of 3-hydroxybutyrate as well as acetoacetate into lipids also suggest the possibility of a previously undetected enzymatic activity for utilization of this ketone body.
UR - http://www.scopus.com/inward/record.url?scp=0030570749&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1996.1171
DO - 10.1006/bbrc.1996.1171
M3 - Article
C2 - 8769135
AN - SCOPUS:0030570749
SN - 0006-291X
VL - 225
SP - 307
EP - 312
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -