The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate
Fatty acid synthesis via the citrate cleavage pathway requires the continual replenishment of oxaloacetate within the mitochondria, probably by carboxylation of pyruvate.Malic enzyme, although present in adipose tissue, is completely localized in the cytoplasm and has insufficient activity to suppor...
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1967-03-01
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Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520389173 |
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doaj-05c7cbbec7684881ab9dde508b593c3a2021-04-23T06:10:25ZengElsevierJournal of Lipid Research0022-22751967-03-01827379The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetateF.J. Ballard0Richard W. Hanson1Fels Research Institute and Department of Biochemistry, Temple University School of Medicine, Philadelphia, Pennsylvania 19140Fels Research Institute and Department of Biochemistry, Temple University School of Medicine, Philadelphia, Pennsylvania 19140Fatty acid synthesis via the citrate cleavage pathway requires the continual replenishment of oxaloacetate within the mitochondria, probably by carboxylation of pyruvate.Malic enzyme, although present in adipose tissue, is completely localized in the cytoplasm and has insufficient activity to support lipogenesis. Pyruvate carboxylase was found to be active in both the mitochondria and cytoplasm of epididymal adipose tissue cells; it was dependent on both ATP and biotin. Alterations in dietary conditions induced no significant changes in mitochondrial pyruvate carboxylase activity, but the soluble activity was depressed in fat-fed animals.The possible importance of the soluble activity in lipogenesis lies in its participation in a soluble malate transhydrogenation cycle with NAD malate dehydrogenase and malic enzyme, whereby a continual supply of NADPH is produced. Consequently, the pyruvate carboxylase in adipose tissue both generates mitochondrial oxaloacetate for the citrate cleavage pathway and supplies soluble NADPH for the conversion of acetyl-CoA to fatty acid.http://www.sciencedirect.com/science/article/pii/S0022227520389173pyruvate carboxylaseadipose tissueratintracellular distributiondietary changesoxaloacetate formation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
F.J. Ballard Richard W. Hanson |
spellingShingle |
F.J. Ballard Richard W. Hanson The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate Journal of Lipid Research pyruvate carboxylase adipose tissue rat intracellular distribution dietary changes oxaloacetate formation |
author_facet |
F.J. Ballard Richard W. Hanson |
author_sort |
F.J. Ballard |
title |
The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
title_short |
The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
title_full |
The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
title_fullStr |
The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
title_full_unstemmed |
The citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
title_sort |
citrate cleavage pathway and lipogenesis in rat adipose tissue: replenishment of oxaloacetate |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
1967-03-01 |
description |
Fatty acid synthesis via the citrate cleavage pathway requires the continual replenishment of oxaloacetate within the mitochondria, probably by carboxylation of pyruvate.Malic enzyme, although present in adipose tissue, is completely localized in the cytoplasm and has insufficient activity to support lipogenesis. Pyruvate carboxylase was found to be active in both the mitochondria and cytoplasm of epididymal adipose tissue cells; it was dependent on both ATP and biotin. Alterations in dietary conditions induced no significant changes in mitochondrial pyruvate carboxylase activity, but the soluble activity was depressed in fat-fed animals.The possible importance of the soluble activity in lipogenesis lies in its participation in a soluble malate transhydrogenation cycle with NAD malate dehydrogenase and malic enzyme, whereby a continual supply of NADPH is produced. Consequently, the pyruvate carboxylase in adipose tissue both generates mitochondrial oxaloacetate for the citrate cleavage pathway and supplies soluble NADPH for the conversion of acetyl-CoA to fatty acid. |
topic |
pyruvate carboxylase adipose tissue rat intracellular distribution dietary changes oxaloacetate formation |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520389173 |
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