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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Main Authors: F.J. Ballard, Richard W. Hanson
Format: Article
Language:English
Published: Elsevier 1967-03-01
Series:Journal of Lipid Research
Subjects:
rat
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520389173
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spelling 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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