Metabolism of saturated fatty acids by Paramecium tetraurelia.

Paramecium requires oleate for growth. The phospholipids of the ciliate contain high concentrations of palmitate and 18- and 20-carbon unsaturated fatty acids. We previously showed that radiolabeled oleate is desaturated and elongated to provide these 18- and 20-carbon unsaturated acids. We now repo...

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Main Authors: D E Rhoads, O Honer-Schmid, E S Kaneshiro
Format: Article
Language:English
Published: Elsevier 1987-12-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520385795
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spelling doaj-6a323c9debc64d2eb59ddb95875710062021-04-25T04:19:57ZengElsevierJournal of Lipid Research0022-22751987-12-01281214241433Metabolism of saturated fatty acids by Paramecium tetraurelia.D E Rhoads0O Honer-Schmid1E S Kaneshiro2Department of Biological Sciences, University of Cincinnati, OH 45221.Department of Biological Sciences, University of Cincinnati, OH 45221.Department of Biological Sciences, University of Cincinnati, OH 45221.Paramecium requires oleate for growth. The phospholipids of the ciliate contain high concentrations of palmitate and 18- and 20-carbon unsaturated fatty acids. We previously showed that radiolabeled oleate is desaturated and elongated to provide these 18- and 20-carbon unsaturated acids. We now report on saturated fatty acid (SFA) metabolism in Paramecium. Radiolabeled palmitate and stearate were incorporated directly into cellular phospholipids with little or no desaturation and/or elongation. Radiolabeled acetate, malonate, pyruvate, citrate, or glucose added to cultures were not incorporated into cellular phospholipid fatty acids indicating that these exogenously supplied putative precursors were not utilized for fatty acid synthesis by Paramecium. Radiolabel from octanoate or hexanoate appeared in fatty acyl groups of phospholipids, possibly by partial beta-oxidation and reincorporation of the label. Under oleate-free conditions in which cultures do not grow, radiolabel from these shorter chain SFA were beta-oxidized and preferentially used for the formation of arachidonate, the major end-product of fatty acid synthesis in Paramecium. Cerulenin inhibited culture growth apparently by inhibiting de novo fatty acid synthesis. Cerulenin-treated cells did not incorporate radioactivity from [1-14C]octanoate into esterified palmitate. However, total saponifiable phospholipid fatty acids, including SFA, per cell increased under these conditions.http://www.sciencedirect.com/science/article/pii/S0022227520385795
collection DOAJ
language English
format Article
sources DOAJ
author D E Rhoads
O Honer-Schmid
E S Kaneshiro
spellingShingle D E Rhoads
O Honer-Schmid
E S Kaneshiro
Metabolism of saturated fatty acids by Paramecium tetraurelia.
Journal of Lipid Research
author_facet D E Rhoads
O Honer-Schmid
E S Kaneshiro
author_sort D E Rhoads
title Metabolism of saturated fatty acids by Paramecium tetraurelia.
title_short Metabolism of saturated fatty acids by Paramecium tetraurelia.
title_full Metabolism of saturated fatty acids by Paramecium tetraurelia.
title_fullStr Metabolism of saturated fatty acids by Paramecium tetraurelia.
title_full_unstemmed Metabolism of saturated fatty acids by Paramecium tetraurelia.
title_sort metabolism of saturated fatty acids by paramecium tetraurelia.
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1987-12-01
description Paramecium requires oleate for growth. The phospholipids of the ciliate contain high concentrations of palmitate and 18- and 20-carbon unsaturated fatty acids. We previously showed that radiolabeled oleate is desaturated and elongated to provide these 18- and 20-carbon unsaturated acids. We now report on saturated fatty acid (SFA) metabolism in Paramecium. Radiolabeled palmitate and stearate were incorporated directly into cellular phospholipids with little or no desaturation and/or elongation. Radiolabeled acetate, malonate, pyruvate, citrate, or glucose added to cultures were not incorporated into cellular phospholipid fatty acids indicating that these exogenously supplied putative precursors were not utilized for fatty acid synthesis by Paramecium. Radiolabel from octanoate or hexanoate appeared in fatty acyl groups of phospholipids, possibly by partial beta-oxidation and reincorporation of the label. Under oleate-free conditions in which cultures do not grow, radiolabel from these shorter chain SFA were beta-oxidized and preferentially used for the formation of arachidonate, the major end-product of fatty acid synthesis in Paramecium. Cerulenin inhibited culture growth apparently by inhibiting de novo fatty acid synthesis. Cerulenin-treated cells did not incorporate radioactivity from [1-14C]octanoate into esterified palmitate. However, total saponifiable phospholipid fatty acids, including SFA, per cell increased under these conditions.
url http://www.sciencedirect.com/science/article/pii/S0022227520385795
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AT ohonerschmid metabolismofsaturatedfattyacidsbyparameciumtetraurelia
AT eskaneshiro metabolismofsaturatedfattyacidsbyparameciumtetraurelia
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