Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis

In trypanosomatids, little is known about the biosynthetic pathways involved in the metabolism of ethanolamine. In an attempt to clarify this point, an exhaustive analysis of the chloroform:methanol extract of T. cruzi trypomastigotes metabolically labeled with [14C]ethanolamine, in comparison with...

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Autores principales: Uhrig, M.L., Couto, A.S., Alves, M.J.M., Colli, W., De Lederkremer, R.M.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00144894_v87_n1_p8_Uhrig
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spelling todo:paper_00144894_v87_n1_p8_Uhrig2023-10-03T14:12:49Z Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis Uhrig, M.L. Couto, A.S. Alves, M.J.M. Colli, W. De Lederkremer, R.M. DAG, diacylglycerol DME, Dulbecco's modified Eagle's medium DMPE, dimethylphosphatidylethanolamine FCS, fetal calf serum GLC, gas-liquid chromatography GLC-MS, gas- liquid chromatography-mass spectrometry GPI, glycosylphosphatidylinositol LPC, lysophosphatidylcholine LPE, lysophosphatidylethanolamine MMPE, monomethylphosphatidylethanolamine PC, phosphatidylcholine PE, phosphatidylethanolamine PLA2, phospholipase A2 PLC, phospholipase C RP-TLC, reverse- phase thin-layer chromatography SAPA Shed acute-phase antigen TAG, triacylglycerol TLC, thin-layer chromatography Trypanosoma cruzi Trypomastigote Zwitterionic phospholipids ethanolamine article chemical analysis gas liquid chromatography host parasite interaction nonhuman priority journal Trypanosoma cruzi trypomastigote Ciconiiformes Trypanosoma Trypanosoma cruzi Trypanosomatidae In trypanosomatids, little is known about the biosynthetic pathways involved in the metabolism of ethanolamine. In an attempt to clarify this point, an exhaustive analysis of the chloroform:methanol extract of T. cruzi trypomastigotes metabolically labeled with [14C]ethanolamine, in comparison with the lipids from [13H]palmitic acid-incorporated parasites, was performed. In both cases, phosphatidylethanolamine and lysophosphatidylethanolamine were detected, while phosphatidylcholine and lysophosphatidylcholine were only labeled with the fatty acid precursor. However, dimethylphosphatidylethanolamine was isolated from parasites labeled with the base precursor, indicating the ability of trypanosomes to methylate phosphatidylethanolamine to dimethylphosphatidylethanolamine. Fatty acids of the labeled phospholipids were analyzed by reverse-phase thin-layer chromatography and fluorography. Interestingly, phospholipids from the trypomastigote stage show palmitic acid (C16:0) and stearic acid (C18:0) as the only labeled components. The same saturated fatty acids were found free and as components of the radioactive triglycerides. No unsaturated fatty acids were detected, in accordance with the results obtained with inositolphospholipids. Conversely, when the fatty acids of phospholipids purified from nonlabeled parasites were analyzed by gas-liquid chromatography and gas-liquid chromatography-mass spectrometry, C18:1 was also detected. A striking finding was the presence of a considerable amount of free lignoceric acid (C24:0). Also, the C24:0 fatty acid was identified in the triglyceride fraction and as a component of phosphatidylcholine. The limited capacity of trypomastigote forms to elongate fatty acids was determined. In contrast with the results reported for other noninfective forms of the parasite, the absence of unsaturated fatty acids due to a low activity of desaturases was observed. Fil:Uhrig, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Couto, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:De Lederkremer, R.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00144894_v87_n1_p8_Uhrig
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic DAG, diacylglycerol
DME, Dulbecco's modified Eagle's medium
DMPE, dimethylphosphatidylethanolamine
FCS, fetal calf serum
GLC, gas-liquid chromatography
GLC-MS, gas- liquid chromatography-mass spectrometry
GPI, glycosylphosphatidylinositol
LPC, lysophosphatidylcholine
LPE, lysophosphatidylethanolamine
MMPE, monomethylphosphatidylethanolamine
PC, phosphatidylcholine
PE, phosphatidylethanolamine
PLA2, phospholipase A2
PLC, phospholipase C
RP-TLC, reverse- phase thin-layer chromatography
SAPA
Shed acute-phase antigen
TAG, triacylglycerol
TLC, thin-layer chromatography
Trypanosoma cruzi
Trypomastigote
Zwitterionic phospholipids
ethanolamine
article
chemical analysis
gas liquid chromatography
host parasite interaction
nonhuman
priority journal
Trypanosoma cruzi
trypomastigote
Ciconiiformes
Trypanosoma
Trypanosoma cruzi
Trypanosomatidae
spellingShingle DAG, diacylglycerol
DME, Dulbecco's modified Eagle's medium
DMPE, dimethylphosphatidylethanolamine
FCS, fetal calf serum
GLC, gas-liquid chromatography
GLC-MS, gas- liquid chromatography-mass spectrometry
GPI, glycosylphosphatidylinositol
LPC, lysophosphatidylcholine
LPE, lysophosphatidylethanolamine
MMPE, monomethylphosphatidylethanolamine
PC, phosphatidylcholine
PE, phosphatidylethanolamine
PLA2, phospholipase A2
PLC, phospholipase C
RP-TLC, reverse- phase thin-layer chromatography
SAPA
Shed acute-phase antigen
TAG, triacylglycerol
TLC, thin-layer chromatography
Trypanosoma cruzi
Trypomastigote
Zwitterionic phospholipids
ethanolamine
article
chemical analysis
gas liquid chromatography
host parasite interaction
nonhuman
priority journal
Trypanosoma cruzi
trypomastigote
Ciconiiformes
Trypanosoma
Trypanosoma cruzi
Trypanosomatidae
Uhrig, M.L.
Couto, A.S.
Alves, M.J.M.
Colli, W.
De Lederkremer, R.M.
Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
topic_facet DAG, diacylglycerol
DME, Dulbecco's modified Eagle's medium
DMPE, dimethylphosphatidylethanolamine
FCS, fetal calf serum
GLC, gas-liquid chromatography
GLC-MS, gas- liquid chromatography-mass spectrometry
GPI, glycosylphosphatidylinositol
LPC, lysophosphatidylcholine
LPE, lysophosphatidylethanolamine
MMPE, monomethylphosphatidylethanolamine
PC, phosphatidylcholine
PE, phosphatidylethanolamine
PLA2, phospholipase A2
PLC, phospholipase C
RP-TLC, reverse- phase thin-layer chromatography
SAPA
Shed acute-phase antigen
TAG, triacylglycerol
TLC, thin-layer chromatography
Trypanosoma cruzi
Trypomastigote
Zwitterionic phospholipids
ethanolamine
article
chemical analysis
gas liquid chromatography
host parasite interaction
nonhuman
priority journal
Trypanosoma cruzi
trypomastigote
Ciconiiformes
Trypanosoma
Trypanosoma cruzi
Trypanosomatidae
description In trypanosomatids, little is known about the biosynthetic pathways involved in the metabolism of ethanolamine. In an attempt to clarify this point, an exhaustive analysis of the chloroform:methanol extract of T. cruzi trypomastigotes metabolically labeled with [14C]ethanolamine, in comparison with the lipids from [13H]palmitic acid-incorporated parasites, was performed. In both cases, phosphatidylethanolamine and lysophosphatidylethanolamine were detected, while phosphatidylcholine and lysophosphatidylcholine were only labeled with the fatty acid precursor. However, dimethylphosphatidylethanolamine was isolated from parasites labeled with the base precursor, indicating the ability of trypanosomes to methylate phosphatidylethanolamine to dimethylphosphatidylethanolamine. Fatty acids of the labeled phospholipids were analyzed by reverse-phase thin-layer chromatography and fluorography. Interestingly, phospholipids from the trypomastigote stage show palmitic acid (C16:0) and stearic acid (C18:0) as the only labeled components. The same saturated fatty acids were found free and as components of the radioactive triglycerides. No unsaturated fatty acids were detected, in accordance with the results obtained with inositolphospholipids. Conversely, when the fatty acids of phospholipids purified from nonlabeled parasites were analyzed by gas-liquid chromatography and gas-liquid chromatography-mass spectrometry, C18:1 was also detected. A striking finding was the presence of a considerable amount of free lignoceric acid (C24:0). Also, the C24:0 fatty acid was identified in the triglyceride fraction and as a component of phosphatidylcholine. The limited capacity of trypomastigote forms to elongate fatty acids was determined. In contrast with the results reported for other noninfective forms of the parasite, the absence of unsaturated fatty acids due to a low activity of desaturases was observed.
format JOUR
author Uhrig, M.L.
Couto, A.S.
Alves, M.J.M.
Colli, W.
De Lederkremer, R.M.
author_facet Uhrig, M.L.
Couto, A.S.
Alves, M.J.M.
Colli, W.
De Lederkremer, R.M.
author_sort Uhrig, M.L.
title Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
title_short Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
title_full Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
title_fullStr Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
title_full_unstemmed Trypanosoma cruzi: Nitrogenous-base-containing phosphatides in trypomastigote forms - Isolation and chemical analysis
title_sort trypanosoma cruzi: nitrogenous-base-containing phosphatides in trypomastigote forms - isolation and chemical analysis
url http://hdl.handle.net/20.500.12110/paper_00144894_v87_n1_p8_Uhrig
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