Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms

In vivo labeling experiments with [3H]palmitic acid, [3H]inositol, and [3H]glucose allowed the identification of two main classes of inositolphospholipids (IPLs) from the trypomastigote stage of Trypanosoma cruzi. Purification of these compounds was achieved by ion-exchange chromatography, high perf...

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Publicado: 1996
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00052760_v1300_n3_p233_Uhrig
http://hdl.handle.net/20.500.12110/paper_00052760_v1300_n3_p233_Uhrig
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spelling paper:paper_00052760_v1300_n3_p233_Uhrig2023-06-08T14:29:56Z Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms Inositolphospholipid T. cruzi Trypomastigote inositol derivative phospholipid ceramide diacylglycerol fatty acid glycerylphosphoinositol glycosylphosphatidylinositol inositol phosphate palmitic acid palmitic acid derivative phosphatidylinositol sphingosine article high performance liquid chromatography ion exchange chromatography isotope labeling life cycle lipid analysis priority journal thin layer chromatography Trypanosoma cruzi animal chemical structure chemistry isolation and purification metabolism Trypanosoma Trypanosoma cruzi Animals Ceramides Chromatography, High Pressure Liquid Chromatography, Thin Layer Diglycerides Fatty Acids Glycosylphosphatidylinositols Inositol Phosphates Molecular Structure Palmitic Acid Palmitic Acids Phosphatidylinositols Sphingosine Trypanosoma cruzi In vivo labeling experiments with [3H]palmitic acid, [3H]inositol, and [3H]glucose allowed the identification of two main classes of inositolphospholipids (IPLs) from the trypomastigote stage of Trypanosoma cruzi. Purification of these compounds was achieved by ion-exchange chromatography, high performance liquid chromatography and thin layer chromatography. Specific phosphatidyl-inositol phospholipase C digestion, dephosphorylation and acid methanolysis showed a ceramide structure for the lower migrating IPL1. Palmitoyldihydrosphingosine and palmitoylsphingosine were detected by reverse-phase thin-layer chromatography. On the other hand, IPL2 showed to be a mixture of diacylglycero- and alkylacylglycero-phospholipids in a 1:1 ratio. After PI-PLC digestion, the lipids were separated by preparative TLC and individually analysed. The diacylglycerol contained mainly C18:0 fatty acid together with a low amount of C16:0. Hexadecylglycerol esterified with the C18:0 fatty acid was the only alkylacylglycerol detected. The C18:2 and C18:1 fatty acids, preponderant in the PI molecules of epimastigote forms, were not detected in trypomastigote forms. This is the first report on inositol phospholipids, putative precursors of lipid anchors in the infective stage of T. cruzi. 1996 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00052760_v1300_n3_p233_Uhrig http://hdl.handle.net/20.500.12110/paper_00052760_v1300_n3_p233_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 Inositolphospholipid
T. cruzi
Trypomastigote
inositol derivative
phospholipid
ceramide
diacylglycerol
fatty acid
glycerylphosphoinositol
glycosylphosphatidylinositol
inositol phosphate
palmitic acid
palmitic acid derivative
phosphatidylinositol
sphingosine
article
high performance liquid chromatography
ion exchange chromatography
isotope labeling
life cycle
lipid analysis
priority journal
thin layer chromatography
Trypanosoma cruzi
animal
chemical structure
chemistry
isolation and purification
metabolism
Trypanosoma
Trypanosoma cruzi
Animals
Ceramides
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Diglycerides
Fatty Acids
Glycosylphosphatidylinositols
Inositol Phosphates
Molecular Structure
Palmitic Acid
Palmitic Acids
Phosphatidylinositols
Sphingosine
Trypanosoma cruzi
spellingShingle Inositolphospholipid
T. cruzi
Trypomastigote
inositol derivative
phospholipid
ceramide
diacylglycerol
fatty acid
glycerylphosphoinositol
glycosylphosphatidylinositol
inositol phosphate
palmitic acid
palmitic acid derivative
phosphatidylinositol
sphingosine
article
high performance liquid chromatography
ion exchange chromatography
isotope labeling
life cycle
lipid analysis
priority journal
thin layer chromatography
Trypanosoma cruzi
animal
chemical structure
chemistry
isolation and purification
metabolism
Trypanosoma
Trypanosoma cruzi
Animals
Ceramides
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Diglycerides
Fatty Acids
Glycosylphosphatidylinositols
Inositol Phosphates
Molecular Structure
Palmitic Acid
Palmitic Acids
Phosphatidylinositols
Sphingosine
Trypanosoma cruzi
Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
topic_facet Inositolphospholipid
T. cruzi
Trypomastigote
inositol derivative
phospholipid
ceramide
diacylglycerol
fatty acid
glycerylphosphoinositol
glycosylphosphatidylinositol
inositol phosphate
palmitic acid
palmitic acid derivative
phosphatidylinositol
sphingosine
article
high performance liquid chromatography
ion exchange chromatography
isotope labeling
life cycle
lipid analysis
priority journal
thin layer chromatography
Trypanosoma cruzi
animal
chemical structure
chemistry
isolation and purification
metabolism
Trypanosoma
Trypanosoma cruzi
Animals
Ceramides
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Diglycerides
Fatty Acids
Glycosylphosphatidylinositols
Inositol Phosphates
Molecular Structure
Palmitic Acid
Palmitic Acids
Phosphatidylinositols
Sphingosine
Trypanosoma cruzi
description In vivo labeling experiments with [3H]palmitic acid, [3H]inositol, and [3H]glucose allowed the identification of two main classes of inositolphospholipids (IPLs) from the trypomastigote stage of Trypanosoma cruzi. Purification of these compounds was achieved by ion-exchange chromatography, high performance liquid chromatography and thin layer chromatography. Specific phosphatidyl-inositol phospholipase C digestion, dephosphorylation and acid methanolysis showed a ceramide structure for the lower migrating IPL1. Palmitoyldihydrosphingosine and palmitoylsphingosine were detected by reverse-phase thin-layer chromatography. On the other hand, IPL2 showed to be a mixture of diacylglycero- and alkylacylglycero-phospholipids in a 1:1 ratio. After PI-PLC digestion, the lipids were separated by preparative TLC and individually analysed. The diacylglycerol contained mainly C18:0 fatty acid together with a low amount of C16:0. Hexadecylglycerol esterified with the C18:0 fatty acid was the only alkylacylglycerol detected. The C18:2 and C18:1 fatty acids, preponderant in the PI molecules of epimastigote forms, were not detected in trypomastigote forms. This is the first report on inositol phospholipids, putative precursors of lipid anchors in the infective stage of T. cruzi.
title Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
title_short Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
title_full Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
title_fullStr Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
title_full_unstemmed Characterization of inositolphospholipids in Tryparzosoma cruzi trypmastigote forms
title_sort characterization of inositolphospholipids in tryparzosoma cruzi trypmastigote forms
publishDate 1996
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00052760_v1300_n3_p233_Uhrig
http://hdl.handle.net/20.500.12110/paper_00052760_v1300_n3_p233_Uhrig
_version_ 1768544530314821632