L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi

A very specific L-arginine transporter showing high affinity has been characterized in Trypanosoma cruzi epimastigotes. Uptake was found to be dependent on L-arginine concentration and it was saturable. Values for maximum velocity and Km ranged between 48.1-57.5 pmol·min-1 per 3 x 107 cells and betw...

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Autores principales: Pereira, C.A., Alonso, G.D., Paveto, M.C., Flawiá, M.M., Torres, H.N.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_10665234_v46_n6_p566_Pereira
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spelling todo:paper_10665234_v46_n6_p566_Pereira2023-10-03T16:02:07Z L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi Pereira, C.A. Alonso, G.D. Paveto, M.C. Flawiá, M.M. Torres, H.N. Amino acid transport Arginine kinase Canavanine Epimastigotes Homoarginine Phosphagen amino acid synthesis amino acid transport arginine canavanine citrulline energy metabolism homoarginine microbe metabolism ornithine phosphoarginine Trypanosoma Trypanosoma cruzi Trypanosoma cruzi A very specific L-arginine transporter showing high affinity has been characterized in Trypanosoma cruzi epimastigotes. Uptake was found to be dependent on L-arginine concentration and it was saturable. Values for maximum velocity and Km ranged between 48.1-57.5 pmol·min-1 per 3 x 107 cells and between 4.2-5.5 μM, respectively The calculated activation energy and Q10 were 31.1 KJ·mol-1, and 1.7, respectively. Uptake velocity significantly increased when cells were preincubated in the absence of L-arginine. Cells retained the labeled amino acid independently of the presence or absence of exogenous L-arginine. The specificity of L-arginine uptake was demonstrated by competition assays in the presence of 80-fold molar excess of natural amino acids and several L-arginine derivatives. The highest levels of inhibition were caused by L-homoarginine. D-arginine, L-canavanine, L-ornithine, and L-citrulline, L-arginine uptake by T. cruzi epimastigotes was not affected by the presence of potassium or sodium ions in the incubation mixture or by pH changes in the range between 5.5-8.5. The major product of L-arginine uptake was characterized as phosphoarginine. Moreover, arginine kinase activity was detected in soluble extracts from T. cruzi epimastigotes. Fil:Pereira, C.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Alonso, G.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Paveto, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Flawiá, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Torres, H.N. 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_10665234_v46_n6_p566_Pereira
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Amino acid transport
Arginine kinase
Canavanine
Epimastigotes
Homoarginine
Phosphagen
amino acid synthesis
amino acid transport
arginine
canavanine
citrulline
energy metabolism
homoarginine
microbe metabolism
ornithine
phosphoarginine
Trypanosoma
Trypanosoma cruzi
Trypanosoma cruzi
spellingShingle Amino acid transport
Arginine kinase
Canavanine
Epimastigotes
Homoarginine
Phosphagen
amino acid synthesis
amino acid transport
arginine
canavanine
citrulline
energy metabolism
homoarginine
microbe metabolism
ornithine
phosphoarginine
Trypanosoma
Trypanosoma cruzi
Trypanosoma cruzi
Pereira, C.A.
Alonso, G.D.
Paveto, M.C.
Flawiá, M.M.
Torres, H.N.
L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
topic_facet Amino acid transport
Arginine kinase
Canavanine
Epimastigotes
Homoarginine
Phosphagen
amino acid synthesis
amino acid transport
arginine
canavanine
citrulline
energy metabolism
homoarginine
microbe metabolism
ornithine
phosphoarginine
Trypanosoma
Trypanosoma cruzi
Trypanosoma cruzi
description A very specific L-arginine transporter showing high affinity has been characterized in Trypanosoma cruzi epimastigotes. Uptake was found to be dependent on L-arginine concentration and it was saturable. Values for maximum velocity and Km ranged between 48.1-57.5 pmol·min-1 per 3 x 107 cells and between 4.2-5.5 μM, respectively The calculated activation energy and Q10 were 31.1 KJ·mol-1, and 1.7, respectively. Uptake velocity significantly increased when cells were preincubated in the absence of L-arginine. Cells retained the labeled amino acid independently of the presence or absence of exogenous L-arginine. The specificity of L-arginine uptake was demonstrated by competition assays in the presence of 80-fold molar excess of natural amino acids and several L-arginine derivatives. The highest levels of inhibition were caused by L-homoarginine. D-arginine, L-canavanine, L-ornithine, and L-citrulline, L-arginine uptake by T. cruzi epimastigotes was not affected by the presence of potassium or sodium ions in the incubation mixture or by pH changes in the range between 5.5-8.5. The major product of L-arginine uptake was characterized as phosphoarginine. Moreover, arginine kinase activity was detected in soluble extracts from T. cruzi epimastigotes.
format JOUR
author Pereira, C.A.
Alonso, G.D.
Paveto, M.C.
Flawiá, M.M.
Torres, H.N.
author_facet Pereira, C.A.
Alonso, G.D.
Paveto, M.C.
Flawiá, M.M.
Torres, H.N.
author_sort Pereira, C.A.
title L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
title_short L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
title_full L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
title_fullStr L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
title_full_unstemmed L-arginine uptake and L-phosphoarginine synthesis in Trypanosoma cruzi
title_sort l-arginine uptake and l-phosphoarginine synthesis in trypanosoma cruzi
url http://hdl.handle.net/20.500.12110/paper_10665234_v46_n6_p566_Pereira
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