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Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila
Protochlamydia amoebophila UWE25 is related to the Chlamydiaceae comprising major pathogens of humans, but thrives as obligate intracellular symbiont in the protozoan host Acanthamoeba sp. The genome of P. amoebophila encodes five paralogous carrier proteins belonging to the nucleotide transporter (...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513512/ https://www.ncbi.nlm.nih.gov/pubmed/16796686 http://dx.doi.org/10.1111/j.1365-2958.2006.05193.x |
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author | Haferkamp, Ilka Schmitz-Esser, Stephan Wagner, Michael Neigel, Nadjeschka Horn, Matthias Neuhaus, H Ekkehard |
author_facet | Haferkamp, Ilka Schmitz-Esser, Stephan Wagner, Michael Neigel, Nadjeschka Horn, Matthias Neuhaus, H Ekkehard |
author_sort | Haferkamp, Ilka |
collection | PubMed |
description | Protochlamydia amoebophila UWE25 is related to the Chlamydiaceae comprising major pathogens of humans, but thrives as obligate intracellular symbiont in the protozoan host Acanthamoeba sp. The genome of P. amoebophila encodes five paralogous carrier proteins belonging to the nucleotide transporter (NTT) family. Here we report on three P. amoebophila NTT isoforms, PamNTT2, PamNTT3 and PamNTT5, which possess several conserved amino acid residues known to be critical for nucleotide transport. We demonstrated that these carrier proteins are able to transport nucleotides, although substrate specificities and mode of transport differ in an unexpected manner and are unique among known NTTs. PamNTT2 is a counter exchange transporter exhibiting submillimolar apparent affinities for all four RNA nucleotides, PamNTT3 catalyses an unidirectional proton-coupled transport confined to UTP, whereas PamNTT5 mediates a proton-energized GTP and ATP import. All NTT genes of P. amoebophila are transcribed during intracellular multiplication in acanthamoebae. The biochemical characterization of all five NTT proteins from P. amoebophila in this and previous studies uncovered that these metabolically impaired bacteria are intimately connected with their host cell’s metabolism in a surprisingly complex manner. |
format | Text |
id | pubmed-1513512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-15135122006-07-24 Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila Haferkamp, Ilka Schmitz-Esser, Stephan Wagner, Michael Neigel, Nadjeschka Horn, Matthias Neuhaus, H Ekkehard Mol Microbiol Research Articles Protochlamydia amoebophila UWE25 is related to the Chlamydiaceae comprising major pathogens of humans, but thrives as obligate intracellular symbiont in the protozoan host Acanthamoeba sp. The genome of P. amoebophila encodes five paralogous carrier proteins belonging to the nucleotide transporter (NTT) family. Here we report on three P. amoebophila NTT isoforms, PamNTT2, PamNTT3 and PamNTT5, which possess several conserved amino acid residues known to be critical for nucleotide transport. We demonstrated that these carrier proteins are able to transport nucleotides, although substrate specificities and mode of transport differ in an unexpected manner and are unique among known NTTs. PamNTT2 is a counter exchange transporter exhibiting submillimolar apparent affinities for all four RNA nucleotides, PamNTT3 catalyses an unidirectional proton-coupled transport confined to UTP, whereas PamNTT5 mediates a proton-energized GTP and ATP import. All NTT genes of P. amoebophila are transcribed during intracellular multiplication in acanthamoebae. The biochemical characterization of all five NTT proteins from P. amoebophila in this and previous studies uncovered that these metabolically impaired bacteria are intimately connected with their host cell’s metabolism in a surprisingly complex manner. Blackwell Publishing Ltd 2006-06 /pmc/articles/PMC1513512/ /pubmed/16796686 http://dx.doi.org/10.1111/j.1365-2958.2006.05193.x Text en © 2006 The Authors; Journal compilation © 2006 Blackwell Publishing Ltd |
spellingShingle | Research Articles Haferkamp, Ilka Schmitz-Esser, Stephan Wagner, Michael Neigel, Nadjeschka Horn, Matthias Neuhaus, H Ekkehard Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title | Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title_full | Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title_fullStr | Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title_full_unstemmed | Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title_short | Tapping the nucleotide pool of the host: novel nucleotide carrier proteins of Protochlamydia amoebophila |
title_sort | tapping the nucleotide pool of the host: novel nucleotide carrier proteins of protochlamydia amoebophila |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513512/ https://www.ncbi.nlm.nih.gov/pubmed/16796686 http://dx.doi.org/10.1111/j.1365-2958.2006.05193.x |
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