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The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum
The apicoplast of Plasmodium falciparum parasites is believed to rely on the import of three-carbon phosphate compounds for use in organelle anabolic pathways, in addition to the generation of energy and reducing power within the organelle. We generated a series of genetic deletions in an apicoplast...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556864/ https://www.ncbi.nlm.nih.gov/pubmed/32815516 http://dx.doi.org/10.7554/eLife.50807 |
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author | Swift, Russell P Rajaram, Krithika Keutcha, Cyrianne Liu, Hans B Kwan, Bobby Dziedzic, Amanda Jedlicka, Anne E Prigge, Sean T |
author_facet | Swift, Russell P Rajaram, Krithika Keutcha, Cyrianne Liu, Hans B Kwan, Bobby Dziedzic, Amanda Jedlicka, Anne E Prigge, Sean T |
author_sort | Swift, Russell P |
collection | PubMed |
description | The apicoplast of Plasmodium falciparum parasites is believed to rely on the import of three-carbon phosphate compounds for use in organelle anabolic pathways, in addition to the generation of energy and reducing power within the organelle. We generated a series of genetic deletions in an apicoplast metabolic bypass line to determine which genes involved in apicoplast carbon metabolism are required for blood-stage parasite survival and organelle maintenance. We found that pyruvate kinase II (PyrKII) is essential for organelle maintenance, but that production of pyruvate by PyrKII is not responsible for this phenomenon. Enzymatic characterization of PyrKII revealed activity against all NDPs and dNDPs tested, suggesting that it may be capable of generating a broad range of nucleotide triphosphates. Conditional mislocalization of PyrKII resulted in decreased transcript levels within the apicoplast that preceded organelle disruption, suggesting that PyrKII is required for organelle maintenance due to its role in nucleotide triphosphate generation. |
format | Online Article Text |
id | pubmed-7556864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75568642020-10-16 The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum Swift, Russell P Rajaram, Krithika Keutcha, Cyrianne Liu, Hans B Kwan, Bobby Dziedzic, Amanda Jedlicka, Anne E Prigge, Sean T eLife Biochemistry and Chemical Biology The apicoplast of Plasmodium falciparum parasites is believed to rely on the import of three-carbon phosphate compounds for use in organelle anabolic pathways, in addition to the generation of energy and reducing power within the organelle. We generated a series of genetic deletions in an apicoplast metabolic bypass line to determine which genes involved in apicoplast carbon metabolism are required for blood-stage parasite survival and organelle maintenance. We found that pyruvate kinase II (PyrKII) is essential for organelle maintenance, but that production of pyruvate by PyrKII is not responsible for this phenomenon. Enzymatic characterization of PyrKII revealed activity against all NDPs and dNDPs tested, suggesting that it may be capable of generating a broad range of nucleotide triphosphates. Conditional mislocalization of PyrKII resulted in decreased transcript levels within the apicoplast that preceded organelle disruption, suggesting that PyrKII is required for organelle maintenance due to its role in nucleotide triphosphate generation. eLife Sciences Publications, Ltd 2020-08-20 /pmc/articles/PMC7556864/ /pubmed/32815516 http://dx.doi.org/10.7554/eLife.50807 Text en © 2020, Swift et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Swift, Russell P Rajaram, Krithika Keutcha, Cyrianne Liu, Hans B Kwan, Bobby Dziedzic, Amanda Jedlicka, Anne E Prigge, Sean T The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title | The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title_full | The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title_fullStr | The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title_full_unstemmed | The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title_short | The NTP generating activity of pyruvate kinase II is critical for apicoplast maintenance in Plasmodium falciparum |
title_sort | ntp generating activity of pyruvate kinase ii is critical for apicoplast maintenance in plasmodium falciparum |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556864/ https://www.ncbi.nlm.nih.gov/pubmed/32815516 http://dx.doi.org/10.7554/eLife.50807 |
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