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Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12 controls utilization of proline as an energy source in Saccharomyces cerevisiae
The amino acid proline functions as a nitrogen source and as a stress protectant in the yeast Saccharomyces cerevisiae. However, utilization of proline as a carbon source in S. cerevisiae cells has not been studied yet. In the process of study on the physiological roles of the found-in-mitochondrial...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348986/ https://www.ncbi.nlm.nih.gov/pubmed/28357320 http://dx.doi.org/10.15698/mic2016.10.535 |
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author | Nishida, Ikuhisa Watanabe, Daisuke Takagi, Hiroshi |
author_facet | Nishida, Ikuhisa Watanabe, Daisuke Takagi, Hiroshi |
author_sort | Nishida, Ikuhisa |
collection | PubMed |
description | The amino acid proline functions as a nitrogen source and as a stress protectant in the yeast Saccharomyces cerevisiae. However, utilization of proline as a carbon source in S. cerevisiae cells has not been studied yet. In the process of study on the physiological roles of the found-in-mitochondrial-proteome (FMP) genes in proline metabolism, we found that Δfmp12 cells could grow better than wild-type cells on agar plate medium containing proline as the sole nitrogen and carbon sources. In contrast, overexpression of FMP12 negatively affected cell growth under the same condition. The Fmp12 protein was localized in the mitochondria and was constitutively expressed. Deletion of the genes that encode mitochondrial enzymes, such as proline dehydrogenase (PUT1), Δ(1)-pyrroline-5-carboxylate dehydrogenase (PUT2), alanine transaminase (ALT1), and α-ketoglutarate dehydrogenase subunit (KGD1), abolished the enhanced cell growth in Δfmp12. These results provided the first evidence that proline can be utilized as a carbon source via the mitochondrial proline metabolic pathway and the subsequent tricarboxylic acid (TCA) cycle in S. cerevisiae. The function of Fmp12, which has a similarity with α-ketoglutarate-dependent dioxygenases of the yeast Candida species and human, might inhibit cell growth by skipping the ATP production step of the TCA cycle. |
format | Online Article Text |
id | pubmed-5348986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-53489862017-03-29 Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12 controls utilization of proline as an energy source in Saccharomyces cerevisiae Nishida, Ikuhisa Watanabe, Daisuke Takagi, Hiroshi Microb Cell Microbiology The amino acid proline functions as a nitrogen source and as a stress protectant in the yeast Saccharomyces cerevisiae. However, utilization of proline as a carbon source in S. cerevisiae cells has not been studied yet. In the process of study on the physiological roles of the found-in-mitochondrial-proteome (FMP) genes in proline metabolism, we found that Δfmp12 cells could grow better than wild-type cells on agar plate medium containing proline as the sole nitrogen and carbon sources. In contrast, overexpression of FMP12 negatively affected cell growth under the same condition. The Fmp12 protein was localized in the mitochondria and was constitutively expressed. Deletion of the genes that encode mitochondrial enzymes, such as proline dehydrogenase (PUT1), Δ(1)-pyrroline-5-carboxylate dehydrogenase (PUT2), alanine transaminase (ALT1), and α-ketoglutarate dehydrogenase subunit (KGD1), abolished the enhanced cell growth in Δfmp12. These results provided the first evidence that proline can be utilized as a carbon source via the mitochondrial proline metabolic pathway and the subsequent tricarboxylic acid (TCA) cycle in S. cerevisiae. The function of Fmp12, which has a similarity with α-ketoglutarate-dependent dioxygenases of the yeast Candida species and human, might inhibit cell growth by skipping the ATP production step of the TCA cycle. Shared Science Publishers OG 2016-09-19 /pmc/articles/PMC5348986/ /pubmed/28357320 http://dx.doi.org/10.15698/mic2016.10.535 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Microbiology Nishida, Ikuhisa Watanabe, Daisuke Takagi, Hiroshi Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12 controls utilization of proline as an energy source in Saccharomyces cerevisiae |
title | Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12
controls utilization of proline as an energy source in Saccharomyces
cerevisiae |
title_full | Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12
controls utilization of proline as an energy source in Saccharomyces
cerevisiae |
title_fullStr | Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12
controls utilization of proline as an energy source in Saccharomyces
cerevisiae |
title_full_unstemmed | Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12
controls utilization of proline as an energy source in Saccharomyces
cerevisiae |
title_short | Putative mitochondrial α-ketoglutarate-dependent dioxygenase Fmp12
controls utilization of proline as an energy source in Saccharomyces
cerevisiae |
title_sort | putative mitochondrial α-ketoglutarate-dependent dioxygenase fmp12
controls utilization of proline as an energy source in saccharomyces
cerevisiae |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348986/ https://www.ncbi.nlm.nih.gov/pubmed/28357320 http://dx.doi.org/10.15698/mic2016.10.535 |
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