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Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome

[Image: see text] Paenarthrobacter nicotinovorans is a soil Gram-positive nicotine-degrading microorganism (NDM) that harbors a 165 kb pAO1 catabolic megaplasmid. The nicotine catabolic genes on pAO1 have been sequenced, but not all the details on the regulation and interplay of this pathway with th...

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Autores principales: Mihăşan, Marius, Boiangiu, Răzvan Ştefan, Guzun, Doina, Babii, Cornelia, Aslebagh, Roshanak, Channaveerappa, Devika, Dupree, Emmalyn, Darie, Costel C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190789/
https://www.ncbi.nlm.nih.gov/pubmed/34124447
http://dx.doi.org/10.1021/acsomega.1c01020
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author Mihăşan, Marius
Boiangiu, Răzvan Ştefan
Guzun, Doina
Babii, Cornelia
Aslebagh, Roshanak
Channaveerappa, Devika
Dupree, Emmalyn
Darie, Costel C.
author_facet Mihăşan, Marius
Boiangiu, Răzvan Ştefan
Guzun, Doina
Babii, Cornelia
Aslebagh, Roshanak
Channaveerappa, Devika
Dupree, Emmalyn
Darie, Costel C.
author_sort Mihăşan, Marius
collection PubMed
description [Image: see text] Paenarthrobacter nicotinovorans is a soil Gram-positive nicotine-degrading microorganism (NDM) that harbors a 165 kb pAO1 catabolic megaplasmid. The nicotine catabolic genes on pAO1 have been sequenced, but not all the details on the regulation and interplay of this pathway with the general metabolism of the cell are available. To address this issue at the protein level, a time-based shotgun proteomics study was performed. P. nicotinovorans was grown in the presence or absence of nicotine, and the cells were harvested at three different time intervals: 7, 10, and 24 h after inoculation. The cells were lysed, separated on SDS-PAGE, and digested by in-gel digestion using trypsin, and the resulting peptide mixture was analyzed using nanoliquid chromatography tandem mass spectrometry. We found an extensive number of proteins that are both plasmidal- and chromosomal-encoded and that work together in the energetic metabolism via the Krebs cycle and nicotine pathway. These data provide insight into the adaptation of the bacterial cells to the nicotine metabolic intermediates and could serve as a basis for future attempts to genetically engineer the pAO1-encoded catabolic pathway for increased bioremediation efficiency or for the production of valuable chemicals. The mass-spectrometry-based proteomics data have been deposited to the PRIDE partner repository with the data set identifier PXD012577.
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spelling pubmed-81907892021-06-11 Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome Mihăşan, Marius Boiangiu, Răzvan Ştefan Guzun, Doina Babii, Cornelia Aslebagh, Roshanak Channaveerappa, Devika Dupree, Emmalyn Darie, Costel C. ACS Omega [Image: see text] Paenarthrobacter nicotinovorans is a soil Gram-positive nicotine-degrading microorganism (NDM) that harbors a 165 kb pAO1 catabolic megaplasmid. The nicotine catabolic genes on pAO1 have been sequenced, but not all the details on the regulation and interplay of this pathway with the general metabolism of the cell are available. To address this issue at the protein level, a time-based shotgun proteomics study was performed. P. nicotinovorans was grown in the presence or absence of nicotine, and the cells were harvested at three different time intervals: 7, 10, and 24 h after inoculation. The cells were lysed, separated on SDS-PAGE, and digested by in-gel digestion using trypsin, and the resulting peptide mixture was analyzed using nanoliquid chromatography tandem mass spectrometry. We found an extensive number of proteins that are both plasmidal- and chromosomal-encoded and that work together in the energetic metabolism via the Krebs cycle and nicotine pathway. These data provide insight into the adaptation of the bacterial cells to the nicotine metabolic intermediates and could serve as a basis for future attempts to genetically engineer the pAO1-encoded catabolic pathway for increased bioremediation efficiency or for the production of valuable chemicals. The mass-spectrometry-based proteomics data have been deposited to the PRIDE partner repository with the data set identifier PXD012577. American Chemical Society 2021-05-25 /pmc/articles/PMC8190789/ /pubmed/34124447 http://dx.doi.org/10.1021/acsomega.1c01020 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mihăşan, Marius
Boiangiu, Răzvan Ştefan
Guzun, Doina
Babii, Cornelia
Aslebagh, Roshanak
Channaveerappa, Devika
Dupree, Emmalyn
Darie, Costel C.
Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title_full Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title_fullStr Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title_full_unstemmed Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title_short Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome
title_sort time-dependent analysis of paenarthrobacter nicotinovorans pao1 nicotine-related proteome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190789/
https://www.ncbi.nlm.nih.gov/pubmed/34124447
http://dx.doi.org/10.1021/acsomega.1c01020
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