Time-Dependent Analysis of Paenarthrobacter nicotinovorans pAO1 Nicotine-Related Proteome.
Marius MihăşanRăzvan Ştefan BoiangiuDoina GuzunCornelia BabiiRoshanak AslebaghDevika ChannaveerappaEmmalyn DupreeCostel C DariePublished in: ACS omega (2021)
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.
Keyphrases
- mass spectrometry
- smoking cessation
- induced apoptosis
- tandem mass spectrometry
- liquid chromatography
- cell cycle arrest
- high performance liquid chromatography
- electronic health record
- gas chromatography
- ultra high performance liquid chromatography
- big data
- signaling pathway
- endoplasmic reticulum stress
- stem cells
- single cell
- genome wide
- dna methylation
- cell death
- oxidative stress
- escherichia coli
- cell proliferation
- high resolution
- solid phase extraction
- bone marrow
- small molecule
- cell therapy
- pi k akt
- transcription factor
- binding protein
- hyaluronic acid
- label free
- klebsiella pneumoniae