Quantitative proteomic analyses reveal the impact of nitrogen starvation on the proteome of the model diatom Phaeodactylum tricornutum
| dc.rights.license | open | en_US |
| hal.structure.identifier | Laboratoire de biogenèse membranaire [LBM] | |
| dc.contributor.author | LUPETTE, Josselin | |
| dc.contributor.author | TARDIF, Marianne | |
| dc.contributor.author | BRUGIERE, Sabine | |
| dc.contributor.author | COUTE, Yohann | |
| dc.contributor.author | SALVAING, Juliette | |
| dc.contributor.author | MARECHAL, Eric | |
| dc.date.accessioned | 2023-01-26T10:39:58Z | |
| dc.date.available | 2023-01-26T10:39:58Z | |
| dc.date.issued | 2022 | |
| dc.identifier.issn | 1615-9861 | en_US |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/171802 | |
| dc.description.abstractEn | Diatoms are one of the largest groups in phytoplankton biodiversity. Understanding their response to nitrogen variations, present from micromolar to near-zero levels in oceans and fresh waters, is essential to comprehend their ecological success. Nitrogen starvation is used in biotechnological processes, to trigger the remodeling of carbon metabolism in the direction of fatty acids and triacylglycerol synthesis. We evaluated whole proteome changes in Phaeodactylum tricornutum after 7 days of cultivation with 5.5-mM nitrate (+N) or without any nitrogen source (-N). On a total of 3768 proteins detected in biological replicates, our analysis pointed to 384 differentially abundant proteins (DAP). Analysis of proteins of lower abundance in -N revealed an arrest of amino acid and protein syntheses, a remodeling of nitrogen metabolism, and a decrease of the proteasome abundance suggesting a decline in unselective whole-proteome decay. Analysis of proteins of higher abundance revealed the setting up of a general nitrogen scavenging system dependent on deaminases. The increase of a plastid palmitoyl-ACP desaturase appeared as a hallmark of carbon metabolism rewiring in the direction of fatty acid and triacylglycerol synthesis. This dataset is also valuable to select gene candidates for improved biotechnological properties. | |
| dc.description.sponsorship | CBH-EUR-GS - ANR-17-EURE-0003 | en_US |
| dc.description.sponsorship | Grenoble Alliance for Integrated Structural Cell Biology - ANR-10-LABX-0049 | en_US |
| dc.description.sponsorship | Infrastructure Française de Protéomique - ANR-10-INBS-0008 | en_US |
| dc.description.sponsorship | IDEX UGA - ANR-15-IDEX-0002 | en_US |
| dc.language.iso | EN | en_US |
| dc.subject.en | Diatom | |
| dc.subject.en | Nitrogen starvation | |
| dc.subject.en | Phaeodactylum | |
| dc.subject.en | Proteome remodelling | |
| dc.subject.en | Quantitative proteomics | |
| dc.title.en | Quantitative proteomic analyses reveal the impact of nitrogen starvation on the proteome of the model diatom Phaeodactylum tricornutum | |
| dc.type | Article de revue | en_US |
| dc.identifier.doi | 10.1002/pmic.202200155 | en_US |
| dc.subject.hal | Sciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire | en_US |
| bordeaux.journal | Proteomics | en_US |
| bordeaux.page | 2200155 | en_US |
| bordeaux.volume | 22 | en_US |
| bordeaux.hal.laboratories | Laboratoire de Biogenèse Membranaire (LBM) - UMR 5200 | en_US |
| bordeaux.issue | 22 | en_US |
| bordeaux.institution | Université de Bordeaux | en_US |
| bordeaux.institution | CNRS | en_US |
| bordeaux.peerReviewed | oui | en_US |
| bordeaux.inpress | non | en_US |
| hal.export | false | |
| dc.rights.cc | Pas de Licence CC | en_US |
| bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Proteomics&rft.date=2022&rft.volume=22&rft.issue=22&rft.spage=2200155&rft.epage=2200155&rft.eissn=1615-9861&rft.issn=1615-9861&rft.au=LUPETTE,%20Josselin&TARDIF,%20Marianne&BRUGIERE,%20Sabine&COUTE,%20Yohann&SALVAING,%20Juliette&rft.genre=article |
