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PXD060374

PXD060374 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleExploring the high light stress response of a Haematococcus pluvialis (Chlorophyceae) mutant with a higher astaxanthin content via proteomic and phosphoproteomic analysis reveals altered chlorophyll biosynthesis, carbon partitioning, and astaxanthin biosynthesis and trafficking
DescriptionWhile the green microalga, Haematococcus pluvialis, is the best natural producer of astaxanthin, efforts to grow it for astaxanthin production are still limited by its low biomass productivity which subsequently results in lower astaxanthin productivity. Despite new methods of direct strain modification to improve growth and astaxanthin production, the limited understanding of how the astaxanthin biosynthesis pathway is regulated has been a significant roadblock to strain improvement. This work aims to address this knowledge gap by exploring the stress response of H. pluvialis during the transition from heterotrophy to high light conditions. A physical radiation (heavy-ion beam) mutagenesis approach was applied to generate H. pluvialis mutants with a higher cell division rate under heterotrophic conditions. The mutant JWHIB 27-38 that grew 25% faster than the wild type was identified. Mutant JWHIB 27-38 also achieved a 69.61% higher lipid content per cell and 86.17% higher astaxanthin per cell than the wild type under high light stress conditions. A proteomics and phosphoproteomics analysis was conducted with JWHIB 27-38 and the wild type at 0, 48, and 72 h of high light stress to elucidate the mechanisms underlying these phenotypes. Maintained upregulation of chlorophyll biosynthesis pathway proteins and phosphoproteins in mutant JWHIB 27-38 during high light stress, such as glutamate-1-semialdehyde 2,1-aminomutase (GSAM) and coproporphyrinogen oxidase (CPOX), may support continued chlorophyll biosynthesis which can allow cells to adapt to high light conditions. Upregulation of fatty acid biosynthetic proteins such as biotin carboxyl carrier protein (BCCP) and 3-ketoacyl-CoA synthase (KCS) in mutant JWHIB 27-38 suggests that carbon is favored toward lipid accumulation. Increased lipid content, along with upregulation of the key astaxanthin biosynthesis protein, phytoene synthase (PSY), may enable the higher astaxanthin content in mutant JWHIB 27-38. Additionally, upregulation of a putative astaxanthin-trafficking protein, AstaP, likely enables the mutant to traffic more astaxanthin to the cell periphery as part of its stress response. These and other significantly differentially expressed proteins may provide promising targets for future strain engineering work to improve astaxanthin productivity.
HostingRepositoryPRIDE
AnnounceDate2026-01-24
AnnouncementXMLSubmission_2026-01-24_14:56:45.126.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD060374
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterKyarii Ramarui
SpeciesList scientific name: Haematococcus lacustris; NCBI TaxID: NEWT:44745;
ModificationListphosphorylated residue; acetylated residue; deamidated residue; iodoacetamide derivatized residue
InstrumentOrbitrap Eclipse
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-01-30 10:40:30ID requested
12026-01-24 14:56:45announced
Publication List
10.6019/PXD060374;
10.1016/J.ALGAL.2026.104546;
Keyword List
submitter keyword: lipid, proteomics, post-translational modification,High light stress, astaxanthin, phosphoproteomics, chlorophyll biosynthesis, cell cycle control
Contact List
Yantao Li
contact affiliationInstitute of Marine and Environmental Technology, University of Maryland Center for Environmental Science and University of Maryland Baltimore County, 701 E Pratt Street, Baltimore MD, 21202, United States.
contact emailyantao@umces.edu
lab head
Kyarii Ramarui
contact affiliationUniversity of Maryland Center for Environmental Science -- Institute of Marine and Environmental Technology
contact emailkramarui@umces.edu
dataset submitter
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