PXD044412 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Metabolite interactions in the bacterial Calvin cycle and implications for flux regulation |
Description | Metabolite-level regulation of enzyme activity is important for microbes to cope with environmental shifts. Knowledge of such regulations can also guide strain engineering to improve industrial phenotypes. Recently developed chemoproteomics workflows allow for genome-wide detection of metabolite-protein interactions that may regulate pathway activity. We applied limited proteolysis small molecule mapping (LiP-SMap) to identify and compare metabolite-protein interactions in the proteomes of two cyanobacteria and two lithoautotrophic bacteria that fix CO2 using the Calvin cycle. Clustering analysis of the hundreds of detected interactions showed that some metabolites interacted in a species-specific manner, such as interactions of glucose-6-phosphate in Cupriavidus necator and of glyoxylate in Synechocystis sp.sp PCC 6803. These are interpreted in light of the different central carbon conversion pathways present. Metabolites interacting with the Calvin cycle enzymes fructose-1,6/sedoheptulose-1,7-bisphosphatase (F/SBPase) and transketolase were tested for effects on catalytic activity in vitro. The Calvin cycle intermediate glyceraldehyde-3-phosphate activated both Synechocystis and Cupriavidus F/SBPase, which suggests a feed-forward activation of the cycle in both photoautotrophs and chemolithoautotrophs. In contrast to the stimulating effect in reduced conditions, glyceraldehyde-3-phosphate inactivated the Synechocystis F/SBPase in oxidized conditions by accelerating protein aggregation. Thus, metabolite-level regulation of the Calvin cycle is more prevalent than previously appreciated and may act in addition to redox regulation. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-22 |
AnnouncementXML | Submission_2024-10-22_06:02:44.427.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Emil Sporre |
SpeciesList | scientific name: Hydrogenophaga pseudoflava; NCBI TaxID: 47421; scientific name: Synechocystis sp. (strain PCC 6803 / Kazusa); NCBI TaxID: 1111708; scientific name: Synechococcus elongatus (strain PCC 7942) (Anacystis nidulans R2); NCBI TaxID: 1140; scientific name: Bacteria; NCBI TaxID: NCBITaxon:2; scientific name: Cupriavidus necator (strain ATCC 17699 / H16 / DSM 428 / Stanier 337) (Ralstonia eutropha); NCBI TaxID: 381666; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-08-07 07:57:39 | ID requested | |
1 | 2023-09-06 08:48:03 | announced | |
⏵ 2 | 2024-10-22 06:02:44 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: Cupriavidus necator, cyanobacteria, prosit, Synechococcus sp. PCC7942, interaction proteomics, encyclopeDIA, Hydrogenophaga pseudoflava, LiP-SMap, carbon fixation, Synechocystis sp. PCC6803, Ralstonia eutropha |
Contact List
Elton Paul Hudson |
contact affiliation | Head of the Department of Protein Science, Division of Systems Biology at the Royal Institute of Technology (KTH), Stockholm, Sweden |
contact email | paul.hudson@scilifelab.se |
lab head | |
Emil Sporre |
contact affiliation | Royal Institute of Technology (KTH) |
contact email | emil.sporre@scilifelab.se |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD044412
- Label: PRIDE project
- Name: Metabolite interactions in the bacterial Calvin cycle and implications for flux regulation