PXD022622 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Comprehensive analysis of C. glutamicum anaplerotic deletion mutants under defined D-glucose conditions |
Description | Wild-type C. glutamicum ATCC 13032 is known to possess two enzymes with anaplerotic (C4-directed) carboxylation activity, namely phosphoenolpyruvate carboxylase (PEPCx) and pyruvate carboxylase (PCx). On the other hand, C3-directed decarboxylation can be catalyzed by the three enzymes phosphoenolpyruvate carboxykinase (PEPCk), oxaloacetate decarboxylase (ODx), and malic enzyme (ME). The resulting high metabolic flexibility at the anaplerotic node compromises the unambigous determination of its carbon and energy flux in C. glutamicum wild type. To circumvent this problem we performed a comprehensive analysis of selected single or double deletion mutants in the anaplerosis of wild-type C. glutamicum under defined D-glucose conditions. By applying well-controlled lab-scale bioreactor experiments in combination with untargeted proteomics, quantitative metabolomics and whole-genome sequencing hitherto unknown, and sometimes counter-intuitive, genotype-phenotype relationships in these mutants could be unraveled. In comparison to the wild type the four mutants C. glutamiucm pyc, C. glutamiucmpyc odx, C. glutamiucm ppc pyc and C. glutamiucm pck showed lowered specific growth rates and D-glucose uptake rates, underlining the importance of PCx and PEPCk activity for a balanced carbon and energy flux at the anaplerotic node. Most interestingly, the strain C. glutamiucm ppc pyc could be evolved to grow on D-glucose as the only source of carbon and energy, whereas this combination was previously considered lethal. The prevented anaplerotic carboxylation activity of PEPCx and PCx was found in the evolved strain to be compensated by an up-regulation of the glyoxylate shunt, potentially in combination with the 2-methylcitrate cycle. |
HostingRepository | PRIDE |
AnnounceDate | 2021-09-09 |
AnnouncementXML | Submission_2021-09-09_14:27:34.099.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Bianca Klein |
SpeciesList | scientific name: Corynebacterium glutamicum ATCC 13032; NCBI TaxID: 196627; |
ModificationList | No PTMs are included in the dataset |
Instrument | TripleTOF 6600 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-11-19 03:31:54 | ID requested | |
⏵ 1 | 2021-09-09 14:27:34 | announced | |
Publication List
Kappelmann J, Klein B, Papenfu, ß M, Lange J, Blombach B, Takors R, Wiechert W, Polen T, Noack S, Anaplerotic Deletion Mutants Under Defined d-Glucose Conditions. Front Bioeng Biotechnol, 8():602936(2020) [pubmed] |
Keyword List
submitter keyword: Corynebacterium glutamicum, anaplerosis, phosphoenolpyruvate carboxylase, pyruvate carboxylase, phosphoenolpyruvate carboxykinase, oxaloacetate decarboxylase, malic enzyme, methylcitrate cycle |
Contact List
Stephan Noack |
contact affiliation | Forschungszentrum Juelich GmbH Institute of Bio- and Geosciences 1 Systems Biotechnology Group: Quantitative Microbial Phenotyping |
contact email | s.noack@fz-juelich.de |
lab head | |
Bianca Klein |
contact affiliation | Forschungszentrum Juelich GmbH |
contact email | b.klein@fz-juelich.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD022622
- Label: PRIDE project
- Name: Comprehensive analysis of C. glutamicum anaplerotic deletion mutants under defined D-glucose conditions