scholarly journals Multiple links connect central carbon metabolism to DNA replication initiation and elongation inBacillus subtilis

DNA Research ◽  
2018 ◽  
Vol 25 (6) ◽  
pp. 641-653 ◽  
Author(s):  
Hamid Nouri ◽  
Anne-Françoise Monnier ◽  
Solveig Fossum-Raunehaug ◽  
Monika Maciąg-Dorszyńska ◽  
Armelle Cabin-Flaman ◽  
...  
Genes ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 447
Author(s):  
Klaudyna Krause ◽  
Monika Maciąg-Dorszyńska ◽  
Anna Wosinski ◽  
Lidia Gaffke ◽  
Joanna Morcinek-Orłowska ◽  
...  

A direct link between DNA replication regulation and central carbon metabolism (CCM) has been previously demonstrated in Bacillus subtilis and Escherichia coli, as effects of certain mutations in genes coding for replication proteins could be specifically suppressed by particular mutations in genes encoding CCM enzymes. However, specific molecular mechanism(s) of this link remained unknown. In this report, we demonstrate that various CCM metabolites can suppress the effects of mutations in different replication genes of E. coli on bacterial growth, cell morphology, and nucleoid localization. This provides evidence that the CCM-replication link is mediated by metabolites rather than direct protein-protein interactions. On the other hand, action of metabolites on DNA replication appears indirect rather than based on direct influence on the replication machinery, as rate of DNA synthesis could not be corrected by metabolites in short-term experiments. This corroborates the recent discovery that in B. subtilis, there are multiple links connecting CCM to DNA replication initiation and elongation. Therefore, one may suggest that although different in detail, the molecular mechanisms of CCM-dependent regulation of DNA replication are similar in E. coli and B. subtilis, making this regulation an important and common constituent of the control of cell physiology in bacteria.


PLoS ONE ◽  
2017 ◽  
Vol 12 (4) ◽  
pp. e0176050 ◽  
Author(s):  
Joanna Tymecka-Mulik ◽  
Lidia Boss ◽  
Monika Maciąg-Dorszyńska ◽  
João F. Matias Rodrigues ◽  
Lidia Gaffke ◽  
...  

2013 ◽  
Vol 12 (1) ◽  
pp. 55 ◽  
Author(s):  
Sylwia Barańska ◽  
Monika Glinkowska ◽  
Anna Herman-Antosiewicz ◽  
Monika Maciąg-Dorszyńska ◽  
Dariusz Nowicki ◽  
...  

2015 ◽  
Vol 84 (1) ◽  
pp. 58-67 ◽  
Author(s):  
Aleksandra Konieczna ◽  
Aneta Szczepańska ◽  
Karolina Sawiuk ◽  
Robert Łyżeń ◽  
Grzegorz Węgrzyn

Gene ◽  
2018 ◽  
Vol 650 ◽  
pp. 1-6 ◽  
Author(s):  
Aneta Wieczorek ◽  
Karolina Fornalewicz ◽  
Łukasz Mocarski ◽  
Robert Łyżeń ◽  
Grzegorz Węgrzyn

Author(s):  
Monika Maciąg ◽  
Dariusz Nowicki ◽  
Agnieszka Szalewska-Pałasz ◽  
Grzegorz Węgrzyn

2011 ◽  
Vol 10 (1) ◽  
pp. 19 ◽  
Author(s):  
Monika Maciąg ◽  
Dariusz Nowicki ◽  
Laurent Janniere ◽  
Agnieszka Szalewska-Pałasz ◽  
Grzegorz Węgrzyn

2019 ◽  
Vol 16 (3) ◽  
pp. 272-277 ◽  
Author(s):  
Rasmus N. Klitgaard ◽  
Anders Løbner-Olesen

Background:One of many strategies to overcome antibiotic resistance is the discovery of compounds targeting cellular processes, which have not yet been exploited.Materials and Methods:Using various genetic tools, we constructed a novel high throughput, cellbased, fluorescence screen for inhibitors of chromosome replication initiation in bacteria.Results:The screen was validated by expression of an intra-cellular cyclic peptide interfering with the initiator protein DnaA and by over-expression of the negative initiation regulator SeqA. We also demonstrated that neither tetracycline nor ciprofloxacin triggers a false positive result. Finally, 400 extracts isolated mainly from filamentous actinomycetes were subjected to the screen.Conclusion:We concluded that the presented screen is applicable for identifying putative inhibitors of DNA replication initiation in a high throughput setup.


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