An assessment of the role of intracellular free Ca2+ in E. coli
| Autor: | I. B. Holland, Helen E. Jones, Annick Jacq, Anthony K. Campbell |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Intracellular Fluid
Cell division Calmodulin Cell Aequorin Biochemistry chemistry.chemical_compound Escherichia coli medicine FtsZ Egtazic Acid Protein Kinase C biology Chemotaxis Cell Cycle Gene Expression Regulation Bacterial General Medicine Cell cycle Calcium Channel Blockers Cell biology EGTA medicine.anatomical_structure Verapamil chemistry Mutation biology.protein Calcium Cell Division Intracellular Bacillus subtilis |
| Zdroj: | Biochimie. 81:901-907 |
| ISSN: | 0300-9084 |
| Popis: | We have previously proposed that fluctuations in Ca(2+) levels should play an important role in bacteria as in eukaryotes in regulating cell cycle events (Norris et al., J. Theor. Biol. 134 (1998) 341-350). This proposal implied the presence of Ca(2+) uptake systems in bacteria, cell cycle mutants simultaneously defective in Ca(2+)-homeostasis, and perturbation of cell cycle processes when cellular Ca(2+) levels are depleted. We review the properties of new cell cycle mutants in E. coli and B. subtilis resistant to inhibitors of calmodulin, PKC or Ca(2+)-channels; the evidence for Ca(2+)-binding proteins including Acp and FtsZ; and Ca(2+)-transporters. In addition, the effects of EGTA and verapamil (a Ca(2+) channel inhibitor) on growth, protein synthesis and cell cycle events in E. coli are described. We also describe new measurements of free Ca(2+)-levels, using aequorin, in E. coli. Several new cell cycle mutants were obtained using this approach, affecting either initiation of DNA replication or in particular cell division at non-permissive temperature. Several of the mutants were also hypersensitive to EGTA and or Ca(2+). However, none of the mutants apparently involved direct alteration of a drug target and surprisingly in some cases involved specific tRNAs or a tRNA synthetase. The results also indicate that the expression of several genes in E. coli may be regulated by Ca(2+). Cell division in particular appears very sensitive to the level of cell Ca(2+), with the frequency of division clearly reduced by EGTA and by verapamil. However, whilst the effect of EGTA was clearly correlated with depletion of cellular Ca(2+) including free Ca(2+), this was not the case with verapamil which appears to change membrane fluidity and the consequent activity of membrane proteins. Measurement of free Ca(2+) in living cells indicated levels of 200-300 nM, tightly regulated in wild type cells in exponential phase, somewhat less so in stationary phase, with apparently La(2+)-sensitive PHB-polyphosphate complexes involved in Ca(2+) influx. The evidence reviewed increasingly supports a role for Ca(2+) in cellular processes in bacteria, however, any direct link to the control of cell cycle events remains to be established. |
| Databáze: | OpenAIRE |
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