We have previously proposed that fluctuations in Ca2+ levels should play an
important role in bacteria as in eukaryotes in regulating cell cycle event
s (Norris et al., J. Theor. Biol. 134 (1998) 341-350). This proposal implie
d the presence of Ca2+ uptake systems in bacteria, cell cycle mutants simul
taneously defective in Ca2+-homeostasis, and perturbation of cell cycle pro
cesses when cellular Ca2+ levels are depleted. We review the properties of
new cell cycle mutants in E. coli and B. subtilis resistant to inhibitors o
f calmodulin, PKC or Ca2+-channels; the evidence for Ca2+-binding proteins
including Acp and FtsZ; and Ca2+-transporters. In addition, the effects of
EGTA and verapamil (a Ca2+ channel inhibitor) on growth, protein synthesis
and cell cycle events in E. coli are described. We also describe new measur
ements of free Ca2+-levels, using aequorin, in E. coli. Several new cell cy
cle mutants were obtained using this approach, affecting either initiation
of DNA replication or in particular cell division at non-permissive tempera
ture. Several of the mutants were also hypersensitive to EGTA and or Ca2+.
However, none of the mutants apparently involved direct alteration of a dru
g target and surprisingly in some cases involved specific tRNAs or a tRNA s
ynthetase. The results also indicate that the expression of several genes i
n E. coli may be regulated by Ca2+. Cell division in particular appears ver
y sensitive to the level of cell Ca2+, with the frequency of division clear
ly reduced by EGTA and by verapamil. However, whilst the effect of EGTA was
clearly correlated with depletion of cellular Ca2+ including free Ca2+, th
is was not the case with verapamil which appears to change membrane fluidit
y and the consequent activity of membrane proteins. Measurement of free Ca2
+ in living cells indicated levels of 200-300 nM, tightly regulated in wild
type cells in exponential phase, somewhat less so in stationary phase, wit
h apparently La2+-sensitive PHB-polyphosphate complexes involved in Ca2+ in
flux. The evidence reviewed increasingly supports a role for Ca2+ in cellul
ar processes in bacteria, however, any direct link to the control of cell c
ycle events remains to be established. (C) 1999 Societe francaise de biochi
mie et biologie moleculaire/Editions scientifiques et medicales Elsevier SA
S.