We present evidence that biological properties of cell membranes are altere
d in dnaA and seqA mutants of Escherichia coli relative to wild-type bacter
ia. We found that bacteriophage lambda forms extremely large plaques on the
dnaA seqA double mutants. On the single mutants, dnaA and seqA, the plaque
s are also bigger than those formed on the wild-type host. However, no sign
ificant differences in intracellular phage lambda development were observed
between wild-type and mutant hosts, indicating that differences in burst s
ize do not account for the observed differences in plaque size. On the othe
r hand, more efficient release of the phage lytic proteins and/or higher se
nsitivity of the cell membranes to these proteins may result in more effici
ent cell lysis. We found that the efficiency of adsorption of bacteriophage
lambda to the dnaA seqA mutant cells is decreased at 0 degrees C, but not
at 30 degrees C, relative to the wild-type strain. A considerable increase
in the permeability of membranes of the mutant cells for P-galactosidase is
demonstrated. The dnaA and seqA mutants are more sensitive to ethanol tan
organic solvent) than wild-type bacteria, and the seqA strain and the doubl
e mutant dnaA seqA are very sensitive to deoxycholate (a detergent). We con
clude that lesions in the genes dna and seqA result in alterations in cell
membranes, such that the permeability and possibly also other properties of
the membranes are significantly altered relative to wild-type bacteria.