Excess production of phage λ delayed early proteins under conditions supporting high Escherichia coli growth rates

Bacteriophage λ is unable to lysogenize Escherichia coli hosts harbouring the rpoA341 mutation due to a drastic reduction in transcription from CII-activated lysogenic promoters ( p E , p 1 and p aQ ). In addition, the level of early transcripts involved in the lytic pathway of λ development is also decreased in this genetic background due to impaired N-dependent antitermination. Here, it is demonstrated that despite the reduced level of early lytic p L - and p R -derived transcripts, lytic growth of bacteriophage λ is not affected in rich media. The level of the late lytic, p R -derived transcripts also remains unaffected by the rpoA341 mutation under these conditions. However, it was found that whilst there is no significant difference in the phage burst size in rpoA + and rpoA341 hosts growing in rich media, phage λ is not able to produce progeny in the rpoA341 mutant growing in minimal medium, in contrast to otherwise isogenic rpoA + bacteria. Provision of an excess of the phage replication proteins O and P in trans or overproduction of the antitermination protein N restore the ability of phage λ to produce progeny in the rpoA341 mutant under the latter conditions. These results suggest that in rich media phage λ produces some early proteins in excess of that needed for its effective propagation and indicate that replication proteins may be limiting factors for phage lytic growth in poor media.