The synthetic plasmid pfdC1 with the replication origin of phage fd an
d fd gene 2 grows autonomously in E. coli cells. DNA sequencing reveal
ed several mutations compared to the fd genome causing reduced express
ion of viral gene 2 protein, which can be toxic for the host cell. Ano
ther adaptation was noticed for E. coli strains with a copy of fd gene
2 on the F-episome and a pfdA-plasmid with a minimal fd replication o
rigin, when maintained at 42 degrees C. The carrier cells adjusted the
ir cellular metabolism to these stress conditions, whereas replication
functions of the plasmid or expression of fd gene 2 on the F-episome
were not changed. The filamentous bacteriophages tend to reduce their
genome size into miniphages, which was also observed for phages with a
n antibiotic resistance gene. Bacteriophages with a transposon inserti
on in the viral gene 2 had a tendency to restore the mutated gene by e
xchange with the functional gene 2 carried in recA-host cells. Mobiliz
ation of pfd-plasmids with RP4 transfer functions was reduced due to i
nterference of replication and transfer in the rolling circle mode. Th
e vectors used in these studies can also be applied as cloning vectors
, which are compatible with many other plasmid vectors.