In order to determine the replication-transposition (RT) efficiency of
Escherichia coli phage Mu in Pseudomonas aeruginosa cells, the change
of Mu DNA copy number after transfer of P. aeruginosa (RP4=Mu) from 4
2 (the condition of RP4=Mu plasmid stability and low phage production
level in P. aeruginosa) to 30-degrees-C (the condition of RP4=Mu plasm
id instability and higher phage production level in P. aeruginosa) was
analysed. It was shown that the temperature shift causes no increase
in Mu DNA copy number, although free phage DNA is revealed after trans
fer of the cells at 30-degrees-C. Considering that the studied cells c
ontained also a linear RP4 DNA and the free Mu DNA hybridized with the
RP4 DNA, we proposed that the mature Mu DNA arises as a result of Mu
genome packaging from the original plasmid. So, the Mu genome RT is un
effective in P. aeruginosa and all of the phage particles released fro
m P. aeruginosa (RP4=Mu) cells contain Mu DNA apparently originated fr
om the DNA of hybrid plasmid RP4=Mu. Moreover, these results suggest t
hat the Mu DNA packaging is not effective in P. aeruginosa (taking int
o account that the P. aeruginosa (RP4=Mu) cells release about 10(-2) p
.f.u./cell and that originally the copy number of RP4=Mu greater-than-
or-equal-to 1).