Temperate bacteriophage Mx8 of Myxococcus xanthus encapsidates termina
lly repetitious DNA, packaged as circular permutations of its 49-kbp g
enome. During both lytic and lysogenic development, Mx8 expresses a no
nessential DNA methylase, Mox, which modifies adenine residues in occu
rrences of XhoI and PstI recognition sites, CTCGAG and CTGCAG, respect
ively, on both phage DNA and the host chromosome. The mox gene is nece
ssary for methylase activity in vivo, because an amber mutation in the
mox gene abolishes activity. The mox gene is the only phage gene requ
ired for methylase activity in vivo, because ectopic expression of mox
as part of the M. xanthus mg/BA operon results in partial methylation
of the host chromosome. The predicted amino acid sequence of Mox is r
elated most closely to that of the methylase involved in the cell cycl
e control of Caulobacter crescentus. We speculate that Mox acts to pro
tect Mx8 phage DNA against restriction upon infection of a subset of n
atural M. xanthus hosts. One natural isolate of M. xanthus, the lysoge
nic source of related phage Mx81, produces a restriction endonuclease
with the cleavage specificity of endonuclease BstBI.