K. Gregg et al., CLONING AND DNA-SEQUENCE ANALYSIS OF THE REGION CONTAINING ATTP OF THE TEMPERATE PHAGE-PHI-AR29 OF PREVOTELLA-RUMINICOLA-AR29, Microbiology, 140, 1994, pp. 2109-2114
Phage phi AR29 was shown to exist as a prophage integrated into the ch
romosome of Prevotella ruminicola AR29. By DNA hybridization studies,
the point of integrative recombination on the phage genome (attP) was
located on a 4.5 kb EcoRV fragment. After preliminary mapping with res
triction endonucleases, a 2.8 kb EcoRV/HindIII fragment was isolated,
cloned in Escherichia coil and sequenced. DNA hybridization localized
the attP site to the vicinity of an internal Dral site. Sequence analy
sis showed the presence of several direct and inverted repeats around
the attP site, with consensus core sequences similar to the integrase
binding sites of phage lambda. Two open reading frames are present adj
acent to attP (ORF1 and ORF2). The predicted polypeptide product of OR
F1 has a region of structural similarity to known integrases. Although
the predicted product of ORF2 shows at best weak homology with known
excisionases, no other ORFs occur in the sequence upstream from ORF1,
leaving ORF2 as the mast likely candidate for this role. However, if O
RF2 does represent an xis gene, then this putative integration module
would possess a notable difference from that of other temperate phages
in the inversion of the positions of int and xis relative to attP. Th
e proposed phi AR29 integration module is being used to develop phage-
based integrative vector systems for the genetic manipulation of rumen
bacteria.