Previous Article | Next Article ![]()
J. Bacteriol., 09 1996, 5164-5173, Vol 178, No. 17
B Christiansen, L Brondsted, FK Vogensen and K Hammer
The integration system of the temperate lactococcal phage TP901-1 was
characterized in Lactococcus lactis subsp. cremoris LM0230 and MG1363 with
the use of deletion derivatives of the integration vector pBC143 (B.
Christiansen, M. G. Johnsen, E. Stenby, F. K. Vogensen, and K. Hammer, J.
Bacteriol. 176:1069-1076, 1994). The phage-encoded elements necessary for
integration were localized on a 2.8-kb NsiI-EcoRI fragment including the
phage attachment site, attP. This fragment was DNA sequenced, and sequence
analysis revealed three putatively expressed open reading frames, Orf1,
Orf2, and Orf3 By the introduction of mutations within the orf1, orf2, and
orf3 genes, it was shown that only Orf1 was necessary for the integration
process. Furthermore, it was found that Orf1, attP, and a 425-bp region
upstream of the orf1 gene are sufficient for integration. Orf1 contains 485
amino acids and is located just upstream of attP. The N-terminal 150 to 180
amino acids of Orf1 showed 38 to 44% similarity to the resolvase group of
site- specific integrases, while no similarity to known proteins was found
in the C-terminal end. Bacteriophage TP901-1 therefore contains a unique
integration system that does not resemble the Int class of site- specific
integrases usually found in temperate bacteriophages. The constructed
integration vector, pBC170, integrates into the chromosomal attachment site
very efficiently and forms stable transformants with a frequency
corresponding to 20% of the transformation efficiency.
Copyright © 1996, American Society for Microbiology
A resolvase-like protein is required for the site-specific integration of the temperate lactococcal bacteriophage TP901-1
Department of Microbiology, Technical University of Denmark, Lyngby, Denmark.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»