Abstract
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 suficent
for integration. Orf1 contains 485 amino acids and is located just
upstream of attP. The N-terminal 150 to 1180 amino acids of Orf1
showed 38 to 44% similarity to the resolvase group of
site-specific integrases, while no similarity to know 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.
Original language | English |
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Journal | Journal of Bacteriology |
Volume | 178 |
Issue number | 17 |
Pages (from-to) | 5164-5173 |
ISSN | 0021-9193 |
Publication status | Published - 1996 |