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Appl. Environ. Microbiol., Dec 1995, 4348-4356, Vol 61, No. 12
MW Lubbers, NR Waterfield, TP Beresford, RW Le Page and AW Jarvis
The 22,163-bp genome of the lactococcal prolate-headed phage c2 was
sequenced. Thirty-nine open reading frames (ORFs), early and late
promoters, and a putative transcription terminator were identified.
Twenty-two ORFs were in the early gene region, and 17 were in the late gene
region. Putative genes for a DNA polymerase, a recombination protein, a
sigma factor protein, a transcription regulatory protein, holin proteins,
and a terminase were identified. Transcription of the early and late genes
proceeded divergently from a noncoding 611-bp region. A 521-bp fragment
contained within the 611-bp intergenic region could act as an origin of
replication in Lactococcus lactis. Three major structural proteins, with
sizes of 175, 90, and 29 kDa, and eight minor proteins, with sizes of 143,
82, 66, 60, 44, 42, 32, and 28 kDa, were identified. Several of these
proteins appeared to be posttranslationally modified by proteolytic
cleavage. The 175- and 90- kDa proteins were identified as the major phage
head proteins, and the 29- and 60-kDa proteins were identified as the major
tail protein and (possibly) the tail adsorption protein, respectively. The
head proteins appeared to be covalently linked multimers of the same 30-kDa
gene product. Phage c2 and prolate-headed lactococcal phage bIL67 (C.
Schouler, S. D. Ehrlich, and M.-C. Chopin, Microbiology 140:3061-3069,
1994) shared 80% nucleotide sequence identity. However, several DNA
deletions or insertions which corresponded to the loss or acquisition of
specific ORFs, respectively, were noted. The identification of direct
nucleotide repeats flanking these sequences indicated that recombination
may be important in the evolution of these phages.(ABSTRACT TRUNCATED AT
250 WORDS)
Copyright © 1995, American Society for Microbiology
Sequencing and analysis of the prolate-headed lactococcal bacteriophage c2 genome and identification of the structural genes
Biological Science Section, New Zealand Dairy Research Institute, Palmerston North, New Zealand.
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