Affiliation:
1. National Institute of Arthritis and Metabolic Diseases, National Institutes of Health, Bethesda, Maryland
Abstract
Lisio, Arnold
L. (National Institutes of Health, Bethesda, Md.),
and Arthur Weissbach
. Repression of λ-associated enzyme synthesis after λ
vir
superinfection of lysogenic hosts. J. Bacteriol.
90:
661–666. 1965.—Phage λ
vir
is a multiple mutant of λ which is capable of overcoming the immunity of a host lysogenic for λ, and initiating normal vegetative replication of the superinfecting phage genome. Superinfection of
Escherichia coli
K-112 (λ
22
) with λ
vir
results in a normal phage yield, lysis time, and H
3
-thymine incorporation compared with infection of the sensitive host, K-112 (S). However, the production of the λ phage-specific early protein, λ-exonuclease, after superinfection of
E. coli
K-112 (λ
22
) with λ
vir
is only 25 to 50% of that obtained from corresponding infection of a nonlysogenic host,
E. coli
K-112 (S). This repression of λ-exonuclease synthesis is dependent on the C
1
cistron of the prophage and is overcome if the lysogenic host cells are induced prior to superinfection. The data are interpreted as evidence for partial repression of λ
vir
by the host immunity.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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