Affiliation:
1. Department of Bacterial Immunology, Walter Reed Army Institute of Research, Washington, D.C. 20012
2. Department of Microbiology, Georgetown University Schools of Medicine and Dentistry, Washington, D.C. 20007
Abstract
Salmonella typhosa
hybrids able to adsorb lambda were obtained by mating
S. typhosa
recipients with
Escherichia coli
K-12 donors. After adsorption of wild-type λ to these
S. typhosa
hybrids, no plaques or infective centers could be detected.
E. coli
K-12
gal
+
genes carried by the defective phage λ
dg
were transduced to
S. typhosa
hybrids with HFT lysates derived from
E. coli
heterogenotes. The lysogenic state which resulted in the
S. typhosa
hybrids after
gal
+
transduction differed from that of
E. coli
. Ability to produce λ, initially present, was permanently segregated by transductants of the
S. typhosa
hybrid.
S. typhosa
lysogens did not lyse upon treatment for phage induction with mitomycin C, ultraviolet light, or heat in the case of thermoinducible λ. A further difference in the behavior of λ in
Salmonella
hybrids was the absence of zygotic induction of the prophage when transferred from
E. coli
K-12 donors to
S. typhosa
. A new λ mutant class, capable of forming plaques on
S. typhosa
hybrids refractory to wild-type λ, was isolated at low frequency by plating λ on
S. typhosa
hybrid WR4254. Such mutants have been designated as λ
sx
, and a mutant allele of λ
sx
was located between the P and Q genes of the λ chromosome. Plaques were formed also on the
S. typhosa
hybrid host with a series of λ
i21
hybrid phages which contain the N gene of phage 21. The significance of these results in terms of
Salmonella
species as hosts for λ is discussed.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
50 articles.
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