» Articles » PMID: 4977240

Mapping of a Temperate Bacteriophage Active on Bacillus Subtilis

Overview
Journal J Virol
Date 1969 Jan 1
PMID 4977240
Citations 60
Authors
Affiliations
Soon will be listed here.
Abstract

Bacteriophage phi105 is a temperate bacteriophage for Bacillus subtilis 168. Temperature-sensitive and plaque mutants of phi105 were isolated. The results of two- and three-factor crosses with these mutants suggest the vegetative map of phi105 to be circular. The location of prophage phi105 between bacterial markers phe-1 and ilvA1 was shown by means of PBS1 transduction. Five markers in the prophage were linearly ordered with respect to the bacterial markers. Linkage between bacterial and prophage markers was demonstrated in transformation experiments with deoxyribonucleic acid extracted from lysogenic bacteria. The data demonstrate that prophage phi105 is linearly inserted into the bacterial chromosome.

Citing Articles

Inactivation of ribosomal protein genes in Bacillus subtilis reveals importance of each ribosomal protein for cell proliferation and cell differentiation.

Akanuma G, Nanamiya H, Natori Y, Yano K, Suzuki S, Omata S J Bacteriol. 2012; 194(22):6282-91.

PMID: 23002217 PMC: 3486396. DOI: 10.1128/JB.01544-12.


Characterization of Temperate Bacillus Bacteriophage phi105.

Birdsell D, Hathaway G, Rutberg L J Virol. 1969; 4(3):264-70.

PMID: 16789103 PMC: 375868. DOI: 10.1128/JVI.4.3.264-270.1969.


Endo.SK1: an inducible site-specific endonuclease from yeast mitochondria.

Ohta K, Nicolas A, Keszenman-Pereyra D, Shibata T Mol Gen Genet. 1996; 250(4):395-404.

PMID: 8602156 DOI: 10.1007/BF02174027.


Anti-SOS effects induced in Bacillus subtilis by a phi 105 mutant prophage.

Rubinstein C, Coso O, Ruzal S, Sanchez-Rivas C Arch Microbiol. 1993; 160(6):486-91.

PMID: 8297212 DOI: 10.1007/BF00245310.


trp RNA-binding attenuation protein (TRAP)-trp leader RNA interactions mediate translational as well as transcriptional regulation of the Bacillus subtilis trp operon.

Merino E, Babitzke P, Yanofsky C J Bacteriol. 1995; 177(22):6362-70.

PMID: 7592410 PMC: 177485. DOI: 10.1128/jb.177.22.6362-6370.1995.


References
1.
HERSHEY A, Burgi E, Ingraham L . COHESION OF DNA MOLECULES ISOLATED FROM PHAGE LAMBDA. Proc Natl Acad Sci U S A. 1963; 49(5):748-55. PMC: 299970. DOI: 10.1073/pnas.49.5.748. View

2.
Anagnostopoulos C, Spizizen J . REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS. J Bacteriol. 1961; 81(5):741-6. PMC: 279084. DOI: 10.1128/jb.81.5.741-746.1961. View

3.
Dubnau D, Goldthwaite C, Smith I, MARMUR J . Genetic mapping in Bacillus subtilis. J Mol Biol. 1967; 27(1):163-85. DOI: 10.1016/0022-2836(67)90358-0. View

4.
Reilly B, Spizizen J . BACTERIOPHAGE DEOXYRIBONUCLEATE INFECTION OF COMPETENT BACILLUS SUBTILIS. J Bacteriol. 1965; 89:782-90. PMC: 277537. DOI: 10.1128/jb.89.3.782-790.1965. View

5.
Weil J, Signer E . Recombination in bacteriophage lambda. II. Site-specific recombination promoted by the integration system. J Mol Biol. 1968; 34(2):273-9. DOI: 10.1016/0022-2836(68)90252-0. View