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. 1973 Nov;116(2):1001–1010. doi: 10.1128/jb.116.2.1001-1010.1973

Production of Bacteriophage by Temperature-Sensitive Sporulation Mutants of Bacillus cereus T1

G N Stelma Jr a, H L Sadoff a
PMCID: PMC285475  PMID: 4126824

Abstract

Five temperature-sensitive sporulation mutants of Bacillus cereus T have been isolated. These mutants are blocked at stage 0 of sporulation at the restrictive temperature (37 C) but are able to sporulate at nearly normal frequencies at the permissive temperature (26 C). A bacteriophage that forms a stable lysogen in the parent strain is induced at increased frequencies in the mutants. This induction is accompanied, in some of the mutants, by a reduction in immunity to the phage. Revertants, selected for their ability to sporulate normally at both temperatures, lose their ability to produce high titers of the phage. In addition to this lytic phage, an apparently defective phage has been found in lysates of the mutants. Strains cured of the plaque-forming phage still carry the defective phage. Comparisons of physical and biological properties of the plaque-forming phage with those of the two Bacillus cereus phages most similar to it have shown that this phage is not identical to either of them. The maximal titer of phage produced in cultures of the parent strain is about 103 plaque-forming units (PFU) per ml at both temperatures. The maximal titers of phage produced by the mutant are 4 × 109 PFU/ml at 37 C and 7 × 108 PFU/ml at 26 C. Both mutant and parent strains release over 90% of the phage they produce after the onset of stationary phase.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALTENBERN R. A., STULL H. B. EDEMA FACTOR AND PHOSPHOLIPASE RELEASE BY A STRAIN OF BACILLUS CEREUS. Can J Microbiol. 1964 Oct;10:717–725. doi: 10.1139/m64-091. [DOI] [PubMed] [Google Scholar]
  2. Bradley D. E. The fluorescent staining of bacteriophage nucleic acids. J Gen Microbiol. 1966 Sep;44(3):383–391. doi: 10.1099/00221287-44-3-383. [DOI] [PubMed] [Google Scholar]
  3. Bradley D. E. Ultrastructure of bacteriophage and bacteriocins. Bacteriol Rev. 1967 Dec;31(4):230–314. doi: 10.1128/br.31.4.230-314.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Carls R. A., Hanson R. S. Isolation and characterization of tricarboxylic acid cycle mutants of Bacillus subtilis. J Bacteriol. 1971 Jun;106(3):848–855. doi: 10.1128/jb.106.3.848-855.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. HANSON R. S., SRINIVASAN V. R., HALVORSON H. O. Biochemistry of sporulation. I. Metabolism of acetate by vegetative and sporulating cells. J Bacteriol. 1963 Feb;85:451–460. doi: 10.1128/jb.85.2.451-460.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. HASHIMOTO T., BLACK S. H., GERHARDT P. Development of fine structure, thermostability, and dipicolinate during sporogenesis in a bacillus. Can J Microbiol. 1960 Apr;6:203–212. doi: 10.1139/m60-022. [DOI] [PubMed] [Google Scholar]
  7. Ito J., Spizizen J. Abortive infection of sporulating Bacillus subtilis 168 by phi 2 bacteriophage. J Virol. 1971 Apr;7(4):515–523. doi: 10.1128/jvi.7.4.515-523.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kawakami M., Landman O. E. Nature of the carrier state of bacteriophage SP-10 in Bacillus subtilis. J Bacteriol. 1968 May;95(5):1804–1812. doi: 10.1128/jb.95.5.1804-1812.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. MEYNELL E. W. Characters of a group of bacillus phages. J Gen Microbiol. 1962 Apr;28:103–117. doi: 10.1099/00221287-28-1-103. [DOI] [PubMed] [Google Scholar]
  10. Pattee P. A. Use of tetrazolium for improved resolution of bacteriophage plaques. J Bacteriol. 1966 Sep;92(3):787–788. doi: 10.1128/jb.92.3.787-788.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Schaeffer P. Sporulation and the production of antibiotics, exoenzymes, and exotonins. Bacteriol Rev. 1969 Mar;33(1):48–71. doi: 10.1128/br.33.1.48-71.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. THORNE C. B. Transduction in Bacillus subtilis. J Bacteriol. 1962 Jan;83:106–111. doi: 10.1128/jb.83.1.106-111.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Thorne C. B. Transducing bacteriophage for Bacillus cereus. J Virol. 1968 Jul;2(7):657–662. doi: 10.1128/jvi.2.7.657-662.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Yelton D. B., Thorne C. B. Comparison of Bacillus cereus bacteriophages CP-51 and CP-53. J Virol. 1971 Aug;8(2):242–253. doi: 10.1128/jvi.8.2.242-253.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Yelton D. B., Thorne C. B. Transduction in Bacillus cereus by each of two bacteriophages. J Bacteriol. 1970 May;102(2):573–579. doi: 10.1128/jb.102.2.573-579.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]

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