pmc logo imageJournal ListSearchpmc logo image
Logo of jbacterJ Bacteriol SubscriptionsJ Bacteriol Web Site
J Bacteriol. 1975 January; 121(1): 296–304.
PMCID: PMC285643
Transformation and transfection in lysogenic strains of Bacillus subtilis: evidence for selective induction of prophage in competent cells.
R E Yasbin, G A Wilson, and F E Young
Abstract
Lysogenic strains of Bacillus subtilis 168 were reduced in their level of transformation as compared to non-lysogenic strains. The level of transformation decreased even further if the competent lysogenic cells were allowed to incubate in growth media prior to selection on minimal agar. This reduction in the frequency of transformation was attributable to the selective elimination of transformed lysogenic cells from the competent population. Concurrent with the decrease in the number of transformants from a lysogenic competent population was the release of bacteriophage by these cells. The lysogenic bacteria demonstrated this dramatic release of bacteriophage only if the cells were grown to competence. Both the selective elimination of transformed lysogens and the induction of prophage was prevented by the inhibition of protein synthesis. Additionally, competent lysogenic cells released significantly higher amounts of exogenous donor transforming deoxyribonucleic acid than did competent non-lysogenic cells or competent lysogenic cells incubated with erythromycin. These data establish that the induction of the prophage from the competent lysogenic cells was responsible for the selective elmination of the lysogenic transformants. A model is presented that accounts for the induction of the prophage from competent lysogenic bacteria via the induction of a repair system. It is postulated that a repair system is induced or derepressed by the accumulation of gaps in the chromosomes of competent bacteria. This hypothetical enzyme(s) is ultimately responsible for the induction of the prophage and the selective elimination of transformants.
Full text
Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1.3M), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
  • Boylan, RJ; Mendelson, NH; Brooks, D; Young, FE. Regulation of the bacterial cell wall: analysis of a mutant of Bacillus subtilis defective in biosynthesis of teichoic acid. J Bacteriol. 1972 Apr;110(1):281–290. [PubMed]
  • Bridges, BA. Evidence for a further dark repair process in bacteria. Nat New Biol. 1972 Nov 8;240(97):52–53. [PubMed]
  • Brown, NC. Inhibition of bacterial DNA replication by 6-(p-hydroxyphenylazo)-uracil: differential effect on repair and semi-conservative synthesis in Bacillus subtilis. J Mol Biol. 1971 Jul 14;59(1):1–16. [PubMed]
  • Burgess, RR. RNA polymerase. Annu Rev Biochem. 1971;40:711–740. [PubMed]
  • Castellazzi, M; George, J; Buttin, G. Prophage induction and cell division in E. coli. I. Further characterization of the thermosensitive mutation tif-1 whose expression mimics the effect of UV irradiation. Mol Gen Genet. 1972;119(2):139–152. [PubMed]
  • Castellazzi, M; George, J; Buttin, G. [Prophage induction and cell division in E. coli. II. Linked (recA, zab) and unlinked (lex) suppressors of tif-1-mediated induction and filamentation.]. Mol Gen Genet. 1972;119(2):153–174. [PubMed]
  • Clark, AJ. Recombination deficient mutants of E. coli and other bacteria. Annu Rev Genet. 1973;7:67–86. [PubMed]
  • Defais, M; Fauquet, P; Radman, M; Errera, M. Ultraviolet reactivation and ultraviolet mutagenesis of lambda in different genetic systems. Virology. 1971 Feb;43(2):495–503. [PubMed]
  • Dooley, DC; Hadden, CT; Nester, EW. Macromolecular synthesis in Bacillus subtilis during development of the competent state. J Bacteriol. 1971 Nov;108(2):668–679. [PubMed]
  • Dubnau, D; Cirigliano, C. Fate of transforming DNA following uptake by competent Bacillus subtilis. Formation and properties of products isolated from transformed cells which are derived entirely from donor DNA. J Mol Biol. 1972 Feb 28;64(1):9–29. [PubMed]
  • Dubnau, D; Cirigliano, C. Fate of transforming deoxyribonucleic acid after uptake by competent Bacillus subtilis: nonrequirement of deoxyribonucleic acid replication for uptake and integration of transforming deoxyribonucleic acid. J Bacteriol. 1973 Mar;113(3):1512–1514. [PubMed]
  • Dubnau, D; Cirigliano, C. Genetic characterization of recombination-deficient mutants of Bacillus subtilis. J Bacteriol. 1974 Feb;117(2):488–493. [PubMed]
  • Dubnau, D; Davidoff-Abelson, R; Scher, B; Cirigliano, C. Fate of transforming deoxyribonucleic acid after uptake by competent Bacillus subtilis: phenotypic characterization of radiation-sensitive recombination-deficient mutants. J Bacteriol. 1973 Apr;114(1):273–286. [PubMed]
  • Garro, AJ. Isolation and properties of Bacillus subtilis strains lysogenized by a clear plaque mutant of bacteriophage phi 105. J Virol. 1973 Jul;12(1):13–17. [PubMed]
  • Garro, AJ. DNA-mediated prophage induction in Bacillus subtilis lysogenic for phi 105c4. J Virol. 1973 Jul;12(1):18–24. [PubMed]
  • Gass, KB; Low, RL; Cozzarelli, NR. Inhibition of a DNA polymerase from Bacillus subtilis by hydroxyphenylazopyrimidines. Proc Natl Acad Sci U S A. 1973 Jan;70(1):103–107. [PubMed]
  • George, J; Devoret, R; Radman, M. Indirect ultraviolet-reactivation of phage lambda. Proc Natl Acad Sci U S A. 1974 Jan;71(1):144–147. [PubMed]
  • Harris, WJ; Barr, GC. Some properties of DNA in competent Bacillus subtilis. J Mol Biol. 1969 Jan;39(2):245–255. [PubMed]
  • Harris, WJ; Barr, GC. Structural features of DNA in competent Bacillus subtilis. Mol Gen Genet. 1971;113(4):316–330. [PubMed]
  • Harris, WJ; Barr, GC. Mechanism of transformation in B. subtilis. Mol Gen Genet. 1971;113(4):331–344. [PubMed]
  • Laird, CD; Wang, L; Bodmer, WF. Recombination and DNA replication in Bacillus subtilis transformation. Mutat Res. 1968 6(2):205–209.Sep–Oct; [PubMed]
  • Mount, DW; Low, KB; Edmiston, SJ. Dominant mutations (lex) in Escherichia coli K-12 which affect radiation sensitivity and frequency of ultraviolet lght-induced mutations. J Bacteriol. 1972 Nov;112(2):886–893. [PubMed]
  • Parsons, LC; Ranhand, JM; Leonard, CG; Colon, AE; Cole, RM. Inhibition of transformation in group H streptococci by lysogeny. J Bacteriol. 1973 Mar;113(3):1217–1222. [PubMed]
  • Pestka, S. Inhibitors of ribosome functions. Annu Rev Microbiol. 1971;25:487–562. [PubMed]
  • Rudin, L; Sjöström, JE; Lindberg, M; Philipson, L. Factors affecting competence for transformation in Staphylococcus aureus. J Bacteriol. 1974 Apr;118(1):155–164. [PubMed]
  • Rutberg, B; Rutberg, L. Growth of bacteriophage phi 105 and its deoxyribonucleic acid in radiation-sensitive mutants of Bacillus subtilis. J Virol. 1971 Dec;8(6):919–921. [PubMed]
  • Samojlenko, I; Harford, N; Mergeay, M. Phenotypic properties of Bacillus subtilis mutants defective in recombination and repair functions. Mol Gen Genet. 1974 May 21;130(2):143–152. [PubMed]
  • SEAMAN, E; TARMY, E; MARMUR, J. INDUCIBLE PHAGES OF BACILLUS SUBTILIS. Biochemistry. 1964 May;3:607–613. [PubMed]
  • Setlow, JK; Boling, ME; Allison, DP; Beattie, KL. Relationship between prophage induction and transformation in Haemophilus influenzae. J Bacteriol. 1973 Jul;115(1):153–161. [PubMed]
  • Sjöström, JE; Lindberg, M; Philipson, L. Competence for transfection in Staphylococcus aureus. J Bacteriol. 1973 Feb;113(2):576–585. [PubMed]
  • Spizizen, J. TRANSFORMATION OF BIOCHEMICALLY DEFICIENT STRAINS OF BACILLUS SUBTILIS BY DEOXYRIBONUCLEATE. Proc Natl Acad Sci U S A. 1958 Oct 15;44(10):1072–1078. [PubMed]
  • Stewart, CR; Pagel, MF. Relationship between transformation in Bacillus subtilis and infection by bacteriophage SP02. J Bacteriol. 1973 Nov;116(2):1082–1083. [PubMed]
  • Streips, UN; Young, FE. Mode of action of the competence-inducing factor of Bacillus stearothermophilus. J Bacteriol. 1971 Jun;106(3):868–875. [PubMed]
  • Wilson, GA; Williams, MT; Baney, HW; Young, FE. Characterization of temperate bacteriophages of Bacillus subtilis by the restriction endonuclease EcoRI: evidence for three different temperate bacteriophages. J Virol. 1974 Oct;14(4):1013–1016. [PubMed]
  • Witkin, EM. Thermal enhancement of ultraviolet mutability in a tif-1 uvrA derivative of Escherichia coli B-r: evidence that ultraviolet mutagenesis depends upon an inducible function. Proc Natl Acad Sci U S A. 1974 May;71(5):1930–1934. [PubMed]
  • Witkin, EM; George, DL. Ultraviolet mutagenesis in polA and UvrA polA derivatives of Escherichia coli B-R: evidence for an inducible error-prone repair system. Genetics. 1973 Apr;73(Suppl):Suppl 73–NaN10. [PubMed]
  • Yasbin, RE; Ganesan, AT; Young, FE. Bacteriophage interference in Bacillus subtilis 168. J Virol. 1974 Apr;13(4):916–921. [PubMed]
  • Yasbin, RE; Wilson, GA; Young, FE. Transformation and transfection in lysogenic strains of Bacillus subtilis 168. J Bacteriol. 1973 Feb;113(2):540–548. [PubMed]
  • Yasbin, RE; Wilson, GA; Young, FE. Effect of lysogeny on transfection and transfection enhancement in Bacillus subtilis. J Bacteriol. 1975 Jan;121(1):305–312. [PubMed]
  • Yasbin, RE; Young, FE. The influence of temperate bacteriophage phi105 on transformation and transfection in Bacillus subtilis. Biochem Biophys Res Commun. 1972 Apr 28;47(2):365–371. [PubMed]
  • YOUNG, FE; SPIZIZEN, J. Physiological and genetic factors affecting transformation of Bacillus subtilis. J Bacteriol. 1961 May;81:823–829. [PubMed]