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. 1967 Jan;93(1):107–114. doi: 10.1128/jb.93.1.107-114.1967

Conditional Mutations Involving Septum Formation in Escherichia coli

James R Walker 1, Arthur B Pardee 1
PMCID: PMC314975  PMID: 5335887

Abstract

The lon mutation is responsible for a defect in cell division of Escherichia coli lightly irradiated with ultraviolet light (UV). These lon mutants can be isolated readily by a procedure described here. Physiological studies were performed with the objective of determining the role of the lon gene. Unirradiated lon mutants grow normally, except that a correlation of this mutation with capsule formation has been noted previously. These two properties can be separated, however. After irradiation, lon grows as long filaments because septum formation is prevented. The filaments eventually lyse. Mass increase and deoxyribonucleic acid and enzyme synthesis appear to proceed normally. Thus, the lesion produced by UV appears to be highly specific. In bacteria that carry both genes (merozygotes), lon+ is dominant to lon. Septum formation is restored to irradiated lon bacteria by introduction of lon+ by conjugation. Also, normal growth can be restored by nutritional variations. It is concluded that lon+ is able to nullify the effects of the UV lesion under conditions where lon cannot. Possibly, capsule precursors that can accumulate in the latter are responsible for the difference because they interfere with repair of the UV lesion.

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Selected References

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

  1. ADLER H. I., HARDIGREE A. A. ANALYSIS OF A GENE CONTROLLING CELL DIVISION AND SENSITIVITY TO RADIATION IN ESCHERICHIA COLI. J Bacteriol. 1964 Mar;87:720–726. doi: 10.1128/jb.87.3.720-726.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. ADLER H. I., HARDIGREE A. A. POSTIRRADIATION GROWTH, DIVISION, AND RECOVERY IN BACTERIA. Radiat Res. 1965 May;25:92–102. [PubMed] [Google Scholar]
  3. Adler H. I., Fisher W. D., Hardigree A. A., Stapleton G. E. Repair of radiation-induced damage to the cell division mechanism of Escherichia coli. J Bacteriol. 1966 Feb;91(2):737–742. doi: 10.1128/jb.91.2.737-742.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Adler H. I., Hardigree A. A. Growth and Division of Filamentous Forms of Escherichia coli. J Bacteriol. 1965 Jul;90(1):223–226. doi: 10.1128/jb.90.1.223-226.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BOYCE R. P., HOWARD-FLANDERS P. RELEASE OF ULTRAVIOLET LIGHT-INDUCED THYMINE DIMERS FROM DNA IN E. COLI K-12. Proc Natl Acad Sci U S A. 1964 Feb;51:293–300. doi: 10.1073/pnas.51.2.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. GRULA E. A., GRULA M. M. Cell division in a species of Erwinia III. Reversal of inhibition of cell division caused by D-amino acids, penicillin, and ultraviolet light. J Bacteriol. 1962 May;83:981–988. doi: 10.1128/jb.83.5.981-988.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Greenberg J. Radiation sensitivity in Escherichia coli: some properties of the radiation-sensitive Hfr K12 mutant, PAM 401. Mutat Res. 1965 Aug;2(4):304–311. doi: 10.1016/0027-5107(65)90064-3. [DOI] [PubMed] [Google Scholar]
  8. HOWARD-FLANDERS P., SIMSON E., THERIOT L. A LOCUS THAT CONTROLS FILAMENT FORMATION AND SENSITIVITY TO RADIATION IN ESCHERICHIA COLI K-12. Genetics. 1964 Feb;49:237–246. doi: 10.1093/genetics/49.2.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kantor G. J., Deering R. A. Ultraviolet radiation studies of filamentous Escherichia coli B. J Bacteriol. 1966 Oct;92(4):1062–1069. doi: 10.1128/jb.92.4.1062-1069.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. MARKOVITZ A. REGULATORY MECHANISMS FOR SYNTHESIS OF CAPSULAR POLYSACCHARIDE IN MUCOID MUTANTS OF ESCHERICHIA COLI K12. Proc Natl Acad Sci U S A. 1964 Feb;51:239–246. doi: 10.1073/pnas.51.2.239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Markovitz A., Rosenbaum N. A regulator gene that is dominant on an episome and recessive on a chromosome. Proc Natl Acad Sci U S A. 1965 Oct;54(4):1084–1091. doi: 10.1073/pnas.54.4.1084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. PARDEE A. B., PRESTIDGE L. S. The initial kinetics of enzyme induction. Biochim Biophys Acta. 1961 Apr 29;49:77–88. doi: 10.1016/0006-3002(61)90871-x. [DOI] [PubMed] [Google Scholar]
  13. RORSCH A., EDELMAN A., COHEN J. A. The gene-controlled radiation sensitivity in Escherichia coli. Biochim Biophys Acta. 1963 Feb 26;68:263–270. doi: 10.1016/0006-3002(63)90141-0. [DOI] [PubMed] [Google Scholar]
  14. RORSCH A., EDELMAN A., van der KAMP, COHEN J. A. Phenotypic and genotypic characterization of radiation sensitivity in Escherichia coli B. Biochim Biophys Acta. 1962 Aug 20;61:278–289. doi: 10.1016/0926-6550(62)90090-7. [DOI] [PubMed] [Google Scholar]
  15. SETLOW R. B., CARRIER W. L. THE DISAPPEARANCE OF THYMINE DIMERS FROM DNA: AN ERROR-CORRECTING MECHANISM. Proc Natl Acad Sci U S A. 1964 Feb;51:226–231. doi: 10.1073/pnas.51.2.226. [DOI] [PMC free article] [PubMed] [Google Scholar]

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