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Effect of Rec mutations on the activity of colicinogenic factors

Journal of Bacteriology
|September 1, 1967
PubMed

Insights

Rec(-) mutations in Escherichia coli prevent colicin E(1) and E(2) production but do not affect colicin V factor properties or plasmid maintenance. These mutations impact spontaneous and induced colicin expression.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Genetics

Background:

  • Colicinogenic factors (Col factors) are plasmids in Escherichia coli that confer the ability to produce colicins, a class of bacteriocins.
  • Rec(-) mutations affect DNA repair mechanisms, potentially influencing plasmid stability and gene expression.

Purpose of the Study:

  • To investigate the impact of Rec(-) mutations on the acceptance, maintenance, and expression of ColE(1), ColE(2), and ColV factors in Escherichia coli.
  • To determine if Rec(-) mutations affect colicin production, plasmid transfer, or immunity conferred by these factors.

Main Methods:

  • Utilizing two specific Rec(-) mutant strains (AB2463 and JC1553) of Escherichia coli.
  • Examining the effects of these mutations on cells harboring ColE(1), ColE(2), and ColV factors.
  • Assessing spontaneous and induced colicin production, plasmid acquisition, maintenance, transfer, and immunity expression.

Main Results:

  • Rec(-) mutations did not affect the colicinogenic properties of the ColV factor.
  • These mutations abolished spontaneous and induced production of colicins E(1) and E(2).
  • Rec(-) mutations did not impair the ability of cells to acquire, maintain, or transfer ColE(1) and ColE(2) factors, nor did they affect immunity expression.

Conclusions:

  • Rec(-) mutations specifically disrupt the production of colicins E(1) and E(2) in Escherichia coli.
  • DNA repair pathways are crucial for the expression of certain colicin types, but not for plasmid maintenance or immunity.
  • Indirect induction of colicin production can occur through mating with irradiated cells, irrespective of the Rec(-) status of the donor strain.

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