F- phenocopies: characterization of expression of the F transfer region in stationary phase
- 1 September 1998
- journal article
- Published by Microbiology Society in Microbiology
- Vol. 144 (9) , 2579-2587
- https://doi.org/10.1099/00221287-144-9-2579
Abstract
The phenomenon of ‘F- phenocopies’ in which F+ cells become transfer-deficient in stationary phase seems contradictory to the proposed role for F transfer in adaptive mutation during stationary phase induced by nutrient limitation. The expression of a range of transfer genes at the transcriptional and translational level in stationary phase has been characterized as well as the degree of nicking at the origin of transfer, oriT. Transfer efficiency rapidly decreased in mid-exponential phase, coincident with a decrease in traM transcripts. Approximately 2 h later, the transcript for traA, encoding F-pilin, also decreased to undetectable levels. The levels of TraA (pilin), TraD, TraJ and TraT remained fairly constant well into stationary phase while the levels of TraM and Tral decreased to undetectable levels in early stationary phase. A null mutation in the gene for the alternative s factor, rpoS, did not affect mating efficiency or transcript levels but did increase the stability of TraM and Tral in stationary phase. Nicking at oriT was detected at maximal levels in early stationary phase and at low levels in late stationary phase. The results suggest that the F-pilus transfer apparatus is maintained in the cell envelope after transcription of the transfer region from the main promoter, Py, has ceased with down-regulation of traM transcription being the first step detected in this process. The presence of a low level of nicking at oriT in stationary phase is consistent with a role for F in promoting adaptive mutation.Keywords
This publication has 37 references indexed in Scilit:
- The cytoplasmic DNA-binding protein TraM binds to the inner membrane protein TraD in vitroJournal of Bacteriology, 1997
- Analysis of the traLEKBP sequence and the TraP protein from three F-like plasmids: F, R100-1 and ColB2Journal of Bacteriology, 1996
- Adaptive reversion of an episomal frameshift mutation in Escherichia coli requires conjugal functions but not actual conjugation.Proceedings of the National Academy of Sciences, 1995
- The FinO protein of IncF plasmids binds FinP antisense RNA and its target, traJ mRNA, and promotes duplex formationMolecular Microbiology, 1994
- Regulation of R100 conjugation requires traM in cis to traJMolecular Microbiology, 1994
- Synthesis of the Escherichia coli K‐12 nucleoid‐associated DNA‐binding protein H‐NS is subjected to growth‐phase control and autoregulationMolecular Microbiology, 1993
- Cointegrate formation mediated by Tn9Journal of Molecular Biology, 1983
- A rapid alkaline extraction procedure for screening recombinant plasmid DNANucleic Acids Research, 1979
- Transposition and fusion of the lac genes to selected promoters in Escherichia coli using bacteriophage lambda and MuJournal of Molecular Biology, 1976
- BACTERIAL CONJUGATIONAnnual Review of Microbiology, 1969