Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1996 Feb;178(3):668–674. doi: 10.1128/jb.178.3.668-674.1996

A regulator of the flagellar regulon of Escherichia coli, flhD, also affects cell division.

B M Prüss 1, P Matsumura 1
PMCID: PMC177710  PMID: 8550498

Abstract

The role of an activator of flagellar transcription in Escherichia coli, flhD, was investigated in the regulation of cell division. When grown in tryptone broth, flhD mutant cells divided exponentially until they reached a cell density of 2.5 x 10(9) cells per ml. Wild-type cells and flhC mutant cells divided exponentially until they reached a cell density of 4 x 10(7) cells per ml. flhD mutant cells divided 5 times more than wild-type cells before they reduced their cell division rate and reached a cell density 37 times higher than that of wild-type or flhC mutant cultures. In stationary phase, the biomasses of all cultures were similar; however, flhD mutant cells were significantly smaller. Additional tryptone, Casamino Acids, and individual amino acids, added at the beginning of growth, allowed wild-type cells to grow to higher cell densities. Serine was determined to have the greatest effect. In contrast, the addition of Casamino Acids did not exhibit an effect upon flhD mutant cells. flhD mutant cells exhibited normal rates of uptake of serine and other amino acids. In both wild-type and flhD mutant cultures, the concentrations of serine in the media dropped from 140 to 20 microM within the first 2 h of growth. Serine concentrations and cell division rates were highly correlated. Wild-type cells reduced their cell division rate at a medium concentration of 50 microM serine, and the addition of serine at this time caused cells to resume a higher rate of division. We conclude that the reduction of the cell division rate in wild-type cells is caused by the depletion of serine from the medium and that flhD mutant cells seem to be unable to sense this depletion.

Full Text

The Full Text of this article is available as a PDF (270.7 KB).

Selected References

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

  1. Amsler C. D., Cho M., Matsumura P. Multiple factors underlying the maximum motility of Escherichia coli as cultures enter post-exponential growth. J Bacteriol. 1993 Oct;175(19):6238–6244. doi: 10.1128/jb.175.19.6238-6244.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bartlett D. H., Frantz B. B., Matsumura P. Flagellar transcriptional activators FlbB and FlaI: gene sequences and 5' consensus sequences of operons under FlbB and FlaI control. J Bacteriol. 1988 Apr;170(4):1575–1581. doi: 10.1128/jb.170.4.1575-1581.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brown T. D., Jones-Mortimer M. C., Kornberg H. L. The enzymic interconversion of acetate and acetyl-coenzyme A in Escherichia coli. J Gen Microbiol. 1977 Oct;102(2):327–336. doi: 10.1099/00221287-102-2-327. [DOI] [PubMed] [Google Scholar]
  4. Bryan R., Glaser D., Shapiro L. Genetic regulatory hierarchy in Caulobacter development. Adv Genet. 1990;27:1–31. doi: 10.1016/s0065-2660(08)60022-x. [DOI] [PubMed] [Google Scholar]
  5. Dingwall A., Zhuang W. Y., Quon K., Shapiro L. Expression of an early gene in the flagellar regulatory hierarchy is sensitive to an interruption in DNA replication. J Bacteriol. 1992 Mar;174(6):1760–1768. doi: 10.1128/jb.174.6.1760-1768.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Erickson H. P. FtsZ, a prokaryotic homolog of tubulin? Cell. 1995 Feb 10;80(3):367–370. doi: 10.1016/0092-8674(95)90486-7. [DOI] [PubMed] [Google Scholar]
  7. Givskov M., Eberl L., Christiansen G., Benedik M. J., Molin S. Induction of phospholipase- and flagellar synthesis in Serratia liquefaciens is controlled by expression of the flagellar master operon flhD. Mol Microbiol. 1995 Feb;15(3):445–454. doi: 10.1111/j.1365-2958.1995.tb02258.x. [DOI] [PubMed] [Google Scholar]
  8. Gober J. W., Marques M. V. Regulation of cellular differentiation in Caulobacter crescentus. Microbiol Rev. 1995 Mar;59(1):31–47. doi: 10.1128/mr.59.1.31-47.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Helmstetter C. E., Eenhuis C., Theisen P., Grimwade J., Leonard A. C. Improved bacterial baby machine: application to Escherichia coli K-12. J Bacteriol. 1992 Jun;174(11):3445–3449. doi: 10.1128/jb.174.11.3445-3449.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Holms W. H. The central metabolic pathways of Escherichia coli: relationship between flux and control at a branch point, efficiency of conversion to biomass, and excretion of acetate. Curr Top Cell Regul. 1986;28:69–105. doi: 10.1016/b978-0-12-152828-7.50004-4. [DOI] [PubMed] [Google Scholar]
  11. Kawamukai M., Matsuda H., Fujii W., Utsumi R., Komano T. Nucleotide sequences of fic and fic-1 genes involved in cell filamentation induced by cyclic AMP in Escherichia coli. J Bacteriol. 1989 Aug;171(8):4525–4529. doi: 10.1128/jb.171.8.4525-4529.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Komeda Y., Iino T. Regulation of expression of the flagellin gene (hag) in Escherichia coli K-12: analysis of hag-lac gene fusions. J Bacteriol. 1979 Sep;139(3):721–729. doi: 10.1128/jb.139.3.721-729.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Komeda Y., Kutsukake K., Iino T. Definition of additional flagellar genes in Escherichia coli K12. Genetics. 1980 Feb;94(2):277–290. doi: 10.1093/genetics/94.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Liu X., Matsumura P. The FlhD/FlhC complex, a transcriptional activator of the Escherichia coli flagellar class II operons. J Bacteriol. 1994 Dec;176(23):7345–7351. doi: 10.1128/jb.176.23.7345-7351.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Macnab R. M. Genetics and biogenesis of bacterial flagella. Annu Rev Genet. 1992;26:131–158. doi: 10.1146/annurev.ge.26.120192.001023. [DOI] [PubMed] [Google Scholar]
  16. McCleary W. R., Stock J. B., Ninfa A. J. Is acetyl phosphate a global signal in Escherichia coli? J Bacteriol. 1993 May;175(10):2793–2798. doi: 10.1128/jb.175.10.2793-2798.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Nishimura A., Hirota Y. A cell division regulatory mechanism controls the flagellar regulon in Escherichia coli. Mol Gen Genet. 1989 Apr;216(2-3):340–346. doi: 10.1007/BF00334374. [DOI] [PubMed] [Google Scholar]
  18. Prüss B. M., Nelms J. M., Park C., Wolfe A. J. Mutations in NADH:ubiquinone oxidoreductase of Escherichia coli affect growth on mixed amino acids. J Bacteriol. 1994 Apr;176(8):2143–2150. doi: 10.1128/jb.176.8.2143-2150.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Prüss B. M., Wolfe A. J. Regulation of acetyl phosphate synthesis and degradation, and the control of flagellar expression in Escherichia coli. Mol Microbiol. 1994 Jun;12(6):973–984. doi: 10.1111/j.1365-2958.1994.tb01085.x. [DOI] [PubMed] [Google Scholar]
  20. Robinson A. C., Collins J. F., Donachie W. D. Prokaryotic and eukaryotic cell-cycle proteins. 1987 Aug 27-Sep 2Nature. 328(6133):766–766. doi: 10.1038/328766a0. [DOI] [PubMed] [Google Scholar]
  21. Shi W., Zhou Y., Wild J., Adler J., Gross C. A. DnaK, DnaJ, and GrpE are required for flagellum synthesis in Escherichia coli. J Bacteriol. 1992 Oct;174(19):6256–6263. doi: 10.1128/jb.174.19.6256-6263.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Shin S., Park C. Modulation of flagellar expression in Escherichia coli by acetyl phosphate and the osmoregulator OmpR. J Bacteriol. 1995 Aug;177(16):4696–4702. doi: 10.1128/jb.177.16.4696-4702.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Silverman M., Simon M. Characterization of Escherichia coli flagellar mutants that are insensitive to catabolite repression. J Bacteriol. 1974 Dec;120(3):1196–1203. doi: 10.1128/jb.120.3.1196-1203.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  25. Yu J., Shapiro L. Early Caulobacter crescentus genes fliL and fliM are required for flagellar gene expression and normal cell division. J Bacteriol. 1992 May;174(10):3327–3338. doi: 10.1128/jb.174.10.3327-3338.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES