Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Feb;177(3):765–773. doi: 10.1128/jb.177.3.765-773.1995

Bacillus subtilis possesses a second determinant with extensive sequence similarity to the Escherichia coli mreB morphogene.

Y Abhayawardhane 1, G C Stewart 1
PMCID: PMC176655  PMID: 7836311

Abstract

A gene with substantial sequence similarity to the mreB morphogene of Bacillus subtilis has been identified at 302 degrees on the chromosomal map by A. Decatur, B. Kunkel, and R. Losick (Harvard University; personal communication). Our characterization has revealed that the protein product of this determinant (termed mbl for mreB-like) is 55 and 53% identical in sequence to the MreB proteins of B. subtilis and Escherichia coli, respectively. The protein is 86% identical to a protein identified as MreB from Bacillus cereus, suggesting that the B. cereus protein is actually Mbl. Insertional inactivation of mbl indicated that this gene is not essential for cell viability or sporulation. Cells bearing mutant mbl alleles display a decreased growth rate and an altered cellular morphology. The cells appear bloated and are frequently twisted. Intergenic suppressor mutations which restore the growth rate to an approximately normal level arise within the mutant population. A second site mutation, designated som-1, was mapped to the hisA-mbl region of the chromosome by transduction.

Full Text

The Full Text of this article is available as a PDF (672.4 KB).

Selected References

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

  1. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  2. Birnboim H. C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523. doi: 10.1093/nar/7.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bork P., Sander C., Valencia A. An ATPase domain common to prokaryotic cell cycle proteins, sugar kinases, actin, and hsp70 heat shock proteins. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7290–7294. doi: 10.1073/pnas.89.16.7290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brandt C., Karamata D. Thermosensitive Bacillus subtilis mutants which lyse at the non-permissive temperature. J Gen Microbiol. 1987 May;133(5):1159–1170. doi: 10.1099/00221287-133-5-1159. [DOI] [PubMed] [Google Scholar]
  5. Butler Y. X., Abhayawardhane Y., Stewart G. C. Amplification of the Bacillus subtilis maf gene results in arrested septum formation. J Bacteriol. 1993 May;175(10):3139–3145. doi: 10.1128/jb.175.10.3139-3145.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dagert M., Ehrlich S. D. Prolonged incubation in calcium chloride improves the competence of Escherichia coli cells. Gene. 1979 May;6(1):23–28. doi: 10.1016/0378-1119(79)90082-9. [DOI] [PubMed] [Google Scholar]
  7. Dedonder R. A., Lepesant J. A., Lepesant-Kejzlarová J., Billault A., Steinmetz M., Kunst F. Construction of a kit of reference strains for rapid genetic mapping in Bacillus subtilis 168. Appl Environ Microbiol. 1977 Apr;33(4):989–993. doi: 10.1128/aem.33.4.989-993.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Doi M., Wachi M., Ishino F., Tomioka S., Ito M., Sakagami Y., Suzuki A., Matsuhashi M. Determinations of the DNA sequence of the mreB gene and of the gene products of the mre region that function in formation of the rod shape of Escherichia coli cells. J Bacteriol. 1988 Oct;170(10):4619–4624. doi: 10.1128/jb.170.10.4619-4624.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Erickson R. J., Copeland J. C. Structure and replication of chromosomes in competent cells of Bacillus subtilis. J Bacteriol. 1972 Mar;109(3):1075–1084. doi: 10.1128/jb.109.3.1075-1084.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gonzy-Tréboul G., Karmazyn-Campelli C., Stragier P. Developmental regulation of transcription of the Bacillus subtilis ftsAZ operon. J Mol Biol. 1992 Apr 20;224(4):967–979. doi: 10.1016/0022-2836(92)90463-t. [DOI] [PubMed] [Google Scholar]
  11. Gupta R. S., Singh B. Cloning of the HSP70 gene from Halobacterium marismortui: relatedness of archaebacterial HSP70 to its eubacterial homologs and a model for the evolution of the HSP70 gene. J Bacteriol. 1992 Jul;174(14):4594–4605. doi: 10.1128/jb.174.14.4594-4605.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Halberg R., Kroos L. Fate of the SpoIIID switch protein during Bacillus subtilis sporulation depends on the mother-cell sigma factor, sigma K. J Mol Biol. 1992 Dec 5;228(3):840–849. doi: 10.1016/0022-2836(92)90868-k. [DOI] [PubMed] [Google Scholar]
  13. Homma M., Kutsukake K., Hasebe M., Iino T., Macnab R. M. FlgB, FlgC, FlgF and FlgG. A family of structurally related proteins in the flagellar basal body of Salmonella typhimurium. J Mol Biol. 1990 Jan 20;211(2):465–477. doi: 10.1016/0022-2836(90)90365-S. [DOI] [PubMed] [Google Scholar]
  14. Honeyman A. L., Stewart G. C. The nucleotide sequence of the rodC operon of Bacillus subtilis. Mol Microbiol. 1989 Sep;3(9):1257–1268. doi: 10.1111/j.1365-2958.1989.tb00276.x. [DOI] [PubMed] [Google Scholar]
  15. Karamata D., McConnell M., Rogers H. J. Mapping of rod mutants of Bacillus subtilis. J Bacteriol. 1972 Jul;111(1):73–79. doi: 10.1128/jb.111.1.73-79.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kunkel B., Kroos L., Poth H., Youngman P., Losick R. Temporal and spatial control of the mother-cell regulatory gene spoIIID of Bacillus subtilis. Genes Dev. 1989 Nov;3(11):1735–1744. doi: 10.1101/gad.3.11.1735. [DOI] [PubMed] [Google Scholar]
  17. Lee S., Price C. W. The minCD locus of Bacillus subtilis lacks the minE determinant that provides topological specificity to cell division. Mol Microbiol. 1993 Feb;7(4):601–610. doi: 10.1111/j.1365-2958.1993.tb01151.x. [DOI] [PubMed] [Google Scholar]
  18. Levin P. A., Margolis P. S., Setlow P., Losick R., Sun D. Identification of Bacillus subtilis genes for septum placement and shape determination. J Bacteriol. 1992 Nov;174(21):6717–6728. doi: 10.1128/jb.174.21.6717-6728.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Lleo M. M., Canepari P., Satta G. Bacterial cell shape regulation: testing of additional predictions unique to the two-competing-sites model for peptidoglycan assembly and isolation of conditional rod-shaped mutants from some wild-type cocci. J Bacteriol. 1990 Jul;172(7):3758–3771. doi: 10.1128/jb.172.7.3758-3771.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Narahara A., Naterstad K., Kristensen T., Lopez R., Bork P., Kolstø A. B. Cloning of a gene from Bacillus cereus with homology to the mreB gene from Escherichia coli. Gene. 1992 Dec 1;122(1):181–185. doi: 10.1016/0378-1119(92)90047-s. [DOI] [PubMed] [Google Scholar]
  21. Okada Y., Wachi M., Hirata A., Suzuki K., Nagai K., Matsuhashi M. Cytoplasmic axial filaments in Escherichia coli cells: possible function in the mechanism of chromosome segregation and cell division. J Bacteriol. 1994 Feb;176(3):917–922. doi: 10.1128/jb.176.3.917-922.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Rosey E. L., Oskouian B., Stewart G. C. Lactose metabolism by Staphylococcus aureus: characterization of lacABCD, the structural genes of the tagatose 6-phosphate pathway. J Bacteriol. 1991 Oct;173(19):5992–5998. doi: 10.1128/jb.173.19.5992-5998.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. SAITO H., MIURA K. I. PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT. Biochim Biophys Acta. 1963 Aug 20;72:619–629. [PubMed] [Google Scholar]
  24. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Tatti K. M., Jones C. H., Moran C. P., Jr Genetic evidence for interaction of sigma E with the spoIIID promoter in Bacillus subtilis. J Bacteriol. 1991 Dec;173(24):7828–7833. doi: 10.1128/jb.173.24.7828-7833.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tinoco I., Jr, Borer P. N., Dengler B., Levin M. D., Uhlenbeck O. C., Crothers D. M., Bralla J. Improved estimation of secondary structure in ribonucleic acids. Nat New Biol. 1973 Nov 14;246(150):40–41. doi: 10.1038/newbio246040a0. [DOI] [PubMed] [Google Scholar]
  27. Varley A. W., Stewart G. C. The divIVB region of the Bacillus subtilis chromosome encodes homologs of Escherichia coli septum placement (minCD) and cell shape (mreBCD) determinants. J Bacteriol. 1992 Nov;174(21):6729–6742. doi: 10.1128/jb.174.21.6729-6742.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Wachi M., Doi M., Okada Y., Matsuhashi M. New mre genes mreC and mreD, responsible for formation of the rod shape of Escherichia coli cells. J Bacteriol. 1989 Dec;171(12):6511–6516. doi: 10.1128/jb.171.12.6511-6516.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wachi M., Doi M., Tamaki S., Park W., Nakajima-Iijima S., Matsuhashi M. Mutant isolation and molecular cloning of mre genes, which determine cell shape, sensitivity to mecillinam, and amount of penicillin-binding proteins in Escherichia coli. J Bacteriol. 1987 Nov;169(11):4935–4940. doi: 10.1128/jb.169.11.4935-4940.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Wachi M., Doi M., Ueda T., Ueki M., Tsuritani K., Nagai K., Matsuhashi M. Sequence of the downstream flanking region of the shape-determining genes mreBCD of Escherichia coli. Gene. 1991 Sep 30;106(1):135–136. doi: 10.1016/0378-1119(91)90578-y. [DOI] [PubMed] [Google Scholar]
  31. Wachi M., Matsuhashi M. Negative control of cell division by mreB, a gene that functions in determining the rod shape of Escherichia coli cells. J Bacteriol. 1989 Jun;171(6):3123–3127. doi: 10.1128/jb.171.6.3123-3127.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Wagner P. M., Stewart G. C. Role and expression of the Bacillus subtilis rodC operon. J Bacteriol. 1991 Jul;173(14):4341–4346. doi: 10.1128/jb.173.14.4341-4346.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Zuberi A. R., Ying C., Bischoff D. S., Ordal G. W. Gene-protein relationships in the flagellar hook-basal body complex of Bacillus subtilis: sequences of the flgB, flgC, flgG, fliE and fliF genes. Gene. 1991 May 15;101(1):23–31. doi: 10.1016/0378-1119(91)90220-6. [DOI] [PubMed] [Google Scholar]

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

RESOURCES