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. 1995 Oct;177(19):5696–5700. doi: 10.1128/jb.177.19.5696-5700.1995

Mutations in GltC that increase Bacillus subtilis gltA expression.

B R Belitsky 1, A L Sonenshein 1
PMCID: PMC177382  PMID: 7559360

Abstract

Mutants with altered forms of GltC, a positive LysR-type regulator of Bacillus subtilis glutamate synthase gene expression, were isolated. The mutant GltC proteins stimulated expression from the wild-type gltA promoter region 1.5- to 2.0-fold and from mutant promoter regions up to 80-fold. Moreover, expression of gltA became much less dependent on a nitrogen source-associated signal.

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Selected References

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  1. Bartowsky E., Normark S. Interactions of wild-type and mutant AmpR of Citrobacter freundii with target DNA. Mol Microbiol. 1993 Nov;10(3):555–565. doi: 10.1111/j.1365-2958.1993.tb00927.x. [DOI] [PubMed] [Google Scholar]
  2. Belitsky B. R., Janssen P. J., Sonenshein A. L. Sites required for GltC-dependent regulation of Bacillus subtilis glutamate synthase expression. J Bacteriol. 1995 Oct;177(19):5686–5695. doi: 10.1128/jb.177.19.5686-5695.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bohannon D. E., Rosenkrantz M. S., Sonenshein A. L. Regulation of Bacillus subtilis glutamate synthase genes by the nitrogen source. J Bacteriol. 1985 Sep;163(3):957–964. doi: 10.1128/jb.163.3.957-964.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bohannon D. E., Sonenshein A. L. Positive regulation of glutamate biosynthesis in Bacillus subtilis. J Bacteriol. 1989 Sep;171(9):4718–4727. doi: 10.1128/jb.171.9.4718-4727.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cho K., Winans S. C. Altered-function mutations in the Agrobacterium tumefaciens OccR protein and in an OccR-regulated promoter. J Bacteriol. 1993 Dec;175(23):7715–7719. doi: 10.1128/jb.175.23.7715-7719.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Colyer T. E., Kredich N. M. Residue threonine-149 of the Salmonella typhimurium CysB transcription activator: mutations causing constitutive expression of positively regulated genes of the cysteine regulon. Mol Microbiol. 1994 Sep;13(5):797–805. doi: 10.1111/j.1365-2958.1994.tb00472.x. [DOI] [PubMed] [Google Scholar]
  7. Dower W. J., Miller J. F., Ragsdale C. W. High efficiency transformation of E. coli by high voltage electroporation. Nucleic Acids Res. 1988 Jul 11;16(13):6127–6145. doi: 10.1093/nar/16.13.6127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dubnau D., Davidoff-Abelson R. Fate of transforming DNA following uptake by competent Bacillus subtilis. I. Formation and properties of the donor-recipient complex. J Mol Biol. 1971 Mar 14;56(2):209–221. doi: 10.1016/0022-2836(71)90460-8. [DOI] [PubMed] [Google Scholar]
  9. Fouet A., Sonenshein A. L. A target for carbon source-dependent negative regulation of the citB promoter of Bacillus subtilis. J Bacteriol. 1990 Feb;172(2):835–844. doi: 10.1128/jb.172.2.835-844.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Györgypal Z., Kondorosi A. Homology of the ligand-binding regions of Rhizobium symbiotic regulatory protein NodD and vertebrate nuclear receptors. Mol Gen Genet. 1991 Apr;226(1-2):337–340. doi: 10.1007/BF00273624. [DOI] [PubMed] [Google Scholar]
  11. Henikoff S., Haughn G. W., Calvo J. M., Wallace J. C. A large family of bacterial activator proteins. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6602–6606. doi: 10.1073/pnas.85.18.6602. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Huang J. Z., Schell M. A. In vivo interactions of the NahR transcriptional activator with its target sequences. Inducer-mediated changes resulting in transcription activation. J Biol Chem. 1991 Jun 15;266(17):10830–10838. [PubMed] [Google Scholar]
  13. Itaya M., Kondo K., Tanaka T. A neomycin resistance gene cassette selectable in a single copy state in the Bacillus subtilis chromosome. Nucleic Acids Res. 1989 Jun 12;17(11):4410–4410. doi: 10.1093/nar/17.11.4410. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kredich N. M. The molecular basis for positive regulation of cys promoters in Salmonella typhimurium and Escherichia coli. Mol Microbiol. 1992 Oct;6(19):2747–2753. doi: 10.1111/j.1365-2958.1992.tb01453.x. [DOI] [PubMed] [Google Scholar]
  15. Kullik I., Toledano M. B., Tartaglia L. A., Storz G. Mutational analysis of the redox-sensitive transcriptional regulator OxyR: regions important for oxidation and transcriptional activation. J Bacteriol. 1995 Mar;177(5):1275–1284. doi: 10.1128/jb.177.5.1275-1284.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. McIver J., Djordjevic M. A., Weinman J. J., Bender G. L., Rolfe B. G. Extension of host range of Rhizobium leguminosarum bv. trifolii caused by point mutations in nodD that result in alterations in regulatory function and recognition of inducer molecules. Mol Plant Microbe Interact. 1989 May-Jun;2(3):97–106. doi: 10.1094/mpmi-2-097. [DOI] [PubMed] [Google Scholar]
  17. Neidle E. L., Hartnett C., Ornston L. N. Characterization of Acinetobacter calcoaceticus catM, a repressor gene homologous in sequence to transcriptional activator genes. J Bacteriol. 1989 Oct;171(10):5410–5421. doi: 10.1128/jb.171.10.5410-5421.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. 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]
  19. Schell M. A. Molecular biology of the LysR family of transcriptional regulators. Annu Rev Microbiol. 1993;47:597–626. doi: 10.1146/annurev.mi.47.100193.003121. [DOI] [PubMed] [Google Scholar]
  20. 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]

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