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. 1996 Aug;178(15):4679–4687. doi: 10.1128/jb.178.15.4679-4687.1996

Iron is required to relieve inhibitory effects on NifL on transcriptional activation by NifA in Klebsiella pneumoniae.

R A Schmitz 1, L He 1, S Kustu 1
PMCID: PMC178239  PMID: 8755900

Abstract

In Klebsiella pneumoniae, products of the nitrogen fixation nifLA operon regulate transcription of the other nif operons. NifA activates transcription by sigma54-holoenzyme. In vivo, NifL antagonizes the action of NifA under aerobic conditions or in the presence of combined nitrogen. In contrast to a previous report, we show that depletion of iron (Fe) from the growth medium with the chelating agent o-phenanthroline (20 microM) mimics aerobiosis or combined nitrogen in giving rise to inhibition of NifA activity even under anaerobic, nitrogen-limiting conditions. Adding back Fe in only twofold molar excess over phenanthroline restores NifA activity, whereas adding other metals fails to do so. By using strains that lack NifL, we showed that NifA activity itself does not require Fe and is not directly affected by phenanthroline. Hence, Fe is required to relieve the inhibition of NifA activity by NifL in vivo. Despite the Fe requirement in vivo, we have found no evidence that NifL contains Fe or an iron-sulfur (Fe-S) cluster. Determination of the molecular mass of an inhibitory form of NifL overproduced under aerobic conditions indicated that it was not posttranslationally modified. When NifL was synthesized in vitro, it inhibited transcriptional activation by NifA even when it was synthesized under anaerobic conditions in the presence of a high Fe concentration or of superoxide dismutase, which is known to protect some Fe-S clusters. Moreover, overproduction of superoxide dismutase in vivo did not relieve NifL, inhibition under aerobic conditions, and attempts to relieve NifL inhibition in vitro by reconstituting Fe-S clusters with the NifS enzyme (Azotobacter vinelandii) were unsuccessful. Since we obtained no evidence that Fe acts directly on NifL or NifA, we postulate that an additional Fe-containing protein, not yet identified, may be required to relieve NifL inhibition under anaerobic, nitrogen-limiting conditions.

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Selected References

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  1. Adman E., Watenpaugh K. D., Jensen L. H. NH---S hydrogen bonds in Peptococcus aerogenes ferredoxin, Clostridium pasteurianum rubredoxin, and Chromatium high potential iron protein. Proc Natl Acad Sci U S A. 1975 Dec;72(12):4854–4858. doi: 10.1073/pnas.72.12.4854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arnold W., Rump A., Klipp W., Priefer U. B., Pühler A. Nucleotide sequence of a 24,206-base-pair DNA fragment carrying the entire nitrogen fixation gene cluster of Klebsiella pneumoniae. J Mol Biol. 1988 Oct 5;203(3):715–738. doi: 10.1016/0022-2836(88)90205-7. [DOI] [PubMed] [Google Scholar]
  3. Berg J. M. Potential metal-binding domains in nucleic acid binding proteins. Science. 1986 Apr 25;232(4749):485–487. doi: 10.1126/science.2421409. [DOI] [PubMed] [Google Scholar]
  4. Berger D. K., Narberhaus F., Kustu S. The isolated catalytic domain of NIFA, a bacterial enhancer-binding protein, activates transcription in vitro: activation is inhibited by NIFL. Proc Natl Acad Sci U S A. 1994 Jan 4;91(1):103–107. doi: 10.1073/pnas.91.1.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  6. Buchanan-Wollaston V., Cannon M. C., Beynon J. L., Cannon F. C. Role of the nifA gene product in the regulation of nif expression in Klebsiella pneumoniae. Nature. 1981 Dec 24;294(5843):776–778. doi: 10.1038/294776a0. [DOI] [PubMed] [Google Scholar]
  7. Buck M., Cannon W., Woodcock J. Transcriptional activation of the Klebsiella pneumoniae nitrogenase promoter may involve DNA loop formation. Mol Microbiol. 1987 Sep;1(2):243–249. doi: 10.1111/j.1365-2958.1987.tb00518.x. [DOI] [PubMed] [Google Scholar]
  8. Carlioz A., Touati D. Isolation of superoxide dismutase mutants in Escherichia coli: is superoxide dismutase necessary for aerobic life? EMBO J. 1986 Mar;5(3):623–630. doi: 10.1002/j.1460-2075.1986.tb04256.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Drummond M. H., Wootton J. C. Sequence of nifL from Klebsiella pneumoniae: mode of action and relationship to two families of regulatory proteins. Mol Microbiol. 1987 Jul;1(1):37–44. doi: 10.1111/j.1365-2958.1987.tb00524.x. [DOI] [PubMed] [Google Scholar]
  10. Fellay R., Frey J., Krisch H. Interposon mutagenesis of soil and water bacteria: a family of DNA fragments designed for in vitro insertional mutagenesis of gram-negative bacteria. Gene. 1987;52(2-3):147–154. doi: 10.1016/0378-1119(87)90041-2. [DOI] [PubMed] [Google Scholar]
  11. Filser M., Merrick M., Cannon F. Cloning and characterisation of nifLA regulatory mutations from Klebsiella pneumoniae. Mol Gen Genet. 1983;191(3):485–491. doi: 10.1007/BF00425767. [DOI] [PubMed] [Google Scholar]
  12. Flint D. H., Smyk-Randall E., Tuminello J. F., Draczynska-Lusiak B., Brown O. R. The inactivation of dihydroxy-acid dehydratase in Escherichia coli treated with hyperbaric oxygen occurs because of the destruction of its Fe-S cluster, but the enzyme remains in the cell in a form that can be reactivated. J Biol Chem. 1993 Dec 5;268(34):25547–25552. [PubMed] [Google Scholar]
  13. Gardner P. R., Fridovich I. Superoxide sensitivity of the Escherichia coli 6-phosphogluconate dehydratase. J Biol Chem. 1991 Jan 25;266(3):1478–1483. [PubMed] [Google Scholar]
  14. Govantes F., Santero E. Transcription termination within the regulatory nifLA operon of Klebsiella pneumoniae. Mol Gen Genet. 1996 Mar 7;250(4):447–454. [PubMed] [Google Scholar]
  15. Grabowski R., Buckel W. Purification and properties of an iron-sulfur-containing and pyridoxal-phosphate-independent L-serine dehydratase from Peptostreptococcus asaccharolyticus. Eur J Biochem. 1991 Jul 1;199(1):89–94. doi: 10.1111/j.1432-1033.1991.tb16095.x. [DOI] [PubMed] [Google Scholar]
  16. Gropp F., Betlach M. C. The bat gene of Halobacterium halobium encodes a trans-acting oxygen inducibility factor. Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5475–5479. doi: 10.1073/pnas.91.12.5475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hill S., Austin S., Eydmann T., Jones T., Dixon R. Azotobacter vinelandii NIFL is a flavoprotein that modulates transcriptional activation of nitrogen-fixation genes via a redox-sensitive switch. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2143–2148. doi: 10.1073/pnas.93.5.2143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hill S., Kennedy C., Kavanagh E., Goldberg R. B., Hanau R. Nitrogen fixation gene (nifL) involved in oxygen regulation of nitrogenase synthesis in K. pneumoniae. Nature. 1981 Apr 2;290(5805):424–426. doi: 10.1038/290424a0. [DOI] [PubMed] [Google Scholar]
  19. Hofmeister A. E., Grabowski R., Linder D., Buckel W. L-serine and L-threonine dehydratase from Clostridium propionicum. Two enzymes with different prosthetic groups. Eur J Biochem. 1993 Jul 15;215(2):341–349. doi: 10.1111/j.1432-1033.1993.tb18040.x. [DOI] [PubMed] [Google Scholar]
  20. Hoover T. R., Santero E., Porter S., Kustu S. The integration host factor stimulates interaction of RNA polymerase with NIFA, the transcriptional activator for nitrogen fixation operons. Cell. 1990 Oct 5;63(1):11–22. doi: 10.1016/0092-8674(90)90284-l. [DOI] [PubMed] [Google Scholar]
  21. Khoroshilova N., Beinert H., Kiley P. J. Association of a polynuclear iron-sulfur center with a mutant FNR protein enhances DNA binding. Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2499–2503. doi: 10.1073/pnas.92.7.2499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lee H. S., Berger D. K., Kustu S. Activity of purified NIFA, a transcriptional activator of nitrogen fixation genes. Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2266–2270. doi: 10.1073/pnas.90.6.2266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Lee H. S., Narberhaus F., Kustu S. In vitro activity of NifL, a signal transduction protein for biological nitrogen fixation. J Bacteriol. 1993 Dec;175(23):7683–7688. doi: 10.1128/jb.175.23.7683-7688.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Liochev S. I., Fridovich I. Effects of overproduction of superoxide dismutases in Escherichia coli on inhibition of growth and on induction of glucose-6-phosphate dehydrogenase by paraquat. Arch Biochem Biophys. 1992 Apr;294(1):138–143. doi: 10.1016/0003-9861(92)90147-o. [DOI] [PubMed] [Google Scholar]
  25. MacNeil D., Zhu J., Brill W. J. Regulation of nitrogen fixation in Klebsiella pneumoniae: isolation and characterization of strains with nif-lac fusions. J Bacteriol. 1981 Jan;145(1):348–357. doi: 10.1128/jb.145.1.348-357.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. McCord J. M., Fridovich I. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J Biol Chem. 1969 Nov 25;244(22):6049–6055. [PubMed] [Google Scholar]
  27. Morett E., Buck M. In vivo studies on the interaction of RNA polymerase-sigma 54 with the Klebsiella pneumoniae and Rhizobium meliloti nifH promoters. The role of NifA in the formation of an open promoter complex. J Mol Biol. 1989 Nov 5;210(1):65–77. doi: 10.1016/0022-2836(89)90291-x. [DOI] [PubMed] [Google Scholar]
  28. Morett E., Buck M. NifA-dependent in vivo protection demonstrates that the upstream activator sequence of nif promoters is a protein binding site. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9401–9405. doi: 10.1073/pnas.85.24.9401. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mott J. E., Grant R. A., Ho Y. S., Platt T. Maximizing gene expression from plasmid vectors containing the lambda PL promoter: strategies for overproducing transcription termination factor rho. Proc Natl Acad Sci U S A. 1985 Jan;82(1):88–92. doi: 10.1073/pnas.82.1.88. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Narberhaus F., Lee H. S., Schmitz R. A., He L., Kustu S. The C-terminal domain of NifL is sufficient to inhibit NifA activity. J Bacteriol. 1995 Sep;177(17):5078–5087. doi: 10.1128/jb.177.17.5078-5087.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Ow D. W., Ausubel F. M. Regulation of nitrogen metabolism genes by nifA gene product in Klebsiella pneumoniae. Nature. 1983 Jan 27;301(5898):307–313. doi: 10.1038/301307a0. [DOI] [PubMed] [Google Scholar]
  32. Ow D. W., Xiong Y., Gu Q., Shen S. C. Mutational analysis of the Klebsiella pneumoniae nitrogenase promoter: sequences essential for positive control by nifA and ntrC (glnG) products. J Bacteriol. 1985 Mar;161(3):868–874. doi: 10.1128/jb.161.3.868-874.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Poole R. K. Oxygen reactions with bacterial oxidases and globins: binding, reduction and regulation. Antonie Van Leeuwenhoek. 1994;65(4):289–310. doi: 10.1007/BF00872215. [DOI] [PubMed] [Google Scholar]
  34. Prentki P., Krisch H. M. In vitro insertional mutagenesis with a selectable DNA fragment. Gene. 1984 Sep;29(3):303–313. doi: 10.1016/0378-1119(84)90059-3. [DOI] [PubMed] [Google Scholar]
  35. Santero E., Hoover T. R., North A. K., Berger D. K., Porter S. C., Kustu S. Role of integration host factor in stimulating transcription from the sigma 54-dependent nifH promoter. J Mol Biol. 1992 Oct 5;227(3):602–620. doi: 10.1016/0022-2836(92)90211-2. [DOI] [PubMed] [Google Scholar]
  36. Santero E., Hoover T., Keener J., Kustu S. In vitro activity of the nitrogen fixation regulatory protein NIFA. Proc Natl Acad Sci U S A. 1989 Oct;86(19):7346–7350. doi: 10.1073/pnas.86.19.7346. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Shand R. F., Betlach M. C. Expression of the bop gene cluster of Halobacterium halobium is induced by low oxygen tension and by light. J Bacteriol. 1991 Aug;173(15):4692–4699. doi: 10.1128/jb.173.15.4692-4699.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Spiro S., Roberts R. E., Guest J. R. FNR-dependent repression of the ndh gene of Escherichia coli and metal ion requirement for FNR-regulated gene expression. Mol Microbiol. 1989 May;3(5):601–608. doi: 10.1111/j.1365-2958.1989.tb00207.x. [DOI] [PubMed] [Google Scholar]
  39. Touati D. Transcriptional and posttranscriptional regulation of manganese superoxide dismutase biosynthesis in Escherichia coli, studied with operon and protein fusions. J Bacteriol. 1988 Jun;170(6):2511–2520. doi: 10.1128/jb.170.6.2511-2520.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Yang C. F., DasSarma S. Transcriptional induction of purple membrane and gas vesicle synthesis in the archaebacterium Halobacterium halobium is blocked by a DNA gyrase inhibitor. J Bacteriol. 1990 Jul;172(7):4118–4121. doi: 10.1128/jb.172.7.4118-4121.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Zheng L., Dean D. R. Catalytic formation of a nitrogenase iron-sulfur cluster. J Biol Chem. 1994 Jul 22;269(29):18723–18726. [PubMed] [Google Scholar]
  42. Zheng L., White R. H., Cash V. L., Dean D. R. Mechanism for the desulfurization of L-cysteine catalyzed by the nifS gene product. Biochemistry. 1994 Apr 19;33(15):4714–4720. doi: 10.1021/bi00181a031. [DOI] [PubMed] [Google Scholar]
  43. Zheng L., White R. H., Cash V. L., Jack R. F., Dean D. R. Cysteine desulfurase activity indicates a role for NIFS in metallocluster biosynthesis. Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2754–2758. doi: 10.1073/pnas.90.7.2754. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. de Lorenzo V., Herrero M., Jakubzik U., Timmis K. N. Mini-Tn5 transposon derivatives for insertion mutagenesis, promoter probing, and chromosomal insertion of cloned DNA in gram-negative eubacteria. J Bacteriol. 1990 Nov;172(11):6568–6572. doi: 10.1128/jb.172.11.6568-6572.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]

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