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. 1995 Feb;177(3):628–635. doi: 10.1128/jb.177.3.628-635.1995

Posttranslational regulation of nitrogenase in Rhodospirillum rubrum strains overexpressing the regulatory enzymes dinitrogenase reductase ADP-ribosyltransferase and dinitrogenase reductase activating glycohydrolase.

S K Grunwald 1, D P Lies 1, G P Roberts 1, P W Ludden 1
PMCID: PMC176637  PMID: 7836296

Abstract

Rhodospirillum rubrum strains that overexpress the enzymes involved in posttranslational nitrogenase regulation, dinitrogenase reductase ADP-ribosyltransferase (DRAT) and dinitrogenase reductase activating glycohydrolase (DRAG), were constructed, and the effect of this overexpression on in vivo DRAT and DRAG regulation was investigated. Broad-host-range plasmid constructs containing a fusion of the R. rubrum nifH promoter and translation initiation sequences to the second codon of draT, the first gene of the dra operon, were constructed. Overexpression plasmid constructs which overexpressed (i) only functional DRAT, (ii) only functional DRAG and presumably the putative downstream open reading frame (ORF)-encoded protein, or (iii) all three proteins were generated and introduced into wild-type R. rubrum. Overexpression of DRAT still allowed proper regulation of nitrogenase activity, with ADP-ribosylation of dinitrogenase reductase by DRAT occurring only upon dark or ammonium stimuli, suggesting that DRAT is still regulated upon overexpression. However, overexpression of DRAG and the downstream ORF altered nitrogenase regulation such that dinitrogenase reductase did not accumulate in the ADP-ribosylated form under inactivation conditions, suggesting that DRAG was constitutively active and that therefore DRAG regulation is altered upon overexpression. Proper DRAG regulation was observed in a strain overexpressing DRAT, DRAG, and the downstream ORF, suggesting that a proper balance of DRAT and DRAG levels is required for proper DRAG regulation.

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Selected References

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  1. Blake M. S., Johnston K. H., Russell-Jones G. J., Gotschlich E. C. A rapid, sensitive method for detection of alkaline phosphatase-conjugated anti-antibody on Western blots. Anal Biochem. 1984 Jan;136(1):175–179. doi: 10.1016/0003-2697(84)90320-8. [DOI] [PubMed] [Google Scholar]
  2. Burris R. H. Nitrogen fixation--assay methods and techniques. Methods Enzymol. 1972;24:415–431. doi: 10.1016/0076-6879(72)24088-5. [DOI] [PubMed] [Google Scholar]
  3. Ditta G., Schmidhauser T., Yakobson E., Lu P., Liang X. W., Finlay D. R., Guiney D., Helinski D. R. Plasmids related to the broad host range vector, pRK290, useful for gene cloning and for monitoring gene expression. Plasmid. 1985 Mar;13(2):149–153. doi: 10.1016/0147-619x(85)90068-x. [DOI] [PubMed] [Google Scholar]
  4. Durner J., Böhm I., Hilz H., Böger P. Posttranslational modification of nitrogenase. Differences between the purple bacterium Rhodospirillum rubrum and the cyanobacterium Anabaena variabilis. Eur J Biochem. 1994 Feb 15;220(1):125–130. doi: 10.1111/j.1432-1033.1994.tb18606.x. [DOI] [PubMed] [Google Scholar]
  5. Figurski D. H., Helinski D. R. Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans. Proc Natl Acad Sci U S A. 1979 Apr;76(4):1648–1652. doi: 10.1073/pnas.76.4.1648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fitzmaurice W. P., Saari L. L., Lowery R. G., Ludden P. W., Roberts G. P. Genes coding for the reversible ADP-ribosylation system of dinitrogenase reductase from Rhodospirillum rubrum. Mol Gen Genet. 1989 Aug;218(2):340–347. doi: 10.1007/BF00331287. [DOI] [PubMed] [Google Scholar]
  7. Fu H. A., Hartmann A., Lowery R. G., Fitzmaurice W. P., Roberts G. P., Burris R. H. Posttranslational regulatory system for nitrogenase activity in Azospirillum spp. J Bacteriol. 1989 Sep;171(9):4679–4685. doi: 10.1128/jb.171.9.4679-4685.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fu H. A., Wirt H. J., Burris R. H., Roberts G. P. Functional expression of a Rhodospirillum rubrum gene encoding dinitrogenase reductase ADP-ribosyltransferase in enteric bacteria. Gene. 1989 Dec 21;85(1):153–160. doi: 10.1016/0378-1119(89)90475-7. [DOI] [PubMed] [Google Scholar]
  9. Gotto J. W., Yoch D. C. Regulation of Rhodospirillum rubrum nitrogenase activity. Properties and interconversion of active and inactive Fe protein. J Biol Chem. 1982 Mar 25;257(6):2868–2873. [PubMed] [Google Scholar]
  10. Gotto J. W., Yoch D. C. Regulation of nitrogenase activity by covalent modification in Chromatium vinosum. Arch Microbiol. 1985 Feb;141(1):40–43. doi: 10.1007/BF00446737. [DOI] [PubMed] [Google Scholar]
  11. Hartmann A., Fu H., Burris R. H. Regulation of nitrogenase activity by ammonium chloride in Azospirillum spp. J Bacteriol. 1986 Mar;165(3):864–870. doi: 10.1128/jb.165.3.864-870.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Honjo T., Nishizuka Y., Hayaishi O. Diphtheria toxin-dependent adenosine diphosphate ribosylation of aminoacyl transferase II and inhibition of protein synthesis. J Biol Chem. 1968 Jun 25;243(12):3553–3555. [PubMed] [Google Scholar]
  13. Kanemoto R. H., Ludden P. W. Amino acid concentrations in Rhodospirillum rubrum during expression and switch-off of nitrogenase activity. J Bacteriol. 1987 Jul;169(7):3035–3043. doi: 10.1128/jb.169.7.3035-3043.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kanemoto R. H., Ludden P. W. Effect of ammonia, darkness, and phenazine methosulfate on whole-cell nitrogenase activity and Fe protein modification in Rhodospirillum rubrum. J Bacteriol. 1984 May;158(2):713–720. doi: 10.1128/jb.158.2.713-720.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kerby R. L., Hong S. S., Ensign S. A., Coppoc L. J., Ludden P. W., Roberts G. P. Genetic and physiological characterization of the Rhodospirillum rubrum carbon monoxide dehydrogenase system. J Bacteriol. 1992 Aug;174(16):5284–5294. doi: 10.1128/jb.174.16.5284-5294.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  17. Lehman L. J., Fitzmaurice W. P., Roberts G. P. The cloning and functional characterization of the nifH gene of Rhodospirillum rubrum. Gene. 1990 Oct 30;95(1):143–147. doi: 10.1016/0378-1119(90)90426-r. [DOI] [PubMed] [Google Scholar]
  18. Li J. D., Hu C. Z., Yoch D. C. Changes in amino acid and nucleotide pools of Rhodospirillum rubrum during switch-off of nitrogenase activity initiated by NH4+ or darkness. J Bacteriol. 1987 Jan;169(1):231–237. doi: 10.1128/jb.169.1.231-237.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Liang J. H., Nielsen G. M., Lies D. P., Burris R. H., Roberts G. P., Ludden P. W. Mutations in the draT and draG genes of Rhodospirillum rubrum result in loss of regulation of nitrogenase by reversible ADP-ribosylation. J Bacteriol. 1991 Nov;173(21):6903–6909. doi: 10.1128/jb.173.21.6903-6909.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Lowery R. G., Ludden P. W. Purification and properties of dinitrogenase reductase ADP-ribosyltransferase from the photosynthetic bacterium Rhodospirillum rubrum. J Biol Chem. 1988 Nov 15;263(32):16714–16719. [PubMed] [Google Scholar]
  21. Lowery R. G., Saari L. L., Ludden P. W. Reversible regulation of the nitrogenase iron protein from Rhodospirillum rubrum by ADP-ribosylation in vitro. J Bacteriol. 1986 May;166(2):513–518. doi: 10.1128/jb.166.2.513-518.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Miller B. E., Norman A. W. Enzyme-linked immunoabsorbent assay (ELISA) and radioimmunoassay (RIA) for the vitamin D-dependent 28,000 dalton calcium-binding protein. Methods Enzymol. 1983;102:291–296. doi: 10.1016/s0076-6879(83)02029-7. [DOI] [PubMed] [Google Scholar]
  23. Moss J., Vaughan M. ADP-ribosylation of guanyl nucleotide-binding regulatory proteins by bacterial toxins. Adv Enzymol Relat Areas Mol Biol. 1988;61:303–379. doi: 10.1002/9780470123072.ch6. [DOI] [PubMed] [Google Scholar]
  24. Murrell S. A., Lowery R. G., Ludden P. W. ADP-ribosylation of dinitrogenase reductase from Clostridium pasteurianum prevents its inhibition of nitrogenase from Azotobacter vinelandii. Biochem J. 1988 Apr 15;251(2):609–612. doi: 10.1042/bj2510609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Nielsen G. M., Bao Y., Roberts G. P., Ludden P. W. Purification and characterization of an oxygen-stable form of dinitrogenase reductase-activating glycohydrolase from Rhodospirillum rubrum. Biochem J. 1994 Sep 15;302(Pt 3):801–806. doi: 10.1042/bj3020801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Paul T. D., Ludden P. W. Adenine nucleotide levels in Rhodospirillum rubrum during switch-off of whole-cell nitrogenase activity. Biochem J. 1984 Dec 15;224(3):961–969. doi: 10.1042/bj2240961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Pierrard J., Ludden P. W., Roberts G. P. Posttranslational regulation of nitrogenase in Rhodobacter capsulatus: existence of two independent regulatory effects of ammonium. J Bacteriol. 1993 Mar;175(5):1358–1366. doi: 10.1128/jb.175.5.1358-1366.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Preston G. G., Ludden P. W. Change in subunit composition of the iron protein of nitrogenase from Rhodospirillum rubrum during activation and inactivation of iron protein. Biochem J. 1982 Sep 1;205(3):489–494. doi: 10.1042/bj2050489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Saari L. L., Triplett E. W., Ludden P. W. Purification and properties of the activating enzyme for iron protein of nitrogenase from the photosynthetic bacterium Rhodospirillum rubrum. J Biol Chem. 1984 Dec 25;259(24):15502–15508. [PubMed] [Google Scholar]
  30. Woehle D. L., Lueddecke B. A., Ludden P. W. ATP-dependent and NAD-dependent modification of glutamine synthetase from Rhodospirillum rubrum in vitro. J Biol Chem. 1990 Aug 15;265(23):13741–13749. [PubMed] [Google Scholar]
  31. Wolle D., Kim C., Dean D., Howard J. B. Ionic interactions in the nitrogenase complex. Properties of Fe-protein containing substitutions for Arg-100. J Biol Chem. 1992 Feb 25;267(6):3667–3673. [PubMed] [Google Scholar]
  32. 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]
  33. Zhang Y., Burris R. H., Ludden P. W., Roberts G. P. Posttranslational regulation of nitrogenase activity by anaerobiosis and ammonium in Azospirillum brasilense. J Bacteriol. 1993 Nov;175(21):6781–6788. doi: 10.1128/jb.175.21.6781-6788.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Zhang Y., Burris R. H., Ludden P. W., Roberts G. P. Posttranslational regulation of nitrogenase activity in Azospirillum brasilense ntrBC mutants: ammonium and anaerobic switch-off occurs through independent signal transduction pathways. J Bacteriol. 1994 Sep;176(18):5780–5787. doi: 10.1128/jb.176.18.5780-5787.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

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