Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1966 Feb;91(2):634–641. doi: 10.1128/jb.91.2.634-641.1966

Nitrate Reductase and Respiratory Adaptation in Bacillus stearothermophilus

R J Downey 1
PMCID: PMC314907  PMID: 4286885

Abstract

Downey, R. J. (University of Notre Dame, Notre Dame, Ind.). Nitrate reductase and respiratory adaptation in Bacillus stearothermophilus. J. Bacteriol. 91:634–641. 1966.—Bacillus stearothermophilus 2184 required nitrate to grow in the absence of oxygen. Like many facultative microorganisms, the growth obtained anaerobically was considerably less than that obtained aerobically, even though the dissimilatory reduction of nitrate is, in effect, anaerobic respiration. The ability to reduce nitrate depended on the induction of nitrate reductase. Although oxygen at low levels did not retard induction of the enzyme, enzyme synthesis was considerably lessened by aeration. A semisynthetic medium containing nitrate supported aerobic growth of the thermophile but did not support anaerobic growth. The adaptation to nitrate resulted in a decrease in the level of cytochrome oxidase normally present in aerobically grown cells. Although the aerobic oxidation of succinate by the respiratory enzymes from aerobically grown cells was inhibited by 2-N-heptyl-4-hydroxyquinoline-N-oxide, the anaerobic oxidation of succinate by nitrate in a similar preparation from nitrate-adapted cells was not. The nitrate reductase in the bacillus was strongly inhibited by cyanide and azide but not by carbon monoxide. The nitrate reductase catalyzed the anaerobic oxidation of reduced nicotinamide adenine dinucleotide, and appeared to transfer electrons from cytochrome b1 to nitrate. Cytochrome c1 did not appear to be involved in the transfer.

Full text

PDF
634

Selected References

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

  1. CHENIAE G., EVANS H. J. Properties of a particulate nitrate reductase from the nodules of the soybean plant. Biochim Biophys Acta. 1959 Sep;35:140–153. doi: 10.1016/0006-3002(59)90343-9. [DOI] [PubMed] [Google Scholar]
  2. Downey R. J. NAPHTHOQUINONE INTERMEDIATE IN THE RESPIRATION OF BACILLUS STEAROTHERMOPHILUS. J Bacteriol. 1962 Nov;84(5):953–960. doi: 10.1128/jb.84.5.953-960.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. FEWSON C. A., NICHOLAS D. J. Nitrate reductase from Pseudomonas aeruginosa. Biochim Biophys Acta. 1961 May 13;49:335–349. doi: 10.1016/0006-3002(61)90133-0. [DOI] [PubMed] [Google Scholar]
  4. LIGHTBOWN J. W., JACKSON F. L. Inhibition of cytochrome systems of heart muscle and certain bacteria by the antagonists of dihydrostreptomycin: 2-alkyl-4-hydroxyquinoline N-oxides. Biochem J. 1956 May;63(1):130–137. doi: 10.1042/bj0630130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. NASON A., EVANS H. J. Triphosphopyridine nucleotide-nitrate reductase in Neurospora. J Biol Chem. 1953 Jun;202(2):655–673. [PubMed] [Google Scholar]
  7. NASON A. Symposium on metabolism of inorganic compounds. II. Enzymatic pathways of nitrate, nitrite, and hydroxylamine metabolisms. Bacteriol Rev. 1962 Mar;26:16–41. doi: 10.1128/br.26.1.16-41.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. PICHINOTY F., D'ORNANO L. Inhibition by oxygen of biosynthesis and activity of nitrate-reductase in Aerobacter aerogenes. Nature. 1961 Aug 26;191:879–881. doi: 10.1038/191879a0. [DOI] [PubMed] [Google Scholar]
  9. SADANA J. C., MCELROY W. D. Nitrate reductase from Achromobacter fischeri; purification and properties: function of flavines and cytochrome. Arch Biochem Biophys. 1957 Mar;67(1):16–34. doi: 10.1016/0003-9861(57)90242-4. [DOI] [PubMed] [Google Scholar]
  10. SENEZ J. C. Some considerations on the energetics of bacterial growth. Bacteriol Rev. 1962 Jun;26:95–107. [PMC free article] [PubMed] [Google Scholar]
  11. STRAAT P. A., NASON A. CHARACTERIZATION OF A NITRATE REDUCTASE FROM THE CHEMOAUTOTROPH NITROBACTER AGILIS. J Biol Chem. 1965 Mar;240:1412–1426. [PubMed] [Google Scholar]
  12. WELKER N. E., CAMPBELL L. L. EFFECT OF CARBON SOURCES ON FORMATION OF ALPHA-AMYLASE BY BACILLUS STEAROTHERMOPHILUS. J Bacteriol. 1963 Oct;86:681–686. doi: 10.1128/jb.86.4.681-686.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. WHITE D. C., SMITH L. LOCALIZATION OF THE ENZYMES THAT CATALYZE HYDROGEN AND ELECTRON TRANSPORT IN HEMOPHILUS PARAINFLUENZAE AND THE NATURE OF THE RESPIRATORY CHAIN SYSTEM. J Biol Chem. 1964 Nov;239:3956–3963. [PubMed] [Google Scholar]

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

RESOURCES