Skip to main content
NCBI home page
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1978 Jan;133(1):392–395. doi: 10.1128/jb.133.1.392-395.1978

ATP hydrolysis in a marine bacterium.

P H Calcott, A R Bhatti
PMCID: PMC222019  PMID: 145434

Abstract

The membrane-bound adenosine triphosphatase of marine pseudomonad B-16, when solubilized, is able to rebind to depleted membrane residues of the bacterium and to those of Escherichia coli.

Full text

PDF
392

Selected References

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

  1. Altendorf K., Zitzmann W. Identification of the DCCD-reactive protein of the energy transducing adenosinetriphosphatase complex from Escherichia coli. FEBS Lett. 1975 Nov 15;59(2):268–272. doi: 10.1016/0014-5793(75)80390-5. [DOI] [PubMed] [Google Scholar]
  2. Bhatti A. R., DeVoe I. W., Ingram J. M. The release and characterization of some periplasm-located enzymes of Pseudomona aeruginosa. Can J Microbiol. 1976 Oct;22(10):1425–1429. doi: 10.1139/m76-211. [DOI] [PubMed] [Google Scholar]
  3. Cox G. B., Gibson F. Studies on electron transport and energy-linked reactions using mutants of Escherichia coli. Biochim Biophys Acta. 1974 Apr 30;346(1):1–25. doi: 10.1016/0304-4173(74)90010-x. [DOI] [PubMed] [Google Scholar]
  4. DAVIS B. J. DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS. Ann N Y Acad Sci. 1964 Dec 28;121:404–427. doi: 10.1111/j.1749-6632.1964.tb14213.x. [DOI] [PubMed] [Google Scholar]
  5. Gow J. A., DeVoe U. W., MacLeod R. A. Dissociation in a marine pseudomonad. Can J Microbiol. 1973 Jun;19(6):695–701. doi: 10.1139/m73-113. [DOI] [PubMed] [Google Scholar]
  6. Grinius L., Slusnyte R., Griniuviene B. ATP synthesis driven by protonmotive force imposed across Escherichia coli cell membranes. FEBS Lett. 1975 Oct 1;57(3):290–293. doi: 10.1016/0014-5793(75)80319-x. [DOI] [PubMed] [Google Scholar]
  7. Houghton R. L., Fisher R. J., Sanadi D. R. Energy-linked and energy-independent transhydrogenase activities in Escherichia coli vesicles. Biochim Biophys Acta. 1975 Jul 8;396(1):17–23. doi: 10.1016/0005-2728(75)90185-1. [DOI] [PubMed] [Google Scholar]
  8. Kanner B. I., Nelson N., Gutnick D. L. Differentiation between mutants of Escherichia coli K defective in oxidative phosphorylation. Biochim Biophys Acta. 1975 Sep 8;396(3):347–359. doi: 10.1016/0005-2728(75)90141-3. [DOI] [PubMed] [Google Scholar]
  9. Kay W. W., Bragg P. D. Salmonella typhimurium HfrA, a mutant in which adenosine triphosphate can drive amino acid transport but not energy-dependent nicotinamide nucleotide transhydrogenation. Biochem J. 1975 Jul;150(1):21–29. doi: 10.1042/bj1500021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kelln R. A., Warren R. A. Pyrimidine metabolism in Pseudomonas acidovorans. Can J Microbiol. 1974 Apr;20(4):427–433. doi: 10.1139/m74-067. [DOI] [PubMed] [Google Scholar]
  11. Knowles C. J., Calcott P. H., MacLeod R. A. Periplasmic CO-binding c-type cytochrome in a marine bacterium. FEBS Lett. 1974 Dec 1;49(1):78–83. doi: 10.1016/0014-5793(74)80636-8. [DOI] [PubMed] [Google Scholar]
  12. Maloney P. C., Kashket E. R., Wilson T. H. A protonmotive force drives ATP synthesis in bacteria. Proc Natl Acad Sci U S A. 1974 Oct;71(10):3896–3900. doi: 10.1073/pnas.71.10.3896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Nieuwenhuis F. J., Kanner B. I., Gutnick D. L., Postma P. W., van Dam K. Energy conservation in membranes of mutants of Escherichia coli defective in oxidative phosphorylation. Biochim Biophys Acta. 1973 Oct 19;325(1):62–71. doi: 10.1016/0005-2728(73)90151-5. [DOI] [PubMed] [Google Scholar]
  14. Patel L., Kaback H. R. The role of the carbodiimide-reactive component of the adenosine-5'-triphosphatase complex in the proton permeability of Escherichia coli membrane vesicles. Biochemistry. 1976 Jun 29;15(13):2741–2746. doi: 10.1021/bi00658a005. [DOI] [PubMed] [Google Scholar]
  15. Poole R. K., Haddock B. A. Energy-linked reduction of nicotinamide--adenine dinucleotide in membranes derived from normal and various respiratory-deficient mutant strains of Escherichia coli K12. Biochem J. 1974 Oct;144(1):77–85. doi: 10.1042/bj1440077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sprott G. D., MacLeod R. A. Nature of the specificity of alcohol coupling to L-alanine transport into isolated membrane vesicles of a marine pseudomonad. J Bacteriol. 1974 Mar;117(3):1043–1054. doi: 10.1128/jb.117.3.1043-1054.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. TORRIANI A., ROTHMAN F. Mutants of Escherichia coli constitutive for alkaline phosphatase. J Bacteriol. 1961 May;81:835–836. doi: 10.1128/jb.81.5.835-836.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES