Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1979 Jan;137(1):524–530. doi: 10.1128/jb.137.1.524-530.1979

Growth of the photosynthetic bacterium Rhodopseudomonas capsulata chemoautotrophically in darkness with H2 as the energy source.

M T Madigan, H Gest
PMCID: PMC218479  PMID: 216663

Abstract

The phototrophic bacterium Rhodopseudomonas capsulata was found to be capable of growing chemoautotrophically under aerobic conditions in darkness. Growth was strictly dependent on the presence of H2 as the source of energy and reducing power, O2 as the terminal electron acceptor for energy transduction, and CO2 as the sole carbon source; under optimal conditions the generation time was about 6 h. Chemoautotrophically grown cells showed a relatively high content of bacteriochlorophyll a and intracytoplasmic membranes (chromatophores). Experiments with various mutants of R. capsulata, affected in electron transport, indicate that either of the two terminal oxidases of this bacterium can participate in the energy-yielding oxidation of H2. The ability of R. capsulata to multiply in at least five different physiological growth modes suggests that it is one of the most metabolically versatile procaryotes known.

Full text

PDF
524

Images in this article

Selected References

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

  1. Baccarini Melandri A., Zannoni D., Melandri B. A. Energy transduction in photosynthetic bacteria. VI. Respiratory sites of energy conservation in membranes from dark-grown cells of Rhodopseudomonas capsulata. Biochim Biophys Acta. 1973 Sep 26;314(3):298–311. doi: 10.1016/0005-2728(73)90114-x. [DOI] [PubMed] [Google Scholar]
  2. COHEN-BAZIRE G., SISTROM W. R., STANIER R. Y. Kinetic studies of pigment synthesis by non-sulfur purple bacteria. J Cell Physiol. 1957 Feb;49(1):25–68. doi: 10.1002/jcp.1030490104. [DOI] [PubMed] [Google Scholar]
  3. GEST H. Oxidation and evolution of molecular hydrogen by microorganisms. Bacteriol Rev. 1954 Mar;18(1):43–73. doi: 10.1128/br.18.1.43-73.1954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Gibson J. L., Tabita F. R. Isolation and preliminary characterization of two forms of ribulose 1,5-bisphosphate carboxylase from Rhodopseudomonas capsulata. J Bacteriol. 1977 Dec;132(3):818–823. doi: 10.1128/jb.132.3.818-823.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hillmer P., Gest H. H2 metabolism in the photosynthetic bacterium Rhodopseudomonas capsulata: production and utilization of H2 by resting cells. J Bacteriol. 1977 Feb;129(2):732–739. doi: 10.1128/jb.129.2.732-739.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Klemme J. H. Untersuchungen zur Photoautotrophie mit molekularem Wasserstoff bei neuisolierten schwefelfreien Purpurbakterien. Arch Mikrobiol. 1968;64(1):29–42. [PubMed] [Google Scholar]
  7. LAW J. H., SLEPECKY R. A. Assay of poly-beta-hydroxybutyric acid. J Bacteriol. 1961 Jul;82:33–36. doi: 10.1128/jb.82.1.33-36.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. 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]
  9. Madigan M. T., Gest H. Growth of a photosynthetic bacterium anaerobically in darkness, supported by "oxidant-dependent" sugar fermentation. Arch Microbiol. 1978 May 30;117(2):119–122. doi: 10.1007/BF00402298. [DOI] [PubMed] [Google Scholar]
  10. Marrs B., Gest H. Genetic mutations affecting the respiratory electron-transport system of the photosynthetic bacterium Rhodopseudomonas capsulata. J Bacteriol. 1973 Jun;114(3):1045–1051. doi: 10.1128/jb.114.3.1045-1051.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. McFadden B. A. The oxygenase activity of ribulose-1,5-bisphosphate carboxylase from Rhodospirillum rubrum. Biochem Biophys Res Commun. 1974 Sep 9;60(1):312–317. doi: 10.1016/0006-291x(74)90206-x. [DOI] [PubMed] [Google Scholar]
  12. PACKER L., VISHNIAC W. Chemosynthetic fixation of carbon dioxide and characteristics of hydrogenase in resting cell suspensions of Hydrogenomonas ruhlandii nov. spec. J Bacteriol. 1955 Aug;70(2):216–223. doi: 10.1128/jb.70.2.216-223.1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. RYTER A., KELLENBERGER E., BIRCHANDERSEN A., MAALOE O. Etude au microscope électronique de plasmas contenant de l'acide désoxyribonucliéique. I. Les nucléoides des bactéries en croissance active. Z Naturforsch B. 1958 Sep;13B(9):597–605. [PubMed] [Google Scholar]
  14. STOPPANI A. O., FULLER R. C., CALVIN M. Carbon dioxide fixation by Rhodopseudomonas capsulatus. J Bacteriol. 1955 May;69(5):491–501. doi: 10.1128/jb.69.5.491-501.1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Schlegel H. G. Physiology and biochemistry of knallgasbacteria. Adv Comp Physiol Biochem. 1966;2:185–236. doi: 10.1016/b978-0-12-395511-1.50008-1. [DOI] [PubMed] [Google Scholar]
  16. Sojka G. A., Freeze H. H., Gest H. Quantitative estimation of bacteriochlorophyll in situ. Arch Biochem Biophys. 1970 Feb;136(2):578–580. doi: 10.1016/0003-9861(70)90231-6. [DOI] [PubMed] [Google Scholar]
  17. Stanier R. Y., Doudoroff M., Kunisawa R., Contopoulou R. THE ROLE OF ORGANIC SUBSTRATES IN BACTERIAL PHOTOSYNTHESIS. Proc Natl Acad Sci U S A. 1959 Aug;45(8):1246–1260. doi: 10.1073/pnas.45.8.1246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Wall J. D., Johansson B. C., Gest H. A pleiotropic mutant of Rhodopseudomonas capsulata defective in nitrogen metabolism. Arch Microbiol. 1977 Dec 15;115(3):259–263. doi: 10.1007/BF00446450. [DOI] [PubMed] [Google Scholar]
  19. Wall J. D., Weaver P. F., Gest H. Gene transfer agents, bacteriophages, and bacteriocins of Rhodopseudomonas capsulata. Arch Microbiol. 1975 Nov 7;105(3):217–224. doi: 10.1007/BF00447140. [DOI] [PubMed] [Google Scholar]
  20. Wall J. D., Weaver P. F., Gest H. Genetic transfer of nitrogenase-hydrogenase activity in Rhodopseudomonas capsulata. Nature. 1975 Dec 18;258(5536):630–631. doi: 10.1038/258630a0. [DOI] [PubMed] [Google Scholar]
  21. Weaver P. F., Wall J. D., Gest H. Characterization of Rhodopseudomonas capsulata. Arch Microbiol. 1975 Nov 7;105(3):207–216. doi: 10.1007/BF00447139. [DOI] [PubMed] [Google Scholar]
  22. Yen H. C., Marrs B. Growth of Rhodopseudomonas capsulata under anaerobic dark conditions with dimethyl sulfoxide. Arch Biochem Biophys. 1977 Jun;181(2):411–418. doi: 10.1016/0003-9861(77)90246-6. [DOI] [PubMed] [Google Scholar]
  23. Zannoni D., Baccarini-Melandri A., Malandri B. A. Energy transduction in photosynthetic bacteria. The nature of cytochrome C oxidase in the respiratory chain of Rhodopseudomonas capsulata. FEBS Lett. 1974 Nov 1;48(1):152–155. doi: 10.1016/0014-5793(74)81085-9. [DOI] [PubMed] [Google Scholar]
  24. Zannoni D., Melandri B. A., Baccarini-Melandri A. Energy tranduction in photosynthetic bacteria. XI. Further resolution of cytochromes of b type and the nature of the co-sensitive oxidase present in the respiratory chain of Rhodopseudomonas capsulata. Biochim Biophys Acta. 1976 Dec 6;449(3):386–400. doi: 10.1016/0005-2728(76)90150-x. [DOI] [PubMed] [Google Scholar]
  25. van Niel C. B. THE CULTURE, GENERAL PHYSIOLOGY, MORPHOLOGY, AND CLASSIFICATION OF THE NON-SULFUR PURPLE AND BROWN BACTERIA. Bacteriol Rev. 1944 Mar;8(1):1–118. doi: 10.1128/br.8.1.1-118.1944. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES