Skip to main content
Log in

Aspects of nitrogen fixation in Chlorobium

  • Original Papers
  • Published:
Archives of Microbiology Aims and scope Submit manuscript

Abstract

Four strains of the green sulfur bacterium Chlorobium were studied in respect to nitrogen nutrition and nitrogen fixation. All strains grew on ammonia, N2, or glutamine as sole nitrogen sources; certain strains also grew on other amino acids. Acetylene-reducing activity was detectable in all strains grown on N2 or on amino acids (except for glutamine). In N2 grown Chlorobium thiosulfatophilum strain 8327 1 mM ammonia served to “switch-off” nitrogenase activity, but the effect of ammonia was much less dramatic in glutamate or limiting ammonia grown cells. The glutamine synthetase inhibitor methionine sulfoximine inhibited ammonia “switch-off” in all but one strain. Cell extracts of glutamate grown strain 8327 reduced acetylene and required Mg2+ and dithionite, but not Mn2+, for activity. Partially purified preparations of Rhodospirillum rubrum nitrogenase reductase (iron protein) activating enzyme slightly stimulated acetylene reduction in extracts of strain 8327, but no evidence for an indigenous Chlorobium activating enzyme was obtained. The results suggest that certain Chlorobium strains are fairly versatile in their nitrogen nutrition and that at least in vivo, nitrogenase activity in green bacteria is controlled by ammonia in a fashion similar to that described in nonsulfur purple bacteria and in Chromatium.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

MSX:

Methionine sulfoximine

MOPS:

3-(N-morpholino) propane sulfonic acid

References

  • Alef K, Kleiner D (1982) Regulatory aspects of inorganic nitrogen metabolism in Rhodospirillaceae. Arch Microbiol 133:239–241

    Google Scholar 

  • Arp DJ, Zumft WG (1983) Overproduction of nitrogenase by nitrogen-limited cultures of Rhodopseudomonas palustris. J Bacteriol 153:1322–1330

    Google Scholar 

  • Belousova AA (1968) Effect of some amino acids on the yield of green sulphur bacteria Chlorobium thiosulfatophilum. Microbiology (English translation of Mikrobiologiya) 37:855–860

    Google Scholar 

  • Biebl H, Pfennig N (1978) Growth yields of green sulfur bacteria in mixed cultures with sulfur and sulfate reducing bacteria. Arch Microbiol 117:9–16

    Google Scholar 

  • Brock TD (1978) Thermophilic microorganisms and life at high temperatures. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Dowling TE, Preston GG, Ludden PW (1982) Heat activation of the Fe protein of nitrogenase from Rhodospirillum rubrum. J Biol Chem 257:13987–13992

    Google Scholar 

  • Evans MCW, Smith RV (1971) Nitrogen fixation by the green photosynthetic bacterium Chloropseudomonas ethylicum. J Gen Microbiol 65:95–98

    Google Scholar 

  • Evans MCW, Telfer A, Cammack R, Smith RV (1971) EPR studies of nitrogenase: ATP dependent oxidation of fraction 1 protein by cyanide. FEBS Letters 15:317–319

    Google Scholar 

  • Falk G, Johansson BoC, Nordlund S (1982) The role of glutamine synthetase in the regulation of nitrogenase activity (switch-off effect) in Rhodospirillum rubrum. Arch Microbiol 132:251–253

    Google Scholar 

  • Gest H, Favinger JL, Madigan MT, (1985) Exploitation of N2-fixation capacity for enrichment of anoxygenic photosynthetic bacteria in ecological studies. FEMS Microbiol Ecology 31:317–322

    Google Scholar 

  • Gest H, Kamen MD (1949) Photoproduction of molecular hydrogen by Rhodospirillum rubrum. Science 109:558–559

    Google Scholar 

  • Gotto JW, Yoch DC (1985) Regulation of nitrogenase activity by covalent modification in Chromatium vinosum. Arch Microbiol 41:40–43

    Google Scholar 

  • Gray BH, Fowler CF, Nugent NA, Rigopoulous N, Fuller RC (1973) Reevaluation of Chloropseudomonas ethylica strain 2-K. Intl J Syst Bacteriol 23:256–264

    Google Scholar 

  • Herbert RA, Siefert E, Pfennig N (1978) Nitrogen assimilation in Rhodopseudomonas acidophila. Arch Microbiol 119:1–5

    Google Scholar 

  • Hillmer P, Gest H (1977) H2 metabolism in the photosynthetic bacterium Rhodopseudomonas capsulata: H2 production by growing cells. J Bacteriol 129:724–731

    Google Scholar 

  • Jones BL, Monty KJ (1979) Glutamine as a feedback inhibitor of the Rhodopseudomonas sphaeroides nitrogenase system. J Bacteriol 139:1007–1013

    Google Scholar 

  • Kamen MD, Gest H (1949) Evidence for a nitrogenase system in the photosynthetic bacterium Rhodospirillum rubrum. Science 109:560

    Google Scholar 

  • Kelly DP (1974) Growth and metabolism of the obligate photolithotroph Chlorobium thiosulfatophilum in the presence of added organic nutrients. Arch Microbiol 100:163–178

    Google Scholar 

  • Keppen OI, Lebedeva NV, Petukhov SA, Rodionov YuV (1985) The activity of nitrogenase in the green sulfur bacterium Chlorobium limicola forma thiosulfatophilum (In Russian). Mikrobiologiya 54:36–41

    Google Scholar 

  • Kovacs KL, Bagyinka Cs, Serebriakova LT (1983) Distribution and orientation of hydrogenase in various photosynthetic bacteria. Curr Microbiol 9:215–218

    Google Scholar 

  • Lindstrom ES, Tove SR, Wilson PW (1950) Nitrogen fixation by the green and purple sulfur bacteria. Science 112:197–198

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    Google Scholar 

  • Ludden PW, Burris RH (1976) Activating factor for the iron protein of nitrogenase from Rhodospirillum rubrum. Science 194:424–426

    Google Scholar 

  • Ludden PW, Burris RH (1978) Purification and properties of nitrogenase from Rhodospirillum rubrum, and evidence for phosphate, ribose and an adenine-like unit covalently bound to the iron protein. Biochem J 175:251–259

    Google Scholar 

  • Madigan MT, Cox SS, Stegeman RA (1984) Nitrogen fixation and nitrogenase activities in members of the family Rhodospirillaceae. J Bacteriol 157:73–78

    Google Scholar 

  • Madigan MT, Gest H (1979) Growth of the photosynthetic bacterium Rhodopseudomonas capsulata chemoautotrophically in darkness with H2 as the energy source. J Bacteriol 137:524–530

    Google Scholar 

  • Masters RA, Madigan MT (1983) Nitrogen metabolism in the phototrophic bacteria Rhodocyclus purpureus and Rhodospirillum tenue. J Bacyeriol 155:222–227

    Google Scholar 

  • Pfennig N, Biebl H (1976) Desulfuromonas acetoxidans, gen. nov., and sp. nov., a new anaerobic, sulfur-reducing, acetate-oxidizing bacterium. Arch Microbiol 110:3–12

    Google Scholar 

  • Pfennig N, Trüper HG (1981) Isolation of members of the families Chromatiaceae and Chlorobiaceae. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The prokaryotes, a handbook on habitats, isolation and identification of bacteria, vol I. Springer, Berlin Heidelberg New York, pp 279–289

    Google Scholar 

  • Postgate JR (1982) The fundamentals of nitrogen fixation. Cambridge University Press, Cambridge, England

    Google Scholar 

  • Reiderer-Henderson MA, Wilson PW (1970) Nitrogen fixation by sulfate-reducing bacteria. J Gen Microbiol 61:27–31

    Google Scholar 

  • Saari LL, Triplett EW, Ludden PW (1984) Purification and properties of the activating enzyme for iron protein of nitrogenase from the photosynthetic bacterium Rhodospirillum rubrum. J Biol Chem 259:15502–15508

    Google Scholar 

  • Simpson FB, Burris RH (1984) A nitrogen pressure of 50 atmospheres does not prevent evolution of hydrogen by nitrogenase. Science 224:1095–1097

    Google Scholar 

  • Smith RV, Telfer A, Evans MCW (1971) Complementary functioning of nitrogenase components from a blue-green alga and a photosynthetic bacterium. J Bacteriol 107:574–575

    Google Scholar 

  • Stackebrandt E, Woese CR (1981) The evolution of prokaryotes. In: Carlile MJ, Collins JR, Moseley BEB (eds) Molecular and cellular aspects of microbial evolution. Cambridge University Press, pp 1–31

  • Stegeman RA, Madigan MT (1985) Nitrogen nutrition and pathway of ammonia assimilation in brown Rhodospirillum species. FEMS Microbiology Letts 26:259–264

    Google Scholar 

  • Sweet WJ, Burris RH (1981) Inhibition of nitrogenase activity by NH +4 in Rhodospirillum rubrum. J Bacteriol 145:824–831

    Google Scholar 

  • Wagner BJ, Miović ML, Gibson J (1973) Utilization of amino acids by Chromatium sp. strain D. Arch Mikrobiol 91:255–272

    Google Scholar 

  • Yoch DC (1979) Manganese, an essential trace element for N2 fixation by Rhodospirillum rubrum and Rhodopseudomonas capsulata: role in nitrogenase regulation. J Bacteriol 140:987–995

    Google Scholar 

  • Yoch DC (1980) Regulation of nitrogenase A and R concentrations in Rhodopseudomonas capsulata by glutamine synthetase. Biochem J 187:273–276

    Google Scholar 

  • Zakhvataeva NV, Kondrateva EN (1971) Fixation of molecular nitrogen by photosynthesizing bacteria in relation to presence of light and ATP and character of exogenous substrate. Dokl Akad Nauk SSSR 196:72–74

    Google Scholar 

  • Zakhvataeva NV, Malofeeva IV, Kondrateva EN (1970) Nitrogen fixation capacity of photosynthesizing bacteria. Microbiology (English translation of Mikrobiologiya) 39:661–666

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This paper is dedicated to Professor Norbert Pfennig on the occasion of his 60th birthday

Rights and permissions

Reprints and permissions

About this article

Cite this article

Heda, G.D., Madigan, M.T. Aspects of nitrogen fixation in Chlorobium . Arch. Microbiol. 143, 330–336 (1986). https://doi.org/10.1007/BF00412798

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00412798

Key words

Navigation