Skip to main content
Log in

A pathway of the autotrophic CO2 fixation in Chloroflexus aurantiacus

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

Abstract

Autotrophically grown cells of Chloroflexus aurantiacus B-3 were shown to possess activity of ATP-dependent malate lyase (acetylating CoA). ATP: malate lyase is supposed to be the specific enzyme of the cycle of the autotrophic CO2 fixation, in which pyruvate synthase, pyruvate phosphate dikinase, phosphoenolpyruvate (PEP) carboxylase and malate dehydrogenase are involved as well. The main product of the CO2 fixation cycle is glyoxylate, which could further be converted into 3-phosphoglyceric acid (3-PGA) in the reactions of either glycerate or serine pathway. The enzymes of both pathways were detected in C. auratiacus B-3. The results of the in vivo studies of glyxoylate and glycine metabolism, as well as the inhibitor analysis using fluoroacetate (FAc), isonicotinic acid hydrazide (INH), and 4-aminopterin (4-AP) confirm the operation of the proposed pathway in Chloroflexus.

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

3-PGA:

3-phosphoglyceric acid

4-AP:

4-aminopterin

FAc:

fluoroacetate

INH:

isonicotinic acid hydrazide

MV:

methyl viologen

PEP:

phosphoenolpyruvate

THF:

tetrahydrofolate

TPP:

thiamine pyrophosphate

References

  • Albers H, Gottschalk G (1976) Acetate metabolism in Rhodopseudomonas gelatinosa and several other Rhodospirillaceae. Arch Microbiol 111: 45–49

    Google Scholar 

  • Bassham JA, Buchanan BB (1982) Pathway of CO2 fixation in plants and bacteria. In: Govindjee (ed) Photosynthesis, vol 2. Academic Press, New York London, pp 218–272

    Google Scholar 

  • Baker BR (1967) Design of active-site-directed irreversible enzyme inhibitor. Academic Press. New York London

    Google Scholar 

  • Blackmore MA, Quayle JR (1970) Microbial growth on oxalate by a route not involving glyoxylate carboligase. Biochem J 118: 53–59

    Google Scholar 

  • Botsford JL, Parks LW (1969) Serine transhydroxymetylase in methionine biosynthesis in Saccharomyces cereviseae. J Bacteriol 97: 1176–1183

    Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254

    Google Scholar 

  • Castenholz RW, Pierson BK (1981) Isolation of members of the family Chloroflexaceae. In: Balows A, Trüper HG, Dworkin M et al. (eds) The prokaryotes, vol 1, Springer, Berlin Heidelberg New York, pp 290–298

    Google Scholar 

  • Codd GA, Stewart WDP (1973) Pathways of glycollate metabolism in the blue-green alga Anabaena cylindrica. Arch Mikrobiol 94: 11–28

    Google Scholar 

  • Den H, Robinson WG, Coon M (1959) Enzymatic conversion of β-hydroxypropionate to malonate semialdehyde. J Biol Chem 234: 1666–1671

    Google Scholar 

  • Dixon GH, Kornberg HL (1959) Assay methods for key enzymes of the glyoxylate cycle. Biochem J 72: 195–198

    Google Scholar 

  • Durham NN, Jacobs CD, Fergusson D (1964) Relationship of a β-alanine-pyruvic aminotransferase to reversal of D-serine inhibition of growth. J Bacteriol 88: 1525–1528

    Google Scholar 

  • Fuchs G (1989) Alternative pathways of autotrophic CO2 fixation. In: Schlegel HG, Bowien B (eds) Autotrophic bacteria. Science Tech Publishers, Madison, Wis., pp 365–382

    Google Scholar 

  • Hayashi O, Yatsuoki N, Tatibana M, Takeshita M, Kuno S (1961) Enzymatic studies on the metabolism of β-alanine. J Biol Chem 236: 781–790

    Google Scholar 

  • Hayashi S, Lin ECC (1967) Purification and properties of glycerate kinase from Escherichia coli. J Biol Chem 242: 1030–1035

    Google Scholar 

  • Holo H (1989) Chloroflexus aurantiacus secretes 3-hydrohypropionate, a possible intermediate in the assimilation of CO2 and acetate. Arch Microbiol 151: 252–256

    Google Scholar 

  • Holo H, Grace D (1987) Polyglucose synthesis in Chloroflexus aurantiacus studied by 13C-NMR. (Evidence for acetate metabolism by a new metabolic pathway in autotrophically grown cells). Arch Microbiol 148: 292–297

    Google Scholar 

  • Holo H, Sirevåg R (1986) Autotrophic growth and CO2 fixation of Chloroflexus aurantiacus. Arch Microbiol 145: 173–180

    Google Scholar 

  • Kondratieva EN (1979) Interrelation between modes of carbon assimilation and energy production in phototrophic purple and green bacteria. In: Quayle JR (ed) Microbial biochemistry, vol 21. University Park Press, Baltimore, pp 117–175

    Google Scholar 

  • Kornberg HL, Gotto AM (1961) The metabolism of C2 compounds om microorganisms. VI. Synthesis of cell constituents from glycollate by Pseudomonas sp. Biochem J 78: 69–72

    Google Scholar 

  • Krakow G, Barkalis SS, Hayashi JA (1961) Glyoxylic acid carboligase: an enzyme present in glycolate-grown Escherichia coli. J Bacteriol 81: 509–518

    Google Scholar 

  • Krasilnikova EN, Pedan LV, Firsov NN, Kondratieva EN (1973) Enzymes of the citric acid cycle in various species of phototrophic bacteria (in Russian) Mikrobiologia 42: 995–1000

    Google Scholar 

  • Krasilnikova EN, Keppen OI, Gorlenko VM, Kondratieva EN (1986) Chloroflexus aurantiacus growth in media with different organic compounds and the pathways of their metabolism (in Russian). Mikrobiologia 55: 425–430

    Google Scholar 

  • Kun E, Gottwald LK, Fanshier DH, Ayling JE (1963) The effects of difluoro-oxaloacetate and difluoromalate on malate dehydrogenases and glutamate-aspartate aminotransferase. J Biol Chem 238: 1456–1463

    Google Scholar 

  • Laakmann-Ditges G, Klemme J-H (1986) Occurrence of two L-threonine (L-serine) dehydratases in the thermophile Chloroflexus aurantiacus. Arch Microbiol 144: 219–221

    Google Scholar 

  • Larsen H (1952) On the culture and general physiology of the green sulfur bacteria. J Bacteriol 64: 187–196

    Google Scholar 

  • Løken Ø, Sirevåg R (1982) Evidence for presence of the glyoxylate cycle in Chloroflexus. Arch Microbiol 132: 276–279

    Google Scholar 

  • Salem AR, Haking J, Quayle JR (1973) Cleavage of malyl-coenzyme A into acetyl-coenzyme A and glyoxylate by Pseudomonas AM1 and other C1-unit-utilizing bacteria. Biochem J 136: 89–96

    Google Scholar 

  • Scrimgeour KJ, Huennekens FM (1962) Serine hydroxymethylase. In: Colowick SP, Kaplan ND (eds) Methods in enzymology, vol 5. Academic Press, New York London, pp 838–851

    Google Scholar 

  • Sirevåg R, Ormerod JG (1970) Carbon dioxide fixation in green sulfur bacteria. Biochem J 120: 399–408

    Google Scholar 

  • Smith BN, Epstein S (1971) Two categories of 13C/12C ratios of higher plants. Plant Physiol 47: 380–384

    Google Scholar 

  • Stafford HA, Magaldi A, Vennesland B (1954) The enzymatic reduction of hydroxypyruvic acid in higher plants. J Biol Chem 207: 621–629

    Google Scholar 

  • Takabe T, Akazawa T (1977) A comparative study of the effect O2 on photosynthetic carbon metabolism by Chlorobium thiosulfatophillum and Chromatium vinosum. Plant Cell Physiol 18: 753–765

    Google Scholar 

  • Thauer RK, Rupprecht E, Jungermann K (1970) Glyoxylate inhibition of clostridial pyruvate synthase. FEBS Lett 9: 271–273

    Google Scholar 

  • Tuboi S, Kikuchi G (1962) Enzymatic cleavage of malate to glyoxylate and acetyl-coenzyme A. Biochim Biophys Acta 62: 188–192

    Google Scholar 

  • Yokota A, Asama K, Kitaoka S (1990) Evidence of reentrance of glycolate carbon into photosynthetic carbon reduction cycle in photosynthesizing Euglena gracilis Z Plant Physiol 94: 388–391

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ivanovsky, R.N., Krasilnikova, E.N. & Fal, Y.I. A pathway of the autotrophic CO2 fixation in Chloroflexus aurantiacus . Arch. Microbiol. 159, 257–264 (1993). https://doi.org/10.1007/BF00248481

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00248481

Key words

Navigation