Skip to main content
Log in

Fermentation of tartrate enantiomers by anaerobic bacteria, and description of two new species of strict anaerobes, Ruminococcus pasteurii and Ilyobacter tartaricus

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

Abstract

Enumerations of tartrate-fermenting anaerobic bacteria with l-, d-, and m-tartrate as substrates revealed that l-tartrate fermenters outnumbered d- and m-tartrate fermenters by one to three orders of magnitude in all three anoxic environments studied.

Highest numbers of tartrate-fermenting bacteria were found in freshwater creek sediments, less in polluted marine channels, and lowest numbers in anoxic sewage digestor sludge. Prevailing bacteria were isolated on every tartrate enantiomer. They all degraded tartrates via oxaloacetate.

d- and m-tartrate-fermenting anaerobes were able to ferment l-tartrate as well, and were assigned to the genera Bacteroides, Acetivibrio, and Ilyobacter. l-Tartrate-fermenting anaerobes only utilized this enantiomer, and were characterized in more detail. Fermentation products on tartrate, citrate, pyruvate, and oxaloacetate were acetate, formate, and carbon dioxide. On fructose and glucose, also ethanol was formed. Freshwater isolates were Gram-positive cocci with large slime capsules, and were described as a new species, Ruminococcus pasteurii. Saltwater isolates were Gram-negative short rods, and were also described as a new species, Ilyobacter tartaricus. The guanosine-plus-cytosine content of the DNA was 45.2% and 33.1%, respectively.

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

References

  • American Public Health Association Inc (ed) (1969) Standard methods for the examination of water and wastewater including bottom sediments and sludge. New York, pp 604–609

  • Barker HA (1936) On the fermentation of some dibasic C4-acids by Aerobacter aerogenes. Proc Acad Sci Amst 39:674

    Google Scholar 

  • Bergmeyer HU (1974) Methoden der enzymatischen Analyse, 3rd edn. Verlag Chmie, Weinheim

    Google Scholar 

  • Buchanan RE, Gibbons NE (1974) Bergey's manual of determinative bacteriology, 8th edn. Williams and Wilkins Co, Baltimore

    Google Scholar 

  • Dagley S, Trudgill PW (1963) The metabolism of tartaric acid by a Pseudomonas. A new pathway. Biochem J 89:22–31

    PubMed  Google Scholar 

  • De Vries W, Rietveld-Struijck TRM, Stouthamer AG (1977) ATP formation associated with fumarate and nitrate reduction in growing cultures of Veillonella alcalescens. Antonie van Leeuwenhoek 43:153–167

    Google Scholar 

  • Hartree EF (1972) Determination of protein: a modification of the Lowry method that gives a linear photometric response. Anal Biochem 48:422–427

    PubMed  Google Scholar 

  • Hurlbert RE, Jakoby WB (1965) Tartaric acid metabolism. I. Subunits of l(+)-tartaric acid dehydrase. J Biol Chem 240:2772–2777

    PubMed  Google Scholar 

  • Krampitz LO, Lynen F (1956) Formation of oxaloacetate from d-tartrate. Fed Proc 15:292–293

    Google Scholar 

  • Krieg NR, Holt JG (1984) Bergey's manual of systematic bacteriology, 9th edn, vol 1. Williams and Wilkins, Baltimore London

    Google Scholar 

  • Kun E (1956) Enzymatic mechanism of oxidation of tartrate. J Biol Chem 221:223–230

    PubMed  Google Scholar 

  • Lang E, Lang H (1972) Spezifische Farbreaktion zum direkten Nachweis der Ameisensäure. Z Analyt Chem 260:8–10

    Google Scholar 

  • La Rivière HWM (1956) Intermediate products in tartrate decomposition by cell-free extracts of Pseudomonas putida under anaerobic conditions. Biochim Biophys Acta 21:190–191

    PubMed  Google Scholar 

  • Mercer WA, Vaughn RH (1951) The characteristics of some thermophilic tartrate-fermenting anaerobes. J Bacteriol 62: 27–37

    PubMed  Google Scholar 

  • Nomura M, Sakaguchi K (1955) The decomposition of l-(+)-tartrate by microorganisms. J Gen Appl Microbiol 1:77–98

    Google Scholar 

  • Pasteur L (1858) Mémoire sur la fermentation de l'acide tartrique. Compt Rend Acad Sci Paris 46:615–618

    Google Scholar 

  • Pfennig N (1978) Rhodocyclus purpureus gen. nov. and sp. nov., a ring-shaped, vitamin B12-requiring member of the family Rhodospirillaceae. Int J Syst Bacteriol 28:283–288

    Google Scholar 

  • Rode H, Giffhorn F (1982) Ferrous-or cobalt ion-dependent d-(-)-tartrate dehydratase of pseudomonads: purification and properties. J Bacteriol 151:1602–1604

    PubMed  Google Scholar 

  • Schink B, Pfennig N (1982) Fermentation of trihydroxybenzenes by Pelobacter acidigallici gen. nov. sp. nov., a new strictly anaerobic, non-sporeforming bacterium. Arch Microbiol 133:195–201

    Google Scholar 

  • Shilo M (1957) The enzymic conversion of the tartaric acids to oxaloacetic acids. J Gen Microbiol 16:472–481

    PubMed  Google Scholar 

  • Shilo M, Stanier RY (1957) The utilization of the tartaric acids by pseudomonads. J Gen Microbiol 16:482–490

    PubMed  Google Scholar 

  • Stieb M, Schink B (1984) Ilyobacter polytropus gen. nov. sp. nov., a new non-sporing strict anaerobe exhibiting a very versatile fermentation metabolism Arch Microbiol (submitted)

  • Stouthamer AH (1979) The search for correlation between theoretical and experimental growth yields. In: Quayle JR (ed) International review of biochemistry, microbial biochemistry, vol 21. University Park Press, Baltimore, pp 1–47

    Google Scholar 

  • Tabachnick J, Vaughn RH (1948) Characteristics of tartratefermenting species of Clostridium. J Bacteriol 56:435–443

    Google Scholar 

  • Van Niel CB (1944) The culture, general physiology, morphology, and classification of the nonsulfar purple and brown bacteria. Bacteriol Rev 8:1–118

    Google Scholar 

  • Vaughn RH, Marsh GL, Stadtman TC, Cantino BC (1946) Decomposition of tartrates by the coliform bacteria. J Bacteriol 52:311–325

    Google Scholar 

  • Widdel F, Pfennig N (1981) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from salive environments. Description of Desulfobacter postgatei gen. nov. sp. nov. Arch Microbiol 129:395–400

    Google Scholar 

  • Windholz M, Budavari S, Stroumtsos LY, Fertig MN (1976) The Merck Index. Merck & Co Inc, Rahway, New Jersey

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Dedicated to Prof. Dr. H. G. Schlegel on occasion of his 60. birthday

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schink, B. Fermentation of tartrate enantiomers by anaerobic bacteria, and description of two new species of strict anaerobes, Ruminococcus pasteurii and Ilyobacter tartaricus . Arch. Microbiol. 139, 409–414 (1984). https://doi.org/10.1007/BF00408388

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00408388

Key words

Navigation