Skip to main content
Log in

Quantitative analysis of growth and volatile fatty acid production by the anaerobic ruminal bacterium Megasphaera elsdenii T81

  • Applied microbial and cell physiology
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

Megasphaera elsdenii T81 grew on either dl-lactate or d-glucose at similar rates (0.85 h−1) but displayed major differences in the fermentation of these substrates. Lactate was fermented at up to 210-mM concentration to yield acetic, propionic, butyric, and valeric acids. The bacterium was able to grow at much higher concentrations of d-glucose (500 mM), but never removed more than 80 mM of glucose from the medium, and nearly 60 % the glucose removed was sequestered as intracellular glycogen, with low yields of even-carbon acids (acetate, butyrate, caproate). In the presence of both substrates, glucose was not used until lactate was nearly exhausted, even by cells pregrown on glucose. Glucose-grown cultures maintained only low extracellular concentrations of acetate, and addition of exogenous acetate increased yields of butyrate, but not caproate. By contrast, exogenous acetate had little effect on lactate fermentation. At pH 6.6, growth rate was halved by exogenous addition of 60 mM propionate, 69 mM butyrate, 44 mM valerate, or 33 mM caproate; at pH 5.9, these values were reduced to 49, 49, 18, and 22 mM, respectively. The results are consistent with this species’ role as an effective ruminal lactate consumer and suggest that this organism may be useful for industrial production of volatile fatty acids from lactate if product tolerance could be improved. The poor fermentation of glucose and sensitivity to caproate suggests that this strain is not practical for industrial caproate production.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

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

    Google Scholar 

  • Gutierrez J, Davis RE, Lindahl IL, Warwick EJ (1959) Bacterial changes in the rumen during the onset of feed-lot bloat of cattle and characteristics of Peptostreptococcus elsdenii n. sp. Appl Microbiol 7:16–22

    CAS  Google Scholar 

  • Hall MB (2011) Isotrichid protozoa influence conversion of glucose to glycogen and other microbial products. J Dairy Sci 94:4589–4602

    Article  CAS  Google Scholar 

  • Hino T, Kuroda S (1993) Presence of lactate dehydrogenase and lactate racemase in Megasphaera elsdenii grown on glucose or lactate. Appl Environ Microbiol 59:255–259

    CAS  Google Scholar 

  • Hino T, Miyazaki K, Kuroda S (1991) Role of extracellular acetate in the fermentation of glucose by a ruminal bacterium, Megasphaera elsdenii. J Gen Appl Microbiol 37:121–129

    Article  CAS  Google Scholar 

  • Hino T, Shimada K, Maruyama T (1994) Substrate preference in a strain of Megasphaera elsdenii, a ruminal bacterium, and its implications in propionate production and growth competition. Appl Environ Microbiol 60:1827–1831

    CAS  Google Scholar 

  • Holtzapple M, Granda C (2009) Carboxylate platform: the MixAlco process part 1: comparison of three biomass conversion platforms. Appl Biochem Biotechnol 156:525–536

    Article  CAS  Google Scholar 

  • Kenealy WR, Waselefsky DM (1985) Studies on the substrate range of Clostridium kluyveri: the use of propanol and succinate. Arch Microbiol 141:187–194

    Article  CAS  Google Scholar 

  • Lange JP, Price R, Ayoub PM, Louis J, Petrus L, Clarke L, Gosselink H (2010) Valeric biofuels: a platform of cellulosic transportation fuels. Angew Chem Int Ed 49:4479–4483

    Article  CAS  Google Scholar 

  • Marounek M, Fliegrova K, Bartos S (1989) Metabolism and some characteristics of ruminal strains of Megasphaera elsdenii. Appl Environ Microbiol 55:1570–1573

    CAS  Google Scholar 

  • Meissner HH, Henning PH, Horn CH, Leeuw KL, Hagg FM, Fouche G (2010) Ruminal acidosis: a review with detailed reference to the controlling agent Megasphaera elsdenii NCIMB 41125. S Afr J Anim Sci 40:79–100

    CAS  Google Scholar 

  • Miller GL, Blum R, Glennon WE, Burton AL (1960) Measurement of carboxymethylcellulase activity. Anal Biochem 1:127–132

    Article  CAS  Google Scholar 

  • Pavlostathis SG, Miller TL, Wolin MJ (1988) Fermentation of insoluble cellulose by continuous cultures of Ruminococcus albus. Appl Environ Microbiol 54:2655–2659

    CAS  Google Scholar 

  • Piknová M, Bíres O, Javorsky P, Pristas P (2006) Limited genetic variability in Megasphaera elsdenii strains. Folia Microbiol (Praha) 51:299–302

    Article  Google Scholar 

  • Rogosa M (1972) Transfer of Peptostreptococcus elsdenii Gutierrez et al. to a new genus, Megasphaera (M. elsdenii (Gutierrez et al.) comb. nov.). Int J Syst Bacteriol 21:187–189

    Article  Google Scholar 

  • Russell JB, Baldwin LR (1979) Comparison of maintenance energy expenditures and growth yields among several rumen bacteria grown in continuous culture. Appl Environ Microbiol 37:537–543

    CAS  Google Scholar 

  • Russell JB, Hino T (1985) Regulation of lactate production in Streptococcus bovis: a spiraling effect that contributes to rumen acidosis. J Dairy Sci 68:1712–1721

    Article  CAS  Google Scholar 

  • Thauer RK, Jungermann K, Decker K (1977) Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev 31:100–180

    Google Scholar 

  • Torii S, Tanaka H (2001) Carboxylic acids. In: Lund H, Hammerich O (eds) Organic electrochemistry, 4th edn. Marcel Dekker, New York, pp 499–535

    Google Scholar 

  • Wallace RJ, Chaudhary ME, McKain N, Walker ND (2004) Metabolic properties of Eubacterium pyruvativorans, a ruminal ‘hyper-ammonia-producing’ anaerobe with metabolic properties analogous to those of Clostridium kluyveri. Microbiology 150:2921–2930

    Article  CAS  Google Scholar 

  • Weimer PJ (2010) End product yields from the extraruminal fermentation of various polysaccharide, protein and nucleic acid components of biofuels feedstocks. Biores Technol 012:3254–3259

    Google Scholar 

  • Weimer PJ, Stevenson DM (2011) Isolation, characterization and quantification of Clostridium kluyveri from the bovine rumen. Appl Microbiol Biotechnol 94:461–466

    Article  Google Scholar 

  • Weimer PJ, Shi Y, Odt CL (1991) A segmented gas/liquid delivery system for continuous culture of microorganisms on solid substrates, and its use for growth of Ruminococcus flavefaciens on cellulose. Appl Microbiol Biotechnol 36:178–183

    Article  CAS  Google Scholar 

  • Wood WA (1961) Fermentation of carbohydrates and related compounds. In: Gunsalus IC, Stanier RY (eds) The bacteria, vol 2. Academic, New York

    Google Scholar 

Download references

Acknowledgments

We thank C.L. Odt for the technical assistance and M.B. Hall for the useful suggestions regarding glycogen analysis. This research was supported by USDA-ARS CRIS project 3655-41000-06-00D.

Conflict of interest

Mention of specific products is for informational purposes only and does not constitute an endorsement or warranty over similar products that may also be suitable.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P. J. Weimer.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Weimer, P.J., Moen, G.N. Quantitative analysis of growth and volatile fatty acid production by the anaerobic ruminal bacterium Megasphaera elsdenii T81. Appl Microbiol Biotechnol 97, 4075–4081 (2013). https://doi.org/10.1007/s00253-012-4645-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-012-4645-4

Keywords

Navigation