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Effect of fermentation sugar on hydrogen peroxide accumulation by Streptococcus lactis C10

Published online by Cambridge University Press:  01 June 2009

Roger C. Grufferty
Affiliation:
Department of Dairy and Food Microbiology, University College, Cork, Irish Republic
Seamus Condon
Affiliation:
Department of Dairy and Food Microbiology, University College, Cork, Irish Republic

Summary

Hydrogen peroxide accumulated in aerated cultures of Streptococcus lactis C10, the amount depending on the sugar being utilized. When the energy source was galactose or (to a lesser extent) lactose or maltose, H2O2 reached autoinhibitory levels. With glucose, H2O2 reached levels which did not cause obvious inhibition, and then declined. Washed cell suspensions utilized several media ingredients including glucose, galactose and yeast extract as substrates for O2 uptake, but cell-free extracts utilized none of these. The only substrate which supported O2 uptake by cell-free extracts was NADH. The activity of NADH oxidase was not affected by several intermediates of carbohydrate metabolism. Evidence was obtained to show that its synthesis was regulated via induction by O2 with an overriding catabolite repression type control, when cells were grown at the expense of glucose.

Type
Original Articles
Copyright
Copyright © Proprietors of Journal of Dairy Research 1983

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References

REFERENCES

Anders, R. F., Hogg, D. M. & Jago, G. R. 1970 Formation of hydrogen peroxide by Group N streptococci and its effect on their growth and metabolism Applied Microbiology 19 602612Google Scholar
Avigad, G., Amaral, D., Asensio, C. & Horecker, B. L. 1962 The D-galactose oxidase of Polyporus circinatus. Journal of Biological Chemistry 237 27362743CrossRefGoogle ScholarPubMed
Broome, M. C., Thomas, M. P., Hillier, A. J. & Jago, G. R. 1980 Pyruvate dehydrogenase activity in Group N streptococci. Australian Journal of Biological Sciences 33 1525CrossRefGoogle ScholarPubMed
Collins, E. B. & Aramaki, K. 1980 Production of hydrogen peroxide by Lactobacillus acidophilus. Journal of Dairy Science 63 353357CrossRefGoogle ScholarPubMed
Dahiya, R. S. & Speck, M. L. 1968 Hydrogen peroxide formation by lactobacilli and its effect on Staphylococcus aureus. Journal of Dairy Science 51 15681572CrossRefGoogle ScholarPubMed
Dempsey, P. M., O'leary, J. & Condon, S. 1975 Polarographie assay of hydrogen peroxide accumulation in microbial cultures. Applied Microbiology 29 170174CrossRefGoogle Scholar
Dobrogosz, W. J. & Stone, R. W. 1962 Oxidative metabolism in Pediococcus pentosaceus. I. Role of oxygen and eatalase. Journal of Bacteriology 84 716723CrossRefGoogle Scholar
Dolin, M. I. 1955 The DPNH-oxidizing enzymes of Streptococcus faecalis. II. The enzymes utilizing oxygen, cytochrome c, peroxide and 2.6-dichlorophenol-indophenol or ferricyanide as oxidants. Archives of Biochemistry and Biophysics 55 415435CrossRefGoogle Scholar
Farrell, M. A. 1935 Studieson the respiratory mechanism of thestreptococci. Journal of Bacteriolriology 29 411435CrossRefGoogle Scholar
Fukul, S. 1961 Crystalline DPNH oxidase from Lactobacillus plantarum No. 11. Agricultural and Biological Chemistry 25 876878Google Scholar
Gilliland, S. E. & Speck, M. L. 1969 Biological response of lactic streptococci and lactobacilli to catalase. Applied Microbiology 17 797800CrossRefGoogle ScholarPubMed
Gilliland, S. E. & Speck, M. L. 1975 Inhibition of psychrotrophic bacteria by lactobacilli and pediococci in non fermented refrigerated foods. Journal of Food Science 40 903905CrossRefGoogle Scholar
Gilliland, S. E. & Speck, M. L. 1977 Instability of Lactobacillus acidophilus in yogurt. Journal of Dairy Science 60 13941398CrossRefGoogle Scholar
Grufferty, R. C. 1981 Oxygen sensitivity of Streptococcus lactis C10. Thesis, University College, Cork, National University of IrelandGoogle Scholar
Gunsalus, I. C. & Umbreit, W. W. 1945 The oxidation of glycerol by Streptococcus faecalis. Journal of Bacteriology 49 347357CrossRefGoogle ScholarPubMed
Juffs, H. S. & Babel, F. J. 1975 Inhibition of psychrotrophic bacteria by lactic cultures in milk stored at low temperatures. Journal of Dairy Science 58 16121619CrossRefGoogle Scholar
Keane, M. I. 1973 Accumulation of hydrogen peroxide by lactic streptococci and sensitivity of strains to levels produced. Thesis, University College, Cork, National University of IrelandGoogle Scholar
Lowry, O. H., Rosebrough, N. J., Farr, A. L. & Randall, R. J. 1951 Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry 193 265275CrossRefGoogle ScholarPubMed
Niven, C. F., Evans, J. B. & White, J. C. 1945 Oxidation of butyric acid by streptococci. Journal of Bacteriology 49 105CrossRefGoogle ScholarPubMed
Oram, J. D. & Reiter, B. 1966 The inhibition of streptococci by lactoperoxidase, thiocyanate and hydrogen peroxide. The effect of the inhibitory system on susceptible and resistant strains of Group N streptococci. Biochemical Journal 100 373381CrossRefGoogle ScholarPubMed
Price, R. J. & Lee, J. S. 1970 Inhibition of Pseudomonas species by hydrogen peroxide producing lactobacilli. Journal of Milk and Food Technology 33 1318CrossRefGoogle Scholar
Strittmatter, C. F. 1959 Flavin-linked oxidative enzymes of Lactobacillus casei. Journal of Biological Chemistry 234 27942800CrossRefGoogle ScholarPubMed
Ratliff, T. L., Stinson, R. S. & Talburt, D. E. 1980 Effect of prostaglandin E1-induced elevation of cyclic AMP on glucose repression in the lactic streptococci. Canadian Journal of Microbiology 26 5863CrossRefGoogle ScholarPubMed
Thomas, T. D., Turner, K. W. & Crow, V. L. 1980 Galactose fermentation by Streptococcus lactis and Streptococcus cremoris: pathways, products and regulation. Journal of Bacteriology 144 672682CrossRefGoogle ScholarPubMed
Walker, G. A. & Kilgour, G. L. 1965 Pyridine nucleotide oxidizing enzymes of Lactobacillus casei. II. Oxidase and peroxidase. Archives of Biochemistry and Biophysics 111 534539CrossRefGoogle ScholarPubMed
Wheater, D. M., Hirsch, A. & Mattick, A. T. R. 1952 Possible identity of ‘lactobacillin’ with hydrogen peroxide produced by lactobacilli. Nature 170 623624CrossRefGoogle ScholarPubMed