Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-26T13:48:13.304Z Has data issue: false hasContentIssue false

Response to phage infection of immobilized lactococci during continuous acidification and inoculation of skim milk*

Published online by Cambridge University Press:  01 June 2009

Flavia M. L. Passos
Affiliation:
Southeast Dairy Foods Research Center, Department of Food Science, North Carolina State University, Raleigh, NC 27695-7624, USA
Todd R. Klaenhammer
Affiliation:
Southeast Dairy Foods Research Center, Department of Food Science, North Carolina State University, Raleigh, NC 27695-7624, USA
Harold E. Swaisgood*
Affiliation:
Southeast Dairy Foods Research Center, Department of Food Science, North Carolina State University, Raleigh, NC 27695-7624, USA
*
For correspondence.

Summary

A laboratory scale bioreactor was used for continuous acidification and inoculation of milk with a proteinase-negative, lactose-fermenting strain, Lactococcus lactis subsp. lactis C2S. Calcium alginate-entrapped cells were immobilized on a spiral stainless steel mesh incorporated into a column bioreactor and used to acidify and inoculate reconstituted skim milk. Characteristics of the immobilized cell bioreactor (ICB) were compared with those of a free cell bioreactor (FCB) during challenge with a virulent phage. Steady state biomass and lactate productivities were respectively 25-fold and 12-fold larger with the ICB than with the FCB. The ICB and the FCB were inoculated with the prolate phage c2 at multiplicities of infection of 0·25 and 0·02 respectively. Within 90 min of the infection, the FCB viable cell concentration dropped by five orders of magnitude and never recovered, while the plaque forming units/ml increased dramatically. In the ICB, released cells decreased immediately after infection, but subsequently increased, while the plaque forming units/ml steadily declined, indicating that phage were being washed out of the bioreactor. Productivity of FCB decreased to zero, whereas productivity of the ICB only decreased ∼ 60% and subsequently recovered to its initial steady state value.

Type
Original articles
Copyright
Copyright © Proprietors of Journal of Dairy Research 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

*

Paper no. FSR-93-16 of the Journal Series of the Department of Food Science, North Carolina State University, Raleigh, NC 27695-7624. The use of trade names in this publication does not imply endorsement by the North Carolina Agricultural Research Service of products named, nor criticism of similar ones not mentioned.

References

REFERENCES

Champagne, C. P., Girard, F. & Morin, N. 1988 Bacteriophage development in an immobilized lactic acid bacteria system. Biotechnology Letters 10 463468CrossRefGoogle Scholar
Fox, P. F. 1989 Proteolysis during cheese manufacture and ripening. Journal of Dairy Science 72 13791400CrossRefGoogle Scholar
Huggins, A. B. 1984 Progress in dairy starter culture technology. Food Technology 38 (6) 4150Google Scholar
Jarvis, A. W. 1989 Bacteriophages of lactic acid bacteria. Journal of Dairy Science 72 34063428CrossRefGoogle Scholar
Klaenhammer, T. R. 1984 Interactions of bacteriophages with lactic streptococci. Advances in Applied Microbiology 30 129CrossRefGoogle Scholar
Klaenhammer, T. B., McKay, L. L. & Baldwin, K. A. 1978 Improved lysis of group N streptococci for isolation and rapid characterization of plasmid deoxyribonucleic acid. Applied and Environmental Microbiology 35 592600CrossRefGoogle Scholar
Klaenhammer, T. R. & Sanozky, R. B. 1985 Conjugal transfer from Streptococcus lactis ME2 of plasmids encoding phage resistance, nisin resistance and lactose-fermenting ability: evidence for a high-frequency conjugate plasmid responsible for abortive infection of virulent bacteriophage. Journal of General Microbiology 131 15311541Google ScholarPubMed
Klein, J., Stock, J. & Vorlop, K.-D. 1983 Pore size and properties of spherical Ca-alginate biocatalysts. European Journal of Applied Microbiology 18 8691CrossRefGoogle Scholar
Olson, N. F. & Johnson, M. E. 1990 Light cheese products: characteristics and economics. Food Technology 44 (6) 9396Google Scholar
Passos, F. M. L. & Swaisgood, H. E. 1993 Development of a spiral mesh bioreactor with immobilized lactococci for continuous inoculation and acidification of milk. Journal of Dairy Science 76 28562867CrossRefGoogle Scholar
Sanders, M. E. 1988 Phage resistance in lactic acid bacteria. Biochimie 70 411421CrossRefGoogle ScholarPubMed
Sanders, M. E. & Klaenhammer, T. R. 1983 Characterization of phage-sensitive mutants from a phage-insensitive strain of Streptococcus lactis: evidence for a plasmid determinant that prevents phage adsorption. Applied and Environmental Microbiology 46 11251133CrossRefGoogle ScholarPubMed
Smidsrød, O. & Skjåk-Bræk, G. 1990 Alginate as immobilization matrix for cells. Trends in Biotechnology 8 7178CrossRefGoogle ScholarPubMed
Steenson, L. R., Klaenhammer, T. R. & Swaisgood, H. E. 1987 Calcium alginate-immobilized cultures of lactic streptococci are protected from bacteriophages. Journal of Dairy Science 70 11211127CrossRefGoogle ScholarPubMed
Stewart, W. W. & Swaisgood, H. E. 1993 Characterization of calcium alginate pore diameter by size-exclusion chromatography using protein standards. Enzyme and Microbial Technology 15 922927CrossRefGoogle Scholar
Swaisgood, H. E. 1991 Immobilized enzymes: applications to bioprocessing of food. In Food Enzymology, vol. 2, pp. 309341 (Ed. Fox, P. F.). London: Elsevier Applied ScienceGoogle Scholar
Terzaghi, B. E. & Sandine, W. E. 1975 Improved medium for lactic streptococci and their bacteriophage. Applied Microbiology 29 807813CrossRefGoogle Scholar
Thomas, T. D. & Pritchard, G. G. 1987 Proteolytic enzymes of dairy starter cultures. FEMS Microbiology Reviews 46 245268CrossRefGoogle Scholar