Developing applications for lactococcal bacteriocins

While much of the applied research carried out to date with bacteriocins has concerned nisin, lactococci produce other bacteriocins with economic potential. An example is the two component bacteriocin lacticin 3147, which is active over a wide pH range and has a broad spectrum of activity against Gram-positive bacteria. Since the genetic determinants for lacticin 3147 are encoded on a large self-transmissible plasmid, the bacteriocin genes may be conveniently transferred to different lactococcal starters. The resulting food-grade strains can then be used to make a significant impact on the safety and quality of a variety of fermented foods, through the inhibition of undesirable microflora. The bacteriocin is heat stable so it can also be used as an ingredient in a powdered form such as a spray-dried fermentate. Given the observation that lacticin 3147 is effective at physiological pH, there is also considerable potential for biomedical applications. Field trials have demonstrat ed its efficacy in the prevention of mastitis infections in dairy cows. In contrast to lacticin 3147, the lactococcin bacteriocins A, B and M have a narrow spectrum of activity limited to lactococci. Strains which produce these inhibitors can be exploited in the acceleration of cheese ripening by assisting the premature lysis of starter cultures.

[1]  R. P. Ross,et al.  Evaluation of Lacticin 3147 and a Teat Seal Containing This Bacteriocin for Inhibition of Mastitis Pathogens , 1998, Applied and Environmental Microbiology.

[2]  K. Baldwin,et al.  Plasmid linkage of a bacteriocin-like substance in Streptococcus lactis subsp. diacetylactis strain WM4: transferability to Streptococcus lactis , 1983, Applied and environmental microbiology.

[3]  G. Venema,et al.  Cloning of two bacteriocin genes from a lactococcal bacteriocin plasmid , 1989, Applied and environmental microbiology.

[4]  C. Hill,et al.  Development of a lacticin 3147-enriched whey powder with inhibitory activity against foodborne pathogens. , 1999, Journal of food protection.

[5]  L. Vuyst,et al.  Bacteriocins of Lactic Acid Bacteria , 1994 .

[6]  R. P. Ross,et al.  Inhibition of Listeria monocytogenes in cottage cheese manufactured with a lacticin 3147‐producing starter culture , 1999, Journal of applied microbiology.

[7]  V. Crow,et al.  Interactions between non-starter microorganisms during cheese manufacture and repening , 1993 .

[8]  R. P. Ross,et al.  An application in cheddar cheese manufacture for a strain of Lactococcus lactis producing a novel broad-spectrum bacteriocin, lacticin 3147 , 1996, Applied and environmental microbiology.

[9]  J. Flynn,et al.  The natural food grade inhibitor, lacticin 3147, reduced the incidence of mastitis after experimental challenge with Streptococcus dysgalactiae in nonlactating dairy cows. , 1999, Journal of dairy science.

[10]  J. Broadbent,et al.  Nisin inhibits several gram-positive, mastitis-causing pathogens. , 1989, Journal of dairy science.

[11]  M. Gasson,et al.  Gene transfer systems and transposition , 1994 .

[12]  R. P. Ross,et al.  Increasing Starter Cell Lysis in Cheddar Cheese Using a Bacteriocin-Producing Adjunct , 1997 .

[13]  I. Peiris Listeria monocytogenes, a Food-Borne Pathogen , 1991, Microbiological reviews.

[14]  M. Coakley,et al.  Application and evaluation of the phage resistance- and bacteriocin-encoding plasmid pMRC01 for the improvement of dairy starter cultures , 1997, Applied and environmental microbiology.

[15]  P. McSweeney Biochemistry of Cheese Ripening , 2004 .

[16]  T. Klaenhammer,et al.  Genetics of bacteriocins produced by lactic acid bacteria. , 1993, FEMS microbiology reviews.

[17]  R. P. Ross,et al.  Bacteriolytic activity caused by the presence of a novel lactococcal plasmid encoding lactococcins A, B, and M , 1995, Applied and environmental microbiology.

[18]  R. P. Ross,et al.  Lacticin 3147, a Broad-Spectrum Bacteriocin Which Selectively Dissipates the Membrane Potential , 1998, Applied and Environmental Microbiology.

[19]  M. Teuber,et al.  Potential of Lactic Streptococci to Produce Bacteriocin , 1983, Applied and environmental microbiology.

[20]  B. Brooker,et al.  Inorganic constituents of cheese: analysis of juice from a one-month-old Cheddar cheese and the use of light and electron microscopy to characterize the crystalline phases , 1988, Journal of Dairy Research.

[21]  P. Fox,et al.  Autolysis and proteolysis in different strains of starter bacteria during Cheddar cheese ripening , 1994, Journal of Dairy Research.

[22]  W. M. Vos,et al.  Genetics and Biotechnology of Lactic Acid Bacteria , 1994, Springer Netherlands.

[23]  T. P. Guinee,et al.  Elevated Temperature Ripening of Reduced Fat Cheddar Made with or Without Lacticin 3147-Producing Starter Culture , 1999 .

[24]  J. Gripon,et al.  Autolysis of two strains of Lactococcus lactis during cheese ripening , 1994 .

[25]  B. Dougherty,et al.  Sequence and analysis of the 60 kb conjugative, bacteriocin‐producing plasmid pMRC01 from Lactococcus lactis DPC3147 , 1998, Molecular microbiology.

[26]  R. P. Ross,et al.  Lacticin 3147 displays activity in buffer against Gram‐positive bacterial pathogens which appear insensitive in standard plate assays , 1999, Letters in applied microbiology.

[27]  T. Coolbear,et al.  The influence of phage-assisted lysis of Lactococcus lactis subsp. lactis ML8 on cheddar cheese ripening , 1995 .

[28]  R. P. Ross,et al.  Design of a Phage-Insensitive Lactococcal Dairy Starter via Sequential Transfer of Naturally Occurring Conjugative Plasmids , 1998, Applied and Environmental Microbiology.

[29]  M. Rea,et al.  Irish kefir‐like grains: their structure, microbial composition and fermentation kinetics , 1996 .