Tm Cogan

Applicability of a bacteriocin-producing Enterococcus faecium as a co-culture in Cheddar cheese manufacture

Two strains, Enterococcus faecium RZS C5 and E. faecium DPC 1146, produce listericidal bacteriocins, so-called enterocins. E. faecium RZS C5 was studied during batch fermentation in both a complex medium (MRS) and in milk to understand the influence of environmental factors, characteristic for milk and cheese, on both growth and bacteriocin production. Fermentation conditions were chosen in view of the applicability of in situ enterocin production during Cheddar cheese production. Enterocin production by E. faecium RZS C5 in MRS started in the early logarithmic growth phase, and enterocin activity decreased during the stationary phase. The effect of pH on enterocin production and decrease of activity was as intense as the effect on bacterial growth. Higher enterocin production took place at pH 5.5 compared with pH 6.5. The use of lactose instead of glucose increased the production of enterocin, and at higher lactose concentration, production increased more and loss of activity decreased. The production in skimmed milk compared to MRS was lower and was detected mainly in the stationary phase. When casein hydrolysate was added to the milk, enterocin production was higher and started earlier, indicating the importance of an additional nitrogen source for growth of E. faecium in milk. For co-cultures of E. faecium RZS C5 with the starters used during Cheddar cheese manufacture, no enterocin activity was detected during the milk fermentation. Furthermore, the applicability of E. faecium RZS C5 and E. faecium DPC 1146 strains was tested in Cheddar cheese manufacture on pilot scale. Enterocin production took place from the beginning of the cheese manufacturing and was stable during the whole ripening phase of the cheese. This indicates that both an early and late contamination of the milk or cheese can be combated with a stable, in situ enterocin production. The use of such a co-culture is an additional safety provision beyond good manufacturing practices.

A rapid PCR based method to distinguish between Lactococcus and Enterococcus.

Phenotypic characterisation of Lactococcus and Enterococcus species remains unreliable as strains of both genera have been isolated which do not conform to the traditional criteria for separation of these genera. A bank of 131 isolates was phenotypically characterised by three methods: (a) traditional broth tests, (b) API Rapid ID 32 Strep and (c) BBL Crystal ID kits. Differences in genus designation between commercial kits were evident for 12 strains (9%), while 7 strains (5%) remained unidentified by either kit. Published 16S rRNA sequences were aligned and used to design genus-specific primers which, when used in separate PCR reactions, were capable of distinguishing all type strains of Lactococcus and Enterococcus. These primers did not react with known species of Streptococcus, Pediococcus, Lactobacillus, Leuconostoc or Tetragenococcus. Isolates which could not be identified by phenotype were assigned to either genus on the basis of the gene primers.

Sources of the adventitious microflora of a smear‐ripened cheese

Aims:  To determine the relationships between the major organisms from the cheese‐making personnel and environment and the surface of a smear cheese.

Spatial and temporal distribution of non-starter lactic acid bacteria in Cheddar cheese

Aims: The aim of this work was to investigate the spatial and temporal distribution of species and strains of non‐starter lactic acid bacteria (NSLAB) within Cheddar cheese.

Bacterial surface-ripened cheeses

Publisher Summary This chapter explains many cheeses that are characterized by the development of microbial growth on their surfaces during ripening. These are called surface-ripened cheeses and are subdivided into mold-ripened and bacterial-ripened cheeses, depending on the major microorganisms involved. Significant numbers of nonpigmented Micrococci have been found on the surface of Comte and Beaufort cheeses during ripening and the flora was dominated by Coryneforms . The smear bacteria also contribute to the ripening process through their proteolytic and lipolytic activities. Many of the food poisoning outbreaks of bacterial origin and of known aetiology are caused by the ingestion of foods containing Staph. aureus enterotoxins. The bacteria on the surface of smear-ripened cheeses are Gram-positive, catalase-positive, salt-tolerant bacteria that can be divided into two categories, Coryneforms and Staphylococci .

Antibiotic resistance and virulence traits of enterococci isolated from Baylough, an Irish artisanal cheese.

Eight representative Enterococcus strains from a collection of over 600 previously isolated from an Irish artisanal cheese were subjected to phenotypic and genotypic analysis of antibiotic resistance and virulence properties. Genes encoding resistance to tetracycline (tet(M) and tet(L)) and/or erythromycin (erm(B)) were detected in five strains. In addition, all strains contained two or more of the virulence genes tested (agg, gel, cyl, esp, ace, efaAfs, and efaAfm). Further investigation into the transferability and environmental dissemination of these resistance and virulence traits will allow risk assessment and safety evaluation of artisanal cheeses.

Survival of surface ripening cultures during storage and monitoring their development on cheese

Aims:  To study the survival of bacteria isolated from the surface of smear cheese and monitor their development during cheese ripening.