Bacteriocins are natural compounds used as food biopreservatives instead of chemical preservatives. Bifidobacterium animalis subsp. lactis (Bifid. lactis) was shown to produce a bacteriocin-like inhibitory substance (BLIS) able to inhibit the growth of Listeria monocytogenes selected as an indicator microorganism. To enhance this production by the strain Bifid. lactis BL 04, skim milk (SM) was used as a fermentation medium either in the presence or in the absence of yeast extract, Tween 80 or inulin as stimulating additives, and the results in terms of bacterial growth and BLIS production were compared with those obtained in a traditional high cost complex medium such as Man, Rogosa and Sharpe (MRS). To this purpose, all the cultivations were carried out in flasks at 200 rpm under anaerobic conditions ensured by a nitrogen flowrate of 1·0 L/min for 48 h, and BLIS production was quantified by means of a modified agar diffusion assay at low values of both temperature and concentration of List. monocytogenes. Although all these ingredients were shown to exert positive influence on BLIS production in both media, yeast extract and SM were by far the best ingredient and the best medium, respectively, allowing for a BLIS production at the late exponential phase of 2000 AU/ml.

The aggregation of proteins after heating of calcium-fortified milks has been an ongoing problem in the dairy industry. This undesirable effect restricts the manufacture of calcium rich dairy products. To overcome this problem, a completely new approach in controlling the heat stability of dairy protein solutions, developed in our lab, has been employed. In this approach, high intensity, low frequency ultrasound is applied for a very short duration after a pre-heating step at ⩾70 °C. The ultrasound breaks apart whey/whey and whey/casein aggregates through the process of acoustic cavitation. Protein aggregates do not reform on subsequent post-heating, thereby making the systems heat stable. In this paper, the acid gelation properties of ultrasonicated calcium-enriched skim milks have also been investigated. It is shown that ultrasonication alone does not change the gelation properties significantly whereas a sequence of preheating (72 °C/1 min) followed by ultrasonication leads to decreased gelation times, decreased gel syneresis and increased skim milk viscosity in comparison to heating alone. Overall, ultrasonication has the potential to provide calcium-fortified dairy products with increased heat stability. However, enhanced gelation properties can only be achieved when ultrasonication is completed in conjunction with heating.

The effects of ultra-high pressure homogenization (UHPH) on skim milk yogurt making properties were investigated. UHPH-treated milk was compared with conventionally homogenised (15 MPa) heat-treated skim milk (90°C for 90 s), and to skim milk treated under the same thermal conditions but fortified with 3% skim milk powder. Results of the present study showed that UHPH is capable of reducing skim milk particle size which leads to the formation of finer dispersions than those obtained by conventional homogenisation combined with heat treatment. In addition, results involving coagulation properties and yogurt characteristics reflected that, when increasing UHPH pressure conditions some parameters such as density of the gel, aggregation rate and water retention are improved.

A 3 X 2 factorial experiment was conducted to investigate the interactions between lactofeed 70 (LF70) (860 g/kg whey permeate, 140 g/kg soya-bean meal; Volac International, UK) and soya-bean meal (SBM) or dried skim milk (DSM) in piglet diets. Three hundred and thirty-six piglets were selected after weaning at 21 days with an initial live weight of 6-35 kg. They were blocked on the basis of live weight and within each block assigned to one of six dietary treatments. The pigs were offered the following starter diets : (1) 300 g/kg LF70 with 215 g/kg SBM and 100 g/kg DSM; (2) 200 g/kg LF70 with 215 g/kg SBM and 100 g/kg DSM; (3) 100 g/kg LF70 with 215 g/kg SBM and 100 g/kg DSM; (4) 300 g/kg LF70 with 325 g/kg DSM; (5) 200 g/kg LF70 with 325 g/kg DSM; (6) 100 g/kg LF70 with 325 g/kg DSM. The starter diets were offered for 25 days. Following this, a weaner diet (14 g/kg lysine, 14-5 MJ/kg digestible energy) was given for a period of 12 days. There was a significant interaction between LF70 level and protein source on average daily gain (ADG P < 0.001) and food conversion ratio (FCR P < 0.05) during the starter period. There was a linear increase in ADG and a linear improvement in FCR with increasing LF70 levels in diets with SBM. However, there was a linear decrease in ADG with increasing LF70 levels in diets with DSM. There was a significant interaction (P < 0.001) between LF70 level and protein source on average daily food intake (ADFI) during the starter period. At high LF70 levels, the inclusion of DSM reduced ADFl compared with SBM. However, there was no difference between DSM and SBM at the medium and low LF70 levels. There was a significant interaction between LF70 level and protein source in organic matter digestibility (OMD) (P < 0.01) and gross energy digestibility (GED) (P < 0.01). The pigs offered diets containing DSM had a significantly lower OMD and GED at low LF70 levels compared with pigs offered diets containing SBM. However, the inclusion of DSM had no significant effect on OMD or GED at the medium and high LF70 levels. There was a quadratic response in nitrogen digestibility (ND) with increasing concentrations of LF70 (P < 0.05). There was an increase in ND to 200 g/kg LF70 inclusion, however there was no further increase in ND above 200 g/kg LF70 inclusion. In conclusion, increasing the inclusion of lactofeed from 100 g/kg to 300 g/kg in starter diets where soya-bean meal comprised the principle protein source improved food efficiency and increased daily gain and daily food intake when compared with diets where dried skim milk comprised the principle protein source.

The reason for the reported difference in spoilage behaviour of skim and whole pasteurised milks was investigated. The rates of growth of psychrotrophic bacteria were not significantly different in the two milks and the bacterial types, all pseudomonads, present at spoilage were also similar. However, when representative spoilage organisms were cultured into freshly pasteurised skim and whole milks, skim milks exhibited predominantly bitter flavours while whole milk showed mostly sour flavours. The different spoilage behaviours can be largely explained by greater proteolysis in skim milk than in whole milk, caused by higher production of protease and greater susceptibility of the protein to protease attack. In addition, lipolysis in whole milk, caused by the substantial quantities of lipase produced by spoilage pseudomonads in this milk, also contributes to the different flavours produced during cold storage of these milk types.