Flavour, aroma and appearance of milks fermented with commercially available kefir grains were compared with similar characteristics of heat treated (90 ΰC/30 min) milks that had been fermented with aroma producing starters in addition to the kefir grains. The starters used were either a mixture of Streptococcus lactis subsp. diacetilactis and Leuconostoc cremoris (lactic culture) or of Str. thermophilus and Lactobacillus bulgaricus (yogurt culture).

Two methods of fermentation were investigated involving removal of the grains followed by (i) a second fermentation of the kefir with the aroma-producing organisms and (ii) combining the kefir with aroma-producing organisms for use as a starter to ferment a further sample of heat-treated milk. Products were assessed by a taste panel and marked for acceptability. Addition of lactic or yogurt cultures resulted in products with increased mean scores for aroma and more acceptable flavours.

A simple and rapid phosphatase test is described which is based on the use of p–nitrophenylphosphate as the substrate. Execution of the test requires few and easy operations: incubation of the milk at 37° C. with a buffered solution of the substrate, followed directly by a visual comparison of the intensity of yellow colour of liberated p–nitrophenol with that of boiled-milk standards containing known amounts of p–nitrophenol. The test permits the detection of minor processing faults with an incubation time of only 30 min. In this form it should prove of value in creamery control. A more searching, but equally simple test is obtained by increasing the period of incubation to 2 hr.

Microfiltration and ultrafiltration were used to manufacture skim milks with an increased or reduced concentration of whey proteins, while keeping the casein and milk salts concentrations constant. The skim milks were heated on a pilot-scale UHT plant at 80, 90 and 120 °C. The heat-induced denaturation and aggregation of β-lactoglobulin (β-lg), α-lactalbumin (α-la) and bovine serum albumin (BSA) were quantified by polyacrylamide gel electrophoresis. Apparent rate constants and reaction orders were calculated for β-lg, α-la and BSA denaturation. Rates of β-lg, α-la and BSA denaturation increased with increasing whey protein concentration. The rate of α-la and BSA denaturation was affected to a greater extent than β-lg by the change in whey protein concentration. After heating at 120 °C for 160 s, the concentration of β-lg and α-la associated with the casein micelles increased as the initial concentration of whey proteins increased.

1. Two Shorthorn cows with rumen fistulas were used to investigate the effect of diets high in concentrates and low in hay on the physical and biochemical processes of the reticulo-rumen.

2. During the initial control period of the investigation the cows received daily 16 lb. hay and 20 lb. concentrates (flaked maize 50%, weatings 35%, decorticated ground-nut cake 15%) and during the final control period 18 lb. hay and 10 lb. concentrates. There were three intervening experimental periods, in each of which the cows received 2 lb. hay daily. In the first experimental period they received, in addition to the hay, 24 lb. concentrates; in the second, 20 lb. concentrates and 5 lb. of dried delignified straw pulp in a finely macerated form; and in the third, 20 lb. concentrates. The experiment lasted 27 weeks.

3. In the experimental periods the mean milk-fat percentage remained below 2·0 for 10 weeks, whereas the mean value for the control periods was about 3·5. Addition of the straw pulp to the diet low in hay brought about no recovery in milk-fat percentage. It is calculated that in the two cows the losses in the yield of fat were 62·2 and 51·2% in the first experimental period and 62·5 and 58·7% in the second. In the experimental periods there were increases in the milk solids-not-fat percentage amounting in the two cows to upwards of 0·75 and 0·40 respectively. The composition of the butterfat was influenced by the diets low in hay, the main changes being a marked fall in the Reichert value, and a rise in the iodine value.

4. Digestibility trials showed that in the initial control period and the first and second experimental periods the mean daily intake of digestible crudefibrewas 2·6,0·6 and 3·0 lb. respectively. A tentative estimate of the extent of digestion in the reticulo-rumen, based on the lignin-ratio method, showed that a marked depression in values for the digestibility of the cellulosic constituents of the diet given during the first experimental period took place in the reticulo-rumen. In all experimental periods, even the first, the digestion of starch in the reticulo-rumen was virtually complete, only traces passing undigested to the remainder of the gut. In these three periods the mean daily intake of ether extract remained at 0·4·0·5 lb.

A milk-related model system, 2 mM-trilinolein in 0·1 M-piperazine-N, N′-bis-2-ethanesulphonic acid buffer, pH 6·8, stabilized by lysophosphatidylcholine was used to assess the effect of milk proteins on lipid oxidation in emulsion, catalysed by Cu2+ ions. In some experiments the trilinolein was replaced by sunflower oil (2 g 1-1). Oxidation at 25°C was assessed by measurement of the rate of O2-utilization and by the thiobarbituric acid assay. The features, relevance and reliability of the model are described in terms of the observed effects in the absence and presence of added protein. Casein was antioxidative at concentrations relevant to those in bovine milk, human milk, infant milk formulations and ‘high linoleic acid’ milk. Whole whey protein was a less effective inhibitor of lipid oxidation at similar concentrations. Purified α-lactalbumin was also marginally antioxidative, and its effect was independent of the molar Cu2+: protein ratio between 1:1 and 3:1.

The non-protein nitrogen (NPN) of samples of Parmigiano-Reggiano cheese ripened for 6 and 15 months was fractionated by ion-exchange chromatography on a Cu2+-Chelex column to separate oligopeptides from free amino acids. Peptide components were isolated by reversed-phase HPLC and identified by fast atom bombardment–mass spectrometry (FAB–MS). Only the NPN fraction of 6 month old cheese samples contained enough peptides to be further characterized. On the basis of FAB–MS spectral results, 39 oligopeptides were identified, the main components being phosphopeptides. Two sets of both intact and partly dephosphorylated peptides, accounting for a total of 19 phosphopeptides, were formed by the hydrolysis of β–casein and belonged to regions 1–20 and 6–28 of β–casein. The formation and potential role of these peptides in cheese is discussed.

High pressure (HP) treatment affects many constituents of milk (for reviews see Huppertz et al. 2002; Needs, 2002); particular in the properties of casein micelles in HP-treated milk differ considerably from their counterparts in untreated milk. In milk treated at 100–200 MPa, average casein micelle size differs little from that of untreated milk (Needs et al. 2000a; Huppertz et al. 2004a; Regnault et al. 2004; Anema et al. 2005), but micelle size in milk treated at 250 MPa for [ges ]15 min is considerably higher than in untreated milk, probably due to HP-induced aggregation of casein micelles (Huppertz et al. 2004a,b; Regnault et al. 2004); after treatment at 300–800 MPa, micelle size is ~50% lower than that in untreated milk (Needs et al. 2000a; Huppertz et al. 2004a,b; Anema et al. 2005). HP-induced changes in average casein micelle size are irreversible on subsequent storage, except for the increase in micelle size after treatment at 250 MPa (Huppertz et al. 2004a).

Mechanisms controlling exchange and partition of minerals and β-casein between micellar and soluble phases during cooling have been studied using suspensions of milk proteins of varying concentrations in the presence of aqueous phases having varying mineral compositions. In these studies the final equilibrium between Ca and phosphate was found to be regulated by formation of Ca phosphates of varying solubilities. The effect of the total casein level on mineral and protein equilibria was also studied. In milk, part of the β-casein content is bound to micelles by hydrophobic bonds; the proportion present in this form was increased by spontaneous micellar demineralization during cooling as well as by addition of a complexant to milk. At low temperatures, an equilibrium between the micellar and the monomeric states was reached which depends upon the total casein level and on the hydrophobic-bonded β-casein content. Not all of these hydrophobic bonds were broken when milk was cooled.

Genes in the sterol regulatory element-binding protein-1 (SREBP1) pathway play a central role in regulation of milk fat synthesis, especially the de-novo synthesis of saturated fatty acids. SCD, a SREBP-responsive gene, is the key enzyme in the synthesis of monounsaturated fatty acids in the mammary gland. In the present study, we discovered SNP in candidate genes associated with this signalling pathway and SCD to identify genetic markers that can be used for genetic and metabolically directed selection in cattle. We resequenced six candidate genes in the SREBP1 pathway (SREBP1, SCAP, INSIG1, INSIG2, MBTPS1, MBTPS2) and two genes for SCD (SCD1 and SCD5) and discovered 47 Tag SNP that were used in a marker-trait association study. Milk and blood samples were collected from Holstein cows in their 1st or 2nd parity at 100–150 days of lactation. Individual fatty acids from C4 to C20, saturated fatty acid (SFA) content, monounsaturated fatty acid content, polyunsaturated fatty acid content and desaturase indexes were measured and used to perform the asociation analysis. Polymorphisms in the SCD5 and INSIG2 genes were the most representative markers associated with SFA/unsaturated fatty acid (UFA) ratio in milk. The analysis of desaturation activity determined that markers in the SCD1 and SCD5 genes showed the most significant effects. DGAT1 K232A marker was included in the study to examine the effect of this marker on the variation of milk fatty acids in our Holstein population. The percentage of variance explained by DGAT1 in the analysis was only 6% of SFA/UFA ratio. Milk fat depression was observed in one of the dairy herds and in this particular dairy one SNP in the SREBP1 gene (rs41912290) accounted for 40% of the phenotypic variance. Our results provide detailed SNP information for key genes in the SREBP1 signalling pathway and SCD that can be used to change milk fat composition by marker-assisted breeding to meet consumer demands regarding human health, as well as furthering understanding of technological aspects of cows' milk.

Ten different types of milk, arranged in 3 sets, were observed to be pseudoplastic fluids with linear behaviour at high shear rates in a coaxial cylinder rheometer; at low rates of shear all the samples could be considered sufficiently Newtonian and a Höppler viscometer was used for their study. Dynamic viscosity coefficients of skimmilk, half-and-half milk, whole milk and their concentrates up to about 30% total solids were determined every 5°C between 0 and 80°C. For every milk type a quadratic equation relating t to log η was obtained. At a given temperature the concentration dependence of η for the 3 milk sets was expressed by a single relation of the same mathematical model as in the previous case. A general expression was derived to enable η to be calculated at any temperature (0–80°C), and for any concentration (0–30% total solids) whatever the fat to solids-not-fat ratio (0·01–0·4). A nomogram was also constructed for the immediate computation of η without any practical loss of accuracy.

The protein fraction of milk contains several components with physiological significance for the development of the newborn. Among them, immunomodulatory peptides and lactoferrin exemplify the complexity of biologically active substances of milk. Immunomodulatory peptides have latent activity within the native protein and are generated after proteolysis during gastrointestinal transit. Once they are generated, they modulate mucosal immunity, possibly by guiding the local immune system until it develops its full functionality. Lactoferrin is another milk bioactive compound with nutritional and health promoting properties; it modulates the microbial intestinal environment, displays anti-microbial activity against various pathogens and stimulates the establishment of beneficial microflora. The following overview focuses on the importance of immunomodulatory peptides and lactoferrin for the maturation of intestine and immune system that are functionally immature in the newborn.

In this method, the curd, formed in a beaker, was retained after cutting by means of a wire grid placed on top of it. This enabled the whey to be poured off easily at timed intervals for measurement of its volume. The method gave results reproducible within 1·5%. Increasing the amount of rennet added to the milk increased the rate of syneresis of the curd slightly. Adding CaCl2 to the milk, raising the temperature and decreasing the pH, all increased the rate of syneresis. Addition of fat, as cream, to skim-milk decreased the rate of syneresis proportionally. The rate of syneresis was decreased if the milk was concentrated by ultrafiltration and increased if the milk was diluted with permeate. In all instances the early stages of syneresis followed first-order kinetics, the rate depending on the amount of whey remaining within the curd. The later stages of syneresis appeared to depend on hydrophobic forces. Probably, the increasing aggregation of the casein within the curd caused the whey to be squeezed out.

Heat-induced gelation, an important functional property of β-lactoglobulin, was studied by measuring the rheological properties of both the A and B variants of the protein during and after heat treatment within a range of pH, temperature and concentration. Gel electrophoresis was used to determine the extent of denaturation and disulphide bond crosslinking of some samples. Both variants formed gel networks on heating at temperatures > 75 °C, and under most conditions the storage modulus (G′) of βlactoglobulin A gels was higher than the G′ of β-lactoglobulin B gels, in particular after cooling to 25 °C. A minimum protein concentration of 50 g/1 was required for gel formation at pH 7·0 in 0·1 M-NaCl by both variants at 80 °C. Increasing the protein concentration above 50 g/1 increased G′, the extent of increase being much greater for the A variant than the B variant. G′ of variant A gels was not much influenced by pH whereas G′ of variant B gels decreased slightly from pH 3 to pH 6 and increased between pH 6 and pH 9. When mixtures of the two variants were gelled G′ increased at the temperature of heating (80 °C) and after cooling (25 °C) as the relative quantity of variant A was increased. Comparisons of the loss of discrete protein bands from electrophoretic gels (native-PAGE, SDS-PAGE and SDS-PAGE of reduced samples) showed that heating β-lactoglobulin solutions of 100 g/1 at pH 7 in 0·1 M-NaCl and at 75, 80 and 85 °C caused a faster loss of both native and SDS-soluble β-lactoglobulin A than of β-lactoglobulin B. It was concluded that the loss of native β-lactoglobulin structure from these solutions during heating was faster than the formation of disulphidelinked aggregates, which was faster than gel formation for both β-lactoglobulin A and β-lactoglobulin B, and that each of these reactions was faster for β-lactoglobulin A than for β-lactoglobulin B. This contrasts with conclusions drawn from some previous studies and may arise from the differences in protein concentration between the present study (∼ 100 g/1) and the previous ones (< ∼ 10 g/1).

The numbers and types of non-starter lactic acid bacteria, lipolytic bacteria and group D streptococci in cheese milks and corresponding Cheddar cheeses have been studied and their relationship to cheese flavour discussed. Different milks, heat-treatments and starters were used, and their association with flavour investigated. The pH and fat, salt and moisture contents of the cheeses were also determined.

The non-starter lactic acid flora consisted mainly of Lactobacillus casei, L. plantarum, L. brevis, L. buchnerii, Pediococcus spp. and Leuconostoc spp. Lactobacillus casei was nearly always present in the milks and cheeses, predominating in most of the cheeses, particularly in those made from milk which received the most severe of the three heat-treatments tested (160°F for 17 sec). Leuconostocs were not found in any of the cheeses. Other species sometimes occurred in approximately equal numbers to L. casei, particularly in cheeses manufactured from the milder heattreated milks. Cheeses made from milk receiving the highest heat-treatment contained fewest bacteria and scored lowest for flavour. The average flavour scores increased as the number of species contributing to the non-starter lactic acid flora at the time of tasting increased.

The lipolytic organisms capable of hydrolysing butterfat consisted mainly of Gram-positive cocci, predominantly Staphylococcus saprophyticus. The group D streptococci occurred infrequently, Streptococcus faecium being the most commonly occurring species.

A definite correlation was found to exist between the starters used and the flavour of the cheeses. The pH of the cheeses was associated with the flavour, but the fat, moisture and salt contents of the cheeses showed no definite effect.

The influence of storage time and temperature on the distribution of individual milk proteins between the micellar and soluble phases has been examined. Storage at 4 or 7 °C is accompanied by a dissociation of micellar caseins, particularly β-casein, into the soluble phase during the first 48 h, but on further storage there is a partial reversal of this process. At higher storage temperatures (10–20 °C) the contents of all the individual caseins in the soluble phase decrease throughout storage. During cheese–making, losses of fat and curd fines in whey were greater with increased soluble phase casein and clotting times were prolonged. Curd structure was weaker, curds were more moist and slightly lower cheese yields were obtained in stored milks with elevated soluble–phase casein. When milks were stored for up to 3 d at 4 °C cheese gradings were virtually unaffected by storage, but higher temperatures (10–15 °C) led to cheeses being downgraded, largely for body and texture defects but also for flavour after 3 d.

Attempts to reverse the pattern of casein dissociation and to minimize the detrimental effects of milk storage on subsequent cheese-making showed that a heat treatment of 30 min at 60 °C was the most beneficial.

Component PP3 is a phosphorylated glycoprotein with an apparent molecular mass of 28 kDa isolated from the proteose peptone fraction of bovine milk. The function of the protein is not known. The primary structure has been determined and shown to contain 135 amino acid residues (EMBL accession no. P80195). It was phosphorylated at Ser29, Ser34, Ser38, Ser40 and Ser46. Two O-linked carbohydrate groups were found at Thr16 and Thr86, while one N-linked carbohydrate group was present at Asn77. Thr16 was only ∼ 50% glycosylated. The amino sugar detected by the amino acid analyser at Thr86 was mainly galactosamine but a small amount of glucosamine was also present. The amino sugars found in the carbohydrate group linked to Asn77 were both glucosamine and galactosamine. A fragment of PP3 has been isolated from milk and shown to correspond to residues 54–135. This fragment was probably generated by plasmin hydrolysing the Arg53–Ser54 bond.

Heating raw milk at 80 °C for 2·5–20 min was found to result in compositional changes in the milk fat globule membrane (MFGM). The yield of protein material increased with the duration of heating, owing to incorporation of skim milk proteins, predominantly β-lactoglobulin, into the membrane. Lipid components of the MFGM were also affected, with losses of triacylglycerols on heating.

The udder health of a research herd of between 160 and 220 Friesian cows run on a commercial basis has been monitored closely, including detailed bacteriological study, over 5 years. The five point mastitis control plan had been in use for several years prior to this study and was continued with minor alterations to the management of the plan, more detailed bacteriological monitoring and increased encouragement to apply it. It has proved possible to make a substantial improvement in the udder health of the herd. The percentage of infected cows fell from 21·9 to 12·0 and the percentage of infected quarters from 7·3 to 3·3. The main benefit has been a drastic reduction in the rate of clinical and subclinical mastitis caused by coagulase-positive staphylococci. However the total incidence of clinical mastitis did not change substantially, averaging around 30 cases/100 cows per year. This was largely because environmental mastitis organisms were responsible for 65 % of all clinical cases. The results showed marked differences in the patterns of infection due to the environmental mastitis pathogens, Gram-negative bacteria and aesculin-hydrolysing streptococci, suggesting different mechanisms of invasion of the gland.

Activation of the antibacterial lactoperoxidase system in milk, i.e. increasing the thiocyanate concentration to 0·25 mM and adding an equimolar amount of H2O2, results in a substantial reduction of the bacterial flora and prevents the multiplication of psychrotrophic bacteria for up to 5 d. This treatment has no effect on the physico-chemical properties of milk and does not lead to the accumulation of resistant bacteria. The practical application of the lactoperoxidase system in prolonging the storage period of raw milk at low temperatures is discussed.