Despite the great interest paid to protein components in colostrum, fat also plays an important role in the supply of essential nutrients to provide energy, increase metabolism, and protect the newborn calf against microbial infections. This work aimed to elucidate levels of different fat components in colostrum, in particular fatty acid (FA), triglyceride (TG), cholesterol, and phospholipid contents. Colostrum samples from primiparous and multiparous (3-5 lactations) Holstein dams, fed the same ration indoors, were collected on the first 5d after parturition, analyzed, and compared with milk samples from the same cows collected at 5mo of lactation. Fat content during the first 5d of milking did not vary. However, the proportion of short-chain saturated FA increased and that of long-chain FA decreased. The concentration of n-3 FA was higher on the first day of calving than on the other days, with clear differences in the number and type of n-3 FA. Conjugated linoleic isomers and trans FA slowly increased from d 1 to 5, reaching a maximum at 5mo of lactation. Changes in the distribution profile of TG were observed as lactation progressed, with a shift from a prevalence of high-carbon-number TG (C48-50) on d 1 to a bimodal distribution (maxima at C38 and C50) on d 5, characteristic of mid-lactation milk. Cholesterol content was high in the first hours after calving and rapidly decreased within 48h. Colostrum sampled on d 1 also had a high content of phospholipids. Phosphatidylethanolamine and sphingomyelin were, respectively, lower and higher in the first 5d than in mid-lactation milk. The influence of lactation number on colostrum fat composition was also considered and significant results were obtained for all FA groups (except for polyunsaturated and n-6 FA) and TG content.

The aim of this study was to investigate the effects of CSN2-CSN3 (beta-kappa-casein) haplotypes, BLG (beta-lactoglobulin) genotypes, content of milk protein fractions, and protein composition on coagulation properties of milk (MCP). Rennet coagulation time (RCT) and curd firmness (a(30)) were measured using a computerized renneting meter, and the contents of major milk protein fractions were quantified by reversed-phase HPLC in individual milk samples of 2,167 Simmental cows. Cow genotypes at CSN2, CSN3, and BLG were ascertained by reversed-phase HPLC, and CSN2-CSN3 haplotype probabilities were estimated for each cow. Phenotypes for MCP were regressed on CSN2-CSN3 haplotype probabilities using linear models that also included the effects of herd-test-day, parity, days in milk, pH, somatic cell score, renneting meter sensor, sire of the cow, BLG genotype, and content of major protein fractions or, alternatively, protein composition. When the statistical model did not account for protein fraction contents or protein composition, haplotypes carrying CSN3 B were associated with shorter RCT and greater a(30) compared with those carrying CSN3 A. Haplotypes carrying CSN2 B had the effect of decreasing RCT and increasing a(30) relative to haplotype A(2)A. When effects of protein fractions content or protein composition were added to the model, no difference across haplotypes due to CSN3 and CSN2 alleles was observed for MCP, with the exception of the effect of CSN2 B on RCT, which remained markedly favorable. Hence, the effect of CSN3 B on MCP is related to a variation in protein composition caused by the allele-specific expression of kappa-casein, rather than to a direct role of the protein variant on the coagulation process. In addition, the favorable effect exerted by CSN2 B on a(30) was caused by the increased beta-casein content in milk. Conversely, CSN2 B is likely to exert a direct genetic effect on RCT, which does not depend upon variation of beta-casein content associated with CSN2 B. Increased RCT was observed for milk yielded by BLG BB cows, even when models accounted for protein composition. Rennet clotting time was favorably affected by kappa-casein content and percentage of kappa-casein to total casein, whereas a(30) increased when contents and percentages of beta-CN and kappa-CN increased. Changes of milk protein composition and allele frequency at casein and whey protein genes affect variation of MCP.

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The objective of this study was to evaluate the ability of mid-infrared predictions of fine milk composition and technological traits to serve as a tool for large-scale phenotyping of the Italian Simmental population. Calibration equations accurately predicted the fatty acid profile of the milk, but we obtained moderate or poor accuracy for detailed protein composition, coagulation properties, curd yield and composition, lactoferrin, and concentration of major minerals. To evaluate the role of infrared predictions as indicator traits of fine milk composition in indirect selective breeding programs, the genetic parameters of the traits predicted using mid-infrared spectra need to be estimated.

Thirty-eight Italian Friesian first-lactation cows were allocated to 2 groups to evaluate the effect of 1) an automatic milking system (AMS) vs. milking in a milking parlor (MP) on milk fat characteristics; and 2) milking interval (< or =480, 481 to 600, 601 to 720, and >720 min) on the same variables. Milk fat was analyzed for content (% vol/vol), natural creaming (% of fat), and free fatty acids (FFA, mEq/100 g of fat). Distribution of milk fat globule size was evaluated to calculate average fat globule diameter (d(1)), volume-surface average diameter (d(32)), specific globule surface area, and mean interglobular distance. Milk yield was recorded to calculate hourly milk and milk fat yield. Milking system had no effect on milk yield, milk fat content, and hourly milk fat yield. Milk from AMS had less natural creaming and more FFA content than milk from MP. Fat globule size, globular surface area, and interglobular distance were not affected by milking system per se. Afternoon MP milkings had more fat content and hourly milk fat yield than AMS milkings when milking interval was >480 min. Milk fat FFA content was greater in AMS milkings when milking interval was < or =480 min than in milkings from MP and from AMS when milking interval was >600 min. Milking interval did not affect fat globule size, expressed as d32. Results from this experiment indicate a limited effect of AMS per se on milk fat quality; a more important factor seems to be the increase in milking frequency, generally associated with AMS.