Thirty high-producing multiparous Holstein cows were used in a completely randomized block design to compare a lysine deficient total mixed ration, which was sufficient in methionine, to the same diet supplemented with a rumen protected lysine product. The CPM-Dairy prediction model was used to estimate the nutrient requirements and adequacy or deficiency of amino acids. During the 21-day prepartum transition period, cows were fed 4 kg (dry basis) of the lysine deficient diet plus Eragrostis curvula hay ad lib. After calving, cows were fed the lysine deficient diet for the first three weeks and were then blocked according to the average production from day 19-21. Fifteen cows were allocated to each treatment and blocked into 15 groups of two each. Data on production parameters were analyzed for all cows and also separately for cows in the 10 highest production blocks. The experimental period was from day 22 to 120 postpartum. Lysine supplementation resulted in an optimal dietary lysine : methionine ratio in metabolisable protein of 7.2 : 2.4. Lysine supplementation did not affect dry matter intake, milk production, milk fat percentage, milk protein percentage, milk urea nitrogen, body weight or body condition score; but decreased the non-casein nitrogen and whey content of milk. Furthermore, milk casein, which is the milk nitrogen fraction most sensitive towards increased duodenal supply of lysine and methionine, was not affected. The rumen protected lysine product evaluated did not improve cow productivity, probably because the product was either unprotected from rumen degradation, or overprotected to the extent that the lysine was not available for absorption in the small intestine; or absorbed but could not be metabolised. Copyright / Dissertation (MSc(Agric))--University of Pretoria, 2009. / Animal and Wildlife Sciences / unrestricted

Rumen protected methionine has been used in an effort to improve the amino acid composition of metabolisable protein since the early 1960’s. The positive response in dairy cows in terms of milk protein composition and milk production, especially during early lactation has been well documented. Rumen protected methionine supplementation contributes to improving the protein efficiency of the dairy cow which improves the overall productivity of the dairy enterprise. Recently a locally developed liquid rumen protected methionine prototype became available. In our study this product was evaluated through a series of experiments in conjunction with two standard, well known methionnine sources, Smartamine ™ M and unprotected DL-methionine that provided a reference to the relative bioavailability of the liquid rumen protected methionine. In the first of the two studies the effect of methionine supplementation on milk yield, milk composition as well as milk protein composition was evaluated through the milk composition technique. The ability of the liquid rumen protected methionine to elevate blood plasma methionine levels was also evaluated through the blood plasma technique after oral dosing and post ruminal infusion of methionine. The liquid rumen protected methionine prototype induced no response in either milk yield or milk composition. Results suggested that the prototype is either not adequately protected against rumen degradation or it is not available for absorption in the small intestine. The inability of the liquid rumen protected methionine prototype to elevate blood plasma methionine after post ruminal infusion further proved that the product is not available for absorption at this site either. In the event that the product’s mode of action or method of protection caused it not to be detected as pure methionine in the blood, an effect on milk yield would have been expected which was not the case. This product proved to have a very low or no bioavailability in comparison to the well researched and proven Smartamine ™ M. / Dissertation (MSc(Agric))--University of Pretoria, 2012. / Animal and Wildlife Sciences / unrestricted

Dairy cows are extremely inefficient at converting dietary nitrogen (N) to productive N. Approximately 25-30% of dietary N is used for milk protein while the remaining N is lost to the environment. According to National Research Council (NRC, 2001) recommendations, dairy cow rations are formulated in terms of metabolizable protein (MP) which often causes many amino acids (AA) to be fed in excess. A better understanding of protein and AA requirements could help to improve the nitrogen efficiency of dairy cows. The objective of this work was to examine the effects of feeding a low protein diet supplemented with rumen protected (RP) AA on production and N efficiency of dairy cows. Twenty-four Holstein and 24 Holstein x Jersey crossbred cows were used in a Youden square design consisting of 3 periods. Cows were randomly assigned to one of 8 treatments: 1) a standard diet containing 17% crude protein (+Con), 2) a 15% crude protein diet (-Con), 3) â Con plus RP methionine (+M, 16g/d), 4) â Con plus RP lysine (+K, 47g/d), 5) â Con plus RP leucine (+L, 181g/d), 6) â Con plus RP methionine and lysine (+MK), 7) â Con plus RP methionine and leucine (+ML), and 8) â Con plus RP methionine, lysine, and leucine (+MKL). Cows fed the â Con as well as the +MKL diet experienced a reduction in milk production and milk protein yield (P < 0.05). Dry matter intake decreased only for those animals on the +ML diet (P < 0.05). Milk urea N (MUN) decreased for all diets when compared to the +Con treatment (P < 0.05). In accordance with the decrease in MUN, N efficiency was numerically increased in the diets supplemented with RP AA, but this improvement was not significant. Phosphorylation of signaling proteins important for protein synthesis were also examined. Animals fed the +MK treatment increased phosphorylated and total forms of eukaryotic elongation factor 2 (eEF2) when compared to the +Con and â Con (P < 0.05), but this increase in abundance did not affect the ratio of phosphorylated to total abundance. Feeding dairy cows a low protein diet supplemented with RP AA has the ability to alleviate the loss in milk production associated with feeding a low protein diet as well as to increase nitrogen efficiency. / Master of Science

The aim of the present study was to investigate, firstly, whether the substitution of dietary starch by rumen-protected fat results in visible changes in the protein metabolism by increasing the urea flux and decreasing of AA levels in blood plasma as indicators for a change of AA oxidation, secondly, whether the fat-fed cows use predominantly long chain FA in the processes of milk fat synthesis or as an energy source in oxidation processes, and thirdly, whether the ratio of glucogenic to lipogenic nutrients could affect the supply of glucose in the metabolism of dairy cows. Two experiments were conducted. In either experiments, about 1.8 kg of starch in the ration of the control group were substituted by about 0.7 kg fat as protected fat (Ca salts of palm, soybean and sunflower oils in addition to protected soybeans) in the ration of the fat group. The first experiment was carried out on 32 multiparous high yielding dairy cows (16 Holstein-Friesian cows in each group) during the first 100 d of lactation. The second experiment was carried out in four periods in a cross-over design. Two cows were used in each period during the 6th to the 10th lactation weeks. The cows were infused intravenously with D-[U-13C6]-Glucose. The substitution of starch by protected fat tended to increase the milk production and milk lactose output and to decrease the microbial protein synthesis in the rumen and plasma glucose level. Also, the levels of ß-HBA and NEFA in plasma, the milk urea content and the total urea-flux were increased (P<0.05). Milk protein content but not yield and plasma levels of insulin, Met, Ser and His decreased (P<0.05) but the branched chain amino acids in plasma increased (P<0.05). The oxidation rate of FA was lower in comparison to other sub`strates. In the second experiment, the enrichment of milk fat and blood CO2 by 13C decreased but the recovery of 13C in milk lactose increased (P<0.065) due to high fat intake. The results indicate that the substitution of starch by protected fat can save glucose in the intermediary metabolism for lactose synthesis in the mammary gland and the cows used fatty acids predominantly for milk fat synthesis and not for oxidation.

Rumen protected Methionine (MET) and Lysine (LYS) are critical for milk protein synthesis in dairy cows. N-acetyl-L-methionine (NALM) is a MET derivative that consists of L-Met protected with an acetyl group that is attached to the α-amino group.N-acetyl-L-lysine (NALL) is a LYS derivative that is similarly protected. The objectives of these studies were to quantify the gastrointestinal availability of NALM and NALL. Three experiments were run as 3 × 3 Latin square using 3 second lactation Holstein cows that have been fitted with cannulas in the rumen and duodenum. The cows were fed diets containing the supplements for two weeks prior to each experiment so that the rumen microbes had time to adjust to the supplement. Each period consisted of 10 d of adaptation followed by 2 d of sampling. A dose of 0, 30, or 60 g of NALM was placed under the rumen mat at the time of feeding every day during experiment 1. The cows were similarly supplied with 0, 60, or 120 g of ƐNALL during experiment 2. The cows were supplemented with 0 g, 120 g ofƐNALL, or 120 g of diNALL during experiment 3. On day one of sampling, a liquid marker (Co-EDTA) was also administered at the time of the protected AA administration. Blood, ruminal, and duodenal samples were taken at hours 0, 1, 3, 6, 9, 12, and 24 post-feeding. There were no differences for milk production, milk protein, milk fat, or DMI for NALM or either NALL. There were no differences for ruminal escape (69.1% and 46.2% respectively) and duodenal appearance (2.16% and 3.40% respectively). The ruminal escape of ƐNALL was not different between the 120 g dose (32.7%) and the 60 g dose (27.2%). Duodenal appearance was higher (P < 0.01) for the 60 g dose (2.86%) than for the 120 g dose (1.19%) of ƐNALL. Acetate, propionate, butyrate, and valerate were higher (P < 0.01) for the supplemented cows during experiment 1 with NALL. There were no differences between ƐNALL and diNALL for rumen escape, duodenal appearance, VFA production, or blood LYS AUC. Results of the experiment verify significant protection of the N-acetyl MET and LYS from rumen degradation.

No description available.

The aim of the present study was to investigate, firstly, whether the substitution of dietary starch by rumen-protected fat results in visible changes in the protein metabolism by increasing the urea flux and decreasing of AA levels in blood plasma as indicators for a change of AA oxidation, secondly, whether the fat-fed cows use predominantly long chain FA in the processes of milk fat synthesis or as an energy source in oxidation processes, and thirdly, whether the ratio of glucogenic to lipogenic nutrients could affect the supply of glucose in the metabolism of dairy cows. Two experiments were conducted. In either experiments, about 1.8 kg of starch in the ration of the control group were substituted by about 0.7 kg fat as protected fat (Ca salts of palm, soybean and sunflower oils in addition to protected soybeans) in the ration of the fat group. The first experiment was carried out on 32 multiparous high yielding dairy cows (16 Holstein-Friesian cows in each group) during the first 100 d of lactation. The second experiment was carried out in four periods in a cross-over design. Two cows were used in each period during the 6th to the 10th lactation weeks. The cows were infused intravenously with D-[U-13C6]-Glucose. The substitution of starch by protected fat tended to increase the milk production and milk lactose output and to decrease the microbial protein synthesis in the rumen and plasma glucose level. Also, the levels of ß-HBA and NEFA in plasma, the milk urea content and the total urea-flux were increased (P<0.05). Milk protein content but not yield and plasma levels of insulin, Met, Ser and His decreased (P<0.05) but the branched chain amino acids in plasma increased (P<0.05). The oxidation rate of FA was lower in comparison to other sub`strates. In the second experiment, the enrichment of milk fat and blood CO2 by 13C decreased but the recovery of 13C in milk lactose increased (P<0.065) due to high fat intake. The results indicate that the substitution of starch by protected fat can save glucose in the intermediary metabolism for lactose synthesis in the mammary gland and the cows used fatty acids predominantly for milk fat synthesis and not for oxidation.