Formulation of dairy cow rations should consider the following points regarding nitrogen utilization by lactating cows. (a) Maintenance of ruminal ammonia nitrogen in excess of 5 mg/100 ml rumen fluid has no effect on microbial protein production. (b)Supplemental nonprotein nitrogen is not utilized in typical dairy and feedlot beef rations containing more than 12 to 13% crude protein(dry matter basis). (c)Nonprotein nitrogen is approximately equal to true protein as a source of nitrogen in typical dairy and feedlot rations containing not more than 12 to 13% crude protein. (d)A scheme based upon metabolizable protein (absorbable protein) for calculating requirements and comparing protein sources is superior to crude or digestible protein designations. Ultimate expression of the requirement may be in terms of crude protein for the sake of simplicity. (e)One kilogram of crude protein, regardless of nitrogen source, equals about .75kg metabolizable protein in typical dairy and feedlot beef rations containing not more than 12 to 13% crude protein. One kilogram of plant protein (true protein) fed in excess of an amount equivalent to 12 to 13% dietary protein equals about .3 kg metabolizable protein. (f)Protein supplementation of lactating cows might be related more to stage of lactation than to milk production. (g)Lactating cows having above average lactational ability may benefit from dietary protein as high as 16 to 17% (dry matter basis) during the first third of lactation. (h)Cows in the latter two-thirds of lactation appear to require 12.5% dietary protein or less. (i)Plant protein (true protein) should be the supplemental sources of nitrogen during the first third of lactation, with NPN providing most, if not all, the supplemental nitrogen during the last two-thirds of lactation.
In this study, we evaluated the effects of dietary supplementation at two stages of lactation with various levels of Mepron85 (M85) and M85 plus DL-methionine (DL-Met) on milk production and composition of Holstein and Brown Swiss cows fed an alfalfa-hay and corn grain-based diet. In experiment 1, control diets were formulated to supplement, in early lactation [days in milk (DIM) = 73.2], concentrations of metabolizable methionine at 104% of the estimated requirements based on the Cornell Net Carbohydrate and Protein System. Treatment groups were fed the control diet plus 10, 20, or 30 g/d of M85 at 116, 128, or 139% of the estimated requirements for metabolizable methionine. The supplementation with 10 g/d in Brown Swiss and 30 g/d of M85 in Holstein cows increased milk yields and fat percentage, but had no effects on protein percentage. These data suggested that the estimated postruminal supply of metabolizable methionine in the control ration was limiting for maximum milk fat synthesis. Conversely, in experiment 2, the cosupplementation with M85 (15 g/d) plus DL-Met (15 g/d) to cows in midlactation (DIM = 140.5) did not influence fat percentage, but increased protein yield and percentage (+0.1%) in both Holstein and Brown Swiss, and lactose percentage (+0.18%) in Holstein cows. The supplementation with 15 g/d of M85 reduced milk and protein yields, whereas 15 g/d of DL-Met reduced protein percentage in four of the five experimental weeks for Holstein cows. We conclude that supplementation with M85, alone or in combination with DL-Met, may be used to influence milk composition, but these effects are influenced by dosage and type of supplemental methionine, breed, and stage of lactation.
Five nonlactating Holstein cows (average weight 574 kg) with cannulas in the rumen and duodenum were fed five total mixed diets at 2.14% (DM) of BW for seven 2-wk periods to estimate the ruminal degradation of protein and fatty acids in whole cottonseed (WCS) and extruded soybeans (ESB). Lanthanum was used as an indigestible marker. Ruminal propionic acid (molar proportion) was larger and butyric acid was smaller for WCS diets than for control or ESB diets. Total VFA (mM) and acetic acid (molar proportion) were similar for all diets. Duodenal flow of nonammonia nitrogen (N) was 13% higher for ESB diets than for WCS diets, but was similar for the control and diets with WCS. The percentage of intake protein that was undegraded was 19% higher for ESB diets than for WCS diets. Ruminal and total apparent digestibilities of ADF were not reduced by the addition of oil seed. In conclusion, the protein from ESB was less degraded in the rumen of cows than protein from WCS. The addition of ESB at 12.7% (DM) or WCS at 25.3% of the diet did not reduce the apparent digestibility of fiber. The unsaturated fatty acids in WCS were not protected from ruminal biohydrogenation, presumably due to mastication of the seed coat.
The influence of ration composition on mean ruminal ammonia concentration was studied by collecting samples of ruminal ingesta from cattle fed rations varying in crude protein and total digestible nutrient content. A minimum of four sampling times distributed throughout the day permitted calculation of mean ruminal ammonia concentrations. Mean ruminal ammonia concentration was positively related to dietary crude protein concentration and negatively related to total digestible nutrient concentration. It is postulated that mean ruminal ammonia concentration may be a useful criterion for predicting efficacy of nonprotein nitrogen supplementation. A quantitative approach for evaluating nonprotein nitrogen supplementation based upon determination of the point at which ruminal ammonia exceeds the requirement (5 mg ammonia nitrogen/100 ml rumen fluid) of the ammonia-utilizing bacteria is proposed. Dietary conditions expected to result in excessive concentrations of ruminal ammonia are defined and recommended upper limits for nonprotein nitrogen supplementation are presented. Theoretical relationships between composition of the unsupplemented ration, amount of nonprotein nitrogen added, and efficiency of nonprotein nitrogen utilization are discussed. The practice of adding nonprotein nitrogen so as to exceed 12 to 13% crude protein in typical dairy or feedlot rations needs to be reevaluated.
Six ruminally cannulated beef steers were used in a 6 x 6 Latin square experiment with a 3 x 2 factorial arrangement of treatments to evaluate the effects of barley supplementation (BS; 10, 30 or 50% of diet DM) and ruminal buffer (RB; Na sesquicarbonate at 0 or 4% of BS DM) addition to bromegrass hay-based diets on digestion. When early- (boot) and late- (full maturity) havested bromegrass and wheat straw substrates were incubated in situ, no interactions (P greater than .10) involving substrate with dietary BS or RB were observed, indicating that forages differing in fermentability responded similarly to different ruminal environments. Averaged across substrates, RB had no effect with 10% BS and a positive effect with 30% BS, but a negative effect with 50% BS diets (BS x RB, quadratic; P less than .05) for in situ DM and NDF disappearance for 18 and 24 h of incubation and for rate of disappearance of potentially degraded DM and NDF. Intakes of DM and digested DM were greater (P less than .01) for RB diets; however, RB had no effect (P greater than .10) on total tract DM and NDF digestibility. Intake and digestibility of DM increased linearly (P less than .01), whereas NDF digestibility decreased linearly (P less than .01) as BS percentage was increased in the diet. Sixty beef steers (avg initial wt 302 kg) were fed the same dietary treatments in a growth experiment. A numerical improvement in DM intake (P = .20) and ADG (P = .06) was observed when RB was provided with the 50% BS diet. Results of these experiments indicate that RB may moderate negative effects occurring on ruminal fiber digestion when grains are used to supplement forage-based diets; however, improvements in ruminal digestion were not translated effectively to improved animal productivity.
Twenty-four Holstein cows in wk 3 through 12 of lactation were used to evaluate distillers dried grains with solubles as a protein source for alfalfa-based diets. Diets were formulated containing 0, 10.1, 20.8, or 31.5% distillers dried grains with solubles. Crude protein in these diets was 13.9, 16.0, 18.1, and 20.3%. Milk yield increased linearly with increasing dietary CP, whereas DMI was not affected. Dry matter intake averaged over 4% of BW for all treatments. Intake of undegraded intake protein was .93, 1.27, 1.63, and 1.97 kg/d. Yields of milk protein, casein, and lactose all increased linearly with increasing dietary CP. The proportion of milk N as whey N decreased, whereas N as NPN increased, with increasing dietary CP. Plasma urea N and essential and branched-chain AA increased linearly, and nonessential AA decreased linearly, with increasing dietary CP. Increasing the concentration of CP in the diet from 13.9 to 18.1% by the addition of distillers dried grains with solubles was beneficial to cows fed alfalfa-based diets in early lactation. Little additional benefit was observed by feeding greater than 18.1% dietary CP.
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