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Impacts of increasing amounts of supplemental soybean meal on intake and digestion by beef steers and performance by beef cows consuming low-quality tallgrass-prairie forage.

Two experiments were conducted to evaluate the impacts of increasing levels of supplemental soybean meal (SBM) on intake, digestion, and performance of beef cattle consuming low-quality prairie forage. In Exp. 1, ruminally fistulated beef steers (n = 20; 369 kg) were assigned to one of five treatments: control (forage only) and .08, .16, .33, and .50% BW/d of supplemental SBM (DM basis). Prairie hay (5.3% CP; 49% DIP) was offered for ad libitum consumption. Forage OM intake (FOMI) and total OM intake (TOMI) were increased (cubic, P = .01) by level of supplemental SBM, but FOMI reached a plateau when the daily level of SBM supplementation reached .16% BW. The concomitant rises in TOMI and OM digestibility (quadratic, P = .02) resulted in an increase (cubic, P = .03) in total digestible OM intake (TDOMI). In Exp. 2, spring-calving Hereford x Angus cows (n = 120; BW = 518 kg; body condition [BC] = 5.3) grazing low-quality, tall-grass-prairie forage were assigned to one of three pastures and one of eight treatments. The supplemental SBM (DM basis) was fed at .08, .12, .16, .20, .24, .32, .40, and .48% BW/d from December 2, 1996, until February 10, 1997 (beginning of the calving season). Performance seemed to reach a plateau when cows received SBM at approximately .30% BW/d. Below this level, cows lost approximately .5 unit of BC for every .1% BW decrease in the amount of supplemental SBM fed. Providing supplemental SBM is an effective means of improving forage intake, digestion, and performance of beef cattle consuming low-quality forages.

Animal Feed↗

Liquid supplement and forage intake by range beef cows.

One hundred eighty crossbred cows were assigned to one of six native range pastures during two winters to evaluate forage and supplement intake as affected by liquid supplement (yr 1: 50% crude protein, 84% from urea; yr 2: 57% crude protein, 91% from urea) delivery method and cow age (2, 3, 4, 5, or 6 yr). Treatments were: 1) no supplement (Control); 2) a lick-wheel feeder containing liquid supplement (ADLIB); and 3) a computer-controlled lick-wheel feeder that dispensed 0.9 kg x cow(-1) x d(-1) of liquid supplement (average 0.5 kg of dry matter x cow(-1) x d(-1); Restricted). Each treatment was applied to two pastures. Forage digestibility was increased (P = 0.03) by supplementation. Supplemented cows lost less (P = 0.05) body condition than unsupplemented cows (average -0.3 vs -0.6). Blood urea nitrogen (BUN) was highest (P = 0.001) for ADLIB (8.7 mg/dL), intermediate for Restricted (6.2 mg/dL), and lowest for Control (2.3 mg/dL). Forage DMI was 31% higher (P = 0.01) in 1995 than in 1996, and was increased (P = 0.02) by supplementation both years. Cows supplemented with ADLIB consumed 23% more forage dry matter than Control cows, whereas Restricted cows consumed 21% more dry matter than ADLIB cows. Supplement intake by cows on ADLIB was greater (P = 0.001) than by cows on Restricted in both years. Supplement intake was lowest (P = 0.002) by 2-yr-old cows, intermediate by 3-yr-olds, and greatest by 4-, 5-, and 6-yr-old cows. Variation in supplement intake by individual cows was higher (P = 0.09) for cows in the Restricted treatment (coefficient of variation [CV] = 117%) than those on ADLIB (CV = 68%) during the first year, but did not differ between supplement treatments (average CV = 62%) in the second year. The proportions of cows consuming less than 0.3 kg/d of supplement dry matter intake (DMI) and consuming less than the target amount of supplement (0.5 kg DMI) were less (P = 0.001) for ADLIB than for Restricted during both years. ADLIB cows spent more (P = 0.001) time at the supplement feeder and had more (P < 0.002) supplement feeding bouts than Restricted cows during both years. During the first year, 2- and 3-yr-old cows spent less (P < 0.01) time at the feeder and had fewer feeding bouts per day than 6-yr-old cows. Age had no effect (P > 0.24) on feeding behavior during the second year. Supplementation of beef cows grazing winter range with 50 to 57% crude protein liquid supplement increased forage digestibility and intake. Restricting supplement access increased forage consumption and variability of supplement intake.

Age Factors↗

Effect of forage quality on digestion and performance responses of cattle to supplementation with cooked molasses blocks.

We evaluated the effect of forage quality on response of cattle to supplementation with cooked molasses blocks. In Exp. 1, 175 heifers had ad libitum access to prairie hay (5.2% CP, DM basis). Treatments were a 2 x 3 factorial: supplementation with 0 or 1.96 kg/d of alfalfa DM, and supplementation with no cooked molasses block or with a low-protein or a high-protein cooked molasses block (14.4 and 27.5% CP, respectively, DM basis). There were no significant interactions between alfalfa and cooked molasses block for intake or gain. Forage intake and ADG were increased (P < 0.05) by alfalfa supplementation. Heifers fed high-protein cooked molasses blocks gained more (P < 0.05) weight than those fed low-protein cooked molasses blocks or no cooked molasses block. Heifers fed high-protein cooked molasses blocks ate more (P < 0.05) forage than those fed low-protein cooked molasses blocks, with heifers fed no cooked molasses block being intermediate. In Exp. 2, responses to cooked molasses blocks containing 33% CP (DM basis) were measured in 18 steers fed: 1) brome (8.4% CP), 2) alfalfa (19.2% CP), or 3) brome supplemented with 1.93 kg/d of alfalfa DM. Forages were available ad libitum. Forage DM intake was not affected by cooked molasses block and was greater (P < 0.05) for alfalfa than the alfalfa/brome mix, which in turn was greater (P < 0.05) than brome. Digestibility of DM was greater (P < 0.05) for alfalfa than brome or the alfalfa/brome mix and was not affected by cooked molasses block supplementation. Supplementation with cooked molasses blocks had only small effects on intake and digestion of medium- to high-quality forages, but it improved gains and feed efficiencies of heifers fed prairie hay ad libitum, with or without supplemental alfalfa.

Animal Feed↗

Non-steady-state modeling of effects of timing and level of concentrate supplementation on ruminal pH and forage intake in high-producing, grazing ewes.

A computer model was developed to predict responses of lactating ewes to concentrate supplementation, whether on pasture or stall-fed, given concentrate once per day or in multiple feedings, and suckling multiple lambs. The model considers effects of concentrate supplementation on organic acid production, saliva flow, ruminal pH, and forage intake. The user defines ewe BW, feed composition, and concentrate feeding times and amounts. The reference ewe has free access to forage and water. Upon consumption, forages and concentrates enter into lag pools for 2.0 and 0.24 h, respectively. Carbohydrates then enter ruminal pools of degradable fiber, undegradable fiber, or nonstructural carbohydrate, from which they are degraded or pass to the lower gut. Rapid dissociation of organic acids from carbohydrate fermentation and buffers from rumination are simulated to determine ruminal pH according to the Henderson-Hasselbach equation. The pH, in turn, affects fiber degradation rates. Forage intake continues during daylight hours until ruminal NDF exceeds 1.0% of BW, or organic acid concentration exceeds 130 mM. A circadian pattern of organic acid concentrations and pH of rumen contents with multiple concentrate feedings was simulated by the model with root mean square prediction error of 7.7 and 3.0 to 4.0% of the observed mean, respectively. However, ignoring fermentation of dietary protein may have caused an underestimation of organic acid production rates. The model predicted the increase in total DMI and the substitution effect on forage intake of increasing levels of concentrate supplementation. Simulations suggested that a single concentrate meal daily was best fed in the evening to minimize the substitution effect, and that there was no benefit in forage intake to feeding 2 kg/d concentrate in more than two meals per day.

Absorption↗

In vitro bacterial growth and in vivo ruminal microbiota populations associated with bloat in steers grazing wheat forage.

The role of ruminal bacteria in the frothy bloat complex common to cattle grazing winter wheat has not been previously determined. Two experiments, one in vitro and another in vivo, were designed to elucidate the effects of fresh wheat forage on bacterial growth, biofilm complexes, rumen fermentation end products, rumen bacterial diversity, and bloat potential. In Exp. 1, 6 strains of ruminal bacteria (Streptococcus bovis strain 26, Prevotella ruminicola strain 23, Eubacterium ruminantium B1C23, Ruminococcus albus SY3, Fibrobacter succinogenes ssp. S85, and Ruminococcus flavefaciens C94) were used in vitro to determine the effect of soluble plant protein from winter wheat forage on specific bacterial growth rate, biofilm complexes, VFA, and ruminal H2 and CH4 in mono or coculture with Methanobrevibacter smithii. The specific growth rate in plant protein medium containing soluble plant protein (3.27% nitrogen) was measured during a 24-h incubation at 39 degrees C in Hungate tubes under a CO2 gas phase. A monoculture of M. smithii was grown similarly, except under H2:CO2 (1:1), in a basal methanogen growth medium supplemented likewise with soluble plant protein. In Exp. 2, 6 ruminally cannulated steers grazing wheat forage were used to evaluate the influence of bloat on the production of biofilm complexes, ruminal microbial biodiversity patterns, and ruminal fluid protein fractions. In Exp. 1, cultures of R. albus (P < 0.01) and R. flavefaciens (P < 0.05) produced the most H2 among strains and resulted in greater (P < 0.01) CH4 production when cocultured with M. smithii than other coculture combinations. Cultures of S. bovis and E. ruminantium + M. smithii produced the most biofilm mass among strains. In Exp. 2, when diets changed from bermudagrass hay to wheat forage, biofilm production increased (P < 0.01). Biofilm production, concentrations of whole ruminal content (P < 0.01), and cheesecloth filtrate protein fractions (P < 0.05) in the ruminal fluid were greater on d 50 for bloated than for nonbloated steers when grazing wheat forage. The molecular analysis of the 16S rDNA showed that 2 different ruminal microbiota populations developed between bloated and nonbloated animals grazing wheat forage. Bloat in cattle grazing wheat pastures may be caused by increased production of biofilm, resulting from a diet-influenced switch in the rumen bacterial population.

Acetates↗

Influence of forage level on response of feedlot steers to salinomycin supplementation.

Two trials were conducted to evaluate the influence of forage level on the response of feedlot cattle to salinomycin. Diets containing 10, 15 and 20% forage were compared with 0 or 11 mg/kg salinomycin. In trial 1, treatment effects on feedlot performance were evaluated using 108 crossbred steers (295 kg) in a crossover design experiment. There were no salinomycin X forage level interactions (P greater than .20). Weight gain response to salinomycin supplementation averaged 5.4, 5.3 and 6.9%, respectively, for diets containing 10, 15 and 20% forage. Corresponding values for feed conversion response to salinomycin supplementation were 5.1, 3.9 and 5.9%. Averaged across forage level, salinomycin supplementation improved rate of weight gain and feed conversion by 5.9 and 5.2%, respectively (P less than .01). In trial 2, treatment effects on characteristics of ruminal and total tract digestion were evaluated in a 6 X 6 Latin-square design trial involving six crossbred steers (191 kg) with cannulae in the rumen and proximal duodenum. There were no interactions between salinomycin supplementation and forage level on characteristics of ruminal digestion (P greater than .20). Salinomycin supplementation did not influence synthesis of microbial N, ruminal digestion of organic matter, acid detergent fiber and starch, or molar proportions of acetate, propionate and butyrate (P greater than .20). Salinomycin supplementation increased passage of non-ammonia N to the small intestine (5.4%, P less than .10) and increased ruminal escape of feed N (24%, P less than .01).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Effects of corn particle size and source on performance of lactating cows fed direct-cut grass-legume forage.

We conducted two experiments to evaluate the effects of corn supplementation, source of corn, and corn particle size on performance and nutrient utilization of lactating dairy cows. In experiment 1, treatments were 1) direct-cut grass-legume forage without supplement, 2) direct-cut forage plus 10 kg DM of ground dry shelled corn-based concentrate, and 3) direct-cut forage plus 10 kg DM of coarsely ground high moisture ear corn-based concentrate. In experiment 2, treatments were 1) direct-cut grass-legume forage plus 10 kg DM of ground dry shelled corn-based concentrate, 2) direct-cut forage plus 10 kg DM of coarsely ground high moisture ear corn-based concentrate, and 3) direct-cut forage plus 10 kg of DM finely ground high moisture ear corn-based concentrate. Both experiments were designed as 3 x 3 Latin squares replicated three times. In experiment 1, yields of milk and milk protein increased with concentrate supplementation, but were not affected by source of corn. Solids-corrected milk yield tended to increase with grain supplementation. Dry matter intake increased with concentrate supplementation, but was not affected by source of corn or corn particle size. Corn supplements decreased ruminal pH and acetate to propionate ratio and increased ruminal propionate concentration. Grain supplements reduced ruminal ammonia concentration, increased concentration of urine allantoin, and increased the urinary allantoin to creatinine ratio. In the second study, fine grinding of high moisture corn reduced fecal starch plus free glucose levels and tended to increase its apparent digestibility. In both experiments, starch plus free glucose intake was higher on the diets with dry corn, but its utilization was not affected by source of corn.

Animal Feed↗

Maximal replacement of forage and concentrate with a new wet corn milling product for lactating dairy cows.

Three experiments were conducted to determine the maximal amount of concentrate and forage that could be replaced with a new wet corn milling product. The corn milling product contained 23.1% crude protein, 9.9% ruminally undegradable protein, 13.7% acid detergent fiber, 40.3% neutral detergent fiber, and 2.6% ether extract (% of dry matter; DM). In experiment 1, 16 Holstein cows were assigned to one of four diets in a replicated 4 x 4 Latin square design with 28-d periods. The four diets contained 54.3% forage (alfalfa:corn silages, 1:1 DM basis) with the wet corn milling product replacing 0, 50, 75, or 100% of the concentrate portion (corn and soybean meal) of the diet (DM basis). The diets containing wet corn milling product resulted in 7.8% lower DM intake, equivalent milk production (28.5 kg/d), and 13.6% greater efficiency of 4% fat-corrected milk (FCM) production than the control diet. There was no effect of diet on ruminal pH. In experiment 2, 16 Holstein cows were assigned to one of four diets in a replicated 4 x 4 Latin square design with 28-d periods. The 100% concentrate replacement diet from experiment 1 was used as control diet. For the test diets, forage was replaced with 15, 30, or 45% of the corn milling product (DM basis). Efficiency of FCM production (1.16) was not affected by diet. Rumination time was reduced for the 30 and 45% forage replacement diets, but ruminal pH was unaffected. In experiment 3, 30 Holstein cows were assigned at parturition to either a control diet (no corn milling product) or a diet containing 40% corn milling feed in place of both forage and concentrate (optimal levels from experiments 1 and 2) for 9 wk. The diet containing corn milling feed resulted in 21% greater efficiency of FCM production than the control diet. These results indicate that a new feed product based on wet corn milling ingredients has the potential to effectively replace all of the concentrate and up to 45% of the forage in the diet for lactating dairy cows.

Animal Feed↗

Dietary forage and nonfiber carbohydrate contents influence B-vitamin intake, duodenal flow, and apparent ruminal synthesis in lactating dairy cows.

The objective of this experiment was to quantify intakes, duodenal flows, and ruminal apparent synthesis (AS) of B-vitamins in lactating dairy cows fed diets varying in forage and nonfiber carbohydrate (NFC) contents. Eight (4 primiparous and 4 multiparous) ruminally and duodenally cannulated Holstein cows were assigned to 4 dietary treatments in a replicated 21-d period, 4 x 4 Latin square design with a 2 x 2 factorial treatment arrangement. Diets, fed as TMR, contained (DM basis) 2 levels of forage (35 and 60%) and 2 levels of NFC (30 and 40%). The forage portion of the diets contained 50% corn silage, 33% alfalfa hay, and 17% grass hay. Soybean hulls and beet pulp (2:1) and corn meal and ground barley (2:1) were included to achieve desired NFC concentrations. No supplemental B-vitamins were fed. B-vitamin AS was calculated as the amount of a specific B-vitamin flowing to the duodenum minus its daily orts-corrected intake. Dry matter and organic matter intakes were higher for cows fed the 35% forage diets and the 40% NFC diets. Increasing dietary forage content decreased ruminal AS of pyridoxine, folic acid, and B12. Increasing dietary NFC content increased ruminal AS of nicotinic acid, nicotinamide, niacin, pyridoxal, B6, and folic acid but decreased AS of B12. Across diets, amounts of B-vitamins synthesized were highest for niacin, followed by riboflavin, B12, thiamin, B6, and folic acid. Biotin AS values were negative for all diets, suggesting either no ruminal synthesis or that destruction by ruminal microflora was greater than synthesis. B-vitamin intake, duodenal flow, and ruminal synthesis are influenced by dietary forage and NFC contents.

Animals↗

Milk from forage as affected by carbohydrate source and degradability with alfalfa silage-based diets.

Milk from forage (MF) is an estimation of the milk produced solely from forage intake. It is calculated by subtracting milk production theoretically allowed by concentrates from total milk production, assuming that maintenance requirements are covered by the forage portion of the diet. Eight multiparous Holstein cows in early lactation were used in a replicated 4 x 4 Latin square design to evaluate the impact on MF of different sources of carbohydrate with forage that was high in RDP. Diets were alfalfa-based total mixed rations that were formulated to provide similar concentrations of NEL and CP while differing in rumen degradability of concentrate carbohydrates. Treatments were 1) cracked corn (control), 2) ground corn (GC), 3) GC plus wheat starch (GC+S), and 4) GC plus dried whey permeate (GC+W). The GC and the GC+S treatments increased MF as calculated on a protein basis (14.8 vs. 10.5 kg) and increased average MF production (8.6 vs. 5.5 kg) compared with the control. Protein of forage was used more efficiently with GC and with GC+S, as shown by the lower differences between allowable MF, which estimates the potential for milk production from forage, and MF on a protein basis for these 2 treatments when compared with the control. Compared with the control, DMI increased with GC and GC+S; GC+W yielded the highest DMI. Milk production with GC+W (35.8 kg/d) was lower than with GC and GC+S (37.5 kg/d) but was higher than the control (34.0 kg/d). Milk fat concentration was higher with GC+W and lower with GC+S; GC and the control had intermediate values. Milk urea was higher with the control diet compared with the other 3 treatments. Results emphasize the advantage of using concentrates of higher degradability in the rumen to improve MF and milk production when feeding silage with high rumen-degradable protein.

Ammonia↗

Effects of rumen acid load from feed and forage particle size on ruminal pH and dry matter intake in the lactating dairy cow.

The objective of this study was to evaluate the effects of level of concentrate acidogenic value (AV) and forage particle size on ruminal pH and feed intake in lactating dairy cows. Two isoenergetic (net energy for lactation = 1.5 +/- 0.01 Mcal/kg) and isonitrogenous (crude protein = 17.4 +/- 0.1% dry matter) concentrates with either a low AV or high AV were formulated and fed in a total mixed ration with either coarsely or finely chopped corn silage and alfalfa haylage ad libitum. Four rumen-fistulated cows (114 +/- 14 d in milk) were randomly assigned to 1 of the 4 treatments in a 4 x 4 Latin square with a 2 x 2 factorial treatment arrangement. Each period consisted of 3-wk (14-d treatment adaptation and 7-d data collection). Increasing the concentrate AV decreased the mean pH (from 6.07 to 5.97) and minimum pH (from 5.49 to 5.34). Cows fed high-AV diets spent a longer time below pH 5.6 (135.1 vs. 236.7 min/d; low-AV diet vs. high-AV diet, respectively) and pH 5.8 (290.0 vs. 480.6 min/d; low-AV diet vs. high-AV diet, respectively) than cows fed low-AV diets. Increasing forage particle size had no effect on the mean and minimum ruminal pH. There was an interaction between concentrate AV and forage particle size on maximum ruminal pH. Increasing forage particle size increased the maximum pH for cows fed the high-AV concentrate (6.69 vs. 6.72; low-AV diet vs. high-AV diet, respectively) and had no effect on the maximum pH for cows fed the low-AV concentrate (6.98 vs. 6.76; low-AV diet vs. high-AV diet, respectively). Increasing the concentrate AV did not affect dry matter intake but reduced neutral detergent fiber intake from 9.7 to 8.8 kg/d. Milk fat content was negatively correlated with time and area below pH 5.6 (time below, r = -0.51; area below, r = -0.56) and pH 5.8 (time below, r = -0.42; area below, r = -0.54). These results suggest that coarse forage particle size can attenuate drops in ruminal pH. However, the ameliorating effects of forage particle size on drops in ruminal pH were more apparent for high-AV diets than for low-AV diets. The AV approach combined with physically effective neutral detergent fiber would therefore improve the formulation of diets and help to mitigate subacute ruminal acidosis in dairy cows.

Animal Feed↗

Use of a standard forage to reduce effects of animal variation on estimates of mean voluntary intake.

Sixty test forages (alfalfa, timothy, bromegrass, and orchardgrass mixtures), of differing cuttings and maturities, were harvested as hay in each of 2 yr (30/yr) from three locations. Each of the 60 hays was chopped and fed to four growing sheep to determine voluntary intake. The duration of the trial was 2 yr with five experimental periods per year. In each period, immediately prior to feeding the test forages, intake of the same standard alfalfa hay (standard forage) was measured for every sheep. Use of intake of the standard forage as a covariate reduced mean square error by 38%. Regression of least squares means of intake of the test forages on chemical composition uniformly yielded higher coefficients of determination when means were generated from an analysis of variance that included intake of the standard forage as a covariate. This procedure can be used to increase the accuracy of estimates of mean voluntary intake or to reduce the number of animals needed to attain the same accuracy that would be achieved without use of the covariate.

Animal Feed↗

Ruminal in vitro degradability of protein in alfalfa harvested as standing forage or baled hay.

Eighty-nine samples, 45 of standing forage and 44 of baled hay, were collected from alfalfa harvested at various maturities over three cuttings each during 2 yr. Alfalfa was cut and conditioned mechanically; samples of standing forage were collected by removing bunches of forage from windrows and freeze-drying them. Forage was allowed to field cure and was harvested at an average 80% DM as small rectangular bales; samples of baled hay were collected by coring bales after storing for 3 to 6 mo. Samples were analyzed for DM, ADF, total N, fractions of total N present as ADIN, N degraded at 0 h, and potentially degradable protein N. Ruminal protein degradation rates and escapes were estimated using an inhibitor in vitro system, assuming that ADIN was unavailable and that ruminal passage rate was .06/h. Standing forage contained smaller fractions of ADIN and N degraded at 0 h, contained a larger fraction of potentially degradable N, and had more rapid degradation rates and lower estimated protein escapes than baled hay. Mean degradation rates and estimated escapes were .171/h and 24% for standing forage and .075/h and 40% for baled hay. There were no differences in degradation rate or estimated escape because of harvest year, and neither was significantly related to maturity or to ADF concentration. Results indicate a significant advantage in ruminal protein escape, compared with grazed alfalfa, for alfalfa harvested and stored as hay.

Animal Feed↗

Nutrient digestion, nitrogen, and amino acid flows in lactating cows fed soybean hulls in place of forage or concentrate.

Five Holstein cows in early lactation were used in a 5 x 5 Latin square design to study substitution of soybean hulls for portions of forage or concentrate in diets. The control diet consisted of (DM basis) 10% alfalfa hay, 40% corn silage, 25% high moisture corn, 23% protein supplement, and 2.3% vitamins and minerals. Soybean hulls were used to replace approximately 25 and 50% of the forage or concentrate DM in the control ration. The DMI decreased linearly as soybean hulls replaced forage. The DM and OM flow to the duodenum and apparent and true digestion of OM in the stomach were similar among treatments. Ruminal pH was similar among treatments, but concentrations of NH3 N decreased linearly when soybean hulls replaced forage. Total VFA concentrations were similar when soybean hulls replaced forage but showed a positive quadratic response when soybean hulls replaced concentrate. Microbial N averaged 59% of NAN flow and showed a negative quadratic response when soybean hulls replaced concentrate. Flows of total AA and total essential AA to the duodenum were not altered when soybean hulls were fed. Yields of milk and milk components were similar among treatments; hulls can be used effectively to replace forage or concentrate in lactation diets.

Amino Acids↗

Changes in total and individual proteins during drying, ensiling, and ruminal fermentation of forages.

Effects of wilting, drying, and ensiling on concentrations of proteins in alfalfa, crown vetch, perennial ryegrass, orchardgrass, and tall fescue were studied using SDS-PAGE. Seven to nine proteins were identified in the samples. Wilting forages for 24 h on a laboratory bench had little effect on the relative amounts of proteins. Drying forage (on a laboratory bench) for 5 d resulted in a 25 to 30% loss in electrophoretically identified proteins. A 45-kDa protein was more susceptible to hydrolysis during drying than were most other proteins. After ensiling, < 10% of the proteins in fresh alfalfa and fescue remained, but crown vetch silage contained 46% of its original proteins. A 54-kDa protein was extremely susceptible to hydrolysis during ensiling, but a 30-kDa protein was relatively resistant. Fresh forage and hay samples were incubated in vitro for 5 h to determine degradation of proteins. In general, the 54-kDa protein was most susceptible, and the 30-kDa protein was least susceptible, to ruminal hydrolysis. Certain proteins in hay were more degradable than those in fresh forage. Among fresh forages, alfalfa and fescue contained the lowest concentrations of undegradable proteins. Differences among forage species were considerably less for hay samples.

Animal Feed↗

Effect of plant maturity and preservation method on in vitro protein degradation of forages.

The influence of maturity and method of conservation on protein degradation was determined for four different forage species. Alfalfa, smooth bromegrass, and reed canarygrass were harvested at three maturities, and whole plant corn was harvested at two maturities. Samples of each forage were freeze-dried or wilted and then ensiled in mini silos at two DM contents. Additional samples of all forages except corn were field-dried to hay. Ground sample was incubated for 0, 2, and 24 h with crude enzyme extract from ruminal contents. Degraded protein as a percentage of total CP was determined as the amount of protein that was soluble in TCA (80 g/L) after degradation. Increased maturity resulted in lower protein degradation for alfalfa, bromegrass, and canarygrass. For example, the most mature alfalfa or bromegrass, respectively, had 77 or 63% as much N that was soluble in TCA after 2 h of incubation with ruminal enzyme than the least mature forage of the same species. Although protein degradation was higher for ensiled than for dried forage, silage DM content had no consistent effect. Freeze-dried material generally had less degraded protein than hay, but protein degradation of bromegrass at 24 h was lower for hay than for freeze-dried samples. Protein degradation of forages was highly variable and depended on plant maturity and conservation method.

Animal Feed↗

Effects of forage percentage and canola seed on ruminal protein metabolism and duodenal flows of amino acids in steers.

The objective was to determine the effects of dietary forage percentage and fat supplementation on ruminal N metabolism, duodenal flows of AA, and digestion of N. Six ruminally and duodenally cannulated steers were offered six isonitrogenous diets for ad libitum intake twice daily in a 6 x 6 Latin square design. Treatments were arranged as a 2 x 3 factorial with two forage percentages (70 vs. 30% of dietary DM as corn silage) and three forms of canola seed supplementation, including no canola seed or canola seed added at 10% of dietary DM as whole seed treated with alkaline H2O2 or as crushed seed. No interactions between dietary forage percentage and canola seed supplementation occurred for any of the measurements. Duodenal flows of NAN and AA were greater for diets containing low forage than for diets containing high forage. However, duodenal flows of total N and NAN did not differ among diets when corrected for differences in intake. Efficiency of bacterial protein synthesis and duodenal flows of bacterial N and AA were increased when treated whole canola seed was supplemented. Apparent total tract digestibility of N was not altered by dietary forage percentage or canola seed supplementation. Results indicate that fat supplementation from canola seed (at 5% of dietary DM), in either form, had no effects on ruminal N metabolism or flows of AA to the duodenum and suggest that treated whole canola seed may stimulate ruminal bacterial protein synthesis.

Amino Acids↗

In situ disappearance of individual proteins and nitrogen from legume forages containing varying amounts of tannins.

In situ degradability of N and proteins were studied in one cultivar of alfalfa and red clover and two cultivars each of birdsfoot trefoil and sericea lespedeza. Concentrations of tannic acid equivalents (percentage of DM) were 0.68 in one cultivar of birds-foot trefoil and 1.77 and 2.78 in the two cultivars of lespedeza. The other forages contained essentially no tannins. Forage samples were digested in situ for 0, 2, 4, 6, and 12 h. The amount of N remaining at 12 h was positively correlated with concentrations of tannin. About 38% of the N remained after 12 h in forages with no or low concentrations of tannins, and 86% remained in the two cultivars of lespedeza. Total electrophoretically identified proteins followed similar trends, but the percentage remaining was less than that for N. For all forages, bands were found at molecular masses of 15, 30, 45, 47, and 54 kDa. The percentage of 54-kDa protein that remained after 12 h was less than that for the other four proteins (23% vs. 37%). No interaction was found between forage cultivar and protein species. These results showed that tannins reduced ruminal degradation of proteins and that specific forage proteins degraded at different rates that were independent of tannin concentration.

Animal Feed↗