Degradation of methionine hydroxy analog in the rumen of lactating cows

Four lactating cows fitted with T-type cannulae in the proximal duodenum were utilized in a 4 X 4 Latin square design to study rumen microbial degradation of methionine hydroxy analog, a methionine supplement. A diet consisting of 55% concentrate and 45% corn silage was fed ad libitum four times daily. The four treatments were 1) control, no methionine hydroxy analog, 2) methionine hydroxy analog in the form of a calcium salt, 3) methionine hydroxy analog in the acid form, and 4) DL-methionine. The amino acids were incorporated into a grain mix, which was top-dressed. All diets were isonitrogenous. Twelve samples of duodenal digesta and fecal matter were collected during the last 3 d of each of the four 14-d periods. Samples were composited for analysis. Microbes either altered or degraded 99% of the methionine hydroxy analog in the rumen, since recovery of the analog in duodenal digesta was less than 1% of the amount fed for both the acid form and the calcium salt.     

Influence of methionine hydroxy analog and DL-methionine on rumen protozoa and volatile fatty acids

Three lactating Holstein cows with rumen cannulae were used in a 3 X 3 Latin square arrangement of treatments to study effects of methionine source on ciliated protozoa numbers and volatile fatty acid concentrations in the rumen. Cows were fed total mixed diets twice daily of 60% grain mix, 21% corn silage, and 19% alfalfa hay (dry basis). Methionine hydroxy analog, DL-methione, and sodium sulfate were added on an equal sulfur basis. Experimental periods were 14 d with four rumen samples taken daily on d 13 and 14. Total ciliated protozoa were higher when cows were fed DL-methionine than when fed methionine hydroxy analog or sodium sulfate. Ruminal concentrations of butyric acid and isobutyric acid were higher for the DL-methionine treatment than for analog or sodium sulfate treatments. Isovaleric acid concentrations were also higher in fluid from cows fed methionine compared with cows fed the analog.     

The in-vitro metabolism of D,L-lactic acid by rumen microorganisms

Bacterial and protozoal fractions, isolated by centrifugation and filtration from the rumen of sheep given various diets, were used to examine the in-vitro metabolism of both the D(-) and L(+) isomers of lactic acid. The rate of disappearance of both the D- and L-lactic acid isomers in protozoal incubations was up to 15 × higher than the rate of disappearance in bacterial incubations, which was relatively constant at between 0.04 and 0.073 lactate per g protein per h for cells recovered from animals receiving various diets. However, the rate of lactate disappearance in the protozoal fraction varied from 0.133 g per g protein per h with a barley/hay diet to 1.12 g per g protein per h with a silage diet. L-Lactate disappeared more rapidly than the D-lactate in all protozoal incubations. It was confirmed that the disappearance of lactate associated with the protozoal fraction did not originate from adherent or associated bacteria. Further fractionation of the protozoal population by differential filtration showed that lactate only disappeared when incubated with entodiniomorphid protozoa and not with holotrich protozoa. Endogenous propionate and butyrate production by the entodiniomorphid ciliates was stimulated by 100% in the presence of lactate. It was calculated that on certain diets up to 30% of the volatile fatty acids formed from lactate could be protozoal in origin.     

The in vitro lipolysis and biohydrogenation of monogalactosyldiglyceride by whole rumen contents and its fractions

The contribution of bacterial, protozoal, participate and cell-free fractions of rumen fluid to the lipolysis of monogalactolipid and the hydrogenation of its acyl constituents has been examined. Each of these fractions hydrolysed monogalactolipid and free fatty acids were the major acyl products. Almost all the radioactivity added as monogalactolipid to rumen fluid was distributed between the particulate and bacterial fractions and half to two-thirds of the radioactivity in each of the four fractions was recovered as free fatty acids. Both 16:3 and 18:3, after release from monogalactolipids, were hydrogenated to 16:2 and 18:2 at short incubation times. As incubation was continued there was a rapid decline in dienoic fatty acids and an increase in saturated and monoenoic fatty acids. There was a greater accumulation of trans-18: 1 than cis-18:1. Only the particulate fraction of rumen fluid gave patterns of hydrogenation similar to that obtained with rumen fluid. Bacteria in free suspension had little ability to hydrogenate trienoic fatty acids beyond the dienoic stage and neither protozoa nor the cell-free supernatant gave significant biohydrogenation of trienoic fatty acids. On the other hand, the presence of monoenoic and dienoic fatty acids in the bacterial, protozoal and cell-free fractions isolated from total rumen fluid after incubation with monogalactolipid indicated their transfer to these fractions after biohydrogenation in the particulate fraction.     

Ruminal escape, gastrointestinal absorption, and response of serum methionine to supplementation of liquid methionine hydroxy analog in dairy cows

Availability of liquid methionine hydroxy analog [D,L-2-hydroxy-4-(methylthio)-butanoic acid] was evaluated in two experiments using four cannulated lactating dairy cows. The first experiment was designed as a 4 x 4 Latin square. Each cow received a pulse dose of 0, 30, 60, or 90 g of the methionine analog in the rumen each day for 10 d. Duodenal samples were collected at 16, 20, and 24 h after dosing for the last 5 d and pooled. The methionine analog was not detected in duodenal contents because it passed rapidly from the rumen relative to the sampling protocol. In the second experiment, cows were offered 90 g of the methionine analog and 600 ml of Cr-EDTA (3.5 g of Cr) mixed with ground corn for a period of 20 min after which any remains of the treatment were placed in the rumen. The concentration of the analog peaked in ruminal and duodenal fluid at 1 and 3 h, respectively. Based on the fractional rate constants for ruminal and duodenal disappearance of the methionine analog and passage of the liquid, it was determined that 50.0 +/- 2.8% of the methionine analog escaped ruminal degradation and became available for intestinal absorption (44.6 +/- 5.7%) or was absorbed from the omasum (5.4 +/- 3.3%). Serum methionine concentration peaked 6 h after analog dosing at a level that was three times the predose level, indicating that the methionine analog that escaped ruminal degradation was absorbed and metabolized to methionine.     

Ruminal metabolism of grass silage soluble nitrogen fractions

The present study was conducted to investigate ruminal N metabolism in dairy cows using ¹⁵N-labeled N sources and dynamic models. The data summarized in this study were obtained from 2 of 4 treatments whose effects were determined in a 4 × 4 Latin square design. Soluble N (SN) isolated from timothy grass silage labeled with ¹⁵N and ammonia N (AN) labeled with ¹⁵N were administered into the rumen contents of 4 ruminally cannulated dairy cows. Ruminal N pool sizes were determined by manual evacuation of rumen contents. The excess ¹⁵N-atom% was determined in N-fractions of rumen digesta grab samples that were collected frequently between 0 to 72 h and used to determine ¹⁵N metabolism in the rumen. Calculations of area under the curve ratios of ¹⁵N were used to estimate proportions of N fractions originating from precursor N pools. A model including soluble nonammonia N (SNAN), AN, bacterial N, and protozoal N pools was developed to predict observed values of ¹⁵N atomic excess pool sizes. The model described the pool sizes accurately based on small residuals between observed and predicted values. An immediate increase in ¹⁵N enrichment of protozoal N suggests physical attachment of bacteria pool to protozoa pool. The mean proportions of bacterial N, protozoal N, and feed N in rumen solid phase were 0.59, 0.20, and 0.21, respectively. These observations suggest that protozoal N accounted for 0.25 of rumen microbial N. About 0.90 of the initial dose of AN was absorbed or taken up by microbes within 2 h. Faster ¹⁵N enrichment of bacterial N with SN than with AN treatment indicates a rapid adsorption of SNAN to microbial cells. Additionally, the recovery of ¹⁵N as microbial and feed N flow from the rumen was approximately 0.36 greater for SN than for the AN treatment, indicating that SNAN was more efficiently used for microbial growth than AN. The present study indicated that about 0.15 of microbial N flowing to the duodenum was of protozoal origin and that 0.95 of the protozoal N originated from engulfed bacterial N. The kinetic variables indicated that 0.125 of SNAN escaped ruminal degradation, which calls into question the use of in situ estimations of protein degradation to predict the flow of rumen undegradable protein.     

Effect of methionine hydroxy analog supplementation on dairy cattle hoof growth and composition

Fifty lactating Holstein cows were assigned randomly to one of two treatments, control and control plus approximately 30 g methionine hydroxy analog, and confined on concrete for 11 mo. The control diet consisted of sorghum silage and concentrate fed as a blended ration. Sulfur contents of dry matter were .12% and .16% for control and methionine hydroxy analog rations. Hoof growth and hardness were measured on front and rear right abaxial claws in the dorsal and lateral regions. Hoof growth rates were measured for four periods; summer-fall, fall-winter, winter-spring, and spring-summer, each 70 to 90 days. Hooves of cows fed methionine hydroxy analog grew faster than those of control cows during spring-summer in all regions. Variations of growth rates of hooves were seasonal and tended to follow variations in daily photoperiod. Wear rates were not affected significantly by treatment. Hooves of cows fed methionine hydroxy analog were softer in the top dorsal region at the end of winter-spring and in the dorsal toe region at the end of spring-summer. All other locations were not affected significantly by treatment. The toe region was harder than the top of the hoof. Cows fed methionine hydroxy analog had less cysteine and proline in hoof than control cows and greater percentages of methionine lysine, tyrosine, and glutamic acid. These results suggest that a decrease of disulfide bonding occurred in the hoof tissue of cows fed methionine hydroxy analog. Cows fed methionine hydroxy analog produced more actual milk, milk fat, and 4% fat-corrected milk during 180 days than did control cows.     

Rumen degradation and availability of various amounts of liquid methionine hydroxy analog in lactating dairy cows

Ruminal escape of various amounts of methionine hydroxy analog [D,L-2-hydroxy-4-(methylthio)-butanoic acid (HMB)] was measured in an experiment designed as a 4 x 4 Latin square using four lactating dairy cows with cannula in the rumen and duodenum. The cows were fed a diet composed of corn silage, alfalfa haylage, rolled barley grain, canola meal, and blood meal, three times per day. The cows were fed the liquid analog each day for 1 wk before the experiment was started. On the day of the experiment, each cow received an intraruminal bolus dose of 0, 25, or 50 g of the liquid analog (Alimet feed supplement, 88% HMB) or 51.2 g of a dry calcium salt of the analog (86% HMB; MHA) mixed with 0.5 kg of ground barley grain. A liquid phase marker (Co-EDTA) was administered as a bolus dose into the rumen at the time of administration of the methionine hydroxy analogs. Rumen and duodenal contents, and blood serum were collected at 0, 1, 3, 6, 9, 12, and 24 h relative to the time of dosing. Rumen and duodenal samples were analyzed for Co and HMB, and serum was analyzed for free methionine. Fractional rate constants for the passage of the liquid marker (k(p)) and the decline of HMB concentration in the rumen (k(rHMB)) were determined by nonlinear regression. Liquid passage from the rumen was similar among the four analog treatments (0.136 +/- 0.012/h; mean +/- SEM). Ruminal escape of HMB as a percentage of the dose (100% x k(p)/k(rHMB)) did not differ between cows receiving 25, 50, and 51.2 g of the methionine analogs (42.5, 41.0, and 34.9 +/- 9.0%, respectively) and averaged 39.5%. Duodenal appearance of HMB as a percentage also did not differ between cows receiving 25, 50, and 51.2 g of the methionine analogs (16.2, 26.8, and 22.7%, respectively) and averaged 22%. Omasal absorption of HMB was variable ranging from 12.3 to 26.3% and averaged 17.6%. Serum methionine concentration peaked at 3 and 6 h after dosing and increased in proportion to the amount of the analog administered. It was concluded that 39.5% of the methionine hydroxy analog escaped rumen degradation, the percentage of the dose that escaped the rumen was not affected by the amount or form of the methionine analog fed, and the analog that escaped ruminal degradation was likely absorbed and metabolized to methionine.     

Evaluation of a real-time PCR assay quantifying the ruminal pool size and duodenal flow of protozoal nitrogen

We have recently developed a real-time polymerase chain reaction (PCR) assay to quantify copies of the genes encoding protozoal 18S rRNA. The assay includes procedures for isolating and concentrating protozoal cells from the rumen for use as a standard to convert 18S rRNA gene copies to a biomass basis. The current objectives were to 1) determine the degree of reduction of bacterial contamination in the protozoal standard, 2) determine if protozoal standards derived from ruminal fluid are appropriate for predicting duodenal flows, and 3) evaluate the assay's determined values for protozoal N in the rumen and flowing to the duodenum compared with independent measurements. Our protozoal collection method reduced non-associated bacterial contamination by 33-fold, the contamination of which could otherwise significantly bias RNA (microbial marker) and N percentages of concentrated protozoal fractions. Based on denaturing gradient gel electrophoresis, the use of protozoal cells isolated from ruminal fluid appears appropriate for use in quantitative assays determining protozoal N flow postruminally. Using real-time PCR, protozoal N was determined to be 4.8 and 12.7% of the rumen microbial N pool and 5.9 and 11.9% of the duodenal flow of microbial N on diets containing low (16%) or high (21%) forage neutral detergent fiber, respectively, which were comparable with independent measures and expectations.     

Microbial transaminase activities and their relationship with bovine rumen metabolites.

Two each adult male crossbred cattle and murrah buffalo were fed a diet of alfalfa hay, chopped wheat straw, and concentrate mixture. Total rumen transaminase activity of cattle was higher than that of buffalo. Rumen protozoal fractions showed higher total transaminase activity than bacterial fractions in both ruminant species. Besides generally studied glutamate oxalacetate transaminase and glutamate pyruvate transaminase, a large number of other microbial transaminases also have been detected in the rumen of both the ruminant species. Bacterial fractions of rumen liquor were devoid of transaminases utilizing tryptophan, threonine, and lysine as their substrates. Ruminal ammonia and nonprotein nitrogen were correlated positively with microbial transaminases in both species. Transamination reactions may be important for assimilation of ruminal ammonia to cellular proteins.     

Partitioning of amino acids flowing to the abomasum into feed, bacterial, protozoal, and endogenous fractions

We partitioned the flow of amino acids (AA) to the abomasum among rumen undegradable protein (RUP) and bacterial, protozoal, and endogenous fractions using four Holstein cows in midlactation that were equipped with ruminal and abomasal cannulas. A 2 x 2 factorial design with four diets, combinations of high or low ruminally degradable organic matter, and rumen degradable protein, was employed. Crude protein (CP) and AA contents of ruminal bacteria and protozoa and abomasal digesta were determined. Equations for the source compositions and in vivo flows of CP and 16 AA were then solved simultaneously with a linear program to estimate the contribution of RUP, bacterial, protozoal, and endogenous CP to AA flows. The flows of RUP and bacterial AA were not affected by diet. Low dietary RDP increased the flow of protozoal AA to the abomasum, but the ruminally degradable organic matter content of the diet did not affect protozoal AA flow. Across diets, RUP, bacterial, protozoal, and endogenous fractions provided 55, 33, 11, and <1% of the CP, and 62, 26, 12, and <1% of the AA that reached the abomasum. The linear program was a useful tool for partitioning AA that flows to the abomasum. The technique may also allow dietary effects on ruminal microbes and the AA profile of protein flowing to the duodenum to be better understood and perhaps manipulated.     

Influences of methionine hydroxy analog on milk and milk fat production, blood serum lipids, and plasma amino acids

Feeding for 150 days of 25 g per day of methionine hydroxy analog was tested on 100 cows (52 treated and 48 controls) in the Brigham Young University herd. Effect of days after parturition of initiating methionine hydroxy analog feeding also was observed. Milk yields were not affected by methionine hydroxy analog, but fat percent and fat yields were increased 21 and 17% by the additive. Abnormally low milk fat by control cows (2.84%) magnified the response to methionine hydroxy analog feeding. Feeding methionine hydroxy analog beginning 0 to 12 days postpartum elicited much larger increases of milk fat than started later (17 to 102 days). Blood from the coccygeal vein of 20 cows from each treatment had 10% more triglycerides from cows fed methionine hydroxy analog than from control cows. Increases of arterio-venous differences across the mammary gland of triglycerides and lipoproteins of blood serum suggested that increases of milk fat could have resulted from greater uptake of performed fat by the udder. Feeding methionine hydroxy analog increased methionine, isoleucine, and leucine in serum of coccygeal vein, but methionine was the only amino acid with significantly higher arteriovenous differences across the mammary gland.     

Assessment of ruminal bacterial populations and protozoal generation time in cows fed different methionine sources

Methionine supplemented as 2-hydroxy-4-(methylthio)-butanoic acid (HMB) has been suggested to alter bacterial or protozoal populations in the rumen. Our objective was to determine if source of Met would change microbial populations in the rumen and to compare those results to samples from the omasum. The ruminal and omasal samples were collected from cows fed control (no Met), dl-Met, HMB, or the isopropyl ester of HMB (HMBi; estimated 50% rumen protection) in a replicated 4 × 4 Latin square design. In one square, changes in protozoal populations were determined using microscopic counts and denaturing gradient gel electrophoresis (DGGE), whereas changes in bacterial populations were determined using DGGE and ribosomal intergenic spacer length polymorphism (RIS-LP). Neither the protozoal counts nor the DGGE banding patterns derived from protozoa were different among the dietary treatments or for ruminal vs. omasal samples. As revealed by both DGGE and RIS-LP, bacterial populations clustered by treatments in ruminal and especially in omasal samples. Using cows from both Latin squares, the flow of protozoal cells from the rumen was quantified by multiplying protozoal cell count in omasal fluid by the omasal fluid flow (using CoEDTA as a liquid flow marker) or was estimated by rumen pool size of cells multiplied by either the ruminal dilution rate of CoEDTA (after termination of CoEDTA dosing) or the passage rate of Yb-marked particles. Compared with the omasal fluid flow measurement (16.4 h), protozoal generation time was approximated much more closely using the particulate than the fluid passage rate from the rumen (generation times of 15.7 and 7.5 h, respectively). There seems to be minimal selective retention of protozoal genera in the rumen in dairy cattle fed every 2 h. Data support the validity of the omasal sampling technique under our conditions.     

Effects of fat and methionine hydroxy analog on prevention or alleviation of fatty liver induced by feed restriction

Two trials were conducted to examine the effects of supplemental methionine, provided as methionine hydroxy analog 13 g/d), or fat (454 g of calcium salts of long-chain fatty acids/d) on hepatic triglyceride concentration. In the first experiment, methionine hydroxy analog or fat was fed during feed restriction to determine if hepatic triglyceride accumulation is affected. The objective of the second experiment was to determine if feeding fat or methionine hydroxy analog influences the rate of triglyceride depletion from the liver of cows in positive energy balance following the induction of fatty liver by feed restriction. In experiment 1, feeding methionine hydroxy analog decreased plasma glucose, increased plasma nonesterified fatty acids, and had no effect on liver triglyceride. Feeding fat increased plasma nonesterified fatty acids and increased hepatic triglyceride during the 10-d feed restriction period. In experiment 2, feeding fat decreased the rate of triglyceride depletion from liver when cows were allowed to resume ad libitum consumption of feed; methionine hydroxy analog had no effect. Results of these studies indicate that feeding supplemental fat or methionine hydroxy analog at levels tested does not prevent or alleviate fatty liver induced by feed restriction.     

Effects of intake of a mixed dairy steers on digestion events

Ruminally cannulated steers were in a 4 X 4 Latin square to determine the effect of amount of feed ingested on fiber digestion and other digestion events. Alfalfa haylage, corn silage, and a corn-soybean meal mix were incorporated in a ratio 45:20:35 (dry matter) and fed at either 100, 85, 70, or 55% of ad libitum intake. Acid-insoluble ash, lanthanum, and chromium-ethylenediaminetetraacetic acid were digestion, particulate, and liquid markers. Apparent digestibility of dry matter, neutral detergent fiber, and cell solubles decreased linearly as feed intake increased. The fiber fraction digested was a larger percentage of the dry matter digested at low than at high intakes of feed. A more rapid rate of cellulose disappearance and a slow rate of passage of particulate matter through the rumen and total digestive tract with decreasing feed intake were key factors responsible for bringing about changes of digestion coefficients. A consistently lower rumen pH of steers at high intakes of feed was thought to account for the slower rate of ruminal fiber disappearance. The lower tract accounted for 11 to 17% of dry matter disappearance, and tended to play a greater role during periods of high feed intake. Rumen and fecal sampling techniques provided similar ruminal rates of solids passage.     

Palatability of Methionine Hydroxy Analog or DL-Methionine for Lactating Dairy Cows

A decrease in grain intake occurred initially after feeding supplemental methionine hydroxy analog (top-dressed or mixed with concentrate) but top-dressing DL-methionine did not affect intakes. After initial adjustment (1 to 3 d), cows generally returned to normal grain intakes on diets supplemented with methionine hydroxy analog. Intake patterns were similar at all methionine hydroxy analog levels, which attained three to four times that recommended for supplementation. Increases in plasma free methionine at methionine hydroxy analog intakes above 40 g/d suggest bypass of additive for intestinal absorption.     

Fungal pretreatment of wheat straw: Effects on the biodegradability of cell walls,structural polysaccharides,lignin and phenolic acids by rumen microorganisms

Disappearance of cell wall components of untreated straw and straw treated with the ligninolytic white-rot fungi Phanerochaete chrysosporium, Dichomitus squalens and Cyathus stercoreus were determined during the course of rumen digestion of samples in nylon bags. The first fungus degraded hemicelluloses and cellulose non-selectively, adversely affecting the digestion rate of crude cell walls. Dichomitus squalens and C. stercoreus preferentially degraded hemicelluloses and lignin, affording cell wall degradation rates 1.5 times higher than in native straw. Furthermore, the extent of cell wall digestion was also significantly enhanced. Both strains improved the extent of cellulose digestion, whereas the potentially degradable xylan fraction remained unchanged. Polysaccharide digestion rates were influenced in different ways depending on the strain tested: straw degraded by C. stercoreus showed an increase in cellulose digestion rate by 50%, whereas residual arabinose units were slowly degraded. Xylan was degraded 1.8 times faster in straw decayed' by D. squalens, while cellulose digestion remained unchanged. Phanerochaete chrysosporium depressed both xylan and cellulose digestion rates. Fungal-treated lignins were solubilised in the rumen faster than in untreated straw, whereas only treatment by C. stercoreus resulted in higher lignin losses. Esterified phenolic acids were extensively degraded by all three fungi. Residual ferulic and p-coumaric acids accumulated during rumen digestion, although only the former decreased in the original straw.     

Rumen digestion kinetics,microbial yield,and omasal flows of nonmicrobial,bacterial, and protozoal amino acids in lactating dairy cattle fed fermentation by-products or urea as a soluble nitrogen source

The objective of this study was to evaluate the effect of a fermentation by-product on rumen function, microbial yield, and composition and flows of nutrients from the rumen in high-producing lactating dairy cattle. Eight ruminally cannulated multiparous Holstein cows averaging (mean ± standard deviation) 60 ± 10 d in milk and 637 ± 38 kg of body weight were randomly assigned to 1 of 2 treatment sequences in a switchback design. Treatment diets contained (dry matter basis) 44% corn silage, 13% alfalfa silage, 12% ground corn, and 31% protein premix, containing either a control mix of urea and wheat middlings (CON) or a commercial fermentation by-product meal (Fermenten, Arm and Hammer Animal Nutrition, Princeton, NJ) at 3% diet inclusion rate (EXP). The trial consisted of three 28-d experimental periods, where each period consisted of 21 d of diet adaptation and 7 d of data and sample collection. A triple-marker technique and double-labeled ¹⁵N¹⁵N-urea were used to were used to measure protozoal, bacterial, and nonmicrobial omasal flow of AA. Rumen pool sizes and omasal flows were used to determine digestion parameters, including fractional rates of carbohydrate digestion, microbial growth, and yield of microbial biomass per gram of degraded substrate. Fermentation by-product inclusion in EXP diets increased microbial N and amino acid N content in microbes relative to microbes from CON cows fed the urea control. Microbial AA profile did not differ between diets. Daily omasal flows of AA were increased in EXP cows as a result of decreased degradation of feed protein. The inclusion of the fermentation by-product increased nonmicrobial AA flow in cows fed EXP versus CON. Average protozoal contribution to microbial N flow was 16.8%, yet protozoa accounted for 21% of the microbial AA flow, with a range of 8 to 46% for individual AA. Cows in this study maintained an average rumen pool size of 320 g of microbial N, and bacterial and protozoal pools were estimated at 4 different theoretical levels of selective protozoa retention. Fractional growth rate of all microbes was estimated to be 0.069 h^?1, with a yield of 0.44 g of microbial biomass per gram of carbohydrate degraded. Results indicated that fermentation by-product can increase omasal flow of AA while maintaining adequate rumen N available for microbial growth and protein synthesis. Simulations from a developmental version of the Cornell Net Carbohydrate and Protein System indicated strong agreement between predicted and observed values, with some areas key for improvement in AA flow and bacterial versus protozoal N partitioning.     

Studies on methionine derivatives as possible sources of protected methionine in ruminant rations

N-Oleoyl-D,L-methionine, D,L-methionine ethyl ester HCI and the methyl ester of methionine hydroxy analogue were examined for their ability to produce methyl mercaptan in the rumen of sheep. Results indicated that all derivatives were more stable than methionine. The derivatives were then examined for their ability, when fed in the diet, to increase the plasma methionine concentration of sheep. Methionine ethyl ester caused a marked rise. Further results suggested that while some of the methionine ester escaped ruminal degradation, it also passed through the rumen wall. The compound was found to be rapidly hydrolysed in the liver to yield methionine. The effects of the other derivatives tested on plasma methionine concentrations were small.     

Disappearance of cell wall monomeric components from fractions chemically isolated from alfalfa leaves and stems following in-situ ruminal digestion

Alfalfa (Medicago sativa L) leaves and stems were incubated in the rumen of an alfalfa-fed steer for 0, 12, 24 and 48 h. Residues were analysed for monosaccharides remaining in chemically isolated fractions. Pectic substances were rapidly and extensively degraded. Xyloglucans also were quite degradable, whereas glucuronoxylans were very resistant to fermentation. Cellulose disappearance was intermediate between that of xylan and xyloglucan. For all non-pectic polysaccharides, leaf material was more degradable than stem, and this difference between leaf and stem was greater for cellulose than for most hemicellulosic fractions. Acetyl groups associated with the oxalate-insoluble fractions were degraded similarly to xylans. Alkali-labile phenolic acid content was lower in stems than in leaves, but contributed only 4 g kg^?1 of leaf DM. Less than 10% of alkali-labile phenolics were associated with hemicelluloses. Structures which limit alfalfa xylan fermentation may include acetyl groups and linkages of uronic acid side chains to phenolic material.