Effects of fumarate on ruminal ammonia accumulation and fiber digestion in vitro and nutrient utilization in dairy does

The objective of this study was to evaluate effects of fumarate on ruminal ammonia accumulation and fiber digestion in vitro and on feed intake and nutrient utilization in dairy does. Batch cultures of mixed rumen microorganisms were used to study effects of different concentrations of fumarate on fermentation with various N sources (ammonia as ammonium bicarbonate, casein amino acids, casein peptides, gelatin peptides) and feeds (bermudagrass hay, mixed diet of 60% bermudagrass hay plus 40% concentrate) for 6 and 24 h, respectively. Substrates were grouped into pairs for separate incubations. Monosodium fumarate was added to incubation tubes to achieve final concentrations of 0, 5, and 10 mM fumarate. More ammonia accumulated at the end of incubation with added ammonium bicarbonate. Ammonia concentration was higher for peptide compared with amino acid incubation, and for casein peptide compared with gelatin peptide. Addition of fumarate linearly decreased ammonia for all N sources and for feed substrates. For all substrate types, fumarate treatment increased acetate, propionate, and total volatile fatty acids (VFA), decreased acetate to propionate ratio, and tended to reduce branched-chain VFA. Digestion of feed neutral detergent fiber (NDF) by rumen microorganisms was improved by fumarate along with elevated endoglucanase and xylanase activities. In an animal metabolism experiment, 8 dairy does (4 per treatment) were used in a completely randomized design for 21 d. Does were fed a hay plus concentrate diet without (control) or with fumarate (6 g/head per day) supplementation to determine feed intake, whole-tract nutrient digestibility, and N utilization. Fumarate treatment did not affect weight change or feed intake but increased whole-tract digestion of gross energy, crude protein, and cellulose. Digested N was increased by fumarate supplementation; however, N retention was unaffected. Plasma glucose concentration was elevated with fumarate but urea N concentration remained unchanged. Fumarate addition had significant effects on rumen microbial fermentation by decreasing ammonia and branched-chain VFA, and by increasing acetate and propionate, and NDF digestion. These effects were reflected in the improvement in whole-tract gross energy, crude protein, and cellulose digestion and elevated plasma glucose concentration when dairy does were supplemented with fumarate.     

Postprandial changes of selected blood and ruminal metabolites in ruminating calves fed diets with or without hay.

Eight ruminally cannulated Holstein bull calves were used in a switchback design to evaluate effects of hay on postprandial changes in ruminal pH, ammonia and VFA, blood ketones, and plasma glucose, NEFA, VFA, and urea N. Calves were fed 4.5 kd/d of calf starter with or without hay for ad libitum consumption. Blood and ruminal fluid were sampled every 2 h for 12 h on d 21 (periods 1 and 2) or d 13 (period 3). Ruminal pH declined from 6.6 at 0 h to 5.3 by 2 h. Changes in ruminal and plasma VFA were consistent with low pH and rapid fermentation of soluble carbohydrate. Ruminal ammonia, molar percentage butyrate, and blood ketones, plasma urea N, and plasma molar percentage butyrate were lower when hay was fed. Postprandial increases in blood beta-hydroxybutyrate and acetoacetate were reduced when hay was fed, and correlated .65 and .50, respectively, to ruminal butyrate. Concentration of beta-hydroxybutyrate averaged 1.24 and 1.87 mmol/L at 4 h postfeeding. These data suggest that rapid consumption of limited amounts of grain increased in ruminal VFA and blood ketones; increase in ketones was smaller when hay was included in the diet.     

Feeding lactose increases ruminal butyrate and plasma beta-hydroxybutyrate in lactating dairy cows

Ruminal fermentation of lactose increases molar proportions of butyrate, which is metabolized by the ruminal epithelium to beta-hydroxybutyrate (BHBA). To determine the effects of dietary whey, and specifically lactose, on concentrations of ruminal and blood volatile fatty acids (VFA) and blood BHBA, 8 Holstein and 4 Brown Swiss multiparous cows (210 +/- 33 d in milk) were blocked by breed and randomly assigned to one of three 4 x 4 Latin squares. Treatments were control (CON; 7.1% of dietary dry matter [DM] as cornstarch), liquid whey (WHEY; 9.4% of diet DM) containing 70% lactose on a DM basis, low lactose (LOLAC; 7.1% lactose), or high lactose (HILAC; 14.3% lactose). Diets contained 53% forage as corn silage, alfalfa hay, and grass hay (DM basis) and a corn and soybean meal-based concentrate. Average dietary percentage of crude protein and energy density (Mcal/kg net energy for lactation) were 16.8 and 1.47, respectively. Feeding lactose increased DM intake. Milk production and composition were not affected by diet with the exception of decreased urea nitrogen in milk from cows fed lactose. Greater proportions of ruminal propionate were observed in cows fed CON relative to those fed WHEY and LOLAC. Increasing dietary lactose increased proportions of ruminal butyrate and decreased acetate and branched-chain VFA. Concurrent with the increase in ruminal butyrate concentrations, there was an increase in plasma BHBA as lactose in the diet increased. Concentrations of VFA in plasma were not affected by diet with the exception of the branched-chain VFA, which were increased in cows fed LOLAC compared with WHEY. These data indicate lactose fermentation increases proportions of ruminal butyrate and plasma BHBA in lactating dairy cows; however, the observed increase in plasma BHBA is not sufficient to subject cows to ketosis.     

Sources of variation in rates of in vitro ruminal protein degradation

Rates and extents of ruminal protein degradation for casein, solvent soybean meal (SSBM), expeller soybean meal (ESBM), and alfalfa hay were estimated from net appearance of NH3 and total amino acids in in vitro media containing 1 mM hydrazine and 30 mg/L of chloramphenicol. Protein was added at 0.13 mg of N/mL of medium, and incubations were conducted for 4 to 6 h, usually with hourly sampling. Inocula were obtained from ruminally cannulated donor cows fed diets of grass silage or alfalfa and corn silages plus concentrates. Preincubation or dialysis of inocula was used to suppress background NH3 and total amino acids; however, preincubation yielded more rapid degradation rates for casein and SSBM and was used in subsequent incubations. Preincubation with added vitamins, VFA, hemin, or N did not alter protein degradation. Protein degradation rates estimated for SSBM, ESBM, and alfalfa were not different when computed from total N release or N release in NH3 plus total amino acids, regardless of whether amino acids were quantified using ninhydrin colorimetry or o-phthalaldehyde fluorescence. Accounting for the release of peptide-N also did not affect estimated degradation. However, casein degradation rates were more rapid when using total N release or accounting for peptide-N, indicating significant accumulation of small peptides during its breakdown. Rates also were more rapid with inocula from lactating cows versus nonlactating cows with lower feed intake. Protein degradation rates were different due to time after feeding: casein rate was more rapid, but SSBM and ESBM rates were slower with inocula obtained after feeding. Several characteristics of ruminal inoculum that influenced breakdown of the rapidly degraded protein casein did not appear to have direct effects on degradation of protein in soybean meal.     

Increased production of biogas from cowdung by adding other agricultural waste materials

It was found that the addition of nitrogenous materials, such as casein, urea or urine, increased the extem of decomposition of cowdung, resulting in higher gas production. The effect appears to be due to the maintenance of pH > 7 during fermentation. With the addition of urea or CaCO₃, materials such as. dry leaves and cane sugar have yielded high proportions of methane in the gas mixtures and these additions also increased the rate of gas production by promoting anaerobic conditions in the medium. Addition of cellulose also increased the rate but the gas mixture obtained had a lower methane content.     

异养小球藻藻渣产沼气研究

为了充分利用异养小球藻发酵及油脂生产过程中出现的藻渣,本文以p H、NH₄⁺、COD（化学需氧量）、总含碳量、VFA（挥发性脂肪酸）含量、产气量为指标,将异养小球藻发酵及油脂生产过程中产生的藻渣作为研究对象进行沼气发酵。结果表明:使用酸热法提油后藻渣为原料的发酵体系在50℃的发酵温度下,1000 m L发酵液56 d的产气量最高,为7700 m L。在发酵过程中,其pH一直下降,酸化过程良好,NH₄⁺、COD、VFA含量、总碳含量变化幅度不大,说明原料利用率相对较高、发酵过程比较稳定。本研究为异养小球藻提油工艺选择及油脂生产过程中废渣的资源化利用提供了参考。      

Effects of urea and starch on rumen fermentation, nutrient passage to the duodenum, and performance of cows.

Four midlactation, multiparous Holstein cows fitted with ruminal and duodenal cannulas were used in a 4 x 4 Latin square design to determine the effects of supplementing urea or starch or both to diets containing fish meal on passage of nutrients to the small intestine and performance of lactating cows. The treatments (in a 2 x 2 factorial arrangement) were 1) control and control plus 2) urea, 3) starch, or 4) starch and urea. Supplementing diets with urea did not affect DMI; ruminal, postruminal, or total tract digestibilities of DM, starch, ADF, or NDF; ruminal fluid VFA concentrations or molar percentages; or ruminal fluid or particulate dilution rates. Feeding additional starch depressed DMI but did not alter ruminal or postruminal digestion of OM or VFA concentrations and molar percentages in ruminal fluid. Ruminal fluid ammonia concentration was increased by feeding urea and decreased by feeding additional starch. Passage of nonammonia N, nonammonia nonmicrobial N, or microbial N to the small intestine and efficiency of microbial CP synthesis were not affected significantly by supplying either urea or additional starch. Feeding urea increased passage of methionine to the small intestine, whereas feeding additional starch increased passage of methionine and arginine. Passage of other amino acids to the small intestine was not altered significantly by feeding urea or additional starch. Production of milk and milk protein was increased, but yields of fat and SNF were not altered by feeding diets supplemented with urea. Production of milk and milk fat was not affected, but yields of CP and SNF were decreased when additional starch was fed to cows.     

Erratum

Cooking and processing of starch-containing foodstuffs results in a portion of the starch becoming resistant to hydrolytic enzymes secreted in the small intestine of man. In order to determine whether this resistant starch (RS) was degraded in the colon, samples of RS and readily digestible starch (RDS) for comparisons were incubated with (a) cell-free supernatants from faecal suspensions and (b) washed faecal bacterial cell suspensions. The data obtained showed that, whereas pancreatic amylase and faecal supernatants hydrolysed RDS, with the production of oligosaccharides, RS totally resisted breakdown. In contrast, both RS and RDS were completely degraded by the washed bacterial cells with the generation of volatile fatty acids (VFA) and organic acids. Hydrolysis and fermentation of RDS was extremely rapid and, as a consequence, oligosaccharides and lactate initially accumulated in the culture medium. RS was broken down more slowly, howevér, and oligosaccharides and lactate never accumulated. The rate of polysaccharide hydrolysis had a significant effect on the quantities of VFA produced, in that 54% of carbohydrate was fermented to VFA in cultures incubated with RDS as sole carbon source as compared to only 30% in cultures incubated with RS. However no qualitative difference was observed in the VFA produced by fermentation of RDS or RS.     

Ginkgo fruit extract as an additive to modify rumen microbiota and fermentation and to mitigate methane production

Ginkgo fruit, an unused byproduct of the ginkgo nut industry, contains antimicrobial compounds known as anacardic acids. Two major cultivars of ginkgo, Kyuju (K) and Tokuro (T), were evaluated for their potential as a feed additive for ruminants. In batch culture, we incubated a mixture of hay and concentrate in diluted rumen fluid with or without 1.6% (fruit equivalent) ginkgo fruit extract. We conducted another series of batch culture studies to determine the dose response of fermentation. We also conducted continuous culture using the rumen simulation technique (RUSITEC) with cultivar K and carried out a pure culture study to monitor the sensitivity of 17 representative rumen bacterial species to ginkgo extract and component phenolics. Although both K and T extracts led to decreased methane and increased propionate production, changes were more apparent with K extract, and were dose-dependent. Total gas production was depressed at doses ≥3.2%, suggesting that 1.6% was the optimal supplementation level. In RUSITEC fermentation supplemented with 1.6% ginkgo K, methane decreased by 53% without affecting total gas or total VFA production, but with decreased acetate and increased propionate. Disappearance of dry matter, neutral detergent fiber, and acid detergent fiber were not affected by ginkgo, but ammonia levels were decreased. Quantitative PCR indicated that the abundance of protozoa, fungi, methanogens, and bacteria related to hydrogen and formate production decreased, but the abundance of bacteria related to propionate production increased. MiSeq analysis (Illumina Inc., San Diego, CA) confirmed these bacterial changes and identified archaeal community changes, including a decrease in Methanobrevibacter and Methanomassiliicoccaceae and an increase in Methanoplanus. Pure culture study results supported the findings for the above bacterial community changes. These results demonstrate that ginkgo fruit can modulate rumen fermentation toward methane mitigation and propionate enhancement via microbial selection.     

Effect of sarsaponin on ruminal fermentation with particular reference to methane production in vitro

This experiment was designed to investigate the effects of different concentrations (0, 1.2, 1.8, 2.4, and 3.2 g/L) of sarsaponin on ruminal microbial methane production using the substrates soluble potato starch, cornstarch, or hay plus concentrate (1.5:1). Ruminal fluid was collected from a dairy cow, mixed with phosphate buffer (1:2) and incubated (30 ml) anaerobically at 38 degrees C for 6 and 24 h with or without sarsaponin. Excluding the lower level of sarsaponin, pH of the medium was slightly decreased. Ammonia-N concentration and numbers of protozoa were decreased in a dose-dependent manner. Total volatile fatty acids and total gas production were increased. Molar proportion of acetate was decreased and propionate was increased with a corresponding decrease in acetate:propionate ratio. Hydrogen production was decreased. As the concentration of sarsaponin increased from 1.2 to 3.2 g/L, fermentation of soluble potato starch, cornstarch, or hay plus concentrate decreased methane production from 20 to 60% (6 h) and 17 to 50% (24 h), 21 to 58% (6 h) and 18 to 52% (24 h), and 23 to 53% (6 h) and 15 to 44% (24 h), respectively. Excluding the lower dose concentration (1.2 g/L) of sarsaponin, in vitro disappearance of dry matter of hay plus concentrate was decreased after 24 h. In conclusion, these results show that sarsaponin stimulated the mixed ruminal microorganism fermentation as well as to inhibit methane production in vitro.     

Fermentation characteristics of corn‐, triticale‐, and wheat‐based dried distillers' grains with solubles in barley‐based diets determined using continuous and batch culture systems

BACKGROUND: Dried distillers' grains with solubles (DDGS) are becoming increasingly available and popular as an alternative livestock feed. This study used continuous and batch culture techniques to compare the in vitro fermentation characteristics of diets containing corn‐, triticale‐ or wheat‐based DDGS at 200 g kg^?1 diet dry matter (DM) against a barley grain‐based control diet. RESULTS: In continuous fermentation of wheat DDGS diet, total volatile fatty acid (VFA) concentration was decreased by 15.7% across sampling times and NH₃ concentration was quadrupled compared with control, whereas fermentations of corn‐ and triticale‐DDGS diets were similar to the barley‐based control. In batch cultures, corn DDGS differed from control only in increased culture pH. Compared with control diet, triticale DDGS yielded lower total gas production (140.94 versus 148.78 mL g^?1 DM) and in vitro DM digestibility (IVDMD; 0.509 versus 0.535). Wheat DDGS diet yielded decreased total gas production (123.49 mL g^?1 DM) and IVDMD (0.468), as well as total VFA production (105.84 versus 134.20 mmol L^?1) and substantially increased ammonia concentration (151.61 versus 58.34 mg L^?1) and acetate:propionate ratio (2.94 versus 1.11). CONCLUSION: Corn‐ and triticale‐ DDGS diets exhibited fermentation characteristics similar to the barley based control diet, consistent with in vivo findings that these diets yielded no adverse effects on production. In vitro ruminal fermentation of wheat DDGS diet differed significantly from control in several aspects including 2.6 to 6X higher ammonia concentrations. Copyright © 2010 Crown in the right of Canada. Published by John Wiley & Sons, Ltd     

柠檬酸盐对秸秆厌氧降解体系产沼气的影响

将马氏甲烷八叠球菌、地农芽胞杆菌、施氏假单胞菌、谢氏丙酸杆菌接种于秸秆厌氧发酵体系中,考察添加柠檬酸盐对沼气产量、纤维素降解率和木质素降解率的影响.研究发现:添加3g/L柠檬酸盐(添加组)促进了体系的产气效率,沼气产量比对照提高了1倍,其总固体(TS)、挥发性固体(VS)含量分别比对照降低11.2％和5.1％.对照挥发性脂肪酸(VFA)浓度在84h达最大值,达到7.07g/L,仅为添加组的80％,其平均积累速率51.6mg/(L·h),比添加组69.2mg/(L·h)降低25.4％,说明添加柠檬酸盐提高了厌氧发酵体系TS、VS的利用率,促进了厌氧体系乙酸和丙酸、丁酸等VFA的合成.同时发现:秸秆厌氧发酵体系的纤维素降解率普遍高于木质素降解率7.5％左右,说明多菌耦合厌氧发酵产沼气体系的降解纤维素能力高于降解木质素的能力.     

黑曲霉B1401固态发酵茶叶加工废料产单宁酶的研究

为促进茶叶加工废料的高效利用,对黑曲霉B1401利用茶叶加工废料固态发酵生产单宁酶进行初步研究。在单因素研究的基础上,运用Plackett-Burman试验和Box-Behnken响应面法优化黑曲霉B1401固态发酵产单宁酶的最佳工艺条件。结果表明:可溶性淀粉0.48%、氮源比(尿素∶硝酸钠)0.74∶0.26(g/g)、接种量30%、装载量5 g、液固比1.8∶1(mL/g)、发酵温度30℃、发酵时间为99 h,在此条件下单宁酶酶活力可达到46.06 U/g。验证试验值44.02 U/g与模型的预测值基本相符,表明该试验方法适合于黑曲霉B1401的固态发酵工艺。     

Cellulose acetate,a new candidate feed supplement for ruminant animals: In vitro evaluations

Cellulose acetate (CA), a derivative of cellulose in which some hydroxyl groups are substituted with acetyl groups, was evaluated as a new cellulosic feed source for ruminants. In the present work, a series of in vitro studies was carried out to determine how CA supplementation affects rumen fermentation and microbiota. Batch culture studies were conducted to select the type of CA suitable for feed use and to define the optimal supplementation level. Rumen fluid from 2 Holstein cows was mixed with McDougall's buffer in test tubes into which grass hay and concentrate containing a fiber source [cellulose (control), water-soluble CA (WSCA), or insoluble CA] had been placed. Each fiber source was supplemented at 10% of total substrate. Tubes were incubated for 24 h to determine fermentation and microbial parameters. Then, the dose response of these parameters to different supplementation levels of WSCA (0, 7.5, 15, 22.5, and 30%) was tested in the same manner. We also operated a continuous culture system with WSCA supplementation and evaluated the effects on digestibility, fermentation, and microbial parameters. The supplementation level of WSCA was set at 15% of total feed. In batch culture studies, WSCA, but not insoluble CA, yielded dose-dependent increases in ruminal acetate levels. In the continuous culture system study, WSCA yielded increases in ruminal acetate levels and in the abundance of bacteria of the genus Prevotella, including Prevotella ruminicola. Dry matter digestibility and total gas production were not affected. These results suggest that WSCA supplementation at 15% of total feed yielded increased acetate levels without negatively affecting feed digestion; these effects may reflect activation of Prevotella species. As ruminal acetate is involved in milk fat synthesis, WSCA can be considered as a candidate feed additive suitable for dairy cattle.     

The effect of cellulose crystallinity on the in vitro digestibility and fermentation kinetics of meadow hay and barley,wheat and rice straws

The effect of cellulose crystallinity on in vitro digestibility (IVD) and fermentation kinetics was investigated in samples of meadow hay and barley, wheat and rice straws. A saturated solution of potassium permanganate was used to isolate the celluloses, and their crystallinity was evaluated in a Fourier transform infrared spectrometer as the ratio of the observed transmittance at two distinct wave frequencies . IVD was determined after 48 h of incubation, and the kinetics of fermentation was studied with fully automated gas production equipment. Despite significant differences (P < 0.05), crystallinity showed low variation (0.30–0.42) among celluloses and correlated positively with IVD (P < 0.05). Although positively correlated with maximal gas production (r = 0.91) and rates of fermentation, IVD (averaging 784 g kg^?1 organic matter (OM)) was also low for all samples as compared with the usually referred values for isolated celluloses. The lowest means were observed for meadow hay and rice straw. The cumulative gas production profiles were well described by a monophasic model (r² = 0.997, RSD (residual standard deviation) = 8.367), but all the curves had a lag phase varying from 3 to 6 h. Cellulose isolated from rice straw showed the lowest maximal gas production (366 ml g^?1 OM) and highest times to reach half of the maximal gas production and maximal rate. Transmission electron microscopy (TEM) of two cellulose samples showing considerable gas production at highest rates as compared with cellulose isolated from rice straw that provided the lowest gas production at the lowest rate revealed generalised bacterial colonisation, the presence of glycocalyx fibres and cell erosion in all samples. Although samples collected after 12 h of fermentation appeared to present lower microbial attack as compared with those incubated for 24 h, TEM did not explain the observed differences in the data. Since crystallinity, IVD, gas production and rates of fermentation were shown to be associated with the nutritional availability of cellulose, further research dealing with extreme values of cellulose crystallinity may be important. © 2003 Society of Chemical Industry     

Differences in microbial activity of digesta from three sections of the porcine large intestine according to in vitro fermentation of carbohydrate‐rich substrates

To determine whether faecal microorganisms can represent the entire large intestinal population, samples from caecum, mid‐colon and rectum of three adult pigs were used for the in vitro fermentation of fructo‐oligosaccharide (FOS), potato starch, wheat bran and oat hulls. The cumulative gas production technique measured fermentation kinetics and end‐products such as total gas, NH₃ and volatile fatty acids (VFA). There were significant differences in the fermentability of substrates, in terms of both kinetics and end‐products. More relevant to this study, there were also differences between pigs in respect of total gas production, the rate of gas production (R_M) and VFA production. For large intestine sections, there were more VFA from mid‐colon and rectal inocula compared with that from the caecum (p < 0.0001). Total gas, R_M and NH₃ were highest for rectal, intermediate for mid‐colon and lowest for caecal inocula (p < 0.0001). It was concluded that, while faecal sampling might overestimate caecal fermentation, its use is valid for in vitro assessment of large intestinal fermentation. However, differences between pigs indicate that a mix of samples from several animals remains important. Copyright © 2004 Society of Chemical Industry     

Effect of carbon-4 and carbon-5 volatile fatty acids on growth of mixed rumen bacteria in vitro

Mixed ruminal bacteria (400 mg cells/liter) were incubated in artificial media containing ammonia, sodium carbonate, macrominerals, vitamins, sulfide, microminerals, acetate, propionate, and butyrate. When mixed carbohydrates (equal parts glucose, maltose, sucrose, cellobiose, and soluble starch) were added at 155 mg/liter per h for 10 h, average bacterial growth rate was slow, and dry weight yield was greater than 23%. Additions of isobutyrate, valerate, isovalerate, and 2 methylbutyrate had little influence on synthesis of bacterial dry weight, deoxyribonucleic acid, ribonucleic acid, or carbohydrate. When a timothy hay inoculum was used, isovalerate and 2 methyl-butyrate increased protein synthesis by 11.2 and 16.4%, but isobutyrate and valerate alone were without effect. All four acids combined increased bacterial protein by 18.7%. Responses with an inoculum of 60% concentrate and mixed hay were smaller and not statistically different from control incubations. Low concentrations of Trypticase (less than 250 mg/liter) improved efficiency of microbial protein synthesis from organic matter, but more was associated with decreased efficiency and utilization of extracellular ammonia.     

Nitrogen balance, microbial protein production, and milk production in dairy cows fed fodder beets and potatoes, or barley

Fourteen multiparous midlactation dairy cows were used in a change-over experiment with 3 periods and 3 diets to evaluate the effects of fodder beets and potatoes on N metabolism, microbial protein production, and milk production. A basal ration of alfalfa/grass silage offered ad libitum, 1 kg of grass hay and 1 kg of heat-treated rapeseed cake was supplemented with 5 kg DM of either rolled barley/raw potatoes 80:20 (BAP), fodder beets/raw potatoes 80:20 (BEP) or rolled barley (BA). Urine and feces were collected quantitatively from 8 cows and ruminal samplings, and evacuations were performed on 4 cannulated cows. Intake and production did not differ between BAP and BA, but the BEP diet lowered intake of both silage and total ration by 0.9 kg DM. Daily yield of energy-corrected milk (ECM) was decreased by 1.7 and 2.3 kg compared with BAP and BA, respectively. Milk urea concentration was 1 mM lower with the BEP diet. The proportion of feed N recovered in milk was 20 to 21% for all diets. With the BEP diet, urinary N amount and proportion were reduced correspondingly to the lower total N intake. Fecal N amount remained unchanged, and hence nitrogen apparent digestibility decreased by 5 percentage units with the BEP diet. Microbial protein production, assessed by allantoin excretion, tended to be highest with the BAP diet. Acetate proportion of VFA was lowered by the BEP diet, while proportions of propionate and butyrate both tended to increase. Different fermentation patterns, probably related to differences in rumen microbiota, could explain why changes in energetic efficiency and milk composition reported in the literature did not occur in the actual experiment when roots replaced barley. Compared with barley, roots appeared to have a greater negative effect on silage intake in conjunction with a prewilted silage with high intake potential allowed ad libitum and this decreased milk production by a magnitude corresponding to the lower intake of ME.     

A comparison between buffalo (Bubalus bubalis) and cow (Bos taurus) rumen fluids in terms of the in vitro fermentation characteristics of three fibrous feedstuffs

Rumen fluids from fistulated buffalos (Italy‐BRF) and cows (Netherlands‐CRF) were used as inocula to determine the fermentation kinetics of three forages. These were corn silage (CS), grass silage (GS) and wheat straw (WS) which had originated from both regions, giving six substrates in total. Fermentation kinetics was assessed by the measurement of cumulative gas production. Organic matter (OM) loss and volatile fatty acid (VFA) concentration at the end of the fermentation period were also determined. Both BRF and CRF ranked the substrates in the same order for total VFA, total gas production and the maximum rate of substrate degradation (CS > GS > WS). However, while the ranking of substrates was the same for both species, the absolute values differed significantly between the two inocula. Gas production, expressed as cumulative volume per unit mass of incubated (OMCV, ml g^?1) and as cumulative volume per unit mass of OM degraded (OM ml g^?1) for CRF was consistently higher than that for BRF for all substrates (p < 0.0001). VFA production, particularly of acetic and butyric acids, was significantly (p < 0.0001) lower for BRF than for CRF, though the digestibility of OM was the same for both inocula. VFA production predicted by the use of stoichiometric equations was generally higher than the observed gas production. These equations also predicted that the calculated amount of OM utilised for microbial growth was higher for BRF than for CRF. This may explain why diets having the same energy content but less protein can be fed to buffalo since they seem to have a lower requirement for protein compared with cattle. This possibility will need to be investigated in vivo. Given the similar ranking of feedstuffs between the two sources of inocula, these results suggest that either inoculum would be suitable for use in the cumulative gas production test as a measure of feedstuff evaluation. However, given the differences in absolute values, it is recommended that inocula from the species which will receive the feedstuff should be used. Copyright © 2004 Society of Chemical Industry     

Urea-N recycling in lactating dairy cows fed diets with 2 different levels of dietary crude protein and starch with or without monensin

Rumensin (monensin; Elanco Animal Health, Greenfield, IN) has been shown to reduce ammonia production and microbial populations in vitro; thus, it would be assumed to reduce ruminal ammonia production and subsequent urea production and consequently affect urea recycling. The objective of this experiment was to determine the effects of 2 levels of dietary crude protein (CP) and 2 levels of starch, with and without Rumensin on urea-N recycling in lactating dairy cattle. Twelve lactating Holstein dairy cows (107 ± 21 d in milk, 647 kg ± 37 kg of body weight) were fed diets characterized as having high (16.7%) or low (15.3%) CP with or without Rumensin, while dietary starch levels (23 vs. 29%) were varied between 2 feeding periods with at least 7 d of adaptation between measurements. Cows assigned to high or low protein and to Rumensin or no Rumensin remained on those treatments to avoid carryover effects. The diets consisted of approximately 40% corn silage, 20% alfalfa hay, and 40% concentrate mix specific to the treatment diets, with 0.5 kg of wheat straw added to the high starch diets to enhance effective fiber intake. The diets were formulated using Cornell Net Carbohydrate and Protein System (version 6.1), and the low-protein diets were formulated to be deficient for rumen ammonia to create conditions that should enhance the demand for urea recycling. The high-protein diets were formulated to be positive for both rumen ammonia and metabolizable protein. Rumen fluid, urine, feces, and milk samples were collected before and after a 72-h continuous jugular infusion of ¹⁵N¹⁵N-urea. Total urine and feces were collected during the urea infusions for N balance measurements. Milk yield and dry matter intake were improved in cows fed the higher level of dietary CP and by Rumensin. Ruminal ammonia and milk and plasma urea nitrogen concentrations corresponded to dietary CP concentration. As has been shown in vitro, Rumensin reduced rumen ammonia concentration by approximately 23% but did not affect urea entry rate or gastrointestinal entry rate. Urea entry rate averaged approximately 57% of total N intake for cattle with and without Rumensin, and gastrointestinal rate was similar at 43 and 42% of N intake for cattle fed and not fed Rumensin, respectively. The cattle fed the high-protein diet had a 25% increase in urea entry rate and no effect of starch level was observed for any recycling parameters. Contrary to our hypothesis, Rumensin did not alter urea production and recycling.