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Kim, Alam, Gu, Park, Jeon, Ha, Cho, and Lee: Effect of Total Mixed Ration with Fermented Feed on Ruminal In vitro Fermentation, Growth Performance and Blood Characteristics of Hanwoo Steers


In this study, two experiments were conducted to evaluate the total mixed ration with fermented feed (TMRF) and total mixed ration (TMR) by rumen in vitro fermentation and their effects on the growth performance and blood characteristics of Hanwoo steers. In experiment 1, three Hanwoo steers (600±47 kg), each permanently fitted with a ruminal cannula were used. In this experiment, three diets designated as T1, TMRF (18.4% fermented feed, tall fescue, mammoth wild rye forage and whole crop barley); T2, TMRF (17.7% fermented feed, rice straw and whole crop barley); and T3, TMR (rice straw, whole crop barley and probiotics, but no fermented feed), which were subjected to rumen in vitro fermentation for 48 h. The results demonstrated that DM disappearance rate gradually increased with advancing fermentation time, but T1 and T2 were higher than the T3 (p<0.05) from 3 h to 12 h, but insignificant (p>0.05) at 24 and 48 h. None of the specific VFAs were affected except for acetic and non volatile lactic acids, which were produced more in T2 than in T1 and T3 at 24 h and 48 h of incubation. A/P was lower in T1 and T2 than inT3 at 24 h (p<0.05) and 48 h (p>0.05) of incubation. These results confirmed that TMRF-related treatment shows a superior performance to that of TMR during the ruminal fermentation period. In experiment 2, the three diets in experiment 1 plus 1 more control diet (concentrates, probiotics and 2% rice straw of body weight) were fed to the 48 Hanwoo steers (160±10 kg) for a period of 168 d. The results demonstrated that the daily and total live weight gain and feed efficiency were higher (p<0.05) in the TMRF and TMR groups than in the control group. SGOT, SGPT and BUN (p<0.05) were reduced in TMRF relative to the control and TMR groups by 168 d which confirmed that TMRF shows better blood profiles than the TMR and control groups. Overall, these results appear to show that TMRF has better in vitro ruminal characteristics than those of TMR; growth performance and blood profiles were also found to be superior in TMRF than in the TMR and control groups. Thus, our findings suggest that TMRF-based feed supplies are favorable for Hanwoo cattle.


The cost of feed production is rising in the livestock husbandry industry, owing largely to dietary dependency on raw material. New feeding habits and strategies employing different roughages are clearly necessary to overcome the problem. The total mixed ration (TMR) has been the subject of great interest from farmers because of its expected benefits in the nutrition, management and production of ruminant animals (Owen, 1984; Howard et al., 1986; Sirohi et al., 2001). Farmers raising homebred fattening cattle are showing increased interest in fibroid material assorted feed, such as the TMR allowance, over concentrates (Kim et al., 2003), because homebred fattening cattle (rapid growing) require more feed intake for rapid body weight gain. It has already been experimentally confirmed that fibroid materials assorted feed is advantageous in maintaining the homeostasis of ruminant stomach pH, reducing the incidence of metabolic disease, and improving milk production (Nock et al., 1986; Harrison et al., 1989; Kellems et al., 991). In recent years, the expediency of feeding cattle a TMR has become widely accepted. The benefits of a TMR include increased feed intake, enhanced use of low-cost alternative feed ingredients, ability to control the forage concentrate ratio, lower incidence of metabolic and digestive disorders, and reduced labor input for feeding (Owen, 1984). TMR is a proper type of feed especially when agricultural by-products with high moisture are to be included (Li et al., 2003). Silage, forage, and hay are the conventional roughages contained in TMR (Chumpawadee and Pimpa, 2009). Including fermented feed in TMR may change its digestibility as well as feed efficiency. However, there is no available information about TMR prepared with fermented feed. Moreover, tall fescue is an imported feed ingredient usually used to prepare TMR, but the use of domestic straw and whole barley, available in Korea, to replace the tall fescue may reduce the feeding cost.
There is currently insufficient information regarding TMR prepared by replacing tall fescue with domestic rice straw and whole barley with fermented feed (TMRF) and its effects on cattle. The principal objective of this study was to evaluate the effects of different TMR with fermented feed over simple TMR on Hanwoo steers.


Experimental feeds and treatments

The total mixed feed was formulated on the basis of standard tables of feed composition in the Korean NIAS (2007). Treatment 1 (TMRF) contained 18.4% fermented feed with TMR (tall fescue, mammoth wild rye forage (Leymus racemosus), whole barley etc.). Treatment 2 (TMRF) contained 17.9% fermented feed with TMR (rice straw, whole barley etc.). Treatment 3 (TMR) contained rice straw, whole barley and probiotics, but no fermented feed added. Control contained available concentrates and probiotics. Probiotics used in the diets were prepared using Lactobacillus acidophilus (KCTC3140) and Saccharomyces cerevisiae (KACC30068), which were sourced from the Korean collection for type culture, Daejeon, Korea. The details of ingredients and composition of the different treatments are provided in Table 1. The chemical compositions were analyzed according to the guidelines of the AOAC (1995). NDF and ADF were analyzed with an Ankom fiber analyzer (ANKOM Tech. Corp, Fairport, NY) based on Van Soest’s method (Van Soest et al., 1991).
Fermented feed was prepared for T1 and T2 with rice bran and wheat bran (50/50 w/w) supplemented with 0.1% Lactobacillus acidophilus KCTC3140 (1.2×107 CFU/ml) and 0.1% Saccharomyces cerevisiae KACC30068 (2.1×106 CFU/ml); it was then appropriately mixed and maintained at the optimal temperature of 37°C for 48 h to achieve proper fermentation in the confined condition. Finally, these fermented feeds were stored outside for 24 h to achieve normal conditions. The chemical composition of the fermented feed contained DM, CP, CF, ADF and NDF were 59.0%, 8.8%, 8.4%, 13.2% and 22.4%, respectively.

Animals, management and experimental procedure

Experiment 1 - For in vitro model

Exp. 1 used only T1, T2 and T3. Rumen fluids were pooled from 3 ruminally-cannulated Hanwoo steers of 24 months of age and body weights of 600±47 kg. The collected fluids were filtered through 4-folded cheese cloth and contained in glass bottles that were placed in a water bath for 1 h at a temperature of 39°C. A vacuum pump was used to remove the upper residue and the middle rumen fluids were collected for experimental use. Constant CO2 gas flow was used to mix the rumen fluid with media and to fill the serum bottles under anaerobic conditions. Particle-free rumen fluid as an inoculums was anaerobically transferred (20% v/v) to a medium (pH 6.7) containing different minerals, in accordance with the method described by Russell and Vansoest (1984); Russell and Strobel (1988). Subsequently, 100 ml of the buffered rumen fluid was anaerobically transferred to 160 ml serum bottles containing either TMR or TMRF, or containing neither (control). Two g (1 g in DM basis) of the different treatment mixed feeds (2 mm screen DM particle) were then added, prior to filling with buffered rumen fluid. The buffer maintained a pH of 6.7 and was autoclaved prior to its addition to the rumen fluid. The filled serum bottles were then sealed with rubber stoppers and aluminum caps and incubated at 39°C in a shaking incubator at 90 rpm for 0, 3, 6, 9, 12, 24 and 48 h with 3 replications for each of the treatments. Samples from in vitro fermentation were taken for analysis after incubation was completed.

Experiment 2 - For growth performance and blood profiles

A total of 48 Hanwoo steers were used for experimentation over 168 d. The experimental cattle were 6 months old, with live weights of 160±10 kg. The pens were constructed of steel frames, and each pen was 5 m×10 m in size. Each pen contained 6 cattle with 12 cattle for each treatment group, and thus 2 pens were required for each treatment. The cattle house faced toward the south to ensure proper light exposure.
Feed was supplied on the basis of the live weight of the cattle. Total mixed feed was allowed to a level of 1.7% of the total live weight of the cattle. The total feed was supplied equally to the cattle twice (9.00 am and 17.00 pm) daily. Cattle were freely given access to fresh, clean drinking water. Trace mineral salts were made freely available for the experimental cattle, except control animals. The experimental cattle were permitted to consume diets for 2 wk to adapt to the feed prior to beginning the experiment. Initially, the live weights of all cattle were measured. Body weights were then measured at intervals of 4 wk, and blood was collected at 8-wk intervals during the experimental period.

Measurements and analytical methods

Experiment 1 - Rumen fermentation parameters

Total gas production was measured at 3, 6, 9, 12, 24, and 48 h using a press and sensor machine of EA-6 from Sun Bee Instruments, Inc., Korea. After 3, 6, 9, 12, 24, and 48 h of incubation, pH values were measured immediately after uncapping each bottle, and fermentation was halted by swirling the bottles on ice. The pH meter used to determine the pH value was an M530P (Schott Instruments D-55122 Mainz, Germany). The in vitro DM disappearance was measured via the two-stage method of Tilley and Terry (1963). Ammonia nitrogen concentration was measured according to the method of Chaney and Marbach (1962) using OD (extinction) at 630 nm by a UV-spectrophotometer (Biochrom Ltd., CB40FJ, England).
VFA concentration was measured with HPLC (Agilent Technolgies 1200 series, Germany). The HPLC apparatus contained a UV detector, the column used was a Meta Carb 87H (Varian), and quantitative analysis was conducted using an Integrator. It evidenced signals of 210 nm and 220 nm. The samples were centrifuged at 16,609×g for 5 min at 4°C prior to use and filtered through 0.2 μm Millipore filters. A standard was developed at 0.999 for VFAs prior to sample analysis.

Experiment 2 - Feed intake and weight gain calculations

Experimental cattle were weighed using a weighing machine every 4th wk of the total 24 wk experimental period. Weight gain per day was calculated by the initial body weight of the cattle deducted from the final body weight, which was divided by the experimental period (d). Feed efficiency was calculated by the weight gain per day divided by the feed intake per day of the cattle. Feed intake was also calculated by the residual feed deducted from the total supplied feed.

Blood collection and analysis

Blood was collected once at 8 wk, and after 3 h of feed supply. Blood samples were collected from the jugular vein. Five ml of blood was collected in a sterilized vacuum tube (Green Cross MS, Korea) containing K3-EDTA, and the tube was gently inverted a couple of times, kept in an ice box, and later centrifuged for 15 min at 890×g at 4°C and maintained for 8 h in a refrigerator at 4°C prior to analysis and separation of serum. The plasma was also transferred to a storage tube and labeled with the date and animal identification and analyzed fresh or stored at −20°C until analysis. Total protein, albumin, creatinine, blood urea nitrogen and glucose concentrations were analyzed using an automatic blood analyzer (Express Plus, Ciba-Corning, CA, USA) according to the biuret method of Flack and Woollen (1984), the bromocresol green method of Doumas et al. (1971), the picric acid method of Husdan and Rapoport (1968), the urease method of Rocch-Ramel (1967), and the hexokinase method of Farrance (1987), respectively. Serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), total cholesterol, high density lipo protein (HDL), low density lipo protein (LDL) and triglyceride concentrations of the blood samples were analyzed by Green Cross MS in Korea.

Statistical analysis

Results obtained from the experiment were analyzed by one-way ANOVA for variance using the GLM (General Linear Model) procedure of the SAS (2004) 9.1 Soft Ware Package and authorized synonymy between averages were determined by Duncan’s multiple range test method. Significant differences were accepted if p<0.05.


Rumen fermentation characteristics (Experiment 1)

Total gas production and pH value

In vitro gas production at different stages, concentrations of NH3-N and pH value in rumen fluid were employed to monitor the ruminal fermentation pattern (Table 2). Total gas production increased gradually from 3 to 48 h in all of the treatment groups. Gas production increased with incubation and fermentation period. Total gas production differed prominently from 12 to 24 h of incubation among the treatment groups. At the beginning of the experiment the pH value was 6.01, and by the end of the experiment it was changed to 4.86±0.06. The pH value at 6 h of incubation was higher in the T2 and T3 treatment groups than in the others (Table 2). pH values measured at 9 to 48 h did not differ significantly (p>0.05).

NH3-N concentration and DM disappearance

Though NH3-N concentration gradually increased with the advancement of incubation, but did not differ between the treatments (p>0.05) (Table 2). DM disappearance was highest in T2 (69.98) followed by T1 (67.76) and T3 (61.50) at 12 h of incubation (p<0.05). DM disappearance rate gradually increased with advancing fermentation time in all of the groups, but the disappearance rate in T1 and T2 was higher than the T3 and achieved significance (p<0.05) from 3 to 12 h, but was insignificant (p>0.05) at 24 and 48 h (Table 2).

Volatile fatty acid, lactate and A/P ratio

The VFAs and lactate concentrations of the different treatments are provided in Table 3. All types of VFA increased gradually from 0 to 48 h and lactic acid was reduced after 9 h of incubation. None of the specific VFAs were affected by the treatments except for acetate and non-VFA lactate which were produced comparatively more in T2 than T1 and T3 at 24 and 48 h of incubation (Table 3). A/P gradually decreased with advancing rumen fermentation period and differed significantly (p<0.05) at 3, 12 and 24 h of incubation (Table 3).

Growth performance and blood profiles (Experiment 2)

Feed intake and weight gain

The initial and final body weights of the experimental Hanwoo steers were on an average 159.6 and 301.3 kg, respectively. At the end of the experiment, the T1 (308.0 kg) weights were the highest and the control weights (284.0 kg) were lowest (p<0.05). The highest live weight gain (LWG) was detected in the T3 group and the lowest was detected in the controls (Table 4). However, the LWG of the T1, T2, and T3 groups were quite similar, and daily live weight gain values were the same in all treatment groups except the controls, which evidenced the lowest weights. TMR and TMRF feed related treatments yielded higher body weight gains than were seen in the control group (p<0.05). Feed intake was higher in the control group than in the other treatment groups (Table 4). Feed efficiency was identical (0.16) in the T1, T2, and T3 groups, but the control group evidenced the lowest values (0.12).

Changes of blood profiles

Changes of blood profile according to different treatment groups are shown in Table 5. Total blood protein content was unchanged from 56 to 168 d (p<0.05) in T1 and T2, but was slightly increased in the T3 group and decreased in the control group. The albumin concentrations were increased prior to the final test in all treatment groups (Table 5). Serum Glutamate Oxaloacetate Transaminase (SGOT) concentrations were unchanged in the T1 and T2 groups from prior to final, but increased only slightly in the T3 and control groups. Serum Glutamate Pyruvate Transaminase (SGPT) concentration levels were reduced in all treatment groups from 56 to 168 d (p<0.05). Creatinine concentrations decreased in the T1 and T2 groups from before the test to the final test, but increased in the T3 and control groups (Table 5). Blood urea nitrogen (BUN) levels were reduced for all of the treatment groups, but T1 and T2 were reduced more and T3 and control decreased less profoundly from 56 d to 168 d. Total cholesterol levels increased from initial to the final test for all of the treatment groups. However, these levels increased more in the TMR and TMRF feed groups relative to the controls (Table 5). High density lipo protein (HDL) increased for all of the treatments including the controls (p>0.05). Low density lipo protein (LDL) also increased for all of the treatments, including the controls. Triglyceride concentrations reduced from the 56 to the 168-d blood test in all the treatment groups, but the controls were nearly identical, and did not change. Glucose levels increased from 56 to 112 d (p<0.05), and then declined at 168 d (p>0.05) in the case of all of the treatment groups, including the controls.


Experiment 1 for in vitro fermentation characteristics

The results of the experiment confirmed that fermental gas production increased with the advancing incubation period. Mao et al. (2007) noted that the total gas production would increase with advancing rumen fermentation period of the substrate. This consistency illustrates the similarity between present and previous research results. The pH values of the present experiment did not differ according to the effects of different TMR and TMRF, but all gradually decreased with the time period. It is assumed that the decrease in pH was due to the increased level of VFA and lactate.
NH3-N is regarded as the most important nitrogen source for microbial protein synthesis in the rumen (Bryant, 1974) and the level in the rumen is generally high when the feeds are more digestible. The differences in NH3-N concentrations among treatments may be directly related to urea and protein degradability in the TMRs. High ammonium nitrogen levels indicates that the soluble fraction of protein is also high. Erdman et al. (1986) reported previously that ammonia nitrogen contents are increased with the increased digestion period in the ruminant stomach. Slyter et al. (1979) and Li et al. (2003b) reported that cattle on TMR related feed content evidence higher ruminal NH3-N levels with the fermentation periods; the results of the present study agrees with the findings of previous studies. TMR increases the concentration of soluble sugars and lactic acid from feed; thus, the higher ruminal degradability of DM and fermented feed reduced pH and sugar concentrations, enhancing lactic acid production, which facilitates DM disappearance (Hristov and McAllister, 2002). DM disappearance is frequently marginal and depends heavily on the microbial fermentation of feed (Patterson et al., 1997; Mandebvu et al., 1999). The findings of the present experiment also revealed the same relationship between fermentation period and DM disappearance, which is consistent with the findings of previous research.
VFA is the first source of energy for ruminant animals, and is influenced by the feed quality, quantity, allowance method etc. (McCarthy et al., 1989; Casper et al., 1990). Acetate and butyrate may be used for energy supply to animals, but propionate can be employed as a primary source of glucose. However, all VFAs constitute an excellent source of energy for fattening cattle. In the present study, VFA increased gradually with increased incubation periods. VFA production has been reported to depend largely on the level of hay in the ration and the quantity of hay consumed (Sasaki et al., 2001). Although the present experiment did not directly use hay, it did use the TMRF and TMR, which induced a comparatively higher level of VFA production with advancing incubation period. However, these alterations were less profound, which is consistent with the findings of Li et al. (2003b). Overton et al. (1995) previously reported that ruminal VFA production depends on feed composition, feed intake and the feeding system used. The TMR and TMR with fermented feed partially affect VFA production which is partially consistent with the aforementioned reports. There is also some evidence to suggest that the rate and extent of carbohydrate degradation are affected by the condition of rumen fermentation and the rate and extent of VFA production (Cheng et al., 1991). Keady and Mayne (2001) also demonstrated that VFA concentrations were similar when the animals consumed diets containing similar carbohydrate compositions. In this study, different sources of fiber in TMR and TMRF were employed; thus, VFA concentrations and VFA profiles also differed in some specific incubation periods. Also, the different sources of fiber in TMR and TMRF caused the concentration of acetate to differ at 24 h of incubation. Lactate concentrations differed at 3, 6, 9 and 12 h of incubation which gradually decreased with the time periods. McGilliard et al. (1983) and Nock et al. (1985) reported that the TMR and TMRF systems helped to maintain the rumen A/P ratio, because TMR and TMRF could provide a more balanced ration with a uniform rate of roughage and concentrate and increased DM intake. Li et al. (2003a) reported previously that TMR feeding resulted in lower A/P ratios, which is good for ruminants. The present findings showed better A/P in the TMRF group (T1 and T2) than in the TMR (T3) group at 12 h of fermentation, which is consistent with the above previous research findings showing a beneficial effect on ruminants.

Experiment 2 for growth performances and blood profile characteristics

Growth performances

Lin et al. (2001; 2004) reported previously that body weight gain and feed conversion rates of Hanwoo steers at the end of the fattening period were improved by the consumption of fermented feedstuffs. The feed efficiency results from the present experiment were consistent with these findings, though the final body weight did not differ among treatment and control. These results demonstrate that TMR and TMRF feed in the ration improve nutrient utilization in ruminal fermentation and is consistent with the opinions of McGilliard et al. (1983) and Nock et al. (1985). For this reason, the control group failed to achieve growth relative to that seen with TMRF and TMR. Apparently the higher moisture content and lower nutritive value of the feed could not be properly utilized in the stomach (Ministry of Agriculture and Forestry, Republic of Korea, 2002). However, TMR or TMRF can modify moisture contents and nutritive values, which may improve feed efficiency as well as body weight gain.

Blood metabolites

Total protein and albumin concentrations are correlated. It is shown in this experiment that higher total protein or blood albumin content is associated with greater body weight gains. It has been previously reported that blood albumin concentration was decreased with increasing synthesis of muscle proteins (Galbraith et al., 1978), although this is inconsistent with the findings of the present study. Rather, our finding show a relationship between increased levels of blood total protein or albumin and increased body weight at 168 d and is consistent with the findings reported previously by Enright et al. (1990). TMRF and TMR groups achieved a better performance than the control group, consistent with the above statements. Low levels of SGOT and SGPT are favorable for healthy cattle at 168 d, and similar results were reflected in our present experimental findings with TMRF. The correlation between serum glucose and creatinine up to 112 d was also greater in the fermented feed treatment group relative to the controls. This is probably related to the reduced Krebs cycle activity associated with fermented feed. Our findings regarding creatinine are consistent with the findings reported by Erkki et al. (1998). A marked correlation between BUN and NH3-N concentrations in the rumen was previously detected (Church, 1972). Thus, animals fed with TMR and TMRF also evidenced higher BUN levels than the controls at 168 d. Protein degradation occurs more rapidly than synthesis or imbalances of fermentable energy and available nitrogen, and thus ammonia will accumulate in the rumen fluid and be absorbed into the blood where it is transported to the liver and converted to urea. Since BUN is generated during the excretion of ammonia in urine via the urea cycle, the lower correlation between serum BUN and protein in steers fed on fermented feed could result principally from the increase in BUN levels and the reduction in protein synthesis, and vice versa (Charles, 1999). Our experiment showed this phenomenon in reverse; namely, a reduction in BUN and an increase in protein levels. However, the findings regarding BUN levels in the present study were consistent with the findings of Ellenberger et al. (1989). Lin et al. (2001, 2004) noted that blood cholesterol concentrations are generally proportional to the increment of body weight. The findings of this experiment did not differ with regard to blood cholesterol concentrations among the control and treatment groups. From a different experimental viewpoint, it was established that HDL is better than LDL for the animal body, but the concentrations of both depend on the levels of weight gain. Body fat is correlated with HDL and LDL concentrations; if body weight or fat increase, ultimately HDL and LDL will also increase. The findings of this study revealed similar HDL levels in TMR and TMRF, which were favorable for animals and similar to the views described above. Lin et al. (2001, 2004) reported that the provision of alcohol-fermented feed to ruminants increased the propionate, triglyceride, cholesterol and glucose concentrations in the blood with increasing weight gain. However, it remains unclear whether or not the alcohol-fermented feed directly increases metabolic efficiency in the stomach; this was inconsistent with the present results, even though this study used TMRF and TMR rather than alcohol-fermented feed. The present results demonstrate that TMRF and TMR can be applied to modulate the nutritional metabolism and growth characteristics of Korean native Hanwoo steers.
According to the findings of fermentation characteristics, a fermented diet produced comparatively better results while tall fescue and rice straw in the diet showed a similar performance to that of TMR during the 48 h incubation period. Growth performances were confirmed better in the fermented and TMR groups and similar both in tall fescue and rice straw than in the control diet group. Blood profile characteristics were nearly similar in fermented, tall fescue and rice straw TMR and control groups by 168 d of the trial; indicating that the tested feeds were as suitable for healthy cattle as the control. Thus, our findings show that the provision of TMRF with domestic straw and whole barley-based feed is favorable and had no detrimental effect on nutritional aspects in Hanwoo cattle. Futher investigation is required to advance methods of improving cattle productivity through the use of TMRF.


This work was carried out with the support of “Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ0063952010)” Rural Development Administration and Korea Institute of planning & Evaluation for Technology in Food, Agriculture & Fisheries, Republic of Korea.

Table 1
Ingredient and chemical composition of the experimental diets for Exp. 2
Con1 T12 T23 T34
Diet ingredients (%)
 Beet pulp - - 9.5 8.5
 Brewer grain 19.0 - - -
 Calcium sulfate 0.26 - - -
 Wheat 6.5 - - -
 Tapioca 5.5 - - -
 Corn (M)5 6.9 0.8 - -
 Corn (F)6 26.47 5.1 4.0 4.3
 Fermented mixture7 - 18.4 17.7 -
 Mammoth wild rye forage - 7.2 - -
 Lime stone 1.52 0.65 0.8 0.9
 Malt hulls 1.5 - - 8.5
 Mineral mixture8 0.25 - - -
 Vitamin premix9 0.35 0.35 0.35 0.1
 Molasses 0.65 5.1 5.5 6.0
 Probiotics 0.2 - - 0.1
 Rice bran - 24.5 19.0 20.5
 Rice straw - - 7.9 8.5
 Salt 0.6 - - -
 Tall fescue - 7.2 - -
 Concentrate mixture 10 30.3 - - -
 Whole crop barley - 25.6 35.6 42.7
 Water - 5.1 - -
Chemical composition of mixed feeds
 DM (%) at 105°C 87.0 64.0 64.0 65.0
 TDN11 69.0 69.0 69.0 69.0
 Crude protein 14.0 13.0 12.0 12.0
 Crude fiber 18.0 17.0 17.0 16.0
 ADF12 - 24.0 24.0 22.0
 NDF13 - 44.0 45.0 45.0
 Calcium 0.8 1.12 0.98 0.95
 Phosphorus 0.12 0.39 0.34 0.42

1 As usual mixed diet.

2 Tall fescue, 184 g/kg fermented feed, mammoth wild rye forage, whole barley forage etc.

3 Rice straw, 177 g/kg fermented feed, whole barley forage etc.

4 Rice straw, probiotics, whole barley forage etc.

5 Corn meal.

6 Corn Flake.

7 Rice bran 50% and wheat bran 50% (w/w) with 0.1% Lactobacillus acidophilus KCTC3140 (1.2×107 CFU/ml) and 0.1% Saccharomyces cerevisiae KACC30068 (2.1×106 CFU/ml) were mixed and maintained at the optimal temperature for fermentation.

8 Guaranteed analysis: 360 g/kg Na, 600 g/kg Cl, 1,600 mg/kg Fe, 5,000 mg/kg Mn, 7,500 mg/kg Zn, 2,500 mg/kg Cu, 70 mg/kg I, and 40 mg/kg Co (Shur-Gain Feeds Inc., Moncton, New Brunswick, Canada).

9 Guaranteed analysis: 10,000,000 IU/kg vitamin A, 1,500,000 IU/kg vitamin D and 15,000 IU/kg vitamin E (Shur-Gain Feeds Inc., Moncton, New Brunswick, Canada).

10 Mixture of 23.64% wheat meal, 28% corn meal, l9% oil seed meal, 7% coconut meal and 22.36% palm meal from Hanwoo TMR feed factory, Ziri-mountain, Sunhan, Jeonnam, Korea.

11 total digestible nutrient.

12 Acid detergent fiber.

13 Neutral detergent fiber.

Table 2
Total gas production, pH values, ammonia-nitrogen concentration and disappearance rate of DM in in vitro ruminal fermentation of experimental diets at different stages for Exp. 1
Incubation time (h) Treatments Level of significance

T11 T22 T33 SEM
Gas production (ml/g DM)4
 3 27.00a 21.34c 24.17b 0.89 *
 6 36.00 33.84 33.84 1.50 NS
 9 38.00 39.50 40.17 1.72 NS
 12 40.50b 47.00ab 51.17a 3.05 *
 24 53.84b 50.17b 61.50a 2.82 *
 48 56.00 60.00 64.67 6.32 NS
pH values
 3 5.59b 5.78a 5.83a 0.03 *
 6 5.23b 5.43a 5.45a 0.04 *
 9 5.12 5.33 5.29 0.06 NS
 12 5.15 5.16 5.09 0.02 NS
 24 4.98 4.97 4.95 0.02 NS
 48 4.92 4.86 4.82 0.03 NS
NH3-N concentration (mg/L)
 3 227.00 226.00 243.33 28.56 NS
 6 243.00 231.33 246.33 16.37 NS
 9 245.67 239.44 262.67 32.94 NS
 12 261.67 254.00 330.67 43.83 NS
 24 291.44 261.44 344.22 25.69 NS
 48 356.44 328.67 345.78 29.38 NS
Disappearance rate of DM (g/kg)
 3 644.80a 628.00a 535.80b 0.02 *
 6 641.80a 637.20a 547.90b 0.02 *
 9 661.20ab 679.90a 586.60b 0.03 *
 12 677.60ab 699.80a 615.00b 0.02 *
 24 713.50 729.90 667.30 0.02 NS
 48 718.10 744.30 703.60 0.01 NS

Values are given as means (n = 3). Different letters (a, b, c) within each row indicate significant differences within the values (p<0.05).

1 Tall fescue, 184 g/kg fermented feed, mammoth wild rye forage, whole barley forage etc.

2 Rice straw, 177 g/kg fermented feed, whole barley forage etc.

3 Rice straw, probiotics, whole barley forage etc.

4 The total gas was produced from 1 g (DM basis) of feed substrates, which were used in each of the serum bottles during in vitro fermentation.

Table 3
Changes of VFA, lactate concentrations and A/P in in vitro fermentation of experimental diets at different incubation periods for Exp. 1
Fermentation period (h) Treatments Level of significance

T11 T22 T33 SEM
Acetic acid (mM/L)
 0 21.17a 19.08a 14.20b 1.35 *
 3 20.97 29.44 23.83 4.24 NS
 6 33.60a 22.43b 22.42b 2.24 *
 9 22.84b 22.73b 30.48a 1.91 *
 12 30.72 36.45 31.95 2.49 NS
 24 44.23b 54.65a 46.13ab 2.99 *
 48 53.78 60.15 52.01 7.28 NS
Propionic acid
 0 5.02 5.01 2.86 1.33 NS
 3 6.15 6.09 6.53 0.78 NS
 6 11.25 9.25 9.96 1.24 NS
 9 10.32 11.60 11.71 1.81 NS
 12 17.93 27.04 25.30 2.79 NS
 24 38.70 43.60 36.03 2.79 NS
 48 46.90 49.91 38.93 4.75 NS
Butyric acid
 0 3.49 2.50 2.78 0.63 NS
 3 4.57 3.20 4.32 0.87 NS
 6 5.62 4.12 5.44 0.63 NS
 9 3.67 3.35 5.04 0.64 NS
 12 5.41 4.71 5.52 0.74 NS
 24 9.98 5.82 6.23 1.58 NS
 48 9.00 7.47 6.16 1.15 NS
Total VFA
 0 29.68a 26.59ab 19.84b 2.39 *
 3 31.69 38.73 34.69 4.83 NS
 6 50.48a 35.80b 37.81b 2.97 *
 9 36.83 37.68 47.23 3.30 NS
 12 54.07 68.20 62.77 4.91 NS
 24 92.91 104.07 88.40 6.41 NS
 48 109.69 117.53 97.10 11.19 NS
Lactic acid
 0 6.28 5.18 4.61 0.62 NS
 3 19.76a 12.39b 11.33b 1.38 *
 6 24.34a 17.28b 15.92b 1.36 *
 9 26.06ab 19.32b 30.29a 3.03 *
 12 21.06a 4.78b 11.62b 2.28 *
 24 4.27 7.60 6.86 1.17 NS
 48 4.42 6.78 5.15 1.32 NS
A/P ratio
 3 3.40 5.47 3.81 0.74 NS
 6 3.83 2.44 2.45 0.60 NS
 9 2.35 2.16 3.08 0.36 NS
 12 2.23a 1.36b 1.32b 0.23 *
 24 1.15 1.27 1.34 0.09 NS
 48 1.15 1.29 1.29 0.12 NS

Values are given as means (n = 3).

a, b Different letters within each row indicate significant differences within the values (p<0.05).

1 Tall fescue, 184 g/kg fermented feed, mammoth wild rye forage, whole barley forage etc.

2 Rice straw, 177 g/kg fermented feed, whole barley forage etc.

3 Rice straw, probiotics, whole barley forage etc.

Table 4
Growth performance and feed efficiency of growing Hanwoo steers by feeding different diets for Exp. 2
Periods/item Treatments Level of significance

Days Unit Con1 T12 T23 T34 SEM
IBW5 Weight 160.33 160.42 158.92 158.58 4.47 NS
28 (kg) 187.92 190.83 182.75 184.67 5.48 NS
56 201.17 206.83 191.67 199.00 5.57 NS
84 210.08 221.50 202.83 212.92 6.08 NS
112 237.00 252.92 247.33 256.08 6.30 NS
140 258.83 275.42 267.58 278.42 6.92 NS
FBW6 284.00 308.00 306.08 307.00 7.83 NS
TLWG7 123.67b 147.58a 147.17a 148.42a 5.69 *
DLWG8 0.74b 0.88a 0.88a 0.88a 0.04 *
DFI 9 6.43 5.63 5.63 5.63 0.35 NS
FE10 Ratio 0.12b 0.16a 0.16a 0.16a 0.01 *

Values are given as means (n = 3).

a, b Different letters within each row indicate significant differences within the values (p<0.05).

1 As usual mixed diet.

2 Tall fescue, 184 g/kg fermented feed, mammoth wild rye forage, whole barley forage etc.

3 Rice straw, 177 g/kg fermented feed, whole barley forage etc.

4 Rice straw, probiotics, whole barley forage etc.

5 Initial body weight (starting).

6 Final body weight (168 d).

7 Total live weight gain.

8 Daily live weight gain.

9 Daily feed intake.

10 Feed efficiency = DLWG/DFI.

Table 5
Blood characteristics of growing Hanwoo steers on different diets for Exp. 2
Items Unit Treatments Level of significance

Con1 T12 T23 T34 SEM
After 56 d
 Total protein g/dl5 6.65a 6.11b 6.48a 6.13b 0.12 *
 Albumin g/dl 3.49 3.40 3.45 3.48 0.09 NS
 SGOT6 IU/L8 66.17b 71.50ab 66.42b 78.00a 3.61 *
 SGPT7 IU/L 25.75 27.67 27.00 26.67 1.45 NS
 Creatinine mg/dl 1.53a 1.36b 1.32b 1.20b 0.06 *
 BUN9 mg/dl 13.57a 11.89ab 9.69c 10.82bc 0.67 *
 Total cholesterol mg/dl 113.92ab 120.25a 104.00ab 101.17b 5.69 *
 HDL10 cholesterol mg/dl 55.50 60.25 53.58 53.75 2.41 NS
 LDL11 cholesterol mg/dl12 11.83 12.67 10.83 11.58 0.72 NS
 Triglyceride mg/dl 27.83 28.08 31.17 26.08 1.87 NS
 Glucose mg/dl 89.75ab 95.08a 88.50b 92.75ab 2.07 *
After 112 d
 Total protein g/dl 6.22 5.92 6.20 5.97 0.14 NS
 Albumin g/dl 3.46b 3.61a 3.63a 3.63a 0.05 *
 SGOT IU/L 63.17 73.08 76.08 77.33 4.52 NS
 SGPT IU/L 22.00b 25.75a 23.75ab 22.25b 1.04 *
 Creatinine mg/dl 1.28 1.34 1.33 1.27 0.05 NS
 BUN mg/dl 10.22ab 11.75a 10.17ab 9.03b 0.56 *
 Total cholesterol mg/dl 129.67a 108.33b 120.58ab 111.00b 5.13 *
 HDL cholesterol mg/dl 66.25a 55.17b 65.00a 59.58ab 2.32 *
 LDL cholesterol mg/dl 12.58 11.42 11.92 10.83 0.58 NS
 Triglyceride mg/dl 28.42a 27.92a 20.17b 18.83b 1.81 *
 Glucose mg/dl 97.25b 101.92ab 100.67ab 105.67a 1.93 *
After 168 d
 Total protein g/dl 6.28ab 6.11b 6.47a 6.31ab 0.09 *
 Albumin g/dl 3.65c 3.72bc 3.89a 3.84ab 0.05 *
 SGOT IU/L 61.75b 71.33a 66.00ab 69.67a 2.44 *
 SGPT IU/L 20.75b 26.50a 23.33b 22.08b 0.98 *
 Creatinine mg/dl 1.28 1.33 1.27 1.23 0.04 NS
 BUN mg/dl 13.30a 9.82b 10.72b 10.38b 0.52 *
 Total cholesterol mg/dl 121.93 135.17 145.42 142.25 8.33 NS
 HDL cholesterol mg/dl 59.25 62.50 61.08 60.58 2.49 NS
 LDL cholesterol mg/dl 16.83 17.92 18.92 19.50 1.36 NS
 Triglyceride mg/dl 27.67 26.25 23.83 23.67 1.56 NS
 Glucose mg/dl 86.50 89.75 91.17 91.50 2.13 NS

Values are given as means (n = 3). Different letters (a, b, c) within each row indicate significant differences within the values (p<0.05).

1 As usual mixed diet.

2 Tall fescue, 184 g/kg fermented feed, mammoth wild rye forage, whole barley forage etc.

3 Rice straw, 177 g/kg fermented feed, whole barley forage etc.

4 Rice straw, probiotics, whole barley forage etc.

5 Gram per deci liter (g/dl).

6 Serum glutamate oxaloacetate transaminase (SGOT).

7 Serum glutamate pyruvate transaminase (SGPT).

8 International unit per liter (IU/L).

9 Blood urea nitrogen (BUN).

10 High density lipoprotein (HDL).

11 Low density lipoprotein (LDL).

12 mg per deci liter (mg/dl).


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