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ANIMAL NUTRITION |
Department of Animal Science, University of California, Davis 95616
| Abstract |
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Key Words: sorghum tempering steam-flake performance digestion
| INTRODUCTION |
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Moisture uptake softens the grain, thereby reducing processing time and energy expenditure needed to produce a quality flake. Furthermore, the greater moisture uptake due to tempering may improve the strength or integrity of the flake, reducing dustiness and fines (McDonough et al., 1998
). Although tempering has increased the NE value of dry-rolled corn, increasing moisture content of grain, per se, may not have an important influence on the NE value of steam-flaked grain (Zinn, 1988
, 1990
). Tempering steam-flaked corn did not influence ruminal or total tract digestion of starch but increased ruminal microbial efficiency. Also, greater starch gelatinization has been obtained with tempered than nontempered flakes of grain sorghum (McDonough et al., 1998
). The utilization by the animal of grain sorghum is improved by steam-flaking. Theurer et al. (1999)
found that sorghum starch digestibilities by steers in all segments of the digestive tract were improved by steam-flaking vs. dry-rolling.
The beneficial effect of tempering on ruminal microbial efficiency (Zinn, 1988
) may have been due to the sarsaponin surfactants contained in the tempering agent (TA). Grobner et al. (1982)
and Zinn et al. (1983)
noted increased ruminal microbial efficiency with sarsaponin supplementation.
Application of a surfactant-based TA during tempering improved animal performance with barley (Wang et al., 2003
) and corn (Zinn et al., 1998
). However, the influence of tempering using saponin-derived surfactant agents on the feeding value of steam-flaked sorghum in feedlot steers has not been evaluated. The objective of this study was to determine the influence of dry-rolling and TA addition before flaking on the feeding value of grain sorghum for feedlot cattle.
| MATERIALS AND METHODS |
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Exp. 1
Animals and Diets.
One hundred fifty crossbred yearling steers (approximately 25% Brahman breed with the remainder represented by Hereford, Angus, Shorthorn, and Charolais breeds in various proportions) with an average initial BW of 336 kg were used in a 115-d experiment to evaluate the influence of tempering on the feeding value of SFS. Steers were blocked by BW and randomly assigned within BW groups to 25 pens (6 steers per pen). Pens were 43 m2 with 22 m2 of overhead shade. Five dietary treatments were compared: 1) dry-rolled sorghum (DRS); 2) steam-flaked sorghum (SFS), no TA; 3) SFS with 0.275 mg/kg of TA (SarTemp, SarTec, Anoka, MN); 4) SFS with 1.375 mg/kg of TA; and 5) SFS with 2.750 mg/kg of TA. Composition of the basal diet is shown in Table 1
. Diets were prepared at weekly intervals and stored in plywood boxes located in front of each pen. Steers were allowed ad libitum access to their experimental diets. Fresh feed was provided twice daily. Steers were implanted with Synovex-S (Fort Dodge Animal Health, Fort Dodge, IA).
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The SFS was prepared as follows. A chest situated directly above the rollers (46 x 61 cm corrugated rolls) was filled to capacity (441 kg) with sorghum and then brought to a constant temperature of 102°C using steam at atmospheric pressure. The sorghum was steamed for approximately 20 min before beginning the rollers. The first approximately 441 kg of SFS was allowed to pass from the rollers before material was collected for use in the experiment. This preliminary period served for warming the rollers and for adjusting the tension of the rollers to provide a flake with a density of 0.36 kg/L. The SFS was allowed to air-dry before it was fed.
Estimation of Dietary NE.
Energy gain (EG) was calculated by the equation: EG = ADG1.097 0.0493W0.75, where EG = the daily energy deposited (Mcal/d) and W = the mean shrunk BW (kg; NRC, 1984
). Maintenance energy (EM) was calculated by the equation: EM = 0.077W0.75 (Lofgreen and Garrett, 1968
). Dietary NEg was derived from NEm by the equation: NEg = 0.877(NEm) –0.41 (NRC, 1984
; Zinn, 1987
). Dry matter intake is related to energy requirements and dietary NEm according to the equation: DMI = EG/(0.877NEm – 0.41) and can be resolved for estimation of dietary NE by means of the quadratic formula:
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where x = NEm; a = –0.41(EM); b = 0.877(EM) + 0.41(DMI) + EG; and c = –0.877(DMI) (Zinn et al., 1998
).
Carcass Data.
Hot carcass weights were obtained at the time of slaughter. After the carcasses were chilled for 48 h, the following measurements were obtained: 1) LM area (ribeye area), by direct grid reading of the eye muscle at the 12th rib; 2) s.c. fat over the eye muscle at the 12th rib taken at a location 3/4 the lateral length from the chine bone end (adjusted by eye for unusual fat distribution); 3) KPH as a percentage of HCW; and 4) marbling score (USDA, 1965
; using 3.0 as minimum slight, 4.0 as minimum small, etc.).
Statistical Design and Analysis.
For calculating steer performance, initial and final full BW were reduced by 4% to account for digestive tract fill. Pens were used as the experimental units. The experiment data were analyzed as a randomized complete block design experiment, with 5 treatments and 5 blocks (Hicks, 1973
). Treatment effects were tested for the following contrasts: DRS vs. SFS and the linear, quadratic, and cubic effects of the TA level.
Exp. 2
Animals and Sampling.
Five crossbred steers (397 kg) with cannulas in the rumen and proximal duodenum (Zinn and Plascencia, 1993
) were used in 5 x 5 Latin square experiment to study treatment effects on the characteristics of digestion. Treatments were the same as those used in Exp. 1 (Table 1
), with 0.40% chromic oxide added as a digesta marker. Steers were maintained in individual pens with access to water at all times. Diets were fed at 0800 and 2000 daily. Dry matter intake was restricted to 6.3 kg/d (1.6% of BW daily). Experimental periods were 2 wk, with 10 d for diet adjustment and 4 d for collection. During collection, duodenal and fecal samples were taken twice daily as follows: d 1, 0750 and 1350; d 2, 0900 and 1500; d 3, 1050 and 1650, and d 4, 1200 and 1800. Individual samples consisted of approximately 700 mL of duodenal chyme and 200 g (wet basis) of fecal material. Samples of each steer and within each collection period were composited for analysis. During the final day of each collection period, ruminal samples were obtained from each steer via ruminal cannula at 4 h after feeding. Ruminal fluid pH was determined on fresh samples. Samples were strained through 4 layers of cheesecloth. Two milliliters of freshly prepared 25% (wt/vol) meta-phosphoric acid was added to 8 mL of strained ruminal fluid. Samples were then centrifuged (17,000 x g for 10 min), and supernatant fluid was stored at –20°C for VFA analysis. Upon completion of the experiment, ruminal fluid was obtained via the ruminal cannula from all steers and composited for isolation of ruminal bacteria via differential centrifugation (Bergen et al., 1968
).
Sample Analysis and Calculations.
Samples were subjected to all or part of the following analysis: DM (oven-drying at 105°C until no further weight loss), ash, ammonia N, Kjeldahl N (AOAC, 1984
), NDF (Goering and Van Soest, 1970
; adjusted for insoluble ash), chromic oxide (Hill and Anderson, 1958
), purines (Zinn and Owens, 1986
), and starch (Zinn, 1990
). Microbial OM and microbial N leaving the abomasum were calculated using purines as a microbial marker (Zinn and Owens, 1986
). Organic matter fermented in the rumen was considered equal to OM intake minus the difference between the amount of total OM reaching the duodenum and microbial OM reaching the duodenum. Feed N escape to the small intestine was considered equal to total N leaving the abomasum minus ammonia N and microbial N and thus included any endogenous additions. Methane production (mol/mol of glucose equivalent fermented) was estimated based on the theoretical fermentation balance for observed molar distribution of VFA (Wolin, 1960
).
Statistical Analysis.
Data were analyzed as a 5 x 5 Latin square (Hicks, 1973
). Treatment effects were tested using the following contrasts: DRS vs. SFS and the linear, quadratic, and cubic effects of the TA level.
| RESULTS AND DISCUSSION |
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Apparently, the primary determinate for enhancement in feeding value of steam-flaked grain is the degree of shear of the starch granules that occurs as grain passes through rolls (Zinn et al., 2002
). For example, Zinn (1990)
observed that when corn was steamed for a constant time (34 min at 105°C), increasing the pressure on the rolls to produce flake densities of 0.41, 0.36, and 0.31 kg/L linearly increased extent of starch digestion both in the rumen and in the total digestive tract. In contrast, doubling the steaming time (67 vs. 34 min) at 105°C before flaking to a density of 0.31 kg/L failed to increase either ruminal or total tract starch digestion, notwithstanding kernel moisture was increased (18%). In contrast, tempering before cold-rolling (in absence of steam) has enhanced ADG, G:F, and dietary NE in cattle fed corn-based finishing diets (Zinn, 1988
; Bradshaw et al., 1996
) and has enhanced G:F and dietary NE in cattle fed barley-based finishing diets (Wang et al., 2003
).
Given that the NEm and NEg values of DRS are 2.00 and 1.35 Mcal/kg, respectively (NRC, 1996
), the corresponding values for SFS are 2.28 and 1.59 Mcal/kg. The NEm value for SFS is in good agreement with Zinn (1991
; 2.34 Mcal/kg) but is greater (4.6%) than the current tabular value (2.18 Mcal/kg; NRC, 1996
). The NRC (1996)
has given SFS 92% the value of steam-flaked corn. This relationship is consistent with Zinn (1991)
.
Treatment effects on carcass characteristics are shown in Table 3
. There were no treatment effects on dressing percentage (P = 0.87), KPH (P = 0.83), LM area (P = 0.42), marbling score (P = 0.50), or retail yield (P = 0.29). However, level of inclusion of TA tended to affect (quadratic component, P < 0.10) fat thickness and liver abscess (linear component, P < 0.10). With corn-based diets, tempering before flaking likewise did not affect carcass characteristics (Zinn, 1988
).
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Steam-flaking sorghum increased (P < 0.01) postruminal digestion of OM (11%), N (10%), and starch (25%) and total tract digestion (P < 0.01) of OM (8.3%), N (8.2%), and starch (8.9%). Increased postruminal digestion of OM, N, and starch has been a consistent response to steam-flaking sorghum (Swingle et al., 1999
; Theurer et al., 1999
) and corn (Zinn, 1988
, 1990
; Barajas and Zinn, 1998
; Zinn et al., 1998
). Rooney and Pflugfelder (1986)
identified protein bodies and the protein matrix surrounding starch granules as the major cause of lower digestibility in grain sorghum. Zinn et al. (2002)
observed that granule shear during flaking, particularly of the protein-rich horny endosperm, exposes more of the protein to the postruminal proteolytic process; that in turn increases exposure of associated starch to the amylolytic process. Hence, a linkage between postruminal protein and starch digestibility would be expected.
Consistent with previous studies (Zinn, 1991
; Swingle et al., 1999
; Theurer et al., 1999
), total tract starch digestion was nearly (99.3%) complete for SFS. However, total tract starch digestion for DRS (91.2%) was less than reported by Theurer et al. (1999
; 96.5%). Applying the equation of Zinn et al. (2007
; total tract starch digestion, % = 100 {1 – [(0.938 – 0.497 FN + 0.0852 FN2) FS/DS]}, where FN = percentage of fecal N and FS and DS = percentages of starch in feces and diet), total tract starch digestion was predicted to be 99.2 and 92.6% for SFS and DRS, respectively, in good agreement with our observations.
Treatment effects on ruminal pH and VFA molar proportions are shown in Table 5
. Grain processing did not affect (P > 0.20) ruminal pH or VFA molar proportions. A comparison of effects of steam-flaking vs. dry-rolling grain sorghum on ruminal pH and VFA molar proportions in feedlot cattle has not been reported previously in the literature. In the case of corn grain, effects of steam-flaking on ruminal pH and VFA molar proportions have not been consistent. In some studies, steam-flaking did not affect ruminal pH or VFA molar proportions (Lee et al., 1982
; Zinn et al., 1998
), whereas in others (Zinn, 1987
; Zinn et al., 1995
), ruminal pH decreased and molar proportions of propionate were increased with steam-flaking. Level of TA addition to SFS affected (cubic component) ruminal pH (P < 0.10) and molar proportions of acetate (P < 0.05), propionate (P < 0.10), and estimated methane production (P < 0.05). Optimal response in terms of estimated methane energy loss was observed at the 1.375 mg/kg level of TA addition. The basis for this effect is not certain. Its practical significance in terms of dietary NE was not apparent in the growth performance response (Exp. 1).
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| Footnotes |
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3 Current address: Universidad Autónoma de Tamaulipas, Cd. Victoria, Mexico. ![]()
1 Corresponding author: razinn{at}ucdavis.edu
Received for publication August 2, 2007. Accepted for publication November 30, 2007.
| LITERATURE CITED |
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