Abstract
Canola meal (CM) contains less crude protein (CP) and more fiber and anti-nutritional factors such as glucosinolates than soybean meal (SBM) and consequently has a lower nutrient digestibility. Therefore, processing strategies that may increase the feeding value of CM warrant study. In two experiments, the effects of extrusion of Brassica napus CM on apparent (AID) and standardized ileal digestibility (SID) of amino acids (AA), apparent total tract digestibility (ATTD) of gross energy (GE) in growing pigs, and growth performance and diet digestibility in weaned pigs were assessed. Solvent-extracted CM was extruded using a single-screw extruder at three screw speeds: 250 (CM-250), 350 (CM-350), or 450 (CM-450) rpm. In exp. 1, in a double 4 × 4 Latin square, eight ileal-cannulated barrows (initial body weight [BW], 68.1 kg) were fed corn starch-based diets containing 50% CM or extruded CM. The CM sample contained 43.2% CP, 33.2% total dietary fiber (TDF), and 8.9 µmol of total glucosinolates/g on a dry matter (DM) basis. Extrusion increased (P < 0.05) the AID of CP, reduced (P < 0.05) apparent hindgut fermentation of CP, and decreased (P < 0.05) predicted net energy (NE) value of diets. Extrusion increased diet AID and CM SID of most indispensable AA by 3.1 to 5.3%-units. In exp. 2, 200 weaned pigs (initial BW, 8.3 kg) were fed diets containing 20% SBM, CM, or extruded CM starting 2 wk postweaning for 3 wk. The CM sample contained 42.7% CP, 28.3% TDF, and 5.3 µmol total glucosinolates/g DM. Wheat-based diets provided 2.3 Mcal NE/kg and 5.1 g SID Lys/Mcal NE. Dietary inclusion of extruded CM replacing SBM decreased (P < 0.05) diet ATTD of DM, GE and CP, and DE value. Average daily feed intake, average daily gain (ADG), and gain:feed (G:F) of pigs did not differ between extruded CM and SBM diets and were not affected by extrusion, but increasing extruder screw speed linearly increased (P < 0.05) ADG for day 1 to 7 and G:F for the entire trial. In conclusion, extrusion increased diet AID and CM SID of AA but not DE and predicted NE values of CM. However, increasing extruder speed did not further increase the SID of most of the AA of CM in growing pigs. Dietary inclusion of 20% CM or extruded CM did not affect the growth performance in weaned pigs.
Keywords: canola meal, digestibility, extrusion, growth performance, pig
Introduction
Annually, over 70 million metric ton of canola or rapeseed is produced globally mostly in temperate climate zones (FAOSTAT, 2021). In Canada, 20 million t canola seed is produced annually (5-yr average), and domestic crushing of canola seed generates 4.6 million metric ton of canola meal (CM; AAFC, 2020; Canola Council of Canada, 2021). After soybean meal (SBM), CM is the most widely fed alternative supplemental protein meal in diets for pigs (Hansen et al., 2020). However, CM has a lower energy value and contains less digestible amino acids (AA) compared with SBM (Newkirk, 2009), partly due to a greater fiber content that reduces digestibility of energy and AA (Bell, 1993).
Dietary inclusion of CM to substitute SBM reduced total tract nutrient digestibility and thus nutrient utilization in weaned pigs (Landero et al., 2011). Nutrient utilization of CM might be enhanced using feed processing (Rojas and Stein, 2017; Lancheros et al., 2020), for example, extrusion. Hydrothermal treatment with high shear force may break weak bonds in polysaccharides, whereas excessive heating may cause protein damage (McDougall et al., 1996). Finally, extrusion decomposes glucosinolates (Huang et al., 1995; Liang et al., 2002); however, extrusion to enhance the nutrient digestibility of CM has rarely been reported.
The null hypotheses of the present study were that: 1) extrusion and extrusion speed would not affect the digestibility of nutrients and energy in growing pigs or glucosinolates content of CM and 2) weaned pigs fed diets containing 20% CM extruded with increasing extruder speeds and formulated to equal net energy (NE) and standardized ileal digestible AA content would not differ in diet ATTD of nutrients and growth performance compared with pigs fed diets containing non-extruded CM or SBM. The objectives were to evaluate the effects of extrusion of Brassica napus CM at different extrusion speeds on: 1) apparent ileal digestibility (AID) and apparent total tract digestibility (ATTD) of crude protein (CP) and gross energy (GE), and digestible energy (DE) and predicted NE values; 2) standardized ileal digestibility (SID) of AA and CP in growing pigs; 3) growth performance and diet digestibility in weaned pigs; and 4) glucosinolates content.
Materials and Methods
Animal use was approved and procedures were reviewed by the University of Alberta Animal Care and Use Committee for Livestock and followed the principles established by the Canadian Council on Animal Care (CCAC, 2009). The animal study was conducted at the Swine Research and Technology Centre, University of Alberta (Edmonton, AB, Canada).
Test ingredient and processing
Dark-seeded, solvent-extracted B. napus CM (exp. 1: Altona, MB, Canada; exp. 2: Lloydminster, AB, Canada) was extruded at the Agri-Food Discovery Place, University of Alberta (Edmonton, AB, Canada), using a single-screw extruder (X-115; Wenger, Sabetha, KS) at three extruder screw speeds: low (250 rpm; CM-250), medium (350 rpm; CM-350), or high (450 rpm; CM-450). The flow rate (300 kg/h), the extruder water to feed rate (1:10), and extrusion temperature (from 80 °C in zone 1 to 100 °C in zone 5) were set for the three extrusion processing conditions. The raw CM and the extruded CM were subsequently ground through a hammer mill fitted with a 2.78-mm screen.
Experimental diets and design
Cannulated pig trial (exp. 1)
Four diets were formulated by replacing 50% of an N-free diet with 50% of one of the four CM samples (Table 1). The four test diets exceeded the NRC (2012) requirements for most of the nutrients. The four CM diets were fed to eight pigs over four periods in a double 4 × 4 Latin square design to achieve eight observations per treatment. The basal ileal endogenous loss (Iend) of AA was measured on the same pigs feeding an N-free diet prior to feeding the four test diets. The Cr2O3 was included as an indigestible marker. A horizontal paddle mixer (model 3061; Marion Process Solutions, Marion, IA) was used to mix mash diets.
Table 1.
Item, % as-fed | CM | N-free |
---|---|---|
Test ingredient2 | 50.00 | — |
Corn starch3 | 42.19 | 84.80 |
Sugar | 2.49 | 5.00 |
Cellulose4 | 1.49 | 3.00 |
Canola oil | 1.00 | 2.00 |
Monocalcium phosphate | 0.80 | 1.60 |
Limestone | 0.60 | 1.20 |
Chromic oxide | 0.50 | 0.50 |
Vitamin premix5 | 0.25 | 0.50 |
Mineral premix6 | 0.25 | 0.50 |
K2CO3 | 0.25 | 0.50 |
Salt | 0.15 | 0.30 |
MgO | 0.05 | 0.10 |
1CM, canola meal.
2To create four diets, the four test ingredients were: CM (ground and not extruded), CM-250, CM-350, or CM-450.
3Melojel (National Starch and Chemical Co., Bridgewater, NJ).
4Solka-floc (International Fiber Corp., North Tonawanda, NY).
5Provided the following per kilogram of diet: vitamin A, 7,500 IU; vitamin D, 750 IU; vitamin E, 50 IU; niacin, 37.5 mg; pantothenic acid, 15 mg; folacin, 2.5 mg; riboflavin, 5 mg; pyridoxine, 1.5 mg; thiamine, 2.5 mg; choline, 2,000 mg; vitamin K, 4 mg; biotin, 0.25 mg; and vitamin B12, 0.02 mg.
6Provided the following per kilogram of diet: Zn, 125 mg as ZnSO4; Cu, 50 mg as CuSO4; Fe, 75 mg as FeSO4; Mn, 25 mg as MnSO4; I, 0.5 mg as Ca(IO3)2; and Se, 0.3 mg as Na2SeO3.
Eight crossbred barrows (initial body weight [BW] 68.1 ± 9.4 kg; Duroc × Large White/Landrace F1; Hypor, Regina, SK, Canada) were housed in individual metabolism pens (1.2 m wide, 1.5 m long, and 0.95 m high) with polyvinyl chloride walls with windows and plastic slatted flooring. All pens were equipped with a stainless-steel feeder attached to the front of the pen and a cup drinker beside the feeder assuring free access to water throughout the experiment. Room temperature was controlled at 20.8 ± 1.3 °C. Pigs were surgically fitted with a simple T-cannula at the distal ileum, approximately 5 cm proximal to the ileocecal sphincter (Sauer et al., 1983; de Lange et al., 1989). After measuring basal Iend of AA, pigs were switched to the first assigned experimental diet. Daily feed allowance was adjusted to 2.8 times the maintenance requirement for DE (2.8 × 110 kcal of DE/kg of BW0.75; NRC, 1998) fed in two equal meals at approximately 0800 and 1500 hours. Each 9-d experimental period consisted of a 5-d acclimation to the experimental diet, followed by a 2-d collection of feces and a 2-d collection of ileal digesta.
Feces were collected from 0800 to 1600 hours by using plastic bags within a collection system that was glued to the skin around the anus (van Kleef et al., 1994). Digesta was collected between 0800 to 1600 hours using plastic bags containing 15 mL of 5% formic acid attached to the opened cannula barrel with rubber band (Li et al., 1993). Plastic bags were replaced as soon as filled with digesta or after every 20 min. Feces and digesta samples were pooled for each pig within the experimental period and stored at −20 °C. Upon completion of the trial, digesta and fecal samples were thawed, homogenized, subsampled, and freeze-dried.
Nursery pig performance trial (exp. 2)
In total, 200 pigs were selected from 241 pigs (Duroc × Large White/landrace F1; Hypor, Regina, SK, Canada), weaned in three groups at 21 ± 2 d of age based on postweaning average daily gain (ADG) and BW on day 12 after weaning. Pigs within gender were divided into heavy and light BW. One heavy and one light barrow and gilt were then randomly placed in 1 of the 50 pens, 4 pigs per pen. Prior to weaning, all pigs received creep-feeding. After weaning, pigs were fed commercial pre-starter (20.6% CP and 2.5 Mcal NE/kg) for 7 d and starter (22.9% CP and 2.4 Mcal NE/kg) diets (Masterfeeds, Edmonton, AB, Canada) for 5 d, respectively. Commercial diets were based on wheat, SBM, oat groats, lactose, and highly digestible protein sources.
A wheat-based control diet and four diets containing 20% test ingredient were formulated by replacing SBM with one of the four CM samples (Table 2). Diets were formulated to provide 2.3 Mcal NE/kg and 5.1 g SID Lys/Mcal NE, and crystalline Thr, Met, and Trp were formulated as ideal ratios to Lys (NRC, 2012). For main ingredients, tabulated NE values (Sauvant et al., 2004) and SID AA (NRC, 2012) were used. Diets did not contain antimicrobials or growth promoters. Acid-insoluble ash (Celite 281; World Minerals, Santa Barbara, CA) was added as an indigestible marker. Diets in mash form were mixed at the University of Alberta feed mill (Edmonton, AB, Canada). Pigs (initial BW: 8.3 ± 1.7 kg) were fed the experimental diets starting from 2 wk after weaning for 3 wk (day 1 to 21).
Table 2.
Extruded CM | |||||
---|---|---|---|---|---|
Item, % as-fed | SBM | CM | CM-250 | CM-350 | CM-450 |
Wheat | 68.32 | 65.89 | 65.89 | 65.89 | 65.89 |
SBM | 20.00 | — | — | — | — |
CM | — | 20.00 | 20.00 | 20.00 | 20.00 |
Menhaden fish meal | 5.00 | 5.00 | 5.00 | 5.00 | 5.00 |
Soy protein concentrate2 | 2.50 | 2.50 | 2.50 | 2.50 | 2.50 |
Canola oil | — | 2.12 | 2.12 | 2.12 | 2.12 |
Limestone | 0.80 | 0.63 | 0.63 | 0.63 | 0.63 |
Celite3 | 0.80 | 0.80 | 0.80 | 0.80 | 0.80 |
Salt | 0.75 | 0.75 | 0.75 | 0.75 | 0.75 |
Mono/di-calcium phosphate | 0.55 | 0.60 | 0.60 | 0.60 | 0.60 |
Vitamin premix4 | 0.50 | 0.50 | 0.50 | 0.50 | 0.50 |
Mineral premix5 | 0.50 | 0.50 | 0.50 | 0.50 | 0.50 |
l-Lys HCl, 78% | 0.15 | 0.46 | 0.46 | 0.46 | 0.46 |
l-Thr, 99% | 0.08 | 0.15 | 0.15 | 0.15 | 0.15 |
l-Trp, 99% | — | 0.07 | 0.07 | 0.07 | 0.07 |
dl-Met, 99% | 0.03 | 0.01 | 0.01 | 0.01 | 0.01 |
Choline chloride, 60% | 0.03 | 0.03 | 0.03 | 0.03 | 0.03 |
Analyzed nutrient content6, % DM | |||||
Moisture | 11.5 | 11.5 | 11.2 | 11.7 | 11.4 |
Starch | 39.1 | 35.8 | 39.3 | 38.9 | 41.8 |
CP (N × 6.25) | 29.6 | 27.8 | 26.7 | 26.2 | 27.0 |
NDF | 9.6 | 13.7 | 14.9 | 14.6 | 13.8 |
ADF | 4.2 | 7.1 | 7.4 | 7.4 | 7.2 |
Ash | 7.04 | 6.38 | 6.49 | 6.68 | 6.45 |
Ether extract | 1.42 | 4.16 | 4.21 | 3.96 | 4.08 |
GE, Mcal/kg DM | 4.46 | 4.60 | 4.60 | 4.59 | 4.61 |
1SBM, soybean meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
2HP300 (Hamlet Protein Inc., Findlay, OH).
3Celite 281 (World Minerals Inc., Santa Barbara, CA) used as acid-insoluble ash.
4Provided the following per kilogram of diet: vitamin A, 7,500 IU; vitamin D, 750 IU; vitamin E, 50 IU; niacin, 37.5 mg; pantothenic acid, 15 mg; folacin, 2.5 mg; riboflavin, 5 mg; pyridoxine, 1.5 mg; thiamine, 2.5 mg; choline, 2,000 mg; vitamin K, 4 mg; biotin, 0.25 mg; and vitamin B12, 0.02 mg.
5Provided the following per kilogram of diet: Zn, 125 mg as ZnSO4; Cu, 50 mg as CuSO4; Fe, 75 mg as FeSO4; Mn, 25 mg as MnSO4; I, 0.5 mg as Ca(IO3)2; and Se, 0.3 mg as Na2SeO3.
6Diets were formulated to provide (as-fed): 2.41 Mcal NE/kg, 1.23% SID Lys, 0.36% SID Met, 0.73% SID Thr, and 0.20% SID Trp.
The study was conducted as a randomized complete block design with 50 pens divided over three nursery rooms filled 2 wk apart. Each room had three or four blocks representing areas within the room with five pens per block. Pens of pigs within a block were randomly allocated to be fed one of the five diets during the 21-d study for a total of 10 replicate pens per diet. Pens (1.1 × 1.5 m) were equipped with a dry feeder providing four feeding spaces, nipple drinker, polyvinyl chloride partition, and plastic slatted flooring. Rooms were ventilated using negative pressure, maintained within the thermo-neutral zone for the pigs, and provided a 12:12 (L:D) h (0600 to 1800 hours) cycle. Pigs had free access to feed and water.
To calculate average daily feed intake (ADFI), ADG and feed efficiency as gain:feed (G:F), individual pigs, pen feed added, and orts remaining were weighed weekly. To calculate ATTD of dry matter (DM), GE, and CP, freshly voided feces were collected immediately upon defecation from 0800 to 1500 hours by grab sampling from pen floors and pooled by pen (>500 g/pen) on days 19 and 20. Feces were frozen at −20 °C. Upon completion of the study, feces were thawed, homogenized, subsampled, and freeze-dried.
Chemical analyses
The CM, diets, lyophilized feces, and digesta were ground using a 1-mm screen in a centrifugal mill (model ZM200; Retsch, Haan, Germany) and analyzed for moisture (method 930.15; AOAC, 2006), CP (method 990.03; N × 6.25; AOAC, 2006), and GE using an adiabatic bomb calorimeter (model 5003; Ika-Werke, Staufen, Germany). The CM samples and diets were analyzed for ash (method 942.05; AOAC, 2006), ether extract (method 920.39A; AOAC, 2006), starch (assay kit STA-20; Sigma, St. Louis, MO), acid detergent fiber (ADF) inclusive of residual ash (method 973.18; AOAC, 2006), and neutral detergent fiber (NDF) assayed without heat-stable amylase and expressed inclusive of residual ash (Holst, 1973). The CM samples were analyzed for Ca (method 968.08; AOAC, 2006), P (method 946.06; AOAC, 2006), and total dietary fiber (TDF), soluble and insoluble dietary fiber (method 991.43; AOAC, 2006). The AA content in test ingredients, diets, and digesta was analyzed by high-performance liquid chromatography (method 982.30E; AOAC, 2006), and chemically available Lys was analyzed by spectrophotometry (method 975.44; AOAC, 2006). For exp. 1, diets, feces, and digesta were analyzed for Cr2O3 by spectrophotometry (model 80-2097-62, KBULtraspec III, Pharmacia, Cambridge, UK) at 440 nm after ashing at 450 °C overnight (Fenton and Fenton, 1979). For exp. 2, diets and feces were analyzed for acid-insoluble ash (Vogtmann et al., 1975 modified by Newkirk et al., 2003). Glucosinolate content in CM was measured by gas-liquid chromatography (Daun and McGregor, 1981) at POS Bio-Sciences (Saskatoon, SK, Canada).
Calculations
The AID and ATTD of DM, CP, and GE in diets were calculated using the index method (Adeola, 2001). The difference between ATTD and AID was considered as apparent hindgut fermentation (AHF). Diet NE values were predicted using equation 5 in Noblet et al. (1994) using the determined diet DE value and analyzed content of ADF, starch, CP, and ether extract, as adopted by NRC (2012). Gain:feed was calculated as ADG divided by ADFI for each week and the entire trial.
The basal Iend of AA and CP (g/kg of DM intake) was calculated using the equation for the N-free diet (Stein et al., 2007; equation 3): . The SID for AA was calculated by correcting the AID for basal Iend using the equation (Stein et al., 2007; equation ): .
Statistical analyses
Nutrient digestibility and growth performance data were analyzed using the MIXED procedure of SAS (ver. 9.4; SAS Inst. Inc., Cary, NC). Normality (PROC UNIVARIATE) and homogeneity of variance (PROC GLM, Hovtest = Levene) of the residuals of each variable were examined prior to analysis of variance (ANOVA). For exp. 1, diet was the fixed effect, and square, period nested in square, and pig nested in square were random effects. For exp. 2, pen was the experimental unit with diet and week as fixed effects and block as random effect. Multiple comparisons between least squares means were performed using the PDIFF statement with TUKEY adjustment.
Growth performance data were analyzed as repeated measures using weekly pen data with first-order ante-dependence variance–covariance structure based on the Bayesian information criterion fit statistics and initial BW as a covariate if significant. Single degree of freedom contrasts were used to compare the digestibility and performance of the SBM diet vs. extruded CM diets, non-extruded vs. extruded CM diets, and to detect linear or quadratic effects of increasing extruder speed on the digestibility and growth performance for each week and the entire trial (Littell et al., 2006). Data are presented as least squares means with pooled SEM. To test the hypotheses, P < 0.05 was considered significant and 0.05 ≤ P < 0.10 was considered as tendency.
Results
Cannulated pig trial (exp. 1)
Pigs remained healthy and consumed their daily feed allowance throughout the trial.
Extrusion did not affect CP and TDF but seemed to increase the ADF content of CM (Table 3). Increasing extruder screw speed to 350 rpm seemed to decrease total glucosinolate content in CM by 1.57 µmol/g DM, with pronounced reduction of 4-methoxy-3-CH3-indolyl, 4-OH-3-CH3-indolyl, and phenylethyl content. Among the four CM diets (Table 4), the coefficient of variation (CV) for CP, ADF, NDF, and GE was 1.7%, 2.1%, 2.8%, and 0.1%, respectively.
Table 3.
Extruded CM | ||||
---|---|---|---|---|
Item, % DM | CM | CM-250 | CM-350 | CM-450 |
Moisture | 7.34 | 7.49 | 7.00 | 6.37 |
CP (N × 6.25) | 43.2 | 42.5 | 42.1 | 42.1 |
GE, Mcal/kg | 4.79 | 4.81 | 4.79 | 4.79 |
Ether extract | 3.2 | 2.7 | 2.7 | 3.6 |
NDF | 26.0 | 33.9 | 26.9 | 28.6 |
ADF | 19.7 | 23.4 | 21.8 | 21.7 |
TDF | 33.2 | 34.6 | 33.6 | 33.9 |
Insoluble fiber | 27.9 | 27.8 | 28.1 | 26.9 |
Soluble fiber | 2.30 | 2.46 | 2.39 | 2.33 |
Ash | 8.05 | 7.98 | 7.91 | 7.97 |
P | 1.15 | 1.11 | 1.12 | 1.10 |
Ca | 0.66 | 0.69 | 0.70 | 0.69 |
Indispensable AA | ||||
Arg | 2.52 | 2.46 | 2.44 | 2.45 |
His | 1.13 | 1.08 | 1.07 | 1.07 |
Ile | 1.79 | 1.75 | 1.73 | 1.75 |
Leu | 2.93 | 2.87 | 2.86 | 2.87 |
Lys | 2.35 | 2.32 | 2.32 | 2.33 |
Met | 0.84 | 0.73 | 0.80 | 0.81 |
Phe | 1.73 | 1.71 | 1.67 | 1.67 |
Thr | 1.72 | 1.68 | 1.73 | 1.74 |
Trp | 0.54 | 0.51 | 0.51 | 0.50 |
Val | 2.21 | 2.22 | 2.17 | 2.17 |
Dispensable AA | ||||
Ala | 1.80 | 1.78 | 1.79 | 1.77 |
Asp | 2.90 | 2.83 | 2.84 | 2.86 |
Cys | 1.05 | 1.08 | 1.03 | 1.03 |
Glu | 6.97 | 6.77 | 7.03 | 7.07 |
Gly | 2.05 | 2.09 | 2.07 | 2.00 |
Pro | 2.50 | 2.46 | 2.54 | 2.58 |
Ser | 1.34 | 1.31 | 1.58 | 1.60 |
Tyr | 1.12 | 1.13 | 1.09 | 1.10 |
Total AA | 38.2 | 37.5 | 37.9 | 38.0 |
Chemically available Lys | 2.26 | 2.23 | 2.22 | 2.23 |
Glucosinolates, µmol/g | ||||
2-OH-3-Butenyl | 3.67 | 3.54 | 3.31 | 3.52 |
Epi-2-OH-3-butenyl | 0.13 | 0.11 | 0.10 | 0.11 |
4-CH3-Sulfinyl-butyl | 0.13 | 0.14 | 0.13 | 0.13 |
2-OH-4-Pentenyl | 0.10 | 0.10 | 0.09 | 0.10 |
5-CH3-Sulfinyl-pentyl | 0.61 | 0.59 | 0.53 | 0.58 |
3-Butenyl | 1.85 | 1.78 | 1.66 | 1.78 |
4-OH-3-CH3-Indolyl | 1.48 | 0.82 | 0.78 | 0.89 |
4-Pentenyl | 0.15 | 0.15 | 0.14 | 0.15 |
3-CH3-Indolyl | 0.38 | 0.35 | 0.31 | 0.36 |
Phenylethyl | 0.29 | 0.21 | 0.17 | 0.18 |
4-Methoxy-3-CH3-indolyl | 0.04 | 0.02 | 0.02 | 0.02 |
1-Methoxy-3-CH3-indolyl | 0.04 | 0.04 | 0.03 | 0.04 |
Total glucosinolates | 8.87 | 7.84 | 7.30 | 7.86 |
1CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
Table 4.
Extruded CM | |||||
---|---|---|---|---|---|
Item, % DM | CM | CM-250 | CM-350 | CM-450 | N-free |
Moisture | 8.2 | 7.6 | 7.6 | 7.2 | 9.36 |
Starch | 38.6 | 35.1 | 35.8 | 36.6 | 66.5 |
CP (N × 6.25) | 21.9 | 22.2 | 22.8 | 22.3 | 0.96 |
NDF | 15.2 | 15.6 | 14.6 | 14.9 | 2.01 |
ADF | 11.8 | 11.9 | 12.1 | 11.5 | 2.16 |
Crude fiber | 8.27 | 7.71 | 7.83 | 7.42 | 1.18 |
Ash | 6.43 | 6.43 | 6.48 | 6.41 | 4.01 |
Ether extract | 2.84 | 2.81 | 2.03 | 2.24 | 3.71 |
GE, Mcal/kg | 4.42 | 4.41 | 4.42 | 4.42 | — |
Indispensable AA | |||||
Arg | 1.25 | 1.27 | 1.27 | 1.27 | 0.01 |
His | 0.56 | 0.56 | 0.57 | 0.56 | 0.00 |
Ile | 0.90 | 0.91 | 0.92 | 0.91 | 0.02 |
Leu | 1.49 | 1.52 | 1.52 | 1.51 | 0.04 |
Lys | 1.17 | 1.22 | 1.22 | 1.21 | 0.03 |
Met | 0.40 | 0.41 | 0.42 | 0.42 | 0.01 |
Phe | 0.87 | 0.88 | 0.88 | 0.88 | 0.02 |
Thr | 0.88 | 0.89 | 0.90 | 0.89 | 0.01 |
Trp | 0.27 | 0.26 | 0.25 | 0.26 | 0.02 |
Val | 1.08 | 1.15 | 1.14 | 1.14 | 0.02 |
Dispensable AA | |||||
Ala | 0.91 | 0.94 | 0.94 | 0.93 | 0.02 |
Asp | 1.48 | 1.50 | 1.50 | 1.50 | 0.02 |
Cys | 0.53 | 0.53 | 0.54 | 0.53 | 0.01 |
Glu | 3.60 | 3.69 | 3.69 | 3.67 | 0.04 |
Gly | 1.03 | 1.09 | 1.07 | 1.06 | 0.01 |
Pro | 1.35 | 1.32 | 1.38 | 1.29 | 0.03 |
Ser | 0.72 | 0.73 | 0.74 | 0.74 | 0.01 |
Tyr | 0.54 | 0.55 | 0.56 | 0.54 | 0.01 |
1Diets contained 50% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
Extrusion increased (P < 0.05; Table 5) the AID of CP, reduced (P < 0.05) the AHF of CP, and decreased (P < 0.05) predicted NE value of diets. Increasing extruder screw speed did not affect the AID, ATTD, and AHF of DM, CP, and GE, and the DE and predicted NE values of CM diets.
Table 5.
P-value | ||||||||
---|---|---|---|---|---|---|---|---|
Extruded CM | Extruder speed4 | |||||||
Item | CM | CM-250 | CM-350 | CM-450 | SEM2 | Extrusion of CM3 | Linear | Quadratic |
AID, % | ||||||||
DM | 69.6 | 70.2 | 67.3 | 69.6 | 1.81 | 0.685 | 0.735 | 0.116 |
CP | 73.5 | 77.0 | 75.0 | 76.9 | 1.57 | 0.046 | 0.952 | 0.190 |
GE | 71.9 | 72.7 | 70.0 | 72.0 | 1.69 | 0.795 | 0.708 | 0.124 |
ATTD, % | ||||||||
DM | 79.7 | 79.5 | 79.4 | 79.1 | 0.60 | 0.521 | 0.424 | 0.794 |
CP | 79.2 | 78.1 | 78.8 | 77.8 | 0.77 | 0.151 | 0.734 | 0.219 |
GE | 80.3 | 80.2 | 80.0 | 79.6 | 0.59 | 0.407 | 0.360 | 0.787 |
AHF5, % | ||||||||
DM | 10.0 | 9.3 | 12.2 | 9.5 | 1.92 | 0.855 | 0.946 | 0.118 |
CP | 5.7 | 1.1 | 3.8 | 1.0 | 1.82 | 0.023 | 0.926 | 0.103 |
GE | 8.4 | 7.5 | 10.0 | 7.6 | 1.77 | 0.977 | 0.960 | 0.122 |
DE, Mcal/kg DM | 3.55 | 3.54 | 3.53 | 3.52 | 0.026 | 0.353 | 0.477 | 0.753 |
NE, Mcal/kg DM | 2.42 | 2.38 | 2.38 | 2.38 | 0.018 | 0.025 | 0.676 | 0.813 |
1Diets contained 50% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
2Least squares means based on eight observations per diet.
3Contrast CM vs. extruded CM.
4Analyzed using contrast for the three extruded CM diets.
5AHF = ATTD – AID.
Extrusion increased (P < 0.05; Table 6) the AID of AA except for Lys, Thr, Cys, Gly, Pro, and Ser of CM diets.
Table 6.
P-value | ||||||||
---|---|---|---|---|---|---|---|---|
Extruded CM | Extruder speed4 | |||||||
Item, % | CM | CM-250 | CM-350 | CM-450 | SEM2 | Extrusion of CM3 | Linear | Quadratic |
Indispensable AA | ||||||||
Arg | 84.2 | 89.6 | 88.5 | 89.6 | 0.93 | <0.001 | 0.985 | 0.193 |
His | 83.1 | 86.2 | 85.3 | 86.2 | 0.98 | 0.005 | 0.979 | 0.321 |
Ile | 76.8 | 80.5 | 78.5 | 79.7 | 1.25 | 0.023 | 0.549 | 0.169 |
Leu | 79.1 | 83.2 | 81.3 | 82.4 | 1.17 | 0.005 | 0.527 | 0.172 |
Lys | 79.8 | 82.6 | 80.2 | 81.9 | 1.15 | 0.086 | 0.574 | 0.061 |
Met | 86.0 | 90.6 | 89.8 | 90.7 | 0.65 | <0.001 | 0.931 | 0.162 |
Phe | 79.5 | 83.5 | 81.7 | 82.8 | 1.12 | 0.004 | 0.592 | 0.173 |
Thr | 73.1 | 75.7 | 73.8 | 75.5 | 1.62 | 0.184 | 0.883 | 0.221 |
Trp | 86.4 | 89.4 | 88.3 | 90.2 | 0.94 | 0.002 | 0.374 | 0.083 |
Val | 73.8 | 79.1 | 76.7 | 78.3 | 1.37 | 0.003 | 0.564 | 0.136 |
Dispensable AA | ||||||||
Ala | 77.9 | 81.5 | 79.0 | 80.7 | 1.35 | 0.044 | 0.594 | 0.099 |
Asp | 73.7 | 80.2 | 77.9 | 80.1 | 1.43 | <0.001 | 0.973 | 0.089 |
Cys | 74.7 | 75.6 | 74.4 | 76.8 | 2.22 | 0.667 | 0.613 | 0.391 |
Glu | 84.8 | 88.6 | 87.7 | 88.7 | 0.94 | <0.001 | 0.969 | 0.248 |
Gly | 71.5 | 75.1 | 71.9 | 74.7 | 1.63 | 0.110 | 0.792 | 0.060 |
Pro | 71.0 | 73.2 | 70.1 | 72.6 | 2.45 | 0.634 | 0.810 | 0.217 |
Ser | 76.1 | 79.0 | 77.3 | 79.1 | 1.59 | 0.093 | 0.962 | 0.213 |
Tyr | 80.6 | 84.0 | 82.6 | 83.5 | 1.12 | 0.009 | 0.617 | 0.249 |
Total AA | 77.8 | 81.7 | 79.7 | 81.3 | 1.28 | 0.013 | 0.813 | 0.137 |
1Diets contained 50% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
2Least square means based on eight observations per treatment.
3Contrast CM vs. three extruded CM.
4Analyzed using contrast for the three extruded CM diets.
Similar to the changes in AID, extrusion increased (P < 0.05; Table 7) the SID of CP and AA except for Lys, Thr, Ala, Cys, Gly, Pro, and Ser in CM. Increasing extruder screw speed did not affect the SID of CP and most of the AA in CM.
Table 7.
P-value | ||||||||
---|---|---|---|---|---|---|---|---|
Extruded CM | Extruder speed5 | |||||||
Item, % | CM | CM-250 | CM-350 | CM-450 | SEM3 | Extrusion of CM4 | Linear | Quadratic |
CP | 78.9 | 82.3 | 80.2 | 82.2 | 1.57 | 0.056 | 0.938 | 0.162 |
Indispensable AA | ||||||||
Arg | 86.9 | 92.2 | 91.0 | 92.2 | 0.96 | <0.001 | 0.985 | 0.193 |
His | 85.9 | 88.9 | 88.0 | 89.0 | 1.03 | 0.005 | 0.979 | 0.297 |
Ile | 80.3 | 84.0 | 81.9 | 83.2 | 1.32 | 0.025 | 0.549 | 0.160 |
Leu | 82.6 | 86.7 | 84.8 | 85.9 | 1.22 | 0.006 | 0.539 | 0.169 |
Lys | 83.1 | 85.8 | 83.4 | 85.2 | 1.18 | 0.110 | 0.589 | 0.060 |
Met | 88.2 | 92.7 | 91.8 | 92.7 | 0.68 | <0.001 | 0.988 | 0.151 |
Phe | 82.9 | 86.9 | 85.1 | 86.2 | 1.15 | 0.005 | 0.592 | 0.173 |
Thr | 79.2 | 81.8 | 79.7 | 81.5 | 1.66 | 0.205 | 0.883 | 0.205 |
Trp | 86.4 | 89.4 | 88.3 | 90.3 | 0.94 | 0.002 | 0.374 | 0.083 |
Val | 77.7 | 82.8 | 80.4 | 82.0 | 1.43 | 0.004 | 0.579 | 0.139 |
Dispensable AA | ||||||||
Ala | 82.4 | 85.8 | 83.3 | 85.1 | 1.38 | 0.055 | 0.617 | 0.096 |
Asp | 78.5 | 84.9 | 82.6 | 84.8 | 1.46 | <0.001 | 0.973 | 0.089 |
Cys | 78.5 | 79.4 | 78.1 | 80.5 | 2.30 | 0.676 | 0.613 | 0.373 |
Glu | 87.0 | 90.7 | 89.7 | 90.8 | 0.97 | 0.001 | 0.960 | 0.246 |
Gly | 79.0 | 82.2 | 79.1 | 82.0 | 1.72 | 0.158 | 0.882 | 0.062 |
Pro | 76.7 | 79.1 | 75.7 | 78.6 | 2.54 | 0.604 | 0.851 | 0.172 |
Ser | 81.7 | 84.5 | 82.7 | 84.5 | 1.58 | 0.110 | 0.999 | 0.204 |
Tyr | 84.5 | 87.8 | 86.3 | 87.3 | 1.13 | 0.011 | 0.660 | 0.212 |
Total AA | 83.2 | 87.9 | 85.9 | 87.6 | 1.41 | 0.004 | 0.838 | 0.142 |
1Diets contained 50% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
2The SID of CP and AA was calculated by correcting the AID of CP and AA with the measured basal Iend (g/kg DM intake): CP, 11.82; Arg, 0.33; His, 0.15; Ile, 0.31 Leu, 0.53; Lys, 0.39; Met, 0.09; Phe, 0.30; Thr, 0.54; Trp, 0.12; Val, 0.42; Ala, 0.40; Asp, 0.70; Cys, 0.20; Glu, 0.77; Gly, 0.77; Pro, 0.78; Ser, 0.40; Tyr, 0.21; and total AA, 7.50.
3Least square means based on eight observations per treatment.
4Contrast CM vs. three extruded CM.
5Analyzed using contrast for the three extruded CM diets.
Nursery pig performance trial (exp. 2)
Extrusion did not affect CP, TDF, or soluble fiber content of CM (Table 8). Increasing extruder screw speed to 350 rpm seemed to decrease the total glucosinolate content in CM by 0.8 µmol/g DM, with pronounced reduction of 4-OH-3-CH3-indolyl, epi-2-OH-3-butenyl, and 4-CH3-sulfinyl-butyl content. Among the four CM diets (Table 2), the CV for CP, ADF, NDF, and GE was 2.5%, 2.0%, 4.0%, and 0.2%, respectively.
Table 8.
Extruded CM | |||||
---|---|---|---|---|---|
Item, % DM | SBM | CM | CM-250 | CM-350 | CM-450 |
Moisture | 11.25 | 9.01 | 8.92 | 8.55 | 8.66 |
CP (N × 6.25) | 55.9 | 42.7 | 42.2 | 41.3 | 42.4 |
TDF | 9.0 | 28.3 | 29.0 | 29.4 | 29.4 |
Insoluble fiber | 8.4 | 26.7 | 27.3 | 27.8 | 27.8 |
Soluble fiber | 0.55 | 1.61 | 1.70 | 1.63 | 1.60 |
Ash | 7.6 | 7.4 | 7.2 | 9.6 | 7.3 |
Ca | 0.72 | 0.77 | 0.77 | 1.85 | 0.77 |
P | 0.70 | 1.09 | 1.09 | 1.07 | 1.09 |
Ether extract | 1.6 | 3.4 | 3.2 | 3.2 | 3.0 |
GE, Mcal/kg | 4.78 | 4.85 | 4.82 | 4.69 | 4.82 |
Indispensable AA | |||||
Arg | 3.84 | 2.36 | 2.32 | 2.34 | 2.35 |
His | 1.39 | 1.07 | 1.06 | 1.06 | 1.07 |
Ile | 2.63 | 1.71 | 1.69 | 1.69 | 1.71 |
Leu | 4.14 | 2.83 | 2.81 | 2.82 | 2.82 |
Lys | 3.44 | 2.38 | 2.36 | 2.36 | 2.39 |
Met | 0.73 | 0.80 | 0.79 | 0.77 | 0.78 |
Phe | 2.82 | 1.69 | 1.67 | 1.68 | 1.67 |
Thr | 2.03 | 1.73 | 1.71 | 1.71 | 1.69 |
Trp | 0.74 | 0.45 | 0.46 | 0.44 | 0.47 |
Val | 2.69 | 2.14 | 2.10 | 2.11 | 2.15 |
Total AA | 52.29 | 37.09 | 36.63 | 36.61 | 36.90 |
Chemically available Lys | 3.36 | 2.25 | 2.22 | 2.24 | 2.26 |
Glucosinolates, µmol/g | |||||
2-OH-3-Butenyl | N/A | 2.51 | 2.37 | 2.25 | 2.33 |
Epi-2-OH-3-Butenyl | N/A | 0.09 | 0.07 | 0.06 | 0.06 |
4-CH3-Sulfinyl-butyl | N/A | 0.08 | 0.07 | 0.05 | 0.07 |
2-OH-4-Pentenyl | N/A | 0.05 | 0.05 | 0.04 | 0.04 |
5-CH3-Sulfinyl-pentyl | N/A | 0.21 | 0.19 | 0.16 | 0.20 |
3-Butenyl | N/A | 1.24 | 1.17 | 1.13 | 1.15 |
4-OH-3-CH3-Indolyl | N/A | 0.68 | 0.49 | 0.42 | 0.50 |
4-Pentenyl | N/A | 0.07 | 0.06 | 0.06 | 0.07 |
3-CH3-Indolyl | N/A | 0.25 | 0.23 | 0.21 | 0.24 |
Phenylethyl | N/A | 0.15 | 0.14 | 0.11 | 0.12 |
4-Methoxy-3-CH3-indolyl | N/A | <0.02 | <0.02 | <0.02 | <0.02 |
1-Methoxy-3-CH3-indolyl | N/A | <0.02 | <0.02 | <0.02 | <0.02 |
Total glucosinolates | N/A | 5.31 | 4.85 | 4.51 | 4.78 |
1SBM, soybean meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed.
Compared with SBM diet, extruded CM diets had lower (P < 0.05; Table 9) ATTD of DM, GE, and CP, and DE value. Extruded CM diets had lower (P < 0.01) ATTD of CP than non-extruded CM diet. Increasing extruder speed did not increase the ATTD of DM, GE, and CP, and DE and predicted NE values of the CM diets.
Table 9.
P-value | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Extruded CM | Extruder speed5 | |||||||||
Item, % | SBM | CM | CM-250 | CM-350 | CM-450 | SEM2 | SBM vs. extruded CM3 | Extrusion of CM4 | Linear | Quadratic |
ATTD | ||||||||||
DM | 84.6 | 81.0 | 79.3 | 79.3 | 80.4 | 0.87 | <0.001 | 0.077 | 0.201 | 0.456 |
GE | 83.8 | 80.4 | 78.4 | 78.6 | 80.0 | 1.09 | <0.001 | 0.125 | 0.162 | 0.544 |
CP | 83.8 | 80.8 | 77.0 | 77.0 | 79.4 | 1.21 | <0.001 | 0.005 | 0.052 | 0.268 |
DE, Mcal/kg of DM | 3.73 | 3.70 | 3.61 | 3.61 | 3.69 | 0.050 | 0.024 | 0.121 | 0.131 | 0.383 |
NE, Mcal/kg of DM | 2.52 | 2.52 | 2.48 | 2.48 | 2.54 | 0.035 | 0.472 | 0.536 | 0.081 | 0.296 |
1Diets contained 20% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed; SBM, soybean meal.
2Least squares means based on 10 pen observations of 4 pigs per diet.
3Contrast SBM diet vs. three extruded CM diets.
4Contrast CM diet vs. three extruded CM diets.
5Analyzed using contrast for the three extruded CM diets.
For growth performance, pigs fed extruded CM diets had ADFI and ADG not different from pigs fed the SBM diet for each week and the entire trial (day 1 to 21; Table 10). Compared with non-extruded CM, extrusion of CM did not affect ADFI, ADG, and G:F for each week and the entire trial. Increasing extruder screw speed linearly increased (P < 0.05) ADG for day 1 to 7 and G:F for the entire trail. Final BWs were 19.6, 19.6, 19.2, 19.8, and 19.9 kg for SBM, CM, CM-250, CM-350, and CM-450 diets, respectively, and did not differ between SBM and extruded CM diets nor was final BW affected by extrusion or extruder screw speed.
Table 10.
P-value3 | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
Extruded CM | Extruder speed6 | |||||||||
Item | SBM | CM | CM-250 | CM-350 | CM-450 | SEM2 | SBM vs. extruded CM4 | Extrusion of CM5 | Linear | Quadratic |
ADFI, g | ||||||||||
Day 1 to 7 | 456 | 506 | 489 | 504 | 507 | 37 | 0.139 | 0.840 | 0.622 | 0.839 |
Day 8 to 14 | 802 | 831 | 806 | 811 | 823 | 37 | 0.712 | 0.568 | 0.646 | 0.899 |
Day 15 to 21 | 1,080 | 1,066 | 1,066 | 1,073 | 1,065 | 37 | 0.696 | 0.930 | 0.971 | 0.820 |
Day 1 to 21 | 780 | 801 | 787 | 796 | 798 | 27 | 0.525 | 0.761 | 0.686 | 0.893 |
ADG, g | ||||||||||
Day 1 to 7 | 319 | 356 | 309 | 393 | 400 | 45 | 0.182 | 0.766 | 0.044 | 0.320 |
Day 8 to 14 | 607 | 588 | 568 | 548 | 582 | 45 | 0.256 | 0.556 | 0.752 | 0.475 |
Day 15 to 21 | 671 | 675 | 675 | 700 | 673 | 45 | 0.752 | 0.848 | 0.976 | 0.507 |
Day 1 to 21 | 532 | 540 | 517 | 547 | 552 | 26 | 0.765 | 0.954 | 0.183 | 0.585 |
G:F | ||||||||||
Day 1 to 7 | 0.70 | 0.70 | 0.63 | 0.78 | 0.78 | 0.076 | 0.604 | 0.663 | 0.058 | 0.243 |
Day 8 to 14 | 0.73 | 0.71 | 0.71 | 0.67 | 0.70 | 0.044 | 0.303 | 0.724 | 0.947 | 0.432 |
Day 15 to 21 | 0.59 | 0.63 | 0.64 | 0.65 | 0.63 | 0.032 | 0.090 | 0.832 | 0.846 | 0.445 |
Day 1 to 21 | 0.68 | 0.68 | 0.66 | 0.70 | 0.70 | 0.023 | 0.469 | 0.717 | 0.046 | 0.244 |
1Diets contained 20% canola meal; CM, canola meal, ground but not extruded; CM-250, CM extruded at 250 rpm screw speed; CM-350, CM extruded at 350 rpm screw speed; CM-450, CM extruded at 450 rpm screw speed; SBM, soybean meal.
2Least squares means based on 10 pen observations of 4 pigs per diet.
3For ADFI, ADG, and feed efficiency, a week effect was observed (P < 0.001), but an interaction between diet and week was not observed (P > 0.05).
4Contrast SBM diet vs. three extruded CM diets.
5Contrast CM diet vs. three extruded CM diets.
6Analyzed using contrast for the three extruded CM diets.
Discussion
Nutritive value and extrusion of CM
Solvent-extracted CM, a coproduct from crushing canola seed to obtain oil for the food and biofuel industries, is an important protein source used in pig nutrition (Woyengo et al., 2016a). In the present study, the analyzed content of dietary fiber, CP, and AA in CM was similar to table values (NRC, 2012) and values reported by others (Adewole et al., 2017; Wang et al., 2017). CM contains high fiber, mostly insoluble due to high lignification of canola seed hulls (Bach Knudsen, 2014) that is associated with low digestibility and utilization of nutrients such as AA in pigs (Schulze et al., 1994; Stein and Shurson, 2009). In addition, CM contains anti-nutritional factors (ANF), mainly glucosinolates that may decrease animal performance by reducing feed intake and affecting thyroid and liver functions (Tripathi and Mishra, 2007). Thus, processing strategies to increase nutrient digestibility and increase the feeding value of CM are important (Zhou et al., 2015).
Extrusion cooking can disrupt cell walls, denature protein, emulsify fat, and reduce ANF, such as trypsin inhibitors and tannins in field pea or lentil grain (Cheftel, 1986; Alonso et al., 1998; Singh et al., 2007; Hugman et al., 2021), and may increase the solubility of the fiber fraction (de Vries et al., 2012). However, in the present study, extrusion did not noticeably increase the solubility of dietary fiber in CM in both exp. 1 and 2. Instead, extrusion slightly increased soluble fiber and TDF content in CM. The nutrient composition of the extruded CM using increasing extruder screw speed did not change greatly, indicating that extrusion of CM in a single-screw extruder at the screw speed settings used in the present study did not affect cell wall structure sufficiently (Liang et al., 2002). However, extrusion in the present study reduced glucosinolates content in CM, similar to previous reports that extrusion reduced glucosinolates content in rapeseed meal mostly due to heating (Huang et al., 1995; Tripathi and Mishra, 2007). Extrusion did not reduce chemically available Lys of CM, indicating that Lys damage due to the Maillard reaction was minimal (Pahm et al., 2008) likely because of low retention time in the barrel of the extruder.
Nutrient and energy digestibility of extruded CM (exp. 1)
Extrusion alters the physical and chemical characteristics of feedstuff and may increase the nutritional quality of coproducts such as triticale distillers dried grains with solubles (Oryschak et al., 2010). The dietary fiber components in dark-seeded B. napus CM are mainly water-insoluble non-starch polysaccharides, lignin, and polyphenols (Slominski et al., 2012) that might be difficult to degrade in the gut of pigs. In exp.1, extrusion did not increase diet ATTD of DM and GE, likely reflecting similar content or unaltered physicochemical properties of dietary fiber, protein, and fat among the four CM samples. These results contrast with extrusion increasing the nutrient digestibility and energy value of rapeseed meal (Keady and O′Doherty, 2000) and increasing the solubility and fermentability of fiber in wheat flour (Cheftel, 1986). The DM digestibility and fermentability were not affected by extrusion and extruder screw speed in exp. 1. The major energy-yielding components in CM are protein and fiber, and their digestibility determines the DM and GE digestibility of CM. Collectively, the three extruded CM samples had increased AID of CP, similar to extrusion increasing the in vitro CP digestibility of corn dried distillers grain and solubles (de Vries et al., 2013). However, extrusion did not alter ATTD of CP of CM, which could be explained by less CP entering the large intestine for fermentation and possibly reduced fermentability of CP for extruded CM. The overall picture emerging from the present study indicates that cell wall structures of solvent-extracted B. napus CM were not disrupted sufficiently, not even with increasing extruder screw speeds.
Heat treatment can disrupt the cell wall structure and denature protein and may thereby increase AA digestibility (Cheftel, 1986; Camire, 1991), as observed in wheat- and barley-based diets containing either SBM or cassava (Vande Ginste and De Schrijver, 1998) or diets containing 93.5% extruded corn fed to growing pigs (Rodriguez et al., 2020). In the present study, extrusion increased AID and SID of most indispensable AA except Lys of solvent-extracted CM, indicating that extruded CM contributed more dietary AA to the pig than non-extruded CM. Several factors such as an increase in susceptibility to digestive enzymes due to protein denaturation during extrusion might contribute to the increased AA digestibility (Hendriks and Sritharan, 2002). In the present study, increasing extruder screw speed from 250 to 450 rpm increased the specific mechanical energy from 111 to 133 kcal/kg. However, increased extruder speed did not further increase the SID of most of the AA of CM in growing pigs, indicating that the additional mechanical energy applied to CM did not open up the protein structure further, contrasting to potential better cooking effect due to greater shear force and increased conversion of mechanical energy into thermal energy (Liang et al., 2002).
Extrusion did not increase the DE value of CM because the AID and ATTD of GE of diets were not affected by extrusion or increasing extruder screw speed. In addition, changes in ADF and NDF content or rendering dietary insoluble fiber to soluble fiber due to extrusion were not observed in the present study. This finding is in contrast with extrusion increasing the soluble portion of TDF in wheat, oats, and rice bran that may consequently increase energy digestibility (Gualberto et al., 1997). Fiber is partly fermented in the gastrointestinal tract of pigs and is strongly and negatively correlated with DE value (Fairbairn et al., 1999; Noblet and Le Goff, 2001; Woyengo et al., 2016b). In the present study, extrusion decreased the predicted NE values of CM diets, possibly due to lower measured starch and ether extract content in the diets. The increased extruder screw speed, hence increased mechanical energy, did not further affect the predicted NE values of CM diets.
Diet nutrient digestibility and growth performance in weaned pigs (exp. 2)
Fiber is not only an energy-yielding nutrient in CM but also hinders nutrient digestion. In the present study, CM contained three times more fiber than dehulled SBM (26.7 to 27.8 vs. 8.4% insoluble fiber) that may account for most of the lower ATTD of DM and GE in diets containing CM than SBM (Montoya and Leterme, 2010). In particular, the limited ability of young pigs to digest fiber compared with growing pigs might worsen the situation (Noblet and Shi, 1994). Even though increasing fiber content in CM diets did not affect feed intake, the lower ATTD for GE and CP for extruded CM diets compared with SBM run parallel with the 16% reduction in the ATTD of GE and 9% reduction in the ATTD of CP for rapeseed meal than SBM (Fernández et al., 1986). Extrusion reduced the ATTD of CP of CM diets, possibly due to less CP entering the large intestine for fermentation as shown in exp. 1 and possible lower fermentability for extruded CM. However, extrusion of CM at increasing extruder screw speeds did not increase the nutrient digestibility in CM, likely due to its inability to open up the cell wall structure and alter fiber digestibility.
Pigs maintained growth performance indicating that inclusion of 20% extruded CM can replace SBM in diets for weaned pigs, contrasting earlier studies that reported that young pigs fed diets containing CM had a lower growth rate than pigs fed diets containing SBM (McIntosh et al., 1986; Baidoo et al., 1987). Formulating diets based on equal NE value and SID AA content and achieving equivalent feed intake are the main factors to maintain growth when including high fiber coproducts into pig diets (Woyengo et al., 2014). For example, feeding up to 20% solvent-extracted B. napus CM by replacing SBM in diets did not reduce the growth performance of weaned pigs even 1 wk after weaning (Landero et al., 2011). In addition, lower glucosinolate content compared with cultivars of rapeseed offers a better feeding value of CM from modern canola cultivars (Canola Council of Canada, 2009). Indeed, total glucosinolate content in the CM samples (4.51 to 5.31 µmol/g CM) was slightly greater than that in previous studies (3.84 µmol glucosinolates/g CM; Landero et al., 2011) but did not affect feed intake in weaned pigs, indicating that weaned pigs can tolerate the increased glucosinolates in diets. For day 15 to 21, G:F tended to be greater for pigs fed the extruded CM diets than the SBM diet, indicating that weaned pigs can utilize extruded CM to support growth or had greater gut fill due to increased fiber intake. The greater fiber intake and related lower nutrient digestibility might increase the mass of undigested residue in the gut (Jørgensen et al., 1996; de Lange et al., 2003). Among the non-extruded and extruded CM using increasing extruder screw speeds, G:F did not differ, indicating that extrusion or increased extruder screw speed did not result in better conversion efficiencies for CM diets to support growth. However, the linear increase in ADG in day 1 to 7 and G:F for the entire trial with increasing extruder screw speed requires further investigations.
In conclusion, extrusion of dark-seeded, solvent-extracted B. napus CM increased the ileal digestibility of most indispensable AA in growing pigs, thereby providing more dietary AA from CM to the pig. However, extrusion did not increase the AID and SID of the first-limiting AA Lys. In addition, increased extruder screw speed and thus increased mechanical energy did not increase energy digestibility in growing pigs and did not improve the growth performance in weaned pigs. Weaned pigs can be fed 20% CM or extruded CM instead of SBM in diets formulated to equal NE and SID AA by adding feed-grade AA without reducing growth performance.
Acknowledgments
The funding from the Canola Cluster sponsored by Agriculture and Agri-Food Canada and Canola Council of Canada is gratefully acknowledged. C.M.E.H. acknowledges funding from the German Research Foundation (HE 7840/1-1). We thank Jiancheng Qi and Urbano dos Santos Ruiz for support during extrusion processing; Zahra Dehghani, Jill Hugman, and Rian Talen for support during the pig trial; and Miladel Casano for assistance in laboratory analyses.
Glossary
Abbreviations
- AA
amino acid
- ADF
acid detergent fiber
- ADFI
average daily feed intake
- ADG
average daily gain
- AHF
apparent hindgut fermentation
- AID
apparent ileal digestibility
- ANF
anti-nutritional factors
- ATTD
apparent total tract digestibility
- BW
body weight
- CP
crude protein
- DM
dry matter
- G:F
gain:feed
- GE
gross energy
- Iend
ileal endogenous loss
- NDF
neutral detergent fiber
- NE
net energy
- SID
standardized ileal digestibility
- TDF
total dietary fiber
Conflict of interest statement
All authors declare no real or perceived conflicts of interest.
Literature Cited
- AAFC. 2020. Canada: outlook for principal field crops. Available from http://multimedia.agr.gc.ca/pack/pdf/fco-ppc_202012-eng.pdf [accessed February 08, 2021]
- Adeola, O. 2001. Digestion and balance techniques in pigs. In: Lewis, A. L., and Southern L. L., editors. Swine nutrition. Boca Raton (FL): CRC Press; p. 903–916. [Google Scholar]
- Adewole, D. I., Rogiewicz A., Dyck B., Nyachoti C. M., and Slominski B. A.. . 2017. Standardized ileal digestible amino acid contents of canola meal from Canadian crushing plants for growing pigs. J. Anim. Sci. 95:2670–2679. doi: 10.2527/jas.2017.1372 [DOI] [PubMed] [Google Scholar]
- Alonso, R., Orúe E., and Marzo F.. . 1998. Effects of extrusion and conventional processing methods on protein and antinutritional factor contents in pea seeds. Food Chem. 63:505–512. doi: 10.1016/s0308-8146(98)00037-5 [DOI] [Google Scholar]
- AOAC. 2006. Official methods of analysis. 18th ed. Arlington (VA): Association of Official Analytical Chemists. [Google Scholar]
- Bach Knudsen, K. E. 2014. Fiber and nonstarch polysaccharide content and variation in common crops used in broiler diets. Poult. Sci. 93:2380–2393. doi: 10.3382/ps.2014-03902 [DOI] [PubMed] [Google Scholar]
- Baidoo, S. K., Mitaru B. N., Aherne F. X., and Blair R.. . 1987. The nutritive value of canola meal for early-weaned pigs. Anim. Feed Sci. Technol. 18:45–53. doi: 10.1016/0377-8401(87)90028-9 [DOI] [Google Scholar]
- Bell, J. M. 1993. Factors affecting nutritional value of canola meal: review. Can. J. Anim. Sci. 73:679–697. doi: 10.1139/cjas-2015-0184 [DOI] [Google Scholar]
- Camire, M. E. 1991. Protein functionality modification by extrusion cooking. J. Am. Oil. Chem. Soc. 68:200–205. doi: 10.1007/BF02657770 [DOI] [Google Scholar]
- Canola Council of Canada. 2009. Canola meal feed industry guide. 4th ed. Winnipeg (MB): Canola Council of Canada. [Google Scholar]
- Canola Council of Canada. 2021. Canadian canola supply & disposition. Available from https://www.canolacouncil.org/markets-stats/statistics/meal-supply-and-disposition/ [accessed February 11, 2021].
- CCAC. 2009. The care and use of farm animals in research, teaching and testing. Ottawa (ON, Canada): Canadian Council on Animal Care. [Google Scholar]
- Cheftel, J. C. 1986. Nutritional effects of extrusion-cooking. Food Chem. 20:263–283. doi: 10.1016/0308-8146(86)90096-8 [DOI] [Google Scholar]
- Daun, J. K., and McGregor D. I.. . 1981. Glucosinolate analysis of rapeseed (canola). In: Method of the grain research laboratory. Winnipeg (MB, Canada): Agriculture Canada, Canadian Grain Commission; p. 111–116. [Google Scholar]
- Fairbairn, S. L., Patience J. F., Classen H. L., and Zijlstra R. T.. . 1999. The energy content of barley fed to growing pigs: characterizing the nature of its variability and developing prediction equations for its estimation. J. Anim. Sci. 77:1502–1512. doi: 10.2527/1999.7761502x [DOI] [PubMed] [Google Scholar]
- FAOSTAT. 2021. Food and agriculture organization of the United Nations. Available from http://www.fao.org/faostat/en/#data/QC [accessed February 11, 2021].
- Fenton, T. W., and Fenton M.. . 1979. An improved procedure for the determination of chromic oxide in feed and feces. Can. J. Anim. Sci. 59:631–634. doi: 10.4141/cjas79-081 [DOI] [Google Scholar]
- Fernández, J. A., Jørgensen J. N., and Just A.. . 1986. Comparative digestibility experiments with growing pigs and adult sows. Anim. Prod. 43:127–132. doi: 10.1017/S0003356100018419 [DOI] [Google Scholar]
- Gualberto, D. G., Bergman C. J., Kazemzadeh M., and Weber C. W.. . 1997. Effect of extrusion processing on the soluble and insoluble fiber, and phytic acid contents of cereal brans. Plant Foods Hum. Nutr. 51:187–198. doi: 10.1023/a:1007941032726 [DOI] [PubMed] [Google Scholar]
- Hansen, J. Ø., Øverland M., Skrede A., Anderson D. M., and Collins S. A.. . 2020. A meta-analysis of the effects of dietary canola/double low rapeseed meal on growth performance of weanling and growing finishing pigs. Anim. Feed Sci. Technol. 259:114302. doi: 10.1016/j.anifeedsci.2019.114302 [DOI] [Google Scholar]
- Hendriks, W. H., and Sritharan K.. . 2002. Apparent ileal and fecal digestibility of dietary protein is different in dogs. J. Nutr. 132(6 Suppl 2):1692S–1694S. doi: 10.1093/jn/132.6.1692S [DOI] [PubMed] [Google Scholar]
- Holst, D. O. 1973. Holst filtration apparatus for Van Soest detergent fiber analyses. J. Assoc. Off. Anal. Chem. 56:1352–1356. doi: 10.1093/jaoac/56.6.1352 [DOI] [Google Scholar]
- Huang, S., Liang M., Lardy G., Huff H. E., Kerley M. S., and Hsieh F.. . 1995. Extrusion processing of rapeseed meal for reducing glucosinolates. Anim. Feed Sci. Technol. 56:1–9. doi: 10.1016/0377-8401(95)00826-9 [DOI] [Google Scholar]
- Hugman, J., Wang L. F., Beltranena E., Htoo J. K., Vasanthan T., and Zijlstra R. T.. . 2021. Energy and amino acid digestibility of raw, steam-pelleted and extruded red lentil in growing pigs. Anim. Feed Sci. Technol. 275:114838. doi: 10.1016/j.anifeedsci.2021.114838 [DOI] [Google Scholar]
- Jørgensen, H., Zhao X.-Q., and Eggum B. O.. . 1996. The influence of dietary fibre and environmental temperature on the development of the gastrointestinal tract, digestibility, degree of fermentation and the hind-gut and energy metabolism in pigs. Br. J. Nutr. 75:365–378. doi: 10.1079/BJN19960140 [DOI] [PubMed] [Google Scholar]
- Keady, U., and O′Doherty J. V.. . 2000. The effect of extrusion on the nutritive value of rapeseed meal for growing and finishing pigs. Irish J. Agr. Food Res. 39:419–431. [Google Scholar]
- van Kleef, D. J., Deuring K., and van Leeuwen P.. . 1994. A new method of faeces collection in the pig. Lab. Anim. 28:78–79. doi: 10.1258/002367794781065942 [DOI] [PubMed] [Google Scholar]
- Lancheros, J. P., Espinosa C. D., and Stein H. H.. . 2020. Effects of particle size reduction, pelleting, and extrusion on the nutritional value of ingredients and diets fed to pigs: a review. Anim. Feed Sci. Technol. 268:114603. doi: 10.1016/j.anifeedsci.2020.114603 [DOI] [Google Scholar]
- Landero, J. L., Beltranena E., Cervantes M., Morales A., and Zijlstra R. T.. . 2011. The effect of feeding solvent-extracted canola meal on growth performance and diet nutrient digestibility in weaned pigs. Anim. Feed Sci. Technol. 170:136–140. doi: 10.1016/j.anifeedsci.2011.08.003 [DOI] [Google Scholar]
- de Lange, C. F. M., Morel P. C. H., and Birkett S. H.. . 2003. Modeling chemical and physical body composition of the growing pig. J. Anim. Sci. 81:E159–165. doi: 10.2527/2003.8114_suppl_2E159x [DOI] [Google Scholar]
- de Lange, C. F. M., Sauer W. C., Mosenthin R., and Souffrant W. B.. . 1989. The effect of feeding different protein-free on the recovery and amino acid composition of endogenous protein collected from the distal ileum and feces in pigs. J. Anim. Sci. 67:746–754. doi: 10.2527/jas1989.673746x [DOI] [PubMed] [Google Scholar]
- Li, S., Sauer W. C., and Fan M. Z.. . 1993. The effect of dietary crude protein level on ileal and fecal amino acid digestibility in early weaned pigs. J. Anim. Physiol. Anim. Nutr. 70:26–37. doi: 10.1111/j.1439-0396.1993.tb00314.x [DOI] [Google Scholar]
- Liang, M., Huang S., Huff H. E., Kerley M. S., and Hsieh F.. . 2002. Extrusion cooking of rapeseed meal for feeding value improvement. Appl. Eng. Agric. 18:325–330. doi: 10.13031/2013.8584 [DOI] [Google Scholar]
- Littell, R. C., Milliken G. A., Stroup W. W., Wolfinger R. D., and Schabenberger O.. . 2006. SAS for mixed models. 2nd ed. Cary (NC): SAS Institute, Inc. [Google Scholar]
- McDougall, G. J., Morrison I. M., Stewart D., and Hillman J. R.. . 1996. Plant cell walls as dietary fibre: range, structure, processing and function. J. Sci. Food Agric. 70:133–150. doi: [DOI] [Google Scholar]
- McIntosh, M. K., Baidoo S. K., Aherne F. X., and Bowland J. P.. . 1986. Canola meal as a protein supplement for 6 to 20 kilogram pigs. Can. J. Anim. Sci. 66:1051–1056. doi: 10.4141/cjas86-115 [DOI] [Google Scholar]
- Montoya, C. A., and Leterme P.. . 2010. Validation of the net energy content of canola meal and full-fat canola seeds in growing pigs. Can. J. Anim. Sci. 90:213–219. doi: 10.4141/CJAS09054 [DOI] [Google Scholar]
- Newkirk, R. 2009. Canola meal feed industry guide. 4th ed. Winnipeg (MB, Canada): Canola Council of Canada. [Google Scholar]
- Newkirk, R. W., Classen H. L., Scott T. A., and Edney M. J.. . 2003. The digestibility and content of amino acids in toasted and non-toasted canola meals. Can. J. Anim. Sci. 83:131–139. doi: 10.4141/A02-028 [DOI] [Google Scholar]
- Noblet, J., Fortune H., Shi X. S., and Dubois S.. . 1994. Prediction of net energy value of feeds for growing pigs. J. Anim. Sci. 72:344–354. doi: 10.2527/1994.722344x [DOI] [PubMed] [Google Scholar]
- Noblet, J., and Le Goff G.. . 2001. Effect of dietary fibre on the energy value of feeds for pigs. Anim. Feed Sci. Technol. 90:35–52. doi: 10.1016/S0377-8401(01)00195-X [DOI] [Google Scholar]
- Noblet, J., and Shi X. S.. . 1994. Effect of body weight on digestive utilization of energy and nutrients of ingredients and diets in pigs. Livest. Prod. Sci. 37:323–338. doi: 10.1016/0301-6226(94)90126-0 [DOI] [Google Scholar]
- NRC. 1998. Nutrient requirements of swine. 10th rev. ed. Washington (DC): National Academies Press. [Google Scholar]
- NRC. 2012. Nutrient requirements of swine. 11th rev. ed. Washington (DC): National Academies Press. [Google Scholar]
- Oryschak, M., Korver D., Zuidhof M., and Beltranena E.. . 2010. Nutritive value of single-screw extruded and nonextruded triticale distillers dried grains with solubles, with and without an enzyme complex, for broilers. Poult. Sci. 89:1411–1423. doi: 10.3382/ps.2009-00619 [DOI] [PubMed] [Google Scholar]
- Pahm, A. A., Pedersen C., and Stein H. H.. . 2008. Application of the reactive lysine procedure to estimate lysine digestibility in distillers dried grains with solubles fed to growing pigs. J. Agric. Food Chem. 56:9441–9446. doi: 10.1021/jf801618g [DOI] [PubMed] [Google Scholar]
- Rodriguez, D. A., Lee S. A., Jones C. K., Htoo J. K., and Stein H. H.. . 2020. Digestibility of amino acids, fiber, and energy by growing pigs, and concentrations of digestible and metabolizable energy in yellow dent corn, hard red winter wheat, and sorghum may be influenced by extrusion. Anim. Feed Sci. Technol. 268:114602. doi: 10.1016/j.anifeedsci.2020.114602 [DOI] [Google Scholar]
- Rojas, O. J., and Stein H. H.. . 2017. Processing of ingredients and diets and effects on nutritional value for pigs. J. Anim. Sci. Biotechnol. 8:48. doi: 10.1186/s40104-017-0177-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sauer, W. C., Jørgensen H., and Berzins R.. . 1983. The modified nylon bag technique for determining apparent digestibilities of protein in feedstuffs for pigs. Can. J. Anim. Sci. 63:233–237. doi: 10.4141/cjas83-027 [DOI] [Google Scholar]
- Sauvant, D., Perez J. M., and Tran G.. . 2004. Tables of composition and nutritional value of feed materials: pigs, poultry, cattle, sheep, goats, rabbits, horses and fish. Wageningen (The Netherlands): Wageningen Academic Publishers. [Google Scholar]
- Schulze, H., van Leeuwen P., Verstegen M. W., Huisman J., Souffrant W. B., and Ahrens F.. . 1994. Effect of level of dietary neutral detergent fiber on ileal apparent digestibility and ileal nitrogen losses in pigs. J. Anim. Sci. 72:2362–2368. doi: 10.2527/1994.7292362x [DOI] [PubMed] [Google Scholar]
- Singh, S., Gamlath S., and Wakeling L.. . 2007. Nutritional aspects of food extrusion: a review. Int. J. Food Sci. Technol. 42:916–929. doi: 10.1111/j.1365-2621.2006.01309.x [DOI] [Google Scholar]
- Slominski, B. A., Jia W., Rogiewicz A., Nyachoti C. M., and Hickling D.. . 2012. Low-fiber canola. Part 1. Chemical and nutritive composition of the meal. J. Agric. Food Chem. 60:12225–12230. doi: 10.1021/jf302117x [DOI] [PubMed] [Google Scholar]
- Stein, H. H., Sève B., Fuller M. F., Moughan P. J., and de Lange C. F.. . 2007. Invited Review: Amino acid bioavailability and digestibility in pig feed ingredients: terminology and application. J. Anim. Sci. 85:172–180. doi: 10.2527/jas.2005-742 [DOI] [PubMed] [Google Scholar]
- Stein, H. H., and Shurson G. C.. . 2009. BOARD-INVITED REVIEW: The use and application of distillers dried grains with solubles in swine diets. J. Anim. Sci. 87:1292–1303. doi: 10.2527/jas.2008-1290 [DOI] [PubMed] [Google Scholar]
- Tripathi, M. K., and Mishra A. S.. . 2007. Glucosinolates in animal nutrition: a review. Anim. Feed Sci. Technol. 132:1–27. doi: 10.1016/j.anifeedsci.2006.03.003 [DOI] [Google Scholar]
- Vande Ginste, J., and De Schrijver R.. . 1998. Expansion and pelleting of starter, grower and finisher diets for pigs: effects on nitrogen retention, ileal and total tract digestibility of protein, phosphorus and calcium and in vitro protein quality. Anim. Feed Sci. Technol. 72:303–314. doi: 10.1016/S0377-8401(97)00192-2 [DOI] [Google Scholar]
- Vogtmann, H., Pfirter H. P., and Prabucki A. L.. . 1975. A new method of determining metabolisability of energy and digestibility of fatty acids in broiler diets. Br. Poult. Sci. 16:531–534. doi: 10.1080/00071667508416222 [DOI] [PubMed] [Google Scholar]
- de Vries, S., Pustjens A. M., Schols H. A., Hendriks W. H., and Gerrits W. J. J.. . 2012. Improving digestive utilization of fiber-rich feedstuff in pigs and poultry by processing and enzyme technologies: a review. Anim. Feed Sci. Technol. 178:123–138. doi: 10.1016/j.anifeedsci.2012.10.004 [DOI] [Google Scholar]
- de Vries, S., Pustjens A. M., Kabel M. A., Salazar-Villanea S., Hendriks W. H., and Gerrits W. J. J.. . 2013. Processing technologies and cell wall degrading enzymes to improve nutritional value of dried distillers grain with solubles for animal feed: an in vitro digestion study. J. Agric. Food Chem. 61:8821–8828. doi: 10.1021/jf4019855 [DOI] [PubMed] [Google Scholar]
- Wang, L. F., Beltranena E., and Zijlstra R. T.. . 2017. Diet nutrient digestibility and growth performance of weaned pigs fed Brassica napus canola meal varying in nutritive quality. Anim. Feed Sci. Technol. 223:90–98. doi: 10.1016/j.anifeedsci.2016.11.011 [DOI] [Google Scholar]
- Woyengo, T. A., Beltranena E., and Zijlstra R. T.. . 2014. Controlling feed cost by including alternative ingredients into pig diets: a review. J. Anim. Sci. 92:1293–1305. doi: 10.2527/jas2013-7169 [DOI] [PubMed] [Google Scholar]
- Woyengo, T. A., Jha R., Beltranena E., and Zijlstra R. T.. . 2016b. In vitro digestion and fermentation characteristics of canola co-products simulate their digestion in the pig intestine. Animal 10:911–918. doi: 10.1017/S1751731115002566 [DOI] [PubMed] [Google Scholar]
- Woyengo, T. A., Sánchez J. E., Yán͂ez J., Beltranena E., Cervantes M., Morales A., and Zijlstra R. T.. . 2016a. Nutrient digestibility of canola co-products for grower pigs. Anim. Feed Sci. Technol. 222:7–16. doi: 10.1016/j.anifeedsci.2016.09.009 [DOI] [Google Scholar]
- Zhou, X., Zijlstra R. T., and Beltranena E.. . 2015. Nutrient digestibility of solvent-extracted Brassica napus and Brassica juncea canola meals and their air-classified fractions fed to ileal-cannulated grower pigs. J. Anim. Sci. 93:217–228. doi: 10.2527/jas.2014-7451 [DOI] [PubMed] [Google Scholar]