TY - JOUR
T1 - Development of an in vitro protein digestibility assay mimicking the chicken digestive tract
AU - Bryan, Dervan D.S.L.
AU - Abbott, Dawn A.
AU - Classen, Henry L.
N1 - Funding Information:
The authors would like to acknowledge the National Science and Engineering Research Council (NSERC), Industrial Research Chair Program for financial support for this project (Grant No. IRCSA 452664-12 ). Funding for this program was derived from Aviagen , Canadian Poultry Research Council , Chicken Farmers of Saskatchewan , NSERC, Ontario Poultry Industry Council , Prairie Pride Natural Foods Ltd. , Saskatchewan Egg Producers , Saskatchewan Hatching Egg Producers , Saskatchewan Turkey Producers , Sofina Foods Inc. and the University of Saskatchewan .
Funding Information:
The authors would like to acknowledge the National Science and Engineering Research Council (NSERC), Industrial Research Chair Program for financial support for this project (Grant No. IRCSA 452664-12). Funding for this program was derived from Aviagen, Canadian Poultry Research Council, Chicken Farmers of Saskatchewan, NSERC, Ontario Poultry Industry Council, Prairie Pride Natural Foods Ltd., Saskatchewan Egg Producers, Saskatchewan Hatching Egg Producers, Saskatchewan Turkey Producers, Sofina Foods Inc. and the University of Saskatchewan.
Publisher Copyright:
© 2018 Chinese Association of Animal Science and Veterinary Medicine
PY - 2018/12
Y1 - 2018/12
N2 - It is difficult to obtain in vivo digestion kinetics data of high protein ingredients using chickens. Collecting kinetics data requires repeated sampling of digesta from the small intestine during the digestion process, which is not easily accomplished due to the anatomical structure of chicken digestive tract. An in vitro technique is proposed for measuring the digestion kinetics of protein sources fed to chickens. The method has a 30 min gastric and 3 h intestinal phase. Five hundred milligram crude protein (CP) equivalent of each meal sample (CP = % N × 6.25) was digested with pepsin (28,260 units) in 50 mL polyethylene centrifuge tubes for 30 min in a shaking water bath (150 strokes/min; 30 mm stroke length) at 41 °C. The 6.5 mL pancreatin was selected as the enzyme concentration for the intestinal phase, during which time 500 μL aliquots were collected at 0, 15, 30, 45, 60, 90, 120, 150, 180 and 240 min. Samples were diluted 1:820 with HCl and sodium acetate buffer, and then mixed with ninhydrin reagent (2:1) at 100 ± 2 °C for 15 min and spectrometric readings taken at 568 nm. To validate the assay, 5 replications of soybean meal (SBM), corn gluten meal (CGM), corn distillers dried grains with solubles (CDDGS), porcine meal (PCM), fish meal (FM) and casein (CA) were digested. The digestion data were modeled with PROC NLIN procedure, and the intra coefficient of variation (CV) assessed using PROC MEANS of SAS 9.4. The digestion values at 180 min were SBM 95 ± 4, FM 93 ± 3, PCM 68 ± 4, CGM 82 ± 3 and CDDGS 70 ± 2. Intra CV for SBM, CGM, CDDGS, PCM and FM were 5%, 5%, 12%, 10% and 2%, respectively. The estimated fractional digestion rates for SBM, CGM, CDDGS, FM and PCM were 0.023, 0.013, 0.009, 0.024 and 0.013, respectively. In conclusion, the proposed in vitro technique estimated the rate and extent of the digestion of CP for the meals with low intra CV.
AB - It is difficult to obtain in vivo digestion kinetics data of high protein ingredients using chickens. Collecting kinetics data requires repeated sampling of digesta from the small intestine during the digestion process, which is not easily accomplished due to the anatomical structure of chicken digestive tract. An in vitro technique is proposed for measuring the digestion kinetics of protein sources fed to chickens. The method has a 30 min gastric and 3 h intestinal phase. Five hundred milligram crude protein (CP) equivalent of each meal sample (CP = % N × 6.25) was digested with pepsin (28,260 units) in 50 mL polyethylene centrifuge tubes for 30 min in a shaking water bath (150 strokes/min; 30 mm stroke length) at 41 °C. The 6.5 mL pancreatin was selected as the enzyme concentration for the intestinal phase, during which time 500 μL aliquots were collected at 0, 15, 30, 45, 60, 90, 120, 150, 180 and 240 min. Samples were diluted 1:820 with HCl and sodium acetate buffer, and then mixed with ninhydrin reagent (2:1) at 100 ± 2 °C for 15 min and spectrometric readings taken at 568 nm. To validate the assay, 5 replications of soybean meal (SBM), corn gluten meal (CGM), corn distillers dried grains with solubles (CDDGS), porcine meal (PCM), fish meal (FM) and casein (CA) were digested. The digestion data were modeled with PROC NLIN procedure, and the intra coefficient of variation (CV) assessed using PROC MEANS of SAS 9.4. The digestion values at 180 min were SBM 95 ± 4, FM 93 ± 3, PCM 68 ± 4, CGM 82 ± 3 and CDDGS 70 ± 2. Intra CV for SBM, CGM, CDDGS, PCM and FM were 5%, 5%, 12%, 10% and 2%, respectively. The estimated fractional digestion rates for SBM, CGM, CDDGS, FM and PCM were 0.023, 0.013, 0.009, 0.024 and 0.013, respectively. In conclusion, the proposed in vitro technique estimated the rate and extent of the digestion of CP for the meals with low intra CV.
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U2 - 10.1016/j.aninu.2018.04.007
DO - 10.1016/j.aninu.2018.04.007
M3 - Article
AN - SCOPUS:85047871485
SN - 2405-6545
VL - 4
SP - 401
EP - 409
JO - Animal Nutrition
JF - Animal Nutrition
IS - 4
ER -