2019
DOI: 10.1080/09712119.2019.1651318
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Amino acid release patterns of growing pig diets formulated with different dietary protein sources

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Cited by 4 publications
(4 citation statements)
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“…In addition, the poor digestibility of plant-based proteins in piglets may be due to incomplete development of digestive enzymes [ 24 ]. Abdallah et al [ 13 ] compared the in vitro digestion of SBM, fish meal, CGM, and fermented SBM over 28 h, and found that the FAA release from CGM diet was significantly lower than the release from the other diets at between 8 and 20 h, and did not reach the same level until 24 to 28 h, which indicates that AA are released more slowly from CGM. In the present study, we found that the peak AA release from CAS during trypsin digestion was within 0 to 4 h, whereas the peak AA release from CGM was at 16 to 20 h. The slow release of AA from CGM proteins, in contrast to the fast release of the added FAA, exaggerates the degree of AA imbalance associated with this diet.…”
Section: Discussionmentioning
confidence: 99%
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“…In addition, the poor digestibility of plant-based proteins in piglets may be due to incomplete development of digestive enzymes [ 24 ]. Abdallah et al [ 13 ] compared the in vitro digestion of SBM, fish meal, CGM, and fermented SBM over 28 h, and found that the FAA release from CGM diet was significantly lower than the release from the other diets at between 8 and 20 h, and did not reach the same level until 24 to 28 h, which indicates that AA are released more slowly from CGM. In the present study, we found that the peak AA release from CAS during trypsin digestion was within 0 to 4 h, whereas the peak AA release from CGM was at 16 to 20 h. The slow release of AA from CGM proteins, in contrast to the fast release of the added FAA, exaggerates the degree of AA imbalance associated with this diet.…”
Section: Discussionmentioning
confidence: 99%
“…Following the methods of Bai et al [ 12 ] and Abdallah et al [ 13 ] which was modified from the method developed by Boisen and Fernández [ 11 ], 1 g of each feed sample (measured to 0.001 g) was placed in 100 mL conical flasks, with three replicates per diet. Ten milliliters of freshly prepared 1 mg/mL pepsin (pH 2) and 0.5 mL chloramphenicol solution (0.5 g chloramphenicol in 100 mL ethanol) were added to the conical flasks, which were sealed and incubated in a water bath oscillator at 39°C for 4 h. At the end of the incubation, the conical flasks were removed, 10 mL phosphate buffer (pH 6.8) was added, and the pH was adjusted to 6.8 using 1 M NaOH.…”
Section: Methodsmentioning
confidence: 99%
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