2020
DOI: 10.1016/j.anifeedsci.2019.114340
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Predicting the standardized ileal digestibility of crude protein in feather meal fed to broiler chickens using a pH-stat and a FT-Raman method

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Cited by 6 publications
(6 citation statements)
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“…Stretching vibrations located at 510 cm −1 , 516–530 cm − 1 , and 535–545 cm −1 have been assigned to gauche–gauche–gauche, gauche–gauche–trans, and trans–gauche–trans, where the –C–S–S–C– torsion angle of 90° was represented as gauche form and that of 180° was represented as trans form [ 45 ]. Due to its low potential energy, the gauche–gauche–gauche form was presumably the most stable among the others [ 46 ]. Quantitative analysis of FT-IR spectroscopy showed stable bands located at 510 cm −1 in CG and SCG and disappeared with the increment of starch addition.…”
Section: Resultsmentioning
confidence: 99%
“…Stretching vibrations located at 510 cm −1 , 516–530 cm − 1 , and 535–545 cm −1 have been assigned to gauche–gauche–gauche, gauche–gauche–trans, and trans–gauche–trans, where the –C–S–S–C– torsion angle of 90° was represented as gauche form and that of 180° was represented as trans form [ 45 ]. Due to its low potential energy, the gauche–gauche–gauche form was presumably the most stable among the others [ 46 ]. Quantitative analysis of FT-IR spectroscopy showed stable bands located at 510 cm −1 in CG and SCG and disappeared with the increment of starch addition.…”
Section: Resultsmentioning
confidence: 99%
“…According to Kim et al (2011) poultry byproduct meal can vary in protein quality [24]. This variation may be due to differences in the origin of the raw material or differences in processing conditions [25].…”
Section: Resultsmentioning
confidence: 99%
“…The optimum temperature of Novozymes 37071 protease is 50 °C; pH is adjusted to 9.0 with a PB-10 pH meter (Sartorius Corporation, Gottingen, Germany), then the amount of Novozymes 37071 protease is set at 5% of protein content. The hydrolysates with different DH can be obtained by controlling enzymolysis time with a pH-stat method [ 12 ]. After the reaction, solutions were heated at 100 °C for 5 min to inactivate the enzymes and centrifuged (CR 22GIII, HITACHI, Tokyo, Japan) at 4000× g for 30 min.…”
Section: Methodsmentioning
confidence: 99%