Ultrafiltration performance and recovery of bioactive peptides after fractionation of tryptic hydrolysate generated from pressure-treated β-lactoglobulin
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Ultrafiltration performance and recovery of bioactive peptides after fractionation of tryptic hydrolysate generated from pressure-treated β-lactoglobulin. / Boukil, Abir; Suwal, Shyam; Chamberland, Julien; Pouliot, Yves; Doyen, Alain.
In: Journal of Membrane Science, Vol. 556, 2018, p. 42-53.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Ultrafiltration performance and recovery of bioactive peptides after fractionation of tryptic hydrolysate generated from pressure-treated β-lactoglobulin
AU - Boukil, Abir
AU - Suwal, Shyam
AU - Chamberland, Julien
AU - Pouliot, Yves
AU - Doyen, Alain
PY - 2018
Y1 - 2018
N2 - High hydrostatic pressure-assisted enzymatic digestion of β-LG accelerated protein digestion but drastically modified the resulting peptide profile, which may affect the performance of ultrafiltration (UF) which is used to fractionate the hydrolysates. Consequently, the aim of this work was to evaluate the change in UF performance of tryptic hydrolysates generated after β-LG pre-pressurization at 0.1 (control), 400 and 600 MPa. Compared to the other conditions, high peptide relative abundance, including abundance of several bioactive peptides, was observed for the 400 MPa hydrolysate. During total recirculation and concentration mode, the permeate flux of the 400 MPa hydrolysate was lower than for other conditions. After peptide desorption from the membrane, ALPHMIR, an antihypertensive peptide, was identified as the main fouling material. For the 400 MPa condition, a larger number of peptides, mainly negatively charged and with higher relative abundance in the hydrolysate, were identified on the membrane surface compared to other conditions. While the repulsion phenomenon should occur between these peptides and the membrane material, both negatively charged, their detection at membrane surface is due to a size effect and hydrophobic interaction rather than a charge mechanism. Consequently, even if pressure treatment of β-LG improved the production of bioactive peptides, it is necessary to optimize hydrodynamic conditions or membrane material during filtration to minimize loss of UF performance.
AB - High hydrostatic pressure-assisted enzymatic digestion of β-LG accelerated protein digestion but drastically modified the resulting peptide profile, which may affect the performance of ultrafiltration (UF) which is used to fractionate the hydrolysates. Consequently, the aim of this work was to evaluate the change in UF performance of tryptic hydrolysates generated after β-LG pre-pressurization at 0.1 (control), 400 and 600 MPa. Compared to the other conditions, high peptide relative abundance, including abundance of several bioactive peptides, was observed for the 400 MPa hydrolysate. During total recirculation and concentration mode, the permeate flux of the 400 MPa hydrolysate was lower than for other conditions. After peptide desorption from the membrane, ALPHMIR, an antihypertensive peptide, was identified as the main fouling material. For the 400 MPa condition, a larger number of peptides, mainly negatively charged and with higher relative abundance in the hydrolysate, were identified on the membrane surface compared to other conditions. While the repulsion phenomenon should occur between these peptides and the membrane material, both negatively charged, their detection at membrane surface is due to a size effect and hydrophobic interaction rather than a charge mechanism. Consequently, even if pressure treatment of β-LG improved the production of bioactive peptides, it is necessary to optimize hydrodynamic conditions or membrane material during filtration to minimize loss of UF performance.
KW - Bioactive Peptides
KW - High hydrostatic pressure
KW - Tryptic hydrolysis
KW - Ultrafiltration membrane fouling
KW - β-lactoglobulin
U2 - 10.1016/j.memsci.2018.03.079
DO - 10.1016/j.memsci.2018.03.079
M3 - Journal article
VL - 556
SP - 42
EP - 53
JO - Journal of Membrane Science
JF - Journal of Membrane Science
SN - 0376-7388
ER -
ID: 204113900