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1 ve approach which can provide added value to whey.
2 hibited higher rate of lactose hydrolysis in whey.
3 or pure lactose and 38% for raw lactose from whey.
4 etection of adulteration of milk with rennet whey.
5 Lactose is obtained as a by-product from whey.
6 both milks, with higher values for the camel whey.
7 tion was used to add value to sweet defatted whey.
8 ud using the fatty acid profiles of milk and whey.
9 mukat/kg for acid (pH 4.4) or sweet (pH 6.6) whey.
10 ile this protein was totally absent in camel whey.
12 low frequencies and voltage OH processes on whey acerola-flavoured drinks should be performed at low
15 cell (PcSC) subset and a more differentiated whey acidic protein-positive (WAP+) cell subset in mamma
17 tured from cow or goat milk, with or without whey adjustment, or hydrolysates of cow whey proteins, w
18 d to the estimated protein concentrations in whey, allowing direct analysis without sample preparatio
19 d beta-lactoglobulin from sheep cheese sweet whey, an under-utilized by-product of cheese manufacture
21 ollowing isocaloric supplements (45-48 g/d): whey and calcium (whey+), whey, soy, or maltodextrin (co
22 e the in vitro gastric digestion behavior of whey and casein proteins in a heat-treated semisolid rea
28 tification of these macromolecules in cheese whey and the detection of adulteration of milk with renn
29 ning extensively hydrolyzed bovine proteins (whey and/or casein) with use of any other formula for CM
30 strains, defined sugar-rich diets containing whey as the protein source or a matched amino acid mixtu
31 criminant analysis to differentiate milk and whey, as they are present in quite different amounts.
32 that the MRPs derived from electro-activated whey at a concentration of 14% had the highest potential
35 dy of newborn infants assigned to a standard whey-based formula containing a total of 10(7) colony-fo
37 improve the properties of the guava-flavored whey beverages (increased concentration of bioactive and
40 ic current intensity (400, 500 or 600mA) and whey concentration (7, 14 or 21% (w/v)) as a function of
42 for the evaluation of milk adulteration with whey, contributing to the quality control of milk in the
46 ing and interfacial properties of acid camel whey, even if acid and sweet bovine whey exhibited the h
47 id camel whey, even if acid and sweet bovine whey exhibited the highest viscoelastic modulus after he
50 bserved for acid whey when compared to sweet whey for both milks, with higher values for the camel wh
52 and 18MPa at 35+/-2 degrees C for 10min) on whey-grape juice drink characteristics was investigated.
55 Culture media containing whey (W; 2.1g/L) or whey hydrolysate (WH; 2.4 g/L) gave the highest HA produ
56 obulin fraction (r-betaLg) was isolated from whey hydrolysates produced with cardosins from Cynara ca
57 n fraction (r-betaLg) was isolated from milk whey hydrolysates produced with cardosins from Cynara ca
59 ubstitute if necessary: partial or extensive whey hydrolyzate (pHF-W, eHF-W), extensive casein hydrol
61 s method can detect as little as 0.5% bovine whey in ricotta cheese from the other three species.
63 ta-lactoglobulin (beta-lg) present in cheese whey is difficult on SDS-PAGE due to their close proximi
65 ingredients, whey protein concentrate (WPC), whey lactalbumin (WLAC) and skim milk powder (SMP) on oa
67 ere randomized to isocaloric diets: Control, Whey, Lactalbumin, Lactoferrin, or pair-fed to lactoferr
68 and interfacial properties of acid and sweet whey obtained from bovine and camel fresh milk was exami
70 oric dairy products (cheese) based either on whey or on caseins, by using pig as an in vivo digestion
71 rol) diet with high protein diets containing whey, or its fractions lactalbumin and lactoferrin, on e
72 nal digestion (SGID) released a selection of whey peptides some of which were transported across a Ca
74 orrelation was found (R(2)>0.99) between cow whey percentages and mass spectrometry measurements thro
76 s transition temperature of camel and bovine whey powder (at 0.13, 0.23, and 0.33 of water activity).
77 ntify adulterated milk powder through adding whey powder by using laser induced breakdown spectroscop
78 to that using commercial annatto powder and whey powder with equal or superior color quality than ob
79 that pressure-treated complexes resulted in whey powder with significantly lower a(*) values than un
80 0.981 and 1.55% for adulteration with sweet whey powder, and 0.985 and 0.55% for adulteration with a
82 ectroscopy results) in both camel and bovine whey powders regardless the pH (neutral (6.7) or acidic
83 lin was the most denatured protein in bovine whey powders regardless the pH value, while this protein
91 thesis that nutritional supplementation with whey protein (22 g), essential amino acids (10.9 g, incl
92 was explained by the proximity of the pI of whey protein (4.9-5.2), where proteins were found to car
93 a reduced energy density product) and adding whey protein (to increase satiety capacity) allows obtai
96 ulation of eugenol (E) by spray-drying using whey protein (WP) or soy lecithin (LE) and maltodextrin
98 airy proteins: beta-lactoglobulin (beta-LG), whey protein (WPI), and caseinate (CAS) was investigated
102 emulsifier type (quillaja saponin, Tween 80, whey protein and casein) and antioxidant type (EDTA, asc
106 in- and lipid oxidation were investigated in whey protein based oleogels with varying water addition.
107 nt study allicin was covalently bound to the whey protein beta-lactoglobulin and the incorporation of
108 of the critical interfacial concentration of whey protein beta-lactoglobulin at oil/water-interfaces
110 to 3-fold greater in formulas containing 60% whey protein compared with 20% whey protein, for both co
113 This study aimed to optimize mixtures of whey protein concentrate (WPC) and two flours of rice an
114 The main object of study is application of whey protein concentrate (WPC) and whey protein hydrolys
115 nd modified starch (MS) together with either whey protein concentrate (WPC) or soy protein isolate (S
119 These microemulsions were then covered with whey protein concentrate (WPC)-maltodextrin or WPC-pecti
122 ardized meal including intrinsically labeled whey protein concentrate and calcium-caseinate proteins.
124 ted a lower emulsifying activity than either whey protein concentrate or soy protein isolate, at each
128 s experiments were performed using different whey protein concentrations and enzyme/substrate (E/S) r
129 cell adhesion molecule 1 were reduced after whey protein consumption (P = 0.011) and after calcium-c
130 e the effect of varying the sucrose, RS, and whey protein content of cereal bars on glucose and insul
131 than 5% immuno-reactivity, whereas those of whey protein control exhibited a sinusoidal immuno-react
132 0.20 mmol/L (P = 0.042), respectively], only whey protein decreased triacylglycerol (-0.23 mmol/L; P
135 ed acid gels with very high firmness without whey protein denaturation; the firmness was similar to g
136 cteria by initial attachment to the unfolded whey protein due to hydrophobic interactions followed by
142 cation of whey protein concentrate (WPC) and whey protein hydrolysate (WPH) for probiotic encapsulati
144 uring digestion of repolymerized thermolysin-whey protein hydrolysate had less than 5% immuno-reactiv
145 capacity and stability of zinc complexes of whey protein hydrolysates (WPH), produced with Everlase
146 esults of the in vitro study showed that the whey protein hydrolysates (WPHs) obtained had angiotensi
148 concentrations of kappa-casein and denatured whey protein in the serum, and a reduction in casein mic
149 ining hydrolyzed and intact (non-hydrolyzed) whey protein in their composition were investigated at t
151 ts completed a water (control) and multidose whey protein ingestion trial designed to augment the pro
152 physicochemical stability of next-generation whey protein ingredients enriched in alpha-lactalbumin.
153 ein macro peptide release showed that native whey protein inhibited the enzymatic action of chymosin,
156 comprising maltodextrin (M), gum arabic (G), whey protein isolate (W), and their combinations were em
157 n oil-in-water (O/W) emulsions containing 2% whey protein isolate (WPI) and 0.1% xanthan (XG)-locust
158 dy aimed to determine ileal digestibility of whey protein isolate (WPI) and zein in healthy volunteer
159 r binding between beta-carotene (beta-C) and whey protein isolate (WPI) as a function of pH (4-9), te
160 ct using maltodextrin (MD), inulin (IN), and whey protein isolate (WPI) as carrier agents were evalua
161 egrees of beeswax for internal structure and whey protein isolate (WPI) as external coating to improv
164 mulsification followed by spray drying using whey protein isolate (WPI) in its natural form, heated (
166 orts on the preparation of riboflavin-loaded whey protein isolate (WPI) microparticles, using desolva
167 ch product (PLu) were conjugated with either whey protein isolate (WPI) or its antioxidant hydrolysat
170 l properties and oxidative stability of 2wt% whey protein isolate (WPI) stabilized oil-in-water (O/W)
174 the order of alpha-lactalbumin (alpha-Lact), whey protein isolate (WPI), and beta-lactoglobulin (beta
175 sed proteins, such as sodium caseinate (SC), whey protein isolate (WPI), gelatin (Gel) and soy protei
177 us and heterologous cross-linked polymers of whey protein isolate (WPI), soy protein isolate (SPI) an
178 ostructured lipid carriers incorporated into whey protein isolate (WPI)-stabilized EO droplets in oil
182 enoids were encapsulated in porcine gelatin, whey protein isolate and concentrate by emulsification O
184 sunflower oil as oil phase and 0.5% or 1.0% whey protein isolate solution as outer water phase was p
186 ting powders based on soy protein isolate or whey protein isolate, both containing sunflower oil (SO)
187 biotic bacteria L. casei were produced using whey protein isolate-gum Arabic complex coacervate as wa
193 od, which consisted of a cellulose nanofiber/whey protein matrix containing titanium dioxide particle
196 omen is limited.We determined the effects of whey protein on energy intake, appetite, gastric emptyin
198 (BE), a source of anthocyanins, with either whey protein or citrus pectin influences the bioavailabi
201 ystem (8% total protein) with varying casein:whey protein ratios (0:100, 20:80, 50:50 and 80:20) were
202 ein solutions containing different casein to whey protein ratios of 80:20, 60:40, 50:50 and 40:60.
203 ts tested were: alpha-lactoalbumin (ALAC), a whey protein rich in tryptophan, effective in some anima
204 charged into a transglutaminase-cross-linked whey protein solution that was subsequently gelled with
206 systems containing enzymatically hydrolyzed whey protein under dry heating conditions was studied.
208 oluble aggregate of kappa-casein protein and whey protein was suggested in alkalization and neutraliz
209 l digests after oral ingestion of casein and whey protein were collected by a nasogastric tube and pr
210 ey protein, partial association of denatured whey protein with the casein micelle, an increase in cas
212 compare the effect of milk proteins (casein, whey protein) and surfactants (Citrem, Tween 20) on the
213 to the binding interaction between the major whey protein, beta-Lactoglobulin (betaLG) and vitamin B1
216 Bovine beta-lactoglobulin (BLG), the main whey protein, has a strong propensity to bind various bi
217 n denaturation of approximately 67% of total whey protein, partial association of denatured whey prot
226 synthesis rates after the ingestion of 25 g whey protein. kg(-1) . d(-1); n = 12) or a HIGH PRO diet
227 s were randomly assigned to consume 2 x 28 g whey protein/d, 2 x 28 g Ca caseinate/d, or 2 x 27 g mal
229 ion (FMD) increased significantly after both whey-protein and calcium-caseinate intakes compared with
230 Hg; P = 0.050 for both)] were observed after whey-protein consumption compared with control intake.
231 ntrations (P < 0.05).In older men and women, whey-protein drinks load-dependently slow gastric emptyi
235 of equal or greater amounts of caseins than whey proteins (80:20, 60:40 and 50:50), while WP aggrega
237 ures 60 degrees C caused denaturation of the whey proteins and aggregation of the fat globules and pr
240 as to study molecular binding of safranal to whey proteins by taking advantage of headspace solid-pha
242 eptidases; however, heat pretreatment of the whey proteins enhanced the degree of hydrolysis and redu
244 o further explore the action of cardosins on whey proteins for the production of bioactive peptides.
247 Alpha-lactalbumin (alpha-LA) is one of the whey proteins in cows' milk that has been identified as
251 ions in secondary and tertiary structures of whey proteins induced by safranal association resulted f
252 Despite the extensive similarities shared by whey proteins of the four species, a mass spectrometry-b
253 e mechanisms mediating the effects of HIU on whey proteins on the molecular level, thus moving furthe
254 t in addition to inhibiting chymosin, native whey proteins present a physical barrier to para-casein
256 milk protein) were produced with a caseins: whey proteins ratio of 40:60, differing only by the whey
257 rrin preserved a higher proportion of native whey proteins than IMFs containing beta-lactoglobulin.
258 ctive of this study was to track the fate of whey proteins through the upper gastrointestinal tract,
263 therefore investigating new applications of whey proteins will contribute towards the valorisation o
264 n vitro results indicate that consumption of whey proteins will deliver bioactive peptides to target
266 nts (milk fat, xanthine oxidase, caseins and whey proteins) in pulsed electric field (PEF)-treated mi
268 a model of complex food containing 15wt% of whey proteins, according to both static (2h at pH = 3, I
273 scopy regarding the safranal binding site on whey proteins, the order of their binding affinity towar
274 Health benefits are routinely attributed to whey proteins, their hydrolysates and peptides based on
276 hout whey adjustment, or hydrolysates of cow whey proteins, were tested for CML levels using a commer
277 eacted to pH changes differently compared to whey proteins, with less digestion of casein at pH 3.0 t
283 Under bio-economic aspects, sweet and acid whey provide a suitable feed medium for the enzymatic ge
286 nificantly higher in the group that received whey RUSF (960 of 1144; 83.9%) than in the group that re
288 treatment of MAM, because the use of a novel whey RUSF resulted in higher recovery rates and improved
289 roved growth than did soy RUSF, although the whey RUSF supplement provided less total protein and ene
292 pplied to the analyses of buffalo and bovine whey starter cultures, thus assessing the applicability
296 roperties of acid camel whey and acid bovine whey were preserved at air water interface even after a
297 ty and foam stability were observed for acid whey when compared to sweet whey for both milks, with hi
298 nificantly lower a(*) values than unbleached whey, whereas no significant differences were observed f
300 he effect of protein supplements from either whey with or without calcium or soy on WM success after