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1.
J Dairy Sci ; 90(4): 1662-73, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17369206

ABSTRACT

The proteins and polar lipids present in milk fat globule membrane (MFGM) fragments are gaining attention for their technological and nutritional properties. These MFGM fragments are preferentially enriched in side streams of the dairy industry, like butter serum, buttermilk, and whey. The objective of this study was to recover MFGM fragments from whey by tangential filtration techniques. Acid buttermilk cheese whey was chosen as a source for purification by tangential membrane filtration because it is relatively rich in MFGM-fragments and because casein micelles are absent. Polyethersulfone and cellulose acetate membranes of different pore sizes were evaluated on polar lipid and MFGM-protein retention upon filtration at 40 degrees C. All fractions were analyzed for dry matter, ash, lipids, proteins, reducing sugars, polar lipid content by HPLC, and for the presence of MFGM proteins by sodium dodecyl sulfate-PAGE. A fouling coefficient was calculated. It was found that a thermocalcic aggregation whey pretreatment was very effective in the clarification of the whey, but resulted in low permeate fluxes and high retention of ash and whey proteins. By means of an experimental design, the influence of pH and temperature on the fouling and the retention of polar lipids (and thus MFGM fragments), proteins, and total lipids upon microfiltration with 0.15 microM cellulose acetate membrane was investigated. All models were highly significant, and no outliers were observed. By increasing the pH from 4.6 to 7.5, polar lipid retention at 50 degrees C increased from 64 to 98%, whereas fouling of the filtration membrane was minimized. A 3-step diafiltration of acid whey under these conditions resulted in a polar lipid concentration of 6.79 g/100 g of dry matter. As such, this study shows that tangential filtration techniques are suited for the purification of MFGM fragments.


Subject(s)
Cultured Milk Products/chemistry , Filtration/methods , Food Handling/methods , Intracellular Membranes/chemistry , Milk Proteins/chemistry , Cellulose/analogs & derivatives , Cheese , Electrophoresis, Polyacrylamide Gel/methods , Glycolipids/chemistry , Glycoproteins/chemistry , Hydrogen-Ion Concentration , Lipid Droplets , Lipids/analysis , Polymers , Sulfones , Temperature , Whey Proteins
2.
J Dairy Sci ; 89(6): 1915-25, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16702255

ABSTRACT

The gross composition of butter serum, the aqueous phase of butter, is comparable to that of buttermilk, except that it has a higher content of material derived from the milk fat globule membrane (MFGM). As such, butter serum is a good source for further purification of MFGM material. The purified fraction could be of interest for its emulsifying and nutritional properties. The effect of sodium citrate and ethanol on the dissociation of butter serum casein micelles, and their effect on casein retention upon tangential microfiltration were investigated. Optimal conditions of casein micelle dissociation were assessed by using an experimental design (response surface full central composite orthogonal design) with temperature and ethanol or sodium citrate concentration as design variables and the Hunter L* value as response variable. For both dissociating agents, a highly significant reduced quadratic model was fit to the data. Microfiltration tests were performed on pure butter serum, and on butter serum in the presence of sodium citrate, under optimal dissociation conditions (50 degrees C, 80 mM). A cellulose acetate membrane with a pore size of 0.15 microm was used. From the filtration curves and fouling coefficients it was clear that the addition of sodium citrate improved the permeation flux, and minimized fouling. All fractions were analyzed for dry matter, protein, lactose, lipid, and polar lipid contents. The protein fraction was further characterized by sodium dodecyl sulfate-PAGE. It was shown that sodium citrate greatly enhanced casein transmission through the membrane, but at the expense of substantial losses of polar lipids.


Subject(s)
Butter/analysis , Caseins/chemistry , Filtration , Micelles , Cellulose/analogs & derivatives , Citrates/pharmacology , Drug Stability , Electrophoresis, Polyacrylamide Gel , Ethanol/pharmacology , Glycolipids/chemistry , Glycolipids/isolation & purification , Glycoproteins/chemistry , Glycoproteins/isolation & purification , Lactose/analysis , Lipid Droplets , Lipids/analysis , Phospholipids/analysis , Proteins/analysis , Sodium Citrate , Temperature
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