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Protein viscosity

Degradation. There is, however, a second, more important, feature. Above the transition temperature we have shown that both xanthan and succinoglycan are more susceptible to degradation (5). This may be because the polymer side chains become dissociated from the main chain, in a similar manner to the unfolding of proteins. Viscosity changes, however, indicate that main chain linkages have become more... [Pg.168]

As functional properties of soy proteins, viscosity and solubility are alike in that they are non-equilibrium properties of the system. In the case of solubility, there is at least evidence of steady state equilibrium which allows for the possibility of some qualitative thermodynamic interpretation. In the case of viscosity, steady state equilibrium is not reached. Thus, thermodynamic interpretation is impossible. Molecular dynamics data are needed. [Pg.108]

To achieve highest resolution the sample volume must not exceed 5% of the total column volume. Gel filtration is independent of sample concentration, although above 50 mg/ml protein viscosity effects may cause fingering. Extremely viscous samples should be diluted. [Pg.88]

MTG conc.(U/g protein) Viscosity of MTG-treated sodium caseinate. [Pg.34]

Various food products, medicines, cosmetics and toothpaste that use the gelling, reactivity with the protein, viscosity, dispersion and suspension. [Pg.1499]

D. K. Klimov and D. Thirumalai. Viscosity dependence of the folding rates of proteins. Phys. Rev. Lett., 79 317-320, 1997. [Pg.259]

Protein molecules extracted from Escherichia coli ribosomes were examined by viscosity, sedimentation, and diffusion experiments for characterization with respect to molecular weight, hydration, and ellipticity. These dataf are examined in this and the following problem. Use Fig. 9.4a to estimate the axial ratio of the molecules, assuming a solvation of 0.26 g water (g protein)"V At 20°C, [r ] = 27.7 cm g" and P2 = 1.36 for aqueous solutions of this polymer. [Pg.655]

Theie aie only a few fat replacement products based on protein. LITA is a com protein—polysaccharide compound the role of the polysaccharide is to stabilize the protein (zein). The final product is 87% protein and 5% polysaccharide. The mixture, spray dried after processing, claims to look like cream on rehydration. It is low in viscosity, flavor, and lubricity, and is stable to mild heating. The protein particle size is 0.3—3 p.m (55). [Pg.120]

Uses of lactose production by appHcation include baby and infant formulations (30%), human food (30%), pharmaceuticals (25%), and fermentation and animal feed (15%) (39). It is used as a diluent in tablets and capsules to correct the balance between carbohydrate and proteins in cow-milk-based breast milk replacers, and to increase osmotic property or viscosity without adding excessive sweetness. It has also been used as a carrier for flavorings. [Pg.45]

Milk. Imitation milks fall into three broad categories filled products based on skim milk, buttermilk, whey, or combinations of these synthetic milks based on soybean products and toned milk based on the combination of soy or groundnut (peanut) protein with animal milk. Few caseinate-based products have been marketed (1,22,23). Milk is the one area where nutrition is of primary concern, especially in the diets of the young. Substitute milks are being made for human and animal markets. In the latter area, the emphasis is for products to serve as milk replacers for calves. The composition of milk and filled-milk products based on skim milk can be found in Table 10. Table 15 gives the composition of a whey /huttermilk-solids-hased calf-milk replacer, which contains carboxymethyl cellulose (CMC) for proper viscosity of the product. [Pg.447]

Physical Properties. The egg is composed of three basic parts shell, whites (albumen), and yolk. Each of these components has its own membranes to keep the component intact and separate from the other components. The vitelline membrane surrounds the yolk, which in turn is surrounded by the chala2iferous layer of albumen, keeping the yolk in place. Egg white (albumen) consists of an outer thin layer next to the shell, an outer thick layer near the shell, an inner thin layer, and finally, an inner thick layer next to the yolk. Thick layers of albumen have a higher level of ovomucin in addition to natural proportions of all the other egg white proteins. This ovomucin breaks into shorter fibers when the egg white is blended on a high speed mixer (3), or when the egg white ages. Viscosity is gready reduced when the egg white is blended in this way. [Pg.454]

Table 1 shows the various physical properties for components of eggs (4). Specific gravity of whites, yolks, and whole egg is the same, ie, density is 1035 kg/m (64.6 Ib/ft = 8.63 Ib/gal) for all three types of egg products shown. The viscosity of blended Hquid egg components varies over a wide range of temperatures at temperatures higher than those indicated in Table 1, the protein starts to denature and coagulate, increasing viscosity. [Pg.454]

Factors to be considered in maldng the selection of chromatography processing steps are cost, sample volume, protein concentration and sample viscosity, degree of purity of protein product, presence of nucleic acids, pyrogens, and proteolytic enzymes. Ease with which different types of adsorbents can be washed free from adsorbed contaminants and denatured proteins must also be considered. [Pg.2064]

Tannins are polyhydroxyphenols. They are soluble in water, aleohols and aeetone and ean eoagulate proteins. They are yielded by extraetion from wood substanee, bark, leaves and fruits. Other components of the extraction solutions are sugars, pectins and other polymeric carbohydrates, amino acids and other substances. The content of non-tannins can reduce wood failure and water resistance of glued bonds. The polymeric carbohydrates especially increase the viscosity of the extracts. [Pg.1070]

Although the viscosity of the sample solution may affect the resolution, for practical reasons highly concentrated protein samples will give the best separations in the case of SEC with respect to the process economy. Although the actual loading capacity depends on the separation problem and on the... [Pg.225]

Szent-Gyorgyi further showed that the viscosity of an actomyosin solution was lowered by the addition of ATP, indicating that ATP decreases myosin s affinity for actin. Kinetic studies demonstrated that myosin ATPase activity was increased substantially by actin. (For this reason, Szent-Gyorgyi gave the name actin to the thin filament protein.) The ATPase turnover number of pure myosin is 0.05/sec. In the presence of actin, however, the turnover number increases to about 10/sec, a number more like that of intact muscle fibers. [Pg.552]

Charged macromolecules, such as proteins or polymers, are often separated elec-trophoretically. The rate of migration through an electric field increases with net charge and field strength. Molecular size of analytes and viscosity of separation media both have inverse relationships with rate of migration. These variables must all be taken into account in order to optimize the conditions for an efficient electrophoretic separation. [Pg.197]

Initially fermentation broth has to be characterised on the viscosity of the fluid. If the presence of the biomass or cells causes trouble, they have to be removed. Tire product is stored inside the cells, the cells must be ruptured and the product must be freed. Intracellular protein can easily be precipitated, settled or filtered. In fact the product in diluted broth may not be economical enough for efficient recovery. Enrichment of the product from the bioreactor effluents for increasing product concentration may reduce the cost of product recovery. There are several economical methods for pure product recovery, such as crystallisation of the product from the concentrated broth or liquid phase. Even small amounts of cellular proteins can be lyophilised or dried from crude solution of biological products such as hormone or enzymes.2,3... [Pg.170]

Filter aids are widely used in die fermentation industry to improve the efficiency of filtration. It is a pre-coated filter medium to prevent blockage or blinding of the filter by solids, which would otherwise wedge diemselves into the pores of the cloth. Filter aid can be added to the fermentation broth to increase the porosity of the cake as it formed. This is only recommended when fermentation product is extracellular. Filter aid adds to the cost of filtration. The minimum quantity needed to achieve the desired result must be established experimentally. Fermentation broths can be pretreated to improve filtration characteristics. Heating to denature proteins enhances the filterability of mycelial broths such as in penicillin production. Alternatively, electrolytes may be added to promote coagulation of colloids into larger, denser particles, which are easier to filter. The filtration process is affected by the viscosity and composition of the broth, and the cell cake.5... [Pg.173]


See other pages where Protein viscosity is mentioned: [Pg.551]    [Pg.2657]    [Pg.143]    [Pg.235]    [Pg.591]    [Pg.719]    [Pg.54]    [Pg.234]    [Pg.308]    [Pg.431]    [Pg.433]    [Pg.433]    [Pg.434]    [Pg.434]    [Pg.435]    [Pg.453]    [Pg.483]    [Pg.10]    [Pg.334]    [Pg.333]    [Pg.77]    [Pg.522]    [Pg.461]    [Pg.442]    [Pg.408]    [Pg.71]    [Pg.72]    [Pg.234]    [Pg.816]    [Pg.26]    [Pg.136]   
See also in sourсe #XX -- [ Pg.325 ]




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Denatured proteins, viscosity

Intrinsic viscosity of proteins

Protein dynamics, solvent viscosity effects

Proteins integral viscosity

Proteins intrinsic viscosity

Soybean proteins viscosity

Surface viscosity, proteins

Viscosity of protein

Viscosity polymeric proteins

Viscosity protein glass transition

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