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With yeast cell walls

Figure 2. Percentage of binding with yeast cell walls and lipid-free yeast walls at 1 g/L and 10 g/L in the model wine by the equilibrium dialysis method. Figure 2. Percentage of binding with yeast cell walls and lipid-free yeast walls at 1 g/L and 10 g/L in the model wine by the equilibrium dialysis method.
The association of endo-/ - (1 3) -glucanases with yeast cell walls... [Pg.255]

Figure 46.3 Confocal image of macrophage (J777A.1) showing nucleus (1) with yeast cell-wall particles (2). Figure 46.3 Confocal image of macrophage (J777A.1) showing nucleus (1) with yeast cell-wall particles (2).
Phaeococcomyces exophialae forms slimy, mucoid, slow-growing, smooth colonies that are grayish black. Budding yeast cells which are at first subhyaline are abundant. With age, some of the cells become darker, with thickened cell walls. Some pseudohyphae usually are present. Hyphal development may become dominant in some isolates of this species with subsequent subculture. [Pg.77]

Figure 1.15. Complement activation via the alternative pathway. Always present in serum are trace amounts of C3b, which may attach to recognition sites on, for example, yeast cell walls. C3b may combine with serum factor B to form C3bB, and this complex is acted upon by factor D to form C3bBb. This latter complex is a C3 convertase and may act upon C3 to form more C3b to amplify the process. The C3bBb-coated particles may activate other complement components (C4-C9) or be recognised by complement receptors on neutrophils. Figure 1.15. Complement activation via the alternative pathway. Always present in serum are trace amounts of C3b, which may attach to recognition sites on, for example, yeast cell walls. C3b may combine with serum factor B to form C3bB, and this complex is acted upon by factor D to form C3bBb. This latter complex is a C3 convertase and may act upon C3 to form more C3b to amplify the process. The C3bBb-coated particles may activate other complement components (C4-C9) or be recognised by complement receptors on neutrophils.
Domain present in yeast cell wall integrity and stress response component proteins Domain with 2 conserved Trp (W) residues f3/y crystallins A20-like zinc fingers ANl-like zinc finger... [Pg.207]

When in later years Krebs reviewed the major points which had to be established if the cycle was to be shown to be operative in cells, the obvious needs were to find the presence of the required enzymes and to detect their substrates. As the substrates are present in the cycle in catalytic amounts their accumulation required the use of inhibitors. Krebs also stressed that rates of oxidation of the individual substrates must be at least as fast as the established rates of oxygen uptake in vivo, an argument first used by Slator (1907) with reference to fermentation A postulated intermediate must be fermented at least as rapidly as glucose is. (See Holmes, 1991). This requirement did not always appear to be met. In the early 1950s there were reports that acetate was oxidized by fresh yeast appreciably more slowly than the overall rate of yeast respiration. It was soon observed that if acetone-dried or freeze-dried yeasts were used in place of fresh yeast, rates of acetate oxidation were increased more than enough to meet the criterion. Acetate could not penetrate fresh yeast cell walls sufficiently rapidly to maintain maximum rates of respiration. If the cell walls were disrupted by drying this limitation was overcome, i.e. if rates of reaction are to be... [Pg.74]

Of the particulate stimuli certain ones are far more active when they are coated with proteins from serum (opsonized) than when they are not. However, others like latex beads elicit formation of Oj" by PMNs without opsonization DeChatelet et al. found that the production of O by PMNs from man and rabbit was stimulated by opsonized but not unopsonized zymosan (fragments of yeast cell walls). Bacteria alone were found to stimulate the formation of O but in the presence of serum bacteria stimulated the formation of O7 three fold However, the stimulatory effect of bacteria appeared to be caused by changes which the bacteria produced by an interaction with constitutents of serum, because serum itself after exposure to the bacteria stimulated production of O by PMNs. The active component from serum was heat sensitive (100°) and not sedimentable at 105,000 g. Whether this material was derived from the components of serum or from the bacteria is not clear but may have been a protein of the complement system. [Pg.40]

Transfection, DNA uptake in eukaryotic systems, often is more problematic then bacterial transformation the mode of DNA uptake is poorly understood and efficiency is much lower. In yeast, cell walls can be digested with degradative enzymes to yield fragile protoplasts, which are then able to take up DNA. Cell walls are resynthesized after removal of the degrading enzymes. Mammalian cells take up DNA after precipitation onto their surface with calcium phosphate [Fugene 6 (Roche) Lipofectin (Life Technologies) Effectene (Qiagen)]. Electroporation is often more efficient for transfection in eukaryotic cell systems, especially in yeasts. [Pg.81]

Cell pellets are washed with 100 ml of 0.5 cold M NaCl in 66 mM potassium phosphate buffer, pH 6.2 (KP 6.2), to recover lysozyme that is electrostatically adsorbed to the yeast cell walls. [Pg.583]

Interactions between mannoproteins from yeast cell walls and aroma compounds have been studied by Langourieux and Crouzet (1997). They performed the experiments with crude mannoproteins extracts and observed no effect on the activity coefficient of isoamyl acetate, and a slight decrease on the activity coefficients of ethyl hexanoate and limonene. However, when they purified the mannoproteins or when they used a model glycopeptide, they did not observe any effect on limonene volatility. If the synthetic peptide was heat treated (50 °C), they observed a slight reduction on the activity coefficient of limonene. This was explained by an increase in the hydrophobicity of the glycopeptide after the thermal treatment. [Pg.428]

The main structural constituents of Saccharomyces cerevisiae yeast cell wall are glucans and mannans with a minor proportion of chitin (Walker 1998). Manno-proteins are located in the outer layer of the yeast cell wall and determine most of the surface properties of the wall. Vasserot et al. (1997) studied the capacity of yeast lees to adsorb anthocyanins in an attempt to reduce the detrimental effects of charcoal on the color of red musts and wines. Experiments based on model wine solutions revealed that yeast lees possess a greater affinity for anthocyanins than... [Pg.455]

Plant and yeast cell walls consist mostly of polysaccharides along with smaller amounts of proteic material. Adsorption of flavanols on isolated plant cell walls (Renard et al. 2001) and on yeast lees (Mazauric and Salmon 2005, 2006) has been demonstrated. The latter also retained anthocyanins, as stated in Chapter 9A. [Pg.494]


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See also in sourсe #XX -- [ Pg.220 , Pg.222 , Pg.224 ]




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Yeast cell walls, interactions with aroma

Yeast cell walls, interactions with aroma compounds

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