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Yeast winemakers

The dry yeasts have excellent storage stabiUty, up to a year or more if packaged under an inert atmosphere (N2, CO2, or vacuum). First introduced into the United States and then AustraUa, they are now being introduced into European winemaking as well. A number of strains of S. cerevisiae S. bayanus and S. fermentati are available. [Pg.392]

The sugars in fruits such as grapes are feimented by yeasts to produce wines. In winemaking, lactic acid bacteria convert malic acid into lactic acid in malolactic fermentation in fruits with high acidity. Acetobacter and Gluconobacter oxidise ethanol in wine to acetic acid (vinegar). [Pg.7]

The next step of the biotechnical sequence, yeast fermentation, is of the utmost importance to the chemistry of winemaking as well as to the formation of flavor substances. We have investigated this previously using 14C-tagged compounds (16). Amino acids, for example, enter the yeast fermentation with a quasi biochemical valence with regard to the formation of metabolic side products like alcohols and esters. In that respect, the composition of the fermentation substrate, the grape must, is highly important to the formation of aroma substances by yeasts. [Pg.13]

Grape juice was fermented inadvertently into wine by natural yeast. To nomadic tribes, especially, it was welcome since it had flavor reminiscent of the fresh fruit or juice. In addition it could be stored and transported easily and remained drinkable from season to season. Eventually wine found its place as an article of commerce with necessary quality requirements. Not until the time of Louis Pasteur did the scientific foundation of winemaking become established and did enology become the science of wine. Since the early Pasteur experiments and discoveries winemaking has developed from a haphazard, ill understood, and risky... [Pg.123]

Unfortunately, in spite of the published literature on wine proteins, we do not know the actual protein levels at which table or dessert wines are stable. The changes in protein content during production and processing of wines are still not known with sufficient accuracy to predict their behavior. The winemaker has to depend on empirical tests if he is to produce protein stable wines. Early separation of new wines from their fermentation yeast greatly improves their chances for protein stability by decreasing the release of yeast autolysis products into the wine. [Pg.132]

Detection of Malo-Lactic Fermentation. It is imperative that the winemaker, to control malo-lactic fermentation, has a satisfactory method for its detection. Disappearance of malic acid is the indication of the fermentation, but the formation of lactic acid is not sufficient evidence since it might also be formed by yeast and by bacteria from other carbohydrate sources. The rate of conversion of malic acid is expected to reflect bacterial metabolism and growth. In New York State wines, Rice and Mattick (41) showed bacterial growth (as measured by viable count) to be more or less exponential to 106-107 cells/ml, preceding disappearance of malic acid. The rate of loss of malic acid is probably also exponential. Malic acid seems to disappear so slowly that its loss is not detected until a bacterial population of about 106-107 cells/ml is reached then it seems to disappear so rapidly that its complete loss is detected within a few days (41). Rice and Mattick (41) also showed a slight increase in bacterial population for a few days following this. [Pg.169]

White wines are normally fermented in containers that can be partially closed so that the surface of the fermenting wine is protected from the air by a blanket of carbon dioxide. For the home winemaker, 5-gallon carboys serve admirably. An hour or so after adding S02, one adds approximately 3% of an actively fermenting pure-culture starter yeast. [Pg.296]

For the home winemaker, the color intensity may be estimated by eye. It is essential to strain or filter the bulk of the yeast and pulp particles before examining the wine because these suspended materials make the wine appear much lighter in color than it actually is. Color intensity is estimated by looking down through the wines (sample and a control wine) contained in equivalent glass test tubes which are illuminated from the bottom. The depths of the wines are adjusted until the two wines appear to have the same brightness, even though the hues may differ considerably. The amount of color in the test wine varies inversely with its depth in the tube. Thus, if the depth of the test wine is twice that of the standard control wine then it contains only one-half as much color. [Pg.299]

The growth of malo-lactic bacteria in wines is favored by moderate temperatures, low acidity, very low levels of S02, and the presence of small amounts of sugar undergoing fermentation by yeast. It is frequently possible to inoculate a wine with a pure culture of a desirable strain of bacteria and obtain the malo-lactic fermentation under controlled conditions. The pure-culture multiplication of the selected strain of bacteria is difficult, however. It is also difficult to control the time of the malo-lactic fermentation—sometimes it occurs when not wanted, and at other times will not go when very much desired. For the home winemaker it is probably most satisfactory to accept the malo-lactic fermentation if it occurs immediately following the alcoholic fermentation. The wines should then be siphoned away from deposits, stored in completely filled containers at cool temperatures, and have added to them about 50 ppm S02. If the malo-lactic fermentation does not take place spontaneously and the wine is reasonably tart, the above described regime of preservation will likely prevent its occurrence. When the malo-lactic transformation takes place in wines in bottles, the results are nearly always bad. The wine becomes slightly carbonated, and the spoiled sauerkraut flavors are emphasized. [Pg.302]

FIGURE 1.1 Scheme of carbonic maceration winemaking. AM, anaerobic metabolism of grape berries YAF, yeast alcoholic fermentation M, maceration qd = pair temperature (q°C) action duration (days). (Figure from CEnologie—fondements scientifi-ques et techniques. Flanzy et al. collection Sciences Techniques Agroalimentaires. Technique Documentation, 1998, p. 780. Reproduced with the permission of the Editor.)... [Pg.7]


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See also in sourсe #XX -- [ Pg.1119 ]




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